Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:288811-289138 | Common:2; Rare:86 | ||||
chr11:308004-308437 | Common:15; Rare:137 | ||||
chr11:320721-320924 | Common:5; Rare:77; Clinvar:1 | ||||
chr11:417278-417487 | Rare:48 | ||||
chr11:420743-421006 | Common:1; Rare:97 | ||||
chr11:421192-421306 | Rare:17 | ||||
chr11:506732-507001 | Common:3; Rare:92 | ||||
chr11:507140-507431 | Common:2; Rare:92 | ||||
chr11:533338-533480 | Rare:58; Clinvar:1; Clinvar (benign):4 | ||||
chr11:537317-537532 | Common:5; Rare:68 | ||||
chr11:560689-561021 | Common:6; Rare:155 | ||||
chr11:576413-576582 | Rare:71 | ||||
chr11:615936-616033 | Common:1; Rare:30 | ||||
chr11:621344-621664 | Common:3; Rare:141 | ||||
chr11:694820-695010 | Rare:113; Clinvar:3; Clinvar (benign):3 |