| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:122077533-122077725 | Rare:81; Clinvar (benign):1 | ||||
| chr5:122078239-122078382 | Rare:28 | ||||
| chr5:122774874-122775115 | Common:1; Rare:90 | ||||
| chr5:122845323-122845625 | Common:3; Rare:103 | ||||
| chr5:123511964-123512198 | Common:1; Rare:66 | ||||
| chr5:124748758-124749046 | Common:3; Rare:64 | ||||
| chr5:126423175-126423493 | Rare:65 | ||||
| chr5:126595171-126595363 | Common:4; Rare:86; Clinvar:5; Clinvar (benign):9 | ||||
| chr5:127030545-127030736 | Common:2; Rare:43 | ||||
| chr5:127517484-127517744 | Common:7; Rare:112 | ||||
| chr5:129094490-129094768 | Common:3; Rare:116 | ||||
| chr5:131170698-131171002 | Common:1; Rare:61; Clinvar (benign):1 | ||||
| chr5:131263897-131264117 | Common:1; Rare:80 | ||||
| chr5:131635160-131635432 | Common:1; Rare:105 | ||||
| chr5:131635440-131635723 | Rare:82 |