| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:143511656-143511903 | Common:4; Rare:52 | ||||
| chr6:143843179-143843467 | Common:2; Rare:97 | ||||
| chr6:144008247-144008458 | Rare:71 | ||||
| chr6:144064552-144064630 | Rare:19 | ||||
| chr6:144095081-144095360 | Common:1; Rare:68 | ||||
| chr6:144150158-144150537 | Common:6; Rare:103 | ||||
| chr6:144285171-144285361 | Common:3; Rare:61 | ||||
| chr6:144285538-144285634 | Rare:23 | ||||
| chr6:145735224-145735318 | Common:2; Rare:37; Clinvar:7; Clinvar (benign):1 | ||||
| chr6:145814793-145814948 | Rare:73 | ||||
| chr6:145964306-145964565 | Rare:88 | ||||
| chr6:149648628-149648972 | Common:3; Rare:92 | ||||
| chr6:149718062-149718191 | Common:3; Rare:47 | ||||
| chr6:151391520-151391786 | Common:3; Rare:65 | ||||
| chr6:151452033-151452538 | Common:4; Rare:176 |