Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 399979 |
|---|---|
| ensemblid | ENSG00000120451.11 |
| hgncid | 21532 |
| symbol | SNX19 |
| name | sorting nexin 19 |
| refseq_nuc | NM_014758.3 |
| refseq_prot | NP_055573.3 |
| ensembl_nuc | ENST00000265909.9 |
| ensembl_prot | ENSP00000265909.4 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 130866250 |
| end | 130916479 |
| strand | - |
| ver | v1.2 |
| region | chr11:130866250-130916479 |
| region5000 | chr11:130861250-130921479 |
| regionname0 | SNX19_chr11_130866250_130916479 |
| regionname5000 | SNX19_chr11_130861250_130921479 |
| 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 | 0/1 | 992 | 179 | 30 | 35 | 72 | 8 | 33 | 53 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0002 | 0/0 | 992 | 80 | 1 | 21 | 50 | 3 | 5 | 36 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0003 | 0/0 | 992 | 53 | 6 | 5 | 40 | 1 | 1 | 34 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0004 | 0/0 | 992 | 35 | 22 | 3 | 8 | 1 | 1 | 8 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0005 | 0/0 | 992 | 17 | 17 | 0 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0006 | 0/0 | 992 | 16 | 14 | 1 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0007 | 0/0 | 992 | 14 | 0 | 0 | 14 | 0 | 0 | 12 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0008 | 0/0 | 992 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0009 | 0/0 | 992 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0010 | 0/0 | 992 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0011 | 0/0 | 992 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0012 | 0/0 | 992 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0013 | 0/0 | 992 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0014 | 0/0 | 992 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0015 | 0/0 | 992 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0016 | 0/0 | 992 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0017 | 0/0 | 992 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0018 | 0/0 | 992 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0019 | 0/0 | 992 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0020 | 0/0 | 992 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0021 | 0/0 | 992 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0022 | 1/0 | 992 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0023 | 0/0 | 992 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| 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 | 0/0 | 2979 | 165 | 24 | 31 | 72 | 7 | 31 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| c0002 | 0/0 | 2979 | 80 | 1 | 21 | 50 | 3 | 5 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| c0003 | 0/0 | 2979 | 53 | 6 | 5 | 40 | 1 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| c0004 | 0/0 | 2979 | 16 | 16 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| c0005 | 0/0 | 2979 | 16 | 5 | 1 | 8 | 1 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| c0006 | 0/0 | 2979 | 15 | 13 | 1 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| c0007 | 0/0 | 2979 | 14 | 0 | 0 | 14 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| c0008 | 0/0 | 2979 | 11 | 11 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| c0009 | 0/0 | 2979 | 7 | 5 | 2 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| c0010 | 0/1 | 2979 | 6 | 0 | 2 | 0 | 1 | 2 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| c0011 | 0/0 | 2979 | 6 | 5 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| c0012 | 0/0 | 2979 | 4 | 0 | 0 | 4 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| c0013 | 0/0 | 2979 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| c0014 | 0/0 | 2979 | 2 | 1 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| c0015 | 0/0 | 2979 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| c0016 | 0/0 | 2979 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| c0017 | 0/0 | 2979 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| c0018 | 0/0 | 2979 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| c0019 | 0/0 | 2979 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| c0020 | 0/0 | 2979 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| c0021 | 0/0 | 2979 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| c0022 | 0/0 | 2979 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| c0023 | 1/0 | 2979 | 1 | 0 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| c0024 | 0/0 | 2979 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| c0025 | 0/0 | 2979 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| c0026 | 0/0 | 2979 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| c0027 | 0/0 | 2979 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| c0028 | 0/0 | 2979 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| c0029 | 0/0 | 2979 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| c0030 | 0/0 | 2979 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| c0031 | 0/0 | 2979 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| 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 | 0/0 | 12713 | 75 | 2 | 18 | 37 | 5 | 13 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0002 | 1/0 | 12713 | 50 | 0 | 15 | 30 | 2 | 2 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0003 | 0/0 | 12709 | 27 | 5 | 4 | 16 | 1 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0004 | 0/0 | 12709 | 22 | 0 | 1 | 20 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0005 | 0/0 | 12713 | 15 | 0 | 0 | 15 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0006 | 0/0 | 12714 | 14 | 0 | 1 | 3 | 1 | 9 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0007 | 0/0 | 12709 | 13 | 4 | 3 | 3 | 0 | 3 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0008 | 0/0 | 12713 | 10 | 8 | 1 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0009 | 0/0 | 12709 | 7 | 5 | 2 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0010 | 0/0 | 12713 | 5 | 4 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0011 | 0/0 | 12712 | 5 | 3 | 2 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0012 | 0/0 | 12713 | 4 | 0 | 2 | 0 | 1 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0013 | 0/0 | 12709 | 4 | 0 | 0 | 4 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0014 | 0/0 | 12713 | 4 | 0 | 0 | 4 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0015 | 0/0 | 12714 | 4 | 0 | 0 | 4 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0016 | 0/1 | 12713 | 4 | 0 | 2 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0017 | 0/0 | 12713 | 4 | 0 | 0 | 4 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0018 | 0/0 | 12713 | 4 | 3 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0019 | 0/0 | 12714 | 4 | 4 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0020 | 0/0 | 12712 | 3 | 3 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0021 | 0/0 | 12713 | 3 | 3 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0022 | 0/0 | 12713 | 3 | 0 | 1 | 1 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0023 | 0/0 | 12713 | 3 | 0 | 0 | 3 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0024 | 0/0 | 12713 | 3 | 0 | 2 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0025 | 0/0 | 12712 | 3 | 0 | 1 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0026 | 0/0 | 12711 | 3 | 0 | 0 | 3 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0027 | 0/0 | 12713 | 3 | 3 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0028 | 0/0 | 12713 | 3 | 0 | 0 | 3 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0029 | 0/0 | 12714 | 3 | 3 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0030 | 0/0 | 12714 | 2 | 2 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0031 | 0/0 | 12713 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0032 | 0/0 | 12709 | 2 | 2 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0033 | 0/0 | 12711 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0034 | 0/0 | 12710 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0035 | 0/0 | 12713 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0036 | 0/0 | 12713 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0037 | 0/0 | 12709 | 2 | 0 | 1 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0038 | 0/0 | 12709 | 2 | 2 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0039 | 0/0 | 12713 | 2 | 2 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0040 | 0/0 | 12714 | 2 | 2 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0041 | 0/0 | 12713 | 2 | 1 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0042 | 0/0 | 12714 | 2 | 0 | 1 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0043 | 0/0 | 12714 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0044 | 0/0 | 12713 | 2 | 0 | 2 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0045 | 0/0 | 12713 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0046 | 0/0 | 12713 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0047 | 0/0 | 12713 | 2 | 0 | 0 | 0 | 0 | 2 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0048 | 0/0 | 12713 | 2 | 2 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0049 | 0/0 | 12713 | 2 | 2 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0050 | 0/0 | 12713 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0051 | 0/0 | 12713 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0052 | 0/0 | 12713 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0053 | 0/0 | 12713 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0054 | 0/0 | 12711 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0055 | 0/0 | 12714 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0056 | 0/0 | 12713 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0057 | 0/0 | 12714 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0058 | 0/0 | 12713 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0059 | 0/0 | 12709 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0060 | 0/0 | 12709 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0061 | 0/0 | 12712 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0062 | 0/0 | 12713 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0063 | 0/0 | 12713 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0064 | 0/0 | 12713 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0065 | 0/0 | 12713 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0066 | 0/0 | 12711 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0067 | 0/0 | 12712 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0068 | 0/0 | 12712 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0069 | 0/0 | 12711 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0070 | 0/0 | 12714 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0071 | 0/0 | 12709 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0072 | 0/0 | 12709 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0073 | 0/0 | 12710 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0074 | 0/0 | 12714 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0075 | 0/0 | 12713 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0076 | 0/0 | 12709 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0077 | 0/0 | 12711 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0078 | 0/0 | 12713 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0079 | 0/0 | 12713 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0080 | 0/0 | 12714 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0081 | 0/0 | 12713 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0082 | 0/0 | 12713 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0083 | 0/0 | 12713 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0084 | 0/0 | 12714 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0085 | 0/0 | 13045 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0086 | 0/0 | 12714 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0087 | 0/0 | 12713 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0088 | 0/0 | 12714 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0089 | 0/0 | 12714 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0090 | 0/0 | 12715 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0091 | 0/0 | 12714 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0092 | 0/0 | 12715 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0093 | 0/0 | 12713 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0094 | 0/0 | 12713 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0095 | 0/0 | 12713 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0096 | 0/0 | 12713 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0097 | 0/0 | 12713 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0098 | 0/0 | 12713 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0099 | 0/0 | 12713 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0100 | 0/0 | 12713 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0101 | 0/0 | 12714 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0102 | 0/0 | 12714 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0103 | 0/0 | 12714 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0104 | 0/0 | 12713 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0105 | 0/0 | 12713 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0106 | 0/0 | 12713 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0107 | 0/0 | 12713 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0108 | 0/0 | 12714 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0109 | 0/0 | 12709 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0110 | 0/0 | 12713 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0111 | 0/0 | 12713 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0112 | 0/0 | 12713 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0113 | 0/0 | 12710 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0114 | 0/0 | 12712 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0115 | 0/0 | 12714 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0116 | 0/0 | 12714 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0117 | 0/0 | 12714 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| t0118 | 0/0 | 12712 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| 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 | 19 | 0 | 2 | 17 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0002 | 0/0 | 13 | 0 | 5 | 5 | 0 | 3 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0003 | 0/0 | 9 | 0 | 5 | 2 | 1 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0004 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0005 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0006 | 0/0 | 7 | 0 | 0 | 4 | 1 | 2 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0007 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0008 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0009 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0010 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0037 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0040 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0070 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| 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 | 0/0 | 2979 | 165 | 24 | 31 | 72 | 7 | 31 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0010 | 0/1 | 2979 | 6 | 0 | 2 | 0 | 1 | 2 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0011 | 0/0 | 2979 | 6 | 5 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0014 | 0/0 | 2979 | 2 | 1 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0002c0002 | 0/0 | 2979 | 80 | 1 | 21 | 50 | 3 | 5 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0003c0003 | 0/0 | 2979 | 53 | 6 | 5 | 40 | 1 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0004c0005 | 0/0 | 2979 | 16 | 5 | 1 | 8 | 1 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0004c0008 | 0/0 | 2979 | 11 | 11 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0004c0009 | 0/0 | 2979 | 7 | 5 | 2 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0004c0025 | 0/0 | 2979 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0005c0004 | 0/0 | 2979 | 16 | 16 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0005c0017 | 0/0 | 2979 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0006c0006 | 0/0 | 2979 | 15 | 13 | 1 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0006c0019 | 0/0 | 2979 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0007c0007 | 0/0 | 2979 | 14 | 0 | 0 | 14 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0008c0012 | 0/0 | 2979 | 4 | 0 | 0 | 4 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0009c0013 | 0/0 | 2979 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0010c0031 | 0/0 | 2979 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0011c0030 | 0/0 | 2979 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0012c0028 | 0/0 | 2979 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0013c0015 | 0/0 | 2979 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0014c0022 | 0/0 | 2979 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0015c0016 | 0/0 | 2979 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0016c0021 | 0/0 | 2979 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0017c0020 | 0/0 | 2979 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0018c0018 | 0/0 | 2979 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0019c0026 | 0/0 | 2979 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0020c0027 | 0/0 | 2979 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0021c0024 | 0/0 | 2979 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0022c0023 | 1/0 | 2979 | 1 | 0 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0023c0029 | 0/0 | 2979 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 15691 | 73 | 2 | 18 | 37 | 5 | 11 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0004 | 0/0 | 15687 | 2 | 0 | 0 | 1 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0006 | 0/0 | 15692 | 13 | 0 | 1 | 2 | 1 | 9 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0007 | 0/0 | 15687 | 13 | 4 | 3 | 3 | 0 | 3 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0011 | 0/0 | 15690 | 4 | 3 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0014 | 0/0 | 15691 | 4 | 0 | 0 | 4 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0015 | 0/0 | 15692 | 4 | 0 | 0 | 4 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0017 | 0/0 | 15691 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0018 | 0/0 | 15691 | 4 | 3 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0028 | 0/0 | 15691 | 3 | 0 | 0 | 3 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0037 | 0/0 | 15687 | 2 | 0 | 1 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0038 | 0/0 | 15687 | 2 | 2 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0042 | 0/0 | 15692 | 2 | 0 | 1 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0043 | 0/0 | 15692 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0044 | 0/0 | 15691 | 2 | 0 | 2 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0045 | 0/0 | 15691 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0046 | 0/0 | 15691 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0047 | 0/0 | 15691 | 2 | 0 | 0 | 0 | 0 | 2 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0056 | 0/0 | 15691 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0075 | 0/0 | 15691 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0076 | 0/0 | 15687 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0077 | 0/0 | 15689 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0078 | 0/0 | 15691 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0080 | 0/0 | 15692 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0086 | 0/0 | 15692 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0087 | 0/0 | 15691 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0088 | 0/0 | 15692 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0089 | 0/0 | 15692 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0090 | 0/0 | 15693 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0091 | 0/0 | 15692 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0092 | 0/0 | 15693 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0093 | 0/0 | 15691 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0095 | 0/0 | 15691 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0096 | 0/0 | 15691 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0097 | 0/0 | 15691 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0098 | 0/0 | 15691 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0099 | 0/0 | 15691 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0100 | 0/0 | 15691 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0101 | 0/0 | 15692 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0104 | 0/0 | 15691 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0105 | 0/0 | 15691 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0106 | 0/0 | 15691 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0108 | 0/0 | 15692 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0111 | 0/0 | 15691 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0114 | 0/0 | 15690 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0001t0115 | 0/0 | 15692 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0010t0016 | 0/1 | 15691 | 4 | 0 | 2 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0010t0102 | 0/0 | 15692 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0010t0107 | 0/0 | 15691 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0011t0010 | 0/0 | 15691 | 5 | 4 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0011t0053 | 0/0 | 15691 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0001c0014t0041 | 0/0 | 15691 | 2 | 1 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0002c0002t0002 | 0/0 | 15691 | 48 | 0 | 15 | 29 | 2 | 2 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0002c0002t0005 | 0/0 | 15691 | 15 | 0 | 0 | 15 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0002c0002t0012 | 0/0 | 15691 | 4 | 0 | 2 | 0 | 1 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0002c0002t0024 | 0/0 | 15691 | 3 | 0 | 2 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0002c0002t0025 | 0/0 | 15690 | 3 | 0 | 1 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0002c0002t0061 | 0/0 | 15690 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0002c0002t0062 | 0/0 | 15691 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0002c0002t0063 | 0/0 | 15691 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0002c0002t0064 | 0/0 | 15691 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0002c0002t0065 | 0/0 | 15691 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0002c0002t0067 | 0/0 | 15690 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0002c0002t0079 | 0/0 | 15691 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0003c0003t0003 | 0/0 | 15687 | 27 | 5 | 4 | 16 | 1 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0003c0003t0004 | 0/0 | 15687 | 20 | 0 | 1 | 19 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0003c0003t0036 | 0/0 | 15691 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0003c0003t0070 | 0/0 | 15692 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0003c0003t0071 | 0/0 | 15687 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0003c0003t0073 | 0/0 | 15688 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0003c0003t0113 | 0/0 | 15688 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0004c0005t0020 | 0/0 | 15690 | 3 | 3 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0004c0005t0022 | 0/0 | 15691 | 3 | 0 | 1 | 1 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0004c0005t0023 | 0/0 | 15691 | 3 | 0 | 0 | 3 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0004c0005t0030 | 0/0 | 15692 | 2 | 2 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0004c0005t0031 | 0/0 | 15691 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0004c0005t0055 | 0/0 | 15692 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0004c0005t0057 | 0/0 | 15692 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0004c0005t0058 | 0/0 | 15691 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0004c0008t0019 | 0/0 | 15692 | 4 | 4 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0004c0008t0029 | 0/0 | 15692 | 3 | 3 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0004c0008t0048 | 0/0 | 15691 | 2 | 2 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0004c0008t0116 | 0/0 | 15692 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0004c0008t0117 | 0/0 | 15692 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0004c0009t0009 | 0/0 | 15687 | 7 | 5 | 2 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0004c0025t0051 | 0/0 | 15691 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0005c0004t0021 | 0/0 | 15691 | 3 | 3 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0005c0004t0027 | 0/0 | 15691 | 3 | 3 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0005c0004t0039 | 0/0 | 15691 | 2 | 2 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0005c0004t0040 | 0/0 | 15692 | 2 | 2 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0005c0004t0049 | 0/0 | 15691 | 2 | 2 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0005c0004t0074 | 0/0 | 15692 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0005c0004t0081 | 0/0 | 15691 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0005c0004t0082 | 0/0 | 15691 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0005c0004t0084 | 0/0 | 15692 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0005c0017t0083 | 0/0 | 15691 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0006c0006t0008 | 0/0 | 15691 | 9 | 7 | 1 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0006c0006t0032 | 0/0 | 15687 | 2 | 2 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0006c0006t0052 | 0/0 | 15691 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0006c0006t0060 | 0/0 | 15687 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0006c0006t0068 | 0/0 | 15690 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0006c0006t0069 | 0/0 | 15689 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0006c0019t0008 | 0/0 | 15691 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0007c0007t0013 | 0/0 | 15687 | 4 | 0 | 0 | 4 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0007c0007t0026 | 0/0 | 15689 | 3 | 0 | 0 | 3 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0007c0007t0033 | 0/0 | 15689 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0007c0007t0034 | 0/0 | 15688 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0007c0007t0054 | 0/0 | 15689 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0007c0007t0059 | 0/0 | 15687 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0007c0007t0066 | 0/0 | 15689 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0008c0012t0017 | 0/0 | 15691 | 3 | 0 | 0 | 3 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0008c0012t0103 | 0/0 | 15692 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0009c0013t0110 | 0/0 | 15691 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0009c0013t0112 | 0/0 | 15691 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0010c0031t0118 | 0/0 | 15690 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0011c0030t0050 | 0/0 | 15691 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0012c0028t0094 | 0/0 | 15691 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0013c0015t0002 | 0/0 | 15691 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0014c0022t0001 | 0/0 | 15691 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0015c0016t0109 | 0/0 | 15687 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0016c0021t0006 | 0/0 | 15692 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0017c0020t0011 | 0/0 | 15690 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0018c0018t0085 | 0/0 | 16023 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0019c0026t0072 | 0/0 | 15687 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0020c0027t0035 | 0/0 | 15691 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0021c0024t0035 | 0/0 | 15691 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0022c0023t0002 | 1/0 | 15691 | 1 | 0 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| a0023c0029t0001 | 0/0 | 15691 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | copy fasta | chr11 | 130861250 | 130921479 |
