Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:123201837-123201967 | Common:1; Rare:42 | ||||
chr3:123585028-123585317 | Common:1; Rare:89 | ||||
chr3:123585489-123585553 | Rare:11 | ||||
chr3:124730359-124730468 | Common:3; Rare:58; Clinvar:1; Clinvar (benign):3 | ||||
chr3:125375251-125375389 | Rare:36 | ||||
chr3:125520153-125520415 | Rare:70 | ||||
chr3:126084103-126084212 | Common:1; Rare:45 | ||||
chr3:127598223-127598458 | Common:3; Rare:68 | ||||
chr3:127823180-127823349 | Common:3; Rare:36 | ||||
chr3:128052139-128052500 | Common:4; Rare:120 | ||||
chr3:128123760-128124122 | Rare:103 | ||||
chr3:128153365-128153491 | Rare:34 | ||||
chr3:128680637-128680933 | Common:3; Rare:93 | ||||
chr3:128879440-128879675 | Common:4; Rare:118; Clinvar:2; Clinvar (benign):2 | ||||
chr3:129161004-129161125 | Rare:50 |