| geneid | 55668 |
|---|---|
| ensemblid | ENSG00000089916.18 |
| hgncid | 20210 |
| symbol | GPATCH2L |
| name | G-patch domain containing 2 like |
| refseq_nuc | NM_017926.4 |
| refseq_prot | NP_060396.2 |
| ensembl_nuc | ENST00000261530.12 |
| ensembl_prot | ENSP00000261530.7 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 76151922 |
| end | 76214343 |
| strand | + |
| ver | v1.2 |
| region | chr14:76151922-76214343 |
| region5000 | chr14:76146922-76219343 |
| regionname0 | GPATCH2L_chr14_76151922_76214343 |
| regionname5000 | GPATCH2L_chr14_76146922_76219343 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 482 | 399 | 74 | 68 | 202 | 12 | 41 | 158 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0002 | 0/0 | 482 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0003 | 0/0 | 482 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0004 | 0/0 | 482 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1449 | 375 | 67 | 64 | 189 | 12 | 41 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| c0002 | 0/0 | 1449 | 12 | 0 | 0 | 12 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| c0003 | 0/0 | 1449 | 4 | 4 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| c0004 | 0/0 | 1449 | 4 | 0 | 3 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| c0005 | 0/0 | 1449 | 3 | 3 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| c0006 | 0/0 | 1449 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| c0007 | 0/0 | 1449 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| c0008 | 0/0 | 1449 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| c0009 | 0/0 | 1449 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 12575 | 89 | 2 | 16 | 52 | 2 | 16 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0002 | 0/0 | 12571 | 51 | 3 | 10 | 35 | 2 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0003 | 0/0 | 12571 | 34 | 0 | 0 | 29 | 0 | 5 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0004 | 0/0 | 12572 | 24 | 3 | 7 | 12 | 0 | 2 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0005 | 0/0 | 12584 | 15 | 0 | 4 | 11 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0006 | 0/0 | 12584 | 14 | 7 | 1 | 5 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0007 | 0/0 | 12584 | 8 | 0 | 5 | 0 | 1 | 2 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0008 | 0/0 | 12571 | 8 | 0 | 0 | 8 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0009 | 0/0 | 12571 | 8 | 0 | 6 | 0 | 0 | 2 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0010 | 0/0 | 12572 | 8 | 0 | 0 | 8 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0011 | 0/0 | 12562 | 7 | 7 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0012 | 0/0 | 12575 | 7 | 0 | 0 | 7 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0013 | 0/0 | 12582 | 6 | 4 | 1 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0014 | 0/0 | 12575 | 6 | 1 | 1 | 2 | 1 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0015 | 0/0 | 12586 | 4 | 3 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0016 | 0/0 | 12571 | 4 | 4 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0017 | 0/0 | 12572 | 4 | 3 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0018 | 0/0 | 12575 | 4 | 0 | 0 | 4 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0019 | 0/0 | 12588 | 3 | 3 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0020 | 0/0 | 12571 | 3 | 3 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0021 | 0/0 | 12571 | 3 | 3 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0022 | 0/0 | 12575 | 3 | 0 | 3 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0023 | 0/0 | 12573 | 3 | 0 | 1 | 0 | 2 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0024 | 0/0 | 12572 | 3 | 0 | 0 | 0 | 3 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0025 | 0/0 | 12572 | 3 | 3 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0026 | 0/0 | 12582 | 2 | 0 | 0 | 0 | 0 | 2 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0027 | 0/0 | 12580 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0028 | 0/0 | 12571 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0029 | 0/0 | 12572 | 2 | 1 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0030 | 0/0 | 12575 | 2 | 0 | 1 | 0 | 1 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0031 | 0/0 | 12575 | 2 | 0 | 0 | 0 | 0 | 2 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0032 | 0/0 | 12573 | 2 | 1 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0033 | 0/0 | 12573 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0034 | 0/0 | 12572 | 2 | 0 | 0 | 0 | 0 | 2 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0035 | 0/0 | 12572 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0036 | 0/0 | 12571 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0037 | 0/0 | 12572 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0038 | 0/0 | 12575 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0039 | 0/0 | 12575 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0040 | 0/0 | 12588 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0041 | 0/0 | 12584 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0042 | 0/0 | 12584 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0043 | 0/0 | 12583 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0044 | 0/0 | 12584 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0045 | 0/0 | 12584 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0046 | 0/0 | 12584 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0047 | 0/0 | 12582 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0048 | 0/0 | 12582 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0049 | 0/0 | 12580 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0050 | 0/0 | 12573 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0051 | 0/0 | 12573 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0052 | 1/0 | 12573 | 1 | 0 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0053 | 0/0 | 12573 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0054 | 0/0 | 12571 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0055 | 0/0 | 12571 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0056 | 0/0 | 12571 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0057 | 0/0 | 12571 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0058 | 0/0 | 12571 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0059 | 0/0 | 12571 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0060 | 0/0 | 12562 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0061 | 0/0 | 12562 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0062 | 0/0 | 12562 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0063 | 0/0 | 12571 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0064 | 0/0 | 12563 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0065 | 0/0 | 12571 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0066 | 0/0 | 12571 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0067 | 0/0 | 12575 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0068 | 0/0 | 12575 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0069 | 0/0 | 12575 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0070 | 0/0 | 12575 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0071 | 0/0 | 12575 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0072 | 0/0 | 12575 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0073 | 0/0 | 12575 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0074 | 0/0 | 12575 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0075 | 0/0 | 12575 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0076 | 0/0 | 12575 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0077 | 0/0 | 12575 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0078 | 0/0 | 12573 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0079 | 0/0 | 12573 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0080 | 0/0 | 12571 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0081 | 0/0 | 12571 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0082 | 0/0 | 12572 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0083 | 0/0 | 12571 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0084 | 0/0 | 12572 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0085 | 0/0 | 12572 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0086 | 0/0 | 12572 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0087 | 0/0 | 12571 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0088 | 0/0 | 12571 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0089 | 0/0 | 12571 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0090 | 0/0 | 12572 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0091 | 0/0 | 12572 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0092 | 0/0 | 12571 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| t0093 | 0/0 | 12575 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 25 | 1 | 5 | 14 | 2 | 3 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0002 | 0/0 | 12 | 0 | 0 | 10 | 0 | 2 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0003 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0004 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0007 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0010 | 0/0 | 4 | 0 | 1 | 1 | 0 | 2 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0011 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0016 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0025 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0037 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0042 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0108 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1449 | 375 | 67 | 64 | 189 | 12 | 41 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0002 | 0/0 | 1449 | 12 | 0 | 0 | 12 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0003 | 0/0 | 1449 | 4 | 4 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0004 | 0/0 | 1449 | 4 | 0 | 3 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0005 | 0/0 | 1449 | 3 | 3 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0008 | 0/0 | 1449 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0002c0009 | 0/0 | 1449 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0003c0006 | 0/0 | 1449 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0004c0007 | 0/0 | 1449 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 14023 | 76 | 2 | 16 | 40 | 2 | 15 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0002 | 0/0 | 14019 | 51 | 3 | 10 | 35 | 2 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0003 | 0/0 | 14019 | 34 | 0 | 0 | 29 | 0 | 5 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0004 | 0/0 | 14020 | 20 | 3 | 4 | 11 | 0 | 2 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0005 | 0/0 | 14032 | 15 | 0 | 4 | 11 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0006 | 0/0 | 14032 | 13 | 6 | 1 | 5 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0007 | 0/0 | 14032 | 8 | 0 | 5 | 0 | 1 | 2 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0008 | 0/0 | 14019 | 8 | 0 | 0 | 8 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0009 | 0/0 | 14019 | 8 | 0 | 6 | 0 | 0 | 2 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0010 | 0/0 | 14020 | 8 | 0 | 0 | 8 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0011 | 0/0 | 14010 | 7 | 7 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0012 | 0/0 | 14023 | 7 | 0 | 0 | 7 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0013 | 0/0 | 14030 | 6 | 4 | 1 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0014 | 0/0 | 14023 | 6 | 1 | 1 | 2 | 1 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0015 | 0/0 | 14034 | 4 | 3 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0017 | 0/0 | 14020 | 4 | 3 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0018 | 0/0 | 14023 | 4 | 0 | 0 | 4 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0020 | 0/0 | 14019 | 3 | 3 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0021 | 0/0 | 14019 | 3 | 3 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0022 | 0/0 | 14023 | 3 | 0 | 3 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0023 | 0/0 | 14021 | 3 | 0 | 1 | 0 | 2 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0024 | 0/0 | 14020 | 3 | 0 | 0 | 0 | 3 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0025 | 0/0 | 14020 | 3 | 3 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0026 | 0/0 | 14030 | 2 | 0 | 0 | 0 | 0 | 2 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0027 | 0/0 | 14028 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0028 | 0/0 | 14019 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0029 | 0/0 | 14020 | 2 | 1 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0030 | 0/0 | 14023 | 2 | 0 | 1 | 0 | 1 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0031 | 0/0 | 14023 | 2 | 0 | 0 | 0 | 0 | 2 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0032 | 0/0 | 14021 | 2 | 1 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0033 | 0/0 | 14021 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0034 | 0/0 | 14020 | 2 | 0 | 0 | 0 | 0 | 2 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0035 | 0/0 | 14020 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0036 | 0/0 | 14019 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0037 | 0/0 | 14020 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0038 | 0/0 | 14023 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0040 | 0/0 | 14036 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0041 | 0/0 | 14032 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0042 | 0/0 | 14032 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0043 | 0/0 | 14031 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0044 | 0/0 | 14032 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0045 | 0/0 | 14032 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0046 | 0/0 | 14032 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0047 | 0/0 | 14030 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0048 | 0/0 | 14030 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0049 | 0/0 | 14028 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0050 | 0/0 | 14021 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0051 | 0/0 | 14021 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0052 | 1/0 | 14021 | 1 | 0 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0053 | 0/0 | 14021 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0054 | 0/0 | 14019 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0055 | 0/0 | 14019 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0056 | 0/0 | 14019 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0057 | 0/0 | 14019 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0058 | 0/0 | 14019 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0059 | 0/0 | 14019 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0060 | 0/0 | 14010 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0061 | 0/0 | 14010 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0062 | 0/0 | 14010 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0063 | 0/0 | 14019 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0064 | 0/0 | 14011 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0065 | 0/0 | 14019 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0066 | 0/0 | 14019 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0067 | 0/0 | 14023 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0068 | 0/0 | 14023 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0069 | 0/0 | 14023 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0070 | 0/0 | 14023 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0071 | 0/0 | 14023 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0072 | 0/0 | 14023 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0073 | 0/0 | 14023 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0074 | 0/0 | 14023 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0075 | 0/0 | 14023 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0076 | 0/0 | 14023 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0077 | 0/0 | 14023 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0078 | 0/0 | 14021 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0079 | 0/0 | 14021 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0080 | 0/0 | 14019 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0081 | 0/0 | 14019 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0082 | 0/0 | 14020 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0083 | 0/0 | 14019 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0084 | 0/0 | 14020 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0085 | 0/0 | 14020 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0086 | 0/0 | 14020 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0087 | 0/0 | 14019 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0088 | 0/0 | 14019 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0090 | 0/0 | 14020 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0091 | 0/0 | 14020 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0092 | 0/0 | 14019 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0001t0093 | 0/0 | 14023 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0002t0001 | 0/0 | 14023 | 12 | 0 | 0 | 12 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0003t0006 | 0/0 | 14032 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0003t0019 | 0/0 | 14036 | 3 | 3 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0004t0004 | 0/0 | 14020 | 4 | 0 | 3 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0005t0016 | 0/0 | 14019 | 3 | 3 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0001c0008t0039 | 0/0 | 14023 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0002c0009t0001 | 0/0 | 14023 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0003c0006t0016 | 0/0 | 14019 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| a0004c0007t0089 | 0/0 | 14019 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | copy fasta | chr14 | 76146922 | 76219343 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 21 | 1 | 5 | 11 | 2 | 2 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0042 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0004 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0002 | 0/0 | 10 | 0 | 0 | 8 | 0 | 2 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0004g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0004g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0004g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0004g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0004g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0004g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0005g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0005g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0005g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0005g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0005g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0005g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0005g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0005g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0005g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0005g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0005g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0006g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0006g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0006g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0006g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0006g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0006g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0006g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0006g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0007g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0007g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0007g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0007g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0007g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0007g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0007g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0008g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0008g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0008g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0008g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0008g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0008g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0008g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0009g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0009g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0009g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0009g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0009g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0009g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0010g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0010g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0010g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0010g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0010g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0010g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0011g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0011g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0011g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0011g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0011g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0011g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0012g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0012g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0012g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0012g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0012g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0013g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0013g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0013g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0013g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0013g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0013g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0014g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0014g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0014g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0014g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0014g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0015g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0015g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0015g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0015g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0017g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0017g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0018g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0018g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0018g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0020g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0020g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0021g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0021g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0021g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0022g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0022g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0022g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0023g0016 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0024g0037 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0024g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0025g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0026g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0026g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0027g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0027g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0028g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0028g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0029g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0029g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0030g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0030g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0031g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0031g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0032g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0032g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0033g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0033g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0034g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0034g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0035g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0035g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0036g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0036g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0037g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0038g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0040g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0041g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0042g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0043g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0044g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0045g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0046g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0047g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0048g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0049g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0050g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0051g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0052g0108 