| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:36986105-36986342 | Common:7; Rare:85 | ||||
| chr6:37257593-37257792 | Rare:47 | ||||
| chr6:41072314-41072980 | Rare:193 | ||||
| chr6:41921089-41921556 | Common:2; Rare:125 | ||||
| chr6:42929239-42929556 | Common:3; Rare:85 | ||||
| chr6:42984281-42984591 | Rare:74 | ||||
| chr6:43013910-43014308 | Common:1; Rare:84 | ||||
| chr6:43059808-43059913 | Rare:34 | ||||
| chr6:43516852-43517109 | Common:5; Rare:96; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43770685-43770778 | Rare:27 | ||||
| chr6:44127345-44127681 | Common:4; Rare:98 | ||||
| chr6:45328161-45328360 | Rare:50 | ||||
| chr6:45422400-45422599 | Common:2; Rare:58 | ||||
| chr6:46652748-46653008 | Rare:68 | ||||
| chr6:49463186-49463387 | Common:1; Rare:61; Clinvar:1; Clinvar (benign):1 |