| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:113966288-113966530 | Common:8; Rare:84 | ||||
| chr12:116910783-116911008 | Common:1; Rare:74 | ||||
| chr12:118136003-118136184 | Common:2; Rare:46 | ||||
| chr12:118372881-118373216 | Common:1; Rare:87 | ||||
| chr12:119667709-119667987 | Common:2; Rare:78 | ||||
| chr12:119877261-119877541 | Common:2; Rare:65 | ||||
| chr12:120194683-120194774 | Rare:32 | ||||
| chr12:120201081-120201366 | Common:2; Rare:90 | ||||
| chr12:120437988-120438205 | Rare:94; Clinvar (benign):2 | ||||
| chr12:120446353-120446483 | Common:1; Rare:60 | ||||
| chr12:120469458-120469873 | Common:5; Rare:138 | ||||
| chr12:120495867-120496228 | Common:7; Rare:121 | ||||
| chr12:120529137-120529247 | Common:1; Rare:29 | ||||
| chr12:120581344-120581577 | Common:1; Rare:79 | ||||
| chr12:121296675-121296884 | Common:1; Rare:64 |