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0053g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0054g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0055g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0056g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0057g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0058g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0059g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0060g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0061g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0062g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0063g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0064g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0065g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0066g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0067g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0068g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0069g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0070g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0071g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0072g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0073g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0074g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0075g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0076g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0077g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0078g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0079g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0080g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0081g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0082g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0083g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0084g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0085g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0086g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0087g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0088g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0090g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0091g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0092g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0001t0093g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0002t0001g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0003t0006g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0003t0019g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0003t0019g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0003t0019g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0004t0004g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0004t0004g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0005t0016g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0005t0016g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0005t0016g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0001c0008t0039g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0002c0009t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0003c0006t0016g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| a0004c0007t0089g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0197 | EUR | GBR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00140 | hp1 | a0001 | c0001 | t0014 | g0020 | EUR | GBR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00140 | hp2 | a0001 | c0001 | t0024 | g0037 | EUR | GBR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00323 | hp2 | a0001 | c0001 | t0007 | g0133 | EUR | FIN | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0253 | EAS | CHS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00408 | hp2 | a0001 | c0001 | t0008 | g0199 | EAS | CHS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00423 | hp1 | a0001 | c0001 | t0027 | g0027 | EAS | CHS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | CHS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00558 | hp2 | a0001 | c0001 | t0005 | g0131 | EAS | CHS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | CHS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | CHS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0248 | EAS | CHS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00621 | hp2 | a0001 | c0001 | t0014 | g0065 | EAS | CHS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00642 | hp2 | a0001 | c0001 | t0075 | g0046 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | CHS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0264 | EAS | CHS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00738 | hp2 | a0001 | c0008 | t0039 | g0258 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00741 | hp1 | a0001 | c0001 | t0023 | g0016 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0195 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01074 | hp1 | a0001 | c0001 | t0080 | g0230 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0223 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0209 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01081 | hp2 | a0001 | c0001 | t0015 | g0112 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0224 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01106 | hp1 | a0001 | c0001 | t0007 | g0162 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01106 | hp2 | a0001 | c0001 | t0056 | g0107 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01109 | hp1 | a0001 | c0001 | t0017 | g0226 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01167 | hp2 | a0001 | c0001 | t0009 | g0018 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01169 | hp2 | a0001 | c0001 | t0009 | g0018 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01175 | hp2 | a0001 | c0001 | t0009 | g0267 | AMR | PUR | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01256 | hp1 | a0001 | c0001 | t0009 | g0268 | AMR | CLM | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01256 | hp2 | a0001 | c0001 | t0022 | g0061 | AMR | CLM | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0215 | AMR | CLM | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01258 | hp1 | a0001 | c0001 | t0009 | g0269 | AMR | CLM | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | CLM | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | CLM | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01346 | hp1 | a0001 | c0001 | t0074 | g0055 | AMR | CLM | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01346 | hp2 | a0001 | c0001 | t0030 | g0257 | AMR | CLM | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01358 | hp1 | a0001 | c0001 | t0009 | g0018 | AMR | CLM | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01358 | hp2 | a0001 | c0001 | t0085 | g0288 | AMR | CLM | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0263 | AMR | CLM | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01361 | hp2 | a0001 | c0001 | t0022 | g0060 | AMR | CLM | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01433 | hp1 | a0001 | c0001 | t0014 | g0020 | AMR | CLM | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0278 | AMR | CLM | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01496 | hp1 | a0001 | c0001 | t0029 | g0182 | AMR | CLM | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01496 | hp2 | a0001 | c0001 | t0006 | g0136 | AMR | CLM | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01515 | hp1 | a0001 | c0001 | t0024 | g0273 | EUR | IBS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0034 | EUR | IBS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01516 | hp1 | a0001 | c0001 | t0030 | g0259 | EUR | IBS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01516 | hp2 | a0001 | c0001 | t0023 | g0016 | EUR | IBS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01517 | hp1 | a0001 | c0001 | t0023 | g0016 | EUR | IBS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01517 | hp2 | a0001 | c0001 | t0024 | g0037 | EUR | IBS | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01891 | hp1 | a0001 | c0001 | t0060 | g0173 | AFR | ACB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01891 | hp2 | a0001 | c0001 | t0054 | g0179 | AFR | ACB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01928 | hp1 | a0001 | c0004 | t0004 | g0036 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01934 | hp1 | a0001 | c0001 | t0022 | g0053 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01934 | hp2 | a0001 | c0001 | t0013 | g0123 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01943 | hp2 | a0001 | c0001 | t0005 | g0128 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01975 | hp1 | a0001 | c0001 | t0005 | g0138 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01975 | hp2 | a0001 | c0001 | t0076 | g0022 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01978 | hp1 | a0001 | c0001 | t0005 | g0027 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01978 | hp2 | a0001 | c0001 | t0007 | g0110 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01981 | hp2 | a0001 | c0001 | t0005 | g0132 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG01993 | hp2 | a0001 | c0004 | t0004 | g0036 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02004 | hp1 | a0001 | c0001 | t0007 | g0024 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02004 | hp2 | a0001 | c0001 | t0083 | g0265 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02015 | hp1 | a0001 | c0001 | t0033 | g0103 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02015 | hp2 | a0001 | c0001 | t0058 | g0216 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02027 | hp1 | a0001 | c0001 | t0006 | g0146 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02027 | hp2 | a0001 | c0001 | t0008 | g0213 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02040 | hp1 | a0001 | c0001 | t0036 | g0243 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02040 | hp2 | a0001 | c0001 | t0008 | g0006 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02055 | hp1 | a0001 | c0001 | t0055 | g0033 | AFR | ACB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02074 | hp1 | a0001 | c0001 | t0028 | g0187 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0281 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02083 | hp1 | a0001 | c0001 | t0093 | g0007 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02132 | hp2 | a0001 | c0001 | t0078 | g0002 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | KHV | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02145 | hp1 | a0001 | c0001 | t0011 | g0172 | AFR | ACB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02145 | hp2 | a0001 | c0001 | t0017 | g0015 | AFR | ACB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02148 | hp1 | a0001 | c0004 | t0004 | g0010 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02148 | hp2 | a0001 | c0001 | t0069 | g0045 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CDX | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02155 | hp2 | a0001 | c0001 | t0028 | g0188 | EAS | CDX | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02165 | hp1 | a0001 | c0001 | t0033 | g0256 | EAS | CDX | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02165 | hp2 | a0001 | c0001 | t0008 | g0006 | EAS | CDX | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02258 | hp1 | a0001 | c0001 | t0011 | g0177 | AFR | ACB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02258 | hp2 | a0001 | c0001 | t0006 | g0151 | AFR | ACB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02293 | hp2 | a0001 | c0001 | t0007 | g0024 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02300 | hp2 | a0001 | c0001 | t0007 | g0141 | AMR | PEL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02451 | hp1 | a0001 | c0001 | t0025 | g0017 | AFR | ACB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02451 | hp2 | a0001 | c0001 | t0032 | g0098 | AFR | ACB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02572 | hp1 | a0001 | c0001 | t0050 | g0165 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0157 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0207 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02615 | hp1 | a0001 | c0001 | t0081 | g0229 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02615 | hp2 | a0001 | c0001 | t0013 | g0137 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02622 | hp1 | a0001 | c0003 | t0019 | g0111 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02622 | hp2 | a0001 | c0001 | t0059 | g0170 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02630 | hp1 | a0001 | c0001 | t0015 | g0113 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02630 | hp2 | a0004 | c0007 | t0089 | g0228 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02647 | hp1 | a0001 | c0001 | t0053 | g0180 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02647 | hp2 | a0001 | c0001 | t0043 | g0134 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02698 | hp2 | a0001 | c0001 | t0007 | g0139 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0153 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0280 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02723 | hp1 | a0001 | c0001 | t0048 | g0127 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02723 | hp2 | a0001 | c0001 | t0062 | g0009 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02809 | hp1 | a0001 | c0001 | t0049 | g0143 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02809 | hp2 | a0003 | c0006 | t0016 | g0106 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02886 | hp1 | a0001 | c0001 | t0020 | g0171 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02886 | hp2 | a0001 | c0001 | t0021 | g0225 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02897 | hp1 | a0001 | c0001 | t0040 | g0154 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02897 | hp2 | a0001 | c0003 | t0006 | g0118 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02922 | hp1 | a0001 | c0001 | t0011 | g0175 | AFR | ESN | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02922 | hp2 | a0001 | c0001 | t0020 | g0028 | AFR | ESN | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02965 | hp1 | a0001 | c0003 | t0019 | g0116 | AFR | ESN | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02965 | hp2 | a0001 | c0005 | t0016 | g0169 | AFR | ESN | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02976 | hp1 | a0001 | c0001 | t0046 | g0159 | AFR | ESN | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02976 | hp2 | a0001 | c0001 | t0011 | g0029 | AFR | ESN | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0010 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03098 | hp1 | a0001 | c0001 | t0092 | g0009 | AFR | MSL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03098 | hp2 | a0001 | c0001 | t0015 | g0114 | AFR | MSL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0155 | AFR | ESN | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03130 | hp2 | a0001 | c0001 | t0017 | g0015 | AFR | ESN | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03139 | hp1 | a0001 | c0001 | t0013 | g0126 | AFR | ESN | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03139 | hp2 | a0001 | c0001 | t0017 | g0015 | AFR | ESN | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03195 | hp1 | a0001 | c0003 | t0019 | g0117 | AFR | ESN | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03195 | hp2 | a0001 | c0001 | t0025 | g0017 | AFR | ESN | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03209 | hp1 | a0001 | c0001 | t0061 | g0289 | AFR | MSL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0152 | AFR | MSL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03239 | hp1 | a0001 | c0001 | t0014 | g0074 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03239 | hp2 | a0001 | c0001 | t0026 | g0164 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03453 | hp1 | a0001 | c0001 | t0029 | g0183 | AFR | MSL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03453 | hp2 | a0001 | c0001 | t0025 | g0017 | AFR | MSL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03490 | hp1 | a0001 | c0001 | t0071 | g0011 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03490 | hp2 | a0001 | c0001 | t0007 | g0129 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03491 | hp2 | a0001 | c0001 | t0006 | g0130 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03540 | hp1 | a0001 | c0001 | t0051 | g0167 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | GWD | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03579 | hp1 | a0001 | c0001 | t0084 | g0260 | AFR | MSL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03579 | hp2 | a0001 | c0001 | t0015 | g0115 | AFR | MSL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03654 | hp1 | a0001 | c0001 | t0031 | g0086 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03654 | hp2 | a0001 | c0001 | t0009 | g0266 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03669 | hp1 | a0001 | c0001 | t0013 | g0227 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03669 | hp2 | a0001 | c0001 | t0070 | g0001 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0234 | SAS | STU | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03704 | hp1 | a0001 | c0001 | t0041 | g0025 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03831 | hp1 | a0001 | c0001 | t0034 | g0270 | SAS | BEB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | BEB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0010 | SAS | BEB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03834 | hp2 | a0001 | c0001 | t0031 | g0087 | SAS | BEB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0235 | SAS | BEB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | BEB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | STU | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | STU | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | BEB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | BEB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | STU | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG04199 | hp2 | a0001 | c0001 | t0026 | g0163 | SAS | STU | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0249 | SAS | STU | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG04204 | hp2 | a0002 | c0009 | t0001 | g0088 | SAS | STU | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG04228 | hp1 | a0001 | c0001 | t0066 | g0246 | SAS | STU | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG04228 | hp2 | a0001 | c0001 | t0009 | g0272 | SAS | STU | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18522 | hp1 | a0001 | c0001 | t0013 | g0135 | AFR | YRI | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | YRI | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18747 | hp1 | a0001 | c0001 | t0005 | g0161 | EAS | CHB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18747 | hp2 | a0001 | c0001 | t0090 | g0275 | EAS | CHB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18906 | hp1 | a0001 | c0001 | t0011 | g0176 | AFR | YRI | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | YRI | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18939 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18939 | hp2 | a0001 | c0001 | t0012 | g0064 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18942 | hp1 | a0001 | c0001 | t0037 | g0038 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18949 | hp1 | a0001 | c0001 | t0008 | g0194 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18950 | hp1 | a0001 | c0001 | t0032 | g0058 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18952 | hp1 | a0001 | c0001 | t0027 | g0160 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18953 | hp1 | a0001 | c0001 | t0035 | g0284 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18954 | hp1 | a0001 | c0001 | t0005 | g0025 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0291 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18960 | hp1 | a0001 | c0001 | t0018 | g0001 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18960 | hp2 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18966 | hp2 | a0001 | c0001 | t0005 | g0145 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18968 | hp1 | a0001 | c0001 | t0012 | g0012 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18968 | hp2 | a0001 | c0004 | t0004 | g0010 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18969 | hp1 | a0001 | c0001 | t0014 | g0089 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18969 | hp2 | a0001 | c0001 | t0035 | g0285 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18970 | hp2 | a0001 | c0001 | t0077 | g0109 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18971 | hp2 | a0001 | c0001 | t0010 | g0040 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18972 | hp2 | a0001 | c0001 | t0006 | g0150 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18974 | hp1 | a0001 | c0001 | t0010 | g0039 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18974 | hp2 | a0001 | c0001 | t0012 | g0012 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18975 | hp1 | a0001 | c0001 | t0010 | g0277 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18978 | hp2 | a0001 | c0001 | t0047 | g0149 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18979 | hp2 | a0001 | c0001 | t0010 | g0040 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18982 | hp1 | a0001 | c0001 | t0005 | g0120 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18982 | hp2 | a0001 | c0001 | t0067 | g0001 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18986 | hp2 | a0001 | c0001 | t0005 | g0140 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18987 | hp1 | a0001 | c0001 | t0072 | g0003 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18987 | hp2 | a0001 | c0001 | t0006 | g0148 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18990 | hp1 | a0001 | c0001 | t0087 | g0002 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18991 | hp1 | a0001 | c0001 | t0018 | g0052 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18991 | hp2 | a0001 | c0001 | t0045 | g0142 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18993 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18994 | hp1 | a0001 | c0001 | t0010 | g0276 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18999 | hp1 | a0001 | c0001 | t0012 | g0077 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA18999 | hp2 | a0001 | c0001 | t0086 | g0287 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0279 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19002 | hp1 | a0001 | c0001 | t0008 | g0214 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19002 | hp2 | a0001 | c0001 | t0012 | g0012 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19003 | hp1 | a0001 | c0001 | t0008 | g0031 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19004 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19005 | hp1 | a0001 | c0001 | t0005 | g0121 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19006 | hp1 | a0001 | c0001 | t0063 | g0191 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19007 | hp1 | a0001 | c0001 | t0036 | g0252 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19011 | hp1 | a0001 | c0001 | t0010 | g0283 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19011 | hp2 | a0001 | c0001 | t0005 | g0026 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19012 | hp2 | a0001 | c0001 | t0044 | g0125 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19030 | hp1 | a0001 | c0001 | t0020 | g0028 | AFR | LWK | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19030 | hp2 | a0001 | c0005 | t0016 | g0181 | AFR | LWK | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19043 | hp1 | a0001 | c0001 | t0088 | g0255 | AFR | LWK | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19043 | hp2 | a0001 | c0001 | t0082 | g0261 | AFR | LWK | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19054 | hp1 | a0001 | c0001 | t0005 | g0122 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19055 | hp1 | a0001 | c0001 | t0091 | g0274 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19055 | hp2 | a0001 | c0001 | t0006 | g0147 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19056 | hp1 | a0001 | c0001 | t0012 | g0011 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19057 | hp1 | a0001 | c0001 | t0010 | g0039 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19062 | hp2 | a0001 | c0001 | t0018 | g0076 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19068 | hp1 | a0001 | c0001 | t0006 | g0124 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19074 | hp1 | a0001 | c0001 | t0005 | g0026 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19074 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19075 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19077 | hp1 | a0001 | c0001 | t0068 | g0013 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19081 | hp1 | a0001 | c0001 | t0010 | g0286 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19081 | hp2 | a0001 | c0001 | t0018 | g0001 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19082 | hp2 | a0001 | c0001 | t0008 | g0219 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19083 | hp2 | a0001 | c0001 | t0005 | g0119 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19085 | hp1 | a0001 | c0001 | t0038 | g0013 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19088 | hp2 | a0001 | c0001 | t0012 | g0049 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19090 | hp1 | a0001 | c0001 | t0037 | g0038 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19240 | hp1 | a0001 | c0001 | t0021 | g0192 | AFR | YRI | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA19240 | hp2 | a0001 | c0001 | t0064 | g0166 | AFR | YRI | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA20905 | hp1 | a0001 | c0001 | t0073 | g0078 | SAS | GIH | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA20905 | hp2 | a0001 | c0001 | t0034 | g0271 | SAS | GIH | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02109 | hp1 | a0001 | c0001 | t0042 | g0158 | AFR | ACB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0282 | AFR | ACB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0262 | AFR | ACB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02486 | hp2 | a0001 | c0001 | t0021 | g0033 | AFR | ACB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02559 | hp1 | a0001 | c0001 | t0065 | g0193 | AFR | ACB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG02559 | hp2 | a0001 | c0001 | t0013 | g0144 | AFR | ACB | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0156 | AFR | MSL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG03471 | hp2 | a0001 | c0001 | t0011 | g0174 | AFR | MSL | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG06807 | hp1 | a0001 | c0001 | t0011 | g0029 | AFR | USA | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| HG06807 | hp2 | a0001 | c0001 | t0057 | g0178 | AFR | USA | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA20300 | hp1 | a0001 | c0005 | t0016 | g0168 | AFR | USA | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | USA | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA21309 | hp1 | a0001 | c0001 | t0079 | g0290 | AFR | LWK | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| NA21309 | hp2 | a0001 | c0001 | t0014 | g0075 | AFR | LWK | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0042 | REF | REF | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0052 | g0108 | REF | REF | GPATCH2L_chr14_76146922_76219343 | GPATCH2L | chr14 | 76146922 | 76219343 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:76171870
