| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:123396540-123396870 | Rare:114 | ||||
| chr4:124712633-124713082 | Common:2; Rare:203 | ||||
| chr4:127632755-127632974 | Common:1; Rare:53 | ||||
| chr4:127782026-127782361 | Common:4; Rare:176 | ||||
| chr4:127880736-127880943 | Common:1; Rare:133 | ||||
| chr4:127881210-127881660 | Common:1; Rare:202 | ||||
| chr4:127965915-127966109 | Common:1; Rare:35; Clinvar (benign):1 | ||||
| chr4:128060530-128060831 | Common:2; Rare:100 | ||||
| chr4:128061188-128061397 | Common:1; Rare:130 | ||||
| chr4:128287615-128288082 | Common:6; Rare:272; Clinvar:1 | ||||
| chr4:128288069-128288469 | Common:11; Rare:205 | ||||
| chr4:128809645-128810200 | Common:5; Rare:210 | ||||
| chr4:128811050-128811399 | Rare:114 | ||||
| chr4:128812030-128812231 | Rare:108 | ||||
| chr4:129093420-129093756 | Common:4; Rare:186 |