| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:42451457-42451946 | Common:3; Rare:178 | ||||
| chr6:42452110-42452557 | Common:2; Rare:153 | ||||
| chr6:42563763-42564343 | Common:1; Rare:168 | ||||
| chr6:42746059-42746389 | Rare:90 | ||||
| chr6:42746770-42747040 | Rare:84 | ||||
| chr6:42747014-42747259 | Rare:95 | ||||
| chr6:42781710-42782082 | Common:17; Rare:98 | ||||
| chr6:42782085-42782413 | Common:4; Rare:107 | ||||
| chr6:42879563-42879997 | Rare:272 | ||||
| chr6:42890801-42890962 | Rare:94 | ||||
| chr6:42929097-42929584 | Common:8; Rare:256 | ||||
| chr6:42979154-42979351 | Common:5; Rare:104; Clinvar:8; Clinvar (benign):2 | ||||
| chr6:42984280-42984650 | Rare:189 | ||||
| chr6:43013855-43014304 | Common:4; Rare:209 | ||||
| chr6:43021531-43021682 | Common:1; Rare:72 |