| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:105107619-105107832 | Common:1; Rare:98; Clinvar:1 | ||||
| chr12:106955663-106955966 | Rare:108 | ||||
| chr12:107685709-107685872 | Rare:60 | ||||
| chr12:109477287-109477437 | Common:3; Rare:54 | ||||
| chr12:109573463-109573869 | Common:3; Rare:125; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr12:110346033-110346425 | Common:2; Rare:100; Clinvar:1; Clinvar (benign):3 | ||||
| chr12:110468711-110468874 | Rare:42 | ||||
| chr12:110502065-110502332 | Common:1; Rare:95 | ||||
| chr12:111685915-111686127 | Rare:73 | ||||
| chr12:111841894-111842260 | Common:3; Rare:103 | ||||
| chr12:112013135-112013490 | Common:1; Rare:129 | ||||
| chr12:112978364-112978653 | Rare:61 | ||||
| chr12:113185438-113185767 | Common:8; Rare:119 | ||||
| chr12:116737940-116738365 | Common:5; Rare:144 | ||||
| chr12:116878609-116878718 | Common:1; Rare:26 |