| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53501526-53501582 | Rare:10 | ||||
| chr12:53625961-53626169 | Common:1; Rare:52 | ||||
| chr12:53676057-53676383 | Common:3; Rare:149 | ||||
| chr12:54259532-54259730 | Rare:37 | ||||
| chr12:54385756-54385905 | Rare:28 | ||||
| chr12:54403909-54404257 | Common:3; Rare:85 | ||||
| chr12:54419160-54419667 | Common:1; Rare:115 | ||||
| chr12:55707495-55707643 | Common:1; Rare:54; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:55707691-55707997 | Common:1; Rare:66; Clinvar:4 | ||||
| chr12:55712063-55712261 | Common:5; Rare:54; Clinvar (benign):1 | ||||
| chr12:55716003-55716225 | Common:1; Rare:96 | ||||
| chr12:55720184-55720452 | Common:4; Rare:35; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:55725844-55726258 | Rare:94 | ||||
| chr12:55728310-55728521 | Rare:60 | ||||
| chr12:55728922-55729222 | Rare:65 |