| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:101407708-101408035 | Common:3; Rare:76 | ||||
| chr12:101877486-101877755 | Common:3; Rare:72 | ||||
| chr12:102120058-102120257 | Rare:79 | ||||
| chr12:103930033-103930557 | Common:9; Rare:176 | ||||
| chr12:103957153-103957381 | Common:7; Rare:60 | ||||
| chr12:103965722-103965990 | Common:2; Rare:57 | ||||
| chr12:104064408-104064555 | Rare:37 | ||||
| chr12:104138170-104138384 | Common:1; Rare:57 | ||||
| chr12:104286768-104287065 | Common:3; Rare:55 | ||||
| chr12:104287204-104287322 | Rare:27 | ||||
| chr12:105107612-105107789 | Common:1; Rare:80 | ||||
| chr12:105236078-105236296 | Common:2; Rare:100 | ||||
| chr12:107685706-107685934 | Rare:75 | ||||
| chr12:108561141-108561469 | Common:4; Rare:81 | ||||
| chr12:108562393-108562664 | Common:8; Rare:114; Clinvar:2; Clinvar (benign):3 |