Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:103385257-103385444 | Common:1; Rare:66 | ||||
chr14:103529026-103529235 | Common:1; Rare:63 | ||||
chr14:103562624-103563004 | Common:5; Rare:137; Clinvar (benign):1 | ||||
chr14:103715435-103715833 | Common:1; Rare:130 | ||||
chr14:103921473-103921755 | Common:3; Rare:82 | ||||
chr14:105065373-105065637 | Common:1; Rare:44 | ||||
chr14:105388791-105389023 | Common:1; Rare:50 | ||||
chr14:105487166-105487216 | Rare:15 | ||||
chr15:23039540-23039668 | Common:1; Rare:58 | ||||
chr15:25438496-25438531 | Rare:11 | ||||
chr15:34336988-34337028 | Rare:5 | ||||
chr15:40039094-40039329 | Rare:98 | ||||
chr15:40106943-40107033 | Rare:12 | ||||
chr15:40307816-40307859 | Rare:7 | ||||
chr15:40307861-40308031 | Common:1; Rare:43 |