| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144791836-144792024 | Common:3; Rare:77 | ||||
| chr8:144792098-144792272 | Common:1; Rare:49 | ||||
| chr8:144792299-144792590 | Common:3; Rare:112 | ||||
| chr8:144798782-144798924 | Common:1; Rare:46 | ||||
| chr8:144827235-144827608 | Common:2; Rare:96 | ||||
| chr8:144852982-144853143 | Rare:58 | ||||
| chr8:144901370-144901600 | Common:1; Rare:68 | ||||
| chr8:144950571-144950676 | Common:1; Rare:32 | ||||
| chr8:144950809-144950912 | Common:1; Rare:36 | ||||
| chr8:145052098-145052504 | Common:11; Rare:103 | ||||
| chr9:29068-29310 | Rare:8 | ||||
| chr9:178932-179151 | Common:6; Rare:49 | ||||
| chr9:214635-214922 | Common:6; Rare:160; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:215081-215226 | Common:2; Rare:83 | ||||
| chr9:273025-273088 | Rare:22 |