Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 283464 |
|---|---|
| ensemblid | ENSG00000151233.11 |
| hgncid | 27482 |
| symbol | GXYLT1 |
| name | glucoside xylosyltransferase 1 |
| refseq_nuc | NM_173601.2 |
| refseq_prot | NP_775872.1 |
| ensembl_nuc | ENST00000398675.8 |
| ensembl_prot | ENSP00000381666.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 42081845 |
| end | 42144874 |
| strand | - |
| ver | v1.2 |
| region | chr12:42081845-42144874 |
| region5000 | chr12:42076845-42149874 |
| regionname0 | GXYLT1_chr12_42081845_42144874 |
| regionname5000 | GXYLT1_chr12_42076845_42149874 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 440 | 395 | 91 | 72 | 184 | 14 | 32 | 145 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0002 | 0/0 | 427 | 3 | 1 | 0 | 2 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1323 | 180 | 58 | 32 | 70 | 6 | 12 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| c0002 | 0/0 | 1323 | 127 | 16 | 22 | 71 | 4 | 14 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| c0003 | 0/0 | 1323 | 85 | 16 | 16 | 43 | 4 | 6 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| c0004 | 0/0 | 1284 | 3 | 1 | 0 | 2 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| c0005 | 0/0 | 1323 | 2 | 0 | 2 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| c0006 | 0/0 | 1323 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| 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 | 6171 | 71 | 14 | 14 | 39 | 3 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0002 | 1/1 | 6170 | 65 | 5 | 15 | 35 | 4 | 4 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0003 | 0/0 | 6171 | 55 | 5 | 9 | 35 | 1 | 5 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0004 | 0/0 | 6171 | 54 | 7 | 13 | 29 | 2 | 3 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0005 | 0/0 | 6171 | 20 | 1 | 3 | 15 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0006 | 0/0 | 6168 | 14 | 0 | 3 | 11 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0007 | 0/0 | 6182 | 12 | 9 | 2 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0008 | 0/0 | 6185 | 10 | 0 | 6 | 1 | 2 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0009 | 0/0 | 6171 | 8 | 8 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0010 | 0/0 | 6168 | 6 | 0 | 0 | 2 | 0 | 4 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0011 | 0/0 | 6171 | 6 | 6 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0012 | 0/0 | 6182 | 6 | 0 | 0 | 6 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0013 | 0/0 | 6170 | 5 | 0 | 0 | 0 | 0 | 5 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0014 | 0/0 | 6172 | 4 | 4 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0015 | 0/0 | 6171 | 4 | 0 | 1 | 0 | 1 | 2 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0016 | 0/0 | 6172 | 3 | 3 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0017 | 0/0 | 6170 | 3 | 3 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0018 | 0/0 | 6171 | 3 | 3 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0019 | 0/0 | 6171 | 2 | 0 | 0 | 0 | 0 | 2 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0020 | 0/0 | 6171 | 2 | 2 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0021 | 0/0 | 6170 | 2 | 2 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0022 | 0/0 | 6170 | 2 | 2 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0023 | 0/0 | 6171 | 2 | 2 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0024 | 0/0 | 6170 | 2 | 2 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0025 | 0/0 | 6171 | 2 | 0 | 0 | 2 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0026 | 0/0 | 6170 | 2 | 1 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0027 | 0/0 | 6170 | 2 | 2 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0028 | 0/0 | 6170 | 2 | 2 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0029 | 0/0 | 6171 | 2 | 0 | 0 | 2 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0030 | 0/0 | 6171 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0031 | 0/0 | 6171 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0032 | 0/0 | 6171 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0033 | 0/0 | 6171 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0034 | 0/0 | 6171 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0035 | 0/0 | 6171 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0036 | 0/0 | 6171 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0037 | 0/0 | 6171 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0038 | 0/0 | 6171 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0039 | 0/0 | 6171 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0040 | 0/0 | 6171 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0041 | 0/0 | 6170 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0042 | 0/0 | 6171 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0043 | 0/0 | 6171 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0044 | 0/0 | 6171 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0045 | 0/0 | 6170 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0046 | 0/0 | 6171 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0047 | 0/0 | 6171 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0048 | 0/0 | 6171 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0049 | 0/0 | 6171 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0050 | 0/0 | 6171 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0051 | 0/0 | 6182 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0052 | 0/0 | 6182 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0053 | 0/0 | 6182 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0054 | 0/0 | 6182 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0055 | 0/0 | 6182 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| t0056 | 0/0 | 6171 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| 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 | 5 | 1 | 1 | 3 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0008 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0325 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0335 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0363 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0364 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1323 | 180 | 58 | 32 | 70 | 6 | 12 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0002 | 0/0 | 1323 | 127 | 16 | 22 | 71 | 4 | 14 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0003 | 0/0 | 1323 | 85 | 16 | 16 | 43 | 4 | 6 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0005 | 0/0 | 1323 | 2 | 0 | 2 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0006 | 0/0 | 1323 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0002c0004 | 0/0 | 1284 | 3 | 1 | 0 | 2 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 1/1 | 7492 | 63 | 5 | 15 | 33 | 4 | 4 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0001t0005 | 0/0 | 7493 | 20 | 1 | 3 | 15 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0001t0006 | 0/0 | 7490 | 14 | 0 | 3 | 11 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0001t0007 | 0/0 | 7504 | 12 | 9 | 2 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0001t0008 | 0/0 | 7507 | 10 | 0 | 6 | 1 | 2 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0001t0009 | 0/0 | 7493 | 8 | 8 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0001t0010 | 0/0 | 7490 | 6 | 0 | 0 | 2 | 0 | 4 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0001t0011 | 0/0 | 7493 | 6 | 6 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0001t0012 | 0/0 | 7504 | 6 | 0 | 0 | 6 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0001t0014 | 0/0 | 7494 | 4 | 4 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0001t0016 | 0/0 | 7494 | 3 | 3 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0001t0017 | 0/0 | 7492 | 3 | 3 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0001t0018 | 0/0 | 7493 | 3 | 3 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0001t0021 | 0/0 | 7492 | 2 | 2 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0001t0022 | 0/0 | 7492 | 2 | 2 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0001t0024 | 0/0 | 7492 | 2 | 2 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0001t0026 | 0/0 | 7492 | 2 | 1 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0001t0027 | 0/0 | 7492 | 2 | 2 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0001t0028 | 0/0 | 7492 | 2 | 2 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0001t0037 | 0/0 | 7493 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0001t0038 | 0/0 | 7493 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0001t0041 | 0/0 | 7492 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0001t0043 | 0/0 | 7493 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0001t0044 | 0/0 | 7493 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0001t0045 | 0/0 | 7492 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0001t0052 | 0/0 | 7504 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0001t0053 | 0/0 | 7504 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0001t0054 | 0/0 | 7504 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0001t0055 | 0/0 | 7504 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0002t0003 | 0/0 | 7493 | 55 | 5 | 9 | 35 | 1 | 5 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0002t0004 | 0/0 | 7493 | 52 | 7 | 11 | 29 | 2 | 3 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0002t0015 | 0/0 | 7493 | 4 | 0 | 1 | 0 | 1 | 2 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0002t0019 | 0/0 | 7493 | 2 | 0 | 0 | 0 | 0 | 2 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0002t0020 | 0/0 | 7493 | 2 | 2 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0002t0025 | 0/0 | 7493 | 2 | 0 | 0 | 2 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0002t0030 | 0/0 | 7493 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0002t0031 | 0/0 | 7493 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0002t0032 | 0/0 | 7493 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0002t0033 | 0/0 | 7493 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0002t0034 | 0/0 | 7493 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0002t0046 | 0/0 | 7493 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0002t0047 | 0/0 | 7493 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0002t0048 | 0/0 | 7493 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0002t0049 | 0/0 | 7493 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0002t0050 | 0/0 | 7493 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0003t0001 | 0/0 | 7493 | 71 | 14 | 14 | 39 | 3 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0003t0013 | 0/0 | 7492 | 5 | 0 | 0 | 0 | 0 | 5 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0003t0023 | 0/0 | 7493 | 2 | 2 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0003t0029 | 0/0 | 7493 | 2 | 0 | 0 | 2 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0003t0035 | 0/0 | 7493 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0003t0036 | 0/0 | 7493 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0003t0039 | 0/0 | 7493 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0003t0040 | 0/0 | 7493 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0003t0042 | 0/0 | 7493 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0005t0004 | 0/0 | 7493 | 2 | 0 | 2 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0001c0006t0056 | 0/0 | 7493 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0002c0004t0002 | 0/0 | 7453 | 2 | 0 | 0 | 2 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| a0002c0004t0051 | 0/0 | 7465 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | copy fasta | chr12 | 42076845 | 42149874 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0001 | 0/0 | 5 | 1 | 1 | 3 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0325 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0335 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0005g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0005g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0005g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0005g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0005g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0005g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0005g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0005g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0005g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0005g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0005g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0005g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0005g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0005g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0005g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0005g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0005g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0005g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0006g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0006g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0006g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0006g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0006g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0006g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0006g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0006g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0006g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0006g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0006g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0007g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0007g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0007g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0007g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0007g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0007g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0007g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0007g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0007g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0007g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0007g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0008g0363 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0008g0364 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0008g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0008g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0008g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0008g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0008g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0008g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0008g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0008g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0009g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0009g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0009g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0009g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0009g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0009g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0010g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0010g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0010g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0010g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0010g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0010g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0011g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0011g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0011g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0011g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0011g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0011g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0012g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0012g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0012g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0012g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0012g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0012g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0014g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0014g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0014g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0014g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0016g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0016g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0016g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0017g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0017g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0017g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0018g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0018g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0018g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0021g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0021g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0022g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0022g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0024g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0024g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0026g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0026g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0027g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0027g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0028g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0028g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0037g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0038g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0041g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0043g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0044g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0045g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0052g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0053g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0054g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0001t0055g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0008 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0003g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0004g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0015g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0015g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0015g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0015g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0019g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0019g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0020g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0020g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0025g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0025g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0030g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0031g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0032g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0033g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0034g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0046g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0047g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0048g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0049g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0002t0050g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0013g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0013g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0013g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0013g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0013g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0023g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0023g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0029g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0029g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0035g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0036g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0039g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0040g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0003t0042g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0005t0004g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0001c0006t0056g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0002c0004t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| a0002c0004t0051g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0340 | EUR | GBR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG00099 | hp2 | a0001 | c0003 | t0001 | g0147 | EUR | GBR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG00140 | hp1 | a0001 | c0002 | t0015 | g0238 | EUR | GBR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0337 | EUR | GBR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG00323 | hp1 | a0001 | c0002 | t0004 | g0073 | EUR | FIN | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG00323 | hp2 | a0001 | c0003 | t0039 | g0252 | EUR | FIN | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | CHS | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG00408 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | CHS | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG00423 | hp1 | a0001 | c0001 | t0006 | g0246 | EAS | CHS | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | CHS | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG00438 | hp1 | a0001 | c0003 | t0001 | g0114 | EAS | CHS | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG00438 | hp2 | a0001 | c0002 | t0030 | g0017 | EAS | CHS | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG00544 | hp1 | a0001 | c0001 | t0005 | g0270 | EAS | CHS | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG00544 | hp2 | a0001 | c0003 | t0001 | g0144 | EAS | CHS | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG00597 | hp1 | a0001 | c0001 | t0005 | g0278 | EAS | CHS | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG00597 | hp2 | a0001 | c0003 | t0001 | g0124 | EAS | CHS | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG00609 | hp1 | a0001 | c0002 | t0003 | g0101 | EAS | CHS | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG00609 | hp2 | a0001 | c0003 | t0001 | g0125 | EAS | CHS | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG00621 | hp1 | a0001 | c0002 | t0003 | g0201 | EAS | CHS | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG00621 | hp2 | a0001 | c0002 | t0004 | g0043 | EAS | CHS | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG00639 | hp1 | a0001 | c0001 | t0007 | g0349 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG00639 | hp2 | a0001 | c0002 | t0003 | g0164 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG00642 | hp1 | a0001 | c0001 | t0008 | g0368 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG00642 | hp2 | a0001 | c0003 | t0001 | g0153 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG00733 | hp1 | a0001 | c0002 | t0004 | g0035 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG00733 | hp2 | a0001 | c0003 | t0001 | g0219 