| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:88580471-88580522 | Common:1; Rare:18 | ||||
| chr12:89524776-89524883 | Common:1; Rare:19 | ||||
| chr12:92145822-92146154 | Common:2; Rare:105 | ||||
| chr12:93377728-93377929 | Rare:54 | ||||
| chr12:95217427-95217831 | Common:3; Rare:109 | ||||
| chr12:95858822-95859021 | Common:2; Rare:50 | ||||
| chr12:98515428-98515648 | Rare:73; Clinvar:1 | ||||
| chr12:98515862-98516069 | Rare:70; Clinvar:5; Clinvar (benign):3 | ||||
| chr12:98644731-98645066 | Common:3; Rare:100 | ||||
| chr12:100267065-100267197 | Common:1; Rare:64 | ||||
| chr12:101407719-101408035 | Common:3; Rare:76 | ||||
| chr12:102120061-102120192 | Rare:48 | ||||
| chr12:103930098-103930509 | Common:8; Rare:144 | ||||
| chr12:103965730-103965927 | Common:2; Rare:48 | ||||
| chr12:104064442-104064555 | Rare:29 |