Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:121928436-121928527 | Rare:25 | ||||
chr10:122112831-122113078 | Common:3; Rare:79 | ||||
chr10:122375187-122375333 | Common:1; Rare:41 | ||||
chr10:122954185-122954476 | Rare:107 | ||||
chr10:123008788-123009011 | Common:5; Rare:60; Clinvar:4; Clinvar (benign):5 | ||||
chr10:124093497-124093681 | Common:2; Rare:32 | ||||
chr10:124791796-124791942 | Common:1; Rare:75 | ||||
chr10:125161005-125161285 | Common:4; Rare:103 | ||||
chr10:125719494-125719744 | Common:1; Rare:86 | ||||
chr10:125823200-125823566 | Common:1; Rare:120; Clinvar:1; Clinvar (benign):1 | ||||
chr10:125896282-125896607 | Common:3; Rare:22 | ||||
chr10:126905312-126905498 | Rare:75 | ||||
chr10:130136344-130136478 | Common:5; Rare:55 | ||||
chr10:132331803-132332178 | Common:16; Rare:120 | ||||
chr10:133308835-133308990 | Rare:72 |