Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:184185940-184186209 | Common:4; Rare:105 | ||||
chr3:184248885-184249021 | Rare:68; Clinvar:5; Clinvar (benign):2 | ||||
chr3:184249451-184249706 | Rare:67 | ||||
chr3:184298947-184299279 | Common:3; Rare:102 | ||||
chr3:185282751-185283006 | Common:2; Rare:65 | ||||
chr3:185585965-185586358 | Common:1; Rare:90 | ||||
chr3:185821102-185821325 | Rare:41 | ||||
chr3:186783248-186783617 | Common:1; Rare:152 | ||||
chr3:186806416-186806567 | Rare:50 | ||||
chr3:186931259-186931359 | Common:1; Rare:27 | ||||
chr3:187139420-187139564 | Rare:55 | ||||
chr3:188153791-188153992 | Common:1; Rare:36 | ||||
chr3:188154060-188154230 | Rare:57 | ||||
chr3:190120881-190120948 | Rare:22 | ||||
chr3:190322426-190322530 | Rare:31 |