|
A | G | 1 | a0002 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.755A>G | p.Tyr252Cys | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 4/10 | 835/14021 | 755/1449 | 252/482 | chr14 | 76171870 | ||
| chr14:76177998
|
G | A | 1 | a0004 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.1063G>A | p.Ala355Thr | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/10 | 1143/14021 | 1063/1449 | 355/482 | chr14 | 76177998 | ||
| chr14:76201798
|
A | G | 1 | a0003 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.1396A>G | p.Thr466Ala | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 1476/14021 | 1396/1449 | 466/482 | chr14 | 76201798 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:76154729
|
T | G | 1 | a0001c0003 | 4 | HG02622.hp1 HG02897.hp2 HG02965.hp1 others(1): Show |
synonymous_variant | LOW | c.366T>G | p.Pro122Pro | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/10 | 446/14021 | 366/1449 | 122/482 | chr14 | 76154729 | ||
| chr14:76154753
|
G | A | 2 | a0001c0005a0003c0006 | 4 | HG02809.hp2 HG02965.hp2 NA19030.hp2 others(1): Show |
synonymous_variant | LOW | c.390G>A | p.Arg130Arg | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/10 | 470/14021 | 390/1449 | 130/482 | chr14 | 76154753 | ||
| chr14:76171895
|
C | T | 1 | a0001c0004 | 4 | HG01928.hp1 HG01993.hp2 HG02148.hp1 others(1): Show |
synonymous_variant | LOW | c.780C>T | p.Phe260Phe | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 4/10 | 860/14021 | 780/1449 | 260/482 | chr14 | 76171895 | ||
| chr14:76172015
|
A | G | 1 | a0001c0002 | 12 | NA18947.hp1 NA18949.hp2 NA18975.hp2 others(9): Show |
synonymous_variant | LOW | c.900A>G | p.Gln300Gln | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 4/10 | 980/14021 | 900/1449 | 300/482 | chr14 | 76172015 | ||
| chr14:76180805
|
C | T | 1 | a0001c0008 | 1 | HG00738.hp2 | synonymous_variant | LOW | c.1149C>T | p.Ala383Ala | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/10 | 1229/14021 | 1149/1449 | 383/482 | chr14 | 76180805 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:76151931
|
A | C | 1 | a0001c0001t0093 | 1 | HG02083.hp1 | 5_prime_UTR_variant | MODIFIER | c.-71A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/10 | 2433 | chr14 | 76151931 | |||||
| chr14:76151940
|
G | T | 1 | a0001c0001t0092 | 1 | HG03098.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-62G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/10 | chr14 | 76151940 | ||||||
| chr14:76201903
|
T | G | 1 | a0001c0001t0038 | 1 | NA19085.hp1 | 3_prime_UTR_variant | MODIFIER | c.*52T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 52 | chr14 | 76201903 | |||||
| chr14:76201940
|
G | A | 1 | a0001c0008t0039 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*89G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 89 | chr14 | 76201940 | |||||
| chr14:76202013
|
A | G | 52 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(49): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
3_prime_UTR_variant | MODIFIER | c.*162A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 162 | chr14 | 76202013 | |||||
| chr14:76202165
|
G | A | 1 | a0001c0001t0066 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*314G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 314 | chr14 | 76202165 | |||||
| chr14:76202424
|
C | T | 1 | a0001c0001t0065 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*573C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 573 | chr14 | 76202424 | |||||
| chr14:76202536
|
T | TACACAC | 2 | a0001c0001t0027a0001c0001t0049 | 3 | HG00423.hp1 HG02809.hp1 NA18952.hp1 |
3_prime_UTR_variant | MODIFIER | c.*707_*712dupCACACA | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 713 | INFO_REALIGN_3_PRIME | chr14 | 76202536 | ||||
| chr14:76202536
|
T | TACACACA others(1): Show |
4 | a0001c0001t0013a0001c0001t0026a0001c0001t0047others(1): Show | 10 | HG01934.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*705_*712dupCACACA others(2): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 713 | INFO_REALIGN_3_PRIME | chr14 | 76202536 | ||||
| chr14:76202536
|
T | TACACACA others(3): Show |
10 | a0001c0001t0005a0001c0001t0006a0001c0001t0007others(7): Show | 43 | HG00323.hp2 HG00558.hp2 HG01106.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*703_*712dupCACACA others(4): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 713 | INFO_REALIGN_3_PRIME | chr14 | 76202536 | ||||
| chr14:76202536
|
T | TACACACA others(5): Show |
1 | a0001c0001t0015 | 4 | HG01081.hp2 HG02630.hp1 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*701_*712dupCACACA others(6): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 713 | INFO_REALIGN_3_PRIME | chr14 | 76202536 | ||||
| chr14:76202536
|
T | TACACACA others(7): Show |
2 | a0001c0001t0040a0001c0003t0019 | 4 | HG02622.hp1 HG02897.hp1 HG02965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*699_*712dupCACACA others(8): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 713 | INFO_REALIGN_3_PRIME | chr14 | 76202536 | ||||
| chr14:76202536
|
TAC | T | 46 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(43): Show | 197 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*711_*712delCA | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 711 | INFO_REALIGN_3_PRIME | chr14 | 76202536 | ||||
| chr14:76202536
|
TACACACA others(3): Show |
T | 1 | a0001c0001t0064 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*703_*712delCACACA others(4): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 703 | INFO_REALIGN_3_PRIME | chr14 | 76202536 | ||||
| chr14:76202562
|
C | CAG | 23 | a0001c0001t0001a0001c0001t0012a0001c0001t0014others(20): Show | 127 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*713_*714dupGA | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 715 | INFO_REALIGN_3_PRIME | chr14 | 76202562 | ||||
| chr14:76202562
|
C | G | 28 | a0001c0001t0003a0001c0001t0004a0001c0001t0009others(25): Show | 108 | HG00140.hp2 HG00408.hp1 HG00621.hp1 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*711C>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 711 | chr14 | 76202562 | |||||
| chr14:76202929
|
A | G | 3 | a0001c0001t0037a0001c0001t0090a0001c0001t0091 | 4 | NA18747.hp2 NA18942.hp1 NA19055.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1078A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 1078 | chr14 | 76202929 | |||||
| chr14:76202966
|
C | A | 43 | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(40): Show | 194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
3_prime_UTR_variant | MODIFIER | c.*1115C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 1115 | chr14 | 76202966 | |||||
| chr14:76203109
|
T | C | 1 | a0001c0001t0080 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1258T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 1258 | chr14 | 76203109 | |||||
| chr14:76203116
|
T | G | 1 | a0001c0001t0081 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1265T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 1265 | chr14 | 76203116 | |||||
| chr14:76203126
|
C | G | 1 | a0001c0001t0026 | 2 | HG03239.hp2 HG04199.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1275C>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 1275 | chr14 | 76203126 | |||||
| chr14:76203131
|
T | C | 1 | a0001c0001t0087 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1280T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 1280 | chr14 | 76203131 | |||||
| chr14:76203315
|
A | G | 73 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(70): Show | 307 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(304): Show |
3_prime_UTR_variant | MODIFIER | c.*1464A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 1464 | chr14 | 76203315 | |||||
| chr14:76203439
|
G | A | 1 | a0001c0001t0008 | 8 | HG00408.hp2 HG02027.hp2 HG02040.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1588G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 1588 | chr14 | 76203439 | |||||
| chr14:76203449
|
G | C | 1 | a0001c0001t0054 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1598G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 1598 | chr14 | 76203449 | |||||
| chr14:76203509
|
T | C | 1 | a0001c0001t0033 | 2 | HG02015.hp1 HG02165.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1658T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 1658 | chr14 | 76203509 | |||||
| chr14:76203550
|
G | A | 1 | a0001c0001t0088 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1699G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 1699 | chr14 | 76203550 | |||||
| chr14:76203693
|
G | A | 7 | a0001c0001t0003a0001c0001t0036a0001c0001t0066others(4): Show | 41 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1842G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 1842 | chr14 | 76203693 | |||||
| chr14:76203853
|
G | A | 1 | a0001c0001t0067 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2002G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 2002 | chr14 | 76203853 | |||||
| chr14:76204150
|
C | T | 1 | a0001c0001t0063 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2299C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 2299 | chr14 | 76204150 | |||||
| chr14:76204245
|
G | T | 1 | a0001c0001t0022 | 3 | HG01256.hp2 HG01361.hp2 HG01934.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2394G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 2394 | chr14 | 76204245 | |||||
| chr14:76204290
|
A | G | 1 | a0001c0001t0018 | 4 | NA18960.hp1 NA18991.hp1 NA19062.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2439A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 2439 | chr14 | 76204290 | |||||
| chr14:76204310
|
C | G | 1 | a0001c0001t0023 | 3 | HG00741.hp1 HG01516.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2459C>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 2459 | chr14 | 76204310 | |||||
| chr14:76204438
|
C | T | 22 | a0001c0001t0001a0001c0001t0012a0001c0001t0014others(19): Show | 126 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*2587C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 2587 | chr14 | 76204438 | |||||
| chr14:76204554
|
G | A | 5 | a0001c0001t0003a0001c0001t0036a0001c0001t0066others(2): Show | 39 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*2703G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 2703 | chr14 | 76204554 | |||||
| chr14:76204597
|
T | G | 1 | a0001c0001t0055 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2746T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 2746 | chr14 | 76204597 | |||||
| chr14:76204661
|
A | G | 1 | a0001c0001t0081 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2810A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 2810 | chr14 | 76204661 | |||||
| chr14:76204784
|
A | G | 1 | a0001c0001t0053 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2933A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 2933 | chr14 | 76204784 | |||||
| chr14:76204956
|
TTTGTTGT others(2): Show |
T | 4 | a0001c0001t0011a0001c0001t0060a0001c0001t0061others(1): Show | 10 | HG01891.hp1 HG02145.hp1 HG02258.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3123_*3131delGTTG others(5): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 3123 | INFO_REALIGN_3_PRIME | chr14 | 76204956 | ||||
| chr14:76205015
|
G | A | 3 | a0001c0001t0037a0001c0001t0090a0001c0001t0091 | 4 | NA18747.hp2 NA18942.hp1 NA19055.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3164G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 3164 | chr14 | 76205015 | |||||
| chr14:76205364
|
G | C | 1 | a0001c0001t0037 | 2 | NA18942.hp1 NA19090.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3513G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 3513 | chr14 | 76205364 | |||||
| chr14:76205484
|
G | A | 1 | a0001c0001t0029 | 2 | HG01496.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3633G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 3633 | chr14 | 76205484 | |||||
| chr14:76205608
|
A | G | 23 | a0001c0001t0001a0001c0001t0012a0001c0001t0014others(20): Show | 127 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*3757A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 3757 | chr14 | 76205608 | |||||
| chr14:76205618
|
G | T | 8 | a0001c0001t0003a0001c0001t0036a0001c0001t0066others(5): Show | 42 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*3767G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 3767 | chr14 | 76205618 | |||||
| chr14:76205711
|
A | C | 8 | a0001c0001t0003a0001c0001t0036a0001c0001t0066others(5): Show | 42 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*3860A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 3860 | chr14 | 76205711 | |||||
| chr14:76205761
|
A | C | 16 | a0001c0001t0004a0001c0001t0009a0001c0001t0010others(13): Show | 59 | HG00140.hp2 HG00673.hp2 HG01074.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*3910A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 3910 | chr14 | 76205761 | |||||
| chr14:76205863
|
T | C | 1 | a0001c0001t0056 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4012T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 4012 | chr14 | 76205863 | |||||
| chr14:76205921
|
G | A | 1 | a0001c0001t0088 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4070G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 4070 | chr14 | 76205921 | |||||
| chr14:76206088
|
T | C | 1 | a0001c0001t0060 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4237T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 4237 | chr14 | 76206088 | |||||
| chr14:76206203
|
C | T | 1 | a0001c0001t0046 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4352C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 4352 | chr14 | 76206203 | |||||
| chr14:76206284
|
T | C | 96 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(93): Show | 400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
3_prime_UTR_variant | MODIFIER | c.*4433T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 4433 | chr14 | 76206284 | |||||
| chr14:76206328
|
A | G | 1 | a0001c0001t0023 | 3 | HG00741.hp1 HG01516.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4477A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 4477 | chr14 | 76206328 | |||||
| chr14:76206431
|
T | C | 1 | a0001c0001t0081 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4580T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 4580 | chr14 | 76206431 | |||||
| chr14:76206664
|
G | A | 1 | a0001c0001t0082 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4813G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 4813 | chr14 | 76206664 | |||||
| chr14:76206770
|
T | C | 1 | a0001c0001t0068 | 1 | NA19077.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4919T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 4919 | chr14 | 76206770 | |||||
| chr14:76206794
|
G | A | 2 | a0001c0005t0016a0003c0006t0016 | 4 | HG02809.hp2 HG02965.hp2 NA19030.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4943G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 4943 | chr14 | 76206794 | |||||
| chr14:76206863
|
G | C | 1 | a0001c0001t0080 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5012G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 5012 | chr14 | 76206863 | |||||
| chr14:76206921
|
T | A | 1 | a0001c0001t0034 | 2 | HG03831.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5070T>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 5070 | chr14 | 76206921 | |||||
| chr14:76206931
|
T | C | 2 | a0001c0001t0009a0001c0001t0083 | 9 | HG01167.hp2 HG01169.hp2 HG01175.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5080T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 5080 | chr14 | 76206931 | |||||
| chr14:76206931
|
T | TC | 14 | a0001c0001t0004a0001c0001t0010a0001c0001t0024others(11): Show | 50 | HG00140.hp2 HG00673.hp2 HG01074.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*5080_*5081insC | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 5081 | chr14 | 76206931 | |||||
| chr14:76206932
|
T | C | 16 | a0001c0001t0004a0001c0001t0009a0001c0001t0010others(13): Show | 59 | HG00140.hp2 HG00673.hp2 HG01074.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*5081T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 5081 | chr14 | 76206932 | |||||
| chr14:76206940
|
A | G | 8 | a0001c0001t0003a0001c0001t0036a0001c0001t0066others(5): Show | 42 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*5089A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 5089 | chr14 | 76206940 | |||||
| chr14:76207007
|
G | A | 1 | a0001c0001t0088 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5156G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 5156 | chr14 | 76207007 | |||||
| chr14:76207016
|
T | C | 8 | a0001c0001t0003a0001c0001t0036a0001c0001t0066others(5): Show | 42 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*5165T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 5165 | chr14 | 76207016 | |||||
| chr14:76207057
|
A | G | 92 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(89): Show | 394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
3_prime_UTR_variant | MODIFIER | c.*5206A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 5206 | chr14 | 76207057 | |||||
| chr14:76207075
|
G | A | 1 | a0001c0001t0007 | 8 | HG00323.hp2 HG01106.hp1 HG01978.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5224G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 5224 | chr14 | 76207075 | |||||
| chr14:76207153
|
A | G | 6 | a0001c0001t0005a0001c0001t0007a0001c0001t0027others(3): Show | 28 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*5302A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 5302 | chr14 | 76207153 | |||||
| chr14:76207242
|
G | A | 2 | a0001c0001t0050a0001c0001t0057 | 2 | HG02572.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5391G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 5391 | chr14 | 76207242 | |||||
| chr14:76207376
|
A | G | 1 | a0001c0001t0080 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5525A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 5525 | chr14 | 76207376 | |||||
| chr14:76207399
|
G | A | 1 | a0001c0001t0088 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5548G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 5548 | chr14 | 76207399 | |||||
| chr14:76207530
|
G | GA | 20 | a0001c0001t0005a0001c0001t0006a0001c0001t0007others(17): Show | 69 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*5689dupA | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 5690 | INFO_REALIGN_3_PRIME | chr14 | 76207530 | ||||
| chr14:76207658
|
G | T | 7 | a0001c0001t0010a0001c0001t0035a0001c0001t0037others(4): Show | 16 | NA18747.hp2 NA18942.hp1 NA18953.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*5807G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 5807 | chr14 | 76207658 | |||||
| chr14:76207678
|
C | T | 1 | a0001c0001t0083 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5827C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 5827 | chr14 | 76207678 | |||||
| chr14:76207736
|
G | A | 1 | a0001c0001t0084 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5885G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 5885 | chr14 | 76207736 | |||||
| chr14:76207777
|
A | G | 1 | a0001c0001t0091 | 1 | NA19055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5926A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 5926 | chr14 | 76207777 | |||||
| chr14:76208216
|
A | T | 1 | a0001c0001t0088 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6365A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 6365 | chr14 | 76208216 | |||||
| chr14:76208274
|
C | T | 22 | a0001c0001t0001a0001c0001t0012a0001c0001t0014others(19): Show | 126 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*6423C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 6423 | chr14 | 76208274 | |||||
| chr14:76208289
|
A | G | 5 | a0001c0001t0023a0001c0001t0030a0001c0001t0033others(2): Show | 9 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*6438A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 6438 | chr14 | 76208289 | |||||
| chr14:76208338
|
T | C | 12 | a0001c0001t0003a0001c0001t0023a0001c0001t0030others(9): Show | 50 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*6487T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 6487 | chr14 | 76208338 | |||||
| chr14:76208430
|
T | C | 22 | a0001c0001t0001a0001c0001t0012a0001c0001t0014others(19): Show | 126 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*6579T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 6579 | chr14 | 76208430 | |||||
| chr14:76208497
|
A | C | 1 | a0001c0001t0036 | 2 | HG02040.hp1 NA19007.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6646A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 6646 | chr14 | 76208497 | |||||
| chr14:76208581
|
G | A | 1 | a0001c0001t0069 | 1 | HG02148.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6730G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 6730 | chr14 | 76208581 | |||||
| chr14:76208581
|
G | C | 5 | a0001c0001t0023a0001c0001t0030a0001c0001t0033others(2): Show | 9 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*6730G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 6730 | chr14 | 76208581 | |||||
| chr14:76208615
|
C | G | 1 | a0001c0001t0076 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6764C>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 6764 | chr14 | 76208615 | |||||
| chr14:76208876
|
A | G | 21 | a0001c0001t0005a0001c0001t0006a0001c0001t0007others(18): Show | 70 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*7025A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 7025 | chr14 | 76208876 | |||||
| chr14:76208947
|
G | A | 3 | a0001c0001t0037a0001c0001t0090a0001c0001t0091 | 4 | NA18747.hp2 NA18942.hp1 NA19055.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7096G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 7096 | chr14 | 76208947 | |||||
| chr14:76208972
|
G | T | 2 | a0001c0001t0069a0001c0001t0075 | 2 | HG00642.hp2 HG02148.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7121G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 7121 | chr14 | 76208972 | |||||
| chr14:76209031
|
G | C | 10 | a0001c0001t0003a0001c0001t0023a0001c0001t0030others(7): Show | 48 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*7180G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 7180 | chr14 | 76209031 | |||||
| chr14:76209066
|
A | G | 5 | a0001c0001t0023a0001c0001t0030a0001c0001t0033others(2): Show | 9 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*7215A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 7215 | chr14 | 76209066 | |||||
| chr14:76209109
|
A | G | 23 | a0001c0001t0001a0001c0001t0012a0001c0001t0014others(20): Show | 127 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*7258A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 7258 | chr14 | 76209109 | |||||
| chr14:76209197
|
G | C | 73 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(70): Show | 307 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(304): Show |
3_prime_UTR_variant | MODIFIER | c.*7346G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 7346 | chr14 | 76209197 | |||||
| chr14:76209201
|
A | G | 1 | a0001c0001t0031 | 2 | HG03654.hp1 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7350A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 7350 | chr14 | 76209201 | |||||
| chr14:76209253
|
C | A | 1 | a0001c0001t0024 | 3 | HG00140.hp2 HG01515.hp1 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7402C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 7402 | chr14 | 76209253 | |||||
| chr14:76209258
|
G | A | 1 | a0004c0007t0089 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7407G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 7407 | chr14 | 76209258 | |||||
| chr14:76209531
|
T | C | 2 | a0001c0001t0025a0001c0001t0084 | 4 | HG02451.hp1 HG03195.hp2 HG03453.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7680T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 7680 | chr14 | 76209531 | |||||
| chr14:76209655
|
T | A | 4 | a0001c0001t0023a0001c0001t0030a0001c0001t0033others(1): Show | 8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7804T>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 7804 | chr14 | 76209655 | |||||
| chr14:76209711
|
G | T | 4 | a0001c0001t0023a0001c0001t0030a0001c0001t0033others(1): Show | 8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7860G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 7860 | chr14 | 76209711 | |||||
| chr14:76210012
|
