| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:136250440-136250786 | Common:6; Rare:218; Clinvar:8; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr3:136752214-136752950 | Common:4; Rare:602 | ||||
| chr3:136861886-136862399 | Common:4; Rare:404 | ||||
| chr3:136862449-136863173 | Common:13; Rare:253 | ||||
| chr3:138115569-138115754 | Common:4; Rare:47 | ||||
| chr3:138174613-138174758 | Common:2; Rare:86 | ||||
| chr3:138174778-138174987 | Common:5; Rare:107 | ||||
| chr3:138187126-138187679 | Common:3; Rare:292 | ||||
| chr3:138187850-138188420 | Common:8; Rare:234 | ||||
| chr3:138329027-138329427 | Rare:163 | ||||
| chr3:138348437-138348734 | Common:2; Rare:173 | ||||
| chr3:138434287-138434653 | Common:9; Rare:169 | ||||
| chr3:138594140-138594600 | Rare:328 | ||||
| chr3:138608084-138609133 | Common:2; Rare:409 | ||||
| chr3:138609134-138609496 | Common:3; Rare:140 |