Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:13912375-13912549 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):2 | ||||
chr19:14074226-14074352 | Rare:25 | ||||
chr19:14157513-14157662 | Common:1; Rare:40 | ||||
chr19:14409638-14409723 | Rare:31 | ||||
chr19:15123141-15123474 | Common:1; Rare:103 | ||||
chr19:15828832-15829127 | Common:3; Rare:47 | ||||
chr19:16078565-16078717 | Rare:27 | ||||
chr19:16283570-16283822 | Common:1; Rare:57 | ||||
chr19:17798326-17798384 | Rare:9 | ||||
chr19:17862901-17862928 | Rare:12 | ||||
chr19:18319689-18319995 | Rare:59 | ||||
chr19:18320994-18321106 | Rare:25 | ||||
chr19:19776411-19776808 | Common:3; Rare:82 | ||||
chr19:19785007-19785057 | Rare:6 | ||||
chr19:21463879-21463961 | Rare:16 |