Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:229625938-229626284 | Rare:113 | ||||
chr1:230642435-230642604 | Common:1; Rare:73 | ||||
chr1:230714087-230714333 | Common:3; Rare:49; Clinvar:5; Clinvar (benign):3 | ||||
chr1:230978753-230979144 | Common:2; Rare:154 | ||||
chr1:231241094-231241367 | Common:2; Rare:132; Clinvar:4; Clinvar (benign):2 | ||||
chr1:231337823-231338065 | Common:2; Rare:85 | ||||
chr1:231528466-231528738 | Common:2; Rare:88 | ||||
chr1:232950501-232950676 | Common:1; Rare:60 | ||||
chr1:233613918-233614141 | Common:2; Rare:55 | ||||
chr1:234373347-234373588 | Common:1; Rare:120; Clinvar (benign):4 | ||||
chr1:234373623-234373792 | Rare:62; Clinvar (benign):3 | ||||
chr1:234608029-234608227 | Common:1; Rare:61 | ||||
chr1:234608245-234608433 | Common:1; Rare:73 | ||||
chr1:235128791-235128951 | Rare:60 | ||||
chr1:235328270-235328611 | Common:2; Rare:95 |