A | G | 11 | a0001c0001t0002a0001c0001t0008a0001c0001t0021others(8): Show | 71 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*8161A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 8161 | chr14 | 76210012 | |||||
| chr14:76210092
|
C | G | 1 | a0001c0001t0066 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8241C>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 8241 | chr14 | 76210092 | |||||
| chr14:76210097
|
C | A | 2 | a0001c0001t0021a0001c0001t0065 | 4 | HG02486.hp2 HG02559.hp1 HG02886.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8246C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 8246 | chr14 | 76210097 | |||||
| chr14:76210098
|
T | C | 5 | a0001c0001t0023a0001c0001t0030a0001c0001t0033others(2): Show | 9 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*8247T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 8247 | chr14 | 76210098 | |||||
| chr14:76210170
|
T | C | 1 | a0001c0001t0053 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8319T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 8319 | chr14 | 76210170 | |||||
| chr14:76210237
|
A | T | 4 | a0001c0001t0023a0001c0001t0030a0001c0001t0033others(1): Show | 8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*8386A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 8386 | chr14 | 76210237 | |||||
| chr14:76210357
|
C | T | 1 | a0004c0007t0089 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8506C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 8506 | chr14 | 76210357 | |||||
| chr14:76210360
|
T | C | 5 | a0001c0001t0023a0001c0001t0030a0001c0001t0033others(2): Show | 9 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*8509T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 8509 | chr14 | 76210360 | |||||
| chr14:76210408
|
G | C | 1 | a0001c0001t0080 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8557G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 8557 | chr14 | 76210408 | |||||
| chr14:76210464
|
C | T | 1 | a0001c0001t0040 | 1 | HG02897.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8613C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 8613 | chr14 | 76210464 | |||||
| chr14:76210484
|
T | C | 22 | a0001c0001t0001a0001c0001t0012a0001c0001t0014others(19): Show | 126 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*8633T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 8633 | chr14 | 76210484 | |||||
| chr14:76210557
|
A | G | 18 | a0001c0001t0005a0001c0001t0006a0001c0001t0007others(15): Show | 63 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*8706A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 8706 | chr14 | 76210557 | |||||
| chr14:76210651
|
T | G | 4 | a0001c0001t0023a0001c0001t0030a0001c0001t0033others(1): Show | 8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*8800T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 8800 | chr14 | 76210651 | |||||
| chr14:76210653
|
C | G | 1 | a0001c0001t0081 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8802C>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 8802 | chr14 | 76210653 | |||||
| chr14:76210662
|
G | A | 4 | a0001c0001t0023a0001c0001t0030a0001c0001t0033others(1): Show | 8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*8811G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 8811 | chr14 | 76210662 | |||||
| chr14:76210714
|
T | C | 79 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(76): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
3_prime_UTR_variant | MODIFIER | c.*8863T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 8863 | chr14 | 76210714 | |||||
| chr14:76210715
|
G | A | 4 | a0001c0001t0023a0001c0001t0030a0001c0001t0033others(1): Show | 8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*8864G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 8864 | chr14 | 76210715 | |||||
| chr14:76210762
|
T | C | 1 | a0001c0001t0070 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8911T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 8911 | chr14 | 76210762 | |||||
| chr14:76210852
|
T | A | 1 | a0001c0001t0071 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9001T>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 9001 | chr14 | 76210852 | |||||
| chr14:76211305
|
G | A | 4 | a0001c0001t0023a0001c0001t0030a0001c0001t0033others(1): Show | 8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*9454G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 9454 | chr14 | 76211305 | |||||
| chr14:76211380
|
G | A | 1 | a0001c0001t0041 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9529G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 9529 | chr14 | 76211380 | |||||
| chr14:76211582
|
G | A | 1 | a0001c0001t0088 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9731G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 9731 | chr14 | 76211582 | |||||
| chr14:76211725
|
T | C | 4 | a0001c0001t0023a0001c0001t0030a0001c0001t0033others(1): Show | 8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*9874T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 9874 | chr14 | 76211725 | |||||
| chr14:76211817
|
G | A | 1 | a0001c0001t0045 | 1 | NA18991.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9966G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 9966 | chr14 | 76211817 | |||||
| chr14:76212155
|
A | G | 1 | a0001c0001t0088 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10304A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 10304 | chr14 | 76212155 | |||||
| chr14:76212250
|
T | C | 1 | a0001c0001t0058 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10399T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 10399 | chr14 | 76212250 | |||||
| chr14:76212351
|
G | A | 1 | a0001c0001t0050 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10500G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 10500 | chr14 | 76212351 | |||||
| chr14:76212377
|
G | A | 1 | a0001c0001t0047 | 1 | NA18978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10526G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 10526 | chr14 | 76212377 | |||||
| chr14:76212412
|
A | C | 1 | a0001c0001t0048 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10561A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 10561 | chr14 | 76212412 | |||||
| chr14:76212413
|
C | A | 6 | a0001c0001t0014a0001c0001t0023a0001c0001t0030others(3): Show | 15 | HG00140.hp1 HG00621.hp2 HG00738.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*10562C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 10562 | chr14 | 76212413 | |||||
| chr14:76212453
|
C | T | 4 | a0001c0001t0011a0001c0001t0060a0001c0001t0061others(1): Show | 10 | HG01891.hp1 HG02145.hp1 HG02258.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*10602C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 10602 | chr14 | 76212453 | |||||
| chr14:76212465
|
T | C | 1 | a0001c0001t0085 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10614T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 10614 | chr14 | 76212465 | |||||
| chr14:76212551
|
T | C | 4 | a0001c0001t0023a0001c0001t0030a0001c0001t0033others(1): Show | 8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*10700T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 10700 | chr14 | 76212551 | |||||
| chr14:76212716
|
T | G | 28 | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(25): Show | 131 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*10865T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 10865 | chr14 | 76212716 | |||||
| chr14:76212759
|
G | A | 95 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(92): Show | 397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
3_prime_UTR_variant | MODIFIER | c.*10908G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 10908 | chr14 | 76212759 | |||||
| chr14:76212800
|
A | C | 1 | a0001c0001t0074 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10949A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 10949 | chr14 | 76212800 | |||||
| chr14:76212823
|
G | A | 4 | a0001c0001t0023a0001c0001t0030a0001c0001t0033others(1): Show | 8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*10972G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 10972 | chr14 | 76212823 | |||||
| chr14:76212844
|
A | G | 2 | a0001c0001t0079a0004c0007t0089 | 2 | HG02630.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10993A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 10993 | chr14 | 76212844 | |||||
| chr14:76212946
|
C | A | 4 | a0001c0001t0023a0001c0001t0030a0001c0001t0033others(1): Show | 8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*11095C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 11095 | chr14 | 76212946 | |||||
| chr14:76213055
|
A | G | 4 | a0001c0001t0023a0001c0001t0030a0001c0001t0033others(1): Show | 8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*11204A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 11204 | chr14 | 76213055 | |||||
| chr14:76213225
|
A | G | 4 | a0001c0001t0023a0001c0001t0030a0001c0001t0033others(1): Show | 8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*11374A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 11374 | chr14 | 76213225 | |||||
| chr14:76213268
|
G | A | 1 | a0001c0001t0051 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11417G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 11417 | chr14 | 76213268 | |||||
| chr14:76213532
|
G | A | 4 | a0001c0001t0023a0001c0001t0030a0001c0001t0033others(1): Show | 8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*11681G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 11681 | chr14 | 76213532 | |||||
| chr14:76213610
|
G | A | 1 | a0001c0001t0073 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11759G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 11759 | chr14 | 76213610 | |||||
| chr14:76213696
|
A | T | 1 | a0001c0001t0035 | 2 | NA18953.hp1 NA18969.hp2 |
3_prime_UTR_variant | MODIFIER | c.*11845A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 11845 | chr14 | 76213696 | |||||
| chr14:76213804
|
G | A | 1 | a0001c0001t0017 | 4 | HG01109.hp1 HG02145.hp2 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*11953G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 11953 | chr14 | 76213804 | |||||
| chr14:76213833
|
C | G | 1 | a0001c0001t0042 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11982C>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 11982 | chr14 | 76213833 | |||||
| chr14:76213860
|
G | A | 4 | a0001c0001t0023a0001c0001t0030a0001c0001t0033others(1): Show | 8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*12009G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 12009 | chr14 | 76213860 | |||||
| chr14:76213891
|
G | C | 19 | a0001c0001t0005a0001c0001t0006a0001c0001t0007others(16): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*12040G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 12040 | chr14 | 76213891 | |||||
| chr14:76213900
|
T | C | 1 | a0001c0001t0086 | 1 | NA18999.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12049T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 12049 | chr14 | 76213900 | |||||
| chr14:76213923
|
T | G | 1 | a0001c0001t0028 | 2 | HG02074.hp1 HG02155.hp2 |
3_prime_UTR_variant | MODIFIER | c.*12072T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 12072 | chr14 | 76213923 | |||||
| chr14:76214035
|
T | G | 1 | a0001c0001t0012 | 7 | NA18939.hp2 NA18968.hp1 NA18974.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*12184T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 12184 | chr14 | 76214035 | |||||
| chr14:76214216
|
T | A | 1 | a0001c0001t0061 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12365T>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 10/10 | 12365 | chr14 | 76214216 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:76151998
|
G | A | 87 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(84): Show | 126 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(123): Show |
splice_region_variant&intron_variant | LOW | c.-11+7G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76151998 | ||||||
| chr14:76152002
|
G | C | 2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | HG01981.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-11+11G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76152002 | ||||||
| chr14:76152097
|
C | T | 87 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(84): Show | 126 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.-11+106C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76152097 | ||||||
| chr14:76152112
|
G | T | 1 | a0001c0001t0003g0291 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-11+121G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76152112 | ||||||
| chr14:76152158
|
C | T | 1 | a0001c0001t0079g0290 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-11+167C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76152158 | ||||||
| chr14:76152221
|
C | T | 1 | a0001c0001t0061g0289 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-11+230C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76152221 | ||||||
| chr14:76152250
|
C | A | 1 | a0003c0006t0016g0106 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-11+259C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76152250 | ||||||
| chr14:76152259
|
CCGAGCCA others(22): Show |
C | 1 | a0001c0001t0085g0288 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-11+271_-11+299del others(29): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 76152259 | |||||
| chr14:76152263
|
G | A | 1 | a0001c0001t0056g0107 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-11+272G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76152263 | ||||||
| chr14:76152416
|
A | G | 249 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(246): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.-11+425A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76152416 | ||||||
| chr14:76152484
|
G | T | 102 | a0001c0001t0004g0005a0001c0001t0004g0010a0001c0001t0004g0041others(99): Show | 121 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.-11+493G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76152484 | ||||||
| chr14:76152495
|
C | G | 3 | a0001c0001t0030g0257a0001c0001t0030g0259a0001c0008t0039g0258 | 3 | HG00738.hp2 HG01346.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.-11+504C>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76152495 | ||||||
| chr14:76152506
|
C | A | 86 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(83): Show | 125 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.-11+515C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76152506 | ||||||
| chr14:76152506
|
C | T | 163 | a0001c0001t0001g0043a0001c0001t0002g0004a0001c0001t0002g0006others(160): Show | 212 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.-11+515C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76152506 | ||||||
| chr14:76152685
|
G | T | 1 | a0001c0001t0033g0256 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-11+694G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76152685 | ||||||
| chr14:76152767
|
G | T | 1 | a0001c0001t0088g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-11+776G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76152767 | ||||||
| chr14:76152824
|
A | C | 125 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(122): Show | 176 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.-11+833A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76152824 | ||||||
| chr14:76152846
|
G | T | 2 | a0001c0001t0010g0286a0001c0001t0086g0287 | 2 | NA18999.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.-11+855G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76152846 | ||||||
| chr14:76152939
|
C | CT | 64 | a0001c0001t0001g0105a0001c0001t0005g0025a0001c0001t0005g0026others(61): Show | 66 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.-11+958dupT | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 76152939 | |||||
| chr14:76152949
|
T | C | 1 | a0001c0001t0050g0165 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-11+958T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76152949 | ||||||
| chr14:76153106
|
G | T | 2 | a0001c0001t0035g0284a0001c0001t0035g0285 | 2 | NA18953.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.-11+1115G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76153106 | ||||||
| chr14:76153267
|
A | C | 3 | a0001c0001t0030g0257a0001c0001t0030g0259a0001c0008t0039g0258 | 3 | HG00738.hp2 HG01346.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.-10-1087A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76153267 | ||||||
| chr14:76153292
|
A | G | 2 | a0001c0001t0017g0015a0001c0001t0017g0226 | 4 | HG01109.hp1 HG02145.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-1062A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76153292 | ||||||
| chr14:76153403
|
T | C | 188 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(185): Show | 241 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.-10-951T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76153403 | ||||||
| chr14:76153406
|
C | T | 1 | a0001c0001t0021g0225 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-10-948C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76153406 | ||||||
| chr14:76153618
|
A | G | 57 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0009others(54): Show | 73 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-10-736A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76153618 | ||||||
| chr14:76154144
|
A | C | 2 | a0001c0001t0010g0286a0001c0001t0086g0287 | 2 | NA18999.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.-10-210A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76154144 | ||||||
| chr14:76154350
|
G | A | 2 | a0001c0001t0002g0184a0001c0001t0002g0185 | 2 | NA18989.hp2 NA19080.hp2 |
splice_region_variant&intron_variant | LOW | c.-10-4G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 1/9 | chr14 | 76154350 | ||||||
| chr14:76155224
|
G | A | 249 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(246): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.662+199G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76155224 | ||||||
| chr14:76155328
|
C | T | 188 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(185): Show | 241 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.662+303C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76155328 | ||||||
| chr14:76155334
|
A | G | 188 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(185): Show | 241 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.662+309A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76155334 | ||||||
| chr14:76155458
|
T | A | 1 | a0001c0001t0001g0044 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.662+433T>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76155458 | ||||||
| chr14:76155693
|
T | C | 57 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0009others(54): Show | 73 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.662+668T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76155693 | ||||||
| chr14:76155877
|
T | G | 1 | a0001c0001t0050g0165 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.662+852T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76155877 | ||||||
| chr14:76155898
|
G | A | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.662+873G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76155898 | ||||||
| chr14:76155999
|
A | G | 4 | a0001c0001t0017g0015a0001c0001t0017g0226a0001c0001t0029g0182others(1): Show | 6 | HG01109.hp1 HG01496.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.662+974A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76155999 | ||||||
| chr14:76156036
|
C | G | 2 | a0001c0001t0002g0221a0001c0001t0002g0222 | 2 | HG00558.hp1 HG00597.hp1 |
intron_variant | MODIFIER | c.662+1011C>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76156036 | ||||||
| chr14:76156264
|
A | G | 29 | a0001c0001t0003g0002a0001c0001t0003g0035a0001c0001t0003g0231others(26): Show | 39 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.662+1239A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76156264 | ||||||
| chr14:76156637
|
T | G | 1 | a0001c0001t0007g0110 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.662+1612T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76156637 | ||||||
| chr14:76156762
|
G | T | 1 | a0001c0001t0002g0220 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.662+1737G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76156762 | ||||||
| chr14:76156785
|
G | A | 8 | a0001c0001t0015g0112a0001c0001t0015g0113a0001c0001t0015g0114others(5): Show | 8 | HG01081.hp2 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.662+1760G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76156785 | ||||||
| chr14:76156860
|
T | A | 1 | a0001c0001t0084g0260 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.662+1835T>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76156860 | ||||||
| chr14:76156875
|
C | T | 1 | a0001c0001t0080g0230 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.662+1850C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76156875 | ||||||
| chr14:76157344
|
AG | A | 4 | a0001c0001t0005g0119a0001c0001t0005g0120a0001c0001t0005g0121others(1): Show | 4 | NA18982.hp1 NA19005.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.662+2321delG | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 76157344 | |||||
| chr14:76157363
|
G | A | 188 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(185): Show | 241 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.662+2338G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76157363 | ||||||
| chr14:76157377
|
G | A | 31 | a0001c0001t0003g0002a0001c0001t0003g0035a0001c0001t0003g0231others(28): Show | 41 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.662+2352G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76157377 | ||||||
| chr14:76157480
|
A | G | 2 | a0001c0002t0001g0023a0001c0002t0001g0104 | 3 | NA18981.hp1 NA19068.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.662+2455A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76157480 | ||||||
| chr14:76157673
|
G | GT | 74 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0222others(71): Show | 82 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.662+2658dupT | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 76157673 | |||||
| chr14:76157683
|
TC | T | 113 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(110): Show | 162 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.662+2659delC | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76157683 | ||||||
| chr14:76157684
|
C | T | 75 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0102others(72): Show | 79 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.662+2659C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76157684 | ||||||
| chr14:76157783
|
A | T | 1 | a0001c0001t0051g0167 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.662+2758A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76157783 | ||||||
| chr14:76158139
|
T | C | 1 | a0001c0001t0081g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.662+3114T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76158139 | ||||||
| chr14:76158198
|
A | C | 1 | a0001c0001t0058g0216 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.662+3173A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76158198 | ||||||
| chr14:76158199
|
T | C | 2 | a0001c0001t0069g0045a0001c0001t0075g0046 | 2 | HG00642.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.662+3174T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76158199 | ||||||
| chr14:76158204
|
T | G | 119 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(116): Show | 168 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.662+3179T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76158204 | ||||||
| chr14:76158357
|
A | G | 168 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(165): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.662+3332A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76158357 | ||||||
| chr14:76158541
|
A | G | 55 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0009others(52): Show | 71 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.662+3516A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76158541 | ||||||
| chr14:76158544
|
A | G | 230 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(227): Show | 300 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.662+3519A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76158544 | ||||||
| chr14:76158682
|
G | A | 168 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(165): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.662+3657G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76158682 | ||||||
| chr14:76158811
|
C | A | 2 | a0001c0001t0017g0015a0001c0001t0017g0226 | 4 | HG01109.hp1 HG02145.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.662+3786C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76158811 | ||||||
| chr14:76158933
|
G | T | 1 | a0001c0001t0081g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.662+3908G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76158933 | ||||||
| chr14:76159099
|
G | T | 230 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(227): Show | 300 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.662+4074G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76159099 | ||||||
| chr14:76159129
|
C | G | 1 | a0001c0001t0053g0180 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.662+4104C>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76159129 | ||||||
| chr14:76159150
|
G | A | 29 | a0001c0001t0003g0002a0001c0001t0003g0035a0001c0001t0003g0231others(26): Show | 39 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.662+4125G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76159150 | ||||||
| chr14:76159189
|
A | T | 2 | a0001c0001t0026g0163a0001c0001t0026g0164 | 2 | HG03239.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.662+4164A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76159189 | ||||||
