| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:152936135-152936391 | Common:4; Rare:67 | ||||
| chr4:158671866-158672365 | Common:5; Rare:117; Clinvar:3; Clinvar (benign):1 | ||||
| chr4:158723214-158723463 | Common:2; Rare:107 | ||||
| chr4:169612581-169612677 | Common:2; Rare:34; Clinvar:1; Clinvar (benign):1 | ||||
| chr4:169620223-169620737 | Common:2; Rare:166 | ||||
| chr4:169757880-169758080 | Rare:57 | ||||
| chr4:170026287-170026581 | Common:4; Rare:109 | ||||
| chr4:173333720-173333870 | Common:1; Rare:40 | ||||
| chr4:173370646-173370986 | Common:2; Rare:86 | ||||
| chr4:174283410-174283965 | Common:2; Rare:99 | ||||
| chr4:174521948-174522259 | Common:6; Rare:77; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr4:174522263-174522659 | Common:1; Rare:119; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr4:176319805-176320028 | Common:2; Rare:85 | ||||
| chr4:177442343-177442514 | Rare:103; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr4:183659132-183659354 | Common:1; Rare:72 |