Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:181088494-181088739 | Common:1; Rare:93 | ||||
chr1:182388768-182389062 | Common:3; Rare:64 | ||||
chr1:182391316-182391480 | Rare:33 | ||||
chr1:182391739-182392078 | Common:4; Rare:125; Clinvar:5; Clinvar (benign):4 | ||||
chr1:182789604-182789778 | Common:2; Rare:53 | ||||
chr1:182839194-182839399 | Common:1; Rare:88 | ||||
chr1:183186025-183186094 | Common:2; Rare:20; Clinvar:2; Clinvar (benign):1 | ||||
chr1:183186112-183186380 | Common:4; Rare:65; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr1:183472248-183472544 | Common:2; Rare:100 | ||||
chr1:183635655-183636114 | Common:5; Rare:128 | ||||
chr1:183653271-183653436 | Common:2; Rare:24 | ||||
chr1:183805007-183805243 | Rare:62 | ||||
chr1:184051681-184051768 | Common:2; Rare:35 | ||||
chr1:184386736-184387193 | Common:4; Rare:127 | ||||
chr1:184754805-184755114 | Common:1; Rare:70 |