| 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 | 19 | 0 | 2 | 17 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0001g0002 | 0/0 | 13 | 0 | 5 | 5 | 0 | 3 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0001g0003 | 0/0 | 9 | 0 | 5 | 2 | 1 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 0 | 4 | 1 | 2 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0001g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0006g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0006g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0006g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0006g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0006g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0006g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0006g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0006g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0006g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0006g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0006g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0007g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0007g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0007g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0007g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0007g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0007g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0007g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0007g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0007g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0007g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0007g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0007g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0007g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0011g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0011g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0011g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0014g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0014g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0014g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0014g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0015g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0015g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0017g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0018g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0018g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0018g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0028g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0028g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0028g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0037g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0038g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0038g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0042g0040 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0043g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0043g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0044g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0044g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0045g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0045g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0046g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0047g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0056g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0075g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0076g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0077g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0078g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0080g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0086g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0087g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0088g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0089g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0090g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0091g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0092g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0093g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0095g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0096g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0097g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0098g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0099g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0100g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0101g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0104g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0105g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0106g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0108g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0111g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0114g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0001t0115g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0010t0016g0037 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0010t0016g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0010t0016g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0010t0102g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0010t0107g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0011t0010g0010 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0011t0010g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0011t0053g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0014t0041g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0001c0014t0041g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0002g0008 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0002g0009 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0002g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0002g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0002g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0005g0004 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0005g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0005g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0005g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0005g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0005g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0012g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0012g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0012g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0024g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0024g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0024g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0025g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0025g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0025g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0061g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0062g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0063g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0064g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0065g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0067g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0002c0002t0079g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0003c0003t0003g0005 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0003c0003t0003g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0003c0003t0003g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0003c0003t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0003c0003t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0003c0003t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0003c0003t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0003c0003t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0003c0003t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0003c0003t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0003c0003t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0003c0003t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0003c0003t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0003c0003t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0003c0003t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0003c0003t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0003c0003t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0003c0003t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0003c0003t0004g0007 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0003c0003t0004g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0003c0003t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0003c0003t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0003c0003t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0003c0003t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0003c0003t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0003c0003t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0003c0003t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0003c0003t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0003c0003t0004g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0003c0003t0036g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0003c0003t0036g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0003c0003t0070g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0003c0003t0071g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0003c0003t0073g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0003c0003t0113g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0004c0005t0020g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0004c0005t0020g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0004c0005t0022g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0004c0005t0022g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0004c0005t0022g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0004c0005t0023g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0004c0005t0030g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0004c0005t0031g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0004c0005t0031g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0004c0005t0055g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0004c0005t0057g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0004c0005t0058g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0004c0008t0019g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0004c0008t0019g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0004c0008t0019g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0004c0008t0019g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0004c0008t0029g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0004c0008t0029g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0004c0008t0029g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0004c0008t0048g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0004c0008t0116g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0004c0008t0117g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0004c0009t0009g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0004c0009t0009g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0004c0009t0009g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0004c0009t0009g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0004c0009t0009g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0004c0009t0009g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0004c0025t0051g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0005c0004t0021g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0005c0004t0021g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0005c0004t0021g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0005c0004t0027g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0005c0004t0027g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0005c0004t0039g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0005c0004t0039g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0005c0004t0040g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0005c0004t0040g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0005c0004t0049g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0005c0004t0049g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0005c0004t0074g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0005c0004t0081g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0005c0004t0082g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0005c0004t0084g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0005c0017t0083g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0006c0006t0008g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0006c0006t0008g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0006c0006t0008g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0006c0006t0008g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0006c0006t0008g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0006c0006t0008g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0006c0006t0008g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0006c0006t0008g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0006c0006t0032g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0006c0006t0032g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0006c0006t0052g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0006c0006t0060g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0006c0006t0068g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0006c0006t0069g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0006c0019t0008g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0007c0007t0013g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0007c0007t0013g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0007c0007t0013g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0007c0007t0026g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0007c0007t0026g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0007c0007t0033g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0007c0007t0034g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0007c0007t0054g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0007c0007t0059g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0007c0007t0066g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0008c0012t0017g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0008c0012t0017g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0008c0012t0103g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0009c0013t0110g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0009c0013t0112g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0010c0031t0118g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0011c0030t0050g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0012c0028t0094g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0013c0015t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0014c0022t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0015c0016t0109g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0016c0021t0006g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0017c0020t0011g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0018c0018t0085g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0019c0026t0072g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0020c0027t0035g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0021c0024t0035g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0022c0023t0002g0070 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| a0023c0029t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0012 | g0074 | EUR | GBR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0218 | EUR | GBR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0208 | EUR | FIN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG00280 | hp2 | a0001 | c0010 | t0016 | g0037 | EUR | FIN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0209 | EUR | FIN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG00323 | hp2 | a0001 | c0001 | t0042 | g0040 | EUR | FIN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG00408 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | CHS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG00423 | hp1 | a0001 | c0001 | t0078 | g0160 | EAS | CHS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG00423 | hp2 | a0003 | c0003 | t0003 | g0146 | EAS | CHS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG00438 | hp1 | a0002 | c0002 | t0005 | g0092 | EAS | CHS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG00544 | hp1 | a0001 | c0001 | t0108 | g0191 | EAS | CHS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG00558 | hp2 | a0003 | c0003 | t0004 | g0272 | EAS | CHS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0011 | EAS | CHS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG00609 | hp1 | a0021 | c0024 | t0035 | g0124 | EAS | CHS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG00609 | hp2 | a0009 | c0013 | t0112 | g0189 | EAS | CHS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG00642 | hp1 | a0002 | c0002 | t0002 | g0008 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG00642 | hp2 | a0001 | c0001 | t0007 | g0152 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG00673 | hp1 | a0001 | c0001 | t0089 | g0255 | EAS | CHS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG00673 | hp2 | a0001 | c0001 | t0106 | g0210 | EAS | CHS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG00733 | hp1 | a0003 | c0003 | t0003 | g0140 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG00733 | hp2 | a0002 | c0002 | t0002 | g0008 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG00735 | hp1 | a0002 | c0002 | t0024 | g0089 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG00738 | hp1 | a0002 | c0002 | t0024 | g0101 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG00738 | hp2 | a0006 | c0006 | t0008 | g0060 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG00741 | hp1 | a0001 | c0001 | t0097 | g0196 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG00741 | hp2 | a0004 | c0009 | t0009 | g0044 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01069 | hp1 | a0002 | c0002 | t0002 | g0087 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01070 | hp2 | a0004 | c0009 | t0009 | g0044 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0088 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01074 | hp1 | a0001 | c0010 | t0016 | g0233 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01074 | hp2 | a0001 | c0001 | t0007 | g0156 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01081 | hp1 | a0001 | c0010 | t0016 | g0232 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01099 | hp1 | a0001 | c0014 | t0041 | g0236 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01099 | hp2 | a0001 | c0001 | t0100 | g0199 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01106 | hp2 | a0002 | c0002 | t0012 | g0019 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01109 | hp1 | a0001 | c0001 | t0011 | g0035 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01167 | hp1 | a0003 | c0003 | t0003 | g0144 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01167 | hp2 | a0002 | c0002 | t0002 | g0113 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01168 | hp1 | a0017 | c0020 | t0011 | g0240 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01168 | hp2 | a0002 | c0002 | t0002 | g0009 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01175 | hp1 | a0002 | c0002 | t0063 | g0103 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01175 | hp2 | a0002 | c0002 | t0012 | g0019 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01243 | hp1 | a0001 | c0011 | t0010 | g0010 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01243 | hp2 | a0001 | c0001 | t0098 | g0197 | AMR | PUR | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01255 | hp1 | a0001 | c0001 | t0037 | g0031 | AMR | CLM | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01256 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | CLM | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | CLM | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01258 | hp2 | a0004 | c0005 | t0022 | g0106 | AMR | CLM | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01261 | hp1 | a0003 | c0003 | t0003 | g0136 | AMR | CLM | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01261 | hp2 | a0002 | c0002 | t0025 | g0104 | AMR | CLM | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01361 | hp2 | a0002 | c0002 | t0002 | g0080 | AMR | CLM | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01433 | hp2 | a0002 | c0002 | t0002 | g0105 | AMR | CLM | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01496 | hp2 | a0001 | c0001 | t0018 | g0277 | AMR | CLM | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01516 | hp1 | a0002 | c0002 | t0002 | g0023 | EUR | IBS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01517 | hp1 | a0002 | c0002 | t0002 | g0023 | EUR | IBS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01517 | hp2 | a0003 | c0003 | t0003 | g0133 | EUR | IBS | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01884 | hp1 | a0001 | c0001 | t0091 | g0250 | AFR | ACB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01884 | hp2 | a0004 | c0008 | t0019 | g0291 | AFR | ACB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01891 | hp1 | a0004 | c0005 | t0030 | g0017 | AFR | ACB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01891 | hp2 | a0005 | c0004 | t0027 | g0032 | AFR | ACB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01934 | hp1 | a0001 | c0001 | t0044 | g0242 | AMR | PEL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01934 | hp2 | a0001 | c0001 | t0007 | g0164 | AMR | PEL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01943 | hp2 | a0002 | c0002 | t0002 | g0109 | AMR | PEL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01952 | hp1 | a0001 | c0001 | t0042 | g0040 | AMR | PEL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01975 | hp1 | a0002 | c0002 | t0002 | g0014 | AMR | PEL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01978 | hp1 | a0001 | c0001 | t0006 | g0039 | AMR | PEL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01978 | hp2 | a0003 | c0003 | t0003 | g0142 | AMR | PEL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01993 | hp1 | a0001 | c0001 | t0044 | g0204 | AMR | PEL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01993 | hp2 | a0002 | c0002 | t0002 | g0107 | AMR | PEL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02004 | hp1 | a0002 | c0002 | t0002 | g0014 | AMR | PEL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02015 | hp1 | a0002 | c0002 | t0064 | g0082 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02027 | hp1 | a0002 | c0002 | t0005 | g0091 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02040 | hp2 | a0007 | c0007 | t0059 | g0118 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02055 | hp1 | a0018 | c0018 | t0085 | g0175 | AFR | ACB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02055 | hp2 | a0001 | c0001 | t0056 | g0056 | AFR | ACB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02056 | hp1 | a0012 | c0028 | t0094 | g0275 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02056 | hp2 | a0002 | c0002 | t0002 | g0083 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02071 | hp1 | a0001 | c0001 | t0007 | g0165 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02071 | hp2 | a0003 | c0003 | t0004 | g0007 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02074 | hp1 | a0003 | c0003 | t0036 | g0143 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0081 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02080 | hp1 | a0001 | c0001 | t0006 | g0259 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02080 | hp2 | a0001 | c0001 | t0101 | g0207 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02083 | hp1 | a0002 | c0002 | t0005 | g0020 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02083 | hp2 | a0002 | c0002 | t0002 | g0111 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02129 | hp2 | a0003 | c0003 | t0004 | g0273 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02155 | hp1 | a0003 | c0003 | t0003 | g0005 | EAS | CDX | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02155 | hp2 | a0002 | c0002 | t0005 | g0069 | EAS | CDX | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02165 | hp1 | a0019 | c0026 | t0072 | g0125 | EAS | CDX | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02257 | hp1 | a0004 | c0008 | t0029 | g0280 | AFR | ACB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02257 | hp2 | a0003 | c0003 | t0071 | g0132 | AFR | ACB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02258 | hp1 | a0001 | c0011 | t0010 | g0010 | AFR | ACB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02258 | hp2 | a0004 | c0025 | t0051 | g0046 | AFR | ACB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02280 | hp1 | a0004 | c0008 | t0117 | g0289 | AFR | ACB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02280 | hp2 | a0006 | c0006 | t0069 | g0065 | AFR | ACB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02293 | hp1 | a0002 | c0002 | t0002 | g0014 | AMR | PEL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02451 | hp1 | a0004 | c0009 | t0009 | g0283 | AFR | ACB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0150 | AFR | ACB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02523 | hp1 | a0002 | c0002 | t0005 | g0095 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02523 | hp2 | a0001 | c0001 | t0017 | g0235 | EAS | KHV | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02572 | hp1 | a0004 | c0005 | t0020 | g0016 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02572 | hp2 | a0005 | c0004 | t0021 | g0050 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02602 | hp2 | a0001 | c0001 | t0037 | g0031 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02615 | hp1 | a0006 | c0006 | t0060 | g0053 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02615 | hp2 | a0001 | c0001 | t0075 | g0148 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02622 | hp1 | a0005 | c0004 | t0027 | g0174 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02622 | hp2 | a0004 | c0005 | t0020 | g0016 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02630 | hp1 | a0001 | c0001 | t0018 | g0278 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02630 | hp2 | a0005 | c0004 | t0039 | g0178 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02647 | hp1 | a0006 | c0006 | t0032 | g0055 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02647 | hp2 | a0001 | c0001 | t0007 | g0168 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02683 | hp1 | a0002 | c0002 | t0012 | g0073 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02698 | hp1 | a0001 | c0001 | t0006 | g0039 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02698 | hp2 | a0003 | c0003 | t0003 | g0141 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0151 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02717 | hp2 | a0004 | c0009 | t0009 | g0287 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02723 | hp1 | a0003 | c0003 | t0003 | g0126 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02723 | hp2 | a0010 | c0031 | t0118 | g0294 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02735 | hp1 | a0001 | c0001 | t0099 | g0198 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02735 | hp2 | a0002 | c0002 | t0024 | g0100 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02738 | hp1 | a0001 | c0001 | t0006 | g0244 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02809 | hp1 | a0006 | c0006 | t0068 | g0061 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02809 | hp2 | a0005 | c0004 | t0021 | g0051 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02818 | hp1 | a0001 | c0001 | t0076 | g0149 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02818 | hp2 | a0005 | c0004 | t0082 | g0177 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02886 | hp1 | a0006 | c0006 | t0008 | g0018 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02886 | hp2 | a0004 | c0008 | t0029 | g0282 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02895 | hp1 | a0001 | c0001 | t0086 | g0187 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02895 | hp2 | a0004 | c0008 | t0048 | g0042 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02896 | hp1 | a0006 | c0006 | t0008 | g0063 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02896 | hp2 | a0001 | c0001 | t0011 | g0194 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02897 | hp1 | a0006 | c0006 | t0008 | g0062 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02897 | hp2 | a0004 | c0008 | t0048 | g0042 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02922 | hp1 | a0005 | c0004 | t0040 | g0179 | AFR | ESN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02922 | hp2 | a0001 | c0011 | t0010 | g0057 | AFR | ESN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02965 | hp1 | a0006 | c0006 | t0008 | g0067 | AFR | ESN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02965 | hp2 | a0005 | c0017 | t0083 | g0173 | AFR | ESN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02970 | hp1 | a0004 | c0008 | t0019 | g0290 | AFR | ESN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02970 | hp2 | a0001 | c0001 | t0115 | g0279 | AFR | ESN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02976 | hp1 | a0006 | c0006 | t0008 | g0059 | AFR | ESN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02976 | hp2 | a0005 | c0004 | t0084 | g0182 | AFR | ESN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03017 | hp2 | a0001 | c0001 | t0093 | g0192 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03041 | hp1 | a0005 | c0004 | t0040 | g0181 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03041 | hp2 | a0001 | c0001 | t0018 | g0043 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03098 | hp1 | a0006 | c0006 | t0032 | g0054 | AFR | MSL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03098 | hp2 | a0001 | c0014 | t0041 | g0237 | AFR | MSL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03130 | hp1 | a0003 | c0003 | t0003 | g0145 | AFR | ESN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03130 | hp2 | a0004 | c0009 | t0009 | g0286 | AFR | ESN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03139 | hp1 | a0003 | c0003 | t0003 | g0135 | AFR | ESN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03139 | hp2 | a0005 | c0004 | t0049 | g0295 | AFR | ESN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03195 | hp1 | a0001 | c0001 | t0018 | g0043 | AFR | ESN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03195 | hp2 | a0006 | c0006 | t0052 | g0048 | AFR | ESN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03209 | hp1 | a0005 | c0004 | t0021 | g0052 | AFR | MSL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03209 | hp2 | a0004 | c0005 | t0020 | g0045 | AFR | MSL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03225 | hp1 | a0005 | c0004 | t0081 | g0176 | AFR | MSL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03225 | hp2 | a0003 | c0003 | t0003 | g0127 | AFR | MSL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03453 | hp1 | a0004 | c0008 | t0019 | g0293 | AFR | MSL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03453 | hp2 | a0001 | c0011 | t0010 | g0010 | AFR | MSL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03486 | hp1 | a0005 | c0004 | t0049 | g0296 | AFR | MSL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03486 | hp2 | a0005 | c0004 | t0039 | g0180 | AFR | MSL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03491 | hp1 | a0001 | c0001 | t0047 | g0041 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03491 | hp2 | a0002 | c0002 | t0065 | g0093 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03492 | hp1 | a0001 | c0010 | t0102 | g0229 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03492 | hp2 | a0001 | c0001 | t0047 | g0041 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03516 | hp1 | a0006 | c0019 | t0008 | g0068 | AFR | ESN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03516 | hp2 | a0005 | c0004 | t0074 | g0147 | AFR | ESN | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03540 | hp1 | a0001 | c0001 | t0038 | g0154 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03540 | hp2 | a0001 | c0001 | t0114 | g0193 | AFR | GWD | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03579 | hp1 | a0001 | c0001 | t0011 | g0035 | AFR | MSL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03579 | hp2 | a0001 | c0011 | t0053 | g0058 | AFR | MSL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03654 | hp1 | a0014 | c0022 | t0001 | g0264 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03654 | hp2 | a0001 | c0001 | t0006 | g0038 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03669 | hp1 | a0001 | c0001 | t0007 | g0162 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03669 | hp2 | a0001 | c0001 | t0104 | g0195 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0102 | SAS | STU | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | STU | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03704 | hp1 | a0001 | c0001 | t0006 | g0246 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03704 | hp2 | a0023 | c0029 | t0001 | g0276 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03710 | hp2 | a0004 | c0005 | t0055 | g0071 | SAS | PJL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03831 | hp1 | a0001 | c0001 | t0006 | g0038 | SAS | BEB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03831 | hp2 | a0001 | c0001 | t0006 | g0261 | SAS | BEB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03834 | hp1 | a0001 | c0010 | t0107 | g0230 | SAS | BEB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03942 | hp2 | a0001 | c0001 | t0006 | g0247 | SAS | BEB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG04115 | hp1 | a0002 | c0002 | t0002 | g0078 | SAS | STU | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG04115 | hp2 | a0001 | c0001 | t0006 | g0262 | SAS | STU | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG04199 | hp1 | a0001 | c0001 | t0007 | g0167 | SAS | STU | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | STU | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | STU | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG04204 | hp2 | a0001 | c0001 | t0088 | g0256 | SAS | STU | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | STU | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0186 | SAS | STU | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18522 | hp1 | a0004 | c0008 | t0116 | g0288 | AFR | YRI | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18522 | hp2 | a0004 | c0009 | t0009 | g0284 | AFR | YRI | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18612 | hp1 | a0002 | c0002 | t0005 | g0004 | EAS | CHB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18612 | hp2 | a0008 | c0012 | t0017 | g0036 | EAS | CHB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18747 | hp1 | a0002 | c0002 | t0005 | g0004 | EAS | CHB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18747 | hp2 | a0007 | c0007 | t0013 | g0122 | EAS | CHB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18906 | hp1 | a0004 | c0009 | t0009 | g0285 | AFR | YRI | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18906 | hp2 | a0001 | c0001 | t0011 | g0220 | AFR | YRI | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0075 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18942 | hp2 | a0003 | c0003 | t0003 | g0030 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18944 | hp1 | a0002 | c0002 | t0005 | g0004 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18945 | hp1 | a0007 | c0007 | t0013 | g0119 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18945 | hp2 | a0002 | c0002 | t0005 | g0004 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18948 | hp1 | a0001 | c0001 | t0028 | g0190 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18948 | hp2 | a0001 | c0001 | t0007 | g0161 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18949 | hp1 | a0001 | c0001 | t0045 | g0206 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18949 | hp2 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18950 | hp2 | a0003 | c0003 | t0003 | g0029 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18952 | hp1 | a0002 | c0002 | t0005 | g0004 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18952 | hp2 | a0003 | c0003 | t0003 | g0029 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18956 | hp2 | a0002 | c0002 | t0002 | g0108 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18957 | hp1 | a0003 | c0003 | t0004 | g0007 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18959 | hp1 | a0007 | c0007 | t0034 | g0028 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18959 | hp2 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18960 | hp1 | a0001 | c0001 | t0006 | g0245 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18960 | hp2 | a0007 | c0007 | t0013 | g0026 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18961 | hp1 | a0002 | c0002 | t0002 | g0079 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18961 | hp2 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18962 | hp1 | a0003 | c0003 | t0003 | g0129 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18963 | hp1 | a0002 | c0002 | t0002 | g0117 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18963 | hp2 | a0002 | c0002 | t0005 | g0004 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18964 | hp1 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18964 | hp2 | a0007 | c0007 | t0033 | g0025 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18965 | hp1 | a0002 | c0002 | t0002 | g0024 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18965 | hp2 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18966 | hp1 | a0001 | c0001 | t0043 | g0254 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18966 | hp2 | a0004 | c0005 | t0031 | g0085 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18967 | hp1 | a0008 | c0012 | t0017 | g0036 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18967 | hp2 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18969 | hp1 | a0001 | c0001 | t0015 | g0015 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18970 | hp1 | a0001 | c0001 | t0007 | g0163 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18970 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18972 | hp1 | a0001 | c0001 | t0014 | g0159 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18972 | hp2 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18973 | hp1 | a0007 | c0007 | t0054 | g0123 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18973 | hp2 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18974 | hp1 | a0002 | c0002 | t0002 | g0076 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18974 | hp2 | a0004 | c0005 | t0058 | g0096 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18975 | hp1 | a0020 | c0027 | t0035 | g0130 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18975 | hp2 | a0001 | c0001 | t0111 | g0252 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18977 | hp2 | a0007 | c0007 | t0034 | g0028 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18978 | hp1 | a0001 | c0001 | t0015 | g0260 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18978 | hp2 | a0004 | c0005 | t0022 | g0114 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18979 | hp1 | a0003 | c0003 | t0004 | g0269 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0090 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18980 | hp1 | a0002 | c0002 | t0002 | g0024 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18981 | hp1 | a0007 | c0007 | t0013 | g0026 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18981 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18983 | hp1 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18983 | hp2 | a0001 | c0001 | t0028 | g0201 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18984 | hp1 | a0002 | c0002 | t0005 | g0115 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18984 | hp2 | a0016 | c0021 | t0006 | g0263 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18985 | hp1 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18985 | hp2 | a0003 | c0003 | t0004 | g0266 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18986 | hp1 | a0001 | c0001 | t0046 | g0034 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18986 | hp2 | a0003 | c0003 | t0003 | g0134 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18988 | hp1 | a0003 | c0003 | t0004 | g0012 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18988 | hp2 | a0007 | c0007 | t0026 | g0120 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18989 | hp1 | a0002 | c0002 | t0005 | g0004 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18990 | hp2 | a0003 | c0003 | t0073 | g0137 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18992 | hp1 | a0001 | c0001 | t0095 | g0228 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18992 | hp2 | a0003 | c0003 | t0004 | g0012 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18993 | hp1 | a0004 | c0005 | t0023 | g0013 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18994 | hp1 | a0002 | c0002 | t0005 | g0020 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18994 | hp2 | a0003 | c0003 | t0004 | g0265 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18998 | hp2 | a0003 | c0003 | t0004 | g0007 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA18999 | hp2 | a0007 | c0007 | t0026 | g0027 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19000 | hp1 | a0001 | c0001 | t0043 | g0258 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19000 | hp2 | a0001 | c0001 | t0046 | g0034 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19001 | hp1 | a0001 | c0001 | t0096 | g0205 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19001 | hp2 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19002 | hp1 | a0003 | c0003 | t0070 | g0138 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19002 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19004 | hp1 | a0001 | c0001 | t0004 | g0225 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19004 | hp2 | a0007 | c0007 | t0026 | g0027 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19006 | hp1 | a0003 | c0003 | t0113 | g0270 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19006 | hp2 | a0002 | c0002 | t0067 | g0098 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19007 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19007 | hp2 | a0001 | c0001 | t0092 | g0257 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19009 | hp1 | a0001 | c0001 | t0015 | g0015 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19009 | hp2 | a0009 | c0013 | t0110 | g0248 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19010 | hp1 | a0007 | c0007 | t0033 | g0025 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19010 | hp2 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19011 | hp2 | a0003 | c0003 | t0004 | g0007 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19012 | hp2 | a0003 | c0003 | t0004 | g0007 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19030 | hp1 | a0004 | c0008 | t0019 | g0292 | AFR | LWK | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19030 | hp2 | a0001 | c0001 | t0007 | g0169 | AFR | LWK | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19043 | hp1 | a0001 | c0001 | t0077 | g0155 | AFR | LWK | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19043 | hp2 | a0001 | c0001 | t0087 | g0185 | AFR | LWK | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19054 | hp1 | a0003 | c0003 | t0036 | g0131 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19055 | hp1 | a0002 | c0002 | t0002 | g0072 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19056 | hp1 | a0001 | c0001 | t0015 | g0015 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19060 | hp1 | a0007 | c0007 | t0066 | g0121 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19060 | hp2 | a0008 | c0012 | t0017 | g0214 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19062 | hp1 | a0001 | c0001 | t0028 | g0226 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19062 | hp2 | a0001 | c0001 | t0105 | g0200 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19063 | hp1 | a0004 | c0005 | t0057 | g0099 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19063 | hp2 | a0008 | c0012 | t0103 | g0202 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19064 | hp2 | a0002 | c0002 | t0062 | g0116 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19067 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19067 | hp2 | a0003 | c0003 | t0004 | g0007 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19068 | hp2 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19070 | hp1 | a0003 | c0003 | t0004 | g0268 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19072 | hp1 | a0004 | c0005 | t0023 | g0013 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19074 | hp1 | a0001 | c0001 | t0014 | g0158 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19074 | hp2 | a0003 | c0003 | t0004 | g0012 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19077 | hp1 | a0004 | c0005 | t0023 | g0013 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19077 | hp2 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19079 | hp1 | a0001 | c0001 | t0045 | g0234 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19079 | hp2 | a0003 | c0003 | t0003 | g0128 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19080 | hp1 | a0001 | c0001 | t0014 | g0157 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19080 | hp2 | a0002 | c0002 | t0025 | g0112 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19083 | hp2 | a0003 | c0003 | t0004 | g0012 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19084 | hp1 | a0003 | c0003 | t0004 | g0267 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19084 | hp2 | a0001 | c0001 | t0014 | g0166 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19085 | hp1 | a0002 | c0002 | t0005 | g0004 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19086 | hp1 | a0002 | c0002 | t0061 | g0097 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19087 | hp1 | a0001 | c0001 | t0090 | g0249 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19087 | hp2 | a0013 | c0015 | t0002 | g0049 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19088 | hp1 | a0003 | c0003 | t0004 | g0271 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19088 | hp2 | a0004 | c0005 | t0031 | g0086 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19090 | hp1 | a0002 | c0002 | t0025 | g0094 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19090 | hp2 | a0003 | c0003 | t0004 | g0007 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19091 | hp2 | a0003 | c0003 | t0003 | g0030 | EAS | JPT | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19240 | hp1 | a0004 | c0005 | t0030 | g0017 | AFR | YRI | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA19240 | hp2 | a0005 | c0004 | t0027 | g0032 | AFR | YRI | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ASW | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA20129 | hp2 | a0006 | c0006 | t0008 | g0066 | AFR | ASW | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA20752 | hp1 | a0001 | c0001 | t0006 | g0251 | EUR | TSI | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA20752 | hp2 | a0006 | c0006 | t0008 | g0064 | EUR | TSI | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA20805 | hp1 | a0004 | c0005 | t0022 | g0110 | EUR | TSI | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA20905 | hp1 | a0001 | c0001 | t0007 | g0170 | SAS | GIH | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA20905 | hp2 | a0001 | c0001 | t0006 | g0212 | SAS | GIH | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG01123 | hp2 | a0003 | c0003 | t0004 | g0274 | AMR | CLM | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02109 | hp1 | a0001 | c0011 | t0010 | g0010 | AFR | ACB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02109 | hp2 | a0003 | c0003 | t0003 | g0139 | AFR | ACB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02559 | hp1 | a0002 | c0002 | t0079 | g0171 | AFR | ACB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG02559 | hp2 | a0004 | c0008 | t0029 | g0281 | AFR | ACB | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03471 | hp1 | a0006 | c0006 | t0008 | g0018 | AFR | MSL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| HG03471 | hp2 | a0001 | c0001 | t0038 | g0153 | AFR | MSL | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA20300 | hp1 | a0001 | c0001 | t0080 | g0241 | AFR | USA | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA20300 | hp2 | a0011 | c0030 | t0050 | g0047 | AFR | USA | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | LWK | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| NA21309 | hp2 | a0015 | c0016 | t0109 | g0172 | AFR | LWK | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0010 | t0016 | g0037 | REF | REF | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| homoSapiens_grch38 | hp1 | a0022 | c0023 | t0002 | g0070 | REF | REF | SNX19_chr11_130861250_130921479 | SNX19 | chr11 | 130861250 | 130921479 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:130879634
|
G | C | 1 | a0017 | 1 | HG01168.hp1 | missense_variant | MODERATE | c.2836C>G | p.Leu946Val | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 10/11 | 3376/15691 | 2836/2979 | 946/992 | chr11 | 130879634 | ||
| chr11:130880747
|
A | C | 17 | a0001a0003a0004others(14): Show | 328 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(325): Show |
missense_variant | MODERATE | c.2633T>G | p.Leu878Arg | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 9/11 | 3173/15691 | 2633/2979 | 878/992 | chr11 | 130880747 | ||
| chr11:130880766
|
G | A | 2 | a0008a0018 | 5 | HG02055.hp1 NA18612.hp2 NA18967.hp1 others(2): Show |
missense_variant | MODERATE | c.2614C>T | p.Arg872Cys | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 9/11 | 3154/15691 | 2614/2979 | 872/992 | chr11 | 130880766 | ||
| chr11:130906629
|
T | C | 14 | a0001a0003a0005others(11): Show | 264 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
missense_variant | MODERATE | c.2258A>G | p.Asn753Ser | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 6/11 | 2798/15691 | 2258/2979 | 753/992 | chr11 | 130906629 | ||
| chr11:130910330
|
C | A | 22 | a0001a0002a0003others(19): Show | 413 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(410): Show |
missense_variant | MODERATE | c.1854G>T | p.Leu618Phe | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 3/11 | 2394/15691 | 1854/2979 | 618/992 | chr11 | 130910330 | ||
| chr11:130914273
|
G | A | 1 | a0016 | 1 | NA18984.hp2 | missense_variant | MODERATE | c.1667C>T | p.Thr556Ile | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 2207/15691 | 1667/2979 | 556/992 | chr11 | 130914273 | ||
| chr11:130914501
|
G | A | 3 | a0003a0019a0020 | 55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
missense_variant | MODERATE | c.1439C>T | p.Pro480Leu | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 1979/15691 | 1439/2979 | 480/992 | chr11 | 130914501 | ||
| chr11:130914559
|
C | T | 1 | a0019 | 1 | HG02165.hp1 | missense_variant | MODERATE | c.1381G>A | p.Val461Ile | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 1921/15691 | 1381/2979 | 461/992 | chr11 | 130914559 | ||
| chr11:130914679
|
C | T | 2 | a0005a0018 | 18 | HG01891.hp2 HG02055.hp1 HG02572.hp2 others(15): Show |
missense_variant | MODERATE | c.1261G>A | p.Gly421Arg | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 1801/15691 | 1261/2979 | 421/992 | chr11 | 130914679 | ||
| chr11:130914694
|
C | A | 1 | a0007 | 14 | HG02040.hp2 NA18747.hp2 NA18945.hp1 others(11): Show |
missense_variant | MODERATE | c.1246G>T | p.Gly416Cys | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 1786/15691 | 1246/2979 | 416/992 | chr11 | 130914694 | ||
| chr11:130914721
|
T | C | 3 | a0003a0019a0020 | 55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
missense_variant | MODERATE | c.1219A>G | p.Ser407Gly | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 1759/15691 | 1219/2979 | 407/992 | chr11 | 130914721 | ||
| chr11:130914752
|
G | C | 3 | a0003a0019a0020 | 55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
missense_variant | MODERATE | c.1188C>G | p.Asp396Glu | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 1728/15691 | 1188/2979 | 396/992 | chr11 | 130914752 | ||
| chr11:130914799
|
C | T | 3 | a0003a0019a0020 | 55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
missense_variant | MODERATE | c.1141G>A | p.Gly381Ser | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 1681/15691 | 1141/2979 | 381/992 | chr11 | 130914799 | ||
| chr11:130914859
|
C | G | 16 | a0001a0003a0005others(13): Show | 294 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(291): Show |
missense_variant | MODERATE | c.1081G>C | p.Val361Leu | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 1621/15691 | 1081/2979 | 361/992 | chr11 | 130914859 | ||
| chr11:130914933
|
A | G | 1 | a0015 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.1007T>C | p.Val336Ala | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 1547/15691 | 1007/2979 | 336/992 | chr11 | 130914933 | ||
| chr11:130914991
|
T | C | 1 | a0014 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.949A>G | p.Ser317Gly | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 1489/15691 | 949/2979 | 317/992 | chr11 | 130914991 | ||
| chr11:130915185
|
C | T | 1 | a0010 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.755G>A | p.Ser252Asn | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 1295/15691 | 755/2979 | 252/992 | chr11 | 130915185 | ||
| chr11:130915359
|
C | T | 1 | a0013 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.581G>A | p.Arg194Gln | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 1121/15691 | 581/2979 | 194/992 | chr11 | 130915359 | ||
| chr11:130915537
|
T | G | 1 | a0012 | 1 | HG02056.hp1 | missense_variant | MODERATE | c.403A>C | p.Met135Leu | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 943/15691 | 403/2979 | 135/992 | chr11 | 130915537 | ||
| chr11:130915665
|
G | C | 1 | a0023 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.275C>G | p.Pro92Arg | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 815/15691 | 275/2979 | 92/992 | chr11 | 130915665 | ||
| chr11:130915689
|
G | A | 1 | a0011 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.251C>T | p.Pro84Leu | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 791/15691 | 251/2979 | 84/992 | chr11 | 130915689 | ||
| chr11:130915862
|
G | C | 1 | a0010 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.78C>G | p.Ser26Arg | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 618/15691 | 78/2979 | 26/992 | chr11 | 130915862 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:130906122
|
A | C | 1 | a0001c0014 | 2 | HG01099.hp1 HG03098.hp2 |
synonymous_variant | LOW | c.2274T>G | p.Thr758Thr | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/11 | 2814/15691 | 2274/2979 | 758/992 | chr11 | 130906122 | ||
| chr11:130906661
|
T | C | 1 | a0001c0010 | 6 | HG00280.hp2 HG01074.hp1 HG01081.hp1 others(3): Show |
synonymous_variant | LOW | c.2226A>G | p.Gln742Gln | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 6/11 | 2766/15691 | 2226/2979 | 742/992 | chr11 | 130906661 | ||
| chr11:130906718
|
A | G | 18 | a0001c0001a0001c0010a0001c0011others(15): Show | 264 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
synonymous_variant | LOW | c.2169T>C | p.Ser723Ser | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 6/11 | 2709/15691 | 2169/2979 | 723/992 | chr11 | 130906718 | ||
| chr11:130907991
|
G | A | 4 | a0003c0003a0019c0026a0020c0027others(1): Show | 56 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
synonymous_variant | LOW | c.2127C>T | p.Thr709Thr | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/11 | 2667/15691 | 2127/2979 | 709/992 | chr11 | 130907991 | ||
| chr11:130908003
|
A | G | 1 | a0006c0019 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.2115T>C | p.Ser705Ser | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/11 | 2655/15691 | 2115/2979 | 705/992 | chr11 | 130908003 | ||
| chr11:130910120
|
C | T | 13 | a0001c0001a0001c0010a0003c0003others(10): Show | 238 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(235): Show |
synonymous_variant | LOW | c.1932G>A | p.Pro644Pro | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/11 | 2472/15691 | 1932/2979 | 644/992 | chr11 | 130910120 | ||
| chr11:130911736
|
G | C | 1 | a0005c0017 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.1710C>G | p.Gly570Gly | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/11 | 2250/15691 | 1710/2979 | 570/992 | chr11 | 130911736 | ||
| chr11:130914443
|
T | A | 1 | a0004c0025 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.1497A>T | p.Pro499Pro | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 2037/15691 | 1497/2979 | 499/992 | chr11 | 130914443 | ||
| chr11:130914538
|
A | G | 1 | a0005c0017 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.1402T>C | p.Leu468Leu | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 1942/15691 | 1402/2979 | 468/992 | chr11 | 130914538 | ||
| chr11:130914593
|
A | G | 3 | a0003c0003a0019c0026a0020c0027 | 55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
synonymous_variant | LOW | c.1347T>C | p.Ile449Ile | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 1887/15691 | 1347/2979 | 449/992 | chr11 | 130914593 | ||
| chr11:130914788
|
G | A | 2 | a0004c0008a0010c0031 | 12 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(9): Show |
synonymous_variant | LOW | c.1152C>T | p.Thr384Thr | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 1692/15691 | 1152/2979 | 384/992 | chr11 | 130914788 | ||
| chr11:130914812
|
C | T | 3 | a0003c0003a0019c0026a0020c0027 | 55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
synonymous_variant | LOW | c.1128G>A | p.Pro376Pro | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 1668/15691 | 1128/2979 | 376/992 | chr11 | 130914812 | ||
| chr11:130915076
|
C | G | 24 | a0001c0001a0001c0010a0001c0011others(21): Show | 313 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(310): Show |
synonymous_variant | LOW | c.864G>C | p.Pro288Pro | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 1404/15691 | 864/2979 | 288/992 | chr11 | 130915076 | ||
| chr11:130915310
|
G | A | 3 | a0003c0003a0019c0026a0020c0027 | 55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
synonymous_variant | LOW | c.630C>T | p.Thr210Thr | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 1170/15691 | 630/2979 | 210/992 | chr11 | 130915310 | ||
| chr11:130915409
|
T | C | 3 | a0003c0003a0019c0026a0020c0027 | 55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
synonymous_variant | LOW | c.531A>G | p.Ala177Ala | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 1071/15691 | 531/2979 | 177/992 | chr11 | 130915409 | ||
| chr11:130915580
|
G | A | 1 | a0007c0007 | 14 | HG02040.hp2 NA18747.hp2 NA18945.hp1 others(11): Show |
synonymous_variant | LOW | c.360C>T | p.Ser120Ser | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 900/15691 | 360/2979 | 120/992 | chr11 | 130915580 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:130866254
|
T | C | 1 | a0001c0001t0056 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12168A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 12168 | chr11 | 130866254 | |||||
| chr11:130866272
|
A | G | 8 | a0001c0001t0092a0007c0007t0013a0007c0007t0026others(5): Show | 15 | HG02040.hp2 NA18747.hp2 NA18945.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*12150T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 12150 | chr11 | 130866272 | |||||
| chr11:130866339
|
C | T | 1 | a0018c0018t0085 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12083G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 12083 | chr11 | 130866339 | |||||
| chr11:130866376
|
T | G | 3 | a0001c0010t0016a0001c0010t0102a0001c0010t0107 | 6 | HG00280.hp2 HG01074.hp1 HG01081.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*12046A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 12046 | chr11 | 130866376 | |||||
| chr11:130866388
|
T | C | 1 | a0001c0001t0099 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12034A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 12034 | chr11 | 130866388 | |||||
| chr11:130866655
|
C | T | 1 | a0002c0002t0065 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11767G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 11767 | chr11 | 130866655 | |||||
| chr11:130866668
|
G | A | 1 | a0006c0006t0032 | 2 | HG02647.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*11754C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 11754 | chr11 | 130866668 | |||||
| chr11:130866739
|
T | C | 1 | a0009c0013t0112 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11683A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 11683 | chr11 | 130866739 | |||||
| chr11:130866790
|
C | T | 4 | a0001c0001t0007a0001c0001t0037a0001c0001t0076others(1): Show | 17 | HG00642.hp2 HG01074.hp2 HG01255.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*11632G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 11632 | chr11 | 130866790 | |||||
| chr11:130866936
|
C | T | 2 | a0001c0001t0007a0001c0001t0037 | 15 | HG00642.hp2 HG01074.hp2 HG01255.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*11486G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 11486 | chr11 | 130866936 | |||||
| chr11:130866960
|
A | AAAGCTCT others(325): Show |
1 | a0018c0018t0085 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11461_*11462insGG others(330): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 11461 | chr11 | 130866960 | |||||
| chr11:130867107
|
G | A | 1 | a0004c0009t0009 | 7 | HG00741.hp2 HG01070.hp2 HG02451.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*11315C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 11315 | chr11 | 130867107 | |||||
| chr11:130867249
|
A | G | 2 | a0001c0001t0105a0001c0001t0106 | 2 | HG00673.hp2 NA19062.hp2 |
3_prime_UTR_variant | MODIFIER | c.*11173T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 11173 | chr11 | 130867249 | |||||
| chr11:130867299
|
G | A | 1 | a0001c0001t0100 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11123C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 11123 | chr11 | 130867299 | |||||
| chr11:130867349
|
T | C | 2 | a0004c0008t0116a0004c0008t0117 | 2 | HG02280.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*11073A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 11073 | chr11 | 130867349 | |||||
| chr11:130867359
|
C | T | 4 | a0001c0001t0007a0001c0001t0037a0001c0001t0076others(1): Show | 17 | HG00642.hp2 HG01074.hp2 HG01255.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*11063G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 11063 | chr11 | 130867359 | |||||
| chr11:130867377
|
T | G | 8 | a0001c0001t0092a0007c0007t0013a0007c0007t0026others(5): Show | 15 | HG02040.hp2 NA18747.hp2 NA18945.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*11045A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 11045 | chr11 | 130867377 | |||||
| chr11:130867386
|
A | G | 109 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(106): Show | 327 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(324): Show |
3_prime_UTR_variant | MODIFIER | c.*11036T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 11036 | chr11 | 130867386 | |||||
| chr11:130867551
|
A | G | 1 | a0009c0013t0112 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10871T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 10871 | chr11 | 130867551 | |||||
| chr11:130867611
|
C | T | 1 | a0001c0001t0046 | 2 | NA18986.hp1 NA19000.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10811G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 10811 | chr11 | 130867611 | |||||
| chr11:130867901
|
G | C | 1 | a0005c0004t0082 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10521C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 10521 | chr11 | 130867901 | |||||
| chr11:130867983
|
C | A | 7 | a0001c0001t0017a0001c0001t0095a0004c0005t0023others(4): Show | 11 | HG02523.hp2 NA18612.hp2 NA18967.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*10439G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 10439 | chr11 | 130867983 | |||||
| chr11:130868016
|
C | G | 2 | a0007c0007t0033a0007c0007t0066 | 3 | NA18964.hp2 NA19010.hp1 NA19060.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10406G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 10406 | chr11 | 130868016 | |||||
| chr11:130868016
|
C | T | 1 | a0004c0009t0009 | 7 | HG00741.hp2 HG01070.hp2 HG02451.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*10406G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 10406 | chr11 | 130868016 | |||||
| chr11:130868058
|
C | G | 1 | a0001c0001t0099 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10364G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 10364 | chr11 | 130868058 | |||||
| chr11:130868357
|
A | G | 1 | a0004c0009t0009 | 7 | HG00741.hp2 HG01070.hp2 HG02451.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*10065T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 10065 | chr11 | 130868357 | |||||
| chr11:130868375
|
C | T | 1 | a0001c0001t0098 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10047G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 10047 | chr11 | 130868375 | |||||
| chr11:130868673
|
A | C | 59 | a0001c0001t0001a0001c0001t0006a0001c0001t0014others(56): Show | 179 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*9749T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 9749 | chr11 | 130868673 | |||||
