| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:41894651-41894826 | Rare:36 | ||||
| chr6:41921059-41921556 | Common:3; Rare:138 | ||||
| chr6:41921559-41921825 | Common:2; Rare:105 | ||||
| chr6:42451281-42451342 | Rare:14 | ||||
| chr6:42451546-42451714 | Common:1; Rare:30 | ||||
| chr6:42452016-42452375 | Common:2; Rare:67 | ||||
| chr6:42879552-42879934 | Common:1; Rare:113 | ||||
| chr6:42929070-42929571 | Common:4; Rare:146 | ||||
| chr6:42929657-42929831 | Common:1; Rare:61 | ||||
| chr6:42984284-42984631 | Rare:88 | ||||
| chr6:43013841-43014329 | Common:2; Rare:118 | ||||
| chr6:43021287-43021654 | Common:6; Rare:112 | ||||
| chr6:43053672-43054017 | Common:2; Rare:122; Clinvar:5; Clinvar (benign):1 | ||||
| chr6:43059806-43059913 | Rare:34 | ||||
| chr6:43076081-43076477 | Rare:128 |