Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:149538-149840 | Common:5; Rare:96 | ||||
chr7:234675-234877 | Common:1; Rare:35 | ||||
chr7:5419115-5419276 | Rare:50 | ||||
chr7:5427797-5427878 | Rare:34 | ||||
chr7:5428016-5428189 | Common:1; Rare:74 | ||||
chr7:5695391-5695719 | Common:2; Rare:84 | ||||
chr7:5823041-5823171 | Common:2; Rare:47 | ||||
chr7:16644755-16644914 | Rare:50 | ||||
chr7:25620562-25620683 | Rare:20 | ||||
chr7:25750812-25750997 | Common:1; Rare:31 | ||||
chr7:26193252-26193696 | Rare:156; Clinvar (benign):2 | ||||
chr7:27099779-27099969 | Common:2; Rare:32 | ||||
chr7:27108681-27108850 | Common:1; Rare:57 | ||||
chr7:27115146-27115418 | Rare:43 | ||||
chr7:29685618-29685835 | Common:8; Rare:51 |