Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23558909-23559155 | Common:5; Rare:123 | ||||
chr1:23559157-23559691 | Common:3; Rare:232 | ||||
chr1:23559698-23559715 | Rare:9 | ||||
chr1:23559842-23560077 | Common:1; Rare:71 | ||||
chr1:23691726-23691897 | Common:4; Rare:71; Clinvar:2; Clinvar (benign):3 | ||||
chr1:23778257-23778639 | Common:10; Rare:151 | ||||
chr1:23800723-23800929 | Common:1; Rare:69 | ||||
chr1:23825396-23825539 | Common:2; Rare:48; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:23867926-23867949 | Rare:8 | ||||
chr1:23868255-23868433 | Common:6; Rare:61; Clinvar:2; Clinvar (benign):5 | ||||
chr1:23959035-23959304 | Common:3; Rare:50 | ||||
chr1:23959641-23959916 | Common:2; Rare:73 | ||||
chr1:23960027-23960128 | Rare:37 | ||||
chr1:23980189-23980497 | Rare:79 | ||||
chr1:24112104-24112311 | Rare:58 |