| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:169010223-169010459 | Common:1; Rare:71 | ||||
| chr4:169612569-169612639 | Common:3; Rare:33; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:169620373-169620713 | Common:2; Rare:120 | ||||
| chr4:169757845-169758063 | Common:1; Rare:67 | ||||
| chr4:173369744-173369935 | Common:1; Rare:63 | ||||
| chr4:173370687-173370976 | Common:2; Rare:73 | ||||
| chr4:174283612-174283975 | Common:1; Rare:74 | ||||
| chr4:174522458-174522637 | Rare:55; Clinvar:2 | ||||
| chr4:174829220-174829567 | Common:1; Rare:74 | ||||
| chr4:175787373-175787724 | Rare:52 | ||||
| chr4:175788020-175788090 | Rare:12 | ||||
| chr4:175788096-175788178 | Rare:11 | ||||
| chr4:175812183-175812885 | Common:11; Rare:161 | ||||
| chr4:175812920-175812965 | Rare:7 | ||||
| chr4:175813001-175813340 | Common:2; Rare:65 |