| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:115841548-115841597 | Common:1; Rare:30 | ||||
| chr5:115841805-115842016 | Common:3; Rare:69 | ||||
| chr5:116085368-116085496 | Rare:36 | ||||
| chr5:119268611-119268821 | Common:1; Rare:58 | ||||
| chr5:122076939-122077229 | Common:1; Rare:64 | ||||
| chr5:126595196-126595361 | Common:4; Rare:73; Clinvar:1; Clinvar (benign):9 | ||||
| chr5:127030529-127030773 | Common:2; Rare:56 | ||||
| chr5:131170704-131171002 | Common:1; Rare:59; Clinvar (benign):1 | ||||
| chr5:131263790-131264094 | Common:2; Rare:108 | ||||
| chr5:131635160-131635422 | Common:1; Rare:99 | ||||
| chr5:132490774-132491002 | Rare:57 | ||||
| chr5:132777218-132777454 | Rare:56 | ||||
| chr5:132866450-132866694 | Common:1; Rare:79; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:133026533-133026825 | Common:5; Rare:69 | ||||
| chr5:133051862-133052107 | Rare:92 |