| chr11:130868695
|
C | A | 22 | a0001c0001t0006a0001c0001t0015a0001c0001t0042others(19): Show | 50 | HG00323.hp2 HG01243.hp1 HG01884.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*9727G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 9727 | chr11 | 130868695 | |||||
| chr11:130868708
|
T | C | 1 | a0004c0005t0030 | 2 | HG01891.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9714A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 9714 | chr11 | 130868708 | |||||
| chr11:130868761
|
C | T | 1 | a0001c0001t0097 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9661G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 9661 | chr11 | 130868761 | |||||
| chr11:130868829
|
T | C | 9 | a0001c0001t0011a0001c0001t0114a0004c0008t0048others(6): Show | 21 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*9593A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 9593 | chr11 | 130868829 | |||||
| chr11:130868873
|
G | A | 3 | a0001c0011t0010a0005c0004t0027a0005c0004t0081 | 9 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*9549C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 9549 | chr11 | 130868873 | |||||
| chr11:130868953
|
C | T | 21 | a0001c0001t0006a0001c0001t0015a0001c0001t0042others(18): Show | 49 | HG00323.hp2 HG00673.hp1 HG01243.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*9469G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 9469 | chr11 | 130868953 | |||||
| chr11:130869051
|
T | A | 63 | a0001c0001t0001a0001c0001t0006a0001c0001t0014others(60): Show | 183 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*9371A>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 9371 | chr11 | 130869051 | |||||
| chr11:130869159
|
A | G | 2 | a0001c0001t0007a0001c0001t0037 | 15 | HG00642.hp2 HG01074.hp2 HG01255.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*9263T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 9263 | chr11 | 130869159 | |||||
| chr11:130869204
|
T | G | 1 | a0004c0008t0117 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9218A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 9218 | chr11 | 130869204 | |||||
| chr11:130869223
|
C | T | 1 | a0001c0001t0045 | 2 | NA18949.hp1 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9199G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 9199 | chr11 | 130869223 | |||||
| chr11:130869238
|
C | T | 36 | a0001c0001t0001a0001c0001t0014a0001c0001t0017others(33): Show | 128 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*9184G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 9184 | chr11 | 130869238 | |||||
| chr11:130869389
|
G | A | 62 | a0001c0001t0001a0001c0001t0006a0001c0001t0014others(59): Show | 182 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*9033C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 9033 | chr11 | 130869389 | |||||
| chr11:130869452
|
C | T | 3 | a0001c0011t0010a0005c0004t0027a0005c0004t0081 | 9 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*8970G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 8970 | chr11 | 130869452 | |||||
| chr11:130869478
|
G | C | 23 | a0001c0001t0006a0001c0001t0015a0001c0001t0042others(20): Show | 51 | HG00323.hp2 HG00673.hp1 HG01243.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*8944C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 8944 | chr11 | 130869478 | |||||
| chr11:130869492
|
T | C | 5 | a0001c0001t0007a0001c0001t0037a0001c0001t0076others(2): Show | 24 | HG00642.hp2 HG00741.hp2 HG01070.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*8930A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 8930 | chr11 | 130869492 | |||||
| chr11:130869536
|
C | G | 3 | a0006c0006t0032a0006c0006t0060a0015c0016t0109 | 4 | HG02615.hp1 HG02647.hp1 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8886G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 8886 | chr11 | 130869536 | |||||
| chr11:130869568
|
C | T | 1 | a0019c0026t0072 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8854G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 8854 | chr11 | 130869568 | |||||
| chr11:130869585
|
T | G | 10 | a0001c0001t0004a0001c0001t0038a0001c0001t0111others(7): Show | 58 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*8837A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 8837 | chr11 | 130869585 | |||||
| chr11:130869638
|
A | C | 2 | a0001c0001t0015a0003c0003t0070 | 5 | NA18969.hp1 NA18978.hp1 NA19002.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*8784T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 8784 | chr11 | 130869638 | |||||
| chr11:130869705
|
C | T | 1 | a0005c0004t0081 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8717G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 8717 | chr11 | 130869705 | |||||
| chr11:130869765
|
A | G | 5 | a0001c0001t0007a0001c0001t0037a0001c0001t0076others(2): Show | 24 | HG00642.hp2 HG00741.hp2 HG01070.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*8657T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 8657 | chr11 | 130869765 | |||||
| chr11:130869769
|
T | C | 8 | a0001c0001t0092a0007c0007t0013a0007c0007t0026others(5): Show | 15 | HG02040.hp2 NA18747.hp2 NA18945.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*8653A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 8653 | chr11 | 130869769 | |||||
| chr11:130869909
|
G | GA | 26 | a0001c0001t0007a0001c0001t0011a0001c0001t0018others(23): Show | 67 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*8512dupT | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 8512 | chr11 | 130869909 | |||||
| chr11:130869909
|
G | GAA | 3 | a0001c0001t0115a0004c0008t0019a0004c0008t0029 | 8 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*8511_*8512dupTT | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 8512 | chr11 | 130869909 | |||||
| chr11:130869942
|
T | TGAA | 16 | a0001c0001t0011a0001c0001t0018a0001c0001t0114others(13): Show | 36 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*8477_*8479dupTTC | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 8479 | chr11 | 130869942 | |||||
| chr11:130869953
|
A | G | 109 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(106): Show | 327 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(324): Show |
3_prime_UTR_variant | MODIFIER | c.*8469T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 8469 | chr11 | 130869953 | |||||
| chr11:130869958
|
T | C | 105 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(102): Show | 320 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(317): Show |
3_prime_UTR_variant | MODIFIER | c.*8464A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 8464 | chr11 | 130869958 | |||||
| chr11:130869992
|
G | T | 64 | a0001c0001t0001a0001c0001t0006a0001c0001t0014others(61): Show | 184 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*8430C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 8430 | chr11 | 130869992 | |||||
| chr11:130870040
|
A | G | 1 | a0002c0002t0063 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8382T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 8382 | chr11 | 130870040 | |||||
| chr11:130870268
|
T | C | 1 | a0006c0006t0060 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8154A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 8154 | chr11 | 130870268 | |||||
| chr11:130870440
|
T | C | 63 | a0001c0001t0001a0001c0001t0006a0001c0001t0014others(60): Show | 183 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*7982A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 7982 | chr11 | 130870440 | |||||
| chr11:130870445
|
G | T | 1 | a0009c0013t0112 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7977C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 7977 | chr11 | 130870445 | |||||
| chr11:130870460
|
C | T | 1 | a0001c0001t0091 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7962G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 7962 | chr11 | 130870460 | |||||
| chr11:130870462
|
T | C | 64 | a0001c0001t0001a0001c0001t0006a0001c0001t0014others(61): Show | 184 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*7960A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 7960 | chr11 | 130870462 | |||||
| chr11:130870529
|
G | A | 13 | a0001c0001t0006a0001c0001t0015a0001c0001t0042others(10): Show | 30 | HG00323.hp2 HG00673.hp1 HG01884.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*7893C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 7893 | chr11 | 130870529 | |||||
| chr11:130870805
|
A | C | 7 | a0004c0008t0048a0004c0008t0116a0004c0008t0117others(4): Show | 16 | HG00738.hp2 HG02280.hp1 HG02809.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*7617T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 7617 | chr11 | 130870805 | |||||
| chr11:130870825
|
T | TG | 14 | a0001c0001t0077a0003c0003t0073a0003c0003t0113others(11): Show | 27 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*7596dupC | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 7596 | chr11 | 130870825 | |||||
| chr11:130870825
|
TG | T | 66 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(63): Show | 211 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(208): Show |
3_prime_UTR_variant | MODIFIER | c.*7596delC | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 7596 | chr11 | 130870825 | |||||
| chr11:130870849
|
T | A | 1 | a0001c0001t0087 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7573A>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 7573 | chr11 | 130870849 | |||||
| chr11:130870896
|
T | C | 1 | a0004c0025t0051 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7526A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 7526 | chr11 | 130870896 | |||||
| chr11:130871072
|
G | A | 67 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(64): Show | 200 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
3_prime_UTR_variant | MODIFIER | c.*7350C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 7350 | chr11 | 130871072 | |||||
| chr11:130871132
|
C | G | 105 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(102): Show | 320 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(317): Show |
3_prime_UTR_variant | MODIFIER | c.*7290G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 7290 | chr11 | 130871132 | |||||
| chr11:130871180
|
G | A | 1 | a0002c0002t0012 | 4 | HG00099.hp1 HG01106.hp2 HG01175.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7242C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 7242 | chr11 | 130871180 | |||||
| chr11:130871205
|
A | G | 1 | a0002c0002t0064 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7217T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 7217 | chr11 | 130871205 | |||||
| chr11:130871295
|
C | T | 4 | a0001c0001t0007a0001c0001t0037a0001c0001t0076others(1): Show | 17 | HG00642.hp2 HG01074.hp2 HG01255.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*7127G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 7127 | chr11 | 130871295 | |||||
| chr11:130871387
|
C | T | 9 | a0001c0001t0004a0001c0001t0038a0003c0003t0003others(6): Show | 56 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*7035G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 7035 | chr11 | 130871387 | |||||
| chr11:130871508
|
T | G | 1 | a0018c0018t0085 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6914A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 6914 | chr11 | 130871508 | |||||
| chr11:130871520
|
G | A | 42 | a0001c0001t0004a0001c0001t0007a0001c0001t0011others(39): Show | 137 | HG00423.hp2 HG00558.hp2 HG00642.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*6902C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 6902 | chr11 | 130871520 | |||||
| chr11:130871578
|
C | T | 3 | a0001c0001t0043a0001c0001t0089a0001c0001t0090 | 4 | HG00673.hp1 NA18966.hp1 NA19000.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6844G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 6844 | chr11 | 130871578 | |||||
| chr11:130871711
|
A | G | 63 | a0001c0001t0001a0001c0001t0006a0001c0001t0014others(60): Show | 183 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*6711T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 6711 | chr11 | 130871711 | |||||
| chr11:130871866
|
A | G | 63 | a0001c0001t0001a0001c0001t0006a0001c0001t0014others(60): Show | 183 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*6556T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 6556 | chr11 | 130871866 | |||||
| chr11:130872010
|
G | A | 1 | a0010c0031t0118 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6412C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 6412 | chr11 | 130872010 | |||||
| chr11:130872045
|
A | G | 62 | a0001c0001t0001a0001c0001t0006a0001c0001t0014others(59): Show | 180 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*6377T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 6377 | chr11 | 130872045 | |||||
| chr11:130872260
|
G | T | 63 | a0001c0001t0001a0001c0001t0006a0001c0001t0014others(60): Show | 183 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*6162C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 6162 | chr11 | 130872260 | |||||
| chr11:130872280
|
G | C | 1 | a0001c0001t0104 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6142C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 6142 | chr11 | 130872280 | |||||
| chr11:130872310
|
C | T | 1 | a0001c0001t0095 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6112G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 6112 | chr11 | 130872310 | |||||
| chr11:130872319
|
C | T | 1 | a0004c0025t0051 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6103G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 6103 | chr11 | 130872319 | |||||
| chr11:130872349
|
G | A | 1 | a0001c0001t0105 | 1 | NA19062.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6073C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 6073 | chr11 | 130872349 | |||||
| chr11:130872508
|
A | G | 1 | a0007c0007t0033 | 2 | NA18964.hp2 NA19010.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5914T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 5914 | chr11 | 130872508 | |||||
| chr11:130872735
|
G | A | 64 | a0001c0001t0001a0001c0001t0006a0001c0001t0014others(61): Show | 184 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*5687C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 5687 | chr11 | 130872735 | |||||
| chr11:130872847
|
T | C | 1 | a0001c0001t0106 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5575A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 5575 | chr11 | 130872847 | |||||
| chr11:130872893
|
T | C | 65 | a0001c0001t0001a0001c0001t0006a0001c0001t0014others(62): Show | 185 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*5529A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 5529 | chr11 | 130872893 | |||||
| chr11:130872906
|
C | T | 1 | a0005c0004t0084 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5516G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 5516 | chr11 | 130872906 | |||||
| chr11:130872917
|
G | A | 24 | a0001c0001t0006a0001c0001t0015a0001c0001t0042others(21): Show | 52 | HG00323.hp2 HG00673.hp1 HG01243.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*5505C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 5505 | chr11 | 130872917 | |||||
| chr11:130872932
|
C | T | 1 | a0001c0001t0042 | 2 | HG00323.hp2 HG01952.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5490G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 5490 | chr11 | 130872932 | |||||
| chr11:130873346
|
T | G | 1 | a0001c0001t0087 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5076A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 5076 | chr11 | 130873346 | |||||
| chr11:130873493
|
T | C | 65 | a0001c0001t0001a0001c0001t0006a0001c0001t0014others(62): Show | 185 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*4929A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 4929 | chr11 | 130873493 | |||||
| chr11:130873539
|
G | A | 3 | a0005c0004t0040a0005c0004t0074a0005c0004t0084 | 4 | HG02922.hp1 HG02976.hp2 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4883C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 4883 | chr11 | 130873539 | |||||
| chr11:130873578
|
C | T | 1 | a0001c0001t0037 | 2 | HG01255.hp1 HG02602.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4844G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 4844 | chr11 | 130873578 | |||||
| chr11:130873939
|
T | C | 3 | a0002c0002t0005a0002c0002t0062a0009c0013t0112 | 17 | HG00438.hp1 HG00609.hp2 HG02027.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*4483A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 4483 | chr11 | 130873939 | |||||
| chr11:130874026
|
G | T | 3 | a0001c0001t0114a0006c0006t0032a0006c0006t0060 | 4 | HG02615.hp1 HG02647.hp1 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4396C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 4396 | chr11 | 130874026 | |||||
| chr11:130874029
|
T | TTA | 12 | a0001c0001t0006a0001c0001t0015a0001c0001t0042others(9): Show | 29 | HG00323.hp2 HG00673.hp1 HG01884.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*4392_*4393insTA | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 4392 | chr11 | 130874029 | |||||
| chr11:130874030
|
T | TA | 53 | a0001c0001t0001a0001c0001t0014a0001c0001t0017others(50): Show | 156 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(153): Show |
3_prime_UTR_variant | MODIFIER | c.*4391_*4392insT | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 4391 | chr11 | 130874030 | |||||
| chr11:130874089
|
C | T | 1 | a0001c0001t0088 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4333G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 4333 | chr11 | 130874089 | |||||
| chr11:130874184
|
C | T | 1 | a0002c0002t0063 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4238G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 4238 | chr11 | 130874184 | |||||
| chr11:130874317
|
C | T | 2 | a0001c0001t0044a0004c0005t0022 | 5 | HG01258.hp2 HG01934.hp1 HG01993.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4105G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 4105 | chr11 | 130874317 | |||||
| chr11:130874348
|
G | A | 1 | a0006c0006t0069 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4074C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 4074 | chr11 | 130874348 | |||||
| chr11:130874353
|
A | G | 1 | a0002c0002t0062 | 1 | NA19064.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4069T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 4069 | chr11 | 130874353 | |||||
| chr11:130874373
|
A | C | 65 | a0001c0001t0001a0001c0001t0006a0001c0001t0014others(62): Show | 185 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*4049T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 4049 | chr11 | 130874373 | |||||
| chr11:130874430
|
G | A | 1 | a0007c0007t0059 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3992C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 3992 | chr11 | 130874430 | |||||
| chr11:130874441
|
C | T | 1 | a0002c0002t0061 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3981G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 3981 | chr11 | 130874441 | |||||
| chr11:130874507
|
G | A | 1 | a0004c0005t0058 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3915C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 3915 | chr11 | 130874507 | |||||
| chr11:130874578
|
G | A | 64 | a0001c0001t0001a0001c0001t0006a0001c0001t0014others(61): Show | 184 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*3844C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 3844 | chr11 | 130874578 | |||||
| chr11:130874595
|
T | G | 65 | a0001c0001t0001a0001c0001t0006a0001c0001t0014others(62): Show | 185 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*3827A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 3827 | chr11 | 130874595 | |||||
| chr11:130874614
|
A | G | 65 | a0001c0001t0001a0001c0001t0006a0001c0001t0014others(62): Show | 185 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*3808T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 3808 | chr11 | 130874614 | |||||
| chr11:130874628
|
C | T | 1 | a0012c0028t0094 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3794G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 3794 | chr11 | 130874628 | |||||
| chr11:130874746
|
A | G | 3 | a0004c0005t0020a0004c0005t0030a0011c0030t0050 | 6 | HG01891.hp1 HG02572.hp1 HG02622.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3676T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 3676 | chr11 | 130874746 | |||||
| chr11:130874775
|
A | G | 65 | a0001c0001t0001a0001c0001t0006a0001c0001t0014others(62): Show | 185 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*3647T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 3647 | chr11 | 130874775 | |||||
| chr11:130874872
|
T | G | 65 | a0001c0001t0001a0001c0001t0006a0001c0001t0014others(62): Show | 185 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*3550A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 3550 | chr11 | 130874872 | |||||
| chr11:130875082
|
G | A | 64 | a0001c0001t0001a0001c0001t0006a0001c0001t0014others(61): Show | 184 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*3340C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 3340 | chr11 | 130875082 | |||||
| chr11:130875150
|
T | C | 65 | a0001c0001t0001a0001c0001t0006a0001c0001t0014others(62): Show | 185 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*3272A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 3272 | chr11 | 130875150 | |||||
| chr11:130875175
|
C | T | 1 | a0001c0001t0093 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3247G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 3247 | chr11 | 130875175 | |||||
| chr11:130875464
|
G | A | 1 | a0001c0001t0078 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2958C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 2958 | chr11 | 130875464 | |||||
| chr11:130875696
|
A | G | 64 | a0001c0001t0001a0001c0001t0006a0001c0001t0014others(61): Show | 184 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*2726T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 2726 | chr11 | 130875696 | |||||
| chr11:130875783
|
T | G | 1 | a0001c0010t0107 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2639A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 2639 | chr11 | 130875783 | |||||
| chr11:130875824
|
C | T | 36 | a0001c0001t0001a0001c0001t0014a0001c0001t0017others(33): Show | 127 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*2598G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 2598 | chr11 | 130875824 | |||||
| chr11:130875845
|
A | C | 3 | a0001c0001t0080a0001c0001t0086a0001c0001t0087 | 3 | HG02895.hp1 NA19043.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2577T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 2577 | chr11 | 130875845 | |||||
| chr11:130876235
|
T | TCCAG | 64 | a0001c0001t0001a0001c0001t0006a0001c0001t0014others(61): Show | 184 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*2186_*2187insCTGG | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 2186 | chr11 | 130876235 | |||||
| chr11:130876251
|
T | C | 36 | a0001c0001t0001a0001c0001t0014a0001c0001t0017others(33): Show | 127 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*2171A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 2171 | chr11 | 130876251 | |||||
| chr11:130876262
|
A | G | 1 | a0004c0008t0048 | 2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2160T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 2160 | chr11 | 130876262 | |||||
| chr11:130876373
|
A | G | 2 | a0001c0014t0041a0018c0018t0085 | 3 | HG01099.hp1 HG02055.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2049T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 2049 | chr11 | 130876373 | |||||
| chr11:130876601
|
AAGGT | A | 103 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(100): Show | 317 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(314): Show |
3_prime_UTR_variant | MODIFIER | c.*1817_*1820delACCT | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 1817 | chr11 | 130876601 | |||||
| chr11:130876631
|
A | C | 2 | a0004c0008t0116a0004c0008t0117 | 2 | HG02280.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1791T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 1791 | chr11 | 130876631 | |||||
| chr11:130876759
|
A | G | 1 | a0003c0003t0071 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1663T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 1663 | chr11 | 130876759 | |||||
| chr11:130876842
|
C | T | 1 | a0001c0011t0053 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1580G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 1580 | chr11 | 130876842 | |||||
| chr11:130876865
|
C | T | 1 | a0002c0002t0024 | 3 | HG00735.hp1 HG00738.hp1 HG02735.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1557G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 1557 | chr11 | 130876865 | |||||
| chr11:130877005
|
T | C | 1 | a0001c0001t0028 | 3 | NA18948.hp1 NA18983.hp2 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1417A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 1417 | chr11 | 130877005 | |||||
| chr11:130877100
|
C | T | 12 | a0001c0011t0010a0001c0011t0053a0005c0004t0021others(9): Show | 23 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1322G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 1322 | chr11 | 130877100 | |||||
| chr11:130877107
|
T | C | 1 | a0001c0001t0047 | 2 | HG03491.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1315A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 1315 | chr11 | 130877107 | |||||
| chr11:130877147
|
G | A | 1 | a0004c0008t0048 | 2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1275C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 1275 | chr11 | 130877147 | |||||
| chr11:130877265
|
C | T | 3 | a0006c0006t0032a0006c0006t0060a0015c0016t0109 | 4 | HG02615.hp1 HG02647.hp1 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1157G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 1157 | chr11 | 130877265 | |||||
| chr11:130877336
|
C | G | 65 | a0001c0001t0001a0001c0001t0006a0001c0001t0014others(62): Show | 185 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*1086G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 1086 | chr11 | 130877336 | |||||
| chr11:130877364
|
A | G | 1 | a0007c0007t0059 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1058T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 1058 | chr11 | 130877364 | |||||
| chr11:130877423
|
A | G | 1 | a0001c0011t0053 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*999T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 999 | chr11 | 130877423 | |||||
| chr11:130877491
|
C | G | 65 | a0001c0001t0001a0001c0001t0006a0001c0001t0014others(62): Show | 185 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*931G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 931 | chr11 | 130877491 | |||||
| chr11:130877633
|
T | C | 1 | a0002c0002t0067 | 1 | NA19006.hp2 | 3_prime_UTR_variant | MODIFIER | c.*789A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 789 | chr11 | 130877633 | |||||
| chr11:130877918
|
G | A | 1 | a0004c0009t0009 | 7 | HG00741.hp2 HG01070.hp2 HG02451.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*504C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 504 | chr11 | 130877918 | |||||
| chr11:130878130
|
AG | A | 9 | a0001c0001t0011a0001c0001t0114a0004c0008t0048others(6): Show | 21 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*291delC | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 291 | chr11 | 130878130 | |||||
| chr11:130878180
|
C | G | 1 | a0001c0001t0080 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*242G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 242 | chr11 | 130878180 | |||||
| chr11:130878236
|
A | G | 68 | a0001c0001t0001a0001c0001t0006a0001c0001t0014others(65): Show | 191 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(188): Show |
3_prime_UTR_variant | MODIFIER | c.*186T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 186 | chr11 | 130878236 | |||||
| chr11:130878332
|
C | G | 5 | a0001c0001t0007a0001c0001t0037a0001c0001t0076others(2): Show | 24 | HG00642.hp2 HG00741.hp2 HG01070.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*90G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 11/11 | 90 | chr11 | 130878332 | |||||
| chr11:130915957
|
G | T | 9 | a0001c0001t0007a0001c0001t0014a0001c0001t0037others(6): Show | 26 | HG00423.hp1 HG00642.hp2 HG01074.hp2 others(23): Show |
5_prime_UTR_variant | MODIFIER | c.-18C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 18 | chr11 | 130915957 | |||||
| chr11:130916164
|
C | A | 2 | a0001c0001t0018a0001c0001t0115 | 5 | HG01496.hp2 HG02630.hp1 HG02970.hp2 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-225G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | chr11 | 130916164 | ||||||
| chr11:130916211
|
C | G | 1 | a0004c0008t0029 | 3 | HG02257.hp1 HG02559.hp2 HG02886.hp2 |
5_prime_UTR_variant | MODIFIER | c.-272G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 272 | chr11 | 130916211 | |||||
| chr11:130916333
|
C | T | 4 | a0004c0005t0020a0004c0005t0030a0004c0025t0051others(1): Show | 7 | HG01891.hp1 HG02258.hp2 HG02572.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-394G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 394 | chr11 | 130916333 | |||||
| chr11:130916391
|
C | T | 1 | a0001c0001t0075 | 1 | HG02615.hp2 | 5_prime_UTR_variant | MODIFIER | c.-452G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 452 | chr11 | 130916391 | |||||
| chr11:130916403
|
G | A | 6 | a0004c0008t0019a0004c0008t0029a0004c0008t0116others(3): Show | 17 | HG00741.hp2 HG01070.hp2 HG01884.hp2 others(14): Show |
5_prime_UTR_variant | MODIFIER | c.-464C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 464 | chr11 | 130916403 | |||||
| chr11:130916413
|
T | C | 8 | a0003c0003t0003a0003c0003t0036a0003c0003t0070others(5): Show | 35 | HG00423.hp2 HG00609.hp1 HG00733.hp1 others(32): Show |
5_prime_UTR_variant | MODIFIER | c.-474A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 474 | chr11 | 130916413 | |||||
| chr11:130916430
|
C | T | 1 | a0005c0004t0074 | 1 | HG03516.hp2 | 5_prime_UTR_variant | MODIFIER | c.-491G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 491 | chr11 | 130916430 | |||||
| chr11:130916441
|
G | C | 1 | a0005c0004t0049 | 2 | HG03139.hp2 HG03486.hp1 |
5_prime_UTR_variant | MODIFIER | c.-502C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 502 | chr11 | 130916441 | |||||
| chr11:130916450
|
C | A | 79 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(76): Show | 240 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(237): Show |
5_prime_UTR_variant | MODIFIER | c.-511G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/11 | 511 | chr11 | 130916450 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:130878565
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2847-11A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 10/10 | chr11 | 130878565 | ||||||
| chr11:130878630
|
C | A | 3 | a0001c0001t0006g0212a0001c0001t0006g0261a0001c0001t0006g0262 | 3 | HG03831.hp2 HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2847-76G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 10/10 | chr11 | 130878630 | ||||||
| chr11:130878816
