Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:2731683-2731930 | Common:1; Rare:59 | ||||
chr7:5427797-5427877 | Rare:33 | ||||
chr7:5427938-5428184 | Common:1; Rare:109 | ||||
chr7:5555121-5555317 | Common:1; Rare:51 | ||||
chr7:5693691-5693809 | Rare:20 | ||||
chr7:5695383-5695730 | Common:3; Rare:85 | ||||
chr7:5823008-5823179 | Common:3; Rare:67 | ||||
chr7:15685901-15686226 | Common:1; Rare:136 | ||||
chr7:18086153-18086311 | Rare:36 | ||||
chr7:22854032-22854262 | Common:5; Rare:76 | ||||
chr7:23680816-23680869 | Rare:14 | ||||
chr7:25620562-25620680 | Rare:20 | ||||
chr7:26193241-26193720 | Rare:170; Clinvar (benign):2 | ||||
chr7:27099923-27099978 | Common:1; Rare:13 | ||||
chr7:27108675-27108851 | Common:1; Rare:59 |