| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:34872817-34872954 | Rare:50 | ||||
| chr20:34955725-34955817 | Common:1; Rare:34; Clinvar:3; Clinvar (benign):3 | ||||
| chr20:35147238-35147407 | Common:1; Rare:59 | ||||
| chr20:35284483-35284870 | Common:3; Rare:116 | ||||
| chr20:35411956-35412214 | Rare:89 | ||||
| chr20:35556058-35556266 | Rare:64 | ||||
| chr20:35699234-35699338 | Rare:31; Clinvar (benign):3 | ||||
| chr20:35699345-35699475 | Rare:43 | ||||
| chr20:35713021-35713245 | Common:2; Rare:45 | ||||
| chr20:35742068-35742641 | Common:5; Rare:179 | ||||
| chr20:35771790-35772060 | Common:2; Rare:84 | ||||
| chr20:36236447-36236491 | Rare:7 | ||||
| chr20:36461133-36461486 | Common:1; Rare:102 | ||||
| chr20:36573388-36573475 | Rare:23 | ||||
| chr20:36746044-36746280 | Common:2; Rare:84 |