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2847-262T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 10/10 | chr11 | 130878816 | ||||||
| chr11:130878931
|
T | C | 1 | a0004c0009t0009g0283 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2847-377A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 10/10 | chr11 | 130878931 | ||||||
| chr11:130879164
|
G | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(76): Show | 130 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.2846+460C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 10/10 | chr11 | 130879164 | ||||||
| chr11:130879222
|
A | G | 2 | a0005c0004t0049g0295a0005c0004t0049g0296 | 2 | HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2846+402T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 10/10 | chr11 | 130879222 | ||||||
| chr11:130879249
|
C | T | 3 | a0001c0014t0041g0236a0001c0014t0041g0237a0018c0018t0085g0175 | 3 | HG01099.hp1 HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2846+375G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 10/10 | chr11 | 130879249 | ||||||
| chr11:130879312
|
C | T | 1 | a0001c0001t0007g0162 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2846+312G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 10/10 | chr11 | 130879312 | ||||||
| chr11:130879361
|
C | A | 42 | a0001c0001t0006g0038a0001c0001t0006g0039a0001c0001t0006g0212others(39): Show | 51 | HG00323.hp2 HG00673.hp1 HG01243.hp1 others(48): Show |
intron_variant | MODIFIER | c.2846+263G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 10/10 | chr11 | 130879361 | ||||||
| chr11:130879452
|
T | C | 5 | a0004c0005t0020g0016a0004c0005t0020g0045a0004c0005t0030g0017others(2): Show | 7 | HG01891.hp1 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2846+172A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 10/10 | chr11 | 130879452 | ||||||
| chr11:130879456
|
TAG | T | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(188): Show | 261 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.2846+166_2846+167d others(4): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 10/10 | chr11 | 130879456 | ||||||
| chr11:130879579
|
G | T | 1 | a0001c0001t0104g0195 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2846+45C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 10/10 | chr11 | 130879579 | ||||||
| chr11:130879820
|
A | G | 237 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(234): Show | 327 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(324): Show |
intron_variant | MODIFIER | c.2759-109T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 9/10 | chr11 | 130879820 | ||||||
| chr11:130879951
|
A | G | 2 | a0005c0004t0021g0050a0005c0004t0039g0180 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2759-240T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 9/10 | chr11 | 130879951 | ||||||
| chr11:130880006
|
A | G | 3 | a0002c0002t0002g0081a0002c0002t0002g0083a0002c0002t0064g0082 | 3 | HG02015.hp1 HG02056.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.2759-295T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 9/10 | chr11 | 130880006 | ||||||
| chr11:130880253
|
G | A | 1 | a0001c0001t0014g0166 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2758+369C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 9/10 | chr11 | 130880253 | ||||||
| chr11:130880354
|
AC | A | 4 | a0001c0010t0016g0037a0001c0010t0016g0233a0001c0010t0102g0229others(1): Show | 5 | HG00280.hp2 HG01074.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.2758+267delG | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 9/10 | chr11 | 130880354 | ||||||
| chr11:130880505
|
T | G | 1 | a0004c0009t0009g0283 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2758+117A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 9/10 | chr11 | 130880505 | ||||||
| chr11:130880558
|
A | G | 4 | a0006c0006t0032g0054a0006c0006t0032g0055a0006c0006t0060g0053others(1): Show | 4 | HG02615.hp1 HG02647.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2758+64T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 9/10 | chr11 | 130880558 | ||||||
| chr11:130880597
|
T | C | 5 | a0004c0005t0020g0016a0004c0005t0020g0045a0004c0005t0030g0017others(2): Show | 7 | HG01891.hp1 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2758+25A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 9/10 | chr11 | 130880597 | ||||||
| chr11:130881007
|
G | C | 1 | a0001c0001t0093g0192 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2574-201C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130881007 | ||||||
| chr11:130881199
|
G | T | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(127): Show | 190 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.2574-393C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130881199 | ||||||
| chr11:130881335
|
C | G | 1 | a0001c0001t0045g0234 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2574-529G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130881335 | ||||||
| chr11:130881335
|
C | T | 2 | a0001c0001t0001g0213a0001c0001t0001g0223 | 2 | HG00735.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2574-529G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130881335 | ||||||
| chr11:130881366
|
A | C | 129 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(126): Show | 189 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.2574-560T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130881366 | ||||||
| chr11:130881372
|
C | T | 1 | a0018c0018t0085g0175 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2574-566G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130881372 | ||||||
| chr11:130881413
|
C | G | 129 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(126): Show | 189 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.2574-607G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130881413 | ||||||
| chr11:130881525
|
T | C | 4 | a0006c0006t0032g0054a0006c0006t0032g0055a0006c0006t0060g0053others(1): Show | 4 | HG02615.hp1 HG02647.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2574-719A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130881525 | ||||||
| chr11:130881535
|
G | C | 1 | a0002c0002t0005g0095 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2574-729C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130881535 | ||||||
| chr11:130881582
|
T | C | 32 | a0001c0001t0011g0035a0001c0001t0011g0194a0001c0001t0011g0220others(29): Show | 36 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.2574-776A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130881582 | ||||||
| chr11:130881874
|
T | G | 1 | a0003c0003t0003g0146 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2574-1068A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130881874 | ||||||
| chr11:130882145
|
A | C | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(123): Show | 186 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.2574-1339T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130882145 | ||||||
| chr11:130882594
|
C | T | 6 | a0004c0009t0009g0044a0004c0009t0009g0283a0004c0009t0009g0284others(3): Show | 7 | HG00741.hp2 HG01070.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2574-1788G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130882594 | ||||||
| chr11:130882657
|
A | T | 1 | a0003c0003t0071g0132 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2574-1851T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130882657 | ||||||
| chr11:130882672
|
A | G | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(235): Show | 328 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(325): Show |
intron_variant | MODIFIER | c.2574-1866T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130882672 | ||||||
| chr11:130882793
|
C | T | 1 | a0001c0011t0053g0058 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2574-1987G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130882793 | ||||||
| chr11:130882802
|
T | C | 4 | a0006c0006t0032g0054a0006c0006t0032g0055a0006c0006t0060g0053others(1): Show | 4 | HG02615.hp1 HG02647.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2574-1996A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130882802 | ||||||
| chr11:130882834
|
G | T | 2 | a0005c0004t0049g0295a0005c0004t0049g0296 | 2 | HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2574-2028C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130882834 | ||||||
| chr11:130883174
|
A | G | 40 | a0001c0001t0004g0186a0001c0001t0004g0225a0001c0001t0038g0153others(37): Show | 58 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.2574-2368T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130883174 | ||||||
| chr11:130883220
|
T | C | 32 | a0001c0001t0011g0035a0001c0001t0011g0194a0001c0001t0011g0220others(29): Show | 36 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.2574-2414A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130883220 | ||||||
| chr11:130883438
|
A | G | 1 | a0001c0001t0043g0254 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2574-2632T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130883438 | ||||||
| chr11:130883446
|
C | T | 2 | a0001c0011t0053g0058a0005c0017t0083g0173 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2574-2640G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130883446 | ||||||
| chr11:130883479
|
C | A | 3 | a0001c0001t0080g0241a0001c0001t0086g0187a0001c0001t0087g0185 | 3 | HG02895.hp1 NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2574-2673G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130883479 | ||||||
| chr11:130883608
|
G | A | 4 | a0006c0006t0032g0054a0006c0006t0032g0055a0006c0006t0060g0053others(1): Show | 4 | HG02615.hp1 HG02647.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2574-2802C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130883608 | ||||||
| chr11:130883672
|
C | T | 1 | a0002c0002t0002g0111 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2574-2866G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130883672 | ||||||
| chr11:130883799
|
G | A | 19 | a0001c0011t0010g0010a0001c0011t0010g0057a0001c0011t0053g0058others(16): Show | 23 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.2574-2993C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130883799 | ||||||
| chr11:130883823
|
A | G | 40 | a0001c0001t0004g0186a0001c0001t0004g0225a0001c0001t0038g0153others(37): Show | 58 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.2574-3017T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130883823 | ||||||
| chr11:130883950
|
T | C | 1 | a0010c0031t0118g0294 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2574-3144A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130883950 | ||||||
| chr11:130884017
|
T | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(96): Show | 152 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.2574-3211A>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884017 | ||||||
| chr11:130884191
|
T | C | 1 | a0005c0004t0082g0177 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2574-3385A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884191 | ||||||
| chr11:130884243
|
G | C | 6 | a0004c0009t0009g0044a0004c0009t0009g0283a0004c0009t0009g0284others(3): Show | 7 | HG00741.hp2 HG01070.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2574-3437C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884243 | ||||||
| chr11:130884351
|
A | G | 10 | a0001c0001t0092g0257a0007c0007t0013g0026a0007c0007t0013g0119others(7): Show | 14 | HG02040.hp2 NA18747.hp2 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.2574-3545T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884351 | ||||||
| chr11:130884352
|
T | C | 19 | a0001c0011t0010g0010a0001c0011t0010g0057a0001c0011t0053g0058others(16): Show | 23 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.2574-3546A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884352 | ||||||
| chr11:130884400
|
G | GAT | 4 | a0006c0006t0032g0054a0006c0006t0032g0055a0006c0006t0060g0053others(1): Show | 4 | HG02615.hp1 HG02647.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2574-3595_2574-359 others(6): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884400 | ||||||
| chr11:130884541
|
C | A | 2 | a0001c0001t0056g0056a0001c0001t0075g0148 | 2 | HG02055.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.2574-3735G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884541 | ||||||
| chr11:130884589
|
C | T | 1 | a0001c0001t0006g0251 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2574-3783G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884589 | ||||||
| chr11:130884590
|
G | A | 1 | a0002c0002t0002g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2574-3784C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884590 | ||||||
| chr11:130884607
|
C | G | 1 | a0001c0001t0080g0241 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2574-3801G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884607 | ||||||
| chr11:130884626
|
G | C | 64 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(61): Show | 74 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.2574-3820C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884626 | ||||||
| chr11:130884627
|
G | A | 18 | a0001c0001t0011g0035a0001c0001t0011g0194a0001c0001t0011g0220others(15): Show | 21 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.2574-3821C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884627 | ||||||
| chr11:130884696
|
G | A | 129 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(126): Show | 189 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.2574-3890C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884696 | ||||||
| chr11:130884713
|
A | G | 40 | a0001c0001t0004g0186a0001c0001t0004g0225a0001c0001t0038g0153others(37): Show | 58 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.2574-3907T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884713 | ||||||
| chr11:130884718
|
A | C | 1 | a0011c0030t0050g0047 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2574-3912T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884718 | ||||||
| chr11:130884763
|
C | T | 1 | a0003c0003t0003g0141 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2574-3957G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884763 | ||||||
| chr11:130884828
|
C | A | 1 | a0001c0001t0078g0160 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2574-4022G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884828 | ||||||
| chr11:130884828
|
C | T | 37 | a0001c0001t0004g0186a0001c0001t0004g0225a0001c0001t0038g0153others(34): Show | 55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.2574-4022G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884828 | ||||||
| chr11:130884871
|
C | CA | 36 | a0001c0001t0004g0186a0001c0001t0004g0225a0001c0001t0111g0252others(33): Show | 46 | HG00423.hp2 HG00438.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.2574-4066dupT | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884871 | ||||||
| chr11:130884871
|
CA | C | 42 | a0001c0001t0007g0151a0001c0001t0007g0152a0001c0001t0007g0161others(39): Show | 51 | HG00099.hp1 HG00642.hp2 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.2574-4066delT | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884871 | ||||||
| chr11:130884878
|
A | G | 1 | a0001c0001t0087g0185 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2574-4072T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884878 | ||||||
| chr11:130884890
|
A | AG | 27 | a0001c0001t0006g0038a0001c0001t0006g0039a0001c0001t0006g0212others(24): Show | 32 | HG00323.hp2 HG00673.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.2574-4085_2574-408 others(5): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884890 | ||||||
| chr11:130884890
|
A | G | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(100): Show | 158 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.2574-4084T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884890 | ||||||
| chr11:130884921
|
A | G | 1 | a0001c0001t0076g0149 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2574-4115T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884921 | ||||||
| chr11:130884955
|
G | T | 5 | a0001c0011t0010g0010a0001c0011t0010g0057a0005c0004t0027g0032others(2): Show | 9 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.2574-4149C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884955 | ||||||
| chr11:130884984
|
G | C | 2 | a0001c0001t0001g0218a0014c0022t0001g0264 | 2 | HG00099.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.2574-4178C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130884984 | ||||||
| chr11:130885149
|
G | C | 28 | a0001c0001t0011g0035a0001c0001t0011g0194a0001c0001t0011g0220others(25): Show | 31 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.2574-4343C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130885149 | ||||||
| chr11:130885345
|
G | A | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(127): Show | 190 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.2574-4539C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130885345 | ||||||
| chr11:130885353
|
G | C | 1 | a0015c0016t0109g0172 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2574-4547C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130885353 | ||||||
| chr11:130885488
|
A | C | 3 | a0007c0007t0033g0025a0007c0007t0059g0118a0007c0007t0066g0121 | 4 | HG02040.hp2 NA18964.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.2574-4682T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130885488 | ||||||
| chr11:130885530
|
A | C | 1 | a0018c0018t0085g0175 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2574-4724T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130885530 | ||||||
| chr11:130885543
|
G | A | 1 | a0001c0001t0087g0185 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2574-4737C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130885543 | ||||||
| chr11:130885680
|
A | G | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(124): Show | 185 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.2574-4874T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130885680 | ||||||
| chr11:130885769
|
C | CCTTAT | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 181 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.2574-4964_2574-496 others(9): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130885769 | ||||||
| chr11:130885805
|
A | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 181 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.2574-4999T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130885805 | ||||||
| chr11:130885844
|
G | A | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 181 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.2574-5038C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130885844 | ||||||
| chr11:130885889
|
G | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 181 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.2574-5083C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130885889 | ||||||
| chr11:130885918
|
T | C | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(100): Show | 157 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.2574-5112A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130885918 | ||||||
| chr11:130885933
|
C | T | 4 | a0005c0004t0040g0179a0005c0004t0040g0181a0005c0004t0074g0147others(1): Show | 4 | HG02922.hp1 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2574-5127G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130885933 | ||||||
| chr11:130885934
|
G | A | 22 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(19): Show | 24 | HG00642.hp2 HG00741.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.2574-5128C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130885934 | ||||||
| chr11:130886034
|
A | T | 1 | a0003c0003t0003g0133 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.2574-5228T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130886034 | ||||||
| chr11:130886057
|
T | C | 1 | a0001c0001t0014g0158 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2574-5251A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130886057 | ||||||
| chr11:130886095
|
C | T | 1 | a0018c0018t0085g0175 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2574-5289G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130886095 | ||||||
| chr11:130886103
|
C | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 181 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.2574-5297G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130886103 | ||||||
| chr11:130886127
|
A | G | 32 | a0001c0001t0011g0035a0001c0001t0011g0194a0001c0001t0011g0220others(29): Show | 36 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.2574-5321T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130886127 | ||||||
| chr11:130886181
|
C | T | 2 | a0001c0001t0006g0039a0001c0001t0091g0250 | 3 | HG01884.hp1 HG01978.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.2574-5375G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130886181 | ||||||
| chr11:130886281
|
T | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 181 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.2574-5475A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130886281 | ||||||
| chr11:130886295
|
T | C | 2 | a0001c0014t0041g0236a0001c0014t0041g0237 | 2 | HG01099.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2574-5489A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130886295 | ||||||
| chr11:130886356
|
C | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 181 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.2574-5550G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130886356 | ||||||
| chr11:130886358
|
C | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 181 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.2574-5552G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130886358 | ||||||
| chr11:130886394
|
G | C | 1 | a0003c0003t0003g0128 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2574-5588C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130886394 | ||||||
| chr11:130886548
|
G | T | 1 | a0001c0001t0001g0231 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2574-5742C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130886548 | ||||||
| chr11:130886559
|
T | C | 1 | a0001c0001t0042g0040 | 2 | HG00323.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.2574-5753A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130886559 | ||||||
| chr11:130886624
|
A | C | 1 | a0001c0001t0001g0231 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2574-5818T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130886624 | ||||||
| chr11:130886737
|
T | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(119): Show | 180 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.2574-5931A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130886737 | ||||||
| chr11:130886769
|
C | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(118): Show | 179 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.2574-5963G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130886769 | ||||||
| chr11:130886940
|
C | A | 28 | a0001c0001t0011g0035a0001c0001t0011g0194a0001c0001t0011g0220others(25): Show | 31 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.2574-6134G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130886940 | ||||||
| chr11:130887148
|
A | G | 51 | a0001c0001t0006g0038a0001c0001t0006g0039a0001c0001t0006g0212others(48): Show | 60 | HG00323.hp2 HG00673.hp1 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.2574-6342T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130887148 | ||||||
| chr11:130887166
|
T | G | 1 | a0005c0004t0084g0182 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2574-6360A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130887166 | ||||||
| chr11:130887266
|
G | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(118): Show | 179 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.2574-6460C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130887266 | ||||||
| chr11:130887277
|
C | CA | 4 | a0005c0004t0040g0179a0005c0004t0040g0181a0005c0004t0074g0147others(1): Show | 4 | HG02922.hp1 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2574-6472dupT | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130887277 | ||||||
| chr11:130887502
|
A | C | 21 | a0001c0011t0010g0010a0001c0011t0010g0057a0001c0011t0053g0058others(18): Show | 25 | HG01099.hp1 HG01243.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.2574-6696T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130887502 | ||||||
| chr11:130887562
|
C | T | 1 | a0002c0002t0002g0022 | 2 | NA18973.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.2574-6756G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130887562 | ||||||
| chr11:130887683
|
T | G | 1 | a0001c0001t0001g0231 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2574-6877A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130887683 | ||||||
| chr11:130887791
|
G | A | 1 | a0005c0004t0021g0051 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2574-6985C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130887791 | ||||||
| chr11:130887844
|
C | T | 1 | a0001c0001t0093g0192 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2574-7038G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130887844 | ||||||
| chr11:130887925
|
T | G | 1 | a0002c0002t0002g0109 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2574-7119A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130887925 | ||||||
| chr11:130887960
|
T | C | 3 | a0008c0012t0017g0036a0008c0012t0017g0214a0008c0012t0103g0202 | 4 | NA18612.hp2 NA18967.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.2574-7154A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130887960 | ||||||
| chr11:130888030
|
C | T | 1 | a0004c0025t0051g0046 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2574-7224G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130888030 | ||||||
| chr11:130888099
|
C | CA | 9 | a0002c0002t0002g0077a0002c0002t0002g0081a0002c0002t0002g0105others(6): Show | 9 | HG01168.hp1 HG01433.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.2574-7294dupT | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130888099 | ||||||
| chr11:130888099
|
CAA | C | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(116): Show | 177 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.2574-7295_2574-729 others(6): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130888099 | ||||||
| chr11:130888136
|
T | C | 1 | a0002c0002t0005g0020 | 2 | HG02083.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.2574-7330A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130888136 | ||||||
| chr11:130888185
|
G | A | 1 | a0003c0003t0003g0140 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2574-7379C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130888185 | ||||||
| chr11:130888218
|
G | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(118): Show | 179 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.2574-7412C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130888218 | ||||||
| chr11:130888257
|
G | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(113): Show | 170 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.2574-7451C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130888257 | ||||||
| chr11:130888258
|
A | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(113): Show | 170 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.2574-7452T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130888258 | ||||||
| chr11:130888271
|
C | T | 1 | a0003c0003t0003g0136 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2574-7465G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130888271 | ||||||
| chr11:130888415
|
C | T | 4 | a0006c0006t0032g0054a0006c0006t0032g0055a0006c0006t0060g0053others(1): Show | 4 | HG02615.hp1 HG02647.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2574-7609G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130888415 | ||||||
| chr11:130888510
|
A | G | 1 | a0002c0002t0005g0091 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2574-7704T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130888510 | ||||||
| chr11:130888554
|
C | T | 7 | a0003c0003t0004g0007a0003c0003t0004g0265a0003c0003t0004g0266others(4): Show | 13 | HG00558.hp2 HG02071.hp2 HG02129.hp2 others(10): Show |
intron_variant | MODIFIER | c.2574-7748G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130888554 | ||||||
| chr11:130888579
|
G | A | 1 | a0004c0005t0057g0099 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2574-7773C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130888579 | ||||||
| chr11:130888584
|
C | T | 1 | a0001c0001t0001g0231 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2574-7778G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130888584 | ||||||
| chr11:130888661
|
G | A | 117 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(114): Show | 171 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.2574-7855C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130888661 | ||||||
| chr11:130888867
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2574-8061G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130888867 | ||||||
| chr11:130889029
|
G | A | 125 | a0001c0001t0001g0203a0001c0001t0004g0225a0001c0001t0006g0038others(122): Show | 162 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(159): Show |
intron_variant | MODIFIER | c.2574-8223C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889029 | ||||||
| chr11:130889034
|
T | A | 2 | a0003c0003t0003g0126a0003c0003t0003g0127 | 2 | HG02723.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2574-8228A>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889034 | ||||||
| chr11:130889047
|
C | T | 1 | a0001c0001t0093g0192 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2574-8241G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889047 | ||||||
| chr11:130889094
|
C | T | 7 | a0001c0011t0053g0058a0001c0014t0041g0236a0001c0014t0041g0237others(4): Show | 7 | HG01099.hp1 HG02055.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2574-8288G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889094 | ||||||
| chr11:130889228
|
C | T | 7 | a0001c0001t0056g0056a0004c0008t0019g0290a0004c0008t0019g0291others(4): Show | 7 | HG01168.hp1 HG01884.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.2574-8422G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889228 | ||||||
| chr11:130889238
|
G | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0183others(52): Show | 87 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.2574-8432C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889238 | ||||||
| chr11:130889244
|
A | T | 295 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(292): Show | 413 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(410): Show |
intron_variant | MODIFIER | c.2574-8438T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889244 | ||||||
| chr11:130889269
|
C | T | 3 | a0001c0001t0007g0163a0001c0001t0046g0034a0007c0007t0034g0028 | 5 | NA18959.hp1 NA18970.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.2574-8463G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889269 | ||||||
| chr11:130889292
|
