| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:115816339-115816356 | Rare:6 | ||||
| chr5:115841476-115841628 | Common:2; Rare:96 | ||||
| chr5:115841849-115842071 | Common:4; Rare:71 | ||||
| chr5:116084965-116085067 | Common:2; Rare:53 | ||||
| chr5:118988501-118988728 | Common:1; Rare:86 | ||||
| chr5:119070840-119071500 | Common:4; Rare:221 | ||||
| chr5:119268572-119268840 | Common:1; Rare:72 | ||||
| chr5:119452387-119452750 | Common:1; Rare:157; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr5:121961901-121962062 | Common:2; Rare:69 | ||||
| chr5:122774838-122775110 | Common:1; Rare:99 | ||||
| chr5:122845315-122845625 | Common:3; Rare:107 | ||||
| chr5:123036621-123036851 | Common:2; Rare:59 | ||||
| chr5:123423336-123423645 | Common:1; Rare:98 | ||||
| chr5:123511982-123512271 | Common:1; Rare:78 | ||||
| chr5:124748816-124748934 | Common:1; Rare:24 |