| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:143450660-143450936 | Common:1; Rare:103; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143677803-143678140 | Common:2; Rare:84 | ||||
| chr6:144095493-144095854 | Common:6; Rare:103 | ||||
| chr6:144285178-144285372 | Common:3; Rare:58 | ||||
| chr6:144330580-144330866 | Common:2; Rare:51 | ||||
| chr6:144583228-144583535 | Common:1; Rare:54 | ||||
| chr6:144659212-144659374 | Rare:19 | ||||
| chr6:145814664-145814953 | Common:1; Rare:131 | ||||
| chr6:145964296-145964592 | Common:1; Rare:104 | ||||
| chr6:149545994-149546132 | Rare:58 | ||||
| chr6:149746454-149746617 | Common:2; Rare:73 | ||||
| chr6:149749606-149749796 | Rare:102 | ||||
| chr6:151391486-151391793 | Common:3; Rare:85 | ||||
| chr6:151452023-151452552 | Common:5; Rare:189; Clinvar (benign):3 | ||||
| chr6:152982994-152983287 | Common:2; Rare:93 |