Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:27434027-27434189 | Rare:51 | ||||
chr13:27450113-27450240 | Common:3; Rare:41 | ||||
chr13:27450383-27450643 | Common:4; Rare:103 | ||||
chr13:27620488-27620828 | Common:2; Rare:108 | ||||
chr13:28138102-28138222 | Rare:40 | ||||
chr13:28658919-28659192 | Rare:113; Clinvar (pathogenic):1 | ||||
chr13:28718775-28719123 | Common:1; Rare:92 | ||||
chr13:29850036-29850435 | Common:3; Rare:126 | ||||
chr13:29850562-29850811 | Common:2; Rare:97 | ||||
chr13:30306980-30307197 | Common:5; Rare:51 | ||||
chr13:30307375-30307605 | Common:3; Rare:77 | ||||
chr13:30463529-30463981 | Common:4; Rare:117 | ||||
chr13:30464027-30464381 | Common:3; Rare:97 | ||||
chr13:30465769-30466119 | Common:1; Rare:106 | ||||
chr13:30616957-30617166 | Rare:40 |