Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:92243249-92243382 | Rare:25 | ||||
chr10:92291026-92291357 | Common:5; Rare:104 | ||||
chr10:92574018-92574113 | Common:1; Rare:27 | ||||
chr10:92592960-92593224 | Common:3; Rare:73 | ||||
chr10:92848344-92848531 | Rare:73 | ||||
chr10:93702354-93702699 | Common:5; Rare:108 | ||||
chr10:93702900-93703028 | Common:1; Rare:21 | ||||
chr10:93757619-93758083 | Common:1; Rare:76; Clinvar:4; Clinvar (benign):1 | ||||
chr10:94362892-94363034 | Common:3; Rare:58 | ||||
chr10:94402352-94402502 | Rare:43 | ||||
chr10:95561330-95561576 | Common:3; Rare:68 | ||||
chr10:95693869-95694199 | Common:5; Rare:108; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr10:95907756-95907967 | Common:3; Rare:63 | ||||
chr10:95908118-95908233 | Rare:22 | ||||
chr10:96129695-96129732 | Rare:11 |