| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:38639811-38639986 | Rare:44 | ||||
| chr6:39934366-39934611 | Common:2; Rare:114; Clinvar:1 | ||||
| chr6:41053050-41053477 | Common:4; Rare:92 | ||||
| chr6:41071878-41071965 | Rare:22 | ||||
| chr6:41735011-41735180 | Common:1; Rare:37 | ||||
| chr6:41921104-41921237 | Rare:36 | ||||
| chr6:41921323-41921505 | Common:2; Rare:43 | ||||
| chr6:42050347-42050581 | Common:1; Rare:83 | ||||
| chr6:42746073-42746335 | Rare:71 | ||||
| chr6:42929201-42929566 | Common:4; Rare:107 | ||||
| chr6:42984343-42984619 | Rare:66 | ||||
| chr6:43013878-43014323 | Common:2; Rare:98 | ||||
| chr6:43308788-43308984 | Common:1; Rare:62 | ||||
| chr6:43427454-43427576 | Rare:35 | ||||
| chr6:43516857-43517130 | Common:4; Rare:106; Clinvar:2; Clinvar (benign):1 |