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG00738 | hp1 | a0001 | c0001 | t0007 | g0346 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG00738 | hp2 | a0001 | c0002 | t0003 | g0199 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01069 | hp1 | a0001 | c0001 | t0008 | g0370 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01069 | hp2 | a0001 | c0001 | t0006 | g0013 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0339 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01070 | hp2 | a0001 | c0002 | t0004 | g0036 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01071 | hp1 | a0001 | c0002 | t0004 | g0037 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01071 | hp2 | a0001 | c0001 | t0006 | g0011 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01074 | hp1 | a0001 | c0002 | t0003 | g0171 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01074 | hp2 | a0001 | c0003 | t0001 | g0130 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01081 | hp1 | a0001 | c0002 | t0004 | g0038 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01081 | hp2 | a0001 | c0001 | t0006 | g0245 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01099 | hp1 | a0001 | c0003 | t0001 | g0221 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01099 | hp2 | a0001 | c0002 | t0004 | g0072 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01106 | hp1 | a0001 | c0005 | t0004 | g0006 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01106 | hp2 | a0001 | c0003 | t0001 | g0253 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01168 | hp2 | a0001 | c0003 | t0001 | g0148 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01169 | hp1 | a0001 | c0001 | t0026 | g0323 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01175 | hp1 | a0001 | c0001 | t0008 | g0365 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01175 | hp2 | a0001 | c0002 | t0003 | g0091 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0294 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01192 | hp2 | a0001 | c0003 | t0001 | g0161 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0145 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01243 | hp2 | a0001 | c0002 | t0004 | g0040 | AMR | PUR | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0334 | AMR | CLM | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01255 | hp2 | a0001 | c0003 | t0035 | g0146 | AMR | CLM | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01256 | hp1 | a0001 | c0001 | t0008 | g0371 | AMR | CLM | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0310 | AMR | CLM | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01257 | hp1 | a0001 | c0002 | t0004 | g0055 | AMR | CLM | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0296 | AMR | CLM | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01258 | hp2 | a0001 | c0001 | t0008 | g0369 | AMR | CLM | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01346 | hp1 | a0001 | c0002 | t0015 | g0183 | AMR | CLM | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01346 | hp2 | a0001 | c0001 | t0008 | g0367 | AMR | CLM | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0326 | AMR | CLM | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01358 | hp2 | a0001 | c0003 | t0001 | g0112 | AMR | CLM | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0336 | AMR | CLM | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01433 | hp2 | a0001 | c0002 | t0047 | g0185 | AMR | CLM | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01496 | hp1 | a0001 | c0005 | t0004 | g0006 | AMR | CLM | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0292 | AMR | CLM | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01515 | hp1 | a0001 | c0001 | t0008 | g0364 | EUR | IBS | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01515 | hp2 | a0001 | c0003 | t0001 | g0222 | EUR | IBS | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01517 | hp1 | a0001 | c0001 | t0008 | g0363 | EUR | IBS | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0321 | EUR | IBS | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01884 | hp1 | a0001 | c0001 | t0014 | g0233 | AFR | ACB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01884 | hp2 | a0001 | c0002 | t0003 | g0087 | AFR | ACB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01891 | hp1 | a0001 | c0001 | t0011 | g0260 | AFR | ACB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01891 | hp2 | a0001 | c0001 | t0007 | g0348 | AFR | ACB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01928 | hp1 | a0001 | c0001 | t0045 | g0304 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01928 | hp2 | a0001 | c0003 | t0040 | g0111 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01934 | hp1 | a0001 | c0003 | t0001 | g0155 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01943 | hp1 | a0001 | c0003 | t0001 | g0128 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01943 | hp2 | a0001 | c0002 | t0003 | g0168 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01952 | hp1 | a0001 | c0003 | t0001 | g0106 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01975 | hp1 | a0001 | c0002 | t0004 | g0075 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01975 | hp2 | a0001 | c0001 | t0005 | g0274 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01978 | hp1 | a0001 | c0001 | t0005 | g0267 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01981 | hp1 | a0001 | c0002 | t0004 | g0039 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG01981 | hp2 | a0001 | c0002 | t0003 | g0173 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02004 | hp1 | a0001 | c0002 | t0003 | g0196 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02004 | hp2 | a0001 | c0003 | t0001 | g0107 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02015 | hp1 | a0001 | c0002 | t0003 | g0163 | EAS | KHV | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02015 | hp2 | a0002 | c0004 | t0002 | g0007 | EAS | KHV | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02040 | hp1 | a0001 | c0003 | t0001 | g0126 | EAS | KHV | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02040 | hp2 | a0001 | c0002 | t0003 | g0010 | EAS | KHV | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02055 | hp1 | a0001 | c0001 | t0009 | g0254 | AFR | ACB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02055 | hp2 | a0001 | c0002 | t0034 | g0025 | AFR | ACB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02071 | hp1 | a0001 | c0001 | t0006 | g0248 | EAS | KHV | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02071 | hp2 | a0001 | c0002 | t0025 | g0098 | EAS | KHV | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02080 | hp1 | a0001 | c0002 | t0048 | g0239 | EAS | KHV | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02080 | hp2 | a0001 | c0002 | t0004 | g0060 | EAS | KHV | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02083 | hp1 | a0001 | c0002 | t0004 | g0054 | EAS | KHV | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02083 | hp2 | a0001 | c0003 | t0001 | g0132 | EAS | KHV | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02129 | hp1 | a0001 | c0002 | t0003 | g0189 | EAS | KHV | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02129 | hp2 | a0001 | c0002 | t0004 | g0042 | EAS | KHV | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02132 | hp1 | a0001 | c0002 | t0003 | g0008 | EAS | KHV | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | KHV | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02135 | hp1 | a0001 | c0002 | t0004 | g0032 | EAS | KHV | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02135 | hp2 | a0001 | c0001 | t0008 | g0372 | EAS | KHV | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02148 | hp1 | a0001 | c0003 | t0001 | g0108 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02148 | hp2 | a0001 | c0002 | t0003 | g0174 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02155 | hp2 | a0001 | c0002 | t0003 | g0181 | EAS | CDX | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02165 | hp1 | a0001 | c0002 | t0003 | g0169 | EAS | CDX | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0320 | EAS | CDX | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02258 | hp1 | a0001 | c0001 | t0022 | g0240 | AFR | ACB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02258 | hp2 | a0001 | c0002 | t0004 | g0047 | AFR | ACB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02273 | hp1 | a0001 | c0002 | t0003 | g0175 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02273 | hp2 | a0001 | c0001 | t0005 | g0273 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02280 | hp1 | a0001 | c0001 | t0014 | g0229 | AFR | ACB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02280 | hp2 | a0001 | c0001 | t0055 | g0362 | AFR | ACB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0288 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02293 | hp2 | a0001 | c0002 | t0004 | g0076 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02300 | hp1 | a0001 | c0001 | t0038 | g0271 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02300 | hp2 | a0001 | c0002 | t0004 | g0082 | AMR | PEL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02451 | hp1 | a0001 | c0001 | t0017 | g0242 | AFR | ACB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02451 | hp2 | a0001 | c0003 | t0001 | g0216 | AFR | ACB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02523 | hp1 | a0001 | c0001 | t0005 | g0276 | EAS | KHV | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02523 | hp2 | a0001 | c0002 | t0003 | g0010 | EAS | KHV | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02572 | hp1 | a0001 | c0002 | t0003 | g0088 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02572 | hp2 | a0001 | c0003 | t0023 | g0206 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02615 | hp1 | a0001 | c0001 | t0009 | g0257 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02615 | hp2 | a0001 | c0002 | t0004 | g0045 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0212 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0213 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02630 | hp1 | a0001 | c0003 | t0001 | g0223 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02630 | hp2 | a0001 | c0001 | t0016 | g0084 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02647 | hp1 | a0001 | c0001 | t0017 | g0235 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02647 | hp2 | a0001 | c0001 | t0007 | g0347 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0307 | SAS | PJL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02683 | hp2 | a0001 | c0002 | t0003 | g0178 | SAS | PJL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02717 | hp1 | a0001 | c0001 | t0037 | g0096 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02717 | hp2 | a0001 | c0002 | t0020 | g0027 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02723 | hp1 | a0001 | c0001 | t0011 | g0261 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02723 | hp2 | a0001 | c0002 | t0004 | g0059 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02735 | hp1 | a0001 | c0002 | t0003 | g0166 | SAS | PJL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0308 | SAS | PJL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02738 | hp1 | a0001 | c0002 | t0049 | g0186 | SAS | PJL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02738 | hp2 | a0001 | c0001 | t0041 | g0333 | SAS | PJL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02809 | hp1 | a0001 | c0001 | t0014 | g0228 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02809 | hp2 | a0002 | c0004 | t0051 | g0342 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02818 | hp1 | a0001 | c0003 | t0001 | g0210 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02818 | hp2 | a0001 | c0001 | t0011 | g0095 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02886 | hp1 | a0001 | c0001 | t0028 | g0328 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02886 | hp2 | a0001 | c0002 | t0004 | g0049 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0324 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02896 | hp2 | a0001 | c0002 | t0004 | g0033 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0300 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02897 | hp2 | a0001 | c0001 | t0011 | g0094 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02922 | hp1 | a0001 | c0001 | t0007 | g0344 | AFR | ESN | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02922 | hp2 | a0001 | c0001 | t0018 | g0262 | AFR | ESN | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02965 | hp1 | a0001 | c0002 | t0031 | g0018 | AFR | ESN | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02965 | hp2 | a0001 | c0001 | t0009 | g0258 | AFR | ESN | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02970 | hp1 | a0001 | c0001 | t0053 | g0354 | AFR | ESN | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0016 | AFR | ESN | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02976 | hp1 | a0001 | c0001 | t0007 | g0351 | AFR | ESN | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02976 | hp2 | a0001 | c0003 | t0023 | g0218 | AFR | ESN | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0205 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG03041 | hp2 | a0001 | c0002 | t0020 | g0026 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG03098 | hp1 | a0001 | c0001 | t0016 | g0085 | AFR | MSL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0301 | AFR | MSL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG03130 | hp1 | a0001 | c0001 | t0009 | g0256 | AFR | ESN | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG03130 | hp2 | a0001 | c0003 | t0001 | g0204 | AFR | ESN | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG03139 | hp1 | a0001 | c0002 | t0004 | g0048 | AFR | ESN | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG03139 | hp2 | a0001 | c0001 | t0011 | g0266 | AFR | ESN | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG03195 | hp1 | a0001 | c0002 | t0003 | g0090 | AFR | ESN | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG03195 | hp2 | a0001 | c0003 | t0001 | g0224 | AFR | ESN | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG03209 | hp1 | a0001 | c0001 | t0043 | g0093 | AFR | MSL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0298 | AFR | MSL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG03225 | hp1 | a0001 | c0001 | t0024 | g0226 | AFR | MSL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG03225 | hp2 | a0001 | c0001 | t0022 | g0241 | AFR | MSL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG03239 | hp1 | a0001 | c0003 | t0013 | g0151 | SAS | PJL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG03239 | hp2 | a0001 | c0002 | t0004 | g0062 | SAS | PJL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG03453 | hp1 | a0001 | c0001 | t0016 | g0086 | AFR | MSL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG03453 | hp2 | a0001 | c0001 | t0027 | g0232 | AFR | MSL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG03486 | hp1 | a0001 | c0001 | t0021 | g0231 | AFR | MSL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0016 | AFR | MSL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG03540 | hp1 | a0001 | c0002 | t0003 | g0089 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG03540 | hp2 | a0001 | c0003 | t0001 | g0225 | AFR | GWD | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG03579 | hp1 | a0001 | c0001 | t0017 | g0234 | AFR | MSL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG03579 | hp2 | a0001 | c0003 | t0001 | g0207 | AFR | MSL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG03654 | hp1 | a0001 | c0003 | t0013 | g0154 | SAS | PJL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG03654 | hp2 | a0001 | c0002 | t0003 | g0251 | SAS | PJL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG03704 | hp1 | a0001 | c0001 | t0010 | g0024 | SAS | PJL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0302 | SAS | PJL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG03831 | hp1 | a0001 | c0001 | t0005 | g0283 | SAS | BEB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG03831 | hp2 | a0001 | c0001 | t0010 | g0020 | SAS | BEB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG03834 | hp1 | a0001 | c0002 | t0003 | g0008 | SAS | BEB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0317 | SAS | BEB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG03927 | hp1 | a0001 | c0002 | t0004 | g0061 | SAS | BEB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG03927 | hp2 | a0001 | c0002 | t0015 | g0200 | SAS | BEB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG03942 | hp1 | a0001 | c0002 | t0003 | g0102 | SAS | BEB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG03942 | hp2 | a0001 | c0001 | t0010 | g0021 | SAS | BEB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG04115 | hp1 | a0001 | c0002 | t0050 | g0159 | SAS | STU | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG04115 | hp2 | a0001 | c0001 | t0010 | g0023 | SAS | STU | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG04184 | hp1 | a0001 | c0002 | t0004 | g0030 | SAS | BEB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG04184 | hp2 | a0001 | c0003 | t0013 | g0259 | SAS | BEB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG04199 | hp1 | a0001 | c0002 | t0019 | g0068 | SAS | STU | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG04199 | hp2 | a0001 | c0003 | t0013 | g0150 | SAS | STU | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG04204 | hp1 | a0001 | c0003 | t0001 | g0208 | SAS | STU | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG04204 | hp2 | a0001 | c0001 | t0007 | g0357 | SAS | STU | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG04228 | hp1 | a0001 | c0002 | t0019 | g0046 | SAS | STU | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG04228 | hp2 | a0001 | c0003 | t0013 | g0152 | SAS | STU | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0361 | AFR | YRI | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18522 | hp2 | a0001 | c0001 | t0009 | g0003 | AFR | YRI | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0327 | EAS | CHB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18612 | hp2 | a0001 | c0001 | t0006 | g0012 | EAS | CHB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | CHB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18747 | hp2 | a0001 | c0003 | t0029 | g0374 | EAS | CHB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18906 | hp1 | a0001 | c0001 | t0009 | g0255 | AFR | YRI | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18906 | hp2 | a0001 | c0001 | t0018 | g0264 | AFR | YRI | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18940 | hp1 | a0001 | c0001 | t0006 | g0250 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18940 | hp2 | a0001 | c0001 | t0005 | g0282 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18941 | hp1 | a0001 | c0003 | t0001 | g0138 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18941 | hp2 | a0001 | c0002 | t0003 | g0176 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18943 | hp1 | a0001 | c0001 | t0006 | g0247 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18943 | hp2 | a0001 | c0002 | t0004 | g0028 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18944 | hp1 | a0001 | c0001 | t0006 | g0012 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18944 | hp2 | a0001 | c0002 | t0004 | g0080 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18946 | hp1 | a0001 | c0001 | t0012 | g0352 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18946 | hp2 | a0001 | c0002 | t0003 | g0167 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18947 | hp1 | a0001 | c0002 | t0004 | g0053 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18948 | hp1 | a0001 | c0002 | t0003 | g0195 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18948 | hp2 | a0001 | c0003 | t0001 | g0211 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18949 | hp2 | a0001 | c0002 | t0004 | g0031 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18950 | hp1 | a0001 | c0002 | t0003 | g0172 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18950 | hp2 | a0001 | c0002 | t0004 | g0074 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18952 | hp1 | a0001 | c0003 | t0001 | g0110 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18952 | hp2 | a0001 | c0002 | t0003 | g0198 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18953 | hp1 | a0001 | c0003 | t0001 | g0157 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18953 | hp2 | a0001 | c0001 | t0005 | g0281 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18954 | hp1 | a0001 | c0003 | t0001 | g0209 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18957 | hp1 | a0001 | c0001 | t0012 | g0350 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18957 | hp2 | a0001 | c0002 | t0004 | g0065 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18959 | hp1 | a0001 | c0002 | t0004 | g0029 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18960 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18961 | hp2 | a0001 | c0001 | t0012 | g0356 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18962 | hp1 | a0001 | c0003 | t0001 | g0122 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18966 | hp1 | a0001 | c0001 | t0006 | g0249 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18966 | hp2 | a0001 | c0001 | t0005 | g0279 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18968 | hp1 | a0001 | c0001 | t0005 | g0277 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18968 | hp2 | a0001 | c0002 | t0003 | g0193 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18969 | hp1 | a0001 | c0003 | t0001 | g0142 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18972 | hp1 | a0001 | c0003 | t0001 | g0104 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18973 | hp1 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18973 | hp2 | a0001 | c0002 | t0004 | g0066 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18974 | hp1 | a0001 | c0003 | t0001 | g0131 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18974 | hp2 | a0001 | c0002 | t0003 | g0162 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18975 | hp1 | a0001 | c0001 | t0006 | g0011 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18975 | hp2 | a0001 | c0003 | t0029 | g0373 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18977 | hp2 | a0001 | c0003 | t0001 | g0141 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18978 | hp1 | a0001 | c0003 | t0001 | g0203 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18980 | hp1 | a0001 | c0003 | t0001 | g0109 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18980 | hp2 | a0001 | c0002 | t0046 | g0182 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18982 | hp2 | a0001 | c0002 | t0004 | g0050 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18983 | hp1 | a0001 | c0003 | t0001 | g0136 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18983 | hp2 | a0001 | c0002 | t0003 | g0160 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18984 | hp1 | a0001 | c0001 | t0012 | g0355 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18984 | hp2 | a0001 | c0003 | t0001 | g0115 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18986 