Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2646 |
| ensemblid | ENSG00000084734.9 |
| hgncid | 4196 |
| symbol | GCKR |
| name | glucokinase regulator |
| refseq_nuc | NM_001486.4 |
| refseq_prot | NP_001477.2 |
| ensembl_nuc | ENST00000264717.7 |
| ensembl_prot | ENSP00000264717.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 27496839 |
| end | 27523684 |
| strand | + |
| ver | v1.2 |
| region | chr2:27496839-27523684 |
| region5000 | chr2:27491839-27528684 |
| regionname0 | GCKR_chr2_27496839_27523684 |
| regionname5000 | GCKR_chr2_27491839_27528684 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 625 | 208 | 69 | 42 | 57 | 7 | 32 | 38 | GCKR_chr2_27491839_27528684 | GCKR | MPGTK others(620): Show |
chr2 | 27491839 | 27528684 |
| a0002 | 1/0 | 625 | 94 | 9 | 18 | 54 | 5 | 7 | 39 | GCKR_chr2_27491839_27528684 | GCKR | MPGTK others(620): Show |
chr2 | 27491839 | 27528684 |
| a0003 | 0/0 | 625 | 5 | 0 | 0 | 4 | 0 | 1 | 3 | GCKR_chr2_27491839_27528684 | GCKR | MPGTK others(620): Show |
chr2 | 27491839 | 27528684 |
| a0004 | 0/0 | 625 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | GCKR_chr2_27491839_27528684 | GCKR | MPGTK others(620): Show |
chr2 | 27491839 | 27528684 |
| a0005 | 0/0 | 625 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | MPGTK others(620): Show |
chr2 | 27491839 | 27528684 |
| a0006 | 0/0 | 625 | 2 | 0 | 1 | 1 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | MPGTK others(620): Show |
chr2 | 27491839 | 27528684 |
| a0007 | 0/0 | 625 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | MPGTK others(620): Show |
chr2 | 27491839 | 27528684 |
| a0008 | 0/0 | 539 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | MPGTK others(534): Show |
chr2 | 27491839 | 27528684 |
| a0009 | 0/0 | 625 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | MPGTK others(620): Show |
chr2 | 27491839 | 27528684 |
| a0010 | 0/0 | 625 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | MPGTK others(620): Show |
chr2 | 27491839 | 27528684 |
| a0011 | 0/0 | 226 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | MPGTK others(221): Show |
chr2 | 27491839 | 27528684 |
| a0012 | 0/0 | 625 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GCKR_chr2_27491839_27528684 | GCKR | MPGTK others(620): Show |
chr2 | 27491839 | 27528684 |
| a0013 | 0/0 | 625 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GCKR_chr2_27491839_27528684 | GCKR | MPGTK others(620): Show |
chr2 | 27491839 | 27528684 |
| a0014 | 0/0 | 625 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GCKR_chr2_27491839_27528684 | GCKR | MPGTK others(620): Show |
chr2 | 27491839 | 27528684 |
| a0015 | 0/0 | 625 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | MPGTK others(620): Show |
chr2 | 27491839 | 27528684 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1875 | 206 | 68 | 42 | 56 | 7 | 32 | GCKR_chr2_27491839_27528684 | GCKR | ATGCC others(1870): Show |
chr2 | 27491839 | 27528684 | ||
| a0001c0010 | 0/0 | 1875 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | ATGCC others(1870): Show |
chr2 | 27491839 | 27528684 | ||
| a0001c0012 | 0/0 | 1875 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | ATGCC others(1870): Show |
chr2 | 27491839 | 27528684 | ||
| a0002c0002 | 1/0 | 1875 | 93 | 9 | 18 | 54 | 5 | 6 | GCKR_chr2_27491839_27528684 | GCKR | ATGCC others(1870): Show |
chr2 | 27491839 | 27528684 | ||
| a0002c0014 | 0/0 | 1875 | 1 | 0 | 0 | 0 | 0 | 1 | GCKR_chr2_27491839_27528684 | GCKR | ATGCC others(1870): Show |
chr2 | 27491839 | 27528684 | ||
| a0003c0003 | 0/0 | 1875 | 3 | 0 | 0 | 3 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | ATGCC others(1870): Show |
chr2 | 27491839 | 27528684 | ||
| a0003c0008 | 0/0 | 1875 | 2 | 0 | 0 | 1 | 0 | 1 | GCKR_chr2_27491839_27528684 | GCKR | ATGCC others(1870): Show |
chr2 | 27491839 | 27528684 | ||
| a0004c0004 | 0/0 | 1875 | 3 | 0 | 0 | 3 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | ATGCC others(1870): Show |
chr2 | 27491839 | 27528684 | ||
| a0005c0007 | 0/0 | 1875 | 2 | 0 | 2 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | ATGCC others(1870): Show |
chr2 | 27491839 | 27528684 | ||
| a0006c0006 | 0/0 | 1875 | 2 | 0 | 1 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | ATGCC others(1870): Show |
chr2 | 27491839 | 27528684 | ||
| a0007c0005 | 0/0 | 1875 | 2 | 2 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | ATGCC others(1870): Show |
chr2 | 27491839 | 27528684 | ||
| a0008c0017 | 0/0 | 1875 | 1 | 0 | 1 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | ATGCC others(1870): Show |
chr2 | 27491839 | 27528684 | ||
| a0009c0015 | 0/0 | 1875 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | ATGCC others(1870): Show |
chr2 | 27491839 | 27528684 | ||
| a0010c0011 | 0/0 | 1875 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | ATGCC others(1870): Show |
chr2 | 27491839 | 27528684 | ||
| a0011c0018 | 0/0 | 1875 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | ATGCC others(1870): Show |
chr2 | 27491839 | 27528684 | ||
| a0012c0016 | 0/0 | 1875 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | ATGCC others(1870): Show |
chr2 | 27491839 | 27528684 | ||
| a0013c0009 | 0/0 | 1875 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | ATGCC others(1870): Show |
chr2 | 27491839 | 27528684 | ||
| a0014c0013 | 0/0 | 1875 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | ATGCC others(1870): Show |
chr2 | 27491839 | 27528684 | ||
| a0015c0019 | 0/0 | 1875 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | ATGCC others(1870): Show |
chr2 | 27491839 | 27528684 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2189 | 193 | 58 | 39 | 56 | 7 | 32 | GCKR_chr2_27491839_27528684 | GCKR | ATTGT others(2184): Show |
chr2 | 27491839 | 27528684 |
| a0001c0001t0002 | 0/0 | 2189 | 11 | 8 | 3 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | ATTGT others(2184): Show |
chr2 | 27491839 | 27528684 |
| a0001c0001t0003 | 0/0 | 2189 | 2 | 2 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | ATTGT others(2184): Show |
chr2 | 27491839 | 27528684 |
| a0001c0010t0001 | 0/0 | 2189 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | ATTGT others(2184): Show |
chr2 | 27491839 | 27528684 |
| a0001c0012t0001 | 0/0 | 2189 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | ATTGT others(2184): Show |
chr2 | 27491839 | 27528684 |
| a0002c0002t0001 | 1/0 | 2189 | 93 | 9 | 18 | 54 | 5 | 6 | GCKR_chr2_27491839_27528684 | GCKR | ATTGT others(2184): Show |
chr2 | 27491839 | 27528684 |
| a0002c0014t0001 | 0/0 | 2189 | 1 | 0 | 0 | 0 | 0 | 1 | GCKR_chr2_27491839_27528684 | GCKR | ATTGT others(2184): Show |
chr2 | 27491839 | 27528684 |
| a0003c0003t0001 | 0/0 | 2189 | 3 | 0 | 0 | 3 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | ATTGT others(2184): Show |
chr2 | 27491839 | 27528684 |
| a0003c0008t0001 | 0/0 | 2189 | 2 | 0 | 0 | 1 | 0 | 1 | GCKR_chr2_27491839_27528684 | GCKR | ATTGT others(2184): Show |
chr2 | 27491839 | 27528684 |
| a0004c0004t0001 | 0/0 | 2189 | 3 | 0 | 0 | 3 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | ATTGT others(2184): Show |
chr2 | 27491839 | 27528684 |
| a0005c0007t0001 | 0/0 | 2189 | 2 | 0 | 2 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | ATTGT others(2184): Show |
chr2 | 27491839 | 27528684 |
| a0006c0006t0001 | 0/0 | 2189 | 2 | 0 | 1 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | ATTGT others(2184): Show |
chr2 | 27491839 | 27528684 |
| a0007c0005t0001 | 0/0 | 2189 | 2 | 2 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | ATTGT others(2184): Show |
chr2 | 27491839 | 27528684 |
| a0008c0017t0001 | 0/0 | 2189 | 1 | 0 | 1 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | ATTGT others(2184): Show |
chr2 | 27491839 | 27528684 |
| a0009c0015t0001 | 0/0 | 2189 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | ATTGT others(2184): Show |
chr2 | 27491839 | 27528684 |
| a0010c0011t0001 | 0/0 | 2189 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | ATTGT others(2184): Show |
chr2 | 27491839 | 27528684 |
| a0011c0018t0001 | 0/0 | 2189 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | ATTGT others(2184): Show |
chr2 | 27491839 | 27528684 |
| a0012c0016t0001 | 0/0 | 2189 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | ATTGT others(2184): Show |
chr2 | 27491839 | 27528684 |
| a0013c0009t0001 | 0/0 | 2189 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | ATTGT others(2184): Show |
chr2 | 27491839 | 27528684 |
| a0014c0013t0001 | 0/0 | 2189 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | ATTGT others(2184): Show |
chr2 | 27491839 | 27528684 |
| a0015c0019t0001 | 0/0 | 2189 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | ATTGT others(2184): Show |
chr2 | 27491839 | 27528684 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 12 | 0 | 7 | 2 | 0 | 3 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0002 | 0/0 | 12 | 0 | 5 | 3 | 2 | 2 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0008 | 0/0 | 5 | 2 | 2 | 0 | 0 | 1 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0011 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0025 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0070 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0002g0007 | 0/0 | 5 | 2 | 3 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0010t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0001c0012t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0005 | 1/0 | 7 | 0 | 3 | 0 | 1 | 2 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0006 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0002c0014t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0003c0003t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0003c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0003c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0003c0008t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0003c0008t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0004c0004t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0004c0004t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0004c0004t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0005c0007t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0005c0007t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0006c0006t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0006c0006t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0007c0005t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0007c0005t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0008c0017t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0009c0015t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0010c0011t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0011c0018t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0012c0016t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0013c0009t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0014c0013t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| a0015c0019t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0080 | EUR | GBR | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | FIN | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0204 | EUR | FIN | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0206 | EUR | FIN | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0095 | EAS | CHS | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG00408 | hp2 | a0003 | c0003 | t0001 | g0127 | EAS | CHS | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | CHS | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0113 | EAS | CHS | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0106 | EAS | CHS | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | CHS | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0140 | EAS | CHS | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CHS | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0179 | AMR | PUR | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | CHS | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0035 | AMR | PUR | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0168 | AMR | PUR | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0034 | AMR | PUR | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0177 | AMR | PUR | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0110 | AMR | PUR | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0034 | AMR | PUR | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01168 | hp1 | a0005 | c0007 | t0001 | g0141 | AMR | PUR | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01169 | hp1 | a0005 | c0007 | t0001 | g0142 | AMR | PUR | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01175 | hp1 | a0006 | c0006 | t0001 | g0107 | AMR | PUR | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0176 | AMR | PUR | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | CLM | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0035 | AMR | CLM | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01358 | hp1 | a0008 | c0017 | t0001 | g0197 | AMR | CLM | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0154 | AMR | CLM | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0155 | AMR | CLM | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0073 | EUR | IBS | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0149 | EUR | IBS | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01891 | hp2 | a0007 | c0005 | t0001 | g0040 | AFR | ACB | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0049 | AMR | PEL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0039 | AMR | PEL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02027 | hp2 | a0009 | c0015 | t0001 | g0004 | EAS | KHV | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02040 | hp1 | a0006 | c0006 | t0001 | g0151 | EAS | KHV | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0152 | EAS | KHV | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0109 | EAS | KHV | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02129 | hp1 | a0001 | c0010 | t0001 | g0001 | EAS | KHV | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | KHV | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02145 | hp2 | a0010 | c0011 | t0001 | g0201 | AFR | ACB | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CDX | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0101 | EAS | CDX | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CDX | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0158 | EAS | KHV | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02523 | hp2 | a0011 | c0018 | t0001 | g0160 | EAS | KHV | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0091 | AFR | GWD | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | GWD | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0038 | AFR | GWD | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0146 | AFR | GWD | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0170 | AFR | ESN | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0187 | AFR | GWD | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | MSL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0038 | AFR | ESN | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ESN | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0036 | AFR | ESN | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | MSL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | MSL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | MSL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03453 | hp2 | a0001 | c0012 | t0001 | g0196 | AFR | MSL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | MSL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03540 | hp1 | a0007 | c0005 | t0001 | g0194 | AFR | GWD | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0182 | SAS | PJL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0148 | SAS | PJL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03669 | hp2 | a0002 | c0014 | t0001 | g0153 | SAS | PJL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | STU | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | STU | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0039 | SAS | PJL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0183 | SAS | PJL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0005 | SAS | BEB | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | BEB | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0005 | SAS | BEB | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | BEB | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | BEB | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG04199 | hp1 | a0003 | c0008 | t0001 | g0031 | SAS | STU | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | STU | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CHB | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0108 | EAS | CHB | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | YRI | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | YRI | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18944 | hp2 | a0012 | c0016 | t0001 | g0037 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18948 | hp2 | a0003 | c0008 | t0001 | g0002 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0139 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18972 | hp2 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18975 | hp2 | a0013 | c0009 | t0001 | g0009 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18982 | hp2 | a0004 | c0004 | t0001 | g0027 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18985 | hp1 | a0004 | c0004 | t0001 | g0067 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18985 | hp2 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA19000 | hp2 | a0004 | c0004 | t0001 | g0001 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0150 | AFR | LWK | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0186 | AFR | LWK | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | LWK | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | LWK | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA19062 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0103 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0205 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA19088 | hp1 | a0014 | c0013 | t0001 | g0024 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA19091 | hp1 | a0003 | c0003 | t0001 | g0115 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | YRI | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0036 | AFR | YRI | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ASW | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ASW | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0178 | EUR | TSI | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0111 | EUR | TSI | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0138 | EUR | TSI | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0005 | EUR | TSI | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | ACB | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0042 | AFR | ACB | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | MSL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | USA | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | USA | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | USA | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA20300 | hp2 | a0015 | c0019 | t0001 | g0175 | AFR | USA | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0041 | AFR | LWK | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | LWK | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0070 | REF | REF | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0005 | REF | REF | GCKR_chr2_27491839_27528684 | GCKR | chr2 | 27491839 | 27528684 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:27496930 | A | G | 1 | a0015 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.26A>G | p.His9Arg | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 1/19 | 92/2189 | 26/1878 | 9/625 | chr2 | 27496930 | |||
| chr2:27497331 | G | A | 1 | a0013 | 1 | NA18975.hp2 | missense_variant | MODERATE | c.148G>A | p.Val50Ile | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 2/19 | 214/2189 | 148/1878 | 50/625 | chr2 | 27497331 | |||
| chr2:27497575 | A | G | 1 | a0003 | 5 | HG00408.hp2 HG04199.hp1 NA18948.hp2 others(2): Show |
missense_variant | MODERATE | c.230A>G | p.Glu77Gly | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 3/19 | 296/2189 | 230/1878 | 77/625 | chr2 | 27497575 | |||
| chr2:27498276 | G | A | 1 | a0004 | 3 | NA18982.hp2 NA18985.hp1 NA19000.hp2 |
