| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:134253261-134253592 | Common:2; Rare:109; Clinvar (benign):1 | ||||
| chr12:389236-389364 | Rare:46 | ||||
| chr12:389483-389703 | Common:6; Rare:99 | ||||
| chr12:401446-401664 | Rare:58 | ||||
| chr12:552415-552511 | Common:1; Rare:34 | ||||
| chr12:610346-610489 | Rare:18 | ||||
| chr12:643213-643418 | Common:5; Rare:50 | ||||
| chr12:643585-643672 | Rare:17 | ||||
| chr12:643863-643891 | Rare:8 | ||||
| chr12:644056-644350 | Common:1; Rare:51 | ||||
| chr12:753003-753278 | Common:2; Rare:78; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:907669-908008 | Common:3; Rare:74; Clinvar:1 | ||||
| chr12:949615-949703 | Rare:28 | ||||
| chr12:991101-991322 | Common:3; Rare:100 | ||||
| chr12:1690873-1691076 | Common:2; Rare:73 |