| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:158671874-158672125 | Common:3; Rare:59 | ||||
| chr4:163166856-163166964 | Common:2; Rare:31 | ||||
| chr4:169620322-169620593 | Common:2; Rare:107 | ||||
| chr4:173334436-173334740 | Rare:61 | ||||
| chr4:183659126-183659337 | Common:1; Rare:65 | ||||
| chr4:184649429-184649756 | Common:4; Rare:108 | ||||
| chr4:184805581-184805871 | Common:2; Rare:50 | ||||
| chr5:218134-218361 | Common:3; Rare:90; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr5:612183-612351 | Rare:66 | ||||
| chr5:892658-892949 | Common:5; Rare:100 | ||||
| chr5:1799795-1799988 | Common:4; Rare:92 | ||||
| chr5:1801300-1801432 | Common:4; Rare:57; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:7868987-7869200 | Common:2; Rare:109; Clinvar (benign):1 | ||||
| chr5:10249878-10250341 | Common:19; Rare:224; Clinvar:3; Clinvar (benign):2 | ||||
| chr5:10353597-10353905 | Common:3; Rare:111 |