| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:124712561-124713057 | Common:1; Rare:140 | ||||
| chr4:127632818-127632972 | Common:1; Rare:38 | ||||
| chr4:127782037-127782342 | Common:2; Rare:82 | ||||
| chr4:127880764-127880939 | Rare:62 | ||||
| chr4:127965896-127966144 | Common:1; Rare:41; Clinvar (benign):1 | ||||
| chr4:128288201-128288341 | Common:5; Rare:52 | ||||
| chr4:128811162-128811317 | Rare:31 | ||||
| chr4:129093411-129093736 | Common:2; Rare:91 | ||||
| chr4:133149099-133149301 | Common:2; Rare:61 | ||||
| chr4:139295793-139296094 | Common:1; Rare:67 | ||||
| chr4:139301192-139301593 | Common:6; Rare:115 | ||||
| chr4:139302460-139302567 | Common:1; Rare:17 | ||||
| chr4:139453642-139454240 | Common:5; Rare:180; Clinvar:10; Clinvar (benign):4 | ||||
| chr4:140154169-140154532 | Common:3; Rare:115 | ||||
| chr4:140373384-140373710 | Common:3; Rare:134 |