| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:119178615-119178823 | Rare:43 | ||||
| chr12:119178866-119179070 | Rare:33; Clinvar:1 | ||||
| chr12:119179337-119179645 | Rare:108; Clinvar:9; Clinvar (benign):3 | ||||
| chr12:119803498-119803734 | Rare:43 | ||||
| chr12:119877267-119877535 | Common:2; Rare:60 | ||||
| chr12:120116627-120116938 | Common:5; Rare:89 | ||||
| chr12:120201093-120201366 | Common:2; Rare:83 | ||||
| chr12:120265684-120265925 | Common:1; Rare:98 | ||||
| chr12:120437881-120438229 | Common:2; Rare:134; Clinvar (benign):2 | ||||
| chr12:120446340-120446478 | Common:1; Rare:62 | ||||
| chr12:120469624-120470042 | Common:4; Rare:131 | ||||
| chr12:120495852-120496550 | Common:7; Rare:230 | ||||
| chr12:120529105-120529202 | Common:2; Rare:37 | ||||
| chr12:120534291-120534360 | Common:1; Rare:26 | ||||
| chr12:120581358-120581586 | Common:1; Rare:79 |