| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144852967-144853166 | Rare:73 | ||||
| chr8:144901381-144901729 | Common:1; Rare:102 | ||||
| chr8:144950593-144950693 | Common:2; Rare:27 | ||||
| chr8:144950814-144950931 | Common:2; Rare:40 | ||||
| chr8:145052153-145052518 | Common:11; Rare:98 | ||||
| chr9:504380-504738 | Common:4; Rare:174 | ||||
| chr9:2015060-2015387 | Common:3; Rare:96 | ||||
| chr9:2621842-2622169 | Common:4; Rare:110; Clinvar:7; Clinvar (benign):2 | ||||
| chr9:2844034-2844382 | Common:7; Rare:136 | ||||
| chr9:3525485-3525820 | Common:1; Rare:108 | ||||
| chr9:3525978-3526119 | Common:1; Rare:69 | ||||
| chr9:3526379-3526545 | Common:4; Rare:84 | ||||
| chr9:4679429-4679742 | Common:1; Rare:138 | ||||
| chr9:4679789-4679840 | Rare:23 | ||||
| chr9:4679855-4680013 | Common:2; Rare:57 |