| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58573305-58573488 | Rare:46 | ||||
| chr19:58573530-58573601 | Rare:19 | ||||
| chr2:677358-677557 | Common:1; Rare:84 | ||||
| chr2:1842853-1842967 | Common:3; Rare:65 | ||||
| chr2:3377811-3377933 | Rare:32 | ||||
| chr2:3519408-3519660 | Common:2; Rare:74 | ||||
| chr2:3558251-3558551 | Common:6; Rare:116 | ||||
| chr2:3575098-3575354 | Common:2; Rare:72; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:9423163-9423676 | Common:1; Rare:138 | ||||
| chr2:9474385-9474626 | Common:8; Rare:82 | ||||
| chr2:9555627-9555992 | Common:2; Rare:119 | ||||
| chr2:9843411-9843514 | Common:3; Rare:24 | ||||
| chr2:9843645-9843749 | Common:3; Rare:39 | ||||
| chr2:10368556-10368796 | Common:2; Rare:48 | ||||
| chr2:11466118-11466184 | Common:1; Rare:18 |