Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:1872109-1872347 | Common:1; Rare:47 | ||||
chr1:7984773-7984960 | Common:2; Rare:56; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr1:8011649-8011762 | Rare:21 | ||||
chr1:8016380-8016492 | Rare:20 | ||||
chr1:8016724-8016886 | Rare:31 | ||||
chr1:8017705-8018019 | Common:1; Rare:44 | ||||
chr1:8019241-8019323 | Common:1; Rare:16 | ||||
chr1:8019365-8019688 | Common:1; Rare:45 | ||||
chr1:8020096-8020598 | Common:2; Rare:82 | ||||
chr1:8021283-8021461 | Rare:32 | ||||
chr1:8025027-8025273 | Common:2; Rare:43 | ||||
chr1:8516067-8516222 | Common:1; Rare:32 | ||||
chr1:8875333-8875624 | Common:1; Rare:61 | ||||
chr1:9687534-9687652 | Common:1; Rare:28 | ||||
chr1:10054014-10054043 | Rare:2 |