| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:105014052-105014214 | Common:3; Rare:70 | ||||
| chr7:105532067-105532231 | Rare:43 | ||||
| chr7:105876461-105876818 | Common:6; Rare:101 | ||||
| chr7:107563894-107564021 | Common:2; Rare:76; Clinvar (benign):3 | ||||
| chr7:107564332-107564592 | Common:2; Rare:49; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:107744058-107744193 | Rare:46 | ||||
| chr7:108569608-108570039 | Common:2; Rare:146 | ||||
| chr7:112206401-112206797 | Common:1; Rare:151 | ||||
| chr7:112790182-112790477 | Common:1; Rare:83 | ||||
| chr7:116526123-116526411 | Common:2; Rare:84 | ||||
| chr7:116954283-116954438 | Common:1; Rare:33 | ||||
| chr7:118183965-118184206 | Common:2; Rare:94 | ||||
| chr7:123748953-123749244 | Common:2; Rare:108 | ||||
| chr7:128455729-128455878 | Common:2; Rare:76 | ||||
| chr7:128791240-128791468 | Common:1; Rare:61 |