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18987 | hp1 | a0001 | c0001 | t0005 | g0268 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18987 | hp2 | a0001 | c0001 | t0006 | g0244 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18988 | hp2 | a0001 | c0003 | t0001 | g0143 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18989 | hp1 | a0001 | c0003 | t0001 | g0135 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18989 | hp2 | a0001 | c0001 | t0010 | g0019 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18990 | hp1 | a0001 | c0003 | t0001 | g0120 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18990 | hp2 | a0001 | c0002 | t0004 | g0071 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18991 | hp1 | a0001 | c0002 | t0004 | g0078 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18991 | hp2 | a0001 | c0001 | t0012 | g0345 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18992 | hp1 | a0001 | c0002 | t0003 | g0170 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18992 | hp2 | a0001 | c0002 | t0025 | g0097 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18993 | hp2 | a0001 | c0002 | t0004 | g0069 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18994 | hp1 | a0001 | c0002 | t0003 | g0179 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18994 | hp2 | a0001 | c0001 | t0005 | g0280 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18995 | hp1 | a0001 | c0002 | t0033 | g0057 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18995 | hp2 | a0001 | c0003 | t0001 | g0116 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18998 | hp1 | a0001 | c0002 | t0004 | g0058 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18999 | hp2 | a0001 | c0002 | t0003 | g0190 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19002 | hp2 | a0001 | c0003 | t0001 | g0140 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19003 | hp1 | a0001 | c0001 | t0054 | g0358 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19003 | hp2 | a0001 | c0002 | t0004 | g0063 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19004 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0332 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19006 | hp1 | a0001 | c0002 | t0003 | g0237 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19007 | hp2 | a0001 | c0003 | t0001 | g0119 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19009 | hp2 | a0001 | c0003 | t0001 | g0133 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19011 | hp1 | a0001 | c0001 | t0044 | g0275 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19011 | hp2 | a0001 | c0003 | t0001 | g0156 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19012 | hp1 | a0001 | c0003 | t0001 | g0149 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19012 | hp2 | a0001 | c0002 | t0003 | g0180 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19030 | hp1 | a0001 | c0002 | t0003 | g0092 | AFR | LWK | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19030 | hp2 | a0001 | c0001 | t0027 | g0158 | AFR | LWK | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19043 | hp1 | a0001 | c0001 | t0014 | g0236 | AFR | LWK | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19043 | hp2 | a0001 | c0003 | t0001 | g0100 | AFR | LWK | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19055 | hp2 | a0001 | c0001 | t0006 | g0243 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19056 | hp1 | a0001 | c0003 | t0001 | g0099 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19056 | hp2 | a0001 | c0002 | t0003 | g0009 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19057 | hp1 | a0001 | c0002 | t0004 | g0056 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19057 | hp2 | a0001 | c0003 | t0001 | g0134 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19058 | hp1 | a0001 | c0002 | t0004 | g0077 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19058 | hp2 | a0001 | c0001 | t0005 | g0331 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19060 | hp1 | a0001 | c0001 | t0010 | g0022 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19060 | hp2 | a0001 | c0002 | t0003 | g0187 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19062 | hp1 | a0001 | c0002 | t0003 | g0194 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19062 | hp2 | a0002 | c0004 | t0002 | g0007 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19066 | hp1 | a0001 | c0003 | t0001 | g0121 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19066 | hp2 | a0001 | c0002 | t0004 | g0044 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19067 | hp2 | a0001 | c0002 | t0003 | g0197 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19068 | hp1 | a0001 | c0002 | t0003 | g0165 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19068 | hp2 | a0001 | c0003 | t0042 | g0113 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19070 | hp1 | a0001 | c0002 | t0003 | g0202 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19070 | hp2 | a0001 | c0002 | t0004 | g0079 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19074 | hp1 | a0001 | c0002 | t0004 | g0051 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19076 | hp1 | a0001 | c0002 | t0004 | g0070 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19076 | hp2 | a0001 | c0001 | t0005 | g0272 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19077 | hp1 | a0001 | c0003 | t0001 | g0117 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19077 | hp2 | a0001 | c0002 | t0004 | g0064 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19079 | hp1 | a0001 | c0001 | t0005 | g0269 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19079 | hp2 | a0001 | c0003 | t0001 | g0139 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19082 | hp1 | a0001 | c0002 | t0004 | g0081 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19082 | hp2 | a0001 | c0002 | t0003 | g0192 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19084 | hp1 | a0001 | c0002 | t0032 | g0041 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19084 | hp2 | a0001 | c0003 | t0036 | g0103 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19085 | hp1 | a0001 | c0003 | t0001 | g0127 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19085 | hp2 | a0001 | c0002 | t0003 | g0177 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19086 | hp1 | a0001 | c0001 | t0012 | g0359 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19086 | hp2 | a0001 | c0002 | t0004 | g0034 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19087 | hp2 | a0001 | c0003 | t0001 | g0137 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19088 | hp1 | a0001 | c0002 | t0004 | g0067 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19088 | hp2 | a0001 | c0003 | t0001 | g0129 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19090 | hp1 | a0001 | c0003 | t0001 | g0118 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19090 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19091 | hp1 | a0001 | c0002 | t0003 | g0009 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19091 | hp2 | a0001 | c0003 | t0001 | g0105 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19240 | hp1 | a0001 | c0001 | t0009 | g0003 | AFR | YRI | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA19240 | hp2 | a0001 | c0001 | t0026 | g0299 | AFR | YRI | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA20129 | hp1 | a0001 | c0001 | t0021 | g0230 | AFR | ASW | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA20129 | hp2 | a0001 | c0003 | t0001 | g0215 | AFR | ASW | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0338 | EUR | TSI | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA20752 | hp2 | a0001 | c0002 | t0003 | g0188 | EUR | TSI | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA20805 | hp1 | a0001 | c0003 | t0001 | g0220 | EUR | TSI | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA20805 | hp2 | a0001 | c0002 | t0004 | g0083 | EUR | TSI | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA20905 | hp1 | a0001 | c0001 | t0008 | g0366 | SAS | GIH | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA20905 | hp2 | a0001 | c0002 | t0015 | g0184 | SAS | GIH | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02109 | hp1 | a0001 | c0003 | t0001 | g0217 | AFR | ACB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02109 | hp2 | a0001 | c0001 | t0028 | g0329 | AFR | ACB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02486 | hp1 | a0001 | c0001 | t0024 | g0227 | AFR | ACB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02486 | hp2 | a0001 | c0002 | t0004 | g0052 | AFR | ACB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02559 | hp1 | a0001 | c0001 | t0009 | g0003 | AFR | ACB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0360 | AFR | ACB | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG03471 | hp1 | a0001 | c0001 | t0018 | g0263 | AFR | MSL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG03471 | hp2 | a0001 | c0001 | t0052 | g0343 | AFR | MSL | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG06807 | hp1 | a0001 | c0001 | t0007 | g0353 | AFR | USA | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| HG06807 | hp2 | a0001 | c0003 | t0001 | g0214 | AFR | USA | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18955 | hp1 | a0001 | c0002 | t0003 | g0191 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA18955 | hp2 | a0001 | c0001 | t0006 | g0013 | EAS | JPT | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA20300 | hp1 | a0001 | c0001 | t0011 | g0265 | AFR | USA | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | USA | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0341 | AFR | LWK | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| NA21309 | hp2 | a0001 | c0006 | t0056 | g0375 | AFR | LWK | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0335 | REF | REF | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0325 | REF | REF | GXYLT1_chr12_42076845_42149874 | GXYLT1 | chr12 | 42076845 | 42149874 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:42144454
|
GGCCCGCG others(32): Show |
G | 1 | a0002 | 3 | HG02015.hp2 HG02809.hp2 NA19062.hp2 |
conservative_inframe_deletion | MODERATE | c.154_192delGGCGGACG others(31): Show |
p.Gly52_Gly64del | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/8 | 420/7492 | 154/1323 | 52/440 | chr12 | 42144454 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:42087930
|
G | A | 1 | a0001c0003 | 85 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(82): Show |
synonymous_variant | LOW | c.1179C>T | p.Asp393Asp | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 1407/7492 | 1179/1323 | 393/440 | chr12 | 42087930 | ||
| chr12:42097577
|
T | A | 1 | a0001c0005 | 2 | HG01106.hp1 HG01496.hp1 |
synonymous_variant | LOW | c.1026A>T | p.Arg342Arg | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/8 | 1254/7492 | 1026/1323 | 342/440 | chr12 | 42097577 | ||
| chr12:42109665
|
T | C | 2 | a0001c0002a0001c0005 | 129 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(126): Show |
synonymous_variant | LOW | c.513A>G | p.Thr171Thr | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/8 | 741/7492 | 513/1323 | 171/440 | chr12 | 42109665 | ||
| chr12:42119162
|
C | T | 1 | a0001c0006 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.324G>A | p.Leu108Leu | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/8 | 552/7492 | 324/1323 | 108/440 | chr12 | 42119162 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:42081850
|
G | A | 2 | a0001c0001t0014a0001c0001t0021 | 6 | HG01884.hp1 HG02280.hp1 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5936C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 5936 | chr12 | 42081850 | |||||
| chr12:42081899
|
T | C | 1 | a0001c0006t0056 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5887A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 5887 | chr12 | 42081899 | |||||
| chr12:42081946
|
G | A | 1 | a0001c0001t0009 | 8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5840C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 5840 | chr12 | 42081946 | |||||
| chr12:42082086
|
G | A | 16 | a0001c0002t0003a0001c0002t0004a0001c0002t0015others(13): Show | 128 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*5700C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 5700 | chr12 | 42082086 | |||||
| chr12:42082139
|
G | A | 1 | a0001c0001t0038 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5647C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 5647 | chr12 | 42082139 | |||||
| chr12:42082182
|
T | A | 2 | a0001c0001t0006a0001c0001t0010 | 20 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*5604A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 5604 | chr12 | 42082182 | |||||
| chr12:42082222
|
T | A | 2 | a0001c0001t0026a0001c0001t0028 | 4 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5564A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 5564 | chr12 | 42082222 | |||||
| chr12:42082233
|
G | A | 1 | a0001c0002t0050 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5553C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 5553 | chr12 | 42082233 | |||||
| chr12:42082411
|
A | G | 3 | a0001c0001t0005a0001c0001t0038a0001c0001t0044 | 22 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*5375T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 5375 | chr12 | 42082411 | |||||
| chr12:42082684
|
C | A | 1 | a0001c0001t0054 | 1 | NA19003.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5102G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 5102 | chr12 | 42082684 | |||||
| chr12:42082811
|
A | C | 30 | a0001c0001t0016a0001c0001t0026a0001c0001t0027others(27): Show | 223 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(220): Show |
3_prime_UTR_variant | MODIFIER | c.*4975T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 4975 | chr12 | 42082811 | |||||
| chr12:42082877
|
C | A | 1 | a0001c0001t0009 | 8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4909G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 4909 | chr12 | 42082877 | |||||
| chr12:42082996
|
T | C | 2 | a0001c0001t0006a0001c0001t0010 | 20 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*4790A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 4790 | chr12 | 42082996 | |||||
| chr12:42083043
|
T | C | 1 | a0001c0001t0017 | 3 | HG02451.hp1 HG02647.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4743A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 4743 | chr12 | 42083043 | |||||
| chr12:42083174
|
C | T | 1 | a0001c0001t0043 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4612G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 4612 | chr12 | 42083174 | |||||
| chr12:42083185
|
T | A | 11 | a0001c0001t0024a0001c0001t0053a0001c0002t0003others(8): Show | 70 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*4601A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 4601 | chr12 | 42083185 | |||||
| chr12:42083186
|
A | T | 4 | a0001c0001t0018a0001c0001t0026a0001c0001t0052others(1): Show | 7 | HG00323.hp2 HG01169.hp1 HG02922.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4600T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 4600 | chr12 | 42083186 | |||||
| chr12:42083554
|
T | A | 2 | a0001c0001t0012a0001c0001t0054 | 7 | NA18946.hp1 NA18957.hp1 NA18961.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4232A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 4232 | chr12 | 42083554 | |||||
| chr12:42083602
|
T | C | 2 | a0001c0001t0006a0001c0001t0010 | 20 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*4184A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 4184 | chr12 | 42083602 | |||||
| chr12:42083625
|
A | G | 1 | a0001c0001t0009 | 8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4161T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 4161 | chr12 | 42083625 | |||||
| chr12:42083725
|
T | C | 1 | a0001c0001t0016 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4061A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 4061 | chr12 | 42083725 | |||||
| chr12:42083768
|
T | C | 4 | a0001c0002t0015a0001c0002t0047a0001c0002t0049others(1): Show | 7 | HG00140.hp1 HG01346.hp1 HG01433.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4018A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 4018 | chr12 | 42083768 | |||||
| chr12:42083873
|
A | T | 1 | a0001c0002t0047 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3913T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 3913 | chr12 | 42083873 | |||||
| chr12:42083978
|
T | TA | 12 | a0001c0001t0005a0001c0001t0009a0001c0001t0011others(9): Show | 51 | HG00544.hp1 HG00597.hp1 HG01884.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*3807dupT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 3807 | chr12 | 42083978 | |||||
| chr12:42083978
|
TA | T | 1 | a0001c0003t0013 | 5 | HG03239.hp1 HG03654.hp1 HG04184.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3807delT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 3807 | chr12 | 42083978 | |||||
| chr12:42084013
|
A | G | 1 | a0001c0001t0037 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3773T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 3773 | chr12 | 42084013 | |||||
| chr12:42084261
|
C | T | 1 | a0001c0001t0016 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3525G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 3525 | chr12 | 42084261 | |||||
| chr12:42084416
|
G | A | 1 | a0001c0006t0056 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3370C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 3370 | chr12 | 42084416 | |||||
| chr12:42084462
|
C | CA | 27 | a0001c0001t0016a0001c0002t0003a0001c0002t0004others(24): Show | 217 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*3323_*3324insT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 3323 | chr12 | 42084462 | |||||
| chr12:42084513
|
C | T | 1 | a0001c0001t0041 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3273G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 3273 | chr12 | 42084513 | |||||
| chr12:42084611
|
G | T | 53 | a0001c0001t0005a0001c0001t0006a0001c0001t0007others(50): Show | 330 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(327): Show |
3_prime_UTR_variant | MODIFIER | c.*3175C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 3175 | chr12 | 42084611 | |||||
| chr12:42084737
|
T | C | 3 | a0001c0001t0026a0001c0001t0027a0001c0001t0028 | 6 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3049A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 3049 | chr12 | 42084737 | |||||
| chr12:42084754
|
A | C | 7 | a0001c0001t0007a0001c0001t0008a0001c0001t0012others(4): Show | 32 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*3032T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 3032 | chr12 | 42084754 | |||||
| chr12:42084855
|
T | C | 1 | a0001c0001t0016 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2931A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 2931 | chr12 | 42084855 | |||||
| chr12:42084881
|
C | A | 1 | a0001c0002t0019 | 2 | HG04199.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2905G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 2905 | chr12 | 42084881 | |||||
| chr12:42084937
|
A | C | 1 | a0001c0002t0047 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2849T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 2849 | chr12 | 42084937 | |||||
| chr12:42084993
|
CTA | C | 3 | a0001c0001t0006a0001c0001t0010a0001c0001t0021 | 22 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2791_*2792delTA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 2791 | chr12 | 42084993 | |||||
| chr12:42085032
|
C | T | 1 | a0001c0003t0023 | 2 | HG02572.hp2 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2754G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 2754 | chr12 | 42085032 | |||||
| chr12:42085377
|
G | A | 1 | a0001c0003t0042 | 1 | NA19068.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2409C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 2409 | chr12 | 42085377 | |||||
| chr12:42085385
|
C | T | 1 | a0001c0002t0046 | 1 | NA18980.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2401G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 2401 | chr12 | 42085385 | |||||
| chr12:42085538
|
G | A | 1 | a0001c0001t0043 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2248C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 2248 | chr12 | 42085538 | |||||
| chr12:42085570
|
T | G | 1 | a0001c0001t0044 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2216A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 2216 | chr12 | 42085570 | |||||
| chr12:42085648
|
A | G | 11 | a0001c0001t0006a0001c0001t0007a0001c0001t0008others(8): Show | 55 | HG00423.hp1 HG00639.hp1 HG00642.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*2138T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 2138 | chr12 | 42085648 | |||||
| chr12:42085791
|
G | C | 1 | a0001c0001t0016 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1995C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 1995 | chr12 | 42085791 | |||||
| chr12:42086067
|
C | T | 1 | a0001c0001t0016 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1719G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 1719 | chr12 | 42086067 | |||||
| chr12:42086175
|
A | G | 1 | a0001c0003t0036 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1611T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 1611 | chr12 | 42086175 | |||||
| chr12:42086434
|
G | A | 1 | a0001c0001t0045 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1352C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 1352 | chr12 | 42086434 | |||||
| chr12:42086570
|
G | C | 1 | a0001c0002t0034 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1216C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 1216 | chr12 | 42086570 | |||||
| chr12:42087088
|
A | G | 1 | a0001c0001t0009 | 8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*698T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 698 | chr12 | 42087088 | |||||
| chr12:42087299
|
A | G | 1 | a0001c0003t0035 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*487T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 487 | chr12 | 42087299 | |||||
| chr12:42087335
|
A | G | 1 | a0001c0002t0032 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*451T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 451 | chr12 | 42087335 | |||||
| chr12:42087562
|
G | GT | 2 | a0001c0001t0014a0001c0001t0021 | 6 | HG01884.hp1 HG02280.hp1 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*223dupA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 223 | chr12 | 42087562 | |||||
| chr12:42087641
|
A | G | 8 | a0001c0001t0007a0001c0001t0008a0001c0001t0012others(5): Show | 33 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*145T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 145 | chr12 | 42087641 | |||||
| chr12:42087722
|
G | A | 1 | a0001c0002t0020 | 2 | HG02717.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*64C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 64 | chr12 | 42087722 | |||||
| chr12:42087743
|
T | C | 8 | a0001c0002t0003a0001c0002t0015a0001c0002t0030others(5): Show | 65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*43A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 8/8 | 43 | chr12 | 42087743 | |||||
