| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:85678704-85678971 | Rare:99 | ||||
| chr6:98832435-98832678 | Common:3; Rare:58 | ||||
| chr6:98838192-98838300 | Common:1; Rare:22 | ||||
| chr6:101393582-101394003 | Common:3; Rare:110 | ||||
| chr6:101399499-101399750 | Common:1; Rare:56 | ||||
| chr6:104527365-104527579 | Common:3; Rare:50 | ||||
| chr6:104941016-104941077 | Rare:14 | ||||
| chr6:107046281-107046622 | Common:1; Rare:55 | ||||
| chr6:107458921-107459049 | Common:1; Rare:47; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr6:111686020-111686325 | Common:4; Rare:45 | ||||
| chr6:112879990-112880374 | Common:1; Rare:96 | ||||
| chr6:113969662-113969993 | Common:1; Rare:64 | ||||
| chr6:116277817-116277888 | Common:1; Rare:9 | ||||
| chr6:116681784-116681983 | Rare:32 | ||||
| chr6:122833306-122833450 | Common:4; Rare:26 |