| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:158172639-158172734 | Rare:15 | ||||
| chr4:158671806-158672141 | Common:4; Rare:93 | ||||
| chr4:158672240-158672322 | Rare:17; Clinvar:1 | ||||
| chr4:169010223-169010365 | Common:1; Rare:50 | ||||
| chr4:173370690-173370986 | Common:2; Rare:76 | ||||
| chr4:173530195-173530462 | Common:2; Rare:61 | ||||
| chr4:174283642-174283953 | Common:1; Rare:59 | ||||
| chr4:183504400-183504743 | Rare:117 | ||||
| chr4:183659167-183659323 | Rare:46 | ||||
| chr4:184649427-184649770 | Common:4; Rare:112 | ||||
| chr4:185203919-185204097 | Rare:60 | ||||
| chr4:185396580-185396843 | Rare:83 | ||||
| chr4:189940592-189940969 | Common:11; Rare:126 | ||||
| chr5:218124-218350 | Common:2; Rare:88; Clinvar:1; Clinvar (benign):3 | ||||
| chr5:443068-443272 | Common:10; Rare:92 |