Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:184181694-184181926 | Rare:52 | ||||
chr3:184248914-184249026 | Rare:51; Clinvar:4; Clinvar (benign):1 | ||||
chr3:184249553-184249678 | Rare:35 | ||||
chr3:184711978-184712229 | Common:1; Rare:85 | ||||
chr3:185824965-185825183 | Rare:63 | ||||
chr3:186806449-186806619 | Rare:60 | ||||
chr3:188153693-188153901 | Common:1; Rare:37 | ||||
chr3:190322431-190322541 | Common:1; Rare:31 | ||||
chr3:191329342-191329488 | Common:1; Rare:45 | ||||
chr3:196287626-196287828 | Common:1; Rare:63 | ||||
chr3:196318174-196318372 | Common:1; Rare:80 | ||||
chr3:196942375-196942668 | Common:1; Rare:121 | ||||
chr3:197949871-197950231 | Common:4; Rare:104; Clinvar (benign):1 | ||||
chr4:499136-499319 | Common:3; Rare:68 | ||||
chr4:673839-673982 | Rare:59 |