| chr12:42144661
|
T | TCCTCCTT others(5): Show |
1 | a0002c0004t0051 | 1 | HG02809.hp2 | 5_prime_UTR_variant | MODIFIER | c.-27_-16dupCGGCGAAG others(4): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/8 | 16 | chr12 | 42144661 | |||||
| chr12:42144668
|
T | TCGCCGCC others(5): Show |
6 | a0001c0001t0007a0001c0001t0012a0001c0001t0052others(3): Show | 22 | HG00639.hp1 HG00738.hp1 HG01891.hp2 others(19): Show |
5_prime_UTR_variant | MODIFIER | c.-34_-23dupGCGGCGGC others(4): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/8 | 23 | chr12 | 42144668 | |||||
| chr12:42144668
|
T | TCGCCGCC others(8): Show |
1 | a0001c0001t0008 | 10 | HG00642.hp1 HG01069.hp1 HG01175.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-37_-23dupGCGGCGGC others(7): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/8 | 23 | chr12 | 42144668 | |||||
| chr12:42144700
|
T | C | 1 | a0001c0003t0029 | 2 | NA18747.hp2 NA18975.hp2 |
5_prime_UTR_variant | MODIFIER | c.-54A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/8 | 54 | chr12 | 42144700 | |||||
| chr12:42144728
|
C | G | 8 | a0001c0002t0004a0001c0002t0019a0001c0002t0020others(5): Show | 62 | HG00323.hp1 HG00621.hp2 HG00733.hp1 others(59): Show |
5_prime_UTR_variant | MODIFIER | c.-82G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/8 | 82 | chr12 | 42144728 | |||||
| chr12:42144766
|
C | A | 1 | a0001c0006t0056 | 1 | NA21309.hp2 | 5_prime_UTR_variant | MODIFIER | c.-120G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/8 | 120 | chr12 | 42144766 | |||||
| chr12:42144767
|
C | T | 1 | a0001c0001t0010 | 6 | HG03704.hp1 HG03831.hp2 HG03942.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-121G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/8 | 121 | chr12 | 42144767 | |||||
| chr12:42144788
|
C | T | 1 | a0001c0002t0031 | 1 | HG02965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-142G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/8 | 142 | chr12 | 42144788 | |||||
| chr12:42144833
|
G | T | 1 | a0001c0002t0030 | 1 | HG00438.hp2 | 5_prime_UTR_variant | MODIFIER | c.-187C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/8 | 187 | chr12 | 42144833 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:42088001
|
G | A | 311 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(308): Show | 325 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(322): Show |
intron_variant | MODIFIER | c.1162-54C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42088001 | ||||||
| chr12:42088099
|
T | G | 1 | a0001c0001t0028g0329 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1162-152A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42088099 | ||||||
| chr12:42088199
|
T | C | 24 | a0001c0002t0004g0028a0001c0002t0004g0029a0001c0002t0004g0030others(21): Show | 24 | HG00621.hp2 HG01975.hp1 HG02071.hp2 others(21): Show |
intron_variant | MODIFIER | c.1162-252A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42088199 | ||||||
| chr12:42088222
|
A | C | 1 | a0001c0001t0002g0307 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1162-275T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42088222 | ||||||
| chr12:42088292
|
C | T | 1 | a0001c0003t0036g0103 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1162-345G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42088292 | ||||||
| chr12:42088510
|
G | A | 1 | a0001c0002t0004g0045 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1162-563C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42088510 | ||||||
| chr12:42088625
|
C | T | 17 | a0001c0001t0006g0011a0001c0001t0006g0012a0001c0001t0006g0013others(14): Show | 20 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1162-678G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42088625 | ||||||
| chr12:42088883
|
G | GAAAGAAC others(70): Show |
1 | a0001c0003t0001g0141 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1162-937_1162-936i others(79): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42088883 | ||||||
| chr12:42088883
|
G | GAAAGAAC others(80): Show |
2 | a0001c0002t0004g0029a0001c0002t0020g0026 | 2 | HG03041.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.1162-937_1162-936i others(89): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42088883 | ||||||
| chr12:42088883
|
G | GAAAGAAC others(81): Show |
49 | a0001c0002t0004g0028a0001c0002t0004g0030a0001c0002t0004g0032others(46): Show | 49 | HG00323.hp1 HG00323.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.1162-937_1162-936i others(90): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42088883 | ||||||
| chr12:42088883
|
G | GAAAGAAC others(82): Show |
125 | a0001c0002t0003g0002a0001c0002t0003g0008a0001c0002t0003g0009others(122): Show | 130 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.1162-937_1162-936i others(91): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42088883 | ||||||
| chr12:42088883
|
G | GAAAGAAC others(83): Show |
22 | a0001c0002t0003g0174a0001c0002t0003g0196a0001c0002t0003g0251others(19): Show | 22 | HG00438.hp1 HG00597.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.1162-937_1162-936i others(92): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42088883 | ||||||
| chr12:42088883
|
G | GAAAGAAC others(84): Show |
5 | a0001c0002t0003g0198a0001c0002t0004g0038a0001c0002t0004g0040others(2): Show | 5 | HG01081.hp1 HG01243.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.1162-937_1162-936i others(93): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42088883 | ||||||
| chr12:42088883
|
G | GAAAGAAC others(85): Show |
2 | a0001c0003t0001g0127a0001c0005t0004g0006 | 3 | HG01106.hp1 HG01496.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1162-937_1162-936i others(94): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42088883 | ||||||
| chr12:42088883
|
G | GAAAGAAC others(86): Show |
2 | a0001c0003t0001g0134a0001c0003t0001g0161 | 2 | HG01192.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1162-937_1162-936i others(95): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42088883 | ||||||
| chr12:42089000
|
A | G | 1 | a0001c0001t0007g0351 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1162-1053T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42089000 | ||||||
| chr12:42089176
|
A | G | 208 | a0001c0002t0003g0002a0001c0002t0003g0008a0001c0002t0003g0009others(205): Show | 214 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.1162-1229T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42089176 | ||||||
| chr12:42089306
|
G | A | 1 | a0001c0001t0005g0341 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1162-1359C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42089306 | ||||||
| chr12:42089312
|
G | A | 1 | a0001c0001t0002g0326 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1162-1365C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42089312 | ||||||
| chr12:42089342
|
T | A | 6 | a0001c0001t0026g0299a0001c0001t0026g0323a0001c0001t0027g0158others(3): Show | 6 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1162-1395A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42089342 | ||||||
| chr12:42089466
|
C | T | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1162-1519G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42089466 | ||||||
| chr12:42089477
|
A | G | 1 | a0001c0001t0006g0245 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1162-1530T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42089477 | ||||||
| chr12:42089516
|
T | A | 4 | a0001c0001t0002g0005a0001c0001t0002g0288a0001c0001t0002g0292others(1): Show | 6 | HG01496.hp2 HG01928.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.1162-1569A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42089516 | ||||||
| chr12:42089573
|
C | T | 1 | a0002c0004t0051g0342 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1162-1626G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42089573 | ||||||
| chr12:42089633
|
C | T | 10 | a0001c0001t0009g0003a0001c0001t0009g0254a0001c0001t0009g0255others(7): Show | 12 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1162-1686G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42089633 | ||||||
| chr12:42089669
|
T | C | 1 | a0001c0002t0004g0030 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1162-1722A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42089669 | ||||||
| chr12:42089786
|
G | C | 4 | a0001c0001t0002g0005a0001c0001t0002g0288a0001c0001t0002g0292others(1): Show | 6 | HG01496.hp2 HG01928.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.1162-1839C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42089786 | ||||||
| chr12:42089888
|
A | T | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1162-1941T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42089888 | ||||||
| chr12:42090032
|
T | C | 1 | a0001c0001t0017g0242 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1162-2085A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42090032 | ||||||
| chr12:42090114
|
G | GA | 361 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0014others(358): Show | 384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.1162-2168dupT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42090114 | ||||||
| chr12:42090114
|
G | GAA | 11 | a0001c0001t0014g0228a0001c0001t0014g0229a0001c0001t0014g0233others(8): Show | 11 | HG01884.hp1 HG02280.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1162-2169_1162-216 others(6): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42090114 | ||||||
| chr12:42090129
|
T | C | 60 | a0001c0002t0003g0002a0001c0002t0003g0008a0001c0002t0003g0009others(57): Show | 65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1162-2182A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42090129 | ||||||
| chr12:42090205
|
T | A | 1 | a0001c0001t0008g0365 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1162-2258A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42090205 | ||||||
| chr12:42090388
|
T | A | 1 | a0001c0001t0027g0232 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1162-2441A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42090388 | ||||||
| chr12:42090568
|
T | C | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1162-2621A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42090568 | ||||||
| chr12:42090771
|
T | A | 2 | a0001c0002t0020g0026a0001c0002t0020g0027 | 2 | HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1162-2824A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42090771 | ||||||
| chr12:42090865
|
A | C | 1 | a0001c0003t0001g0161 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1162-2918T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42090865 | ||||||
| chr12:42090886
|
T | C | 8 | a0001c0002t0004g0028a0001c0002t0004g0032a0001c0002t0004g0042others(5): Show | 8 | HG00621.hp2 HG02129.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.1162-2939A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42090886 | ||||||
| chr12:42090954
|
T | C | 1 | a0001c0002t0020g0026 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1162-3007A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42090954 | ||||||
| chr12:42090956
|
A | AATTT | 10 | a0001c0001t0009g0003a0001c0001t0009g0254a0001c0001t0009g0255others(7): Show | 12 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1162-3010_1162-300 others(8): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42090956 | ||||||
| chr12:42090978
|
T | C | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1162-3031A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42090978 | ||||||
| chr12:42091052
|
G | A | 59 | a0001c0002t0004g0028a0001c0002t0004g0029a0001c0002t0004g0030others(56): Show | 60 | HG00323.hp1 HG00621.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.1162-3105C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42091052 | ||||||
| chr12:42091287
|
AT | A | 8 | a0001c0002t0003g0194a0001c0002t0015g0183a0001c0002t0015g0184others(5): Show | 8 | HG00140.hp1 HG01346.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.1162-3341delA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42091287 | ||||||
| chr12:42091292
|
T | A | 1 | a0001c0002t0004g0042 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1162-3345A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42091292 | ||||||
| chr12:42091293
|
T | A | 15 | a0001c0001t0016g0085a0001c0001t0016g0086a0001c0002t0003g0169others(12): Show | 15 | HG00544.hp2 HG00597.hp2 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.1162-3346A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42091293 | ||||||
| chr12:42091294
|
T | A | 204 | a0001c0001t0011g0094a0001c0001t0011g0095a0001c0001t0016g0084others(201): Show | 210 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.1162-3347A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42091294 | ||||||
| chr12:42091295
|
A | T | 6 | a0001c0001t0010g0019a0001c0001t0010g0020a0001c0001t0010g0021others(3): Show | 6 | HG03704.hp1 HG03831.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.1162-3348T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42091295 | ||||||
| chr12:42091361
|
T | C | 1 | a0001c0001t0002g0314 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1162-3414A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42091361 | ||||||
| chr12:42091414
|
GAT | G | 4 | a0001c0002t0015g0183a0001c0002t0015g0184a0001c0002t0015g0200others(1): Show | 4 | HG00140.hp1 HG01346.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.1162-3469_1162-346 others(6): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42091414 | ||||||
| chr12:42091415
|
A | AT | 17 | a0001c0001t0006g0011a0001c0001t0006g0012a0001c0001t0006g0013others(14): Show | 20 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1162-3469dupA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42091415 | ||||||
| chr12:42091434
|
G | A | 1 | a0001c0002t0031g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1162-3487C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42091434 | ||||||
| chr12:42091486
|
A | G | 4 | a0001c0001t0011g0094a0001c0001t0011g0095a0001c0001t0037g0096others(1): Show | 4 | HG02717.hp1 HG02818.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1162-3539T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42091486 | ||||||
| chr12:42091503
|
C | G | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1162-3556G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42091503 | ||||||
| chr12:42091633
|
TC | T | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1162-3687delG | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42091633 | ||||||
| chr12:42091649
|
T | C | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1162-3702A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42091649 | ||||||
| chr12:42091665
|
T | C | 2 | a0001c0001t0011g0265a0001c0001t0011g0266 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1162-3718A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42091665 | ||||||
| chr12:42091717
|
C | A | 311 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(308): Show | 325 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(322): Show |
intron_variant | MODIFIER | c.1162-3770G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42091717 | ||||||
| chr12:42091856
|
C | T | 32 | a0001c0001t0007g0016a0001c0001t0007g0344a0001c0001t0007g0346others(29): Show | 33 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.1162-3909G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42091856 | ||||||
| chr12:42091885
|
T | C | 6 | a0001c0001t0010g0019a0001c0001t0010g0020a0001c0001t0010g0021others(3): Show | 6 | HG03704.hp1 HG03831.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.1162-3938A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42091885 | ||||||
| chr12:42092670
|
A | G | 44 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(41): Show | 48 | HG00544.hp1 HG00597.hp1 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.1162-4723T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42092670 | ||||||
| chr12:42092686
|
T | C | 1 | a0001c0003t0001g0224 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1162-4739A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42092686 | ||||||
| chr12:42092693
|
G | A | 3 | a0001c0001t0021g0230a0001c0001t0021g0231a0002c0004t0051g0342 | 3 | HG02809.hp2 HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1162-4746C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42092693 | ||||||
| chr12:42092774
|
C | T | 1 | a0001c0001t0022g0240 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1161+4668G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42092774 | ||||||
| chr12:42092800
|
C | T | 311 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(308): Show | 325 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(322): Show |
intron_variant | MODIFIER | c.1161+4642G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42092800 | ||||||
| chr12:42092840
|
G | A | 6 | a0001c0001t0009g0003a0001c0001t0009g0254a0001c0001t0009g0255others(3): Show | 8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1161+4602C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42092840 | ||||||
| chr12:42092905
|
T | C | 1 | a0001c0001t0008g0366 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1161+4537A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42092905 | ||||||
| chr12:42092920
|
G | T | 1 | a0001c0002t0003g0167 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1161+4522C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42092920 | ||||||
| chr12:42092960
|
G | A | 32 | a0001c0001t0007g0016a0001c0001t0007g0344a0001c0001t0007g0346others(29): Show | 33 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.1161+4482C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42092960 | ||||||
| chr12:42092986
|
A | G | 1 | a0001c0001t0037g0096 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1161+4456T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42092986 | ||||||
| chr12:42093037
|
T | C | 1 | a0001c0002t0004g0039 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1161+4405A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42093037 | ||||||
| chr12:42093200
|
C | T | 32 | a0001c0001t0007g0016a0001c0001t0007g0344a0001c0001t0007g0346others(29): Show | 33 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.1161+4242G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42093200 | ||||||
| chr12:42093344
|
G | A | 6 | a0001c0001t0009g0003a0001c0001t0009g0254a0001c0001t0009g0255others(3): Show | 8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1161+4098C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42093344 | ||||||
| chr12:42093346
|
C | A | 1 | a0001c0001t0002g0291 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1161+4096G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42093346 | ||||||
| chr12:42093348
|
G | A | 1 | a0001c0003t0001g0130 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1161+4094C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42093348 | ||||||
| chr12:42093415
|
A | C | 5 | a0001c0001t0017g0234a0001c0001t0017g0235a0001c0001t0017g0242others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1161+4027T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42093415 | ||||||
| chr12:42093466
|
T | C | 4 | a0001c0001t0011g0094a0001c0001t0011g0095a0001c0001t0037g0096others(1): Show | 4 | HG02717.hp1 HG02818.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1161+3976A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42093466 | ||||||
| chr12:42093495
|
T | C | 1 | a0001c0002t0003g0178 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1161+3947A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42093495 | ||||||
| chr12:42093517
|
C | A | 85 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0104others(82): Show | 85 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1161+3925G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42093517 | ||||||
| chr12:42093853
|
A | C | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1161+3589T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42093853 | ||||||
| chr12:42094055
|
T | TAAA | 6 | a0001c0001t0009g0003a0001c0001t0009g0254a0001c0001t0009g0255others(3): Show | 8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1161+3384_1161+338 others(7): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42094055 | ||||||
| chr12:42094067
|
A | G | 6 | a0001c0001t0014g0228a0001c0001t0014g0229a0001c0001t0014g0233others(3): Show | 6 | HG01884.hp1 HG02280.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1161+3375T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42094067 | ||||||
| chr12:42094275
|
C | A | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1161+3167G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42094275 | ||||||
| chr12:42094351
|
C | CA | 46 | a0001c0001t0026g0299a0001c0001t0026g0323a0001c0001t0028g0328others(43): Show | 50 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1161+3090dupT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42094351 | ||||||
| chr12:42094351
|
C | CAA | 16 | a0001c0002t0003g0009a0001c0002t0003g0101a0001c0002t0003g0102others(13): Show | 17 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.1161+3089_1161+309 others(6): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42094351 | ||||||
| chr12:42094351
|
CA | C | 36 | a0001c0001t0002g0300a0001c0001t0002g0306a0001c0001t0002g0308others(33): Show | 38 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.1161+3090delT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42094351 | ||||||
| chr12:42094461
|
C | G | 2 | a0001c0001t0011g0260a0001c0001t0011g0261 | 2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1161+2981G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42094461 | ||||||
| chr12:42094505
|
A | G | 2 | a0001c0001t0007g0344a0001c0001t0052g0343 | 2 | HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1161+2937T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42094505 | ||||||
| chr12:42094734
|
A | T | 1 | a0001c0001t0011g0261 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1161+2708T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42094734 | ||||||
| chr12:42094832
|
G | T | 2 | a0001c0001t0011g0260a0001c0001t0011g0261 | 2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1161+2610C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42094832 | ||||||
| chr12:42094847
|
C | T | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1161+2595G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42094847 | ||||||
| chr12:42094867
|
T | C | 2 | a0001c0002t0004g0082a0001c0002t0004g0083 | 2 | HG02300.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1161+2575A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42094867 | ||||||
| chr12:42094914
|
T | C | 2 | a0001c0002t0020g0026a0001c0002t0020g0027 | 2 | HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1161+2528A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42094914 | ||||||
| chr12:42094940
|
T | C | 2 | a0001c0001t0002g0302a0001c0001t0002g0317 | 2 | HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1161+2502A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42094940 | ||||||
| chr12:42095009
|
