| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:111766814-111766995 | Rare:59 | ||||
| chr12:112013127-112013478 | Common:1; Rare:124 | ||||
| chr12:112108761-112108907 | Common:1; Rare:35 | ||||
| chr12:113185447-113185739 | Common:7; Rare:107 | ||||
| chr12:113221029-113221319 | Common:2; Rare:82 | ||||
| chr12:113966318-113966527 | Common:8; Rare:73 | ||||
| chr12:116910886-116910990 | Rare:43 | ||||
| chr12:118103889-118104117 | Common:1; Rare:54 | ||||
| chr12:118135947-118136175 | Common:2; Rare:73 | ||||
| chr12:118372908-118373151 | Common:1; Rare:51 | ||||
| chr12:119877248-119877518 | Common:3; Rare:61 | ||||
| chr12:120116747-120116938 | Common:2; Rare:64 | ||||
| chr12:120194690-120194760 | Rare:26 | ||||
| chr12:120201081-120201366 | Common:2; Rare:90 | ||||
| chr12:120437988-120438147 | Rare:60; Clinvar (benign):1 |