| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:111092276-111092602 | Common:2; Rare:162; Clinvar:2; Clinvar (benign):5 | ||||
| chr5:111512423-111512778 | Common:3; Rare:130 | ||||
| chr5:111757714-111757815 | Common:1; Rare:40 | ||||
| chr5:112707492-112707677 | Common:3; Rare:74; Clinvar:40; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr5:112861187-112861415 | Common:4; Rare:94 | ||||
| chr5:112921602-112921686 | Common:2; Rare:27 | ||||
| chr5:115262797-115262888 | Common:1; Rare:41 | ||||
| chr5:115601761-115602154 | Common:1; Rare:102 | ||||
| chr5:115625972-115626274 | Rare:96 | ||||
| chr5:115841490-115842024 | Common:7; Rare:240 | ||||
| chr5:116084777-116085088 | Common:8; Rare:118 | ||||
| chr5:119070876-119071143 | Common:2; Rare:85 | ||||
| chr5:119268604-119268851 | Common:1; Rare:64 | ||||
| chr5:121961728-121962045 | Common:15; Rare:112 | ||||
| chr5:122078253-122078382 | Rare:24 |