| chr14:76159316
|
T | G | 4 | a0001c0001t0013g0123a0001c0001t0013g0227a0001c0001t0026g0163others(1): Show | 4 | HG01934.hp2 HG03239.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.662+4291T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76159316 | ||||||
| chr14:76159339
|
G | T | 6 | a0001c0001t0023g0016a0001c0001t0030g0257a0001c0001t0030g0259others(3): Show | 8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.662+4314G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76159339 | ||||||
| chr14:76159375
|
G | A | 3 | a0001c0001t0003g0231a0001c0001t0003g0232a0001c0001t0003g0233 | 3 | HG00673.hp1 HG02083.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.662+4350G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76159375 | ||||||
| chr14:76159474
|
A | G | 1 | a0001c0001t0005g0122 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.662+4449A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76159474 | ||||||
| chr14:76159475
|
C | T | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.662+4450C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76159475 | ||||||
| chr14:76159524
|
T | C | 2 | a0001c0001t0002g0186a0001c0001t0002g0217 | 2 | NA18951.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.662+4499T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76159524 | ||||||
| chr14:76159567
|
A | G | 31 | a0001c0001t0003g0002a0001c0001t0003g0035a0001c0001t0003g0231others(28): Show | 41 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.662+4542A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76159567 | ||||||
| chr14:76159738
|
C | T | 6 | a0001c0001t0023g0016a0001c0001t0030g0257a0001c0001t0030g0259others(3): Show | 8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.662+4713C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76159738 | ||||||
| chr14:76159860
|
T | G | 1 | a0001c0001t0003g0234 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.662+4835T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76159860 | ||||||
| chr14:76159934
|
C | T | 1 | a0001c0001t0080g0230 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.662+4909C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76159934 | ||||||
| chr14:76159965
|
T | C | 1 | a0001c0001t0006g0124 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.662+4940T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76159965 | ||||||
| chr14:76159989
|
C | T | 87 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(84): Show | 126 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.662+4964C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76159989 | ||||||
| chr14:76160040
|
G | A | 230 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(227): Show | 300 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.662+5015G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76160040 | ||||||
| chr14:76160057
|
C | T | 1 | a0001c0001t0002g0185 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.662+5032C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76160057 | ||||||
| chr14:76160082
|
C | T | 1 | a0001c0001t0088g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.662+5057C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76160082 | ||||||
| chr14:76160126
|
A | G | 1 | a0001c0001t0081g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.662+5101A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76160126 | ||||||
| chr14:76160129
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.662+5104G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76160129 | ||||||
| chr14:76160155
|
A | G | 1 | a0001c0001t0032g0098 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.662+5130A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76160155 | ||||||
| chr14:76160173
|
G | A | 230 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(227): Show | 300 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.662+5148G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76160173 | ||||||
| chr14:76160247
|
C | T | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.662+5222C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76160247 | ||||||
| chr14:76160333
|
C | T | 6 | a0001c0001t0023g0016a0001c0001t0030g0257a0001c0001t0030g0259others(3): Show | 8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.662+5308C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76160333 | ||||||
| chr14:76160360
|
T | C | 228 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(225): Show | 298 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.662+5335T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76160360 | ||||||
| chr14:76160430
|
A | G | 1 | a0001c0001t0002g0186 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.662+5405A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76160430 | ||||||
| chr14:76160771
|
A | G | 3 | a0001c0001t0030g0257a0001c0001t0030g0259a0001c0008t0039g0258 | 3 | HG00738.hp2 HG01346.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.662+5746A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76160771 | ||||||
| chr14:76160787
|
C | T | 1 | a0001c0001t0003g0253 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.662+5762C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76160787 | ||||||
| chr14:76160958
|
A | G | 230 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(227): Show | 300 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.663-5705A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76160958 | ||||||
| chr14:76161322
|
C | CTTTAT | 230 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(227): Show | 300 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.663-5337_663-5336i others(7): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 76161322 | |||||
| chr14:76161576
|
T | C | 42 | a0001c0001t0004g0005a0001c0001t0004g0010a0001c0001t0004g0041others(39): Show | 59 | HG00140.hp2 HG00673.hp2 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.663-5087T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76161576 | ||||||
| chr14:76161592
|
C | T | 1 | a0001c0001t0007g0162 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.663-5071C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76161592 | ||||||
| chr14:76161625
|
A | G | 7 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0094others(4): Show | 8 | HG01257.hp1 HG01928.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.663-5038A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76161625 | ||||||
| chr14:76161660
|
T | G | 1 | a0001c0001t0003g0235 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.663-5003T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76161660 | ||||||
| chr14:76161836
|
G | T | 6 | a0001c0001t0023g0016a0001c0001t0030g0257a0001c0001t0030g0259others(3): Show | 8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.663-4827G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76161836 | ||||||
| chr14:76161896
|
C | T | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.663-4767C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76161896 | ||||||
| chr14:76162014
|
T | C | 230 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(227): Show | 300 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.663-4649T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76162014 | ||||||
| chr14:76162062
|
T | C | 2 | a0001c0001t0079g0290a0004c0007t0089g0228 | 2 | HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.663-4601T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76162062 | ||||||
| chr14:76162129
|
C | CAG | 230 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(227): Show | 300 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.663-4533_663-4532d others(4): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 76162129 | |||||
| chr14:76162169
|
C | T | 1 | a0001c0001t0005g0161 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.663-4494C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76162169 | ||||||
| chr14:76162188
|
C | T | 1 | a0001c0001t0027g0160 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.663-4475C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76162188 | ||||||
| chr14:76162281
|
C | T | 6 | a0001c0001t0023g0016a0001c0001t0030g0257a0001c0001t0030g0259others(3): Show | 8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.663-4382C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76162281 | ||||||
| chr14:76162315
|
G | C | 3 | a0001c0005t0016g0168a0001c0005t0016g0169a0001c0005t0016g0181 | 3 | HG02965.hp2 NA19030.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.663-4348G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76162315 | ||||||
| chr14:76162345
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.663-4318G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76162345 | ||||||
| chr14:76162471
|
C | T | 42 | a0001c0001t0004g0005a0001c0001t0004g0010a0001c0001t0004g0041others(39): Show | 59 | HG00140.hp2 HG00673.hp2 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.663-4192C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76162471 | ||||||
| chr14:76162520
|
A | G | 1 | a0001c0001t0080g0230 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.663-4143A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76162520 | ||||||
| chr14:76162650
|
T | C | 29 | a0001c0001t0003g0002a0001c0001t0003g0035a0001c0001t0003g0231others(26): Show | 39 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.663-4013T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76162650 | ||||||
| chr14:76162703
|
T | G | 230 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(227): Show | 300 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.663-3960T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76162703 | ||||||
| chr14:76162925
|
T | G | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.663-3738T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76162925 | ||||||
| chr14:76163045
|
C | A | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.663-3618C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76163045 | ||||||
| chr14:76163138
|
C | T | 42 | a0001c0001t0004g0005a0001c0001t0004g0010a0001c0001t0004g0041others(39): Show | 59 | HG00140.hp2 HG00673.hp2 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.663-3525C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76163138 | ||||||
| chr14:76163174
|
T | C | 230 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(227): Show | 300 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.663-3489T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76163174 | ||||||
| chr14:76163327
|
G | A | 311 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(308): Show | 401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.663-3336G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76163327 | ||||||
| chr14:76163330
|
A | G | 1 | a0001c0001t0050g0165 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.663-3333A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76163330 | ||||||
| chr14:76163338
|
G | A | 2 | a0001c0001t0004g0223a0001c0001t0004g0224 | 2 | HG01074.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.663-3325G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76163338 | ||||||
| chr14:76163526
|
A | G | 1 | a0003c0006t0016g0106 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.663-3137A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76163526 | ||||||
| chr14:76163579
|
G | A | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.663-3084G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76163579 | ||||||
| chr14:76163761
|
A | G | 1 | a0001c0001t0054g0179 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.663-2902A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76163761 | ||||||
| chr14:76163790
|
G | A | 229 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(226): Show | 299 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.663-2873G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76163790 | ||||||
| chr14:76164154
|
T | G | 1 | a0001c0001t0001g0099 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.663-2509T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76164154 | ||||||
| chr14:76164725
|
A | G | 310 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(307): Show | 400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
intron_variant | MODIFIER | c.663-1938A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76164725 | ||||||
| chr14:76164793
|
G | A | 1 | a0001c0001t0077g0109 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.663-1870G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76164793 | ||||||
| chr14:76165092
|
G | A | 2 | a0001c0001t0020g0028a0001c0001t0020g0171 | 3 | HG02886.hp1 HG02922.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.663-1571G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76165092 | ||||||
| chr14:76165363
|
G | A | 2 | a0001c0001t0028g0187a0001c0001t0028g0188 | 2 | HG02074.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.663-1300G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76165363 | ||||||
| chr14:76165365
|
G | A | 1 | a0001c0001t0044g0125 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.663-1298G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76165365 | ||||||
| chr14:76165490
|
CA | C | 10 | a0001c0001t0001g0093a0001c0001t0002g0215a0001c0001t0004g0224others(7): Show | 12 | HG01099.hp1 HG01169.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.663-1158delA | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 76165490 | |||||
| chr14:76165546
|
G | A | 305 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(302): Show | 394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.663-1117G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76165546 | ||||||
| chr14:76165592
|
A | G | 12 | a0001c0001t0010g0039a0001c0001t0010g0040a0001c0001t0010g0276others(9): Show | 15 | NA18747.hp2 NA18942.hp1 NA18953.hp1 others(12): Show |
intron_variant | MODIFIER | c.663-1071A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76165592 | ||||||
| chr14:76165689
|
T | C | 1 | a0001c0001t0057g0178 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.663-974T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76165689 | ||||||
| chr14:76165718
|
T | C | 7 | a0001c0001t0002g0004a0001c0001t0002g0186a0001c0001t0002g0189others(4): Show | 14 | HG00438.hp2 HG02056.hp2 NA18945.hp2 others(11): Show |
intron_variant | MODIFIER | c.663-945T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76165718 | ||||||
| chr14:76165750
|
A | G | 1 | a0001c0001t0004g0041 | 2 | NA18960.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.663-913A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76165750 | ||||||
| chr14:76165892
|
C | G | 2 | a0001c0001t0020g0028a0001c0001t0020g0171 | 3 | HG02886.hp1 HG02922.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.663-771C>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76165892 | ||||||
| chr14:76165921
|
A | G | 2 | a0001c0001t0033g0103a0001c0001t0033g0256 | 2 | HG02015.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.663-742A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76165921 | ||||||
| chr14:76165992
|
G | C | 230 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(227): Show | 300 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.663-671G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76165992 | ||||||
| chr14:76166113
|
A | G | 2 | a0001c0001t0079g0290a0004c0007t0089g0228 | 2 | HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.663-550A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76166113 | ||||||
| chr14:76166120
|
T | A | 168 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(165): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.663-543T>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76166120 | ||||||
| chr14:76166154
|
C | T | 1 | a0001c0001t0081g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.663-509C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76166154 | ||||||
| chr14:76166218
|
G | T | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.663-445G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76166218 | ||||||
| chr14:76166438
|
T | G | 42 | a0001c0001t0004g0005a0001c0001t0004g0010a0001c0001t0004g0041others(39): Show | 59 | HG00140.hp2 HG00673.hp2 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.663-225T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76166438 | ||||||
| chr14:76166637
|
T | A | 3 | a0001c0005t0016g0168a0001c0005t0016g0169a0001c0005t0016g0181 | 3 | HG02965.hp2 NA19030.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.663-26T>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 2/9 | chr14 | 76166637 | ||||||
| chr14:76166735
|
C | T | 1 | a0001c0001t0008g0214 | 1 | NA19002.hp1 | splice_region_variant&intron_variant | LOW | c.727+8C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76166735 | ||||||
| chr14:76166899
|
T | C | 1 | a0001c0001t0081g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.727+172T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76166899 | ||||||
| chr14:76167053
|
A | C | 1 | a0001c0001t0053g0180 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.727+326A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76167053 | ||||||
| chr14:76167303
|
T | C | 2 | a0001c0001t0004g0223a0001c0001t0004g0224 | 2 | HG01074.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.727+576T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76167303 | ||||||
| chr14:76167343
|
G | A | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.727+616G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76167343 | ||||||
| chr14:76167344
|
T | TG | 3 | a0001c0001t0063g0191a0001c0002t0001g0023a0001c0002t0001g0104 | 4 | NA18981.hp1 NA19006.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.727+621dupG | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 76167344 | |||||
| chr14:76167396
|
C | T | 1 | a0001c0001t0063g0191 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.727+669C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76167396 | ||||||
| chr14:76167397
|
T | C | 1 | a0001c0001t0063g0191 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.727+670T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76167397 | ||||||
| chr14:76167399
|
A | T | 1 | a0001c0001t0063g0191 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.727+672A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76167399 | ||||||
| chr14:76167421
|
A | G | 1 | a0001c0001t0008g0213 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.727+694A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76167421 | ||||||
| chr14:76167467
|
C | T | 87 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(84): Show | 126 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.727+740C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76167467 | ||||||
| chr14:76167580
|
A | AT | 4 | a0001c0005t0016g0168a0001c0005t0016g0169a0001c0005t0016g0181others(1): Show | 4 | HG02809.hp2 HG02965.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.727+858dupT | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 76167580 | |||||
| chr14:76167613
|
G | A | 87 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(84): Show | 126 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.727+886G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76167613 | ||||||
| chr14:76167614
|
T | C | 87 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(84): Show | 126 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.727+887T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76167614 | ||||||
| chr14:76167624
|
G | A | 230 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(227): Show | 300 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.727+897G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76167624 | ||||||
| chr14:76167652
|
C | T | 1 | a0001c0001t0081g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.727+925C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76167652 | ||||||
| chr14:76167668
|
G | A | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.727+941G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76167668 | ||||||
| chr14:76167920
|
A | G | 1 | a0001c0001t0036g0252 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.727+1193A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76167920 | ||||||
| chr14:76168121
|
A | C | 31 | a0001c0001t0003g0002a0001c0001t0003g0035a0001c0001t0003g0231others(28): Show | 41 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.727+1394A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76168121 | ||||||
| chr14:76168299
|
G | C | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.727+1572G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76168299 | ||||||
| chr14:76168310
|
C | T | 3 | a0001c0001t0030g0257a0001c0001t0030g0259a0001c0008t0039g0258 | 3 | HG00738.hp2 HG01346.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.727+1583C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76168310 | ||||||
| chr14:76168333
|
A | T | 12 | a0001c0001t0011g0029a0001c0001t0011g0172a0001c0001t0011g0174others(9): Show | 13 | HG01891.hp1 HG02145.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.727+1606A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76168333 | ||||||
| chr14:76168453
|
A | G | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.727+1726A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76168453 | ||||||
| chr14:76168793
|
G | A | 1 | a0001c0001t0084g0260 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.727+2066G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76168793 | ||||||
| chr14:76168962
|
A | G | 2 | a0001c0001t0028g0187a0001c0001t0028g0188 | 2 | HG02074.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.727+2235A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76168962 | ||||||
| chr14:76169034
|
T | C | 65 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(62): Show | 67 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.727+2307T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76169034 | ||||||
| chr14:76169242
|
C | T | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.727+2515C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76169242 | ||||||
| chr14:76169332
|
G | C | 42 | a0001c0001t0004g0005a0001c0001t0004g0010a0001c0001t0004g0041others(39): Show | 59 | HG00140.hp2 HG00673.hp2 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.728-2511G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76169332 | ||||||
| chr14:76169491
|
A | G | 168 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(165): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.728-2352A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76169491 | ||||||
| chr14:76169561
|
A | G | 1 | a0001c0008t0039g0258 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.728-2282A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76169561 | ||||||
| chr14:76169616
|
C | T | 29 | a0001c0001t0003g0002a0001c0001t0003g0035a0001c0001t0003g0231others(26): Show | 39 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.728-2227C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76169616 | ||||||
| chr14:76169712
|
C | T | 8 | a0001c0001t0004g0010a0001c0001t0004g0223a0001c0001t0004g0224others(5): Show | 12 | HG00140.hp2 HG01074.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.728-2131C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76169712 | ||||||
| chr14:76169715
|
C | G | 1 | a0001c0001t0046g0159 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.728-2128C>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76169715 | ||||||
| chr14:76169784
|
G | T | 1 | a0001c0008t0039g0258 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.728-2059G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76169784 | ||||||
| chr14:76169853
|
A | T | 1 | a0001c0001t0063g0191 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.728-1990A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76169853 | ||||||
| chr14:76169854
|
T | A | 1 | a0001c0001t0063g0191 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.728-1989T>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76169854 | ||||||
| chr14:76169855
|
C | T | 1 | a0001c0001t0063g0191 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.728-1988C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76169855 | ||||||
| chr14:76169856
|
T | G | 1 | a0001c0001t0063g0191 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.728-1987T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76169856 | ||||||
| chr14:76169937
|
G | GAAATACA others(7): Show |
1 | a0001c0001t0063g0191 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.728-1905_728-1892d others(16): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 76169937 | |||||
| chr14:76169943
|
C | T | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.728-1900C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76169943 | ||||||
| chr14:76169998
|
A | G | 305 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(302): Show | 394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.728-1845A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76169998 | ||||||
| chr14:76170019
|
T | G | 168 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(165): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.728-1824T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76170019 | ||||||
| chr14:76170128
|
A | G | 87 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(84): Show | 126 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.728-1715A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76170128 | ||||||
| chr14:76170355
|
G | A | 1 | a0001c0001t0012g0049 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.728-1488G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76170355 | ||||||
| chr14:76170393
|
T | G | 2 | a0001c0001t0021g0192a0001c0001t0065g0193 | 2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.728-1450T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76170393 | ||||||
