| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:119498363-119498620 | Common:4; Rare:89 | ||||
| chr3:120596138-120596354 | Common:2; Rare:71 | ||||
| chr3:120742511-120742771 | Common:2; Rare:72 | ||||
| chr3:121749721-121750021 | Common:1; Rare:68 | ||||
| chr3:121834999-121835194 | Common:3; Rare:63; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122383204-122383345 | Common:2; Rare:41 | ||||
| chr3:122384074-122384268 | Rare:74 | ||||
| chr3:122564264-122564424 | Common:1; Rare:47 | ||||
| chr3:123585504-123585536 | Rare:5 | ||||
| chr3:124730359-124730457 | Common:3; Rare:51; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:125375255-125375425 | Rare:50 | ||||
| chr3:127598212-127598446 | Common:3; Rare:64 | ||||
| chr3:128123767-128123984 | Rare:54 | ||||
| chr3:128153365-128153496 | Rare:37 | ||||
| chr3:128879431-128879675 | Common:4; Rare:121; Clinvar:2; Clinvar (benign):2 |