Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:119596491-119596734 | Common:1; Rare:67 | ||||
chr10:119596934-119597325 | Common:2; Rare:108 | ||||
chr10:119651210-119651382 | Common:2; Rare:71 | ||||
chr10:119818446-119818736 | Rare:96 | ||||
chr10:119892616-119892772 | Common:2; Rare:61 | ||||
chr10:120851200-120851447 | Common:5; Rare:94 | ||||
chr10:121927899-121928200 | Common:2; Rare:92 | ||||
chr10:121928427-121928551 | Rare:35 | ||||
chr10:122112746-122113054 | Common:4; Rare:94 | ||||
chr10:122954179-122954496 | Rare:114 | ||||
chr10:123008791-123009028 | Common:5; Rare:66; Clinvar:4; Clinvar (benign):5 | ||||
chr10:124092369-124092510 | Rare:37 | ||||
chr10:124418905-124419121 | Common:4; Rare:95; Clinvar:1; Clinvar (benign):1 | ||||
chr10:124791742-124791938 | Common:1; Rare:103 | ||||
chr10:124801730-124801846 | Rare:38 |