| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:177897219-177897281 | Rare:15 | ||||
| chr3:179739910-179740164 | Common:2; Rare:47 | ||||
| chr3:182880713-182880980 | Rare:51 | ||||
| chr3:182895843-182896113 | Common:2; Rare:51 | ||||
| chr3:184242623-184242901 | Common:1; Rare:80; Clinvar:4; Clinvar (benign):2 | ||||
| chr3:184322630-184322954 | Rare:81 | ||||
| chr3:184323774-184324346 | Common:2; Rare:108 | ||||
| chr3:187041352-187041688 | Common:3; Rare:49 | ||||
| chr3:187288464-187288775 | Common:6; Rare:67 | ||||
| chr3:188940317-188940532 | Rare:47 | ||||
| chr3:188947924-188948185 | Common:2; Rare:45 | ||||
| chr3:190604978-190605110 | Common:2; Rare:13 | ||||
| chr3:194583894-194584034 | Common:7; Rare:49 | ||||
| chr3:195105421-195105656 | Common:2; Rare:40 | ||||
| chr3:195657892-195658126 | Common:12; Rare:40 |