| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:125780988-125781234 | Rare:46 | ||||
| chr6:125790858-125791012 | Common:2; Rare:53 | ||||
| chr6:125918551-125918823 | Rare:31 | ||||
| chr6:125918904-125919419 | Common:1; Rare:124 | ||||
| chr6:125956661-125956980 | Common:1; Rare:89 | ||||
| chr6:125986392-125986690 | Rare:116 | ||||
| chr6:127118966-127119068 | Rare:17 | ||||
| chr6:127119758-127119858 | Rare:25 | ||||
| chr6:127119860-127119922 | Rare:12 | ||||
| chr6:127266751-127266925 | Common:2; Rare:79 | ||||
| chr6:127342398-127342572 | Common:1; Rare:33 | ||||
| chr6:127343337-127343645 | Common:2; Rare:70 | ||||
| chr6:128520569-128520791 | Common:1; Rare:84 | ||||
| chr6:128883074-128883355 | Common:2; Rare:77; Clinvar:8; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr6:129491068-129491364 | Rare:54 |