Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:120851200-120851450 | Common:5; Rare:96 | ||||
chr10:121598309-121598605 | Common:1; Rare:98; Clinvar:2 | ||||
chr10:121927874-121928200 | Common:2; Rare:102 | ||||
chr10:121928429-121928536 | Rare:28 | ||||
chr10:121974690-121974894 | Common:2; Rare:61 | ||||
chr10:121994557-121994667 | Common:1; Rare:15 | ||||
chr10:122019170-122019848 | Common:5; Rare:115 | ||||
chr10:122112862-122113173 | Common:3; Rare:96 | ||||
chr10:122126866-122127034 | Common:1; Rare:37 | ||||
chr10:122374425-122374784 | Common:2; Rare:113 | ||||
chr10:122375198-122375245 | Rare:12 | ||||
chr10:122879541-122879696 | Common:3; Rare:45 | ||||
chr10:122954185-122954508 | Common:1; Rare:119 | ||||
chr10:123008788-123009028 | Common:5; Rare:66; Clinvar:4; Clinvar (benign):5 | ||||
chr10:124092365-124092510 | Rare:37 |