| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:49550554-49550731 | Rare:39 | ||||
| chr6:52362000-52362246 | Common:4; Rare:77 | ||||
| chr6:52362626-52362707 | Rare:15 | ||||
| chr6:52420098-52420360 | Common:3; Rare:113; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52576992-52577260 | Common:5; Rare:99 | ||||
| chr6:52995267-52995832 | Common:4; Rare:230 | ||||
| chr6:53061667-53061952 | Rare:63 | ||||
| chr6:53065561-53065791 | Rare:60 | ||||
| chr6:53348889-53349222 | Common:2; Rare:125 | ||||
| chr6:54307632-54307937 | Common:1; Rare:59 | ||||
| chr6:54846623-54846805 | Common:1; Rare:45 | ||||
| chr6:56542761-56542954 | Common:1; Rare:33 | ||||
| chr6:56543037-56543128 | Rare:16 | ||||
| chr6:56692605-56692729 | Common:1; Rare:33 | ||||
| chr6:56692832-56693052 | Common:1; Rare:53 |