| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:31875433-31875561 | Rare:24 | ||||
| chr12:31887182-31887358 | Common:1; Rare:30 | ||||
| chr12:31896582-31896839 | Common:2; Rare:42 | ||||
| chr12:42098223-42098334 | Rare:31 | ||||
| chr12:46383303-46383706 | Common:3; Rare:129 | ||||
| chr12:48198161-48198361 | Common:4; Rare:50 | ||||
| chr12:49764785-49765052 | Rare:57 | ||||
| chr12:52007621-52008001 | Common:3; Rare:73 | ||||
| chr12:52036262-52036338 | Rare:15 | ||||
| chr12:53307165-53307472 | Common:3; Rare:71; Clinvar (benign):1 | ||||
| chr12:54081269-54081396 | Rare:29 | ||||
| chr12:54081932-54082069 | Common:1; Rare:34 | ||||
| chr12:56111244-56111517 | Rare:67 | ||||
| chr12:56133622-56133800 | Rare:41 | ||||
| chr12:56634993-56635120 | Rare:22 |