| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53231784-53232188 | Rare:155 | ||||
| chr12:53232097-53232497 | Common:5; Rare:140 | ||||
| chr12:53251002-53252383 | Common:22; Rare:927 | ||||
| chr12:53252332-53253000 | Common:16; Rare:531 | ||||
| chr12:53267714-53267900 | Rare:50 | ||||
| chr12:53267901-53268568 | Common:14; Rare:368 | ||||
| chr12:53295269-53295669 | Common:8; Rare:461 | ||||
| chr12:53295909-53296145 | Common:2; Rare:61 | ||||
| chr12:53299043-53299443 | Common:2; Rare:98 | ||||
| chr12:53309895-53310295 | Common:3; Rare:156 | ||||
| chr12:53321110-53321497 | Common:6; Rare:479; Clinvar:10; Clinvar (pathogenic):9 | ||||
| chr12:53321491-53321900 | Common:5; Rare:278; Clinvar:13 | ||||
| chr12:53324187-53324552 | Common:1; Rare:79 | ||||
| chr12:53324483-53325120 | Common:5; Rare:334 | ||||
| chr12:53325140-53325490 | Common:1; Rare:53 |