| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52706374-52706690 | Common:1; Rare:86 | ||||
| chr3:53347510-53347685 | Common:2; Rare:51 | ||||
| chr3:53846417-53846572 | Rare:49 | ||||
| chr3:53891794-53892071 | Common:4; Rare:92 | ||||
| chr3:55487522-55487625 | Rare:23; Clinvar:3 | ||||
| chr3:55487630-55487669 | Rare:7 | ||||
| chr3:56557076-56557234 | Common:2; Rare:61 | ||||
| chr3:57079247-57079382 | Common:2; Rare:46 | ||||
| chr3:57227615-57227936 | Common:4; Rare:106 | ||||
| chr3:57555995-57556349 | Rare:96 | ||||
| chr3:57597278-57597787 | Common:5; Rare:152 | ||||
| chr3:57755979-57756323 | Common:1; Rare:85 | ||||
| chr3:57889885-57890090 | Rare:45; Clinvar (benign):2 | ||||
| chr3:58306451-58306578 | Common:3; Rare:47 | ||||
| chr3:58332800-58332973 | Common:3; Rare:49 |