| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:77862600-77862935 | Common:9; Rare:339 | ||||
| chr4:78057312-78057663 | Common:6; Rare:186 | ||||
| chr4:78057706-78057912 | Common:1; Rare:51; Clinvar:3; Clinvar (benign):1 | ||||
| chr4:78057934-78058077 | Common:3; Rare:64; Clinvar:3; Clinvar (benign):3 | ||||
| chr4:78551524-78551889 | Rare:237 | ||||
| chr4:78552345-78552718 | Common:15; Rare:130 | ||||
| chr4:78775790-78776434 | Common:5; Rare:559 | ||||
| chr4:78776609-78777264 | Common:7; Rare:150 | ||||
| chr4:78939288-78939592 | Common:4; Rare:204 | ||||
| chr4:80072620-80072990 | Common:4; Rare:103; Clinvar:2; Clinvar (benign):4 | ||||
| chr4:80073012-80073470 | Common:3; Rare:186; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:80266360-80266840 | Common:3; Rare:128 | ||||
| chr4:80335364-80336787 | Common:6; Rare:561 | ||||
| chr4:81153500-81154090 | Common:10; Rare:298 | ||||
| chr4:81471771-81472202 | Common:4; Rare:284 |