| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:95218165-95218269 | Common:2; Rare:25 | ||||
| chr12:95474039-95474247 | Common:2; Rare:101 | ||||
| chr12:95548803-95548918 | Common:1; Rare:41 | ||||
| chr12:95858817-95859061 | Common:3; Rare:74 | ||||
| chr12:96400559-96400645 | Rare:38 | ||||
| chr12:98515411-98515880 | Common:1; Rare:166; Clinvar:5; Clinvar (benign):1 | ||||
| chr12:98593462-98593767 | Common:2; Rare:101; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:98644737-98645293 | Common:5; Rare:161 | ||||
| chr12:99154588-99155005 | Common:1; Rare:90 | ||||
| chr12:99984182-99984458 | Rare:56 | ||||
| chr12:100267060-100267320 | Common:1; Rare:110 | ||||
| chr12:100573501-100573761 | Rare:82 | ||||
| chr12:100593528-100593671 | Rare:21 | ||||
| chr12:101280025-101280195 | Common:1; Rare:50 | ||||
| chr12:101407668-101408076 | Common:3; Rare:102 |