Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:120742503-120742772 | Common:2; Rare:76 | ||||
chr3:121749655-121750065 | Common:2; Rare:101 | ||||
chr3:121834987-121835231 | Common:3; Rare:81; Clinvar:6; Clinvar (benign):2 | ||||
chr3:122383184-122383310 | Common:1; Rare:40 | ||||
chr3:122384046-122384281 | Common:3; Rare:85 | ||||
chr3:122416075-122416229 | Rare:42 | ||||
chr3:123066949-123067125 | Rare:44 | ||||
chr3:123201680-123201967 | Common:1; Rare:79 | ||||
chr3:123585035-123585530 | Common:2; Rare:141 | ||||
chr3:124730376-124730468 | Common:2; Rare:48; Clinvar:1; Clinvar (benign):2 | ||||
chr3:125375255-125375426 | Rare:50 | ||||
chr3:126704081-126704287 | Common:2; Rare:61 | ||||
chr3:127598212-127598458 | Common:3; Rare:73 | ||||
chr3:127823175-127823335 | Common:3; Rare:31 | ||||
chr3:128123767-128124031 | Rare:69 |