| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:47904638-47904816 | Rare:31 | ||||
| chr12:47904887-47905174 | Common:1; Rare:87; Clinvar:1 | ||||
| chr12:47905309-47905534 | Rare:52 | ||||
| chr12:47963411-47963666 | Common:2; Rare:64 | ||||
| chr12:48105347-48105513 | Rare:53 | ||||
| chr12:48105660-48106230 | Common:4; Rare:156 | ||||
| chr12:48106236-48106451 | Rare:53 | ||||
| chr12:48119180-48119448 | Common:2; Rare:50; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:48119455-48119595 | Common:1; Rare:25 | ||||
| chr12:48119611-48119857 | Common:1; Rare:48 | ||||
| chr12:48119907-48120003 | Rare:14 | ||||
| chr12:48157055-48157155 | Rare:22 | ||||
| chr12:48157305-48157746 | Common:4; Rare:95 | ||||
| chr12:48183520-48183817 | Common:1; Rare:75 | ||||
| chr12:48350732-48351104 | Common:5; Rare:129 |