| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:184733355-184733548 | Common:4; Rare:55 | ||||
| chr4:184733973-184734481 | Common:12; Rare:207 | ||||
| chr4:184825909-184826246 | Common:7; Rare:105 | ||||
| chr4:184826535-184826605 | Rare:18 | ||||
| chr4:185143022-185143370 | Common:5; Rare:108; Clinvar:1; Clinvar (benign):4 | ||||
| chr4:185203499-185203571 | Rare:21 | ||||
| chr4:185203863-185204189 | Common:3; Rare:105 | ||||
| chr4:185210598-185210697 | Rare:22 | ||||
| chr4:185395920-185396092 | Rare:54 | ||||
| chr4:185396201-185396349 | Common:1; Rare:52 | ||||
| chr4:185396356-185396897 | Common:1; Rare:188 | ||||
| chr4:185425676-185425853 | Common:2; Rare:52 | ||||
| chr4:185425857-185426272 | Common:4; Rare:130 | ||||
| chr4:185811676-185811895 | Common:1; Rare:47 | ||||
| chr4:186144061-186144089 | Rare:3 |