T | C | 1 | a0001c0001t0001g0213 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2574-8486A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889292 | ||||||
| chr11:130889305
|
CTT | C | 3 | a0006c0006t0008g0060a0006c0006t0008g0062a0006c0006t0008g0063 | 3 | HG00738.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2574-8501_2574-850 others(6): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889305 | ||||||
| chr11:130889310
|
T | C | 43 | a0001c0001t0007g0151a0001c0001t0007g0152a0001c0001t0011g0194others(40): Show | 50 | HG00642.hp2 HG00738.hp2 HG01243.hp1 others(47): Show |
intron_variant | MODIFIER | c.2574-8504A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889310 | ||||||
| chr11:130889328
|
G | T | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0033others(185): Show | 275 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(272): Show |
intron_variant | MODIFIER | c.2574-8522C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889328 | ||||||
| chr11:130889369
|
A | G | 3 | a0002c0002t0002g0014a0002c0002t0002g0107a0002c0002t0002g0109 | 5 | HG01943.hp2 HG01975.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.2574-8563T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889369 | ||||||
| chr11:130889409
|
C | A | 6 | a0007c0007t0013g0026a0007c0007t0013g0122a0007c0007t0026g0027others(3): Show | 10 | NA18747.hp2 NA18959.hp1 NA18960.hp2 others(7): Show |
intron_variant | MODIFIER | c.2574-8603G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889409 | ||||||
| chr11:130889490
|
C | T | 1 | a0002c0002t0002g0107 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2574-8684G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889490 | ||||||
| chr11:130889515
|
G | A | 38 | a0001c0001t0038g0154a0001c0010t0016g0232a0001c0010t0016g0233others(35): Show | 59 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.2574-8709C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889515 | ||||||
| chr11:130889526
|
A | T | 1 | a0001c0001t0087g0185 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2574-8720T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889526 | ||||||
| chr11:130889530
|
C | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(118): Show | 190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.2574-8724G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889530 | ||||||
| chr11:130889531
|
T | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(118): Show | 190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.2574-8725A>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889531 | ||||||
| chr11:130889532
|
T | TGCC | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(118): Show | 190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.2574-8727_2574-872 others(7): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889532 | ||||||
| chr11:130889600
|
T | C | 1 | a0002c0002t0062g0116 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2574-8794A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889600 | ||||||
| chr11:130889611
|
C | T | 3 | a0001c0001t0076g0149a0001c0001t0077g0155a0005c0004t0049g0295 | 3 | HG02818.hp1 HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2574-8805G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889611 | ||||||
| chr11:130889805
|
C | T | 1 | a0005c0004t0082g0177 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2574-8999G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889805 | ||||||
| chr11:130889819
|
T | C | 1 | a0009c0013t0112g0189 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2574-9013A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889819 | ||||||
| chr11:130889904
|
T | C | 1 | a0002c0002t0002g0109 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2574-9098A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130889904 | ||||||
| chr11:130890043
|
G | C | 2 | a0001c0011t0010g0010a0001c0011t0010g0057 | 5 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.2574-9237C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130890043 | ||||||
| chr11:130890092
|
A | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 228 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.2574-9286T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130890092 | ||||||
| chr11:130890099
|
T | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(154): Show | 234 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.2574-9293A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130890099 | ||||||
| chr11:130890100
|
G | A | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 233 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.2574-9294C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130890100 | ||||||
| chr11:130890185
|
T | C | 2 | a0001c0001t0080g0241a0001c0001t0086g0187 | 2 | HG02895.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2574-9379A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130890185 | ||||||
| chr11:130890205
|
C | T | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(155): Show | 235 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.2574-9399G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130890205 | ||||||
| chr11:130890297
|
A | C | 16 | a0006c0006t0008g0018a0006c0006t0008g0059a0006c0006t0008g0060others(13): Show | 17 | HG00738.hp2 HG01168.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.2574-9491T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130890297 | ||||||
| chr11:130890308
|
C | T | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(155): Show | 235 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.2574-9502G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130890308 | ||||||
| chr11:130890390
|
T | C | 1 | a0001c0001t0017g0235 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2574-9584A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130890390 | ||||||
| chr11:130890471
|
T | C | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(156): Show | 236 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.2574-9665A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130890471 | ||||||
| chr11:130890577
|
T | C | 10 | a0007c0007t0013g0026a0007c0007t0013g0119a0007c0007t0013g0122others(7): Show | 14 | HG02040.hp2 NA18747.hp2 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.2574-9771A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130890577 | ||||||
| chr11:130890599
|
A | T | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(156): Show | 236 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.2574-9793T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130890599 | ||||||
| chr11:130890667
|
T | C | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(156): Show | 236 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.2574-9861A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130890667 | ||||||
| chr11:130890698
|
G | T | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(154): Show | 234 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.2574-9892C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130890698 | ||||||
| chr11:130890699
|
C | T | 2 | a0003c0003t0004g0267a0003c0003t0004g0268 | 2 | NA19070.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.2574-9893G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130890699 | ||||||
| chr11:130890882
|
A | AT | 295 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(292): Show | 413 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(410): Show |
intron_variant | MODIFIER | c.2574-10077dupA | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130890882 | ||||||
| chr11:130890890
|
C | CT | 21 | a0001c0001t0001g0215a0002c0002t0002g0090a0002c0002t0005g0020others(18): Show | 23 | HG00438.hp1 HG00738.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.2574-10085dupA | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130890890 | ||||||
| chr11:130890890
|
C | CTT | 153 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(150): Show | 230 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.2574-10086_2574-10 others(8): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130890890 | ||||||
| chr11:130890979
|
G | A | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(156): Show | 236 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.2574-10173C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130890979 | ||||||
| chr11:130891048
|
A | G | 5 | a0004c0005t0020g0016a0004c0005t0020g0045a0004c0005t0030g0017others(2): Show | 7 | HG01891.hp1 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2574-10242T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130891048 | ||||||
| chr11:130891077
|
T | C | 36 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(33): Show | 39 | HG00423.hp1 HG00642.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.2574-10271A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130891077 | ||||||
| chr11:130891104
|
G | T | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(156): Show | 236 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.2574-10298C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130891104 | ||||||
| chr11:130891249
|
G | T | 4 | a0004c0008t0019g0290a0004c0008t0019g0291a0004c0008t0019g0292others(1): Show | 4 | HG01884.hp2 HG02970.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2574-10443C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130891249 | ||||||
| chr11:130891283
|
C | T | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 233 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.2574-10477G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130891283 | ||||||
| chr11:130891337
|
T | C | 2 | a0005c0004t0049g0295a0005c0004t0049g0296 | 2 | HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2574-10531A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130891337 | ||||||
| chr11:130891359
|
C | T | 21 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(18): Show | 22 | HG00423.hp1 HG00642.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.2574-10553G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130891359 | ||||||
| chr11:130891367
|
T | TG | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(156): Show | 236 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.2574-10562dupC | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130891367 | ||||||
| chr11:130891685
|
G | A | 1 | a0001c0001t0007g0170 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2574-10879C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130891685 | ||||||
| chr11:130891718
|
A | G | 2 | a0005c0004t0049g0295a0005c0004t0049g0296 | 2 | HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2574-10912T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130891718 | ||||||
| chr11:130891720
|
A | T | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(156): Show | 236 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.2574-10914T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130891720 | ||||||
| chr11:130891790
|
C | A | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 233 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.2574-10984G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130891790 | ||||||
| chr11:130891831
|
T | A | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(156): Show | 236 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.2574-11025A>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130891831 | ||||||
| chr11:130891846
|
C | CTT | 125 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(122): Show | 196 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.2574-11042_2574-11 others(8): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130891846 | ||||||
| chr11:130891846
|
C | CTTT | 33 | a0001c0001t0001g0218a0001c0001t0001g0243a0001c0001t0001g0253others(30): Show | 39 | HG00099.hp2 HG00323.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.2574-11043_2574-11 others(9): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130891846 | ||||||
| chr11:130891864
|
A | G | 1 | a0002c0002t0079g0171 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2574-11058T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130891864 | ||||||
| chr11:130891888
|
T | G | 1 | a0004c0008t0048g0042 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2574-11082A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130891888 | ||||||
| chr11:130891995
|
G | C | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(156): Show | 236 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.2574-11189C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130891995 | ||||||
| chr11:130892140
|
G | A | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(156): Show | 236 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.2573+11115C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130892140 | ||||||
| chr11:130892162
|
G | A | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(155): Show | 235 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.2573+11093C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130892162 | ||||||
| chr11:130892229
|
C | T | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(156): Show | 236 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.2573+11026G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130892229 | ||||||
| chr11:130892230
|
C | T | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(156): Show | 236 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.2573+11025G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130892230 | ||||||
| chr11:130892245
|
C | T | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(156): Show | 236 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.2573+11010G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130892245 | ||||||
| chr11:130892285
|
C | T | 1 | a0010c0031t0118g0294 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2573+10970G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130892285 | ||||||
| chr11:130892580
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2573+10675A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130892580 | ||||||
| chr11:130892603
|
T | C | 28 | a0001c0001t0001g0218a0001c0001t0001g0243a0001c0001t0001g0253others(25): Show | 34 | HG00099.hp2 HG00323.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.2573+10652A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130892603 | ||||||
| chr11:130892610
|
C | G | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(156): Show | 236 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.2573+10645G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130892610 | ||||||
| chr11:130892634
|
A | G | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(156): Show | 236 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.2573+10621T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130892634 | ||||||
| chr11:130892655
|
C | T | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(156): Show | 236 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.2573+10600G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130892655 | ||||||
| chr11:130892667
|
T | C | 1 | a0001c0001t0014g0159 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2573+10588A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130892667 | ||||||
| chr11:130892674
|
G | A | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(156): Show | 236 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.2573+10581C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130892674 | ||||||
| chr11:130892751
|
C | T | 16 | a0006c0006t0008g0018a0006c0006t0008g0059a0006c0006t0008g0060others(13): Show | 17 | HG00738.hp2 HG01168.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.2573+10504G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130892751 | ||||||
| chr11:130892860
|
T | A | 1 | a0002c0002t0002g0022 | 2 | NA18973.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.2573+10395A>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130892860 | ||||||
| chr11:130893025
|
G | C | 9 | a0005c0004t0021g0050a0005c0004t0021g0051a0005c0004t0021g0052others(6): Show | 9 | HG02572.hp2 HG02630.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2573+10230C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130893025 | ||||||
| chr11:130893066
|
T | C | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(156): Show | 236 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.2573+10189A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130893066 | ||||||
| chr11:130893075
|
G | A | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(156): Show | 236 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.2573+10180C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130893075 | ||||||
| chr11:130893121
|
C | G | 1 | a0004c0025t0051g0046 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2573+10134G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130893121 | ||||||
| chr11:130893218
|
C | T | 4 | a0005c0004t0027g0032a0005c0004t0027g0174a0005c0004t0081g0176others(1): Show | 5 | HG01891.hp2 HG02055.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2573+10037G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130893218 | ||||||
| chr11:130893257
|
G | C | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(156): Show | 236 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.2573+9998C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130893257 | ||||||
| chr11:130893445
|
A | C | 25 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(22): Show | 27 | HG00423.hp1 HG00642.hp2 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.2573+9810T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130893445 | ||||||
| chr11:130893559
|
A | C | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(157): Show | 237 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.2573+9696T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130893559 | ||||||
| chr11:130893595
|
G | A | 4 | a0005c0004t0027g0032a0005c0004t0027g0174a0005c0004t0081g0176others(1): Show | 5 | HG01891.hp2 HG02055.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2573+9660C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130893595 | ||||||
| chr11:130893618
|
G | A | 52 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(49): Show | 60 | HG00423.hp1 HG00642.hp2 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.2573+9637C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130893618 | ||||||
| chr11:130893689
|
G | A | 2 | a0005c0004t0049g0295a0005c0004t0049g0296 | 2 | HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2573+9566C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130893689 | ||||||
| chr11:130893692
|
TAATA | T | 3 | a0006c0006t0032g0054a0006c0006t0032g0055a0006c0006t0060g0053 | 3 | HG02615.hp1 HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2573+9559_2573+956 others(8): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130893692 | ||||||
| chr11:130893817
|
C | T | 1 | a0007c0007t0059g0118 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2573+9438G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130893817 | ||||||
| chr11:130893877
|
C | T | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(156): Show | 236 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.2573+9378G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130893877 | ||||||
| chr11:130894051
|
G | A | 17 | a0004c0008t0019g0290a0004c0008t0019g0291a0004c0008t0019g0292others(14): Show | 19 | HG00741.hp2 HG01070.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.2573+9204C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894051 | ||||||
| chr11:130894100
|
C | G | 59 | a0001c0001t0038g0153a0001c0001t0038g0154a0001c0011t0010g0010others(56): Show | 81 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.2573+9155G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894100 | ||||||
| chr11:130894114
|
CA | C | 42 | a0001c0001t0038g0153a0001c0001t0038g0154a0001c0011t0010g0010others(39): Show | 63 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.2573+9140delT | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894114 | ||||||
| chr11:130894122
|
A | G | 10 | a0007c0007t0013g0026a0007c0007t0013g0119a0007c0007t0013g0122others(7): Show | 14 | HG02040.hp2 NA18747.hp2 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.2573+9133T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894122 | ||||||
| chr11:130894197
|
G | T | 128 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(125): Show | 199 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.2573+9058C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894197 | ||||||
| chr11:130894503
|
A | C | 10 | a0007c0007t0013g0026a0007c0007t0013g0119a0007c0007t0013g0122others(7): Show | 14 | HG02040.hp2 NA18747.hp2 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.2573+8752T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894503 | ||||||
| chr11:130894514
|
T | C | 41 | a0001c0001t0038g0153a0001c0001t0038g0154a0001c0014t0041g0236others(38): Show | 59 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.2573+8741A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894514 | ||||||
| chr11:130894523
|
C | G | 31 | a0001c0001t0001g0218a0001c0001t0001g0243a0001c0001t0001g0253others(28): Show | 37 | HG00099.hp2 HG00323.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.2573+8732G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894523 | ||||||
| chr11:130894554
|
G | T | 59 | a0001c0001t0001g0218a0001c0001t0001g0243a0001c0001t0001g0253others(56): Show | 68 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.2573+8701C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894554 | ||||||
| chr11:130894581
|
ATTGT | A | 17 | a0005c0004t0021g0050a0005c0004t0021g0051a0005c0004t0021g0052others(14): Show | 18 | HG01891.hp2 HG02055.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.2573+8670_2573+867 others(8): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894581 | ||||||
| chr11:130894631
|
C | T | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(171): Show | 253 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.2573+8624G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894631 | ||||||
| chr11:130894635
|
G | A | 2 | a0005c0004t0049g0295a0005c0004t0049g0296 | 2 | HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2573+8620C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894635 | ||||||
| chr11:130894645
|
A | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(63): Show | 115 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.2573+8610T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894645 | ||||||
| chr11:130894670
|
C | T | 17 | a0005c0004t0021g0050a0005c0004t0021g0051a0005c0004t0021g0052others(14): Show | 18 | HG01891.hp2 HG02055.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.2573+8585G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894670 | ||||||
| chr11:130894852
|
C | T | 47 | a0001c0001t0007g0152a0001c0014t0041g0236a0001c0014t0041g0237others(44): Show | 54 | HG00642.hp2 HG00741.hp2 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.2573+8403G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894852 | ||||||
| chr11:130894944
|
C | T | 1 | a0001c0001t0006g0262 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2573+8311G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894944 | ||||||
| chr11:130894953
|
A | G | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(176): Show | 255 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.2573+8302T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894953 | ||||||
| chr11:130894962
|
G | A | 1 | a0001c0001t0075g0148 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2573+8293C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894962 | ||||||
| chr11:130894989
|
G | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 261 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.2573+8266C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894989 | ||||||
| chr11:130894990
|
C | T | 1 | a0001c0011t0053g0058 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2573+8265G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130894990 | ||||||
| chr11:130895008
|
T | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 261 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.2573+8247A>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895008 | ||||||
| chr11:130895136
|
G | A | 38 | a0001c0001t0038g0153a0001c0001t0038g0154a0003c0003t0003g0005others(35): Show | 56 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.2573+8119C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895136 | ||||||
| chr11:130895145
|
G | A | 2 | a0001c0014t0041g0236a0001c0014t0041g0237 | 2 | HG01099.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2573+8110C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895145 | ||||||
| chr11:130895183
|
T | C | 1 | a0002c0002t0002g0023 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2573+8072A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895183 | ||||||
| chr11:130895365
|
T | G | 3 | a0001c0011t0010g0010a0001c0011t0010g0057a0001c0011t0053g0058 | 6 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2573+7890A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895365 | ||||||
| chr11:130895482
|
T | C | 2 | a0006c0006t0008g0062a0006c0006t0008g0063 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2573+7773A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895482 | ||||||
| chr11:130895492
|
G | A | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(176): Show | 255 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.2573+7763C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895492 | ||||||
| chr11:130895503
|
C | T | 1 | a0002c0002t0024g0089 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2573+7752G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895503 | ||||||
| chr11:130895555
|
A | T | 2 | a0003c0003t0003g0126a0003c0003t0003g0127 | 2 | HG02723.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2573+7700T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895555 | ||||||
| chr11:130895567
|
G | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 261 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.2573+7688C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895567 | ||||||
| chr11:130895589
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 261 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.2573+7666A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895589 | ||||||
| chr11:130895590
|
G | A | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(176): Show | 255 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.2573+7665C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895590 | ||||||
| chr11:130895627
|
T | C | 4 | a0005c0004t0027g0032a0005c0004t0027g0174a0005c0004t0081g0176others(1): Show | 5 | HG01891.hp2 HG02055.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2573+7628A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895627 | ||||||
| chr11:130895734
|
T | C | 1 | a0001c0001t0087g0185 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2573+7521A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895734 | ||||||
| chr11:130895738
|
A | G | 1 | a0010c0031t0118g0294 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2573+7517T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895738 | ||||||
| chr11:130895742
|
T | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 261 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.2573+7513A>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895742 | ||||||
| chr11:130895780
|
A | T | 16 | a0006c0006t0008g0018a0006c0006t0008g0059a0006c0006t0008g0060others(13): Show | 17 | HG00738.hp2 HG01168.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.2573+7475T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895780 | ||||||
| chr11:130895790
|
T | C | 1 | a0002c0002t0005g0069 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2573+7465A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895790 | ||||||
| chr11:130895811
|
A | G | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(176): Show | 258 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.2573+7444T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895811 | ||||||
| chr11:130895828
|
C | G | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 261 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.2573+7427G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895828 | ||||||
| chr11:130895833
|
A | T | 3 | a0002c0002t0012g0019a0002c0002t0012g0073a0002c0002t0012g0074 | 4 | HG00099.hp1 HG01106.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.2573+7422T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895833 | ||||||
| chr11:130895834
|
T | C | 3 | a0002c0002t0012g0019a0002c0002t0012g0073a0002c0002t0012g0074 | 4 | HG00099.hp1 HG01106.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.2573+7421A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895834 | ||||||
| chr11:130895917
|
T | C | 1 | a0002c0002t0025g0104 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2573+7338A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895917 | ||||||
| chr11:130895929
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 261 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.2573+7326A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130895929 | ||||||
| chr11:130896023
|
C | T | 2 | a0002c0002t0002g0087a0002c0002t0002g0088 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2573+7232G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896023 | ||||||
| chr11:130896074
|
A | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 261 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.2573+7181T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896074 | ||||||
| chr11:130896110
|
G | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 261 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.2573+7145C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896110 | ||||||
| chr11:130896149
|
G | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 261 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.2573+7106C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896149 | ||||||
| chr11:130896171
|
C | T | 1 | a0001c0001t0087g0185 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2573+7084G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896171 | ||||||
| chr11:130896205
|
G | C | 116 | a0001c0001t0001g0243a0001c0001t0001g0253a0001c0001t0006g0038others(113): Show | 146 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.2573+7050C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896205 | ||||||
| chr11:130896205
|
G | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(63): Show | 115 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.2573+7050C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896205 | ||||||
| chr11:130896237
|
A | G | 4 | a0002c0002t0002g0072a0002c0002t0002g0084a0004c0005t0031g0085others(1): Show | 4 | NA18966.hp2 NA18985.hp1 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.2573+7018T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896237 | ||||||
| chr11:130896240
|
T | G | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 261 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.2573+7015A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896240 | ||||||
| chr11:130896310
|
