| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:82364175-82364337 | Common:2; Rare:46 | ||||
| chr6:83193183-83193416 | Common:3; Rare:78 | ||||
| chr6:83430982-83431160 | Common:4; Rare:55 | ||||
| chr6:85449307-85449829 | Common:4; Rare:114 | ||||
| chr6:85449890-85450339 | Common:1; Rare:130 | ||||
| chr6:85450365-85450478 | Rare:28 | ||||
| chr6:85537016-85537258 | Rare:37 | ||||
| chr6:85593390-85593419 | Rare:5 | ||||
| chr6:85593700-85594107 | Common:2; Rare:124 | ||||
| chr6:85642785-85643098 | Common:3; Rare:103 | ||||
| chr6:85643750-85643898 | Common:1; Rare:50 | ||||
| chr6:87155240-87155624 | Rare:110 | ||||
| chr6:87472893-87473012 | Common:2; Rare:45; Clinvar:1; Clinvar (benign):4 | ||||
| chr6:87589922-87590183 | Common:3; Rare:135; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr6:87701842-87701947 | Common:1; Rare:31 |