| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:119197639-119197896 | Common:1; Rare:79 | ||||
| chr5:119268611-119268837 | Common:1; Rare:60 | ||||
| chr5:119355819-119355917 | Common:1; Rare:34 | ||||
| chr5:119452364-119452626 | Common:1; Rare:102; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr5:119452664-119452804 | Rare:66; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:121851757-121851901 | Common:3; Rare:39 | ||||
| chr5:121961812-121962068 | Common:2; Rare:94 | ||||
| chr5:122129476-122129581 | Rare:27 | ||||
| chr5:122774905-122775169 | Rare:108 | ||||
| chr5:122844146-122844263 | Common:1; Rare:19 | ||||
| chr5:122845315-122845669 | Common:3; Rare:122 | ||||
| chr5:123036642-123036949 | Common:2; Rare:77 | ||||
| chr5:123511976-123512295 | Common:1; Rare:87 | ||||
| chr5:124746268-124746574 | Common:2; Rare:52 | ||||
| chr5:124746628-124746984 | Common:5; Rare:68 |