| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:95217514-95217831 | Common:1; Rare:89 | ||||
| chr12:95474039-95474294 | Common:2; Rare:110 | ||||
| chr12:96194577-96194620 | Rare:10 | ||||
| chr12:98593606-98594130 | Common:1; Rare:185; Clinvar:7; Clinvar (benign):7 | ||||
| chr12:101407686-101408020 | Common:3; Rare:74 | ||||
| chr12:102120061-102120204 | Rare:53 | ||||
| chr12:103930101-103930495 | Common:8; Rare:137 | ||||
| chr12:103965722-103965910 | Common:2; Rare:49 | ||||
| chr12:104064435-104064555 | Rare:29 | ||||
| chr12:106955516-106955967 | Rare:164 | ||||
| chr12:107685706-107685895 | Rare:67 | ||||
| chr12:109477293-109477437 | Common:3; Rare:49 | ||||
| chr12:109573478-109573794 | Common:3; Rare:95; Clinvar:4; Clinvar (benign):5 | ||||
| chr12:109880434-109880653 | Common:1; Rare:59 | ||||
| chr12:109900159-109900394 | Rare:77 |