| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:184181786-184182011 | Rare:52 | ||||
| chr3:184185934-184186276 | Common:5; Rare:135 | ||||
| chr3:184248905-184249057 | Common:2; Rare:70; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:184249515-184249741 | Common:1; Rare:67 | ||||
| chr3:184298979-184299395 | Common:4; Rare:122 | ||||
| chr3:184314443-184314673 | Common:3; Rare:66 | ||||
| chr3:184325275-184325555 | Common:1; Rare:75 | ||||
| chr3:185282924-185283015 | Common:1; Rare:21 | ||||
| chr3:186567291-186567441 | Common:3; Rare:38 | ||||
| chr3:186783287-186783634 | Common:1; Rare:155 | ||||
| chr3:186806429-186806541 | Rare:35 | ||||
| chr3:186930671-186930766 | Rare:24 | ||||
| chr3:186931322-186931360 | Rare:13 | ||||
| chr3:187139426-187139579 | Rare:59 | ||||
| chr3:188153767-188154021 | Common:1; Rare:45 |