Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:190322278-190322552 | Common:2; Rare:71 | ||||
chr3:190388141-190388265 | Rare:42 | ||||
chr3:191329298-191329702 | Common:3; Rare:120 | ||||
chr3:192917840-192918038 | Common:2; Rare:85 | ||||
chr3:193593090-193593404 | Rare:97; Clinvar:2; Clinvar (benign):2 | ||||
chr3:194486966-194487150 | Common:4; Rare:91 | ||||
chr3:195543223-195543497 | Common:3; Rare:108 | ||||
chr3:195895933-195895990 | Rare:20 | ||||
chr3:196318163-196318340 | Common:1; Rare:77 | ||||
chr3:196432385-196432639 | Common:1; Rare:101 | ||||
chr3:196503689-196504046 | Common:7; Rare:114 | ||||
chr3:196712228-196712324 | Common:2; Rare:29 | ||||
chr3:196942388-196942677 | Common:1; Rare:120 | ||||
chr3:197029779-197029916 | Common:1; Rare:45 | ||||
chr3:197298525-197298751 | Rare:69 |