| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:95217397-95217746 | Common:4; Rare:95 | ||||
| chr12:95548796-95548924 | Common:3; Rare:46 | ||||
| chr12:96035550-96035735 | Common:2; Rare:40 | ||||
| chr12:96194220-96194482 | Common:5; Rare:93 | ||||
| chr12:96907162-96907298 | Common:1; Rare:51 | ||||
| chr12:98515475-98515823 | Rare:115; Clinvar:5 | ||||
| chr12:98593420-98593783 | Common:2; Rare:127; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:98644676-98644907 | Common:3; Rare:72 | ||||
| chr12:98644925-98645296 | Common:4; Rare:109 | ||||
| chr12:100267047-100267277 | Common:1; Rare:112 | ||||
| chr12:101407697-101408068 | Common:3; Rare:90 | ||||
| chr12:101877482-101877734 | Common:3; Rare:67 | ||||
| chr12:102120060-102120256 | Rare:78 | ||||
| chr12:103930085-103930557 | Common:8; Rare:163 | ||||
| chr12:103957147-103957294 | Common:3; Rare:45 |