| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123233078-123233497 | Common:3; Rare:143; Clinvar:1 | ||||
| chr12:123364768-123364964 | Common:4; Rare:89 | ||||
| chr12:123383920-123384190 | Rare:63 | ||||
| chr12:123584334-123584813 | Common:8; Rare:160 | ||||
| chr12:123633593-123633860 | Common:1; Rare:129; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972561-123973298 | Common:8; Rare:238 | ||||
| chr12:124863833-124864080 | Common:1; Rare:71 | ||||
| chr12:131828213-131828401 | Common:5; Rare:61 | ||||
| chr12:131929018-131929284 | Common:10; Rare:81; Clinvar:1 | ||||
| chr12:132144326-132144486 | Rare:64 | ||||
| chr12:132710736-132710877 | Common:3; Rare:60 | ||||
| chr12:132956244-132956431 | Common:1; Rare:41 | ||||
| chr13:19633865-19633959 | Rare:34 | ||||
| chr13:19782927-19783088 | Common:2; Rare:57 | ||||
| chr13:19863482-19863930 | Common:6; Rare:169 |