| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:51967319-51967719 | Common:7; Rare:317 | ||||
| chr3:51973500-51974401 | Common:4; Rare:700 | ||||
| chr3:51974770-51975430 | Common:10; Rare:569 | ||||
| chr3:51982387-51983010 | Common:2; Rare:108 | ||||
| chr3:51982911-51983166 | Rare:82 | ||||
| chr3:51983089-51983884 | Common:10; Rare:681 | ||||
| chr3:51995769-51996140 | Common:16; Rare:480 | ||||
| chr3:52055607-52056800 | Common:8; Rare:918 | ||||
| chr3:52154254-52154989 | Common:30; Rare:676; Clinvar (benign):1 | ||||
| chr3:52197872-52198272 | Common:5; Rare:519 | ||||
| chr3:52238286-52238907 | Common:1; Rare:161 | ||||
| chr3:52238851-52239388 | Common:13; Rare:556 | ||||
| chr3:52239481-52239881 | Common:1; Rare:88 | ||||
| chr3:52245498-52246355 | Common:9; Rare:475 | ||||
| chr3:52277514-52278520 | Common:6; Rare:816 |