| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:87401702-87401833 | Rare:44 | ||||
| chr5:87404905-87405083 | Rare:43 | ||||
| chr5:87412777-87413127 | Common:4; Rare:114 | ||||
| chr5:88882961-88883374 | Rare:100; Clinvar:6; Clinvar (benign):3 | ||||
| chr5:88889302-88889337 | Rare:7 | ||||
| chr5:90409690-90410024 | Common:6; Rare:112 | ||||
| chr5:90474715-90474894 | Common:1; Rare:68 | ||||
| chr5:90529506-90529828 | Common:1; Rare:128 | ||||
| chr5:90558566-90558818 | Common:5; Rare:68; Clinvar (benign):1 | ||||
| chr5:91380200-91380412 | Common:1; Rare:65 | ||||
| chr5:91383280-91383498 | Common:2; Rare:71 | ||||
| chr5:94111509-94111731 | Common:2; Rare:80 | ||||
| chr5:94617929-94618305 | Rare:70 | ||||
| chr5:94618534-94618696 | Rare:43 | ||||
| chr5:95554942-95555231 | Rare:76 |