| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49828392-49828575 | Common:1; Rare:64 | ||||
| chr12:50283440-50283672 | Common:3; Rare:72 | ||||
| chr12:50400770-50400963 | Rare:55 | ||||
| chr12:50763920-50764326 | Common:1; Rare:109 | ||||
| chr12:51026313-51026595 | Common:6; Rare:116; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:51048098-51048359 | Common:2; Rare:87 | ||||
| chr12:51172784-51172877 | Common:2; Rare:20 | ||||
| chr12:51238658-51238914 | Common:8; Rare:114 | ||||
| chr12:51590796-51590925 | Common:1; Rare:34 | ||||
| chr12:52006690-52006946 | Rare:52 | ||||
| chr12:52051149-52051493 | Common:1; Rare:111 | ||||
| chr12:52904934-52905202 | Common:4; Rare:81 | ||||
| chr12:52948803-52949253 | Common:2; Rare:124; Clinvar:1 | ||||
| chr12:52949793-52950051 | Rare:55 | ||||
| chr12:53006145-53006486 | Common:4; Rare:123 |