| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:115816649-115816912 | Common:1; Rare:70 | ||||
| chr5:115841484-115841619 | Common:2; Rare:85 | ||||
| chr5:115841789-115842046 | Common:4; Rare:85 | ||||
| chr5:116084816-116085073 | Common:8; Rare:101 | ||||
| chr5:116085368-116085461 | Rare:21 | ||||
| chr5:119070869-119071207 | Common:3; Rare:107 | ||||
| chr5:119071293-119071477 | Rare:74 | ||||
| chr5:119268584-119268837 | Common:1; Rare:70 | ||||
| chr5:119355825-119356021 | Common:2; Rare:50 | ||||
| chr5:121961850-121962044 | Common:2; Rare:69 | ||||
| chr5:122774905-122775113 | Rare:76 | ||||
| chr5:122845508-122845617 | Common:3; Rare:41 | ||||
| chr5:126595183-126595327 | Common:2; Rare:69; Clinvar:4; Clinvar (benign):7 | ||||
| chr5:127030537-127030709 | Common:2; Rare:39 | ||||
| chr5:127290683-127290796 | Rare:30 |