Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:119582196-119582502 | Common:1; Rare:46 | ||||
chr10:119596438-119596544 | Rare:39 | ||||
chr10:119596639-119597302 | Common:4; Rare:165 | ||||
chr10:119651209-119651436 | Common:6; Rare:91; Clinvar:1; Clinvar (benign):4 | ||||
chr10:119651535-119651850 | Common:1; Rare:105; Clinvar:9; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
chr10:119725793-119726199 | Common:3; Rare:137 | ||||
chr10:119818611-119818896 | Rare:100 | ||||
chr10:119819082-119819323 | Common:1; Rare:36 | ||||
chr10:119892536-119892942 | Common:4; Rare:154 | ||||
chr10:120851207-120851514 | Common:6; Rare:110 | ||||
chr10:121927868-121928189 | Common:2; Rare:100 | ||||
chr10:121928429-121928522 | Rare:27 | ||||
chr10:122461952-122462118 | Rare:45; Clinvar:2; Clinvar (pathogenic):1 | ||||
chr10:122879519-122879687 | Common:3; Rare:47 | ||||
chr10:122954015-122954506 | Common:1; Rare:174 |