Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:110007661-110008016 | Rare:108 | ||||
chr10:110304897-110305049 | Common:2; Rare:56 | ||||
chr10:110871558-110871831 | Rare:77 | ||||
chr10:110919359-110919629 | Common:7; Rare:74 | ||||
chr10:112446892-112447284 | Common:3; Rare:97 | ||||
chr10:113854631-113854860 | Common:1; Rare:56 | ||||
chr10:119080757-119080923 | Rare:63 | ||||
chr10:119165648-119165776 | Rare:62; Clinvar (benign):3 | ||||
chr10:119178769-119179013 | Common:3; Rare:86 | ||||
chr10:119818628-119818731 | Rare:37 | ||||
chr10:119892536-119892769 | Common:3; Rare:89 | ||||
chr10:120851207-120851429 | Common:5; Rare:80 | ||||
chr10:121927967-121928068 | Rare:34 | ||||
chr10:121928418-121928535 | Rare:34 | ||||
chr10:122954202-122954464 | Rare:96 |