Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:153963466-153963946 | Common:11; Rare:542 | ||||
chr1:153963983-153964383 | Common:2; Rare:136 | ||||
chr1:153967180-153967544 | Common:5; Rare:364 | ||||
chr1:153967545-153967963 | Common:3; Rare:351 | ||||
chr1:153967984-153969538 | Common:12; Rare:866 | ||||
chr1:153976864-153977309 | Common:4; Rare:510 | ||||
chr1:153977536-153977845 | Rare:226 | ||||
chr1:153977830-153978180 | Rare:110 | ||||
chr1:153984737-153985653 | Common:1; Rare:235 | ||||
chr1:153985614-153986651 | Common:9; Rare:710 | ||||
chr1:153986714-153987114 | Common:8; Rare:152 | ||||
chr1:153990548-153990872 | Common:11; Rare:537 | ||||
chr1:154172810-154173501 | Common:3; Rare:322; Clinvar:5; Clinvar (benign):8; Clinvar (pathogenic):6 | ||||
chr1:154176117-154176370 | Common:1; Rare:65; Clinvar:2; Clinvar (benign):4 | ||||
chr1:154182204-154182610 | Rare:155 |