missense_variant | MODERATE | c.307G>A | p.Val103Met | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 4/19 | 373/2189 | 307/1878 | 103/625 | chr2 | 27498276 | |||
| chr2:27503548 | C | T | 1 | a0011 | 1 | HG02523.hp2 | stop_gained | HIGH | c.679C>T | p.Arg227* | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 9/19 | 745/2189 | 679/1878 | 227/625 | chr2 | 27503548 | |||
| chr2:27503570 | A | C | 1 | a0008 | 1 | HG01358.hp1 | missense_variant | MODERATE | c.701A>C | p.Gln234Pro | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 9/19 | 767/2189 | 701/1878 | 234/625 | chr2 | 27503570 | |||
| chr2:27506530 | T | G | 1 | a0007 | 2 | HG01891.hp2 HG03540.hp1 |
missense_variant | MODERATE | c.919T>G | p.Tyr307Asp | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 11/19 | 985/2189 | 919/1878 | 307/625 | chr2 | 27506530 | |||
| chr2:27508073 | T | C | 10 | a0001 a0003 a0004 others(7): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
missense_variant&splice_region_variant | MODERATE | c.1337T>C | p.Leu446Pro | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 15/19 | 1403/2189 | 1337/1878 | 446/625 | chr2 | 27508073 | |||
| chr2:27518804 | T | A | 1 | a0010 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.1439T>A | p.Leu480Gln | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 17/19 | 1505/2189 | 1439/1878 | 480/625 | chr2 | 27518804 | |||
| chr2:27518825 | A | G | 1 | a0012 | 1 | NA18944.hp2 | missense_variant | MODERATE | c.1460A>G | p.Asn487Ser | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 17/19 | 1526/2189 | 1460/1878 | 487/625 | chr2 | 27518825 | |||
| chr2:27518876 | A | G | 1 | a0005 | 2 | HG01168.hp1 HG01169.hp1 |
missense_variant | MODERATE | c.1511A>G | p.His504Arg | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 17/19 | 1577/2189 | 1511/1878 | 504/625 | chr2 | 27518876 | |||
| chr2:27522505 | C | T | 1 | a0008 | 1 | HG01358.hp1 | stop_gained | HIGH | c.1618C>T | p.Arg540* | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 18/19 | 1684/2189 | 1618/1878 | 540/625 | chr2 | 27522505 | |||
| chr2:27522506 | G | A | 1 | a0006 | 2 | HG01175.hp1 HG02040.hp1 |
missense_variant | MODERATE | c.1619G>A | p.Arg540Gln | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 18/19 | 1685/2189 | 1619/1878 | 540/625 | chr2 | 27522506 | |||
| chr2:27522589 | G | A | 1 | a0009 | 1 | HG02027.hp2 | missense_variant | MODERATE | c.1702G>A | p.Glu568Lys | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 18/19 | 1768/2189 | 1702/1878 | 568/625 | chr2 | 27522589 | |||
| chr2:27523429 | A | G | 1 | a0014 | 1 | NA19088.hp1 | missense_variant | MODERATE | c.1868A>G | p.Asp623Gly | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 19/19 | 1934/2189 | 1868/1878 | 623/625 | chr2 | 27523429 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:27497372 | G | A | 1 | a0003c0003 | 3 | HG00408.hp2 NA19062.hp1 NA19091.hp1 |
synonymous_variant | LOW | c.189G>A | p.Glu63Glu | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 2/19 | 255/2189 | 189/1878 | 63/625 | chr2 | 27497372 | |||
| chr2:27498323 | G | A | 1 | a0001c0010 | 1 | HG02129.hp1 | splice_region_variant&synonymous_variant | LOW | c.354G>A | p.Ser118Ser | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 4/19 | 420/2189 | 354/1878 | 118/625 | chr2 | 27498323 | |||
| chr2:27522468 | T | C | 1 | a0002c0014 | 1 | HG03669.hp2 | synonymous_variant | LOW | c.1581T>C | p.Ser527Ser | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 18/19 | 1647/2189 | 1581/1878 | 527/625 | chr2 | 27522468 | |||
| chr2:27523400 | T | C | 1 | a0001c0012 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.1839T>C | p.Thr613Thr | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 19/19 | 1905/2189 | 1839/1878 | 613/625 | chr2 | 27523400 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:27496896 | C | T | 1 | a0001c0001t0003 | 2 | HG03041.hp2 NA19030.hp2 |
5_prime_UTR_variant | MODIFIER | c.-9C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 1/19 | 9 | chr2 | 27496896 | ||||||
| chr2:27523543 | G | A | 2 | a0001c0001t0002 a0001c0001t0003 |
13 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*104G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 19/19 | 104 | chr2 | 27523543 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:27497406 | AAG | A | 10 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(7): Show |
13 | HG00733.hp1 HG01167.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.216+9_216+10delGA | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr2 | 27497406 | ||||||
| chr2:27497495 | C | G | 3 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 |
3 | HG02257.hp2 HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.217-67C>G | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 2/18 | chr2 | 27497495 | |||||||
| chr2:27497518 | C | T | 12 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(9): Show |
18 | HG01074.hp2 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.217-44C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 2/18 | chr2 | 27497518 | |||||||
| chr2:27497675 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.285+45C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 3/18 | chr2 | 27497675 | |||||||
| chr2:27497888 | C | T | 1 | a0002c0002t0001g0205 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.285+258C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 3/18 | chr2 | 27497888 | |||||||
| chr2:27498016 | G | T | 1 | a0002c0002t0001g0204 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.286-239G>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 3/18 | chr2 | 27498016 | |||||||
| chr2:27498189 | A | G | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0010c0011t0001g0201 |
3 | HG02145.hp2 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.286-66A>G | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 3/18 | chr2 | 27498189 | |||||||
| chr2:27498197 | A | C | 4 | a0001c0001t0001g0011 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
7 | HG00738.hp2 HG02451.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.286-58A>C | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 3/18 | chr2 | 27498197 | |||||||
| chr2:27498324 | G | A | 1 | a0001c0001t0001g0048 | 1 | NA18967.hp1 | splice_donor_variant&intron_variant | HIGH | c.354+1G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 4/18 | chr2 | 27498324 | |||||||
| chr2:27498455 | C | G | 17 | a0001c0001t0001g0040 a0001c0001t0001g0188 a0001c0001t0001g0189 others(14): Show |
17 | HG01358.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.354+132C>G | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 4/18 | chr2 | 27498455 | |||||||
| chr2:27498464 | A | C | 1 | a0008c0017t0001g0197 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.354+141A>C | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 4/18 | chr2 | 27498464 | |||||||
| chr2:27498613 | G | C | 1 | a0001c0001t0001g0017 | 3 | HG02735.hp2 HG03017.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.355-111G>C | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 4/18 | chr2 | 27498613 | |||||||
| chr2:27498803 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG01884.hp1 | splice_region_variant&intron_variant | LOW | c.428+6C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 5/18 | chr2 | 27498803 | |||||||
| chr2:27498917 | T | A | 1 | a0008c0017t0001g0197 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.428+120T>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 5/18 | chr2 | 27498917 | |||||||
| chr2:27498966 | T | C | 1 | a0002c0002t0001g0049 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.428+169T>C | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 5/18 | chr2 | 27498966 | |||||||
| chr2:27499104 | T | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(90): Show |
128 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.429-38T>C | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 5/18 | chr2 | 27499104 | |||||||
| chr2:27499313 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.496-84T>C | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 6/18 | chr2 | 27499313 | |||||||
| chr2:27499320 | C | A | 2 | a0002c0002t0001g0041 a0002c0002t0001g0042 |
2 | HG02559.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.496-77C>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 6/18 | chr2 | 27499320 | |||||||
| chr2:27499549 | G | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(76): Show |
114 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.549+99G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 7/18 | chr2 | 27499549 | |||||||
| chr2:27499753 | G | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG00733.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.549+303G>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 7/18 | chr2 | 27499753 | |||||||
| chr2:27499882 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.549+432C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 7/18 | chr2 | 27499882 | |||||||
| chr2:27499988 | C | G | 3 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 |
3 | HG01891.hp1 HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.549+538C>G | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 7/18 | chr2 | 27499988 | |||||||
| chr2:27501377 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.644+148A>G | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 8/18 | chr2 | 27501377 | |||||||
| chr2:27501392 | T | G | 1 | a0002c0002t0001g0094 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.644+163T>G | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 8/18 | chr2 | 27501392 | |||||||
| chr2:27501402 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.644+173T>C | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 8/18 | chr2 | 27501402 | |||||||
| chr2:27501668 | C | G | 3 | a0002c0002t0001g0039 a0002c0002t0001g0182 a0002c0002t0001g0183 |
4 | HG02004.hp2 HG03654.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.644+439C>G | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 8/18 | chr2 | 27501668 | |||||||
| chr2:27501708 | G | A | 1 | a0002c0002t0001g0095 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.644+479G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 8/18 | chr2 | 27501708 | |||||||
