| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48583137-48583446 | Rare:85; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr3:52046229-52046373 | Rare:24 | ||||
| chr3:52065349-52065488 | Common:1; Rare:26 | ||||
| chr3:52890969-52891245 | Common:1; Rare:44 | ||||
| chr3:62587316-62587429 | Common:2; Rare:24 | ||||
| chr3:75435013-75435388 | Common:5; Rare:127 | ||||
| chr3:80770342-80770635 | Common:5; Rare:58 | ||||
| chr3:105368750-105368969 | Common:1; Rare:41 | ||||
| chr3:107240630-107240724 | Rare:38 | ||||
| chr3:111739386-111739402 | Rare:1 | ||||
| chr3:112640384-112640484 | Rare:20 | ||||
| chr3:115790841-115791039 | Common:2; Rare:30 | ||||
| chr3:121919201-121919352 | Common:1; Rare:25 | ||||
| chr3:125916333-125916615 | Common:4; Rare:85 | ||||
| chr3:129794488-129794767 | Common:1; Rare:46 |