| chr14:76170444
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.728-1399A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76170444 | ||||||
| chr14:76170530
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.728-1313G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76170530 | ||||||
| chr14:76170594
|
G | T | 12 | a0001c0001t0010g0039a0001c0001t0010g0040a0001c0001t0010g0276others(9): Show | 15 | NA18747.hp2 NA18942.hp1 NA18953.hp1 others(12): Show |
intron_variant | MODIFIER | c.728-1249G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76170594 | ||||||
| chr14:76170670
|
A | G | 1 | a0001c0001t0057g0178 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.728-1173A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76170670 | ||||||
| chr14:76170733
|
T | C | 1 | a0001c0001t0081g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.728-1110T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76170733 | ||||||
| chr14:76170858
|
G | T | 1 | a0001c0001t0075g0046 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.728-985G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76170858 | ||||||
| chr14:76171050
|
G | A | 3 | a0001c0001t0002g0009a0001c0001t0062g0009a0001c0001t0092g0009 | 4 | HG02723.hp2 HG03098.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.728-793G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76171050 | ||||||
| chr14:76171197
|
G | A | 1 | a0001c0001t0010g0276 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.728-646G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76171197 | ||||||
| chr14:76171277
|
T | TA | 50 | a0001c0001t0001g0051a0001c0001t0004g0005a0001c0001t0004g0010others(47): Show | 69 | HG00140.hp2 HG00673.hp2 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.728-551dupA | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 76171277 | |||||
| chr14:76171294
|
A | G | 235 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(232): Show | 307 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.728-549A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76171294 | ||||||
| chr14:76171346
|
G | T | 1 | a0001c0001t0001g0050 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.728-497G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76171346 | ||||||
| chr14:76171366
|
G | A | 88 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(85): Show | 127 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.728-477G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76171366 | ||||||
| chr14:76171445
|
C | T | 2 | a0001c0001t0033g0103a0001c0001t0033g0256 | 2 | HG02015.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.728-398C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76171445 | ||||||
| chr14:76171449
|
C | A | 1 | a0001c0001t0080g0230 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.728-394C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76171449 | ||||||
| chr14:76171511
|
A | G | 8 | a0001c0001t0011g0029a0001c0001t0011g0172a0001c0001t0011g0174others(5): Show | 9 | HG01891.hp1 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.728-332A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76171511 | ||||||
| chr14:76171583
|
CAA | C | 60 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(57): Show | 62 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.728-254_728-253del others(2): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 76171583 | |||||
| chr14:76171718
|
G | T | 1 | a0001c0001t0001g0092 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.728-125G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76171718 | ||||||
| chr14:76171729
|
GA | G | 15 | a0001c0001t0004g0263a0001c0001t0004g0264a0001c0001t0006g0155others(12): Show | 17 | HG00673.hp2 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.728-100delA | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 76171729 | |||||
| chr14:76171815
|
A | G | 1 | a0001c0001t0080g0230 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.728-28A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 3/9 | chr14 | 76171815 | ||||||
| chr14:76172123
|
A | G | 173 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(170): Show | 243 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.904+104A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 4/9 | chr14 | 76172123 | ||||||
| chr14:76172243
|
T | G | 310 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(307): Show | 400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
intron_variant | MODIFIER | c.904+224T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 4/9 | chr14 | 76172243 | ||||||
| chr14:76172271
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.904+252C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 4/9 | chr14 | 76172271 | ||||||
| chr14:76172651
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.904+632T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 4/9 | chr14 | 76172651 | ||||||
| chr14:76172683
|
T | C | 35 | a0001c0001t0003g0002a0001c0001t0003g0035a0001c0001t0003g0231others(32): Show | 47 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.904+664T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 4/9 | chr14 | 76172683 | ||||||
| chr14:76172976
|
A | G | 42 | a0001c0001t0004g0005a0001c0001t0004g0010a0001c0001t0004g0041others(39): Show | 59 | HG00140.hp2 HG00673.hp2 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.905-570A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 4/9 | chr14 | 76172976 | ||||||
| chr14:76173079
|
T | C | 1 | a0001c0001t0005g0128 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.905-467T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 4/9 | chr14 | 76173079 | ||||||
| chr14:76173129
|
G | A | 1 | a0001c0001t0022g0053 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.905-417G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 4/9 | chr14 | 76173129 | ||||||
| chr14:76173221
|
T | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(83): Show | 125 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.905-325T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 4/9 | chr14 | 76173221 | ||||||
| chr14:76173226
|
G | T | 168 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(165): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.905-320G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 4/9 | chr14 | 76173226 | ||||||
| chr14:76173271
|
T | C | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.905-275T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 4/9 | chr14 | 76173271 | ||||||
| chr14:76173782
|
A | C | 55 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0009others(52): Show | 71 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.984+157A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76173782 | ||||||
| chr14:76173837
|
CA | C | 219 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(216): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.984+224delA | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 76173837 | |||||
| chr14:76173850
|
C | T | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.984+225C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76173850 | ||||||
| chr14:76173877
|
T | G | 3 | a0001c0001t0013g0227a0001c0001t0026g0163a0001c0001t0026g0164 | 3 | HG03239.hp2 HG03669.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.984+252T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76173877 | ||||||
| chr14:76174035
|
T | TA | 63 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(60): Show | 65 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.984+422dupA | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 76174035 | |||||
| chr14:76174167
|
A | T | 87 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(84): Show | 126 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.984+542A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76174167 | ||||||
| chr14:76174218
|
A | G | 1 | a0001c0001t0044g0125 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.984+593A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76174218 | ||||||
| chr14:76174225
|
T | C | 1 | a0001c0001t0046g0159 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.984+600T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76174225 | ||||||
| chr14:76174277
|
C | G | 1 | a0001c0001t0001g0102 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.984+652C>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76174277 | ||||||
| chr14:76174475
|
C | T | 29 | a0001c0001t0003g0002a0001c0001t0003g0035a0001c0001t0003g0231others(26): Show | 39 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.984+850C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76174475 | ||||||
| chr14:76174556
|
C | T | 2 | a0001c0001t0034g0270a0001c0001t0034g0271 | 2 | HG03831.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.984+931C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76174556 | ||||||
| chr14:76174928
|
C | T | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.984+1303C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76174928 | ||||||
| chr14:76175246
|
G | A | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.985-1377G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76175246 | ||||||
| chr14:76175256
|
G | A | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.985-1367G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76175256 | ||||||
| chr14:76175361
|
G | A | 41 | a0001c0001t0004g0005a0001c0001t0004g0010a0001c0001t0004g0041others(38): Show | 58 | HG00140.hp2 HG00673.hp2 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.985-1262G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76175361 | ||||||
| chr14:76175391
|
C | G | 1 | a0001c0001t0014g0089 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.985-1232C>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76175391 | ||||||
| chr14:76175796
|
G | GT | 4 | a0001c0001t0002g0014a0001c0001t0002g0210a0001c0001t0002g0211others(1): Show | 6 | NA18979.hp1 NA18981.hp2 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.985-824dupT | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 76175796 | |||||
| chr14:76175959
|
A | G | 1 | a0001c0001t0054g0179 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.985-664A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76175959 | ||||||
| chr14:76176173
|
A | G | 2 | a0001c0001t0050g0165a0001c0001t0057g0178 | 2 | HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.985-450A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76176173 | ||||||
| chr14:76176367
|
A | G | 3 | a0001c0005t0016g0168a0001c0005t0016g0169a0001c0005t0016g0181 | 3 | HG02965.hp2 NA19030.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.985-256A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76176367 | ||||||
| chr14:76176414
|
G | A | 230 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(227): Show | 300 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.985-209G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76176414 | ||||||
| chr14:76176426
|
A | G | 1 | a0001c0001t0002g0034 | 2 | HG01261.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.985-197A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76176426 | ||||||
| chr14:76176427
|
TGTAGG | T | 87 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(84): Show | 126 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.985-192_985-188del others(5): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 76176427 | |||||
| chr14:76176454
|
A | G | 6 | a0001c0001t0006g0124a0001c0001t0006g0146a0001c0001t0006g0147others(3): Show | 6 | HG02027.hp1 NA18972.hp2 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.985-169A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76176454 | ||||||
| chr14:76176556
|
T | C | 1 | a0001c0001t0003g0236 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.985-67T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 5/9 | chr14 | 76176556 | ||||||
| chr14:76176814
|
G | A | 6 | a0001c0001t0023g0016a0001c0001t0030g0257a0001c0001t0030g0259others(3): Show | 8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.1052+124G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | chr14 | 76176814 | ||||||
| chr14:76176855
|
G | A | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1052+165G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | chr14 | 76176855 | ||||||
| chr14:76176901
|
T | A | 1 | a0001c0001t0054g0179 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1052+211T>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | chr14 | 76176901 | ||||||
| chr14:76176972
|
A | AT | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1052+293dupT | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr14 | 76176972 | |||||
| chr14:76177000
|
C | A | 1 | a0001c0001t0007g0129 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1052+310C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | chr14 | 76177000 | ||||||
| chr14:76177019
|
T | C | 1 | a0001c0001t0081g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1052+329T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | chr14 | 76177019 | ||||||
| chr14:76177084
|
C | T | 6 | a0001c0001t0001g0044a0001c0001t0001g0091a0001c0001t0031g0086others(3): Show | 6 | HG02135.hp1 HG03654.hp1 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.1052+394C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | chr14 | 76177084 | ||||||
| chr14:76177152
|
C | A | 1 | a0001c0001t0081g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1052+462C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | chr14 | 76177152 | ||||||
| chr14:76177191
|
G | T | 1 | a0001c0001t0003g0233 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1052+501G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | chr14 | 76177191 | ||||||
| chr14:76177304
|
C | T | 1 | a0001c0001t0085g0288 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1052+614C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | chr14 | 76177304 | ||||||
| chr14:76177333
|
G | A | 1 | a0001c0001t0081g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1052+643G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | chr14 | 76177333 | ||||||
| chr14:76177384
|
C | T | 1 | a0001c0005t0016g0169 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1053-604C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | chr14 | 76177384 | ||||||
| chr14:76177662
|
T | C | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1053-326T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | chr14 | 76177662 | ||||||
| chr14:76177697
|
G | GT | 7 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0097others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1053-282dupT | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr14 | 76177697 | |||||
| chr14:76177697
|
G | GTTT | 43 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0119others(40): Show | 45 | HG00323.hp2 HG00558.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.1053-284_1053-282d others(5): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr14 | 76177697 | |||||
| chr14:76177697
|
G | GTTTT | 17 | a0001c0001t0005g0027a0001c0001t0005g0145a0001c0001t0006g0150others(14): Show | 17 | HG00423.hp1 HG01106.hp1 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.1053-285_1053-282d others(6): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr14 | 76177697 | |||||
| chr14:76177706
|
TG | T | 70 | a0001c0001t0001g0063a0001c0001t0003g0002a0001c0001t0003g0035others(67): Show | 97 | HG00140.hp2 HG00408.hp1 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.1053-281delG | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | chr14 | 76177706 | ||||||
| chr14:76177707
|
G | T | 234 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(231): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.1053-281G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | chr14 | 76177707 | ||||||
| chr14:76177709
|
T | G | 30 | a0001c0001t0003g0002a0001c0001t0003g0035a0001c0001t0003g0231others(27): Show | 40 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.1053-279T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | chr14 | 76177709 | ||||||
| chr14:76177713
|
G | T | 63 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(60): Show | 65 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.1053-275G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | chr14 | 76177713 | ||||||
| chr14:76177760
|
A | G | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1053-228A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | chr14 | 76177760 | ||||||
| chr14:76177923
|
C | T | 1 | a0001c0001t0002g0209 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1053-65C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 6/9 | chr14 | 76177923 | ||||||
| chr14:76178280
|
G | A | 168 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(165): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1107+238G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76178280 | ||||||
| chr14:76178504
|
G | A | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1107+462G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76178504 | ||||||
| chr14:76178550
|
A | G | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1107+508A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76178550 | ||||||
| chr14:76178740
|
C | T | 1 | a0001c0001t0080g0230 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1107+698C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76178740 | ||||||
| chr14:76178752
|
C | T | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1107+710C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76178752 | ||||||
| chr14:76178795
|
C | T | 3 | a0001c0001t0001g0013a0001c0001t0038g0013a0001c0001t0068g0013 | 3 | NA18971.hp1 NA19077.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1107+753C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76178795 | ||||||
| chr14:76178813
|
C | A | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1107+771C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76178813 | ||||||
| chr14:76178963
|
A | AT | 2 | a0001c0001t0001g0008a0001c0001t0001g0084 | 5 | NA18941.hp1 NA18972.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.1107+928dupT | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr14 | 76178963 | |||||
| chr14:76178979
|
G | A | 3 | a0001c0001t0013g0227a0001c0001t0026g0163a0001c0001t0026g0164 | 3 | HG03239.hp2 HG03669.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1107+937G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76178979 | ||||||
| chr14:76179063
|
G | GT | 225 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(222): Show | 295 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.1107+1033dupT | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr14 | 76179063 | |||||
| chr14:76179171
|
G | A | 87 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(84): Show | 126 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.1107+1129G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76179171 | ||||||
| chr14:76179180
|
A | G | 2 | a0001c0001t0024g0037a0001c0001t0024g0273 | 3 | HG00140.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1107+1138A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76179180 | ||||||
| chr14:76179311
|
A | G | 3 | a0001c0005t0016g0168a0001c0005t0016g0169a0001c0005t0016g0181 | 3 | HG02965.hp2 NA19030.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1107+1269A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76179311 | ||||||
| chr14:76179420
|
A | T | 1 | a0001c0001t0088g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1108-1344A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76179420 | ||||||
| chr14:76179706
|
A | C | 1 | a0001c0001t0002g0208 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1108-1058A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76179706 | ||||||
| chr14:76179738
|
A | G | 1 | a0001c0001t0006g0130 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1108-1026A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76179738 | ||||||
| chr14:76179927
|
G | A | 1 | a0001c0001t0021g0192 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1108-837G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76179927 | ||||||
| chr14:76180005
|
C | T | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(166): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1108-759C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76180005 | ||||||
| chr14:76180030
|
C | CA | 7 | a0001c0001t0002g0009a0001c0001t0008g0219a0001c0001t0011g0172others(4): Show | 8 | HG02145.hp1 HG02622.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1108-718dupA | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr14 | 76180030 | |||||
| chr14:76180030
|
C | CAAA | 45 | a0001c0001t0003g0250a0001c0001t0004g0005a0001c0001t0004g0010others(42): Show | 64 | HG00140.hp2 HG00673.hp2 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.1108-720_1108-718d others(5): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr14 | 76180030 | |||||
| chr14:76180030
|
C | CAAAA | 172 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(169): Show | 223 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.1108-721_1108-718d others(6): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr14 | 76180030 | |||||
| chr14:76180030
|
C | CAAAAA | 11 | a0001c0001t0001g0043a0001c0001t0001g0066a0001c0001t0001g0067others(8): Show | 11 | HG00558.hp2 HG00621.hp2 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.1108-722_1108-718d others(7): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr14 | 76180030 | |||||
| chr14:76180069
|
G | A | 1 | a0001c0001t0088g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1108-695G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76180069 | ||||||
| chr14:76180283
|
G | A | 1 | a0001c0001t0010g0277 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1108-481G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76180283 | ||||||
| chr14:76180289
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1108-475A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76180289 | ||||||
| chr14:76180355
|
G | A | 41 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0014others(38): Show | 56 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.1108-409G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76180355 | ||||||
| chr14:76180490
|
T | A | 1 | a0003c0006t0016g0106 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1108-274T>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76180490 | ||||||
| chr14:76180535
|
A | T | 31 | a0001c0001t0003g0002a0001c0001t0003g0035a0001c0001t0003g0231others(28): Show | 41 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.1108-229A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76180535 | ||||||
| chr14:76180567
|
T | C | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1108-197T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76180567 | ||||||
| chr14:76180569
|
C | T | 6 | a0001c0001t0001g0057a0001c0001t0023g0016a0001c0001t0030g0257others(3): Show | 8 | HG00738.hp1 HG00738.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.1108-195C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76180569 | ||||||
| chr14:76180693
|
T | G | 1 | a0001c0001t0001g0069 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1108-71T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76180693 | ||||||
| chr14:76180711
|
A | T | 2 | a0001c0001t0021g0192a0001c0001t0065g0193 | 2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1108-53A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76180711 | ||||||
| chr14:76180719
|
C | T | 1 | a0001c0002t0001g0085 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1108-45C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76180719 | ||||||
| chr14:76180745
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1108-19G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 7/9 | chr14 | 76180745 | ||||||
| chr14:76180854
|
T | C | 1 | a0001c0001t0088g0255 | 1 | NA19043.hp1 | splice_region_variant&intron_variant | LOW | c.1193+5T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76180854 | ||||||
| chr14:76181000
|
T | C | 1 | a0001c0001t0080g0230 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1193+151T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76181000 | ||||||
| chr14:76181229
|
A | G | 231 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(228): Show | 301 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.1193+380A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76181229 | ||||||
| chr14:76181239
|
A | G | 8 | a0001c0001t0015g0112a0001c0001t0015g0113a0001c0001t0015g0114others(5): Show | 8 | HG01081.hp2 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1193+390A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76181239 | ||||||
| chr14:76181254
|
T | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(228): Show | 301 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.1193+405T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76181254 | ||||||
| chr14:76181267
|
T | C | 1 | a0001c0005t0016g0169 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1193+418T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76181267 | ||||||
| chr14:76181302
|
A | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(228): Show | 301 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.1193+453A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76181302 | ||||||
| chr14:76181323
|
A | G | 1 | a0001c0001t0033g0256 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1193+474A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76181323 | ||||||
| chr14:76181521
|
T | A | 1 | a0001c0001t0080g0230 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1193+672T>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76181521 | ||||||
| chr14:76181547
|
C | T | 87 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(84): Show | 126 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.1193+698C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76181547 | ||||||