| chr2:27501821 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.644+592T>C | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 8/18 | chr2 | 27501821 | |||||||
| chr2:27502205 | G | A | 2 | a0002c0002t0001g0096 a0002c0002t0001g0097 |
2 | NA18948.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.644+976G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 8/18 | chr2 | 27502205 | |||||||
| chr2:27502500 | G | T | 1 | a0001c0001t0001g0181 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.645-1014G>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 8/18 | chr2 | 27502500 | |||||||
| chr2:27502525 | C | G | 1 | a0001c0001t0001g0180 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.645-989C>G | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 8/18 | chr2 | 27502525 | |||||||
| chr2:27502541 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.645-973G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 8/18 | chr2 | 27502541 | |||||||
| chr2:27502542 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.645-972C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 8/18 | chr2 | 27502542 | |||||||
| chr2:27502566 | C | T | 1 | a0008c0017t0001g0197 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.645-948C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 8/18 | chr2 | 27502566 | |||||||
| chr2:27502578 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.645-936C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 8/18 | chr2 | 27502578 | |||||||
| chr2:27502705 | C | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(79): Show |
117 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.645-809C>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 8/18 | chr2 | 27502705 | |||||||
| chr2:27502894 | C | T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(72): Show |
107 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.645-620C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 8/18 | chr2 | 27502894 | |||||||
| chr2:27503223 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.645-291G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 8/18 | chr2 | 27503223 | |||||||
| chr2:27503239 | AAGGAGCA others(4): Show |
A | 1 | a0002c0002t0001g0099 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.645-273_645-263del others(11): Show |
GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr2 | 27503239 | ||||||
| chr2:27503743 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.750+124T>C | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 9/18 | chr2 | 27503743 | |||||||
| chr2:27503763 | C | G | 1 | a0002c0002t0001g0095 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.750+144C>G | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 9/18 | chr2 | 27503763 | |||||||
| chr2:27503978 | A | C | 4 | a0002c0002t0001g0176 a0002c0002t0001g0177 a0002c0002t0001g0178 others(1): Show |
4 | HG00642.hp1 HG01070.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.750+359A>C | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 9/18 | chr2 | 27503978 | |||||||
| chr2:27504267 | C | T | 1 | a0015c0019t0001g0175 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.750+648C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 9/18 | chr2 | 27504267 | |||||||
| chr2:27504358 | CT | C | 5 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0046 others(2): Show |
6 | HG00733.hp1 HG02155.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.750+755delT | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr2 | 27504358 | ||||||
| chr2:27504447 | C | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(75): Show |
113 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.750+828C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 9/18 | chr2 | 27504447 | |||||||
| chr2:27504450 | C | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.750+831C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 9/18 | chr2 | 27504450 | |||||||
| chr2:27504555 | C | G | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG00733.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.750+936C>G | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 9/18 | chr2 | 27504555 | |||||||
| chr2:27504809 | G | C | 1 | a0001c0001t0001g0018 | 3 | HG02622.hp1 HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.751-909G>C | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 9/18 | chr2 | 27504809 | |||||||
| chr2:27504896 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.751-822C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 9/18 | chr2 | 27504896 | |||||||
| chr2:27504933 | T | C | 1 | a0001c0001t0001g0102 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.751-785T>C | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 9/18 | chr2 | 27504933 | |||||||
| chr2:27505125 | C | CA | 73 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(70): Show |
102 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.751-571dupA | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr2 | 27505125 | ||||||
| chr2:27505125 | C | CAA | 8 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0057 others(5): Show |
9 | HG01981.hp2 HG02965.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.751-572_751-571dup others(2): Show |
GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr2 | 27505125 | ||||||
| chr2:27505125 | CA | C | 17 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(14): Show |
24 | HG01074.hp2 HG01099.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.751-571delA | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr2 | 27505125 | ||||||
| chr2:27505192 | C | G | 1 | a0001c0001t0001g0089 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.751-526C>G | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 9/18 | chr2 | 27505192 | |||||||
| chr2:27505218 | A | C | 2 | a0002c0002t0001g0110 a0002c0002t0001g0168 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.751-500A>C | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 9/18 | chr2 | 27505218 | |||||||
| chr2:27505224 | A | G | 5 | a0001c0001t0001g0050 a0002c0002t0001g0037 a0002c0002t0001g0167 others(2): Show |
5 | HG01081.hp2 NA18944.hp2 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.751-494A>G | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 9/18 | chr2 | 27505224 | |||||||
| chr2:27505312 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.751-406C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 9/18 | chr2 | 27505312 | |||||||
| chr2:27505403 | C | CA | 9 | a0001c0001t0001g0029 a0001c0001t0001g0040 a0001c0001t0001g0104 others(6): Show |
10 | HG01891.hp2 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.751-299dupA | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr2 | 27505403 | ||||||
| chr2:27505403 | C | CAA | 18 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(15): Show |
25 | HG01074.hp2 HG01099.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.751-300_751-299dup others(2): Show |
GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr2 | 27505403 | ||||||
| chr2:27505435 | CAAAGA | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0043 |
3 | HG02257.hp1 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.751-273_751-269del others(5): Show |
GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr2 | 27505435 | ||||||
| chr2:27505637 | G | A | 1 | a0002c0002t0001g0111 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.751-81G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 9/18 | chr2 | 27505637 | |||||||
| chr2:27505716 | A | G | 1 | a0001c0001t0001g0166 | 1 | NA18993.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.751-2A>G | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 9/18 | chr2 | 27505716 | |||||||
| chr2:27505875 | C | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0174 |
2 | HG01109.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.869+39C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 10/18 | chr2 | 27505875 | |||||||
| chr2:27505888 | G | T | 1 | a0001c0001t0001g0165 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.869+52G>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 10/18 | chr2 | 27505888 | |||||||
| chr2:27505910 | C | G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(65): Show |
100 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.869+74C>G | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 10/18 | chr2 | 27505910 | |||||||
| chr2:27505945 | G | A | 1 | a0001c0012t0001g0196 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.869+109G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 10/18 | chr2 | 27505945 | |||||||
| chr2:27505960 | T | C | 6 | a0002c0002t0001g0003 a0002c0002t0001g0099 a0002c0002t0001g0100 others(3): Show |
12 | HG00558.hp1 HG00609.hp1 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.869+124T>C | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 10/18 | chr2 | 27505960 | |||||||
| chr2:27506019 | C | A | 1 | a0002c0002t0001g0095 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.869+183C>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 10/18 | chr2 | 27506019 | |||||||
| chr2:27506189 | C | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.870-292C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 10/18 | chr2 | 27506189 | |||||||
| chr2:27506326 | C | T | 1 | a0001c0001t0001g0028 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.870-155C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 10/18 | chr2 | 27506326 | |||||||
| chr2:27506409 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.870-72C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 10/18 | chr2 | 27506409 | |||||||
| chr2:27506410 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0180 |
2 | HG01261.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.870-71G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 10/18 | chr2 | 27506410 | |||||||
| chr2:27506456 | T | C | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG00733.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.870-25T>C | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 10/18 | chr2 | 27506456 | |||||||
| chr2:27506613 | G | A | 68 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(65): Show |
