| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:184448740-184449240 | Common:3; Rare:151 | ||||
| chr3:184490971-184491238 | Common:3; Rare:38 | ||||
| chr3:184496877-184497318 | Common:10; Rare:195 | ||||
| chr3:184513481-184513679 | Common:8; Rare:49 | ||||
| chr3:184513740-184514140 | Common:4; Rare:85 | ||||
| chr3:184559240-184559650 | Common:4; Rare:72 | ||||
| chr3:184565784-184566184 | Common:16; Rare:173 | ||||
| chr3:184568770-184569330 | Common:9; Rare:289 | ||||
| chr3:184710656-184711390 | Common:6; Rare:402; Clinvar (benign):1 | ||||
| chr3:184737120-184737610 | Common:5; Rare:72 | ||||
| chr3:185524570-185525080 | Common:3; Rare:88 | ||||
| chr3:185537390-185537820 | Common:1; Rare:161 | ||||
| chr3:185544952-185545257 | Common:1; Rare:49 | ||||
| chr3:185549843-185550165 | Rare:49 | ||||
| chr3:185558400-185558670 | Common:1; Rare:45 |