| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:119070840-119071229 | Common:4; Rare:119 | ||||
| chr5:119071282-119071639 | Common:1; Rare:125 | ||||
| chr5:119268563-119268837 | Common:1; Rare:76 | ||||
| chr5:122845508-122845621 | Common:3; Rare:44 | ||||
| chr5:123036533-123036575 | Rare:15 | ||||
| chr5:123036579-123036762 | Common:1; Rare:52 | ||||
| chr5:123511980-123512280 | Common:1; Rare:81 | ||||
| chr5:124748753-124749003 | Common:2; Rare:55 | ||||
| chr5:126595143-126595337 | Common:4; Rare:91; Clinvar:5; Clinvar (benign):9; Clinvar (pathogenic):3 | ||||
| chr5:127030501-127030793 | Common:2; Rare:74 | ||||
| chr5:127290676-127290797 | Rare:31 | ||||
| chr5:128083647-128083768 | Common:2; Rare:49 | ||||
| chr5:131165164-131165367 | Common:1; Rare:80; Clinvar (benign):1 | ||||
| chr5:131170692-131171013 | Common:1; Rare:68; Clinvar (benign):2 | ||||
| chr5:131252946-131253064 | Common:1; Rare:27 |