| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49188506-49188621 | Common:2; Rare:15 | ||||
| chr12:49188981-49189197 | Rare:61; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264775-49265085 | Common:4; Rare:110 | ||||
| chr12:49568096-49568216 | Common:2; Rare:42 | ||||
| chr12:49828359-49828538 | Common:1; Rare:67 | ||||
| chr12:50283452-50283665 | Common:2; Rare:65 | ||||
| chr12:50763948-50764297 | Common:1; Rare:91 | ||||
| chr12:50924426-50924739 | Common:3; Rare:84 | ||||
| chr12:51026313-51026510 | Common:3; Rare:89; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:51048115-51048359 | Common:1; Rare:83 | ||||
| chr12:52006697-52006942 | Rare:51 | ||||
| chr12:52043460-52043766 | Common:4; Rare:66 | ||||
| chr12:52051115-52051558 | Common:1; Rare:145 | ||||
| chr12:53006173-53006495 | Common:4; Rare:122 | ||||
| chr12:53048887-53049228 | Common:1; Rare:74 |