100 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.968+34G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 11/18 | chr2 | 27506613 | |||||||
| chr2:27506665 | G | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0174 |
2 | HG01109.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.968+86G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 11/18 | chr2 | 27506665 | |||||||
| chr2:27507138 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1067-97A>G | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 12/18 | chr2 | 27507138 | |||||||
| chr2:27507182 | T | G | 1 | a0015c0019t0001g0175 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1067-53T>G | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 12/18 | chr2 | 27507182 | |||||||
| chr2:27507207 | C | T | 1 | a0001c0012t0001g0196 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1067-28C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 12/18 | chr2 | 27507207 | |||||||
| chr2:27507384 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1143+73C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 13/18 | chr2 | 27507384 | |||||||
| chr2:27507528 | C | T | 1 | a0001c0001t0001g0014 | 3 | HG02280.hp2 HG02451.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1144-153C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 13/18 | chr2 | 27507528 | |||||||
| chr2:27507883 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1241-94C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 14/18 | chr2 | 27507883 | |||||||
| chr2:27507950 | G | A | 8 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0191 others(5): Show |
12 | HG01884.hp1 HG01981.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1241-27G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 14/18 | chr2 | 27507950 | |||||||
| chr2:27508094 | AAAGG | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0002g0045 |
4 | HG06807.hp1 NA18906.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1338+21_1338+24del others(4): Show |
GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 15/18 | chr2 | 27508094 | |||||||
| chr2:27508124 | C | A | 1 | a0001c0001t0001g0218 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1339-44C>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 15/18 | chr2 | 27508124 | |||||||
| chr2:27508301 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0002g0045 |
4 | HG06807.hp1 NA18906.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1422+50G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27508301 | |||||||
| chr2:27508309 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1422+58A>G | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27508309 | |||||||
| chr2:27508345 | T | C | 50 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(47): Show |
71 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.1422+94T>C | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27508345 | |||||||
| chr2:27508459 | G | T | 1 | a0002c0002t0001g0161 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1422+208G>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27508459 | |||||||
| chr2:27508509 | C | T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(67): Show |
103 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1422+258C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27508509 | |||||||
| chr2:27508666 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1422+415C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27508666 | |||||||
| chr2:27508726 | T | C | 4 | a0002c0002t0001g0033 a0002c0002t0001g0139 a0002c0002t0001g0140 others(1): Show |
5 | HG00609.hp2 NA18959.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.1422+475T>C | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27508726 | |||||||
| chr2:27508872 | C | CT | 6 | a0001c0001t0001g0180 a0001c0001t0001g0199 a0001c0001t0001g0202 others(3): Show |
6 | HG02647.hp2 HG03209.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1422+633dupT | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 27508872 | ||||||
| chr2:27508872 | C | CTT | 60 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(57): Show |
83 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.1422+632_1422+633d others(4): Show |
GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 27508872 | ||||||
| chr2:27508916 | A | G | 1 | a0008c0017t0001g0197 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1422+665A>G | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27508916 | |||||||
| chr2:27509288 | C | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG00733.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.1422+1037C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27509288 | |||||||
| chr2:27509531 | C | T | 1 | a0002c0002t0001g0159 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1422+1280C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27509531 | |||||||
| chr2:27509703 | A | AT | 56 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(53): Show |
77 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.1422+1458dupT | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 27509703 | ||||||
| chr2:27509775 | C | CA | 20 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(17): Show |
27 | HG01074.hp2 HG01099.hp1 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.1422+1540dupA | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 27509775 | ||||||
| chr2:27509775 | C | CAA | 65 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(62): Show |
96 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.1422+1539_1422+154 others(6): Show |
GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 27509775 | ||||||
| chr2:27509775 | CA | C | 67 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(64): Show |
89 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.1422+1540delA | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 27509775 | ||||||
| chr2:27509944 | AATTATT | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0002g0045 |
4 | HG06807.hp1 NA18906.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1422+1706_1422+171 others(10): Show |
GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 27509944 | ||||||
| chr2:27509977 | C | T | 1 | a0008c0017t0001g0197 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1422+1726C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27509977 | |||||||
| chr2:27509978 | G | A | 3 | a0002c0002t0001g0176 a0005c0007t0001g0141 a0005c0007t0001g0142 |
3 | HG01168.hp1 HG01169.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1422+1727G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27509978 | |||||||
| chr2:27510012 | AT | A | 6 | a0001c0001t0001g0064 a0001c0001t0001g0082 a0001c0001t0001g0165 others(3): Show |
6 | HG01069.hp1 HG01168.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1422+1775delT | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 27510012 | ||||||
| chr2:27510158 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1422+1907G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27510158 | |||||||
| chr2:27510178 | T | C | 1 | a0001c0001t0001g0199 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1422+1927T>C | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27510178 | |||||||
| chr2:27510255 | C | T | 1 | a0008c0017t0001g0197 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1422+2004C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27510255 | |||||||
| chr2:27510279 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1422+2028G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27510279 | |||||||
| chr2:27510401 | A | G | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1422+2150A>G | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27510401 | |||||||
| chr2:27510489 | C | T | 1 | a0001c0012t0001g0196 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1422+2238C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27510489 | |||||||
| chr2:27510550 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1422+2299C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27510550 | |||||||
| chr2:27510585 | G | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(70): Show |
107 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.1422+2334G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27510585 | |||||||
| chr2:27510627 | G | C | 1 | a0002c0002t0001g0095 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1422+2376G>C | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27510627 | |||||||
| chr2:27510657 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1422+2406G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27510657 | |||||||
| chr2:27510663 | C | T | 1 | a0002c0002t0001g0161 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1422+2412C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27510663 | |||||||
| chr2:27510673 | G | A | 3 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0171 |
3 | NA18942.hp2 NA18984.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1422+2422G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27510673 | |||||||
| chr2:27510752 | A | T | 1 | a0002c0002t0001g0161 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1422+2501A>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27510752 | |||||||
| chr2:27510765 | G | T | 2 | a0001c0001t0003g0186 a0001c0001t0003g0187 |
2 | HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1422+2514G>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27510765 | |||||||
| chr2:27510797 | C | T | 1 | a0002c0002t0001g0156 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1422+2546C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27510797 | |||||||
| chr2:27511020 | TTTTATTT others(5): Show |
T | 13 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0094 others(10): Show |
24 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.1422+2783_1422+279 others(16): Show |
GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 27511020 | ||||||
| chr2:27511041 | T | A | 1 | a0002c0002t0001g0145 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1422+2790T>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27511041 | |||||||
| chr2:27511087 | G | A | 1 | a0001c0012t0001g0196 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1422+2836G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27511087 | |||||||
