| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:101407668-101408083 | Common:3; Rare:104 | ||||
| chr12:102120048-102120254 | Rare:82 | ||||
| chr12:103841320-103841497 | Common:3; Rare:61 | ||||
| chr12:103930007-103930571 | Common:9; Rare:183 | ||||
| chr12:103957123-103957369 | Common:8; Rare:67 | ||||
| chr12:103965664-103965986 | Common:2; Rare:77 | ||||
| chr12:104064435-104064573 | Rare:32 | ||||
| chr12:104138142-104138354 | Rare:45 | ||||
| chr12:105107619-105107803 | Common:1; Rare:89; Clinvar:1 | ||||
| chr12:105236068-105236312 | Common:2; Rare:112 | ||||
| chr12:106303298-106303484 | Common:1; Rare:44 | ||||
| chr12:106357451-106357823 | Common:4; Rare:65; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:106357939-106357969 | Rare:16 | ||||
| chr12:106358019-106358083 | Common:1; Rare:22 | ||||
| chr12:106774120-106774381 | Common:3; Rare:63 |