| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:42979197-42979344 | Common:3; Rare:41; Clinvar:3; Clinvar (benign):1 | ||||
| chr6:42984284-42984640 | Rare:94 | ||||
| chr6:43013784-43014338 | Common:2; Rare:139 | ||||
| chr6:43014362-43014532 | Common:3; Rare:37 | ||||
| chr6:43053824-43054000 | Common:1; Rare:50; Clinvar:5 | ||||
| chr6:43076166-43076481 | Rare:104 | ||||
| chr6:43182099-43182233 | Rare:38 | ||||
| chr6:43229337-43229537 | Rare:69 | ||||
| chr6:43308803-43308932 | Rare:46 | ||||
| chr6:43427454-43427572 | Rare:33 | ||||
| chr6:43427755-43427932 | Rare:48 | ||||
| chr6:43477472-43477597 | Rare:26 | ||||
| chr6:43516791-43517133 | Common:6; Rare:128; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575911-43576234 | Common:2; Rare:128; Clinvar:8 | ||||
| chr6:43628824-43628922 | Rare:37 |