A | AC | 214 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086others(211): Show | 220 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.1161+2432dupG | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42095009 | ||||||
| chr12:42095155
|
T | C | 10 | a0001c0001t0009g0003a0001c0001t0009g0254a0001c0001t0009g0255others(7): Show | 12 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1161+2287A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42095155 | ||||||
| chr12:42095354
|
C | T | 6 | a0001c0001t0009g0003a0001c0001t0009g0254a0001c0001t0009g0255others(3): Show | 8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1161+2088G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42095354 | ||||||
| chr12:42095357
|
T | C | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1161+2085A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42095357 | ||||||
| chr12:42095393
|
C | T | 9 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086others(6): Show | 9 | HG01169.hp1 HG02109.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1161+2049G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42095393 | ||||||
| chr12:42095680
|
T | C | 1 | a0001c0003t0001g0209 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1161+1762A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42095680 | ||||||
| chr12:42095718
|
CT | C | 32 | a0001c0001t0007g0016a0001c0001t0007g0344a0001c0001t0007g0346others(29): Show | 33 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.1161+1723delA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42095718 | ||||||
| chr12:42095720
|
AT | A | 4 | a0001c0001t0011g0094a0001c0001t0011g0095a0001c0001t0037g0096others(1): Show | 4 | HG02717.hp1 HG02818.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1161+1721delA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42095720 | ||||||
| chr12:42095798
|
T | C | 1 | a0001c0001t0014g0229 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1161+1644A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42095798 | ||||||
| chr12:42095811
|
A | G | 216 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086others(213): Show | 222 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.1161+1631T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42095811 | ||||||
| chr12:42095875
|
T | G | 1 | a0001c0002t0003g0194 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1161+1567A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42095875 | ||||||
| chr12:42095876
|
A | T | 1 | a0001c0002t0003g0194 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1161+1566T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42095876 | ||||||
| chr12:42095877
|
T | A | 1 | a0001c0002t0003g0194 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1161+1565A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42095877 | ||||||
| chr12:42095886
|
C | T | 1 | a0001c0001t0021g0230 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1161+1556G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42095886 | ||||||
| chr12:42095902
|
C | T | 32 | a0001c0001t0007g0016a0001c0001t0007g0344a0001c0001t0007g0346others(29): Show | 33 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.1161+1540G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42095902 | ||||||
| chr12:42095991
|
C | T | 2 | a0001c0001t0002g0285a0001c0001t0002g0291 | 2 | NA18969.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.1161+1451G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42095991 | ||||||
| chr12:42096017
|
G | A | 1 | a0001c0002t0003g0194 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1161+1425C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096017 | ||||||
| chr12:42096110
|
A | C | 1 | a0001c0001t0014g0229 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1161+1332T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096110 | ||||||
| chr12:42096125
|
T | C | 1 | a0001c0001t0014g0236 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1161+1317A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096125 | ||||||
| chr12:42096199
|
C | T | 206 | a0001c0002t0003g0002a0001c0002t0003g0008a0001c0002t0003g0009others(203): Show | 212 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.1161+1243G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096199 | ||||||
| chr12:42096283
|
T | A | 1 | a0001c0002t0004g0047 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1161+1159A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096283 | ||||||
| chr12:42096336
|
G | T | 6 | a0001c0001t0008g0363a0001c0001t0008g0364a0001c0001t0008g0365others(3): Show | 6 | HG00642.hp1 HG01069.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.1161+1106C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096336 | ||||||
| chr12:42096410
|
A | C | 2 | a0001c0001t0022g0240a0001c0001t0022g0241 | 2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1161+1032T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096410 | ||||||
| chr12:42096420
|
G | T | 1 | a0001c0002t0003g0194 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1161+1022C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096420 | ||||||
| chr12:42096464
|
A | G | 6 | a0001c0001t0007g0016a0001c0001t0007g0346a0001c0001t0007g0347others(3): Show | 7 | HG00738.hp1 HG02647.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1161+978T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096464 | ||||||
| chr12:42096478
|
A | C | 1 | a0001c0003t0001g0148 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1161+964T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096478 | ||||||
| chr12:42096502
|
C | A | 85 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0104others(82): Show | 85 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1161+940G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096502 | ||||||
| chr12:42096504
|
T | G | 1 | a0001c0002t0003g0194 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1161+938A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096504 | ||||||
| chr12:42096578
|
G | A | 1 | a0001c0002t0003g0174 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1161+864C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096578 | ||||||
| chr12:42096610
|
G | A | 207 | a0001c0002t0003g0002a0001c0002t0003g0008a0001c0002t0003g0009others(204): Show | 213 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.1161+832C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096610 | ||||||
| chr12:42096618
|
T | C | 1 | a0001c0003t0001g0219 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1161+824A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096618 | ||||||
| chr12:42096673
|
A | G | 6 | a0001c0001t0009g0003a0001c0001t0009g0254a0001c0001t0009g0255others(3): Show | 8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1161+769T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096673 | ||||||
| chr12:42096746
|
C | T | 1 | a0001c0002t0003g0194 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1161+696G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096746 | ||||||
| chr12:42096747
|
T | C | 1 | a0001c0002t0003g0194 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1161+695A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096747 | ||||||
| chr12:42096749
|
C | T | 1 | a0001c0002t0003g0194 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1161+693G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096749 | ||||||
| chr12:42096914
|
G | A | 1 | a0001c0001t0002g0320 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1161+528C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42096914 | ||||||
| chr12:42097004
|
T | C | 4 | a0001c0002t0004g0028a0001c0002t0004g0051a0001c0002t0004g0056others(1): Show | 4 | NA18943.hp2 NA18998.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.1161+438A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42097004 | ||||||
| chr12:42097030
|
A | C | 2 | a0001c0001t0011g0260a0001c0001t0011g0261 | 2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1161+412T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42097030 | ||||||
| chr12:42097073
|
C | T | 2 | a0001c0001t0026g0299a0001c0001t0026g0323 | 2 | HG01169.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1161+369G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42097073 | ||||||
| chr12:42097149
|
G | A | 209 | a0001c0001t0024g0226a0001c0001t0024g0227a0001c0002t0003g0002others(206): Show | 215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.1161+293C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42097149 | ||||||
| chr12:42097153
|
G | A | 1 | a0001c0002t0003g0177 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1161+289C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42097153 | ||||||
| chr12:42097214
|
T | C | 34 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(31): Show | 36 | HG00544.hp1 HG00597.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.1161+228A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42097214 | ||||||
| chr12:42097234
|
A | G | 1 | a0001c0001t0053g0354 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1161+208T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42097234 | ||||||
| chr12:42097283
|
T | C | 5 | a0001c0001t0017g0234a0001c0001t0017g0235a0001c0001t0017g0242others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1161+159A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42097283 | ||||||
| chr12:42097301
|
G | A | 17 | a0001c0001t0006g0011a0001c0001t0006g0012a0001c0001t0006g0013others(14): Show | 20 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1161+141C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42097301 | ||||||
| chr12:42097388
|
A | G | 6 | a0001c0001t0026g0299a0001c0001t0026g0323a0001c0001t0027g0158others(3): Show | 6 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1161+54T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42097388 | ||||||
| chr12:42097390
|
C | T | 1 | a0001c0003t0001g0153 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1161+52G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 7/7 | chr12 | 42097390 | ||||||
| chr12:42098383
|
T | G | 3 | a0001c0002t0020g0026a0001c0002t0020g0027a0001c0002t0034g0025 | 3 | HG02055.hp2 HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.865-350A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098383 | ||||||
| chr12:42098456
|
T | TCA | 312 | a0001c0001t0002g0313a0001c0001t0005g0004a0001c0001t0005g0267others(309): Show | 326 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(323): Show |
intron_variant | MODIFIER | c.865-424_865-423ins others(2): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098456 | ||||||
| chr12:42098760
|
C | CAT | 21 | a0001c0001t0005g0276a0001c0001t0005g0341a0001c0001t0007g0016others(18): Show | 22 | HG00642.hp1 HG00738.hp1 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.865-729_865-728dup others(2): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | ||||||
| chr12:42098760
|
C | CATAT | 23 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0269others(20): Show | 25 | HG00544.hp1 HG00597.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.865-731_865-728dup others(4): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | ||||||
| chr12:42098760
|
C | CATATAT | 9 | a0001c0001t0005g0268a0001c0001t0007g0357a0001c0001t0010g0024others(6): Show | 10 | HG01106.hp1 HG01496.hp1 HG03704.hp1 others(7): Show |
intron_variant | MODIFIER | c.865-733_865-728dup others(6): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | ||||||
| chr12:42098760
|
C | CATATATA others(1): Show |
11 | a0001c0001t0006g0245a0001c0001t0007g0349a0001c0001t0009g0257others(8): Show | 11 | HG00639.hp1 HG01081.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.865-735_865-728dup others(8): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | ||||||
| chr12:42098760
|
C | CATATATA others(3): Show |
11 | a0001c0001t0006g0244a0001c0001t0014g0233a0001c0002t0004g0033others(8): Show | 11 | HG01884.hp1 HG02258.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.865-737_865-728dup others(10): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | ||||||
| chr12:42098760
|
C | CATATATA others(5): Show |
28 | a0001c0001t0006g0011a0001c0001t0006g0012a0001c0001t0006g0013others(25): Show | 31 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.865-739_865-728dup others(12): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | ||||||
| chr12:42098760
|
C | CATATATA others(7): Show |
20 | a0001c0002t0003g0179a0001c0002t0004g0035a0001c0002t0004g0042others(17): Show | 20 | HG00733.hp1 HG01074.hp2 HG02129.hp2 others(17): Show |
intron_variant | MODIFIER | c.865-741_865-728dup others(14): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | ||||||
| chr12:42098760
|
C | CATATATA others(9): Show |
38 | a0001c0001t0006g0247a0001c0001t0006g0248a0001c0001t0006g0250others(35): Show | 40 | HG00438.hp1 HG00438.hp2 HG01975.hp1 others(37): Show |
intron_variant | MODIFIER | c.865-743_865-728dup others(16): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | ||||||
| chr12:42098760
|
C | CATATATA others(11): Show |
12 | a0001c0002t0003g0089a0001c0002t0003g0177a0001c0002t0003g0192others(9): Show | 12 | HG00323.hp2 HG00621.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.865-745_865-728dup others(18): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | ||||||
| chr12:42098760
|
C | CATATATA others(13): Show |
20 | a0001c0001t0010g0023a0001c0002t0003g0002a0001c0002t0003g0008others(17): Show | 24 | HG00408.hp2 HG00609.hp2 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.865-747_865-728dup others(20): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | ||||||
| chr12:42098760
|
C | CATATATA others(15): Show |
23 | a0001c0001t0010g0019a0001c0001t0014g0228a0001c0002t0003g0163others(20): Show | 23 | HG00544.hp2 HG00597.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.865-749_865-728dup others(22): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | ||||||
| chr12:42098760
|
C | CATATATA others(17): Show |
17 | a0001c0001t0009g0258a0001c0002t0003g0009a0001c0002t0003g0090others(14): Show | 18 | HG01099.hp1 HG01981.hp2 HG02004.hp1 others(15): Show |
intron_variant | MODIFIER | c.865-751_865-728dup others(24): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | ||||||
| chr12:42098760
|
C | CATATATA others(19): Show |
22 | a0001c0001t0009g0256a0001c0001t0014g0229a0001c0001t0014g0236others(19): Show | 22 | HG00099.hp2 HG01074.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.865-728_865-727ins others(26): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | ||||||
| chr12:42098760
|
C | CATATATA others(21): Show |
12 | a0001c0001t0010g0022a0001c0002t0003g0174a0001c0002t0003g0190others(9): Show | 12 | HG00140.hp1 HG01346.hp1 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.865-728_865-727ins others(28): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | ||||||
| chr12:42098760
|
C | CATATATA others(23): Show |
6 | a0001c0001t0009g0254a0001c0002t0003g0101a0001c0002t0003g0160others(3): Show | 6 | HG00609.hp1 HG00733.hp2 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.865-728_865-727ins others(30): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | ||||||
| chr12:42098760
|
C | CATATATA others(25): Show |
4 | a0001c0002t0003g0199a0001c0003t0001g0132a0001c0003t0001g0134others(1): Show | 4 | HG00738.hp2 HG02083.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.865-728_865-727ins others(32): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | ||||||
| chr12:42098760
|
C | CATATATA others(27): Show |
6 | a0001c0002t0003g0164a0001c0002t0004g0036a0001c0002t0004g0037others(3): Show | 6 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.865-728_865-727ins others(34): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | ||||||
| chr12:42098760
|
C | CATATATA others(29): Show |
1 | a0001c0002t0003g0188 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.865-728_865-727ins others(36): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | ||||||
| chr12:42098760
|
CAT | C | 61 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0014others(58): Show | 70 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.865-729_865-728del others(2): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | ||||||
| chr12:42098760
|
CATAT | C | 3 | a0001c0001t0002g0297a0001c0001t0027g0158a0001c0001t0027g0232 | 3 | HG00423.hp2 HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.865-731_865-728del others(4): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | ||||||
| chr12:42098760
|
CATATAT | C | 4 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.865-733_865-728del others(6): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | ||||||
| chr12:42098760
|
CATATATA others(3): Show |
C | 1 | a0001c0002t0003g0165 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.865-737_865-728del others(10): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | ||||||
| chr12:42098760
|
CATATATA others(11): Show |
C | 1 | a0001c0003t0001g0161 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.865-745_865-728del others(18): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098760 | ||||||
| chr12:42098762
|
T | TATATATA others(45): Show |
1 | a0001c0003t0001g0203 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.865-730_865-729ins others(52): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098762 | ||||||
| chr12:42098782
|
T | TAA | 3 | a0001c0001t0011g0094a0001c0001t0011g0095a0001c0001t0037g0096 | 3 | HG02717.hp1 HG02818.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.865-750_865-749ins others(2): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098782 | ||||||
| chr12:42098782
|
T | TATATATA others(13): Show |
1 | a0001c0003t0001g0153 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.865-750_865-749ins others(20): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098782 | ||||||
| chr12:42098784
|
T | A | 10 | a0001c0001t0002g0310a0001c0001t0002g0326a0001c0001t0011g0094others(7): Show | 10 | HG01169.hp1 HG01256.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.865-751A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098784 | ||||||
| chr12:42098784
|
T | TATATATA others(3): Show |
1 | a0001c0001t0043g0093 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.865-752_865-751ins others(10): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098784 | ||||||
| chr12:42098784
|
T | TATATATA others(3): Show |
2 | a0001c0001t0011g0265a0001c0001t0011g0266 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.865-752_865-751ins others(10): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098784 | ||||||
| chr12:42098784
|
T | TATATATA others(8): Show |
1 | a0001c0002t0003g0189 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.865-752_865-751ins others(15): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42098784 | ||||||
| chr12:42099009
|
G | T | 1 | a0001c0001t0002g0320 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.865-976C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42099009 | ||||||
| chr12:42099102
|
C | G | 1 | a0001c0003t0001g0223 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.865-1069G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42099102 | ||||||
| chr12:42099159
|
T | C | 1 | a0001c0001t0002g0302 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.865-1126A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42099159 | ||||||
| chr12:42099619
|
G | A | 2 | a0001c0001t0022g0240a0001c0001t0022g0241 | 2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.865-1586C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42099619 | ||||||
| chr12:42099651
|
G | A | 2 | a0001c0003t0001g0161a0001c0006t0056g0375 | 2 | HG01192.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.865-1618C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42099651 | ||||||
| chr12:42099710
|
C | A | 1 | a0001c0005t0004g0006 | 2 | HG01106.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.865-1677G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42099710 | ||||||
| chr12:42099875
|
T | C | 3 | a0001c0003t0001g0220a0001c0003t0001g0221a0001c0003t0001g0222 | 3 | HG01099.hp1 HG01515.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.865-1842A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42099875 | ||||||
| chr12:42100151
|
A | G | 28 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(25): Show | 30 | HG00544.hp1 HG00597.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.865-2118T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42100151 | ||||||
| chr12:42100264
|
T | G | 7 | a0001c0001t0012g0345a0001c0001t0012g0350a0001c0001t0012g0352others(4): Show | 7 | NA18946.hp1 NA18957.hp1 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.865-2231A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42100264 | ||||||
| chr12:42100314
|
A | T | 1 | a0001c0003t0001g0220 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.865-2281T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42100314 | ||||||
| chr12:42100429
|
T | C | 51 | a0001c0001t0006g0011a0001c0001t0006g0012a0001c0001t0006g0013others(48): Show | 55 | HG00423.hp1 HG00639.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.865-2396A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42100429 | ||||||
| chr12:42100440
|
T | C | 1 | a0001c0001t0014g0236 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.865-2407A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42100440 | ||||||
| chr12:42100554
|
GA | G | 6 | a0001c0001t0009g0003a0001c0001t0009g0254a0001c0001t0009g0255others(3): Show | 8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.865-2522delT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42100554 | ||||||
| chr12:42100655
|
A | T | 6 | a0001c0001t0009g0003a0001c0001t0009g0254a0001c0001t0009g0255others(3): Show | 8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.865-2622T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42100655 | ||||||
| chr12:42100704
|
A | C | 1 | a0001c0005t0004g0006 | 2 | HG01106.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.865-2671T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42100704 | ||||||
| chr12:42100886
|
TATACACA others(3): Show |
T | 20 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(17): Show | 22 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(19): Show |
intron_variant | MODIFIER | c.865-2863_865-2854d others(12): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42100886 | ||||||
| chr12:42101098
|
C | T | 1 | a0001c0001t0002g0305 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.865-3065G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42101098 | ||||||
| chr12:42101125
|
A | G | 1 | a0001c0003t0001g0155 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.865-3092T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42101125 | ||||||
| chr12:42101303
|
G | C | 1 | a0001c0003t0001g0153 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.865-3270C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42101303 | ||||||
| chr12:42101324
|
G | A | 2 | a0001c0001t0011g0260a0001c0001t0011g0261 | 2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.865-3291C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42101324 | ||||||
| chr12:42101459
|
