| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:119268596-119268798 | Common:1; Rare:57 | ||||
| chr5:120464194-120464367 | Common:1; Rare:54 | ||||
| chr5:121961639-121962044 | Common:15; Rare:135 | ||||
| chr5:122845516-122845621 | Common:3; Rare:40 | ||||
| chr5:123512195-123512198 | Rare:1 | ||||
| chr5:124745996-124746154 | Common:1; Rare:36 | ||||
| chr5:124748755-124749051 | Common:3; Rare:65 | ||||
| chr5:126423324-126423479 | Rare:40 | ||||
| chr5:126595171-126595324 | Common:2; Rare:71; Clinvar:5; Clinvar (benign):7 | ||||
| chr5:126776874-126777184 | Common:2; Rare:123; Clinvar:4; Clinvar (benign):4 | ||||
| chr5:127073465-127073584 | Common:3; Rare:42 | ||||
| chr5:127290654-127290852 | Rare:42 | ||||
| chr5:131165206-131165382 | Common:2; Rare:76; Clinvar (benign):1 | ||||
| chr5:131170692-131171006 | Common:1; Rare:66; Clinvar (benign):2 | ||||
| chr5:131635172-131635430 | Common:1; Rare:99 |