| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:143927315-143927513 | Common:6; Rare:73; Clinvar:6; Clinvar (benign):13 | ||||
| chr8:143939468-143939789 | Common:4; Rare:101 | ||||
| chr8:144060680-144060820 | Rare:42 | ||||
| chr8:144078492-144078722 | Common:1; Rare:74 | ||||
| chr8:144078742-144078879 | Rare:47 | ||||
| chr8:144082503-144082679 | Common:2; Rare:63 | ||||
| chr8:144103649-144103881 | Common:1; Rare:77 | ||||
| chr8:144413227-144413244 | Rare:7 | ||||
| chr8:144413511-144413685 | Rare:61; Clinvar:1 | ||||
| chr8:144428487-144428763 | Common:3; Rare:104 | ||||
| chr8:144477902-144478104 | Common:4; Rare:73 | ||||
| chr8:144508943-144509106 | Rare:45 | ||||
| chr8:144792284-144792585 | Common:3; Rare:113 | ||||
| chr8:145052174-145052504 | Common:10; Rare:88 | ||||
| chr9:2015194-2015387 | Rare:50 |