| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32853670-32853811 | Rare:66; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:32854023-32854227 | Common:2; Rare:53 | ||||
| chr6:32977530-32977785 | Common:2; Rare:87; Clinvar (benign):1 | ||||
| chr6:33075812-33076008 | Common:2; Rare:21 | ||||
| chr6:33200356-33200420 | Rare:17 | ||||
| chr6:33200656-33200920 | Common:2; Rare:81 | ||||
| chr6:33271664-33272122 | Common:2; Rare:161 | ||||
| chr6:33289323-33289617 | Common:3; Rare:52 | ||||
| chr6:33298869-33299071 | Rare:46 | ||||
| chr6:33418056-33418455 | Common:2; Rare:94 | ||||
| chr6:33420037-33420267 | Rare:50 | ||||
| chr6:34248984-34249230 | Rare:57 | ||||
| chr6:34696717-34696981 | Common:1; Rare:61 | ||||
| chr6:34757311-34757545 | Common:1; Rare:67 | ||||
| chr6:34887946-34888116 | Common:1; Rare:44 |