| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:42746805-42747288 | Rare:109 | ||||
| chr6:42782311-42782431 | Common:2; Rare:23 | ||||
| chr6:42879479-42879980 | Common:2; Rare:152 | ||||
| chr6:42890250-42890570 | Common:2; Rare:103 | ||||
| chr6:42890773-42891060 | Common:1; Rare:103 | ||||
| chr6:42928859-42929519 | Common:4; Rare:174 | ||||
| chr6:42929620-42929850 | Common:2; Rare:88 | ||||
| chr6:42979146-42979334 | Common:3; Rare:58; Clinvar:5; Clinvar (benign):1 | ||||
| chr6:42984273-42984609 | Rare:83 | ||||
| chr6:43013865-43014297 | Common:2; Rare:98 | ||||
| chr6:43021487-43021650 | Common:2; Rare:72 | ||||
| chr6:43053780-43054073 | Common:1; Rare:81; Clinvar:5 | ||||
| chr6:43059365-43059631 | Common:2; Rare:88 | ||||
| chr6:43059813-43059929 | Common:1; Rare:39 | ||||
| chr6:43076103-43076321 | Rare:70 |