| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:122526898-122527291 | Common:3; Rare:134 | ||||
| chr12:122975133-122975240 | Common:1; Rare:24 | ||||
| chr12:122980406-122980734 | Common:1; Rare:110 | ||||
| chr12:123233093-123233490 | Common:2; Rare:132; Clinvar:1 | ||||
| chr12:123364820-123364969 | Common:2; Rare:59 | ||||
| chr12:123584311-123584616 | Common:6; Rare:104 | ||||
| chr12:123602023-123602156 | Common:3; Rare:47 | ||||
| chr12:123633624-123633851 | Common:1; Rare:104; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:132687311-132687713 | Common:4; Rare:149; Clinvar:5; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132829069-132829255 | Rare:87 | ||||
| chr12:132887558-132887834 | Rare:79 | ||||
| chr12:132956262-132956431 | Common:1; Rare:35 | ||||
| chr12:133130238-133130616 | Common:7; Rare:116 | ||||
| chr13:19782923-19783088 | Common:2; Rare:59 | ||||
| chr13:20525801-20525936 | Common:1; Rare:58 |