| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:124746571-124746684 | Rare:24 | ||||
| chr5:124746769-124747016 | Common:5; Rare:46 | ||||
| chr5:124748766-124749001 | Common:2; Rare:54 | ||||
| chr5:126423160-126423610 | Common:1; Rare:107 | ||||
| chr5:126595145-126595448 | Common:5; Rare:114; Clinvar:5; Clinvar (benign):10; Clinvar (pathogenic):3 | ||||
| chr5:126600849-126601008 | Common:1; Rare:76 | ||||
| chr5:126601235-126601635 | Common:1; Rare:165 | ||||
| chr5:126776855-126777187 | Common:3; Rare:125; Clinvar:4; Clinvar (benign):5 | ||||
| chr5:127030515-127030844 | Common:2; Rare:88 | ||||
| chr5:127290648-127290846 | Rare:45 | ||||
| chr5:127290857-127291043 | Common:1; Rare:39; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:127517481-127517710 | Common:7; Rare:102 | ||||
| chr5:128083250-128083470 | Rare:72 | ||||
| chr5:128083513-128083778 | Common:2; Rare:110 | ||||
| chr5:128536917-128537583 | Common:13; Rare:347; Clinvar:24; Clinvar (benign):30 |