Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:119080629-119080923 | Common:4; Rare:94 | ||||
chr10:119596454-119596737 | Common:1; Rare:82 | ||||
chr10:119651243-119651412 | Common:6; Rare:64; Clinvar:1; Clinvar (benign):4 | ||||
chr10:119651586-119651826 | Common:1; Rare:83; Clinvar:7; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
chr10:119651828-119651853 | Rare:8; Clinvar:2 | ||||
chr10:119892543-119892833 | Common:3; Rare:115 | ||||
chr10:120851068-120851433 | Common:9; Rare:111 | ||||
chr10:121927953-121928047 | Rare:41 | ||||
chr10:122019187-122019501 | Rare:54 | ||||
chr10:122954197-122954496 | Rare:109 | ||||
chr10:123008791-123009028 | Common:5; Rare:66; Clinvar:4; Clinvar (benign):5 | ||||
chr10:124092369-124092591 | Common:1; Rare:55 | ||||
chr10:124093497-124093657 | Common:2; Rare:30 | ||||
chr10:124743116-124743333 | Common:1; Rare:40 | ||||
chr10:125719480-125719739 | Common:1; Rare:88 |