A | G | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.865-3426T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42101459 | ||||||
| chr12:42101562
|
T | C | 1 | a0001c0003t0001g0121 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.865-3529A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42101562 | ||||||
| chr12:42101575
|
C | CT | 6 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086others(3): Show | 6 | HG02630.hp2 HG02717.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.865-3543dupA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42101575 | ||||||
| chr12:42101575
|
CT | C | 34 | a0001c0001t0005g0274a0001c0001t0007g0016a0001c0001t0007g0344others(31): Show | 35 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.865-3543delA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42101575 | ||||||
| chr12:42101582
|
T | A | 1 | a0001c0002t0003g0195 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.865-3549A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42101582 | ||||||
| chr12:42101585
|
T | A | 1 | a0001c0001t0014g0229 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.865-3552A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42101585 | ||||||
| chr12:42101657
|
C | T | 1 | a0001c0001t0014g0229 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.865-3624G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42101657 | ||||||
| chr12:42101696
|
C | T | 2 | a0001c0001t0018g0263a0001c0001t0018g0264 | 2 | HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.865-3663G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42101696 | ||||||
| chr12:42101728
|
T | C | 1 | a0001c0002t0025g0097 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.865-3695A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42101728 | ||||||
| chr12:42101873
|
CAAAATGC others(7): Show |
C | 17 | a0001c0001t0006g0011a0001c0001t0006g0012a0001c0001t0006g0013others(14): Show | 20 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.865-3854_865-3841d others(16): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42101873 | ||||||
| chr12:42102022
|
C | T | 3 | a0001c0001t0008g0366a0001c0001t0008g0368a0001c0001t0008g0370 | 3 | HG00642.hp1 HG01069.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.864+3796G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42102022 | ||||||
| chr12:42102114
|
A | C | 5 | a0001c0003t0013g0150a0001c0003t0013g0151a0001c0003t0013g0152others(2): Show | 5 | HG03239.hp1 HG03654.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.864+3704T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42102114 | ||||||
| chr12:42102175
|
T | C | 208 | a0001c0002t0003g0002a0001c0002t0003g0008a0001c0002t0003g0009others(205): Show | 214 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.864+3643A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42102175 | ||||||
| chr12:42102238
|
T | C | 2 | a0001c0002t0025g0097a0001c0002t0025g0098 | 2 | HG02071.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.864+3580A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42102238 | ||||||
| chr12:42102256
|
C | G | 5 | a0001c0002t0004g0029a0001c0002t0004g0063a0001c0002t0004g0064others(2): Show | 5 | NA18957.hp2 NA18959.hp1 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.864+3562G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42102256 | ||||||
| chr12:42102270
|
T | C | 1 | a0001c0001t0012g0359 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.864+3548A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42102270 | ||||||
| chr12:42102389
|
C | T | 11 | a0001c0003t0001g0099a0001c0003t0001g0110a0001c0003t0001g0115others(8): Show | 11 | NA18948.hp2 NA18952.hp1 NA18983.hp1 others(8): Show |
intron_variant | MODIFIER | c.864+3429G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42102389 | ||||||
| chr12:42102401
|
T | G | 10 | a0001c0003t0001g0203a0001c0003t0001g0208a0001c0003t0001g0209others(7): Show | 10 | HG01099.hp1 HG01515.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.864+3417A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42102401 | ||||||
| chr12:42102436
|
A | G | 28 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(25): Show | 30 | HG00544.hp1 HG00597.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.864+3382T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42102436 | ||||||
| chr12:42102486
|
G | C | 3 | a0001c0002t0020g0026a0001c0002t0020g0027a0001c0002t0034g0025 | 3 | HG02055.hp2 HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.864+3332C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42102486 | ||||||
| chr12:42102500
|
A | G | 1 | a0001c0006t0056g0375 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.864+3318T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42102500 | ||||||
| chr12:42102840
|
A | G | 1 | a0001c0003t0001g0131 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.864+2978T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42102840 | ||||||
| chr12:42102880
|
G | A | 1 | a0001c0001t0002g0335 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.864+2938C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42102880 | ||||||
| chr12:42102891
|
TATTTA | T | 5 | a0001c0001t0017g0234a0001c0001t0017g0235a0001c0001t0017g0242others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.864+2922_864+2926d others(7): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42102891 | ||||||
| chr12:42102949
|
T | A | 3 | a0001c0002t0003g0192a0001c0002t0003g0197a0001c0002t0003g0201 | 3 | HG00621.hp1 NA19067.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.864+2869A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42102949 | ||||||
| chr12:42103061
|
A | G | 1 | a0001c0003t0001g0161 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.864+2757T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42103061 | ||||||
| chr12:42103062
|
G | C | 17 | a0001c0001t0006g0011a0001c0001t0006g0012a0001c0001t0006g0013others(14): Show | 20 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.864+2756C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42103062 | ||||||
| chr12:42103111
|
C | G | 1 | a0001c0001t0002g0286 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.864+2707G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42103111 | ||||||
| chr12:42103211
|
G | A | 32 | a0001c0001t0007g0016a0001c0001t0007g0344a0001c0001t0007g0346others(29): Show | 33 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.864+2607C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42103211 | ||||||
| chr12:42103239
|
G | A | 1 | a0001c0001t0012g0356 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.864+2579C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42103239 | ||||||
| chr12:42103266
|
A | T | 1 | a0001c0002t0004g0045 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.864+2552T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42103266 | ||||||
| chr12:42103303
|
G | A | 6 | a0001c0001t0026g0299a0001c0001t0026g0323a0001c0001t0027g0158others(3): Show | 6 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.864+2515C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42103303 | ||||||
| chr12:42103318
|
A | G | 312 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(309): Show | 326 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(323): Show |
intron_variant | MODIFIER | c.864+2500T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42103318 | ||||||
| chr12:42103322
|
A | G | 317 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(314): Show | 331 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(328): Show |
intron_variant | MODIFIER | c.864+2496T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42103322 | ||||||
| chr12:42103350
|
T | C | 11 | a0001c0001t0006g0011a0001c0001t0006g0012a0001c0001t0006g0013others(8): Show | 14 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.864+2468A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42103350 | ||||||
| chr12:42103581
|
T | C | 2 | a0001c0001t0022g0240a0001c0001t0022g0241 | 2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.864+2237A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42103581 | ||||||
| chr12:42104025
|
G | A | 7 | a0001c0002t0015g0183a0001c0002t0015g0184a0001c0002t0015g0200others(4): Show | 7 | HG00140.hp1 HG01346.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.864+1793C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42104025 | ||||||
| chr12:42104081
|
C | T | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.864+1737G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42104081 | ||||||
| chr12:42104254
|
C | CT | 25 | a0001c0001t0007g0016a0001c0001t0007g0344a0001c0001t0007g0346others(22): Show | 26 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.864+1563_864+1564i others(3): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42104254 | ||||||
| chr12:42104254
|
C | CTT | 7 | a0001c0001t0012g0345a0001c0001t0012g0350a0001c0001t0012g0352others(4): Show | 7 | NA18946.hp1 NA18957.hp1 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.864+1563_864+1564i others(4): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42104254 | ||||||
| chr12:42104255
|
A | AT | 254 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(251): Show | 262 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.864+1562dupA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42104255 | ||||||
| chr12:42104255
|
A | ATT | 20 | a0001c0001t0006g0011a0001c0001t0006g0012a0001c0001t0006g0013others(17): Show | 23 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.864+1561_864+1562d others(4): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42104255 | ||||||
| chr12:42104255
|
A | T | 32 | a0001c0001t0007g0016a0001c0001t0007g0344a0001c0001t0007g0346others(29): Show | 33 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.864+1563T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42104255 | ||||||
| chr12:42104298
|
A | G | 9 | a0001c0001t0002g0005a0001c0001t0002g0288a0001c0001t0002g0290others(6): Show | 11 | HG01496.hp2 HG01928.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.864+1520T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42104298 | ||||||
| chr12:42104435
|
G | C | 1 | a0001c0001t0002g0338 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.864+1383C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42104435 | ||||||
| chr12:42104557
|
TA | T | 297 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(294): Show | 311 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.864+1260delT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42104557 | ||||||
| chr12:42104598
|
A | G | 312 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(309): Show | 326 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(323): Show |
intron_variant | MODIFIER | c.864+1220T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42104598 | ||||||
| chr12:42104672
|
GC | G | 3 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0157 | 3 | NA18953.hp1 NA18972.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.864+1145delG | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42104672 | ||||||
| chr12:42104779
|
G | A | 1 | a0001c0001t0002g0292 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.864+1039C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42104779 | ||||||
| chr12:42105146
|
C | T | 1 | a0001c0003t0001g0132 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.864+672G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42105146 | ||||||
| chr12:42105156
|
A | G | 2 | a0001c0001t0021g0230a0001c0001t0021g0231 | 2 | HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.864+662T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42105156 | ||||||
| chr12:42105274
|
A | C | 1 | a0001c0002t0031g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.864+544T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42105274 | ||||||
| chr12:42105280
|
G | C | 1 | a0001c0003t0001g0115 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.864+538C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42105280 | ||||||
| chr12:42105405
|
AT | A | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.864+412delA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42105405 | ||||||
| chr12:42105412
|
G | A | 1 | a0001c0001t0014g0236 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.864+406C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42105412 | ||||||
| chr12:42105553
|
G | C | 1 | a0001c0001t0043g0093 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.864+265C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42105553 | ||||||
| chr12:42105593
|
C | T | 312 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(309): Show | 326 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(323): Show |
intron_variant | MODIFIER | c.864+225G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42105593 | ||||||
| chr12:42105599
|
T | C | 1 | a0001c0002t0003g0251 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.864+219A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42105599 | ||||||
| chr12:42105670
|
C | G | 2 | a0001c0001t0009g0003a0001c0001t0009g0255 | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.864+148G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42105670 | ||||||
| chr12:42105736
|
T | A | 208 | a0001c0002t0003g0002a0001c0002t0003g0008a0001c0002t0003g0009others(205): Show | 214 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.864+82A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42105736 | ||||||
| chr12:42105737
|
T | C | 208 | a0001c0002t0003g0002a0001c0002t0003g0008a0001c0002t0003g0009others(205): Show | 214 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.864+81A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 5/7 | chr12 | 42105737 | ||||||
| chr12:42106207
|
C | T | 6 | a0001c0001t0009g0003a0001c0001t0009g0254a0001c0001t0009g0255others(3): Show | 8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.613-138G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42106207 | ||||||
| chr12:42106212
|
A | G | 1 | a0001c0006t0056g0375 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.613-143T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42106212 | ||||||
| chr12:42106255
|
C | T | 2 | a0001c0001t0053g0354a0002c0004t0051g0342 | 2 | HG02809.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.613-186G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42106255 | ||||||
| chr12:42106388
|
G | C | 2 | a0001c0001t0022g0240a0001c0001t0022g0241 | 2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.613-319C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42106388 | ||||||
| chr12:42106408
|
C | G | 1 | a0001c0002t0004g0060 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.613-339G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42106408 | ||||||
| chr12:42106520
|
T | C | 22 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(19): Show | 24 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(21): Show |
intron_variant | MODIFIER | c.613-451A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42106520 | ||||||
| chr12:42106692
|
T | C | 6 | a0001c0001t0009g0003a0001c0001t0009g0254a0001c0001t0009g0255others(3): Show | 8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.613-623A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42106692 | ||||||
| chr12:42106742
|
T | C | 1 | a0001c0001t0014g0236 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.613-673A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42106742 | ||||||
| chr12:42106743
|
C | CT | 19 | a0001c0001t0002g0284a0001c0001t0002g0286a0001c0001t0002g0289others(16): Show | 19 | HG01192.hp1 HG02055.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.613-675dupA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42106743 | ||||||
| chr12:42106743
|
C | T | 1 | a0001c0001t0014g0236 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.613-674G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42106743 | ||||||
| chr12:42106743
|
CT | C | 10 | a0001c0001t0002g0309a0001c0001t0006g0243a0001c0001t0014g0228others(7): Show | 10 | HG01515.hp2 HG01884.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.613-675delA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42106743 | ||||||
| chr12:42106748
|
T | C | 33 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(30): Show | 35 | HG00544.hp1 HG00597.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.613-679A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42106748 | ||||||
| chr12:42106808
|
T | G | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.613-739A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42106808 | ||||||
| chr12:42106855
|
C | T | 2 | a0001c0002t0004g0036a0001c0002t0004g0037 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.613-786G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42106855 | ||||||
| chr12:42106907
|
G | A | 1 | a0001c0001t0014g0233 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.613-838C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42106907 | ||||||
| chr12:42106985
|
G | A | 1 | a0001c0001t0014g0236 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.613-916C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42106985 | ||||||
| chr12:42107028
|
C | T | 1 | a0001c0002t0004g0045 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.613-959G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42107028 | ||||||
| chr12:42107029
|
G | A | 1 | a0001c0002t0034g0025 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.613-960C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42107029 | ||||||
| chr12:42107115
|
C | T | 1 | a0001c0003t0042g0113 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.613-1046G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42107115 | ||||||
| chr12:42107344
|
C | T | 312 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(309): Show | 326 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(323): Show |
intron_variant | MODIFIER | c.613-1275G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42107344 | ||||||
| chr12:42107438
|
C | T | 28 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(25): Show | 30 | HG00544.hp1 HG00597.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.613-1369G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42107438 | ||||||
| chr12:42107461
|
C | T | 1 | a0001c0003t0001g0127 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.613-1392G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42107461 | ||||||
| chr12:42107471
|
A | G | 244 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(241): Show | 258 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(255): Show |
intron_variant | MODIFIER | c.613-1402T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42107471 | ||||||
| chr12:42107808
|
C | G | 1 | a0001c0002t0004g0074 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.613-1739G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42107808 | ||||||
| chr12:42107838
|
G | C | 1 | a0001c0002t0050g0159 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.612+1728C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42107838 | ||||||
| chr12:42107881
|
C | A | 1 | a0001c0002t0004g0045 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.612+1685G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42107881 | ||||||
| chr12:42108043
|
AT | A | 3 | a0001c0001t0014g0228a0001c0001t0014g0229a0001c0001t0014g0233 | 3 | HG01884.hp1 HG02280.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.612+1522delA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42108043 | ||||||
| chr12:42108200
|
C | T | 32 | a0001c0001t0007g0016a0001c0001t0007g0344a0001c0001t0007g0346others(29): Show | 33 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.612+1366G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42108200 | ||||||
| chr12:42108255
|
G | C | 1 | a0001c0003t0001g0161 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.612+1311C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42108255 | ||||||
| chr12:42108320
|
T | C | 26 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(23): Show | 28 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(25): Show |
intron_variant | MODIFIER | c.612+1246A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42108320 | ||||||
| chr12:42108489
|
A | ACC | 4 | a0001c0001t0026g0299a0001c0001t0026g0323a0001c0001t0028g0328others(1): Show | 4 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.612+1076_612+1077i others(4): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42108489 | ||||||
| chr12:42108757
|
T | A | 85 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0104others(82): Show | 85 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.612+809A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42108757 | ||||||
| chr12:42108817
|
G | A | 6 | a0001c0001t0026g0299a0001c0001t0026g0323a0001c0001t0027g0158others(3): Show | 6 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.612+749C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42108817 | ||||||
| chr12:42108980
|
C | T | 6 | a0001c0001t0009g0003a0001c0001t0009g0254a0001c0001t0009g0255others(3): Show | 8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.612+586G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42108980 | ||||||
| chr12:42108993
|
T | C | 1 | a0001c0001t0010g0024 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.612+573A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42108993 | ||||||
| chr12:42109232
|
G | A | 7 | a0001c0001t0005g0277a0001c0001t0026g0299a0001c0001t0026g0323others(4): Show | 7 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.612+334C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42109232 | ||||||
| chr12:42109309
|
C | T | 1 | a0001c0002t0004g0063 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.612+257G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42109309 | ||||||
| chr12:42109452
|
C | T | 321 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0301others(318): Show | 335 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.612+114G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42109452 | ||||||
| chr12:42109523
|
T | A | 17 | a0001c0001t0006g0011a0001c0001t0006g0012a0001c0001t0006g0013others(14): Show | 20 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.612+43A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42109523 | ||||||
| chr12:42109523
|
T | TA | 7 | a0001c0001t0011g0095a0001c0001t0014g0233a0001c0001t0037g0096others(4): Show | 7 | HG01884.hp1 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.612+42dupT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42109523 | ||||||
| chr12:42109523
|
TA | T | 35 | a0001c0001t0002g0285a0001c0001t0002g0324a0001c0001t0002g0334others(32): Show | 35 | HG00323.hp2 HG01070.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.612+42delT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 4/7 | chr12 | 42109523 | ||||||
| chr12:42109702
|
T | TA | 32 | a0001c0001t0007g0016a0001c0001t0007g0344a0001c0001t0007g0346others(29): Show | 33 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.487-12_487-11insT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42109702 | ||||||
| chr12:42109703
|
