| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:119452649-119452756 | Rare:53; Clinvar:1 | ||||
| chr5:120464211-120464356 | Common:1; Rare:43 | ||||
| chr5:121961748-121962066 | Common:2; Rare:113 | ||||
| chr5:122774763-122775169 | Common:1; Rare:149 | ||||
| chr5:122845503-122845625 | Common:3; Rare:48 | ||||
| chr5:123036626-123036950 | Common:2; Rare:82 | ||||
| chr5:123423317-123423618 | Rare:105 | ||||
| chr5:123511962-123512230 | Common:1; Rare:74 | ||||
| chr5:124746273-124746581 | Common:2; Rare:52 | ||||
| chr5:126423343-126423609 | Rare:77 | ||||
| chr5:126595187-126595368 | Common:4; Rare:80; Clinvar:3; Clinvar (benign):9 | ||||
| chr5:126776917-126777187 | Common:1; Rare:104; Clinvar:4; Clinvar (benign):2 | ||||
| chr5:127030501-127030768 | Common:2; Rare:64 | ||||
| chr5:127073471-127073554 | Common:3; Rare:26 | ||||
| chr5:128082976-128083425 | Common:8; Rare:139 |