| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144509019-144509077 | Rare:14 | ||||
| chr8:144787290-144787374 | Rare:26 | ||||
| chr8:144792342-144792562 | Common:3; Rare:82 | ||||
| chr8:145052198-145052504 | Common:10; Rare:87 | ||||
| chr9:2015060-2015395 | Common:3; Rare:97 | ||||
| chr9:2017535-2017718 | Rare:59 | ||||
| chr9:2621842-2622163 | Common:4; Rare:105; Clinvar:7; Clinvar (benign):2 | ||||
| chr9:2844047-2844329 | Common:5; Rare:104 | ||||
| chr9:3525751-3526119 | Common:1; Rare:134 | ||||
| chr9:3526425-3526554 | Common:1; Rare:65 | ||||
| chr9:4662017-4662323 | Common:5; Rare:101 | ||||
| chr9:4679437-4679834 | Common:1; Rare:174 | ||||
| chr9:4984741-4985090 | Common:1; Rare:128 | ||||
| chr9:5437832-5437982 | Common:1; Rare:53 | ||||
| chr9:5628898-5629230 | Common:1; Rare:162 |