Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:118754897-118755322 | Common:1; Rare:143 | ||||
chr10:119080757-119080927 | Rare:66 | ||||
chr10:119178790-119179021 | Common:3; Rare:77 | ||||
chr10:119818522-119818731 | Rare:73 | ||||
chr10:119892536-119892769 | Common:3; Rare:89 | ||||
chr10:120851189-120851411 | Common:4; Rare:75 | ||||
chr10:121927945-121928068 | Rare:48 | ||||
chr10:121928438-121928500 | Rare:18 | ||||
chr10:121974741-121974881 | Common:1; Rare:46 | ||||
chr10:122374453-122374768 | Common:1; Rare:101 | ||||
chr10:122879541-122879674 | Common:3; Rare:38 | ||||
chr10:122954185-122954484 | Rare:110 | ||||
chr10:123008791-123009035 | Common:5; Rare:69; Clinvar:4; Clinvar (benign):5 | ||||
chr10:124461733-124461865 | Common:4; Rare:50 | ||||
chr10:124801611-124801854 | Rare:77 |