Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:119651243-119651386 | Common:4; Rare:56; Clinvar (benign):2 | ||||
chr10:119892555-119892777 | Common:3; Rare:84 | ||||
chr10:120851200-120851411 | Common:4; Rare:73 | ||||
chr10:121927967-121928068 | Rare:34 | ||||
chr10:121928429-121928479 | Rare:17 | ||||
chr10:121928481-121928519 | Rare:6 | ||||
chr10:122112718-122113046 | Common:4; Rare:105 | ||||
chr10:122374518-122374774 | Common:1; Rare:88 | ||||
chr10:122879532-122879659 | Common:2; Rare:36 | ||||
chr10:122954174-122954484 | Rare:111 | ||||
chr10:122980389-122980435 | Common:1; Rare:9 | ||||
chr10:123008791-123009032 | Common:5; Rare:68; Clinvar:4; Clinvar (benign):5 | ||||
chr10:124791756-124791944 | Common:1; Rare:98 | ||||
chr10:124801730-124801827 | Rare:33 | ||||
chr10:125719456-125719727 | Rare:86 |