T | A | 373 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0014others(370): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.487-12A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42109703 | ||||||
| chr12:42109798
|
C | T | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.487-107G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42109798 | ||||||
| chr12:42109838
|
C | T | 1 | a0001c0002t0004g0082 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.487-147G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42109838 | ||||||
| chr12:42109927
|
C | A | 6 | a0001c0001t0007g0016a0001c0001t0007g0346a0001c0001t0007g0347others(3): Show | 7 | HG00738.hp1 HG02647.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.487-236G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42109927 | ||||||
| chr12:42109933
|
C | A | 3 | a0001c0001t0018g0262a0001c0001t0018g0263a0001c0001t0018g0264 | 3 | HG02922.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.487-242G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42109933 | ||||||
| chr12:42109992
|
C | A | 208 | a0001c0002t0003g0002a0001c0002t0003g0008a0001c0002t0003g0009others(205): Show | 214 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.487-301G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42109992 | ||||||
| chr12:42110142
|
G | C | 208 | a0001c0002t0003g0002a0001c0002t0003g0008a0001c0002t0003g0009others(205): Show | 214 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.487-451C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42110142 | ||||||
| chr12:42110145
|
T | C | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.487-454A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42110145 | ||||||
| chr12:42110195
|
T | C | 5 | a0001c0001t0014g0228a0001c0001t0014g0229a0001c0001t0014g0233others(2): Show | 5 | HG01884.hp1 HG02280.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.487-504A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42110195 | ||||||
| chr12:42110198
|
C | T | 2 | a0001c0001t0011g0265a0001c0001t0011g0266 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.487-507G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42110198 | ||||||
| chr12:42110270
|
C | A | 1 | a0001c0002t0003g0181 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.487-579G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42110270 | ||||||
| chr12:42110395
|
G | A | 2 | a0001c0001t0024g0226a0001c0001t0024g0227 | 2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.487-704C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42110395 | ||||||
| chr12:42110396
|
A | G | 1 | a0001c0002t0003g0190 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.487-705T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42110396 | ||||||
| chr12:42110523
|
T | C | 2 | a0001c0001t0011g0265a0001c0001t0011g0266 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.487-832A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42110523 | ||||||
| chr12:42110553
|
T | G | 4 | a0001c0001t0011g0094a0001c0001t0011g0095a0001c0001t0037g0096others(1): Show | 4 | HG02717.hp1 HG02818.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.487-862A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42110553 | ||||||
| chr12:42110633
|
T | C | 85 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0104others(82): Show | 85 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.487-942A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42110633 | ||||||
| chr12:42110681
|
G | A | 1 | a0001c0001t0014g0233 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.487-990C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42110681 | ||||||
| chr12:42110765
|
T | G | 2 | a0001c0001t0011g0265a0001c0001t0011g0266 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.487-1074A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42110765 | ||||||
| chr12:42110877
|
T | G | 123 | a0001c0002t0003g0002a0001c0002t0003g0008a0001c0002t0003g0009others(120): Show | 129 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.487-1186A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42110877 | ||||||
| chr12:42111051
|
T | C | 1 | a0001c0006t0056g0375 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.487-1360A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111051 | ||||||
| chr12:42111181
|
G | A | 2 | a0001c0001t0011g0265a0001c0001t0011g0266 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.487-1490C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111181 | ||||||
| chr12:42111185
|
G | A | 26 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(23): Show | 28 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(25): Show |
intron_variant | MODIFIER | c.487-1494C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111185 | ||||||
| chr12:42111185
|
G | T | 1 | a0001c0002t0003g0195 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.487-1494C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111185 | ||||||
| chr12:42111198
|
G | A | 3 | a0001c0001t0014g0228a0001c0001t0014g0229a0001c0001t0014g0233 | 3 | HG01884.hp1 HG02280.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.487-1507C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111198 | ||||||
| chr12:42111215
|
C | G | 6 | a0001c0001t0009g0003a0001c0001t0009g0254a0001c0001t0009g0255others(3): Show | 8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.487-1524G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111215 | ||||||
| chr12:42111247
|
G | A | 2 | a0001c0001t0009g0258a0001c0001t0016g0085 | 2 | HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.487-1556C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111247 | ||||||
| chr12:42111259
|
C | A | 1 | a0001c0001t0002g0339 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.487-1568G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111259 | ||||||
| chr12:42111289
|
A | T | 1 | a0002c0004t0051g0342 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.487-1598T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111289 | ||||||
| chr12:42111291
|
T | A | 3 | a0001c0001t0007g0346a0001c0001t0007g0351a0001c0001t0007g0353 | 3 | HG00738.hp1 HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.487-1600A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111291 | ||||||
| chr12:42111305
|
C | T | 1 | a0001c0003t0001g0153 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.487-1614G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111305 | ||||||
| chr12:42111309
|
C | T | 208 | a0001c0002t0003g0002a0001c0002t0003g0008a0001c0002t0003g0009others(205): Show | 214 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.487-1618G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111309 | ||||||
| chr12:42111321
|
C | T | 1 | a0001c0001t0002g0315 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.487-1630G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111321 | ||||||
| chr12:42111434
|
T | A | 10 | a0001c0001t0009g0003a0001c0001t0009g0254a0001c0001t0009g0255others(7): Show | 12 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.487-1743A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111434 | ||||||
| chr12:42111440
|
G | A | 3 | a0001c0001t0005g0272a0001c0001t0005g0280a0001c0001t0005g0331 | 3 | NA18994.hp2 NA19058.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.487-1749C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111440 | ||||||
| chr12:42111546
|
C | T | 1 | a0001c0006t0056g0375 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.487-1855G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111546 | ||||||
| chr12:42111559
|
C | T | 1 | a0001c0002t0004g0060 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.487-1868G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111559 | ||||||
| chr12:42111582
|
C | A | 312 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(309): Show | 326 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(323): Show |
intron_variant | MODIFIER | c.487-1891G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111582 | ||||||
| chr12:42111603
|
G | A | 1 | a0001c0001t0014g0236 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.487-1912C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111603 | ||||||
| chr12:42111644
|
G | A | 7 | a0001c0001t0002g0321a0001c0001t0024g0226a0001c0001t0024g0227others(4): Show | 7 | HG01169.hp1 HG01517.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.487-1953C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111644 | ||||||
| chr12:42111659
|
C | A | 1 | a0001c0002t0003g0170 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.487-1968G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111659 | ||||||
| chr12:42111702
|
T | G | 3 | a0001c0001t0018g0262a0001c0001t0018g0263a0001c0001t0018g0264 | 3 | HG02922.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.487-2011A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111702 | ||||||
| chr12:42111717
|
C | T | 2 | a0001c0001t0027g0158a0001c0001t0027g0232 | 2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.487-2026G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111717 | ||||||
| chr12:42111718
|
G | A | 3 | a0001c0001t0017g0234a0001c0001t0017g0235a0001c0001t0017g0242 | 3 | HG02451.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.487-2027C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111718 | ||||||
| chr12:42111725
|
CAA | C | 8 | a0001c0002t0004g0054a0001c0002t0004g0069a0001c0002t0004g0070others(5): Show | 8 | HG02083.hp1 NA18944.hp2 NA18990.hp2 others(5): Show |
intron_variant | MODIFIER | c.487-2036_487-2035d others(4): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111725 | ||||||
| chr12:42111748
|
C | T | 2 | a0001c0001t0022g0240a0001c0001t0022g0241 | 2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.487-2057G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111748 | ||||||
| chr12:42111773
|
G | A | 6 | a0001c0001t0014g0228a0001c0001t0014g0229a0001c0001t0014g0233others(3): Show | 6 | HG01884.hp1 HG02280.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.487-2082C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111773 | ||||||
| chr12:42111794
|
C | T | 1 | a0001c0001t0002g0288 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.487-2103G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111794 | ||||||
| chr12:42111803
|
C | T | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.487-2112G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111803 | ||||||
| chr12:42111804
|
G | A | 1 | a0001c0001t0002g0339 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.487-2113C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111804 | ||||||
| chr12:42111813
|
G | C | 84 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0104others(81): Show | 84 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.487-2122C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111813 | ||||||
| chr12:42111823
|
C | T | 1 | a0001c0001t0014g0236 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.487-2132G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111823 | ||||||
| chr12:42111824
|
G | A | 1 | a0001c0002t0046g0182 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.487-2133C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111824 | ||||||
| chr12:42111860
|
T | C | 217 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086others(214): Show | 223 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.487-2169A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111860 | ||||||
| chr12:42111884
|
C | G | 1 | a0001c0002t0034g0025 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.487-2193G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111884 | ||||||
| chr12:42111913
|
C | T | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.487-2222G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111913 | ||||||
| chr12:42111914
|
A | G | 223 | a0001c0001t0014g0228a0001c0001t0014g0229a0001c0001t0014g0233others(220): Show | 229 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.487-2223T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111914 | ||||||
| chr12:42111935
|
A | G | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.487-2244T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111935 | ||||||
| chr12:42111972
|
G | T | 2 | a0001c0001t0011g0265a0001c0001t0011g0266 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.487-2281C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42111972 | ||||||
| chr12:42112019
|
G | A | 10 | a0001c0001t0009g0003a0001c0001t0009g0254a0001c0001t0009g0255others(7): Show | 12 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.487-2328C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112019 | ||||||
| chr12:42112044
|
TAGCAAAC others(21): Show |
T | 1 | a0001c0005t0004g0006 | 2 | HG01106.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.487-2381_487-2354d others(30): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112044 | ||||||
| chr12:42112157
|
C | A | 1 | a0001c0001t0002g0310 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.487-2466G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112157 | ||||||
| chr12:42112277
|
G | C | 6 | a0001c0001t0010g0019a0001c0001t0010g0020a0001c0001t0010g0021others(3): Show | 6 | HG03704.hp1 HG03831.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.487-2586C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112277 | ||||||
| chr12:42112346
|
G | C | 1 | a0001c0002t0047g0185 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.487-2655C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112346 | ||||||
| chr12:42112363
|
G | A | 23 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(20): Show | 25 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(22): Show |
intron_variant | MODIFIER | c.487-2672C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112363 | ||||||
| chr12:42112380
|
A | G | 9 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086others(6): Show | 9 | HG01169.hp1 HG02109.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.487-2689T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112380 | ||||||
| chr12:42112468
|
C | T | 6 | a0001c0001t0007g0016a0001c0001t0007g0346a0001c0001t0007g0347others(3): Show | 7 | HG00738.hp1 HG02647.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.487-2777G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112468 | ||||||
| chr12:42112513
|
A | G | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.487-2822T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112513 | ||||||
| chr12:42112517
|
C | T | 6 | a0001c0002t0003g0087a0001c0002t0003g0088a0001c0002t0003g0089others(3): Show | 6 | HG01175.hp2 HG01884.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.487-2826G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112517 | ||||||
| chr12:42112609
|
C | T | 32 | a0001c0001t0007g0016a0001c0001t0007g0344a0001c0001t0007g0346others(29): Show | 33 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.487-2918G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112609 | ||||||
| chr12:42112610
|
G | A | 10 | a0001c0001t0009g0003a0001c0001t0009g0254a0001c0001t0009g0255others(7): Show | 12 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.487-2919C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112610 | ||||||
| chr12:42112647
|
G | C | 6 | a0001c0001t0026g0299a0001c0001t0026g0323a0001c0001t0027g0158others(3): Show | 6 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.487-2956C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112647 | ||||||
| chr12:42112684
|
C | T | 1 | a0001c0003t0001g0208 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.487-2993G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112684 | ||||||
| chr12:42112686
|
G | C | 1 | a0001c0003t0001g0208 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.487-2995C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112686 | ||||||
| chr12:42112687
|
A | G | 1 | a0001c0003t0001g0208 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.487-2996T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112687 | ||||||
| chr12:42112735
|
GAACTTCC others(1139): Show |
G | 10 | a0001c0001t0009g0003a0001c0001t0009g0254a0001c0001t0009g0255others(7): Show | 12 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.487-4190_487-3045d others(2): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112735 | ||||||
| chr12:42112898
|
T | A | 9 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086others(6): Show | 9 | HG01169.hp1 HG02109.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.487-3207A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112898 | ||||||
| chr12:42112949
|
A | C | 2 | a0001c0001t0010g0021a0001c0001t0010g0024 | 2 | HG03704.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.487-3258T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112949 | ||||||
| chr12:42112996
|
T | A | 217 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086others(214): Show | 223 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.487-3305A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42112996 | ||||||
| chr12:42113016
|
A | T | 19 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(16): Show | 21 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(18): Show |
intron_variant | MODIFIER | c.487-3325T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113016 | ||||||
| chr12:42113090
|
T | G | 1 | a0001c0002t0004g0045 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.487-3399A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113090 | ||||||
| chr12:42113113
|
A | T | 1 | a0001c0003t0001g0208 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.487-3422T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113113 | ||||||
| chr12:42113151
|
C | T | 208 | a0001c0002t0003g0002a0001c0002t0003g0008a0001c0002t0003g0009others(205): Show | 214 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.487-3460G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113151 | ||||||
| chr12:42113168
|
A | C | 2 | a0001c0001t0011g0265a0001c0001t0011g0266 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.487-3477T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113168 | ||||||
| chr12:42113201
|
A | G | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.487-3510T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113201 | ||||||
| chr12:42113220
|
G | C | 217 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086others(214): Show | 223 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.487-3529C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113220 | ||||||
| chr12:42113251
|
G | A | 1 | a0001c0002t0003g0173 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.487-3560C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113251 | ||||||
| chr12:42113315
|
C | A | 2 | a0001c0001t0007g0351a0001c0001t0007g0353 | 2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.487-3624G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113315 | ||||||
| chr12:42113326
|
C | A | 5 | a0001c0001t0017g0234a0001c0001t0017g0235a0001c0001t0017g0242others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.487-3635G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113326 | ||||||
| chr12:42113390
|
T | C | 1 | a0001c0001t0007g0349 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.487-3699A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113390 | ||||||
| chr12:42113393
|
C | T | 1 | a0001c0001t0002g0297 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.487-3702G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113393 | ||||||
| chr12:42113400
|
A | G | 2 | a0001c0001t0022g0240a0001c0001t0022g0241 | 2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.487-3709T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113400 | ||||||
| chr12:42113499
|
A | G | 22 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(19): Show | 24 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(21): Show |
intron_variant | MODIFIER | c.487-3808T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113499 | ||||||
| chr12:42113522
|
G | A | 1 | a0001c0001t0006g0250 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.487-3831C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113522 | ||||||
| chr12:42113556
|
C | G | 4 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086others(1): Show | 4 | HG02040.hp1 HG02630.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.487-3865G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113556 | ||||||
| chr12:42113556
|
C | T | 1 | a0001c0002t0003g0164 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.487-3865G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113556 | ||||||
| chr12:42113624
|
T | G | 2 | a0001c0001t0007g0344a0001c0001t0052g0343 | 2 | HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.487-3933A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113624 | ||||||
| chr12:42113637
|
C | T | 12 | a0001c0001t0006g0011a0001c0001t0006g0012a0001c0001t0006g0013others(9): Show | 15 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.487-3946G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113637 | ||||||
| chr12:42113672
|
C | CAAT | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.487-3984_487-3982d others(5): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113672 | ||||||
| chr12:42113678
|
T | A | 32 | a0001c0001t0007g0016a0001c0001t0007g0344a0001c0001t0007g0346others(29): Show | 33 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.487-3987A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113678 | ||||||
| chr12:42113699
|
T | C | 1 | a0001c0002t0004g0062 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.487-4008A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113699 | ||||||
| chr12:42113707
|
T | C | 45 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(42): Show | 47 | HG00544.hp1 HG00597.hp1 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.487-4016A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113707 | ||||||
| chr12:42113712
|
C | A | 14 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086others(11): Show | 14 | HG02630.hp2 HG03098.hp1 HG03453.hp1 others(11): Show |
intron_variant | MODIFIER | c.487-4021G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113712 | ||||||
| chr12:42113740
|
G | A | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.487-4049C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113740 | ||||||
| chr12:42113775
|
G | A | 2 | a0001c0001t0022g0240a0001c0001t0022g0241 | 2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.487-4084C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113775 | ||||||
| chr12:42113887
|
T | C | 10 | a0001c0001t0009g0003a0001c0001t0009g0254a0001c0001t0009g0255others(7): Show | 12 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.487-4196A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113887 | ||||||
| chr12:42113899
|
T | C | 10 | a0001c0001t0009g0003a0001c0001t0009g0254a0001c0001t0009g0255others(7): Show | 12 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.487-4208A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113899 | ||||||
| chr12:42113917
|
A | G | 5 | a0001c0001t0014g0228a0001c0001t0014g0229a0001c0001t0014g0233others(2): Show | 5 | HG01884.hp1 HG02280.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.487-4226T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113917 | ||||||
