| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:122526911-122527260 | Common:3; Rare:109 | ||||
| chr12:122980571-122980969 | Common:2; Rare:114 | ||||
| chr12:123233096-123233490 | Common:2; Rare:130; Clinvar:1 | ||||
| chr12:123364825-123364981 | Common:3; Rare:58 | ||||
| chr12:123584284-123584676 | Common:8; Rare:138 | ||||
| chr12:123602039-123602163 | Common:3; Rare:48 | ||||
| chr12:123633624-123633869 | Common:2; Rare:116; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972571-123972895 | Common:6; Rare:114 | ||||
| chr12:130871730-130872120 | Common:4; Rare:163 | ||||
| chr12:131710795-131711107 | Rare:82 | ||||
| chr12:132887555-132887843 | Rare:84 | ||||
| chr12:133130265-133130592 | Common:7; Rare:101 | ||||
| chr13:21140394-21140622 | Rare:106 | ||||
| chr13:21176516-21176708 | Common:1; Rare:89 | ||||
| chr13:23579252-23579405 | Common:2; Rare:46 |