Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:120880683-120880737 | Common:2; Rare:3 | ||||
chr10:120890884-120890909 | Rare:6 | ||||
chr10:121927151-121927284 | Rare:29 | ||||
chr10:121927288-121927315 | Rare:3 | ||||
chr10:122112108-122112164 | Common:1; Rare:6 | ||||
chr10:122114256-122114561 | Common:2; Rare:66 | ||||
chr10:122115451-122115527 | Rare:19 | ||||
chr10:122140558-122140790 | Common:4; Rare:40 | ||||
chr10:122183315-122183589 | Common:2; Rare:38 | ||||
chr10:122310453-122310547 | Common:1; Rare:15 | ||||
chr10:122401095-122401193 | Rare:20 | ||||
chr10:122429043-122429270 | Common:3; Rare:41 | ||||
chr10:122462038-122462119 | Rare:19; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr10:122488597-122489001 | Common:2; Rare:97; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
chr10:122489114-122489399 | Common:1; Rare:51 |