| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144078492-144078722 | Common:1; Rare:74 | ||||
| chr8:144082520-144082670 | Common:2; Rare:52 | ||||
| chr8:144094942-144095227 | Common:3; Rare:92; Clinvar (benign):2 | ||||
| chr8:144095834-144096247 | Common:2; Rare:165; Clinvar (benign):3 | ||||
| chr8:144103686-144103896 | Common:1; Rare:75 | ||||
| chr8:144104153-144104526 | Common:3; Rare:127 | ||||
| chr8:144318723-144318899 | Rare:55 | ||||
| chr8:144413548-144413708 | Rare:48; Clinvar:1 | ||||
| chr8:144428487-144428638 | Common:2; Rare:55 | ||||
| chr8:144502867-144503077 | Common:2; Rare:48 | ||||
| chr8:144503287-144503602 | Common:2; Rare:75 | ||||
| chr8:144503977-144504155 | Rare:36 | ||||
| chr8:144755429-144755684 | Common:1; Rare:93 | ||||
| chr8:144787279-144787386 | Rare:37 | ||||
| chr8:144792294-144792585 | Common:3; Rare:109 |