| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123584315-123584586 | Common:6; Rare:71 | ||||
| chr12:123633629-123633845 | Common:1; Rare:100; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:131929074-131929300 | Common:9; Rare:64; Clinvar:1 | ||||
| chr12:132144309-132144480 | Rare:69 | ||||
| chr13:19863602-19863929 | Common:5; Rare:130 | ||||
| chr13:24512745-24512847 | Common:3; Rare:33 | ||||
| chr13:30307001-30307203 | Common:4; Rare:48 | ||||
| chr13:36346279-36346470 | Common:2; Rare:50; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:39038047-39038415 | Common:1; Rare:93 | ||||
| chr13:40789372-40789630 | Common:2; Rare:86; Clinvar:5; Clinvar (benign):2 | ||||
| chr13:41061226-41061575 | Common:3; Rare:119 | ||||
| chr13:45341094-45341442 | Common:4; Rare:172 | ||||
| chr13:49247728-49247969 | Common:1; Rare:57 | ||||
| chr13:49444005-49444281 | Common:1; Rare:95 | ||||
| chr13:50081989-50082262 | Common:1; Rare:78 |