| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:120465486-120465631 | Common:1; Rare:42 | ||||
| chr5:121961808-121962055 | Common:2; Rare:90 | ||||
| chr5:122311223-122311791 | Common:4; Rare:96 | ||||
| chr5:122311867-122312266 | Common:2; Rare:127; Clinvar:1 | ||||
| chr5:122845516-122845621 | Common:3; Rare:40 | ||||
| chr5:123511966-123512286 | Common:1; Rare:93 | ||||
| chr5:124745986-124746070 | Common:1; Rare:16 | ||||
| chr5:124746251-124746863 | Common:4; Rare:113 | ||||
| chr5:124746867-124746972 | Common:3; Rare:18 | ||||
| chr5:124748758-124749052 | Common:3; Rare:65 | ||||
| chr5:126595160-126595370 | Common:4; Rare:98; Clinvar:5; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr5:126600852-126601005 | Common:1; Rare:72 | ||||
| chr5:126776879-126777219 | Common:3; Rare:131; Clinvar:4; Clinvar (benign):6 | ||||
| chr5:127290750-127290812 | Rare:14 | ||||
| chr5:127517504-127517759 | Common:6; Rare:108 |