| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:42979154-42979324 | Common:3; Rare:54; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:42984279-42984673 | Rare:218 | ||||
| chr6:43013867-43014316 | Common:4; Rare:193 | ||||
| chr6:43021499-43021674 | Common:3; Rare:153 | ||||
| chr6:43053634-43054014 | Common:4; Rare:247; Clinvar:10; Clinvar (benign):2 | ||||
| chr6:43059817-43060038 | Common:2; Rare:110 | ||||
| chr6:43060357-43060580 | Rare:43 | ||||
| chr6:43076168-43076505 | Rare:175 | ||||
| chr6:43171053-43171582 | Rare:288 | ||||
| chr6:43182105-43182317 | Common:1; Rare:56 | ||||
| chr6:43229357-43229604 | Rare:133 | ||||
| chr6:43297747-43298550 | Common:2; Rare:205 | ||||
| chr6:43369359-43369854 | Common:6; Rare:313 | ||||
| chr6:43427321-43427603 | Common:1; Rare:99 | ||||
| chr6:43427778-43427961 | Rare:94 |