| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:111757172-111757338 | Common:5; Rare:33 | ||||
| chr5:111757391-111757451 | Rare:20 | ||||
| chr5:115841505-115841627 | Common:2; Rare:77 | ||||
| chr5:115841791-115842016 | Common:3; Rare:74 | ||||
| chr5:119268552-119268829 | Common:1; Rare:78 | ||||
| chr5:119355798-119356021 | Common:2; Rare:61 | ||||
| chr5:122774882-122775103 | Common:1; Rare:84 | ||||
| chr5:122845456-122845621 | Common:3; Rare:61 | ||||
| chr5:126776917-126777184 | Common:1; Rare:103; Clinvar:4; Clinvar (benign):2 | ||||
| chr5:127030537-127030749 | Common:2; Rare:47 | ||||
| chr5:127517484-127517724 | Common:7; Rare:106 | ||||
| chr5:131170698-131170996 | Common:1; Rare:60; Clinvar (benign):1 | ||||
| chr5:131635211-131635446 | Common:1; Rare:86 | ||||
| chr5:131796943-131797215 | Rare:77 | ||||
| chr5:132490774-132491020 | Rare:64 |