| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:121961808-121962053 | Common:2; Rare:89 | ||||
| chr5:122774905-122775145 | Rare:98 | ||||
| chr5:122845256-122845625 | Common:3; Rare:121 | ||||
| chr5:123423342-123423609 | Rare:79 | ||||
| chr5:123511976-123512093 | Common:1; Rare:25 | ||||
| chr5:124745996-124746038 | Rare:9 | ||||
| chr5:124746628-124746959 | Common:3; Rare:65 | ||||
| chr5:124748758-124749051 | Common:3; Rare:65 | ||||
| chr5:126595107-126595401 | Common:5; Rare:120; Clinvar:8; Clinvar (benign):11; Clinvar (pathogenic):3 | ||||
| chr5:126600839-126601002 | Common:1; Rare:76 | ||||
| chr5:126776652-126776781 | Rare:29 | ||||
| chr5:126776872-126777197 | Common:3; Rare:128; Clinvar:4; Clinvar (benign):6 | ||||
| chr5:127030529-127030793 | Common:2; Rare:64 | ||||
| chr5:127073441-127073544 | Common:3; Rare:32 | ||||
| chr5:127290705-127290839 | Rare:29 |