| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:100535224-100535418 | Rare:47 | ||||
| chr5:100903223-100903374 | Rare:30 | ||||
| chr5:103120104-103120404 | Common:1; Rare:72 | ||||
| chr5:108748673-108748993 | Common:2; Rare:112 | ||||
| chr5:109689274-109689438 | Common:4; Rare:82 | ||||
| chr5:109689636-109689966 | Common:3; Rare:126 | ||||
| chr5:110738929-110739072 | Common:2; Rare:54 | ||||
| chr5:112707379-112707665 | Common:6; Rare:126; Clinvar:69; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr5:115841481-115842068 | Common:8; Rare:256 | ||||
| chr5:116084918-116085076 | Common:6; Rare:74 | ||||
| chr5:116085366-116085462 | Rare:23 | ||||
| chr5:116574806-116574973 | Common:2; Rare:60 | ||||
| chr5:118988498-118988670 | Common:1; Rare:75 | ||||
| chr5:119070872-119071497 | Common:3; Rare:214 | ||||
| chr5:119268611-119268837 | Common:1; Rare:60 |