| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:107744058-107744173 | Rare:37 | ||||
| chr7:107929137-107929524 | Common:3; Rare:115; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:107937256-107937360 | Rare:27; Clinvar (benign):1 | ||||
| chr7:108002906-108003361 | Common:3; Rare:131 | ||||
| chr7:108526095-108526480 | Common:5; Rare:117 | ||||
| chr7:108569576-108569998 | Common:2; Rare:154 | ||||
| chr7:111091073-111091130 | Rare:9 | ||||
| chr7:112206339-112206719 | Common:2; Rare:119 | ||||
| chr7:112450844-112451011 | Common:1; Rare:45 | ||||
| chr7:112451253-112451305 | Rare:11 | ||||
| chr7:114086191-114086520 | Common:2; Rare:121 | ||||
| chr7:114922003-114922387 | Common:3; Rare:99 | ||||
| chr7:116499434-116499790 | Common:3; Rare:119 | ||||
| chr7:116499961-116500392 | Common:3; Rare:106 | ||||
| chr7:116525653-116525805 | Rare:32 |