| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:44219496-44219670 | Common:2; Rare:45 | ||||
| chr6:44223401-44223640 | Common:1; Rare:67 | ||||
| chr6:44387455-44387575 | Common:2; Rare:26 | ||||
| chr6:44387625-44387782 | Common:2; Rare:50 | ||||
| chr6:45377628-45377665 | Rare:17 | ||||
| chr6:45377798-45378209 | Common:2; Rare:132 | ||||
| chr6:46129777-46130173 | Common:5; Rare:126 | ||||
| chr6:46652675-46653018 | Rare:84 | ||||
| chr6:47477606-47478073 | Common:3; Rare:120; Clinvar:5; Clinvar (benign):4 | ||||
| chr6:49463122-49463449 | Common:1; Rare:94; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:52284682-52285085 | Common:2; Rare:137 | ||||
| chr6:52420122-52420404 | Common:3; Rare:114; Clinvar:1; Clinvar (benign):3 | ||||
| chr6:52576987-52577297 | Common:5; Rare:116 | ||||
| chr6:52995267-52995819 | Common:4; Rare:228 | ||||
| chr6:53065561-53065684 | Rare:26 |