Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:2971542-2971711 | Common:1; Rare:49 | ||||
chr6:2999642-3000032 | Common:10; Rare:83 | ||||
chr6:3068256-3068585 | Common:1; Rare:106 | ||||
chr6:3118591-3118743 | Common:2; Rare:51 | ||||
chr6:3157407-3157706 | Common:7; Rare:97; Clinvar (benign):1 | ||||
chr6:3258887-3259088 | Rare:80 | ||||
chr6:4021174-4021445 | Rare:116 | ||||
chr6:5003644-5003849 | Common:5; Rare:68 | ||||
chr6:5003998-5004102 | Common:2; Rare:52 | ||||
chr6:5260675-5261017 | Common:3; Rare:117; Clinvar (benign):4 | ||||
chr6:5261276-5261585 | Common:9; Rare:83 | ||||
chr6:6004010-6004112 | Common:1; Rare:23 | ||||
chr6:7313052-7313354 | Common:5; Rare:115 | ||||
chr6:7389740-7389926 | Common:1; Rare:51 | ||||
chr6:7910606-7910885 | Common:4; Rare:111 |