| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:50999377-50999549 | Common:1; Rare:33 | ||||
| chr12:51048211-51048393 | Common:1; Rare:83 | ||||
| chr12:51218073-51218406 | Common:5; Rare:71 | ||||
| chr12:51239176-51239355 | Rare:43 | ||||
| chr12:51270267-51270439 | Common:3; Rare:49 | ||||
| chr12:51590683-51590939 | Common:1; Rare:69 | ||||
| chr12:52051152-52051518 | Common:1; Rare:122 | ||||
| chr12:52186161-52186349 | Common:1; Rare:23 | ||||
| chr12:52948844-52949566 | Common:3; Rare:200; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr12:52949805-52950030 | Rare:48 | ||||
| chr12:52950746-52951109 | Common:1; Rare:82 | ||||
| chr12:52951556-52951741 | Rare:53; Clinvar:1 | ||||
| chr12:53006117-53006443 | Common:4; Rare:108 | ||||
| chr12:53047026-53047250 | Common:1; Rare:54 | ||||
| chr12:53049867-53050128 | Common:1; Rare:67 |