G | A | 4 | a0005c0004t0027g0032a0005c0004t0027g0174a0005c0004t0081g0176others(1): Show | 5 | HG01891.hp2 HG02055.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2573+6945C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896310 | ||||||
| chr11:130896330
|
T | C | 39 | a0001c0001t0038g0153a0001c0001t0038g0154a0003c0003t0003g0005others(36): Show | 57 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.2573+6925A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896330 | ||||||
| chr11:130896347
|
T | C | 17 | a0005c0004t0021g0050a0005c0004t0021g0051a0005c0004t0021g0052others(14): Show | 18 | HG01891.hp2 HG02055.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.2573+6908A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896347 | ||||||
| chr11:130896637
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 261 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.2573+6618A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896637 | ||||||
| chr11:130896643
|
C | T | 26 | a0001c0001t0001g0243a0001c0001t0001g0253a0001c0001t0006g0038others(23): Show | 32 | HG00323.hp2 HG00673.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.2573+6612G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896643 | ||||||
| chr11:130896650
|
T | A | 1 | a0015c0016t0109g0172 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2573+6605A>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896650 | ||||||
| chr11:130896674
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 261 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.2573+6581A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896674 | ||||||
| chr11:130896713
|
C | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 261 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.2573+6542G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896713 | ||||||
| chr11:130896821
|
A | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 261 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.2573+6434T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896821 | ||||||
| chr11:130896866
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 261 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.2573+6389A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896866 | ||||||
| chr11:130896937
|
A | ACT | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 261 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.2573+6317_2573+631 others(6): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896937 | ||||||
| chr11:130896945
|
C | T | 10 | a0007c0007t0013g0026a0007c0007t0013g0119a0007c0007t0013g0122others(7): Show | 14 | HG02040.hp2 NA18747.hp2 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.2573+6310G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896945 | ||||||
| chr11:130896946
|
G | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 261 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.2573+6309C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896946 | ||||||
| chr11:130896968
|
A | C | 1 | a0001c0001t0001g0239 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2573+6287T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896968 | ||||||
| chr11:130896991
|
T | C | 1 | a0001c0001t0014g0166 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2573+6264A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130896991 | ||||||
| chr11:130897038
|
G | A | 3 | a0001c0011t0010g0010a0001c0011t0010g0057a0001c0011t0053g0058 | 6 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2573+6217C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130897038 | ||||||
| chr11:130897050
|
A | C | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(178): Show | 260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.2573+6205T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130897050 | ||||||
| chr11:130897050
|
A | T | 1 | a0003c0003t0003g0141 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2573+6205T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130897050 | ||||||
| chr11:130897083
|
C | G | 4 | a0005c0004t0027g0032a0005c0004t0027g0174a0005c0004t0081g0176others(1): Show | 5 | HG01891.hp2 HG02055.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2573+6172G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130897083 | ||||||
| chr11:130897163
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 261 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.2573+6092A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130897163 | ||||||
| chr11:130897187
|
T | C | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(178): Show | 260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.2573+6068A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130897187 | ||||||
| chr11:130897192
|
G | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 261 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.2573+6063C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130897192 | ||||||
| chr11:130897244
|
C | T | 3 | a0001c0001t0080g0241a0001c0001t0086g0187a0001c0001t0087g0185 | 3 | HG02895.hp1 NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2573+6011G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130897244 | ||||||
| chr11:130897303
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 261 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.2573+5952A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130897303 | ||||||
| chr11:130897352
|
A | G | 4 | a0005c0004t0027g0032a0005c0004t0027g0174a0005c0004t0081g0176others(1): Show | 5 | HG01891.hp2 HG02055.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2573+5903T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130897352 | ||||||
| chr11:130897363
|
G | A | 17 | a0005c0004t0021g0050a0005c0004t0021g0051a0005c0004t0021g0052others(14): Show | 18 | HG01891.hp2 HG02055.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.2573+5892C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130897363 | ||||||
| chr11:130897373
|
T | TAC | 3 | a0001c0001t0080g0241a0001c0001t0086g0187a0001c0001t0087g0185 | 3 | HG02895.hp1 NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2573+5880_2573+588 others(6): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130897373 | ||||||
| chr11:130897411
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 261 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.2573+5844A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130897411 | ||||||
| chr11:130897506
|
C | T | 10 | a0007c0007t0013g0026a0007c0007t0013g0119a0007c0007t0013g0122others(7): Show | 14 | HG02040.hp2 NA18747.hp2 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.2573+5749G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130897506 | ||||||
| chr11:130897560
|
C | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 261 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.2573+5695G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130897560 | ||||||
| chr11:130897591
|
G | T | 39 | a0001c0001t0038g0153a0001c0001t0038g0154a0003c0003t0003g0005others(36): Show | 57 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.2573+5664C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130897591 | ||||||
| chr11:130897593
|
C | T | 2 | a0001c0001t0090g0249a0009c0013t0110g0248 | 2 | NA19009.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.2573+5662G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130897593 | ||||||
| chr11:130897840
|
T | G | 6 | a0004c0009t0009g0044a0004c0009t0009g0283a0004c0009t0009g0284others(3): Show | 7 | HG00741.hp2 HG01070.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2573+5415A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130897840 | ||||||
| chr11:130897857
|
G | C | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(176): Show | 258 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.2573+5398C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130897857 | ||||||
| chr11:130898152
|
G | GT | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(176): Show | 258 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.2573+5102dupA | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130898152 | ||||||
| chr11:130898369
|
C | T | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(178): Show | 260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.2573+4886G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130898369 | ||||||
| chr11:130898442
|
C | T | 1 | a0001c0001t0111g0252 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2573+4813G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130898442 | ||||||
| chr11:130898468
|
C | T | 1 | a0001c0001t0006g0038 | 2 | HG03654.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.2573+4787G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130898468 | ||||||
| chr11:130898530
|
T | G | 4 | a0001c0001t0018g0043a0001c0001t0018g0277a0001c0001t0018g0278others(1): Show | 5 | HG01496.hp2 HG02630.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2573+4725A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130898530 | ||||||
| chr11:130898673
|
A | C | 4 | a0005c0004t0040g0179a0005c0004t0040g0181a0005c0004t0074g0147others(1): Show | 4 | HG02922.hp1 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2573+4582T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130898673 | ||||||
| chr11:130898673
|
A | G | 13 | a0005c0004t0021g0050a0005c0004t0021g0051a0005c0004t0021g0052others(10): Show | 14 | HG01891.hp2 HG02055.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.2573+4582T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130898673 | ||||||
| chr11:130899138
|
T | C | 57 | a0001c0011t0010g0010a0001c0011t0010g0057a0001c0011t0053g0058others(54): Show | 79 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.2573+4117A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130899138 | ||||||
| chr11:130899294
|
T | C | 1 | a0001c0001t0028g0226 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2573+3961A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130899294 | ||||||
| chr11:130899343
|
T | C | 3 | a0002c0002t0002g0081a0002c0002t0002g0083a0002c0002t0064g0082 | 3 | HG02015.hp1 HG02056.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.2573+3912A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130899343 | ||||||
| chr11:130899479
|
A | G | 2 | a0005c0004t0027g0174a0005c0004t0081g0176 | 2 | HG02622.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2573+3776T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130899479 | ||||||
| chr11:130899506
|
C | T | 1 | a0016c0021t0006g0263 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2573+3749G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130899506 | ||||||
| chr11:130899710
|
C | T | 10 | a0007c0007t0013g0026a0007c0007t0013g0119a0007c0007t0013g0122others(7): Show | 14 | HG02040.hp2 NA18747.hp2 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.2573+3545G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130899710 | ||||||
| chr11:130899791
|
A | C | 17 | a0004c0008t0029g0282a0006c0006t0008g0018a0006c0006t0008g0059others(14): Show | 18 | HG00738.hp2 HG01168.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.2573+3464T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130899791 | ||||||
| chr11:130899843
|
T | C | 1 | a0003c0003t0004g0272 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2573+3412A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130899843 | ||||||
| chr11:130900056
|
G | C | 1 | a0015c0016t0109g0172 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2573+3199C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130900056 | ||||||
| chr11:130900088
|
C | T | 10 | a0007c0007t0013g0026a0007c0007t0013g0119a0007c0007t0013g0122others(7): Show | 14 | HG02040.hp2 NA18747.hp2 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.2573+3167G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130900088 | ||||||
| chr11:130900124
|
T | C | 1 | a0003c0003t0003g0129 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2573+3131A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130900124 | ||||||
| chr11:130900185
|
T | G | 1 | a0001c0001t0001g0219 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2573+3070A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130900185 | ||||||
| chr11:130900247
|
G | A | 1 | a0001c0001t0011g0220 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2573+3008C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130900247 | ||||||
| chr11:130900284
|
C | T | 1 | a0002c0002t0002g0111 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2573+2971G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130900284 | ||||||
| chr11:130900364
|
A | G | 1 | a0006c0006t0008g0059 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2573+2891T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130900364 | ||||||
| chr11:130900441
|
G | A | 1 | a0003c0003t0004g0272 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2573+2814C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130900441 | ||||||
| chr11:130900461
|
C | T | 4 | a0002c0002t0002g0081a0002c0002t0002g0083a0002c0002t0064g0082others(1): Show | 4 | HG00609.hp1 HG02015.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.2573+2794G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130900461 | ||||||
| chr11:130900663
|
A | G | 2 | a0001c0014t0041g0236a0001c0014t0041g0237 | 2 | HG01099.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2573+2592T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130900663 | ||||||
| chr11:130900690
|
T | C | 4 | a0002c0002t0002g0105a0004c0005t0022g0106a0004c0005t0022g0110others(1): Show | 4 | HG01258.hp2 HG01433.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.2573+2565A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130900690 | ||||||
| chr11:130900828
|
A | G | 2 | a0001c0014t0041g0236a0001c0014t0041g0237 | 2 | HG01099.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2573+2427T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130900828 | ||||||
| chr11:130900872
|
G | A | 1 | a0001c0001t0014g0157 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2573+2383C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130900872 | ||||||
| chr11:130900873
|
A | G | 1 | a0001c0001t0014g0157 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2573+2382T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130900873 | ||||||
| chr11:130900916
|
C | A | 16 | a0006c0006t0008g0018a0006c0006t0008g0059a0006c0006t0008g0060others(13): Show | 17 | HG00738.hp2 HG01168.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.2573+2339G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130900916 | ||||||
| chr11:130901481
|
A | G | 1 | a0002c0002t0002g0080 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2573+1774T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130901481 | ||||||
| chr11:130901488
|
G | A | 3 | a0004c0005t0020g0016a0004c0005t0020g0045a0004c0025t0051g0046 | 4 | HG02258.hp2 HG02572.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2573+1767C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130901488 | ||||||
| chr11:130901519
|
T | G | 2 | a0003c0003t0003g0141a0003c0003t0003g0142 | 2 | HG01978.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.2573+1736A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130901519 | ||||||
| chr11:130901600
|
C | T | 26 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(23): Show | 28 | HG00423.hp1 HG00642.hp2 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.2573+1655G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130901600 | ||||||
| chr11:130901767
|
G | T | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(208): Show | 296 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.2573+1488C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130901767 | ||||||
| chr11:130901770
|
G | T | 1 | a0001c0001t0093g0192 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2573+1485C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130901770 | ||||||
| chr11:130901818
|
A | AG | 17 | a0005c0004t0021g0050a0005c0004t0021g0051a0005c0004t0021g0052others(14): Show | 18 | HG01891.hp2 HG02055.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.2573+1436dupC | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130901818 | ||||||
| chr11:130901856
|
T | C | 4 | a0005c0004t0021g0050a0005c0004t0021g0051a0005c0004t0021g0052others(1): Show | 4 | HG02572.hp2 HG02630.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2573+1399A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130901856 | ||||||
| chr11:130901873
|
T | C | 69 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(66): Show | 118 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.2573+1382A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130901873 | ||||||
| chr11:130901921
|
T | C | 3 | a0001c0001t0080g0241a0001c0001t0086g0187a0001c0001t0087g0185 | 3 | HG02895.hp1 NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2573+1334A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130901921 | ||||||
| chr11:130901942
|
A | C | 4 | a0005c0004t0040g0179a0005c0004t0040g0181a0005c0004t0074g0147others(1): Show | 4 | HG02922.hp1 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2573+1313T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130901942 | ||||||
| chr11:130902054
|
G | A | 1 | a0004c0009t0009g0287 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2573+1201C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130902054 | ||||||
| chr11:130902166
|
G | A | 1 | a0005c0004t0081g0176 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2573+1089C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130902166 | ||||||
| chr11:130902298
|
A | C | 4 | a0004c0008t0019g0290a0004c0008t0019g0291a0004c0008t0019g0292others(1): Show | 4 | HG01884.hp2 HG02970.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2573+957T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130902298 | ||||||
| chr11:130902391
|
C | T | 1 | a0001c0001t0001g0223 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2573+864G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130902391 | ||||||
| chr11:130902488
|
T | C | 1 | a0001c0001t0007g0152 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2573+767A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130902488 | ||||||
| chr11:130902521
|
G | A | 5 | a0004c0009t0009g0044a0004c0009t0009g0284a0004c0009t0009g0285others(2): Show | 6 | HG00741.hp2 HG01070.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2573+734C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130902521 | ||||||
| chr11:130902658
|
C | G | 11 | a0004c0008t0019g0290a0004c0008t0019g0291a0004c0008t0019g0292others(8): Show | 12 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.2573+597G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130902658 | ||||||
| chr11:130902896
|
A | G | 6 | a0002c0002t0002g0011a0002c0002t0002g0076a0002c0002t0002g0077others(3): Show | 9 | HG00597.hp1 HG04115.hp1 NA18961.hp1 others(6): Show |
intron_variant | MODIFIER | c.2573+359T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130902896 | ||||||
| chr11:130903012
|
A | G | 1 | a0015c0016t0109g0172 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2573+243T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130903012 | ||||||
| chr11:130903091
|
T | G | 2 | a0001c0001t0001g0221a0001c0001t0001g0222 | 2 | HG03710.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.2573+164A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130903091 | ||||||
| chr11:130903154
|
T | C | 2 | a0005c0004t0049g0295a0005c0004t0049g0296 | 2 | HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2573+101A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130903154 | ||||||
| chr11:130903164
|
C | T | 27 | a0005c0004t0021g0050a0005c0004t0021g0051a0005c0004t0021g0052others(24): Show | 32 | HG01891.hp2 HG02040.hp2 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.2573+91G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130903164 | ||||||
| chr11:130903172
|
G | T | 2 | a0005c0004t0049g0295a0005c0004t0049g0296 | 2 | HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2573+83C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130903172 | ||||||
| chr11:130903181
|
G | A | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(142): Show | 206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.2573+74C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130903181 | ||||||
| chr11:130903205
|
C | T | 2 | a0001c0001t0038g0153a0001c0001t0038g0154 | 2 | HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2573+50G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 8/10 | chr11 | 130903205 | ||||||
| chr11:130903501
|
T | C | 4 | a0005c0004t0021g0050a0005c0004t0021g0051a0005c0004t0021g0052others(1): Show | 4 | HG02572.hp2 HG02630.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2444-117A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903501 | ||||||
| chr11:130903593
|
T | C | 2 | a0001c0014t0041g0236a0001c0014t0041g0237 | 2 | HG01099.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2444-209A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903593 | ||||||
| chr11:130903643
|
A | G | 1 | a0001c0001t0017g0235 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2444-259T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903643 | ||||||
| chr11:130903696
|
CAT | C | 4 | a0002c0002t0002g0024a0002c0002t0002g0075a0004c0025t0051g0046others(1): Show | 5 | HG02258.hp2 HG02280.hp2 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.2444-314_2444-313d others(4): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903696 | ||||||
| chr11:130903710
|
T | C | 2 | a0004c0005t0020g0016a0004c0005t0020g0045 | 3 | HG02572.hp1 HG02622.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2444-326A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903710 | ||||||
| chr11:130903712
|
C | T | 1 | a0001c0001t0006g0247 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2444-328G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903712 | ||||||
| chr11:130903714
|
C | T | 2 | a0004c0005t0020g0016a0004c0005t0020g0045 | 3 | HG02572.hp1 HG02622.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2444-330G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903714 | ||||||
| chr11:130903716
|
T | C | 5 | a0001c0001t0006g0247a0001c0014t0041g0236a0001c0014t0041g0237others(2): Show | 6 | HG01099.hp1 HG02572.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2444-332A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903716 | ||||||
| chr11:130903716
|
T | TAC | 23 | a0001c0001t0043g0258a0001c0001t0092g0257a0002c0002t0002g0014others(20): Show | 26 | HG01167.hp1 HG01261.hp1 HG01517.hp2 others(23): Show |
intron_variant | MODIFIER | c.2444-334_2444-333d others(4): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903716 | ||||||
| chr11:130903716
|
T | TACAC | 41 | a0001c0011t0010g0010a0001c0011t0010g0057a0002c0002t0002g0111others(38): Show | 66 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.2444-336_2444-333d others(6): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903716 | ||||||
| chr11:130903716
|
T | TACACAC | 8 | a0003c0003t0004g0266a0003c0003t0004g0273a0003c0003t0036g0143others(5): Show | 8 | HG02074.hp1 HG02129.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2444-338_2444-333d others(8): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903716 | ||||||
| chr11:130903716
|
T | TACACACA others(1): Show |
3 | a0003c0003t0004g0274a0003c0003t0036g0131a0004c0009t0009g0283 | 3 | HG01123.hp2 HG02451.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.2444-340_2444-333d others(10): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903716 | ||||||
| chr11:130903716
|
T | TACACACA others(3): Show |
1 | a0004c0009t0009g0286 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2444-342_2444-333d others(12): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903716 | ||||||
| chr11:130903716
|
T | TACACACA others(7): Show |
1 | a0004c0009t0009g0044 | 2 | HG00741.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.2444-346_2444-333d others(16): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903716 | ||||||
| chr11:130903716
|
T | TACACACA others(9): Show |
1 | a0004c0009t0009g0287 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2444-348_2444-333d others(18): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903716 | ||||||
| chr11:130903716
|
TAC | T | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(99): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.2444-334_2444-333d others(4): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903716 | ||||||
| chr11:130903716
|
TACAC | T | 8 | a0001c0001t0001g0227a0001c0001t0037g0031a0001c0001t0044g0242others(5): Show | 9 | HG01074.hp1 HG01081.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.2444-336_2444-333d others(6): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903716 | ||||||
| chr11:130903716
|
TACACAC | T | 8 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(5): Show | 9 | HG00544.hp1 HG00642.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2444-338_2444-333d others(8): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903716 | ||||||
| chr11:130903716
|
TACACACA others(3): Show |
T | 1 | a0001c0001t0028g0190 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2444-342_2444-333d others(12): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903716 | ||||||
| chr11:130903718
|
C | T | 3 | a0001c0001t0006g0247a0001c0014t0041g0236a0001c0014t0041g0237 | 3 | HG01099.hp1 HG03098.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.2444-334G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903718 | ||||||
| chr11:130903747
|
A | G | 1 | a0001c0001t0056g0056 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2444-363T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903747 | ||||||
| chr11:130903764
|
CTACT | C | 3 | a0001c0011t0010g0010a0001c0011t0010g0057a0001c0011t0053g0058 | 6 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2444-384_2444-381d others(6): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903764 | ||||||
| chr11:130903925
|
AAGTGGGG others(4): Show |
A | 10 | a0005c0004t0021g0050a0005c0004t0021g0051a0005c0004t0021g0052others(7): Show | 10 | HG02572.hp2 HG02630.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.2444-552_2444-542d others(13): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130903925 | ||||||
| chr11:130904079
|
G | A | 1 | a0001c0001t0076g0149 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2444-695C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130904079 | ||||||
| chr11:130904182
|
G | A | 3 | a0001c0011t0010g0010a0001c0011t0010g0057a0001c0011t0053g0058 | 6 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2444-798C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130904182 | ||||||
| chr11:130904381
|
C | T | 1 | a0004c0009t0009g0283 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2444-997G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130904381 | ||||||
| chr11:130904439
|
A | T | 1 | a0003c0003t0004g0265 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2444-1055T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130904439 | ||||||
| chr11:130904536
|
G | A | 17 | a0005c0004t0021g0050a0005c0004t0021g0051a0005c0004t0021g0052others(14): Show | 18 | HG01891.hp2 HG02055.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.2444-1152C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130904536 | ||||||
| chr11:130904595
|
C | T | 1 | a0009c0013t0112g0189 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2444-1211G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130904595 | ||||||
| chr11:130904642
|
T | C | 1 | a0001c0014t0041g0237 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2444-1258A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130904642 | ||||||
| chr11:130904642
|
TAAG | T | 38 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(35): Show | 56 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2444-1261_2444-125 others(7): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130904642 | ||||||
| chr11:130904689
|
G | C | 17 | a0005c0004t0021g0050a0005c0004t0021g0051a0005c0004t0021g0052others(14): Show | 18 | HG01891.hp2 HG02055.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.2443+1264C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130904689 | ||||||
| chr11:130904694
|
A | AT | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(137): Show | 201 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.2443+1258dupA | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130904694 | ||||||
| chr11:130904694
|
A | ATT | 41 | a0001c0001t0006g0246a0001c0001t0014g0157a0001c0001t0014g0158others(38): Show | 59 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.2443+1257_2443+125 others(6): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130904694 | ||||||
| chr11:130904704
|
G | T | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(182): Show | 264 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.2443+1249C>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130904704 | ||||||
| chr11:130904798
|
G | A | 14 | a0005c0004t0021g0050a0005c0004t0021g0051a0005c0004t0021g0052others(11): Show | 15 | HG01891.hp2 HG02055.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.2443+1155C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130904798 | ||||||
| chr11:130904809
|
A | T | 1 | a0001c0001t0001g0188 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2443+1144T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130904809 | ||||||
| chr11:130905028
|
G | C | 1 | a0015c0016t0109g0172 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2443+925C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130905028 | ||||||
| chr11:130905045
|
C | T | 1 | a0005c0017t0083g0173 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2443+908G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130905045 | ||||||
| chr11:130905105
|
G | A | 1 | a0001c0001t0001g0238 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.2443+848C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130905105 | ||||||
| chr11:130905207
|
C | CCTGGAAG others(11): Show |
1 | a0001c0001t0006g0246 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2443+728_2443+745d others(20): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130905207 | ||||||
| chr11:130905360
|
CA | C | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(182): Show | 264 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.2443+592delT | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130905360 | ||||||
| chr11:130905453
|
CAT | C | 10 | a0007c0007t0013g0026a0007c0007t0013g0119a0007c0007t0013g0122others(7): Show | 14 | HG02040.hp2 NA18747.hp2 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.2443+498_2443+499d others(4): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130905453 | ||||||
| chr11:130905561
|
C | G | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(182): Show | 264 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.2443+392G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130905561 | ||||||
| chr11:130905584
|
A | G | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(182): Show | 264 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.2443+369T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130905584 | ||||||
| chr11:130905601
|