| chr2:27511120 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1422+2869C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27511120 | |||||||
| chr2:27511591 | C | T | 1 | a0008c0017t0001g0197 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1422+3340C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27511591 | |||||||
| chr2:27511617 | G | A | 1 | a0001c0001t0001g0017 | 3 | HG02735.hp2 HG03017.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1422+3366G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27511617 | |||||||
| chr2:27511681 | T | C | 1 | a0008c0017t0001g0197 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1422+3430T>C | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27511681 | |||||||
| chr2:27511776 | T | C | 1 | a0002c0002t0001g0157 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1422+3525T>C | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27511776 | |||||||
| chr2:27511844 | C | T | 1 | a0008c0017t0001g0197 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1422+3593C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27511844 | |||||||
| chr2:27512025 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0002g0045 |
4 | HG06807.hp1 NA18906.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1422+3774G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27512025 | |||||||
| chr2:27512105 | G | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(142): Show |
202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.1422+3854G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27512105 | |||||||
| chr2:27512126 | C | A | 12 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(9): Show |
14 | HG00733.hp1 HG01109.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.1422+3875C>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27512126 | |||||||
| chr2:27512154 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1422+3903G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27512154 | |||||||
| chr2:27512166 | G | A | 5 | a0002c0002t0001g0035 a0002c0002t0001g0177 a0002c0002t0001g0178 others(2): Show |
6 | HG00323.hp1 HG00642.hp1 HG00733.hp2 others(3): Show |
intron_variant | MODIFIER | c.1422+3915G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27512166 | |||||||
| chr2:27512235 | C | CA | 93 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(90): Show |
131 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.1422+4005dupA | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 27512235 | ||||||
| chr2:27512235 | C | CAA | 42 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0016 others(39): Show |
61 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.1422+4004_1422+400 others(6): Show |
GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 27512235 | ||||||
| chr2:27512235 | C | CAAA | 15 | a0001c0001t0001g0015 a0001c0001t0001g0040 a0001c0001t0001g0048 others(12): Show |
17 | HG00544.hp1 HG00621.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.1422+4003_1422+400 others(7): Show |
GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 27512235 | ||||||
| chr2:27512392 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1422+4141G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27512392 | |||||||
| chr2:27512428 | G | A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0124 |
2 | HG02040.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.1422+4177G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27512428 | |||||||
| chr2:27512534 | CA | C | 31 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(28): Show |
40 | HG00733.hp1 HG01074.hp2 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.1422+4299delA | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 27512534 | ||||||
| chr2:27512593 | G | C | 1 | a0001c0001t0001g0104 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1422+4342G>C | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27512593 | |||||||
| chr2:27512999 | G | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0120 a0001c0001t0001g0125 |
4 | NA18963.hp2 NA18978.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.1422+4748G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27512999 | |||||||
| chr2:27513083 | T | G | 1 | a0001c0001t0001g0207 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1422+4832T>G | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27513083 | |||||||
| chr2:27513482 | C | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0002g0045 |
4 | HG06807.hp1 NA18906.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1422+5231C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27513482 | |||||||
| chr2:27513522 | C | T | 2 | a0001c0001t0001g0080 a0001c0001t0001g0206 |
2 | HG00099.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.1423-5266C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27513522 | |||||||
| chr2:27513527 | C | CA | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(138): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.1423-5247dupA | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 27513527 | ||||||
| chr2:27513909 | T | TTG | 13 | a0001c0001t0001g0027 a0001c0001t0001g0052 a0001c0001t0001g0053 others(10): Show |
13 | HG01433.hp1 HG01496.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1423-4841_1423-484 others(6): Show |
GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 27513909 | ||||||
| chr2:27513909 | T | TTGTG | 3 | a0002c0002t0001g0042 a0002c0002t0001g0112 a0008c0017t0001g0197 |
3 | HG01358.hp1 HG02559.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1423-4843_1423-484 others(8): Show |
GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 27513909 | ||||||
| chr2:27513909 | TTG | T | 8 | a0001c0001t0001g0014 a0001c0001t0001g0024 a0001c0001t0001g0174 others(5): Show |
10 | HG00408.hp1 HG01109.hp2 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.1423-4841_1423-484 others(6): Show |
GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 27513909 | ||||||
| chr2:27513909 | TTGTG | T | 10 | a0001c0001t0001g0090 a0001c0001t0001g0123 a0001c0001t0001g0212 others(7): Show |
11 | HG00597.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1423-4843_1423-484 others(8): Show |
GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 27513909 | ||||||
| chr2:27513909 | TTGTGTG | T | 16 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0046 others(13): Show |
17 | HG00733.hp1 HG01167.hp1 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.1423-4845_1423-484 others(10): Show |
GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 27513909 | ||||||
| chr2:27513909 | TTGTGTGT others(1): Show |
T | 59 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(56): Show |
87 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1423-4847_1423-484 others(12): Show |
GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 27513909 | ||||||
| chr2:27513909 | TTGTGTGT others(3): Show |
T | 6 | a0001c0001t0001g0021 a0001c0001t0001g0031 a0001c0001t0001g0093 others(3): Show |
7 | HG01361.hp1 HG01433.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1423-4849_1423-484 others(14): Show |
GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 27513909 | ||||||
| chr2:27513947 | G | T | 1 | a0001c0001t0001g0185 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1423-4841G>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27513947 | |||||||
| chr2:27514253 | G | A | 1 | a0002c0002t0001g0146 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1423-4535G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27514253 | |||||||
| chr2:27514253 | G | GTATA | 4 | a0001c0001t0001g0093 a0001c0001t0001g0174 a0001c0001t0001g0189 others(1): Show |
4 | HG01109.hp2 HG02109.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1423-4524_1423-452 others(8): Show |
GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 27514253 | ||||||
| chr2:27514263 | A | G | 3 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0002g0045 |
4 | HG06807.hp1 NA18906.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1423-4525A>G | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27514263 | |||||||
| chr2:27514266 | T | C | 1 | a0001c0001t0001g0199 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1423-4522T>C | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27514266 | |||||||
| chr2:27514314 | A | G | 74 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(71): Show |
108 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.1423-4474A>G | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27514314 | |||||||
| chr2:27514516 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1423-4272A>G | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27514516 | |||||||
| chr2:27514687 | T | A | 1 | a0001c0001t0001g0192 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1423-4101T>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27514687 | |||||||
| chr2:27515033 | A | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(70): Show |
107 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.1423-3755A>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27515033 | |||||||
| chr2:27515229 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1423-3559C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27515229 | |||||||
| chr2:27515339 | G | A | 1 | a0003c0003t0001g0127 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1423-3449G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27515339 | |||||||
| chr2:27515412 | A | T | 1 | a0001c0001t0001g0058 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1423-3376A>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27515412 | |||||||
| chr2:27515420 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0198 |
5 | HG00738.hp2 HG02717.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1423-3368C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27515420 | |||||||
| chr2:27515438 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0002g0045 |
4 | HG06807.hp1 NA18906.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1423-3350G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27515438 | |||||||
| chr2:27515648 | A | T | 1 | a0001c0012t0001g0196 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1423-3140A>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27515648 | |||||||
