| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:134253306-134253601 | Common:2; Rare:99; Clinvar (benign):1 | ||||
| chr11:134331650-134332080 | Common:10; Rare:101 | ||||
| chr11:134412196-134412320 | Rare:40 | ||||
| chr12:389198-389350 | Rare:60 | ||||
| chr12:389449-389709 | Common:6; Rare:108 | ||||
| chr12:401387-401774 | Common:2; Rare:103 | ||||
| chr12:459710-460138 | Common:3; Rare:213 | ||||
| chr12:542930-543240 | Rare:84 | ||||
| chr12:752304-752615 | Common:1; Rare:94 | ||||
| chr12:949200-949458 | Rare:54 | ||||
| chr12:949620-950087 | Common:6; Rare:131 | ||||
| chr12:989960-990097 | Rare:30 | ||||
| chr12:990255-990655 | Common:5; Rare:140 | ||||
| chr12:991030-991410 | Common:7; Rare:149 | ||||
| chr12:1530226-1530362 | Common:1; Rare:40 |