| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:76084893-76085123 | Common:6; Rare:44 | ||||
| chr12:76348071-76348210 | Rare:42; Clinvar (pathogenic):1 | ||||
| chr12:76348305-76348611 | Common:2; Rare:103; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:76559005-76559102 | Rare:17 | ||||
| chr12:76559551-76560051 | Common:4; Rare:161 | ||||
| chr12:76763515-76763625 | Common:2; Rare:18 | ||||
| chr12:76763826-76764326 | Common:5; Rare:199 | ||||
| chr12:76764469-76764607 | Rare:44 | ||||
| chr12:76878843-76879247 | Common:1; Rare:127 | ||||
| chr12:77065476-77065934 | Common:3; Rare:150 | ||||
| chr12:77065952-77065979 | Common:1; Rare:6 | ||||
| chr12:77066018-77066130 | Rare:28 | ||||
| chr12:79045469-79045503 | Common:2; Rare:19 | ||||
| chr12:79689539-79689636 | Rare:28 | ||||
| chr12:79689750-79690058 | Common:1; Rare:95 |