| chr2:27515733 | A | T | 1 | a0001c0012t0001g0196 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1423-3055A>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27515733 | |||||||
| chr2:27515745 | G | GTA | 10 | a0001c0001t0001g0044 a0001c0001t0001g0083 a0001c0001t0001g0169 others(7): Show |
10 | HG01099.hp1 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1423-3023_1423-302 others(6): Show |
GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 27515745 | ||||||
| chr2:27515745 | GTA | G | 40 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0051 others(37): Show |
60 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.1423-3023_1423-302 others(6): Show |
GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 27515745 | ||||||
| chr2:27515745 | GTATA | G | 3 | a0001c0001t0001g0043 a0001c0001t0001g0046 a0001c0001t0001g0047 |
3 | HG00733.hp1 HG01167.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1423-3025_1423-302 others(8): Show |
GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 27515745 | ||||||
| chr2:27515763 | ATATT | A | 11 | a0001c0001t0001g0020 a0001c0001t0001g0093 a0001c0001t0001g0116 others(8): Show |
12 | HG01358.hp1 HG01433.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1423-3023_1423-302 others(8): Show |
GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 27515763 | ||||||
| chr2:27515764 | TA | T | 3 | a0001c0001t0001g0001 a0002c0002t0001g0100 a0002c0002t0001g0145 |
3 | HG02004.hp1 NA19066.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1423-3023delA | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27515764 | |||||||
| chr2:27515765 | A | T | 33 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(30): Show |
47 | HG00597.hp1 HG00639.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.1423-3023A>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27515765 | |||||||
| chr2:27515765 | AT | A | 12 | a0001c0001t0001g0019 a0001c0001t0001g0174 a0001c0001t0001g0208 others(9): Show |
15 | HG00642.hp2 HG01074.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1423-3007delT | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 27515765 | ||||||
| chr2:27515765 | ATT | A | 14 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(11): Show |
17 | HG00597.hp2 HG01884.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1423-3008_1423-300 others(6): Show |
GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 27515765 | ||||||
| chr2:27515765 | ATTTT | A | 46 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(43): Show |
64 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.1423-3010_1423-300 others(8): Show |
GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 27515765 | ||||||
| chr2:27515766 | T | TA | 3 | a0001c0001t0002g0045 a0001c0010t0001g0001 a0012c0016t0001g0037 |
3 | HG02129.hp1 HG06807.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.1423-3022_1423-302 others(5): Show |
GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27515766 | |||||||
| chr2:27515767 | T | A | 11 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0018 others(8): Show |
14 | HG01069.hp1 HG01071.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.1423-3021T>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27515767 | |||||||
| chr2:27515768 | T | A | 4 | a0001c0001t0001g0174 a0001c0001t0001g0208 a0002c0002t0001g0157 others(1): Show |
4 | HG01109.hp2 HG02630.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1423-3020T>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27515768 | |||||||
| chr2:27515769 | T | A | 2 | a0001c0001t0001g0209 a0001c0001t0003g0186 |
2 | HG01981.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1423-3019T>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27515769 | |||||||
| chr2:27515770 | T | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0174 |
4 | HG00558.hp2 HG01109.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.1423-3018T>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27515770 | |||||||
| chr2:27515771 | T | A | 10 | a0001c0001t0001g0040 a0001c0001t0001g0048 a0001c0001t0001g0114 others(7): Show |
10 | HG01261.hp2 HG01891.hp2 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.1423-3017T>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27515771 | |||||||
| chr2:27515772 | T | A | 1 | a0001c0001t0001g0174 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1423-3016T>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27515772 | |||||||
| chr2:27515940 | A | AT | 81 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(78): Show |
110 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.1423-2831dupT | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 27515940 | ||||||
| chr2:27515940 | A | ATT | 6 | a0001c0001t0001g0048 a0001c0001t0001g0120 a0001c0001t0001g0125 others(3): Show |
6 | HG00673.hp2 HG01358.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1423-2832_1423-283 others(6): Show |
GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 27515940 | ||||||
| chr2:27515940 | A | T | 5 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0132 others(2): Show |
6 | HG02056.hp1 HG03453.hp2 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.1423-2848A>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27515940 | |||||||
| chr2:27515971 | C | A | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG02257.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1423-2817C>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27515971 | |||||||
| chr2:27515987 | C | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(70): Show |
107 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.1423-2801C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27515987 | |||||||
| chr2:27516239 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1423-2549G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27516239 | |||||||
| chr2:27516280 | CTTGTTTT others(4): Show |
C | 1 | a0001c0001t0001g0211 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1423-2505_1423-249 others(15): Show |
GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 27516280 | ||||||
| chr2:27516283 | G | GT | 49 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(46): Show |
60 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1423-2480dupT | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 27516283 | ||||||
| chr2:27516283 | G | GTT | 8 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0189 others(5): Show |
8 | HG00733.hp1 HG01167.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.1423-2481_1423-248 others(6): Show |
GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 27516283 | ||||||
| chr2:27516283 | GT | G | 13 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(10): Show |
13 | HG00280.hp1 HG01081.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1423-2480delT | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 27516283 | ||||||
| chr2:27516283 | GTTTTTTT others(5): Show |
G | 1 | a0001c0001t0001g0180 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1423-2491_1423-248 others(16): Show |
GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 27516283 | ||||||
| chr2:27516439 | C | T | 34 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(31): Show |
51 | HG00597.hp1 HG01074.hp1 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.1423-2349C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27516439 | |||||||
| chr2:27516456 | A | T | 1 | a0001c0001t0001g0074 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1423-2332A>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27516456 | |||||||
| chr2:27516493 | C | G | 2 | a0001c0001t0001g0163 a0001c0001t0001g0173 |
2 | HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1423-2295C>G | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27516493 | |||||||
| chr2:27516510 | G | C | 1 | a0002c0002t0001g0034 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1423-2278G>C | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27516510 | |||||||
| chr2:27516511 | T | TC | 10 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0051 others(7): Show |
14 | HG01074.hp2 HG01496.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1423-2276dupC | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 27516511 | ||||||
| chr2:27516575 | G | A | 1 | a0007c0005t0001g0194 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1423-2213G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27516575 | |||||||
| chr2:27516654 | T | A | 2 | a0001c0001t0001g0075 a0001c0001t0001g0078 |
2 | NA18963.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1423-2134T>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27516654 | |||||||
| chr2:27516669 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1423-2119G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27516669 | |||||||
| chr2:27516732 | A | C | 1 | a0001c0001t0001g0021 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1423-2056A>C | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27516732 | |||||||
| chr2:27516742 | G | T | 1 | a0001c0001t0001g0180 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1423-2046G>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27516742 | |||||||
| chr2:27517013 | CT | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(128): Show |
186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.1423-1757delT | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 27517013 | ||||||
| chr2:27517013 | CTT | C | 15 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(12): Show |
17 | HG00733.hp1 HG01109.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.1423-1758_1423-175 others(6): Show |
GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 27517013 | ||||||
| chr2:27517053 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1423-1735G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27517053 | |||||||
| chr2:27517381 | A | G | 1 | a0002c0002t0001g0143 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1423-1407A>G | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27517381 | |||||||
| chr2:27517461 | C | T | 11 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(8): Show |
