| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:106284874-106285285 | Common:2; Rare:164 | ||||
| chr7:107469902-107470344 | Common:1; Rare:100 | ||||
| chr7:107480869-107481211 | Common:1; Rare:60 | ||||
| chr7:107563840-107564048 | Common:2; Rare:120; Clinvar:2; Clinvar (benign):6 | ||||
| chr7:107564326-107564456 | Common:1; Rare:22; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:107580091-107580521 | Common:4; Rare:140 | ||||
| chr7:107743582-107743914 | Common:5; Rare:127 | ||||
| chr7:107744018-107744171 | Rare:46 | ||||
| chr7:107903233-107903544 | Rare:75; Clinvar (benign):2 | ||||
| chr7:108001696-108001813 | Common:1; Rare:54; Clinvar:1 | ||||
| chr7:108526032-108526475 | Common:5; Rare:130 | ||||
| chr7:108569580-108570103 | Common:3; Rare:178 | ||||
| chr7:111090947-111091171 | Rare:43 | ||||
| chr7:112206339-112206778 | Common:2; Rare:149 | ||||
| chr7:112450123-112450474 | Common:7; Rare:96 |