| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:131027618-131027937 | Common:2; Rare:63 | ||||
| chr3:131087917-131088029 | Common:1; Rare:17 | ||||
| chr3:131381451-131381825 | Common:3; Rare:100 | ||||
| chr3:131502754-131503024 | Common:1; Rare:108 | ||||
| chr3:132317392-132317459 | Rare:21 | ||||
| chr3:132417169-132417743 | Common:6; Rare:187 | ||||
| chr3:132654290-132654485 | Common:2; Rare:34 | ||||
| chr3:132659756-132659907 | Common:3; Rare:34 | ||||
| chr3:132660060-132660262 | Common:2; Rare:34 | ||||
| chr3:132722018-132722344 | Common:2; Rare:122; Clinvar:22; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr3:133038131-133038419 | Common:1; Rare:100 | ||||
| chr3:133573815-133574045 | Rare:79 | ||||
| chr3:133628440-133628640 | Common:1; Rare:55 | ||||
| chr3:133661789-133662015 | Rare:54 | ||||
| chr3:133746152-133746407 | Common:1; Rare:48; Clinvar:2; Clinvar (benign):1 |