C | T | 26 | a0001c0001t0001g0243a0001c0001t0001g0253a0001c0001t0006g0038others(23): Show | 32 | HG00323.hp2 HG00673.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.2443+352G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130905601 | ||||||
| chr11:130905671
|
A | T | 1 | a0001c0001t0001g0033 | 2 | HG01109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2443+282T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130905671 | ||||||
| chr11:130905690
|
T | A | 1 | a0004c0025t0051g0046 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2443+263A>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130905690 | ||||||
| chr11:130905793
|
C | T | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(182): Show | 264 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.2443+160G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130905793 | ||||||
| chr11:130905808
|
C | T | 2 | a0001c0001t0080g0241a0001c0001t0086g0187 | 2 | HG02895.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2443+145G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130905808 | ||||||
| chr11:130905887
|
C | A | 1 | a0004c0025t0051g0046 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2443+66G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130905887 | ||||||
| chr11:130905887
|
C | T | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(225): Show | 314 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.2443+66G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | 130905887 | ||||||
| chr11:130906458
|
C | A | 17 | a0004c0008t0019g0290a0004c0008t0019g0291a0004c0008t0019g0292others(14): Show | 19 | HG00741.hp2 HG01070.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.2262+167G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 6/10 | chr11 | 130906458 | ||||||
| chr11:130906507
|
G | A | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(182): Show | 264 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.2262+118C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 6/10 | chr11 | 130906507 | ||||||
| chr11:130906525
|
C | T | 1 | a0001c0001t0076g0149 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2262+100G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 6/10 | chr11 | 130906525 | ||||||
| chr11:130906542
|
C | T | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(182): Show | 264 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.2262+83G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 6/10 | chr11 | 130906542 | ||||||
| chr11:130906548
|
A | G | 1 | a0001c0011t0053g0058 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2262+77T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 6/10 | chr11 | 130906548 | ||||||
| chr11:130906559
|
A | G | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(182): Show | 264 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.2262+66T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 6/10 | chr11 | 130906559 | ||||||
| chr11:130906751
|
T | A | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(225): Show | 314 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.2166-30A>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/10 | chr11 | 130906751 | ||||||
| chr11:130906795
|
C | T | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(182): Show | 264 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.2166-74G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/10 | chr11 | 130906795 | ||||||
| chr11:130906806
|
A | C | 4 | a0001c0001t0018g0043a0001c0001t0018g0277a0001c0001t0018g0278others(1): Show | 5 | HG01496.hp2 HG02630.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2166-85T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/10 | chr11 | 130906806 | ||||||
| chr11:130906806
|
A | T | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(178): Show | 259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.2166-85T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/10 | chr11 | 130906806 | ||||||
| chr11:130906957
|
A | C | 4 | a0005c0004t0040g0179a0005c0004t0040g0181a0005c0004t0074g0147others(1): Show | 4 | HG02922.hp1 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2166-236T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/10 | chr11 | 130906957 | ||||||
| chr11:130906970
|
T | C | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(182): Show | 264 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.2166-249A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/10 | chr11 | 130906970 | ||||||
| chr11:130907023
|
A | T | 1 | a0001c0001t0004g0186 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2166-302T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/10 | chr11 | 130907023 | ||||||
| chr11:130907144
|
T | A | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(182): Show | 264 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.2166-423A>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/10 | chr11 | 130907144 | ||||||
| chr11:130907283
|
G | A | 11 | a0004c0008t0019g0290a0004c0008t0019g0291a0004c0008t0019g0292others(8): Show | 12 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.2166-562C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/10 | chr11 | 130907283 | ||||||
| chr11:130907313
|
T | C | 1 | a0002c0002t0025g0112 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2166-592A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/10 | chr11 | 130907313 | ||||||
| chr11:130907329
|
G | GACAC | 36 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(33): Show | 54 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.2166-612_2166-609d others(6): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/10 | chr11 | 130907329 | ||||||
| chr11:130907341
|
T | C | 38 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(35): Show | 56 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2165+612A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/10 | chr11 | 130907341 | ||||||
| chr11:130907349
|
T | C | 38 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(35): Show | 56 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2165+604A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/10 | chr11 | 130907349 | ||||||
| chr11:130907536
|
T | C | 1 | a0001c0001t0001g0231 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2165+417A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/10 | chr11 | 130907536 | ||||||
| chr11:130907665
|
G | A | 3 | a0004c0008t0048g0042a0004c0008t0116g0288a0004c0008t0117g0289 | 4 | HG02280.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2165+288C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/10 | chr11 | 130907665 | ||||||
| chr11:130907694
|
T | C | 38 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(35): Show | 56 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2165+259A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/10 | chr11 | 130907694 | ||||||
| chr11:130907778
|
G | A | 27 | a0004c0008t0019g0290a0004c0008t0019g0291a0004c0008t0019g0292others(24): Show | 33 | HG00741.hp2 HG01070.hp2 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.2165+175C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/10 | chr11 | 130907778 | ||||||
| chr11:130907918
|
G | A | 38 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(35): Show | 56 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2165+35C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 5/10 | chr11 | 130907918 | ||||||
| chr11:130908432
|
C | T | 10 | a0007c0007t0013g0026a0007c0007t0013g0119a0007c0007t0013g0122others(7): Show | 14 | HG02040.hp2 NA18747.hp2 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.2035-349G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130908432 | ||||||
| chr11:130908502
|
A | G | 1 | a0001c0001t0006g0245 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2035-419T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130908502 | ||||||
| chr11:130908589
|
A | T | 1 | a0002c0002t0002g0072 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2035-506T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130908589 | ||||||
| chr11:130908615
|
A | G | 38 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(35): Show | 56 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2035-532T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130908615 | ||||||
| chr11:130908632
|
T | A | 2 | a0001c0001t0056g0056a0001c0001t0075g0148 | 2 | HG02055.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.2035-549A>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130908632 | ||||||
| chr11:130908709
|
AC | A | 38 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(35): Show | 56 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2035-627delG | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130908709 | ||||||
| chr11:130908983
|
C | A | 2 | a0001c0010t0016g0232a0001c0010t0016g0233 | 2 | HG01074.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.2035-900G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130908983 | ||||||
| chr11:130909001
|
G | A | 1 | a0001c0001t0045g0234 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2035-918C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130909001 | ||||||
| chr11:130909010
|
C | T | 38 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(35): Show | 56 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2035-927G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130909010 | ||||||
| chr11:130909095
|
T | C | 38 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(35): Show | 56 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2034+923A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130909095 | ||||||
| chr11:130909157
|
G | A | 38 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(35): Show | 56 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2034+861C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130909157 | ||||||
| chr11:130909173
|
G | C | 38 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(35): Show | 56 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2034+845C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130909173 | ||||||
| chr11:130909244
|
ACCCAGTT others(3): Show |
A | 4 | a0005c0004t0040g0179a0005c0004t0040g0181a0005c0004t0074g0147others(1): Show | 4 | HG02922.hp1 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2034+764_2034+773d others(12): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130909244 | ||||||
| chr11:130909262
|
T | C | 1 | a0001c0011t0053g0058 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2034+756A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130909262 | ||||||
| chr11:130909378
|
T | C | 38 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(35): Show | 56 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2034+640A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130909378 | ||||||
| chr11:130909515
|
C | A | 26 | a0001c0001t0001g0243a0001c0001t0001g0253a0001c0001t0006g0038others(23): Show | 32 | HG00323.hp2 HG00673.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.2034+503G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130909515 | ||||||
| chr11:130909584
|
C | T | 38 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(35): Show | 56 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2034+434G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130909584 | ||||||
| chr11:130909620
|
G | A | 1 | a0002c0002t0002g0113 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2034+398C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130909620 | ||||||
| chr11:130909726
|
C | T | 38 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(35): Show | 56 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2034+292G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130909726 | ||||||
| chr11:130909751
|
A | G | 38 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(35): Show | 56 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2034+267T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130909751 | ||||||
| chr11:130909773
|
T | C | 125 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(122): Show | 182 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.2034+245A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130909773 | ||||||
| chr11:130909779
|
C | T | 38 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(35): Show | 56 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2034+239G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130909779 | ||||||
| chr11:130909869
|
G | A | 1 | a0005c0004t0021g0052 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2034+149C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130909869 | ||||||
| chr11:130909892
|
T | G | 16 | a0006c0006t0008g0018a0006c0006t0008g0059a0006c0006t0008g0060others(13): Show | 17 | HG00738.hp2 HG01168.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.2034+126A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130909892 | ||||||
| chr11:130909908
|
C | T | 38 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(35): Show | 56 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2034+110G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130909908 | ||||||
| chr11:130910009
|
T | A | 12 | a0001c0001t0007g0161a0001c0001t0007g0162a0001c0001t0007g0163others(9): Show | 12 | HG00423.hp1 HG01934.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.2034+9A>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 4/10 | chr11 | 130910009 | ||||||
| chr11:130910373
|
TC | T | 14 | a0001c0001t0001g0183a0001c0001t0006g0244a0001c0001t0087g0185others(11): Show | 17 | HG02040.hp2 HG02738.hp1 HG03195.hp2 others(14): Show |
splice_region_variant&intron_variant | LOW | c.1814-4delG | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130910373 | ||||||
| chr11:130910374
|
C | CA | 7 | a0001c0001t0015g0260a0001c0001t0017g0235a0001c0001t0075g0148others(4): Show | 7 | HG01099.hp1 HG02523.hp2 HG02615.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.1814-5_1814-4insT | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130910374 | ||||||
| chr11:130910374
|
CCA | C | 3 | a0001c0011t0010g0010a0001c0011t0010g0057a0001c0011t0053g0058 | 6 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1814-6_1814-5delTG | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130910374 | ||||||
| chr11:130910374
|
CCAAAA | C | 37 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(34): Show | 55 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(52): Show |
splice_region_variant&intron_variant | LOW | c.1814-9_1814-5delTT others(3): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130910374 | ||||||
| chr11:130910375
|
C | A | 240 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(237): Show | 334 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(331): Show |
splice_region_variant&intron_variant | LOW | c.1814-5G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130910375 | ||||||
| chr11:130910517
|
G | A | 2 | a0001c0001t0056g0056a0001c0001t0075g0148 | 2 | HG02055.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1814-147C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130910517 | ||||||
| chr11:130910580
|
A | T | 37 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(34): Show | 55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1814-210T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130910580 | ||||||
| chr11:130910588
|
T | G | 37 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(34): Show | 55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1814-218A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130910588 | ||||||
| chr11:130910692
|
C | T | 37 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(34): Show | 55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1814-322G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130910692 | ||||||
| chr11:130910700
|
C | T | 38 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(35): Show | 57 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.1814-330G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130910700 | ||||||
| chr11:130910721
|
T | C | 37 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(34): Show | 55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1814-351A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130910721 | ||||||
| chr11:130910754
|
A | G | 37 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(34): Show | 55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1814-384T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130910754 | ||||||
| chr11:130910876
|
C | T | 37 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(34): Show | 55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1814-506G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130910876 | ||||||
| chr11:130910933
|
A | G | 37 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(34): Show | 55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1814-563T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130910933 | ||||||
| chr11:130910970
|
A | G | 37 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(34): Show | 55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1814-600T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130910970 | ||||||
| chr11:130911012
|
T | C | 1 | a0002c0002t0005g0115 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1813+621A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130911012 | ||||||
| chr11:130911075
|
A | G | 37 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(34): Show | 55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1813+558T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130911075 | ||||||
| chr11:130911079
|
T | C | 37 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(34): Show | 55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1813+554A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130911079 | ||||||
| chr11:130911126
|
C | T | 26 | a0001c0001t0001g0243a0001c0001t0001g0253a0001c0001t0006g0038others(23): Show | 32 | HG00323.hp2 HG00673.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.1813+507G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130911126 | ||||||
| chr11:130911194
|
C | CA | 12 | a0004c0008t0019g0292a0005c0004t0039g0180a0007c0007t0013g0026others(9): Show | 16 | HG02040.hp2 HG03486.hp2 NA18747.hp2 others(13): Show |
intron_variant | MODIFIER | c.1813+438dupT | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130911194 | ||||||
| chr11:130911194
|
C | CAAA | 32 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(29): Show | 50 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.1813+436_1813+438d others(5): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130911194 | ||||||
| chr11:130911210
|
AG | A | 3 | a0001c0001t0001g0183a0001c0001t0001g0184a0004c0009t0009g0283 | 3 | HG02451.hp1 NA18977.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1813+422delC | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130911210 | ||||||
| chr11:130911211
|
G | A | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(289): Show | 410 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(407): Show |
intron_variant | MODIFIER | c.1813+422C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130911211 | ||||||
| chr11:130911235
|
AT | A | 295 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(292): Show | 413 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(410): Show |
intron_variant | MODIFIER | c.1813+397delA | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130911235 | ||||||
| chr11:130911331
|
G | A | 1 | a0004c0008t0019g0292 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1813+302C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130911331 | ||||||
| chr11:130911371
|
A | G | 1 | a0006c0006t0060g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1813+262T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130911371 | ||||||
| chr11:130911462
|
T | C | 1 | a0002c0002t0062g0116 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1813+171A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130911462 | ||||||
| chr11:130911533
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1813+100G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130911533 | ||||||
| chr11:130911580
|
C | G | 37 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(34): Show | 55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1813+53G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130911580 | ||||||
| chr11:130911587
|
C | T | 2 | a0003c0003t0003g0126a0003c0003t0003g0127 | 2 | HG02723.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1813+46G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130911587 | ||||||
| chr11:130911611
|
A | T | 1 | a0002c0002t0005g0069 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1813+22T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 2/10 | chr11 | 130911611 | ||||||
| chr11:130911780
|
C | T | 37 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(34): Show | 55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1675-9G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130911780 | ||||||
| chr11:130911788
|
T | C | 1 | a0001c0001t0001g0238 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1675-17A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130911788 | ||||||
| chr11:130911790
|
G | C | 37 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(34): Show | 55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1675-19C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130911790 | ||||||
| chr11:130911799
|
A | C | 2 | a0004c0008t0116g0288a0004c0008t0117g0289 | 2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1675-28T>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130911799 | ||||||
| chr11:130911807
|
G | A | 1 | a0004c0008t0019g0293 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1675-36C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130911807 | ||||||
| chr11:130911872
|
C | A | 37 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(34): Show | 55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1675-101G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130911872 | ||||||
| chr11:130911908
|
T | G | 1 | a0001c0001t0007g0168 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1675-137A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130911908 | ||||||
| chr11:130912151
|
T | C | 2 | a0001c0001t0006g0261a0001c0001t0006g0262 | 2 | HG03831.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1675-380A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912151 | ||||||
| chr11:130912163
|
G | A | 37 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(34): Show | 55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1675-392C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912163 | ||||||
| chr11:130912169
|
A | G | 37 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(34): Show | 55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1675-398T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912169 | ||||||
| chr11:130912192
|
G | C | 37 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(34): Show | 55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1675-421C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912192 | ||||||
| chr11:130912206
|
A | T | 37 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(34): Show | 55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1675-435T>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912206 | ||||||
| chr11:130912237
|
A | G | 4 | a0004c0005t0020g0016a0004c0005t0020g0045a0004c0005t0030g0017others(1): Show | 6 | HG01891.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1675-466T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912237 | ||||||
| chr11:130912264
|
C | G | 37 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(34): Show | 55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1675-493G>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912264 | ||||||
| chr11:130912330
|
T | G | 1 | a0001c0001t0001g0239 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1675-559A>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912330 | ||||||
| chr11:130912369
|
G | A | 17 | a0004c0008t0019g0290a0004c0008t0019g0291a0004c0008t0019g0292others(14): Show | 19 | HG00741.hp2 HG01070.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1675-598C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912369 | ||||||
| chr11:130912422
|
C | T | 17 | a0005c0004t0021g0050a0005c0004t0021g0051a0005c0004t0021g0052others(14): Show | 18 | HG01891.hp2 HG02055.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.1675-651G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912422 | ||||||
| chr11:130912449
|
G | A | 37 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(34): Show | 55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1675-678C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912449 | ||||||
| chr11:130912454
|
T | C | 3 | a0001c0011t0010g0010a0001c0011t0010g0057a0001c0011t0053g0058 | 6 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1675-683A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912454 | ||||||
| chr11:130912460
|
G | A | 6 | a0004c0009t0009g0044a0004c0009t0009g0283a0004c0009t0009g0284others(3): Show | 7 | HG00741.hp2 HG01070.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1675-689C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912460 | ||||||
| chr11:130912532
|
T | C | 1 | a0001c0001t0007g0169 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1675-761A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912532 | ||||||
| chr11:130912553
|
C | T | 4 | a0001c0001t0018g0043a0001c0001t0018g0277a0001c0001t0018g0278others(1): Show | 5 | HG01496.hp2 HG02630.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1675-782G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912553 | ||||||
| chr11:130912674
|
A | G | 37 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(34): Show | 55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1675-903T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912674 | ||||||
| chr11:130912716
|
G | A | 1 | a0001c0001t0007g0170 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1675-945C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912716 | ||||||
| chr11:130912754
|
G | A | 13 | a0006c0006t0008g0018a0006c0006t0008g0059a0006c0006t0008g0060others(10): Show | 14 | HG00738.hp2 HG01168.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1675-983C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912754 | ||||||
| chr11:130912794
|
G | C | 1 | a0002c0002t0002g0117 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1675-1023C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912794 | ||||||
| chr11:130912862
|
T | C | 1 | a0004c0008t0048g0042 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1675-1091A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912862 | ||||||
| chr11:130912877
|
G | A | 5 | a0004c0009t0009g0044a0004c0009t0009g0284a0004c0009t0009g0285others(2): Show | 6 | HG00741.hp2 HG01070.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1675-1106C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130912877 | ||||||
| chr11:130913063
|
A | G | 27 | a0004c0008t0019g0290a0004c0008t0019g0291a0004c0008t0019g0292others(24): Show | 33 | HG00741.hp2 HG01070.hp2 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.1674+1203T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130913063 | ||||||
| chr11:130913364
|
T | C | 1 | a0001c0001t0080g0241 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1674+902A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130913364 | ||||||
| chr11:130913446
|
C | T | 2 | a0004c0005t0020g0016a0004c0005t0020g0045 | 3 | HG02572.hp1 HG02622.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1674+820G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130913446 | ||||||
| chr11:130913595
|
TGG | T | 37 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(34): Show | 55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1674+669_1674+670d others(4): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130913595 | ||||||
| chr11:130913648
|
C | A | 37 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(34): Show | 55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1674+618G>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130913648 | ||||||
| chr11:130913802
|
A | G | 37 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(34): Show | 55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1674+464T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130913802 | ||||||
| chr11:130913833
|
G | A | 37 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(34): Show | 55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1674+433C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130913833 | ||||||
| chr11:130913870
|
T | C | 37 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(34): Show | 55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1674+396A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130913870 | ||||||
| chr11:130913884
|
A | G | 26 | a0001c0001t0001g0243a0001c0001t0001g0253a0001c0001t0006g0038others(23): Show | 32 | HG00323.hp2 HG00673.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.1674+382T>C | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130913884 | ||||||
| chr11:130913891
|
T | C | 1 | a0001c0001t0044g0242 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1674+375A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130913891 | ||||||
| chr11:130913894
|
G | GAAATAT | 37 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(34): Show | 55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1674+371_1674+372i others(8): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130913894 | ||||||
| chr11:130913922
|
AC | A | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(224): Show | 313 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(310): Show |
intron_variant | MODIFIER | c.1674+343delG | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130913922 | ||||||
| chr11:130913980
|
C | T | 37 | a0003c0003t0003g0005a0003c0003t0003g0029a0003c0003t0003g0030others(34): Show | 55 | HG00423.hp2 HG00558.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1674+286G>A | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130913980 | ||||||
| chr11:130914009
|
G | A | 2 | a0005c0004t0040g0181a0005c0004t0084g0182 | 2 | HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1674+257C>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130914009 | ||||||
| chr11:130914112
|
TA | T | 26 | a0001c0001t0001g0243a0001c0001t0001g0253a0001c0001t0006g0038others(23): Show | 32 | HG00323.hp2 HG00673.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.1674+153delT | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130914112 | ||||||
| chr11:130914116
|
T | A | 26 | a0001c0001t0001g0243a0001c0001t0001g0253a0001c0001t0006g0038others(23): Show | 32 | HG00323.hp2 HG00673.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.1674+150A>T | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130914116 | ||||||
| chr11:130914127
|
G | C | 1 | a0003c0003t0003g0146 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1674+139C>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130914127 | ||||||
| chr11:130914172
|
T | C | 17 | a0004c0008t0019g0290a0004c0008t0019g0291a0004c0008t0019g0292others(14): Show | 19 | HG00741.hp2 HG01070.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1674+94A>G | SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 1/10 | chr11 | 130914172 |