| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:125781058-125781201 | Rare:24 | ||||
| chr6:125918904-125919431 | Common:1; Rare:129 | ||||
| chr6:125956661-125957020 | Common:1; Rare:99 | ||||
| chr6:125986421-125986716 | Rare:114 | ||||
| chr6:126340061-126340308 | Rare:75 | ||||
| chr6:127118966-127119066 | Rare:16 | ||||
| chr6:127266783-127266899 | Common:1; Rare:43 | ||||
| chr6:127343337-127343429 | Rare:18 | ||||
| chr6:127343494-127343659 | Common:2; Rare:41 | ||||
| chr6:127459351-127459593 | Common:2; Rare:28 | ||||
| chr6:128520474-128520774 | Common:3; Rare:96 | ||||
| chr6:128882747-128883335 | Common:2; Rare:133; Clinvar:7; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr6:131135419-131135760 | Common:4; Rare:136 | ||||
| chr6:131628054-131628461 | Common:3; Rare:110 | ||||
| chr6:132401350-132401663 | Common:3; Rare:98 |