| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:42452034-42452425 | Common:2; Rare:91 | ||||
| chr6:42564058-42564222 | Rare:27 | ||||
| chr6:42746062-42746352 | Rare:84 | ||||
| chr6:42746835-42747003 | Rare:37 | ||||
| chr6:42879577-42879940 | Rare:106 | ||||
| chr6:42890784-42890915 | Common:1; Rare:52 | ||||
| chr6:42929161-42929271 | Common:2; Rare:32 | ||||
| chr6:42929394-42929797 | Common:3; Rare:157 | ||||
| chr6:42984284-42984640 | Rare:94 | ||||
| chr6:43013820-43014305 | Common:2; Rare:123 | ||||
| chr6:43040283-43040565 | Common:1; Rare:93; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:43053766-43054011 | Common:2; Rare:80; Clinvar:5; Clinvar (benign):1 | ||||
| chr6:43059345-43059360 | Rare:6 | ||||
| chr6:43059800-43059926 | Common:1; Rare:40 | ||||
| chr6:43182105-43182233 | Rare:37 |