| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:119070840-119071477 | Common:4; Rare:214 | ||||
| chr5:119268573-119268838 | Common:1; Rare:72 | ||||
| chr5:119333293-119333610 | Common:3; Rare:68 | ||||
| chr5:121961826-121962044 | Common:2; Rare:79 | ||||
| chr5:122774870-122775113 | Common:1; Rare:92 | ||||
| chr5:122845514-122845625 | Common:3; Rare:45 | ||||
| chr5:123036607-123036821 | Common:2; Rare:62 | ||||
| chr5:123423279-123423618 | Rare:117 | ||||
| chr5:123511975-123512280 | Common:1; Rare:85 | ||||
| chr5:126595143-126595324 | Common:3; Rare:84; Clinvar:5; Clinvar (benign):8; Clinvar (pathogenic):3 | ||||
| chr5:126776649-126776726 | Rare:18 | ||||
| chr5:126776902-126777221 | Common:2; Rare:123; Clinvar:4; Clinvar (benign):5 | ||||
| chr5:127030539-127030764 | Common:2; Rare:52 | ||||
| chr5:127073465-127073522 | Common:1; Rare:14 | ||||
| chr5:127517490-127517704 | Common:7; Rare:96 |