Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:110871622-110871960 | Rare:109 | ||||
chr10:110919279-110919645 | Common:7; Rare:97; Clinvar:1 | ||||
chr10:112183739-112183779 | Common:1; Rare:14 | ||||
chr10:112446858-112447280 | Common:3; Rare:107 | ||||
chr10:113854372-113854610 | Rare:45 | ||||
chr10:118046690-118047022 | Common:4; Rare:108 | ||||
chr10:118755004-118755305 | Common:1; Rare:93 | ||||
chr10:119080757-119080923 | Rare:63 | ||||
chr10:119165650-119165776 | Rare:60; Clinvar (benign):3 | ||||
chr10:119178769-119178940 | Common:3; Rare:70 | ||||
chr10:119596944-119597059 | Rare:31 | ||||
chr10:119892544-119892777 | Common:3; Rare:89 | ||||
chr10:122954202-122954506 | Common:1; Rare:112 | ||||
chr10:123008799-123009011 | Common:5; Rare:60; Clinvar:4; Clinvar (benign):5 | ||||
chr10:125719471-125719734 | Common:1; Rare:85 |