Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:110872250-110872622 | Common:1; Rare:125 | ||||
chr10:110919141-110919645 | Common:8; Rare:132; Clinvar:1 | ||||
chr10:112183708-112183852 | Common:3; Rare:55 | ||||
chr10:112376141-112376249 | Rare:14 | ||||
chr10:112446877-112447295 | Common:3; Rare:105 | ||||
chr10:113679751-113679925 | Common:3; Rare:67 | ||||
chr10:113854344-113854885 | Common:1; Rare:123 | ||||
chr10:114526764-114526964 | Common:2; Rare:51 | ||||
chr10:118046713-118047001 | Common:4; Rare:94 | ||||
chr10:118754921-118755305 | Common:1; Rare:122 | ||||
chr10:119080767-119080973 | Common:1; Rare:90 | ||||
chr10:119165650-119165781 | Rare:61; Clinvar (benign):3 | ||||
chr10:119178786-119178902 | Common:2; Rare:52 | ||||
chr10:119892544-119892765 | Common:3; Rare:83 | ||||
chr10:120851311-120851411 | Rare:41 |