| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:124745996-124746041 | Rare:10 | ||||
| chr5:124748738-124748997 | Common:2; Rare:59 | ||||
| chr5:126423324-126423620 | Rare:85 | ||||
| chr5:126595178-126595345 | Common:3; Rare:79; Clinvar:5; Clinvar (benign):8 | ||||
| chr5:126776917-126777184 | Common:1; Rare:103; Clinvar:4; Clinvar (benign):2 | ||||
| chr5:127030478-127030736 | Common:3; Rare:63 | ||||
| chr5:127290756-127290839 | Rare:14 | ||||
| chr5:127517507-127517704 | Common:5; Rare:90 | ||||
| chr5:128338932-128339259 | Rare:81; Clinvar:9; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
| chr5:128538202-128538265 | Common:1; Rare:16 | ||||
| chr5:128965072-128965206 | Rare:31 | ||||
| chr5:128965340-128965590 | Common:2; Rare:65 | ||||
| chr5:129094426-129094784 | Common:4; Rare:152 | ||||
| chr5:129460108-129460351 | Common:4; Rare:49 | ||||
| chr5:131170692-131171008 | Common:1; Rare:67; Clinvar (benign):2 |