| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:50842884-50842973 | Rare:25 | ||||
| chr12:51026281-51026466 | Common:2; Rare:81; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:51048217-51048379 | Common:1; Rare:76 | ||||
| chr12:51172439-51172728 | Common:1; Rare:51 | ||||
| chr12:51172765-51173185 | Common:2; Rare:93 | ||||
| chr12:51238637-51238914 | Common:8; Rare:116 | ||||
| chr12:51239121-51239312 | Common:2; Rare:56 | ||||
| chr12:51270275-51270354 | Common:2; Rare:21 | ||||
| chr12:51270358-51270540 | Common:3; Rare:46 | ||||
| chr12:51324106-51324213 | Rare:29 | ||||
| chr12:51324288-51324328 | Rare:8 | ||||
| chr12:51424629-51425000 | Common:2; Rare:88 | ||||
| chr12:51468940-51469076 | Rare:19 | ||||
| chr12:51590787-51590947 | Common:1; Rare:41 | ||||
| chr12:51590969-51591283 | Rare:80; Clinvar:1 |