| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:119268611-119268837 | Common:1; Rare:60 | ||||
| chr5:119355823-119356021 | Common:2; Rare:51 | ||||
| chr5:122845323-122845621 | Common:3; Rare:100 | ||||
| chr5:123036288-123036500 | Common:1; Rare:64 | ||||
| chr5:123511980-123512280 | Common:1; Rare:81 | ||||
| chr5:124746284-124746599 | Common:2; Rare:54 | ||||
| chr5:124748758-124749051 | Common:3; Rare:65 | ||||
| chr5:126595160-126595337 | Common:3; Rare:87; Clinvar:5; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr5:126776915-126777184 | Common:1; Rare:105; Clinvar:4; Clinvar (benign):2 | ||||
| chr5:127030509-127030710 | Common:2; Rare:48 | ||||
| chr5:127517490-127517757 | Common:7; Rare:112 | ||||
| chr5:129094470-129094778 | Common:3; Rare:130 | ||||
| chr5:131170657-131171028 | Common:1; Rare:89; Clinvar (benign):2 | ||||
| chr5:131635048-131635424 | Common:1; Rare:128 | ||||
| chr5:131796936-131797215 | Rare:80 |