17 | HG01074.hp2 HG01496.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1423-1327C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27517461 | |||||||
| chr2:27517525 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1423-1263C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27517525 | |||||||
| chr2:27517537 | C | G | 71 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(68): Show |
105 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1423-1251C>G | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27517537 | |||||||
| chr2:27517562 | G | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0174 |
2 | HG01109.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1423-1226G>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27517562 | |||||||
| chr2:27517689 | C | T | 1 | a0001c0012t0001g0196 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1423-1099C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27517689 | |||||||
| chr2:27517809 | A | C | 1 | a0008c0017t0001g0197 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1423-979A>C | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27517809 | |||||||
| chr2:27518005 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1423-783T>C | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27518005 | |||||||
| chr2:27518099 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1423-689G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27518099 | |||||||
| chr2:27518205 | C | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(136): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.1423-583C>G | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27518205 | |||||||
| chr2:27518238 | A | G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(147): Show |
207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1423-550A>G | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27518238 | |||||||
| chr2:27518370 | T | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(157): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1423-418T>C | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27518370 | |||||||
| chr2:27518583 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0210 |
3 | HG02572.hp2 HG03209.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1423-205G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27518583 | |||||||
| chr2:27518626 | A | G | 1 | a0010c0011t0001g0201 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1423-162A>G | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27518626 | |||||||
| chr2:27518688 | T | C | 11 | a0001c0001t0001g0009 a0001c0001t0001g0030 a0001c0001t0001g0054 others(8): Show |
15 | HG02027.hp1 HG02071.hp2 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.1423-100T>C | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27518688 | |||||||
| chr2:27518766 | C | G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0090 |
6 | HG01081.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1423-22C>G | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 16/18 | chr2 | 27518766 | |||||||
| chr2:27518943 | G | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG00733.hp1 HG01167.hp1 |
splice_region_variant&intron_variant | LOW | c.1572+6G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 17/18 | chr2 | 27518943 | |||||||
| chr2:27519307 | T | C | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1572+370T>C | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 17/18 | chr2 | 27519307 | |||||||
| chr2:27519521 | C | T | 1 | a0008c0017t0001g0197 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1572+584C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 17/18 | chr2 | 27519521 | |||||||
| chr2:27519581 | C | T | 6 | a0001c0001t0002g0007 a0001c0001t0002g0055 a0001c0001t0002g0066 others(3): Show |
10 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1572+644C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 17/18 | chr2 | 27519581 | |||||||
| chr2:27519678 | G | A | 2 | a0002c0002t0001g0178 a0008c0017t0001g0197 |
2 | HG01358.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1572+741G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 17/18 | chr2 | 27519678 | |||||||
| chr2:27519736 | T | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(160): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1572+799T>C | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 17/18 | chr2 | 27519736 | |||||||
| chr2:27519880 | C | G | 1 | a0002c0002t0001g0183 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1572+943C>G | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 17/18 | chr2 | 27519880 | |||||||
| chr2:27520104 | G | T | 4 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0050 others(1): Show |
6 | HG00738.hp1 HG01081.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1572+1167G>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 17/18 | chr2 | 27520104 | |||||||
| chr2:27520287 | A | G | 70 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(67): Show |
91 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1572+1350A>G | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 17/18 | chr2 | 27520287 | |||||||
| chr2:27520295 | G | C | 1 | a0001c0001t0001g0130 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1572+1358G>C | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 17/18 | chr2 | 27520295 | |||||||
| chr2:27520348 | A | G | 71 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(68): Show |
92 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1572+1411A>G | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 17/18 | chr2 | 27520348 | |||||||
| chr2:27520532 | G | C | 1 | a0001c0001t0001g0021 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1572+1595G>C | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 17/18 | chr2 | 27520532 | |||||||
| chr2:27520556 | G | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(62): Show |
95 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.1572+1619G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 17/18 | chr2 | 27520556 | |||||||
| chr2:27520763 | C | T | 65 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(62): Show |
95 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.1573-1697C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 17/18 | chr2 | 27520763 | |||||||
| chr2:27520801 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1573-1659C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 17/18 | chr2 | 27520801 | |||||||
| chr2:27520901 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1573-1559G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 17/18 | chr2 | 27520901 | |||||||
| chr2:27520915 | A | T | 1 | a0001c0001t0001g0068 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1573-1545A>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 17/18 | chr2 | 27520915 | |||||||
| chr2:27521081 | A | T | 6 | a0001c0001t0002g0007 a0001c0001t0002g0055 a0001c0001t0002g0066 others(3): Show |
10 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1573-1379A>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 17/18 | chr2 | 27521081 | |||||||
| chr2:27521222 | A | G | 56 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(53): Show |
77 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.1573-1238A>G | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 17/18 | chr2 | 27521222 | |||||||
| chr2:27521258 | C | T | 1 | a0002c0002t0001g0149 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1573-1202C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 17/18 | chr2 | 27521258 | |||||||
| chr2:27521497 | ATT | A | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(138): Show |
196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.1573-947_1573-946d others(4): Show |
GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr2 | 27521497 | ||||||
| chr2:27521691 | A | G | 1 | a0008c0017t0001g0197 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1573-769A>G | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 17/18 | chr2 | 27521691 | |||||||
| chr2:27521984 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1573-476A>G | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 17/18 | chr2 | 27521984 | |||||||
| chr2:27522070 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1573-390G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 17/18 | chr2 | 27522070 | |||||||
| chr2:27522262 | C | T | 1 | a0001c0012t0001g0196 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1573-198C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 17/18 | chr2 | 27522262 | |||||||
| chr2:27522412 | G | A | 2 | a0001c0001t0001g0122 a0001c0001t0001g0131 |
2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1573-48G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 17/18 | chr2 | 27522412 | |||||||
| chr2:27522692 | A | G | 1 | a0002c0014t0001g0153 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1707+98A>G | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 18/18 | chr2 | 27522692 | |||||||
| chr2:27522897 | G | GT | 5 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0002c0002t0001g0147 others(2): Show |
6 | HG01175.hp1 HG02257.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.1707+319dupT | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 27522897 | ||||||
| chr2:27522897 | GT | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(132): Show |
190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.1707+319delT | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 27522897 | ||||||
| chr2:27523079 | A | G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(65): Show |
98 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.1708-190A>G | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 18/18 | chr2 | 27523079 | |||||||
| chr2:27523206 | G | A | 2 | a0001c0001t0001g0059 a0001c0001t0001g0077 |
2 | HG01975.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1708-63G>A | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 18/18 | chr2 | 27523206 | |||||||
| chr2:27523226 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0210 |
3 | HG02572.hp2 HG03209.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1708-43C>T | GCKR | ENSG00000084734.9 | transcript | ENST00000264717.7 | protein_coding | 18/18 | chr2 | 27523226 |