| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:47478067-47478247 | Common:2; Rare:67; Clinvar:2; Clinvar (benign):3 | ||||
| chr6:49463205-49463434 | Common:1; Rare:66; Clinvar (benign):1 | ||||
| chr6:52284676-52285036 | Common:2; Rare:128 | ||||
| chr6:52420231-52420364 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52995267-52995812 | Common:4; Rare:227 | ||||
| chr6:53348853-53349211 | Common:2; Rare:148 | ||||
| chr6:56542788-56543098 | Common:2; Rare:52 | ||||
| chr6:57172550-57172758 | Common:1; Rare:67 | ||||
| chr6:57222264-57222399 | Rare:52 | ||||
| chr6:57317529-57317674 | Rare:41 | ||||
| chr6:73521180-73521460 | Common:1; Rare:59 | ||||
| chr6:73521547-73521627 | Rare:22 | ||||
| chr6:73653956-73654162 | Common:3; Rare:57; Clinvar:2 | ||||
| chr6:73695949-73696242 | Common:1; Rare:68 | ||||
| chr6:75206050-75206348 | Common:2; Rare:70 |