GSM1631492 | case | Homo sapiens | ACSL1,IL1RN,NTF3,TTN | RNA_seq | GCUGGGUGUCCCAUUGAAA,GCUGGGUGUCCCAUUGAAA,GCUGGGUGUCCCAUUGAAA,GCUGGGUGUCCCAUUGAAA,GUGUACUCUCUGAGGUGCUC,GACGCAGAUAAGAACCAGUU,GCAUCAAGUCAGCCAUCAGC,GAGUCACCCUCCUGGAAAC,GAGCGCGGAGCCAUCUGGCC,GCGCGGCGCGGAAGGGGUUA,GCGGCGCGGCGCGGGCCGGC,GCGGUUAUAACCAGCCAACC,GCCUUGGUGAAGUCUCCUUUG,GAUGUUAAAAUCCGAAAAUGC,GGGCACAGUCCUCAGGUUUG,GAUGAGCUCUCUUCAACGUUA | 16 | chr12:102957632:+,chr11:109971250:+,chr2:113117713:+,chr2:113117780:+,chr2:113117749:+,chr12:5432049:+,chr12:5432022:+,chr16:67842357:+,chr12:5432070:-,chr2:178807596:-,chr2:178807675:+,chr12:102957632:+,chr2:178807753:-,chr12:102957632:+,chr2:178807907:-,chr12:102957632:+ | 26030444 | GSE66756 | HEK293FT | cell line | Topology construct: INT |
GSM1631493 | case | Homo sapiens | ACSL1,IL1RN,NTF3,TTN | RNA_seq | GCUGGGUGUCCCAUUGAAA,GCUGGGUGUCCCAUUGAAA,GCUGGGUGUCCCAUUGAAA,GCUGGGUGUCCCAUUGAAA,GUGUACUCUCUGAGGUGCUC,GACGCAGAUAAGAACCAGUU,GCAUCAAGUCAGCCAUCAGC,GAGUCACCCUCCUGGAAAC,GAGCGCGGAGCCAUCUGGCC,GCGCGGCGCGGAAGGGGUUA,GCGGCGCGGCGCGGGCCGGC,GCGGUUAUAACCAGCCAACC,GCCUUGGUGAAGUCUCCUUUG,GAUGUUAAAAUCCGAAAAUGC,GGGCACAGUCCUCAGGUUUG,GAUGAGCUCUCUUCAACGUUA | 16 | chr12:102957632:+,chr11:109971250:+,chr2:113117713:+,chr2:113117780:+,chr2:113117749:+,chr12:5432049:+,chr12:5432022:+,chr16:67842357:+,chr12:5432070:-,chr2:178807596:-,chr2:178807675:+,chr12:102957632:+,chr2:178807753:-,chr12:102957632:+,chr2:178807907:-,chr12:102957632:+ | 26030444 | GSE66756 | HEK293FT | cell line | Topology construct: INT |