| chr14:76181693
|
T | C | 1 | a0001c0001t0064g0166 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1193+844T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76181693 | ||||||
| chr14:76181754
|
T | C | 1 | a0001c0001t0081g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1193+905T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76181754 | ||||||
| chr14:76181764
|
A | G | 2 | a0001c0001t0017g0015a0001c0001t0017g0226 | 4 | HG01109.hp1 HG02145.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1193+915A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76181764 | ||||||
| chr14:76181858
|
A | G | 1 | a0001c0001t0003g0249 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1193+1009A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76181858 | ||||||
| chr14:76181905
|
A | G | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1193+1056A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76181905 | ||||||
| chr14:76181937
|
A | C | 2 | a0001c0001t0013g0126a0001c0001t0048g0127 | 2 | HG02723.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1193+1088A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76181937 | ||||||
| chr14:76182174
|
G | A | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1193+1325G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76182174 | ||||||
| chr14:76182281
|
C | T | 1 | a0001c0001t0053g0180 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1193+1432C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76182281 | ||||||
| chr14:76182321
|
C | T | 233 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(230): Show | 304 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.1193+1472C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76182321 | ||||||
| chr14:76182343
|
C | T | 1 | a0001c0001t0011g0177 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1193+1494C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76182343 | ||||||
| chr14:76182348
|
C | A | 1 | a0001c0001t0001g0047 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1193+1499C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76182348 | ||||||
| chr14:76182351
|
C | T | 1 | a0001c0001t0002g0209 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1193+1502C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76182351 | ||||||
| chr14:76182363
|
G | GA | 58 | a0001c0001t0001g0097a0001c0001t0002g0004a0001c0001t0002g0006others(55): Show | 75 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.1193+1535dupA | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76182363 | |||||
| chr14:76182363
|
G | GAA | 192 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(189): Show | 250 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.1193+1534_1193+153 others(6): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76182363 | |||||
| chr14:76182363
|
G | GAAA | 36 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0021others(33): Show | 46 | HG00423.hp2 HG01074.hp1 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.1193+1533_1193+153 others(7): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76182363 | |||||
| chr14:76182363
|
G | GAAAA | 7 | a0001c0001t0023g0016a0001c0001t0030g0257a0001c0001t0030g0259others(4): Show | 9 | HG00741.hp1 HG01346.hp2 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.1193+1532_1193+153 others(8): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76182363 | |||||
| chr14:76182421
|
A | AT | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(166): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1193+1584dupT | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76182421 | |||||
| chr14:76182422
|
T | A | 1 | a0001c0001t0049g0143 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1193+1573T>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76182422 | ||||||
| chr14:76182441
|
T | C | 1 | a0003c0006t0016g0106 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1193+1592T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76182441 | ||||||
| chr14:76182443
|
G | A | 1 | a0001c0001t0013g0144 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1193+1594G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76182443 | ||||||
| chr14:76182585
|
C | CA | 8 | a0001c0001t0002g0210a0001c0001t0008g0194a0001c0001t0008g0219others(5): Show | 8 | HG02965.hp2 HG03540.hp1 NA18949.hp1 others(5): Show |
intron_variant | MODIFIER | c.1193+1757dupA | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76182585 | |||||
| chr14:76182585
|
CA | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(118): Show | 176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.1193+1757delA | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76182585 | |||||
| chr14:76182585
|
CAA | C | 76 | a0001c0001t0001g0073a0001c0001t0001g0081a0001c0001t0001g0084others(73): Show | 80 | HG00423.hp1 HG00558.hp2 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.1193+1756_1193+175 others(6): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76182585 | |||||
| chr14:76182585
|
CAAAAA | C | 29 | a0001c0001t0003g0002a0001c0001t0003g0035a0001c0001t0003g0231others(26): Show | 39 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1193+1753_1193+175 others(9): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76182585 | |||||
| chr14:76182636
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1193+1787A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76182636 | ||||||
| chr14:76182702
|
C | T | 1 | a0001c0001t0022g0060 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1193+1853C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76182702 | ||||||
| chr14:76182718
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1193+1869A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76182718 | ||||||
| chr14:76182782
|
G | A | 1 | a0001c0001t0033g0103 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1193+1933G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76182782 | ||||||
| chr14:76182822
|
A | G | 6 | a0001c0001t0023g0016a0001c0001t0030g0257a0001c0001t0030g0259others(3): Show | 8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.1193+1973A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76182822 | ||||||
| chr14:76182946
|
A | C | 2 | a0001c0001t0002g0221a0001c0001t0002g0222 | 2 | HG00558.hp1 HG00597.hp1 |
intron_variant | MODIFIER | c.1193+2097A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76182946 | ||||||
| chr14:76182968
|
G | T | 2 | a0001c0001t0004g0005a0001c0001t0004g0279 | 7 | NA18939.hp1 NA18943.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.1193+2119G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76182968 | ||||||
| chr14:76183099
|
T | C | 2 | a0001c0001t0033g0103a0001c0001t0033g0256 | 2 | HG02015.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.1193+2250T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76183099 | ||||||
| chr14:76183373
|
G | A | 1 | a0001c0001t0050g0165 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1193+2524G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76183373 | ||||||
| chr14:76183485
|
A | AT | 5 | a0001c0001t0002g0184a0001c0001t0002g0185a0001c0001t0002g0206others(2): Show | 5 | HG01081.hp1 HG02602.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1193+2644dupT | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76183485 | |||||
| chr14:76183485
|
A | T | 2 | a0001c0001t0079g0290a0004c0007t0089g0228 | 2 | HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1193+2636A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76183485 | ||||||
| chr14:76183558
|
A | G | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1193+2709A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76183558 | ||||||
| chr14:76183583
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1193+2734C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76183583 | ||||||
| chr14:76183596
|
C | A | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1193+2747C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76183596 | ||||||
| chr14:76183723
|
G | A | 1 | a0001c0001t0002g0211 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1193+2874G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76183723 | ||||||
| chr14:76183758
|
C | T | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1193+2909C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76183758 | ||||||
| chr14:76183759
|
G | A | 2 | a0001c0001t0014g0065a0001c0001t0014g0089 | 2 | HG00621.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1193+2910G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76183759 | ||||||
| chr14:76183789
|
T | C | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1193+2940T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76183789 | ||||||
| chr14:76184022
|
T | TGG | 38 | a0001c0001t0003g0002a0001c0001t0003g0231a0001c0001t0003g0232others(35): Show | 47 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.1193+3174_1193+317 others(6): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76184022 | |||||
| chr14:76184023
|
G | GGGGT | 7 | a0001c0001t0001g0096a0001c0001t0003g0035a0001c0001t0003g0239others(4): Show | 8 | HG01346.hp2 HG01516.hp1 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.1193+3175_1193+317 others(8): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76184023 | |||||
| chr14:76184023
|
GGT | G | 22 | a0001c0001t0002g0034a0001c0001t0002g0201a0001c0001t0003g0234others(19): Show | 24 | HG00323.hp2 HG01106.hp1 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.1193+3216_1193+321 others(6): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76184023 | |||||
| chr14:76184023
|
GGTGT | G | 77 | a0001c0001t0001g0007a0001c0001t0001g0042a0001c0001t0001g0043others(74): Show | 96 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.1193+3214_1193+321 others(8): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76184023 | |||||
| chr14:76184023
|
GGTGTGT | G | 117 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(114): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.1193+3212_1193+321 others(10): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76184023 | |||||
| chr14:76184024
|
GTGT | G | 3 | a0001c0001t0001g0091a0001c0001t0002g0203a0001c0001t0002g0217 | 3 | HG02071.hp1 HG02135.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.1193+3176_1193+317 others(7): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76184024 | ||||||
| chr14:76184025
|
T | G | 54 | a0001c0001t0002g0202a0001c0001t0003g0245a0001c0001t0005g0026others(51): Show | 58 | HG00423.hp1 HG00558.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.1193+3176T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76184025 | ||||||
| chr14:76184027
|
T | G | 49 | a0001c0001t0002g0034a0001c0001t0002g0201a0001c0001t0003g0234others(46): Show | 52 | HG00323.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.1193+3178T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76184027 | ||||||
| chr14:76184029
|
T | G | 88 | a0001c0001t0001g0007a0001c0001t0001g0042a0001c0001t0001g0043others(85): Show | 108 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.1193+3180T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76184029 | ||||||
| chr14:76184031
|
T | G | 125 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(122): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.1193+3182T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76184031 | ||||||
| chr14:76184033
|
T | G | 3 | a0001c0001t0001g0057a0001c0001t0013g0227a0001c0001t0088g0255 | 3 | HG00738.hp1 HG03669.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1193+3184T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76184033 | ||||||
| chr14:76184087
|
G | A | 1 | a0001c0001t0028g0188 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1193+3238G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76184087 | ||||||
| chr14:76184421
|
T | C | 230 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(227): Show | 300 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.1193+3572T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76184421 | ||||||
| chr14:76184501
|
G | A | 1 | a0001c0001t0080g0230 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1193+3652G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76184501 | ||||||
| chr14:76184609
|
G | A | 1 | a0001c0001t0002g0196 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1193+3760G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76184609 | ||||||
| chr14:76184678
|
A | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0072 | 2 | HG02698.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1193+3829A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76184678 | ||||||
| chr14:76184721
|
A | G | 1 | a0001c0001t0004g0041 | 2 | NA18960.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1193+3872A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76184721 | ||||||
| chr14:76184788
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1193+3939T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76184788 | ||||||
| chr14:76184793
|
G | A | 6 | a0001c0001t0023g0016a0001c0001t0030g0257a0001c0001t0030g0259others(3): Show | 8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.1193+3944G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76184793 | ||||||
| chr14:76185307
|
A | C | 1 | a0001c0001t0001g0063 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1193+4458A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76185307 | ||||||
| chr14:76185321
|
G | A | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1193+4472G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76185321 | ||||||
| chr14:76185739
|
G | A | 308 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(305): Show | 397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.1193+4890G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76185739 | ||||||
| chr14:76185927
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1193+5078G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76185927 | ||||||
| chr14:76185972
|
C | T | 1 | a0001c0001t0079g0290 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1193+5123C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76185972 | ||||||
| chr14:76186096
|
G | C | 1 | a0001c0001t0003g0253 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1193+5247G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76186096 | ||||||
| chr14:76186127
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1193+5278G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76186127 | ||||||
| chr14:76186341
|
A | G | 1 | a0001c0001t0002g0200 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1193+5492A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76186341 | ||||||
| chr14:76186921
|
C | T | 1 | a0002c0009t0001g0088 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1193+6072C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76186921 | ||||||
| chr14:76187025
|
G | GT | 66 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(63): Show | 70 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1193+6188dupT | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76187025 | |||||
| chr14:76187025
|
GT | G | 87 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(84): Show | 126 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.1193+6188delT | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76187025 | |||||
| chr14:76187143
|
T | C | 66 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(63): Show | 70 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1193+6294T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76187143 | ||||||
| chr14:76187188
|
A | G | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1193+6339A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76187188 | ||||||
| chr14:76187240
|
T | G | 1 | a0001c0001t0015g0112 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1193+6391T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76187240 | ||||||
| chr14:76187241
|
T | C | 1 | a0001c0001t0015g0112 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1193+6392T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76187241 | ||||||
| chr14:76187283
|
T | C | 66 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(63): Show | 70 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1193+6434T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76187283 | ||||||
| chr14:76187408
|
A | C | 1 | a0004c0007t0089g0228 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1193+6559A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76187408 | ||||||
| chr14:76187744
|
T | C | 66 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(63): Show | 70 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1193+6895T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76187744 | ||||||
| chr14:76187851
|
C | T | 58 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(55): Show | 60 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1193+7002C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76187851 | ||||||
| chr14:76188138
|
T | C | 235 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(232): Show | 307 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.1193+7289T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76188138 | ||||||
| chr14:76188235
|
A | G | 1 | a0001c0001t0080g0230 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1193+7386A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76188235 | ||||||
| chr14:76188285
|
G | A | 1 | a0001c0001t0056g0107 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1193+7436G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76188285 | ||||||
| chr14:76188344
|
C | T | 1 | a0001c0001t0002g0190 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1193+7495C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76188344 | ||||||
| chr14:76188360
|
A | C | 1 | a0001c0001t0090g0275 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1193+7511A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76188360 | ||||||
| chr14:76188479
|
T | C | 235 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(232): Show | 307 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.1194-7399T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76188479 | ||||||
| chr14:76188535
|
C | CTTTTGCC others(2): Show |
235 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(232): Show | 307 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.1194-7339_1194-733 others(13): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76188535 | |||||
| chr14:76188547
|
G | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0084 | 5 | NA18941.hp1 NA18972.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.1194-7331G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76188547 | ||||||
| chr14:76188798
|
T | C | 13 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0050others(10): Show | 14 | HG00140.hp1 HG01256.hp2 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.1194-7080T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76188798 | ||||||
| chr14:76188826
|
T | C | 66 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(63): Show | 70 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1194-7052T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76188826 | ||||||
| chr14:76188831
|
G | C | 66 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(63): Show | 70 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1194-7047G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76188831 | ||||||
| chr14:76188834
|
T | C | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1194-7044T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76188834 | ||||||
| chr14:76189147
|
AGTTTT | A | 66 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(63): Show | 70 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1194-6727_1194-672 others(9): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76189147 | |||||
| chr14:76189170
|
T | C | 3 | a0001c0001t0030g0257a0001c0001t0030g0259a0001c0008t0039g0258 | 3 | HG00738.hp2 HG01346.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1194-6708T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76189170 | ||||||
| chr14:76189181
|
G | C | 2 | a0001c0001t0011g0029a0001c0001t0060g0173 | 3 | HG01891.hp1 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1194-6697G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76189181 | ||||||
| chr14:76189268
|
G | A | 1 | a0001c0001t0043g0134 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1194-6610G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76189268 | ||||||
| chr14:76189330
|
C | A | 87 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(84): Show | 126 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.1194-6548C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76189330 | ||||||
| chr14:76189364
|
GTCT | G | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1194-6508_1194-650 others(7): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76189364 | |||||
| chr14:76189473
|
G | C | 1 | a0001c0001t0022g0053 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1194-6405G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76189473 | ||||||
| chr14:76189643
|
A | G | 1 | a0001c0001t0080g0230 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1194-6235A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76189643 | ||||||
| chr14:76189785
|
A | G | 2 | a0001c0001t0079g0290a0004c0007t0089g0228 | 2 | HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1194-6093A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76189785 | ||||||
| chr14:76189857
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1194-6021T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76189857 | ||||||
| chr14:76189969
|
C | A | 1 | a0001c0001t0013g0144 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1194-5909C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76189969 | ||||||
| chr14:76189989
|
C | T | 1 | a0002c0009t0001g0088 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1194-5889C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76189989 | ||||||
| chr14:76190072
|
G | A | 6 | a0001c0001t0023g0016a0001c0001t0030g0257a0001c0001t0030g0259others(3): Show | 8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.1194-5806G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76190072 | ||||||
| chr14:76190114
|
A | AT | 235 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(232): Show | 307 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.1194-5755dupT | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76190114 | |||||
| chr14:76190160
|
T | G | 42 | a0001c0001t0004g0005a0001c0001t0004g0010a0001c0001t0004g0041others(39): Show | 59 | HG00140.hp2 HG00673.hp2 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.1194-5718T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76190160 | ||||||
| chr14:76190166
|
C | T | 1 | a0001c0001t0048g0127 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1194-5712C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76190166 | ||||||
| chr14:76190208
|
C | T | 1 | a0001c0001t0088g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1194-5670C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76190208 | ||||||
| chr14:76190299
|
C | G | 1 | a0001c0001t0051g0167 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1194-5579C>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76190299 | ||||||
| chr14:76190323
|
C | G | 235 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(232): Show | 307 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.1194-5555C>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76190323 | ||||||
| chr14:76190434
|
A | C | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1194-5444A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76190434 | ||||||
| chr14:76190436
|
A | G | 1 | a0001c0001t0088g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1194-5442A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76190436 | ||||||
| chr14:76190488
|
A | G | 1 | a0001c0001t0015g0115 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1194-5390A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76190488 | ||||||
| chr14:76190860
|
A | G | 7 | a0001c0001t0009g0018a0001c0001t0009g0266a0001c0001t0009g0267others(4): Show | 9 | HG01167.hp2 HG01169.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.1194-5018A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76190860 | ||||||
| chr14:76190929
|
G | T | 1 | a0001c0001t0082g0261 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1194-4949G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76190929 | ||||||
| chr14:76190941
|
T | C | 1 | a0001c0001t0088g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1194-4937T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76190941 | ||||||
| chr14:76191070
|
A | G | 1 | a0001c0001t0001g0063 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1194-4808A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76191070 | ||||||
| chr14:76191127
|
C | T | 234 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(231): Show | 306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.1194-4751C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76191127 | ||||||
| chr14:76191132
|
CTTG | C | 7 | a0001c0001t0011g0029a0001c0001t0011g0172a0001c0001t0011g0174others(4): Show | 8 | HG01891.hp1 HG02145.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1194-4740_1194-473 others(7): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76191132 | |||||
| chr14:76191413
|
G | A | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(166): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1194-4465G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76191413 | ||||||
| chr14:76191610
|
C | A | 4 | a0001c0001t0023g0016a0001c0001t0030g0257a0001c0001t0030g0259others(1): Show | 6 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.1194-4268C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76191610 | ||||||
