| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:82247704-82247841 | Common:1; Rare:43 | ||||
| chr6:82364229-82364292 | Common:1; Rare:18 | ||||
| chr6:83067882-83068183 | Common:2; Rare:78 | ||||
| chr6:83193210-83193397 | Common:3; Rare:67 | ||||
| chr6:85449909-85450277 | Common:1; Rare:110 | ||||
| chr6:85593714-85593965 | Common:1; Rare:86 | ||||
| chr6:85642834-85643289 | Common:4; Rare:160 | ||||
| chr6:85643817-85643931 | Common:2; Rare:36 | ||||
| chr6:87155261-87155601 | Rare:89 | ||||
| chr6:87472900-87473010 | Common:1; Rare:43; Clinvar (benign):4 | ||||
| chr6:87589924-87590165 | Common:2; Rare:119; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr6:87701878-87702002 | Rare:40 | ||||
| chr6:87702214-87702528 | Common:1; Rare:97 | ||||
| chr6:88963540-88963830 | Common:2; Rare:96 | ||||
| chr6:89080581-89080784 | Common:1; Rare:89 |