| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:39977463-39977727 | Common:2; Rare:81 | ||||
| chr4:40056651-40056935 | Common:4; Rare:91 | ||||
| chr4:40057197-40057289 | Common:1; Rare:26 | ||||
| chr4:40629462-40629629 | Rare:28 | ||||
| chr4:40629715-40630112 | Common:1; Rare:93 | ||||
| chr4:40750028-40750270 | Common:2; Rare:61 | ||||
| chr4:41990411-41990578 | Common:1; Rare:62 | ||||
| chr4:44678352-44678706 | Common:1; Rare:130 | ||||
| chr4:47913887-47913954 | Rare:19 | ||||
| chr4:48016510-48016795 | Common:3; Rare:77 | ||||
| chr4:48269766-48269985 | Common:2; Rare:53 | ||||
| chr4:48341152-48341535 | Common:2; Rare:153 | ||||
| chr4:48341694-48342014 | Common:1; Rare:100 | ||||
| chr4:52659268-52659439 | Common:1; Rare:55 | ||||
| chr4:54229025-54229363 | Common:1; Rare:71; Clinvar (benign):4 |