Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:156213229-156213355 | Common:2; Rare:24 | ||||
chr1:156282756-156282965 | Common:3; Rare:67 | ||||
chr1:156338152-156338583 | Common:2; Rare:157 | ||||
chr1:156572510-156572655 | Rare:55 | ||||
chr1:156591655-156592016 | Common:5; Rare:161; Clinvar (pathogenic):1 | ||||
chr1:156593212-156593553 | Common:1; Rare:80 | ||||
chr1:156601407-156601501 | Common:1; Rare:41 | ||||
chr1:156728368-156728494 | Common:1; Rare:26 | ||||
chr1:156728559-156728899 | Rare:95 | ||||
chr1:156728909-156728957 | Rare:16 | ||||
chr1:156729079-156729103 | Rare:12 | ||||
chr1:156741022-156741419 | Common:2; Rare:104 | ||||
chr1:156750419-156750491 | Rare:15 | ||||
chr1:156751847-156751981 | Rare:39 | ||||
chr1:156752039-156752269 | Common:1; Rare:65 |