| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109946658-109946730 | Rare:16 | ||||
| chr12:109979074-109979262 | Rare:32 | ||||
| chr12:110282601-110282796 | Rare:56; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:110283040-110283318 | Rare:53 | ||||
| chr12:110283773-110283913 | Rare:30 | ||||
| chr12:110284239-110284577 | Common:2; Rare:70 | ||||
| chr12:110429035-110429324 | Common:1; Rare:56 | ||||
| chr12:110452932-110453398 | Rare:91 | ||||
| chr12:110461290-110461382 | Rare:15 | ||||
| chr12:110489760-110490061 | Common:1; Rare:54 | ||||
| chr12:110492279-110492583 | Rare:61 | ||||
| chr12:110493096-110493351 | Common:1; Rare:51 | ||||
| chr12:110500568-110500793 | Common:2; Rare:35 | ||||
| chr12:110559975-110560260 | Common:1; Rare:57 | ||||
| chr12:110698670-110699016 | Rare:63 |