| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:115841534-115842027 | Common:7; Rare:211 | ||||
| chr5:119070837-119071145 | Common:3; Rare:95 | ||||
| chr5:119268617-119268834 | Common:1; Rare:60 | ||||
| chr5:119355832-119356021 | Common:2; Rare:48 | ||||
| chr5:122077087-122077257 | Common:1; Rare:30 | ||||
| chr5:122078094-122078674 | Common:1; Rare:124 | ||||
| chr5:122845514-122845654 | Common:3; Rare:59 | ||||
| chr5:123511790-123512125 | Common:2; Rare:98 | ||||
| chr5:123512429-123512449 | Rare:3 | ||||
| chr5:127030539-127030761 | Common:2; Rare:52 | ||||
| chr5:131170655-131170999 | Common:1; Rare:81; Clinvar (benign):1 | ||||
| chr5:132556904-132557037 | Rare:57; Clinvar:1 | ||||
| chr5:132866587-132866681 | Rare:24; Clinvar (benign):1 | ||||
| chr5:133051653-133052100 | Common:2; Rare:161 | ||||
| chr5:133968478-133968741 | Rare:107 |