Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:93074327-93074727 | Common:3; Rare:152 | ||||
chr10:93496369-93496643 | Common:4; Rare:68 | ||||
chr10:93702421-93702744 | Common:5; Rare:111 | ||||
chr10:93893842-93894024 | Common:1; Rare:69 | ||||
chr10:93993970-93994340 | Common:3; Rare:91; Clinvar:4; Clinvar (benign):2 | ||||
chr10:94362849-94363098 | Common:4; Rare:105 | ||||
chr10:94402333-94402574 | Rare:81 | ||||
chr10:94402689-94403298 | Common:7; Rare:331 | ||||
chr10:94545439-94545881 | Common:5; Rare:119 | ||||
chr10:95290974-95291196 | Common:2; Rare:96 | ||||
chr10:95561366-95561613 | Common:4; Rare:77 | ||||
chr10:95656649-95656986 | Rare:91; Clinvar:5 | ||||
chr10:95693858-95694186 | Common:5; Rare:110; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr10:95755997-95756587 | Common:5; Rare:238 | ||||
chr10:95907798-95907960 | Common:3; Rare:54 |