Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161258600-161258799 | Common:2; Rare:44 | ||||
chr1:161306129-161306372 | Common:1; Rare:81; Clinvar:5; Clinvar (benign):1 | ||||
chr1:161307449-161307627 | Rare:42 | ||||
chr1:161314180-161314503 | Common:4; Rare:120; Clinvar:10; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
chr1:161523876-161524253 | Common:9; Rare:140 | ||||
chr1:161524391-161524540 | Common:3; Rare:48 | ||||
chr1:161706605-161707313 | Common:5; Rare:141 | ||||
chr1:161725815-161726056 | Common:1; Rare:96 | ||||
chr1:161726106-161726468 | Common:1; Rare:106 | ||||
chr1:161749581-161749949 | Common:1; Rare:129 | ||||
chr1:161749973-161750061 | Rare:34 | ||||
chr1:161750188-161750312 | Rare:36 | ||||
chr1:161766104-161766604 | Common:6; Rare:139; Clinvar (pathogenic):1 | ||||
chr1:161766643-161766680 | Rare:11 | ||||
chr1:162497649-162497935 | Common:3; Rare:82 |