| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:79537103-79537197 | Rare:24; Clinvar:1 | ||||
| chr6:79537344-79537681 | Common:2; Rare:110; Clinvar:4 | ||||
| chr6:79631164-79631392 | Common:2; Rare:53 | ||||
| chr6:80004355-80004744 | Common:7; Rare:92 | ||||
| chr6:80106434-80106708 | Common:1; Rare:91; Clinvar (pathogenic):1 | ||||
| chr6:82247683-82247852 | Common:1; Rare:54 | ||||
| chr6:82363937-82364059 | Rare:34 | ||||
| chr6:82364139-82364544 | Common:2; Rare:105 | ||||
| chr6:83193174-83193429 | Common:3; Rare:81 | ||||
| chr6:83193977-83194199 | Common:1; Rare:48 | ||||
| chr6:83431026-83431115 | Common:2; Rare:30 | ||||
| chr6:83859644-83859853 | Rare:83 | ||||
| chr6:85449939-85450048 | Rare:22 | ||||
| chr6:85594055-85594357 | Common:1; Rare:60 | ||||
| chr6:85642716-85643207 | Common:4; Rare:160 |