| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:143288104-143288451 | Common:1; Rare:115 | ||||
| chr7:143408834-143408960 | Rare:30 | ||||
| chr7:143882823-143882964 | Rare:38 | ||||
| chr7:143885353-143885454 | Common:1; Rare:36 | ||||
| chr7:143902073-143902292 | Common:7; Rare:69 | ||||
| chr7:144355346-144355478 | |||||
| chr7:144835976-144836109 | Common:1; Rare:39; Clinvar (benign):1 | ||||
| chr7:149028362-149028606 | Common:3; Rare:93 | ||||
| chr7:149090657-149090907 | Rare:70 | ||||
| chr7:149126220-149126465 | Common:7; Rare:85 | ||||
| chr7:149873943-149874047 | Common:2; Rare:47 | ||||
| chr7:150323488-150323614 | Rare:35 | ||||
| chr7:150368676-150369119 | Common:4; Rare:126 | ||||
| chr7:150379074-150379335 | Common:1; Rare:92 | ||||
| chr7:150450519-150450759 | Common:1; Rare:43 |