Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:172497874-172498096 | Common:1; Rare:52; Clinvar:2; Clinvar (benign):1 | ||||
chr2:173532797-173533165 | Common:6; Rare:122 | ||||
chr2:177239195-177239303 | Rare:22 | ||||
chr2:187520527-187520561 | Rare:7 | ||||
chr2:191846508-191846594 | Common:2; Rare:33 | ||||
chr2:197693557-197693568 | Rare:1 | ||||
chr2:202376074-202376225 | Rare:81 | ||||
chr2:206085170-206085267 | Rare:23 | ||||
chr2:207239557-207239671 | Rare:22 | ||||
chr2:212903448-212903704 | Rare:35 | ||||
chr2:212935939-212935959 | Rare:3 | ||||
chr2:217897957-217898269 | Common:4; Rare:53 | ||||
chr2:218033945-218034022 | Rare:18 | ||||
chr2:218272482-218272635 | Common:1; Rare:53 | ||||
chr2:218277366-218277549 | Rare:57 |