| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144852970-144853174 | Rare:124 | ||||
| chr8:144901406-144901708 | Common:2; Rare:147 | ||||
| chr8:144902051-144902390 | Common:3; Rare:103 | ||||
| chr8:144950816-144951060 | Common:5; Rare:116 | ||||
| chr8:145052163-145052556 | Common:21; Rare:210 | ||||
| chr9:470060-470324 | Common:31; Rare:174 | ||||
| chr9:706690-707226 | Common:8; Rare:357 | ||||
| chr9:2015050-2015389 | Common:3; Rare:100 | ||||
| chr9:2016570-2016830 | Rare:128 | ||||
| chr9:2017273-2017652 | Common:3; Rare:107 | ||||
| chr9:2621277-2621602 | Common:8; Rare:245 | ||||
| chr9:2621600-2621950 | Common:2; Rare:222; Clinvar:3 | ||||
| chr9:2621967-2622156 | Common:4; Rare:61; Clinvar:6; Clinvar (benign):2 | ||||
| chr9:2844031-2844362 | Common:11; Rare:255 | ||||
| chr9:3525790-3526240 | Common:2; Rare:254 |