| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:24495227-24495545 | Common:4; Rare:128; Clinvar:11; Clinvar (pathogenic):2 | ||||
| chr6:24495510-24495890 | Common:4; Rare:100 | ||||
| chr6:24666720-24667327 | Common:8; Rare:454 | ||||
| chr6:24719850-24720836 | Common:14; Rare:494 | ||||
| chr6:24721150-24721440 | Common:15; Rare:111 | ||||
| chr6:24774722-24775027 | Common:4; Rare:168 | ||||
| chr6:24775218-24775514 | Common:2; Rare:126 | ||||
| chr6:25726560-25726778 | Common:1; Rare:61 | ||||
| chr6:25930573-25930840 | Common:1; Rare:47 | ||||
| chr6:25962708-25962850 | Common:2; Rare:23 | ||||
| chr6:26043674-26043960 | Common:6; Rare:212 | ||||
| chr6:26045157-26045585 | Common:3; Rare:227 | ||||
| chr6:26056246-26056534 | Common:6; Rare:212 | ||||
| chr6:26103711-26104189 | Common:11; Rare:347 | ||||
| chr6:26123614-26124512 | Common:14; Rare:683 |