| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:34392289-34392466 | Rare:75 | ||||
| chr6:34425957-34426168 | Common:4; Rare:87; Clinvar:1; Clinvar (benign):8 | ||||
| chr6:34696545-34696988 | Common:1; Rare:117 | ||||
| chr6:34887928-34888129 | Common:1; Rare:53 | ||||
| chr6:35688882-35689116 | Common:1; Rare:79 | ||||
| chr6:35921042-35921275 | Common:1; Rare:95 | ||||
| chr6:36547358-36547589 | Common:1; Rare:103 | ||||
| chr6:36594126-36594398 | Common:4; Rare:111 | ||||
| chr6:36676409-36676524 | Common:2; Rare:16 | ||||
| chr6:36678564-36678721 | Common:1; Rare:43 | ||||
| chr6:36874774-36874831 | Rare:30 | ||||
| chr6:36874930-36875233 | Common:1; Rare:52 | ||||
| chr6:37257572-37257792 | Rare:52 | ||||
| chr6:37353895-37354090 | Common:3; Rare:49 | ||||
| chr6:37433142-37433288 | Common:2; Rare:47 |