| chr14:76191732
|
A | T | 1 | a0001c0001t0047g0149 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1194-4146A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76191732 | ||||||
| chr14:76191783
|
T | C | 87 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(84): Show | 126 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.1194-4095T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76191783 | ||||||
| chr14:76191829
|
T | C | 1 | a0001c0001t0053g0180 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1194-4049T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76191829 | ||||||
| chr14:76191931
|
T | TC | 4 | a0001c0001t0017g0015a0001c0001t0017g0226a0001c0001t0029g0182others(1): Show | 6 | HG01109.hp1 HG01496.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1194-3944dupC | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76191931 | |||||
| chr14:76191968
|
G | T | 1 | a0001c0001t0007g0110 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1194-3910G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76191968 | ||||||
| chr14:76192119
|
C | CT | 64 | a0001c0001t0001g0044a0001c0001t0001g0099a0001c0001t0005g0025others(61): Show | 68 | HG00423.hp1 HG00558.hp2 HG01081.hp2 others(65): Show |
intron_variant | MODIFIER | c.1194-3741dupT | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76192119 | |||||
| chr14:76192119
|
CT | C | 13 | a0001c0001t0001g0011a0001c0001t0001g0062a0001c0001t0001g0090others(10): Show | 13 | HG00099.hp1 HG01099.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.1194-3741delT | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76192119 | |||||
| chr14:76192174
|
G | C | 2 | a0001c0001t0017g0015a0001c0001t0017g0226 | 4 | HG01109.hp1 HG02145.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1194-3704G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76192174 | ||||||
| chr14:76192318
|
T | A | 1 | a0001c0001t0018g0076 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1194-3560T>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76192318 | ||||||
| chr14:76192480
|
T | C | 1 | a0001c0001t0002g0198 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1194-3398T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76192480 | ||||||
| chr14:76192522
|
G | A | 1 | a0001c0001t0081g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1194-3356G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76192522 | ||||||
| chr14:76192547
|
C | T | 1 | a0001c0001t0053g0180 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1194-3331C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76192547 | ||||||
| chr14:76192597
|
C | T | 4 | a0001c0001t0005g0119a0001c0001t0005g0120a0001c0001t0005g0121others(1): Show | 4 | NA18982.hp1 NA19005.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.1194-3281C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76192597 | ||||||
| chr14:76192861
|
T | G | 1 | a0001c0001t0084g0260 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1194-3017T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76192861 | ||||||
| chr14:76193024
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1194-2854G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76193024 | ||||||
| chr14:76193226
|
A | T | 1 | a0001c0001t0056g0107 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1194-2652A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76193226 | ||||||
| chr14:76193380
|
G | A | 3 | a0001c0001t0013g0227a0001c0001t0026g0163a0001c0001t0026g0164 | 3 | HG03239.hp2 HG03669.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1194-2498G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76193380 | ||||||
| chr14:76193499
|
T | A | 1 | a0001c0001t0001g0105 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1194-2379T>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76193499 | ||||||
| chr14:76193555
|
A | C | 1 | a0001c0001t0002g0207 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1194-2323A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76193555 | ||||||
| chr14:76193709
|
T | C | 1 | a0001c0001t0001g0056 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1194-2169T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76193709 | ||||||
| chr14:76193878
|
A | G | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(166): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1194-2000A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76193878 | ||||||
| chr14:76194081
|
C | T | 1 | a0001c0001t0005g0138 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1194-1797C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76194081 | ||||||
| chr14:76194097
|
C | CTG | 4 | a0001c0001t0002g0014a0001c0001t0002g0210a0001c0001t0002g0211others(1): Show | 6 | NA18979.hp1 NA18981.hp2 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.1194-1779_1194-177 others(6): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76194097 | |||||
| chr14:76194177
|
C | T | 1 | a0001c0001t0001g0079 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1194-1701C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76194177 | ||||||
| chr14:76194484
|
A | AGT | 93 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0009others(90): Show | 118 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1194-1374_1194-137 others(6): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76194484 | |||||
| chr14:76194484
|
A | AGTGT | 13 | a0001c0001t0001g0048a0001c0001t0002g0014a0001c0001t0002g0189others(10): Show | 15 | HG00642.hp2 HG00733.hp2 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.1194-1376_1194-137 others(8): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76194484 | |||||
| chr14:76194484
|
A | AGTGTGT | 5 | a0001c0001t0030g0257a0001c0001t0030g0259a0001c0001t0077g0109others(2): Show | 5 | HG01074.hp1 HG01346.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1194-1378_1194-137 others(10): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76194484 | |||||
| chr14:76194484
|
A | AGTGTGTG others(1): Show |
83 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(80): Show | 122 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1194-1380_1194-137 others(12): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76194484 | |||||
| chr14:76194484
|
A | AGTGTGTG others(3): Show |
6 | a0001c0001t0005g0119a0001c0001t0005g0121a0001c0001t0005g0161others(3): Show | 8 | HG01109.hp1 HG02145.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.1194-1382_1194-137 others(14): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76194484 | |||||
| chr14:76194484
|
A | AGTGTGTG others(5): Show |
33 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(30): Show | 35 | HG00323.hp2 HG00423.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.1194-1384_1194-137 others(16): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76194484 | |||||
| chr14:76194484
|
A | AGTGTGTG others(7): Show |
4 | a0001c0001t0005g0131a0001c0001t0006g0136a0001c0001t0029g0183others(1): Show | 4 | HG00558.hp2 HG01496.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1194-1386_1194-137 others(18): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76194484 | |||||
| chr14:76194484
|
A | AGTGTGTG others(9): Show |
14 | a0001c0001t0006g0152a0001c0001t0006g0153a0001c0001t0013g0123others(11): Show | 14 | HG01081.hp2 HG01934.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1194-1388_1194-137 others(20): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76194484 | |||||
| chr14:76194484
|
A | AGTGTGTG others(11): Show |
5 | a0001c0001t0013g0135a0001c0001t0013g0144a0001c0001t0026g0163others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1194-1390_1194-137 others(22): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76194484 | |||||
| chr14:76194484
|
A | AGTGTGTG others(13): Show |
5 | a0001c0001t0006g0155a0001c0001t0006g0156a0001c0001t0006g0157others(2): Show | 5 | HG02109.hp1 HG02572.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1194-1392_1194-137 others(24): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76194484 | |||||
| chr14:76194484
|
A | AGTGTGTG others(15): Show |
1 | a0001c0001t0006g0151 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1194-1373_1194-137 others(26): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76194484 | |||||
| chr14:76194502
|
T | TGTGTGTG others(5): Show |
1 | a0001c0001t0081g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1194-1373_1194-137 others(16): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76194502 | |||||
| chr14:76194513
|
A | G | 235 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(232): Show | 307 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.1194-1365A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76194513 | ||||||
| chr14:76194521
|
G | A | 1 | a0001c0001t0080g0230 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1194-1357G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76194521 | ||||||
| chr14:76194544
|
T | C | 66 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(63): Show | 70 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1194-1334T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76194544 | ||||||
| chr14:76194670
|
G | T | 1 | a0001c0001t0015g0114 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1194-1208G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76194670 | ||||||
| chr14:76194721
|
TTA | T | 4 | a0001c0001t0017g0015a0001c0001t0017g0226a0001c0001t0029g0182others(1): Show | 6 | HG01109.hp1 HG01496.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1194-1153_1194-115 others(6): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76194721 | |||||
| chr14:76194746
|
T | G | 1 | a0001c0001t0080g0230 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1194-1132T>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76194746 | ||||||
| chr14:76194756
|
TGTG | T | 4 | a0001c0001t0017g0015a0001c0001t0017g0226a0001c0001t0029g0182others(1): Show | 6 | HG01109.hp1 HG01496.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1194-1119_1194-111 others(7): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 76194756 | |||||
| chr14:76194851
|
C | T | 2 | a0001c0001t0033g0103a0001c0001t0033g0256 | 2 | HG02015.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.1194-1027C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76194851 | ||||||
| chr14:76195024
|
C | T | 1 | a0001c0001t0013g0137 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1194-854C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76195024 | ||||||
| chr14:76195175
|
A | G | 1 | a0004c0007t0089g0228 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1194-703A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76195175 | ||||||
| chr14:76195265
|
T | C | 1 | a0001c0001t0004g0263 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1194-613T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76195265 | ||||||
| chr14:76195518
|
C | G | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1194-360C>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 8/9 | chr14 | 76195518 | ||||||
| chr14:76196010
|
G | A | 4 | a0001c0001t0017g0015a0001c0001t0017g0226a0001c0001t0029g0182others(1): Show | 6 | HG01109.hp1 HG01496.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1288+38G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76196010 | ||||||
| chr14:76196027
|
T | C | 66 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(63): Show | 70 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1288+55T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76196027 | ||||||
| chr14:76196033
|
G | GT | 66 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(63): Show | 70 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1288+65dupT | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 76196033 | |||||
| chr14:76196103
|
C | T | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(166): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1288+131C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76196103 | ||||||
| chr14:76196421
|
A | G | 1 | a0001c0001t0014g0075 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1288+449A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76196421 | ||||||
| chr14:76196437
|
G | GT | 43 | a0001c0001t0002g0186a0001c0001t0002g0202a0001c0001t0004g0010others(40): Show | 54 | HG00140.hp2 HG00408.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.1288+485dupT | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 76196437 | |||||
| chr14:76196437
|
G | GTT | 53 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0009others(50): Show | 68 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.1288+484_1288+485d others(4): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 76196437 | |||||
| chr14:76196437
|
G | GTTT | 9 | a0001c0001t0002g0032a0001c0001t0002g0197a0001c0001t0015g0112others(6): Show | 10 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.1288+483_1288+485d others(5): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 76196437 | |||||
| chr14:76196438
|
T | TTTTG | 10 | a0001c0001t0005g0161a0001c0001t0006g0155a0001c0001t0006g0156others(7): Show | 10 | HG01934.hp2 HG02109.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1288+469_1288+470i others(6): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 76196438 | |||||
| chr14:76196439
|
T | TTTG | 45 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(42): Show | 47 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.1288+469_1288+470i others(5): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 76196439 | |||||
| chr14:76196440
|
T | TTG | 4 | a0001c0001t0017g0015a0001c0001t0017g0226a0001c0001t0029g0182others(1): Show | 6 | HG01109.hp1 HG01496.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1288+469_1288+470i others(4): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 76196440 | |||||
| chr14:76196559
|
A | G | 235 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(232): Show | 307 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.1288+587A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76196559 | ||||||
| chr14:76196676
|
A | G | 2 | a0001c0001t0079g0290a0004c0007t0089g0228 | 2 | HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1288+704A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76196676 | ||||||
| chr14:76197008
|
C | T | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(166): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1288+1036C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76197008 | ||||||
| chr14:76197095
|
C | G | 1 | a0001c0001t0008g0199 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1288+1123C>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76197095 | ||||||
| chr14:76197208
|
A | T | 235 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(232): Show | 307 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.1288+1236A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76197208 | ||||||
| chr14:76197234
|
T | C | 1 | a0001c0001t0080g0230 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1288+1262T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76197234 | ||||||
| chr14:76197495
|
T | C | 235 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(232): Show | 307 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.1288+1523T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76197495 | ||||||
| chr14:76197525
|
C | T | 2 | a0001c0001t0014g0065a0001c0001t0014g0089 | 2 | HG00621.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1288+1553C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76197525 | ||||||
| chr14:76197566
|
A | G | 2 | a0001c0001t0029g0182a0001c0001t0029g0183 | 2 | HG01496.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1288+1594A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76197566 | ||||||
| chr14:76197592
|
C | T | 4 | a0001c0001t0017g0015a0001c0001t0017g0226a0001c0001t0029g0182others(1): Show | 6 | HG01109.hp1 HG01496.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1288+1620C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76197592 | ||||||
| chr14:76197595
|
A | T | 235 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(232): Show | 307 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.1288+1623A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76197595 | ||||||
| chr14:76197863
|
G | C | 1 | a0001c0001t0033g0256 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1288+1891G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76197863 | ||||||
| chr14:76197937
|
T | A | 2 | a0001c0001t0036g0243a0001c0001t0036g0252 | 2 | HG02040.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1288+1965T>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76197937 | ||||||
| chr14:76197959
|
G | C | 3 | a0001c0001t0002g0201a0001c0001t0002g0202a0001c0001t0002g0204 | 3 | NA19060.hp1 NA19063.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1288+1987G>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76197959 | ||||||
| chr14:76198051
|
C | A | 6 | a0001c0001t0023g0016a0001c0001t0030g0257a0001c0001t0030g0259others(3): Show | 8 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.1288+2079C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76198051 | ||||||
| chr14:76198096
|
A | C | 66 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(63): Show | 70 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1288+2124A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76198096 | ||||||
| chr14:76198105
|
A | AG | 303 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(300): Show | 392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.1288+2135dupG | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 76198105 | |||||
| chr14:76198120
|
C | A | 1 | a0001c0001t0080g0230 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1288+2148C>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76198120 | ||||||
| chr14:76198184
|
C | T | 1 | a0001c0001t0088g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1288+2212C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76198184 | ||||||
| chr14:76198276
|
G | A | 1 | a0001c0001t0044g0125 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1288+2304G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76198276 | ||||||
| chr14:76198533
|
G | A | 1 | a0001c0001t0006g0153 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1288+2561G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76198533 | ||||||
| chr14:76198730
|
A | G | 2 | a0001c0001t0050g0165a0001c0001t0057g0178 | 2 | HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1288+2758A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76198730 | ||||||
| chr14:76198732
|
CGA | C | 8 | a0001c0001t0015g0112a0001c0001t0015g0113a0001c0001t0015g0114others(5): Show | 8 | HG01081.hp2 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1288+2771_1288+277 others(6): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 76198732 | |||||
| chr14:76198762
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1288+2790A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76198762 | ||||||
| chr14:76198793
|
C | CT | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(166): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1288+2823dupT | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 76198793 | |||||
| chr14:76198808
|
C | T | 2 | a0001c0001t0002g0184a0001c0001t0002g0185 | 2 | NA18989.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1288+2836C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76198808 | ||||||
| chr14:76198825
|
C | T | 4 | a0001c0005t0016g0168a0001c0005t0016g0169a0001c0005t0016g0181others(1): Show | 4 | HG02809.hp2 HG02965.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1288+2853C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76198825 | ||||||
| chr14:76199134
|
C | T | 234 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(231): Show | 306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.1289-2557C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76199134 | ||||||
| chr14:76199189
|
A | T | 66 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(63): Show | 70 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1289-2502A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76199189 | ||||||
| chr14:76199397
|
C | T | 42 | a0001c0001t0004g0005a0001c0001t0004g0010a0001c0001t0004g0041others(39): Show | 59 | HG00140.hp2 HG00673.hp2 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.1289-2294C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76199397 | ||||||
| chr14:76199486
|
T | A | 11 | a0001c0001t0004g0263a0001c0001t0004g0264a0001c0001t0009g0018others(8): Show | 13 | HG00673.hp2 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.1289-2205T>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76199486 | ||||||
| chr14:76199553
|
T | C | 2 | a0001c0001t0050g0165a0001c0001t0057g0178 | 2 | HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1289-2138T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76199553 | ||||||
| chr14:76199629
|
T | C | 1 | a0001c0001t0006g0155 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1289-2062T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76199629 | ||||||
| chr14:76199664
|
GTGTTGGT others(5): Show |
G | 2 | a0001c0001t0028g0187a0001c0001t0028g0188 | 2 | HG02074.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.1289-2023_1289-201 others(16): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 76199664 | |||||
| chr14:76199701
|
T | C | 1 | a0001c0001t0001g0079 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1289-1990T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76199701 | ||||||
| chr14:76199891
|
A | G | 2 | a0001c0001t0017g0015a0001c0001t0017g0226 | 4 | HG01109.hp1 HG02145.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1289-1800A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76199891 | ||||||
| chr14:76199913
|
A | C | 66 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(63): Show | 70 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1289-1778A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76199913 | ||||||
| chr14:76199929
|
T | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(166): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1289-1762T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76199929 | ||||||
| chr14:76199930
|
G | A | 8 | a0001c0001t0004g0010a0001c0001t0004g0223a0001c0001t0004g0224others(5): Show | 12 | HG00140.hp2 HG01074.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.1289-1761G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76199930 | ||||||
| chr14:76199956
|
G | T | 1 | a0001c0001t0032g0098 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1289-1735G>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76199956 | ||||||
| chr14:76200019
|
A | G | 3 | a0001c0001t0012g0012a0001c0001t0012g0049a0001c0001t0012g0064 | 5 | NA18939.hp2 NA18968.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.1289-1672A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76200019 | ||||||
| chr14:76200302
|
T | C | 1 | a0001c0001t0001g0019 | 2 | HG00423.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.1289-1389T>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76200302 | ||||||
| chr14:76200453
|
G | GTA | 66 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(63): Show | 70 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1289-1234_1289-123 others(6): Show |
GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 76200453 | |||||
| chr14:76200547
|
C | T | 1 | a0001c0001t0014g0074 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1289-1144C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76200547 | ||||||
| chr14:76200575
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1289-1116C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76200575 | ||||||
| chr14:76200831
|
C | T | 8 | a0001c0001t0015g0112a0001c0001t0015g0113a0001c0001t0015g0114others(5): Show | 8 | HG01081.hp2 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1289-860C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76200831 | ||||||
| chr14:76200925
|
A | G | 1 | a0001c0001t0035g0285 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1289-766A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76200925 | ||||||
| chr14:76201012
|
A | T | 1 | a0001c0001t0003g0035 | 2 | NA18988.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1289-679A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76201012 | ||||||
| chr14:76201014
|
C | T | 1 | a0001c0001t0009g0266 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1289-677C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76201014 | ||||||
| chr14:76201175
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1289-516G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76201175 | ||||||
| chr14:76201363
|
C | T | 1 | a0001c0004t0004g0036 | 2 | HG01928.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.1289-328C>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76201363 | ||||||
| chr14:76201409
|
A | G | 1 | a0001c0001t0057g0178 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1289-282A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76201409 | ||||||
| chr14:76201417
|
A | G | 1 | a0001c0001t0057g0178 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1289-274A>G | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76201417 | ||||||
| chr14:76201469
|
G | A | 62 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(59): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1289-222G>A | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76201469 | ||||||
| chr14:76201599
|
A | C | 29 | a0001c0001t0003g0002a0001c0001t0003g0035a0001c0001t0003g0231others(26): Show | 39 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1289-92A>C | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76201599 | ||||||
| chr14:76201680
|
A | T | 1 | a0001c0001t0006g0146 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1289-11A>T | GPATCH2L | ENSG00000089916.18 | transcript | ENST00000261530.12 | protein_coding | 9/9 | chr14 | 76201680 |