| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:91182612-91182898 | Rare:59; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:93570865-93571047 | Rare:51 | ||||
| chr12:98601265-98601388 | Rare:36; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:101877531-101877762 | Common:3; Rare:60 | ||||
| chr12:102120069-102120232 | Rare:62 | ||||
| chr12:103930063-103930489 | Common:8; Rare:142 | ||||
| chr12:103965705-103965914 | Common:2; Rare:53 | ||||
| chr12:105107641-105107786 | Common:1; Rare:68 | ||||
| chr12:106955625-106955971 | Common:2; Rare:125 | ||||
| chr12:109477287-109477431 | Common:3; Rare:51 | ||||
| chr12:109573483-109573852 | Common:3; Rare:106; Clinvar:4; Clinvar (benign):5 | ||||
| chr12:109900207-109900316 | Rare:47 | ||||
| chr12:110450271-110450425 | Common:2; Rare:55 | ||||
| chr12:111686016-111686090 | Rare:23 | ||||
| chr12:111841915-111842241 | Common:2; Rare:89 |