| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:118988406-118988806 | Common:8; Rare:667 | ||||
| chr5:119070609-119071900 | Common:30; Rare:1403 | ||||
| chr5:119268091-119268260 | Common:3; Rare:36 | ||||
| chr5:119268462-119268866 | Common:10; Rare:578 | ||||
| chr5:119269052-119269526 | Common:6; Rare:173 | ||||
| chr5:119452228-119452783 | Common:4; Rare:488; Clinvar:11; Clinvar (benign):15; Clinvar (pathogenic):3 | ||||
| chr5:120464000-120465284 | Common:6; Rare:667 | ||||
| chr5:120465358-120465792 | Common:14; Rare:345 | ||||
| chr5:120465710-120466375 | Common:4; Rare:228 | ||||
| chr5:121961610-121962153 | Common:51; Rare:653 | ||||
| chr5:122129410-122129581 | Common:1; Rare:46 | ||||
| chr5:122774759-122775165 | Common:3; Rare:397 | ||||
| chr5:122775278-122775688 | Common:12; Rare:196 | ||||
| chr5:122844339-122845289 | Common:4; Rare:296 | ||||
| chr5:122845267-122845721 | Common:18; Rare:613 |