| chr12:42113959
|
C | T | 1 | a0001c0001t0005g0269 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.487-4268G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113959 | ||||||
| chr12:42113987
|
A | G | 15 | a0001c0001t0007g0348a0001c0001t0007g0349a0001c0001t0007g0357others(12): Show | 17 | HG00639.hp1 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.487-4296T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113987 | ||||||
| chr12:42113996
|
C | T | 1 | a0001c0002t0004g0045 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.487-4305G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42113996 | ||||||
| chr12:42114061
|
A | G | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.487-4370T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114061 | ||||||
| chr12:42114084
|
G | T | 32 | a0001c0001t0007g0016a0001c0001t0007g0344a0001c0001t0007g0346others(29): Show | 33 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.487-4393C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114084 | ||||||
| chr12:42114118
|
A | G | 2 | a0001c0003t0001g0124a0001c0003t0001g0144 | 2 | HG00544.hp2 HG00597.hp2 |
intron_variant | MODIFIER | c.487-4427T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114118 | ||||||
| chr12:42114149
|
C | T | 312 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(309): Show | 326 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(323): Show |
intron_variant | MODIFIER | c.487-4458G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114149 | ||||||
| chr12:42114183
|
G | A | 208 | a0001c0002t0003g0002a0001c0002t0003g0008a0001c0002t0003g0009others(205): Show | 214 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.487-4492C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114183 | ||||||
| chr12:42114252
|
T | G | 1 | a0001c0002t0003g0010 | 2 | HG02040.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.487-4561A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114252 | ||||||
| chr12:42114278
|
T | A | 3 | a0001c0001t0018g0262a0001c0001t0018g0263a0001c0001t0018g0264 | 3 | HG02922.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.487-4587A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114278 | ||||||
| chr12:42114377
|
C | T | 1 | a0001c0002t0003g0173 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.486+4623G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114377 | ||||||
| chr12:42114381
|
A | G | 1 | a0001c0003t0001g0122 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.486+4619T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114381 | ||||||
| chr12:42114410
|
A | C | 3 | a0001c0001t0018g0262a0001c0001t0018g0263a0001c0001t0018g0264 | 3 | HG02922.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.486+4590T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114410 | ||||||
| chr12:42114433
|
C | A | 1 | a0001c0001t0002g0326 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.486+4567G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114433 | ||||||
| chr12:42114568
|
A | T | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.486+4432T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114568 | ||||||
| chr12:42114576
|
C | G | 1 | a0001c0003t0013g0150 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.486+4424G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114576 | ||||||
| chr12:42114600
|
T | A | 4 | a0001c0003t0001g0210a0001c0003t0001g0213a0001c0003t0001g0223others(1): Show | 4 | HG02622.hp2 HG02630.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.486+4400A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114600 | ||||||
| chr12:42114600
|
T | C | 7 | a0001c0001t0012g0345a0001c0001t0012g0350a0001c0001t0012g0352others(4): Show | 7 | NA18946.hp1 NA18957.hp1 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.486+4400A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114600 | ||||||
| chr12:42114654
|
A | G | 2 | a0001c0001t0026g0299a0001c0001t0026g0323 | 2 | HG01169.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.486+4346T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114654 | ||||||
| chr12:42114696
|
G | A | 2 | a0001c0001t0027g0158a0001c0001t0027g0232 | 2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.486+4304C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114696 | ||||||
| chr12:42114756
|
A | G | 1 | a0001c0001t0053g0354 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.486+4244T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114756 | ||||||
| chr12:42114796
|
A | G | 1 | a0001c0001t0014g0233 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.486+4204T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114796 | ||||||
| chr12:42114855
|
G | C | 1 | a0001c0001t0002g0298 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.486+4145C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114855 | ||||||
| chr12:42114864
|
C | T | 210 | a0001c0001t0021g0230a0001c0001t0021g0231a0001c0002t0003g0002others(207): Show | 216 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.486+4136G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114864 | ||||||
| chr12:42114997
|
A | G | 6 | a0001c0001t0026g0299a0001c0001t0026g0323a0001c0001t0027g0158others(3): Show | 6 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.486+4003T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42114997 | ||||||
| chr12:42115060
|
G | T | 1 | a0001c0001t0041g0333 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.486+3940C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115060 | ||||||
| chr12:42115062
|
T | C | 1 | a0001c0001t0041g0333 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.486+3938A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115062 | ||||||
| chr12:42115084
|
T | C | 6 | a0001c0001t0009g0003a0001c0001t0009g0254a0001c0001t0009g0255others(3): Show | 8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.486+3916A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115084 | ||||||
| chr12:42115125
|
G | A | 33 | a0001c0001t0007g0016a0001c0001t0007g0344a0001c0001t0007g0346others(30): Show | 34 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.486+3875C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115125 | ||||||
| chr12:42115213
|
C | A | 7 | a0001c0001t0017g0234a0001c0001t0017g0235a0001c0001t0017g0242others(4): Show | 7 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.486+3787G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115213 | ||||||
| chr12:42115254
|
C | G | 10 | a0001c0001t0009g0003a0001c0001t0009g0254a0001c0001t0009g0255others(7): Show | 12 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.486+3746G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115254 | ||||||
| chr12:42115259
|
T | C | 2 | a0001c0001t0027g0158a0001c0001t0027g0232 | 2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.486+3741A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115259 | ||||||
| chr12:42115311
|
C | T | 1 | a0001c0001t0012g0359 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.486+3689G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115311 | ||||||
| chr12:42115339
|
T | C | 5 | a0001c0001t0017g0234a0001c0001t0017g0235a0001c0001t0017g0242others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.486+3661A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115339 | ||||||
| chr12:42115343
|
T | C | 19 | a0001c0001t0006g0011a0001c0001t0006g0012a0001c0001t0006g0013others(16): Show | 22 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.486+3657A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115343 | ||||||
| chr12:42115364
|
T | C | 1 | a0001c0001t0012g0350 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.486+3636A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115364 | ||||||
| chr12:42115416
|
A | C | 1 | a0001c0001t0002g0337 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.486+3584T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115416 | ||||||
| chr12:42115419
|
A | C | 1 | a0001c0001t0002g0123 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.486+3581T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115419 | ||||||
| chr12:42115431
|
T | G | 2 | a0001c0001t0011g0260a0001c0001t0011g0261 | 2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.486+3569A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115431 | ||||||
| chr12:42115480
|
G | C | 217 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086others(214): Show | 223 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.486+3520C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115480 | ||||||
| chr12:42115494
|
C | A | 320 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0301others(317): Show | 334 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.486+3506G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115494 | ||||||
| chr12:42115521
|
T | C | 1 | a0001c0002t0003g0092 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.486+3479A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115521 | ||||||
| chr12:42115577
|
T | C | 34 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(31): Show | 36 | HG00544.hp1 HG00597.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.486+3423A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115577 | ||||||
| chr12:42115578
|
G | A | 34 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(31): Show | 36 | HG00544.hp1 HG00597.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.486+3422C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115578 | ||||||
| chr12:42115598
|
C | G | 2 | a0001c0002t0004g0033a0001c0003t0042g0113 | 2 | HG02896.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.486+3402G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115598 | ||||||
| chr12:42115767
|
T | C | 6 | a0001c0001t0026g0299a0001c0001t0026g0323a0001c0001t0027g0158others(3): Show | 6 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.486+3233A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115767 | ||||||
| chr12:42115814
|
G | A | 1 | a0001c0006t0056g0375 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.486+3186C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115814 | ||||||
| chr12:42115828
|
G | C | 317 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(314): Show | 331 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(328): Show |
intron_variant | MODIFIER | c.486+3172C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115828 | ||||||
| chr12:42115839
|
A | G | 1 | a0001c0001t0002g0314 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.486+3161T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115839 | ||||||
| chr12:42115845
|
A | C | 1 | a0001c0003t0001g0161 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.486+3155T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115845 | ||||||
| chr12:42115860
|
T | C | 123 | a0001c0002t0003g0002a0001c0002t0003g0008a0001c0002t0003g0009others(120): Show | 129 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.486+3140A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115860 | ||||||
| chr12:42115895
|
A | G | 210 | a0001c0001t0007g0344a0001c0001t0052g0343a0001c0002t0003g0002others(207): Show | 216 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.486+3105T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115895 | ||||||
| chr12:42115901
|
A | G | 210 | a0001c0001t0007g0344a0001c0001t0052g0343a0001c0002t0003g0002others(207): Show | 216 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.486+3099T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115901 | ||||||
| chr12:42115919
|
T | C | 6 | a0001c0001t0026g0299a0001c0001t0026g0323a0001c0001t0027g0158others(3): Show | 6 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.486+3081A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115919 | ||||||
| chr12:42115936
|
A | C | 2 | a0001c0001t0007g0344a0001c0001t0052g0343 | 2 | HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.486+3064T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115936 | ||||||
| chr12:42115939
|
C | T | 213 | a0001c0001t0007g0344a0001c0001t0016g0084a0001c0001t0016g0085others(210): Show | 219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.486+3061G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115939 | ||||||
| chr12:42115949
|
T | A | 317 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(314): Show | 331 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(328): Show |
intron_variant | MODIFIER | c.486+3051A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115949 | ||||||
| chr12:42115960
|
C | T | 6 | a0001c0001t0009g0003a0001c0001t0009g0254a0001c0001t0009g0255others(3): Show | 8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.486+3040G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115960 | ||||||
| chr12:42115962
|
C | G | 49 | a0001c0001t0006g0011a0001c0001t0006g0012a0001c0001t0006g0013others(46): Show | 53 | HG00423.hp1 HG00639.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.486+3038G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115962 | ||||||
| chr12:42115962
|
C | T | 1 | a0001c0003t0001g0224 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.486+3038G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115962 | ||||||
| chr12:42115977
|
A | G | 2 | a0001c0001t0007g0344a0001c0001t0052g0343 | 2 | HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.486+3023T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115977 | ||||||
| chr12:42115984
|
T | C | 2 | a0001c0001t0007g0344a0001c0001t0052g0343 | 2 | HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.486+3016A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115984 | ||||||
| chr12:42115985
|
A | C | 2 | a0001c0001t0007g0344a0001c0001t0052g0343 | 2 | HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.486+3015T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42115985 | ||||||
| chr12:42116011
|
C | G | 2 | a0001c0001t0027g0158a0001c0001t0027g0232 | 2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.486+2989G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116011 | ||||||
| chr12:42116071
|
A | T | 1 | a0001c0003t0001g0224 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.486+2929T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116071 | ||||||
| chr12:42116078
|
C | T | 24 | a0001c0001t0006g0011a0001c0001t0006g0012a0001c0001t0006g0013others(21): Show | 29 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.486+2922G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116078 | ||||||
| chr12:42116150
|
C | A | 3 | a0001c0001t0002g0309a0001c0003t0001g0204a0001c0003t0001g0217 | 3 | HG02109.hp1 HG03130.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.486+2850G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116150 | ||||||
| chr12:42116192
|
G | A | 1 | a0001c0001t0002g0308 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.486+2808C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116192 | ||||||
| chr12:42116211
|
T | G | 2 | a0001c0002t0004g0049a0001c0002t0031g0018 | 2 | HG02886.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.486+2789A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116211 | ||||||
| chr12:42116237
|
A | G | 1 | a0001c0002t0004g0055 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.486+2763T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116237 | ||||||
| chr12:42116251
|
A | T | 44 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(41): Show | 48 | HG00544.hp1 HG00597.hp1 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.486+2749T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116251 | ||||||
| chr12:42116327
|
A | G | 1 | a0001c0001t0014g0228 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.486+2673T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116327 | ||||||
| chr12:42116339
|
C | A | 2 | a0001c0001t0012g0356a0001c0003t0036g0103 | 2 | NA18961.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.486+2661G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116339 | ||||||
| chr12:42116340
|
G | A | 6 | a0001c0001t0026g0299a0001c0001t0026g0323a0001c0001t0027g0158others(3): Show | 6 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.486+2660C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116340 | ||||||
| chr12:42116345
|
C | T | 3 | a0001c0001t0014g0228a0001c0001t0014g0229a0001c0001t0014g0233 | 3 | HG01884.hp1 HG02280.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.486+2655G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116345 | ||||||
| chr12:42116360
|
A | T | 1 | a0001c0002t0004g0045 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.486+2640T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116360 | ||||||
| chr12:42116363
|
A | G | 6 | a0001c0001t0009g0003a0001c0001t0009g0254a0001c0001t0009g0255others(3): Show | 8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.486+2637T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116363 | ||||||
| chr12:42116392
|
G | A | 28 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(25): Show | 30 | HG00544.hp1 HG00597.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.486+2608C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116392 | ||||||
| chr12:42116400
|
C | G | 6 | a0001c0001t0014g0228a0001c0001t0014g0229a0001c0001t0014g0233others(3): Show | 6 | HG01884.hp1 HG02280.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.486+2600G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116400 | ||||||
| chr12:42116414
|
T | G | 364 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0014others(361): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.486+2586A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116414 | ||||||
| chr12:42116419
|
CA | C | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.486+2580delT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116419 | ||||||
| chr12:42116432
|
C | A | 1 | a0001c0006t0056g0375 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.486+2568G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116432 | ||||||
| chr12:42116463
|
C | A | 62 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0014others(59): Show | 71 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.486+2537G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116463 | ||||||
| chr12:42116463
|
C | T | 1 | a0001c0001t0014g0236 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.486+2537G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116463 | ||||||
| chr12:42116498
|
A | G | 32 | a0001c0001t0007g0016a0001c0001t0007g0344a0001c0001t0007g0346others(29): Show | 33 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.486+2502T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116498 | ||||||
| chr12:42116522
|
A | G | 1 | a0001c0001t0006g0246 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.486+2478T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116522 | ||||||
| chr12:42116534
|
C | T | 17 | a0001c0001t0006g0011a0001c0001t0006g0012a0001c0001t0006g0013others(14): Show | 20 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.486+2466G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116534 | ||||||
| chr12:42116543
|
G | A | 208 | a0001c0002t0003g0002a0001c0002t0003g0008a0001c0002t0003g0009others(205): Show | 214 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.486+2457C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116543 | ||||||
| chr12:42116574
|
C | A | 11 | a0001c0001t0006g0011a0001c0001t0006g0012a0001c0001t0006g0013others(8): Show | 14 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.486+2426G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116574 | ||||||
| chr12:42116574
|
C | T | 12 | a0001c0002t0004g0050a0001c0002t0004g0053a0001c0002t0004g0054others(9): Show | 12 | HG00323.hp1 HG01099.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.486+2426G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116574 | ||||||
| chr12:42116591
|
C | G | 2 | a0001c0001t0011g0265a0001c0001t0011g0266 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.486+2409G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116591 | ||||||
| chr12:42116604
|
C | A | 1 | a0002c0004t0002g0007 | 2 | HG02015.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.486+2396G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116604 | ||||||
| chr12:42116605
|
A | G | 1 | a0002c0004t0002g0007 | 2 | HG02015.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.486+2395T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116605 | ||||||
| chr12:42116608
|
C | T | 2 | a0001c0002t0020g0026a0001c0002t0020g0027 | 2 | HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.486+2392G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116608 | ||||||
| chr12:42116641
|
A | C | 1 | a0001c0001t0018g0263 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.486+2359T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116641 | ||||||
| chr12:42116685
|
G | C | 11 | a0001c0001t0006g0011a0001c0001t0006g0012a0001c0001t0006g0013others(8): Show | 14 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.486+2315C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116685 | ||||||
| chr12:42116687
|
A | G | 3 | a0001c0001t0018g0262a0001c0001t0018g0263a0001c0001t0018g0264 | 3 | HG02922.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.486+2313T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116687 | ||||||
| chr12:42116806
|
C | A | 1 | a0001c0001t0002g0330 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.486+2194G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116806 | ||||||
| chr12:42116849
|
T | C | 1 | a0001c0001t0027g0158 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.486+2151A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116849 | ||||||
| chr12:42116851
|
C | T | 3 | a0001c0001t0017g0234a0001c0001t0017g0235a0001c0001t0017g0242 | 3 | HG02451.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.486+2149G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116851 | ||||||
| chr12:42116872
|
C | A | 1 | a0001c0001t0005g0280 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.486+2128G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116872 | ||||||
| chr12:42116872
|
C | G | 208 | a0001c0002t0003g0002a0001c0002t0003g0008a0001c0002t0003g0009others(205): Show | 214 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.486+2128G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116872 | ||||||
| chr12:42116891
|
A | G | 17 | a0001c0001t0006g0011a0001c0001t0006g0012a0001c0001t0006g0013others(14): Show | 20 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.486+2109T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116891 | ||||||
| chr12:42116944
|
A | G | 1 | a0001c0006t0056g0375 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.486+2056T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116944 | ||||||
| chr12:42116969
|
T | C | 1 | a0001c0001t0005g0278 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.486+2031A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42116969 | ||||||
| chr12:42117022
|
A | G | 312 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(309): Show | 326 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(323): Show |
intron_variant | MODIFIER | c.486+1978T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42117022 | ||||||
| chr12:42117045
|
A | G | 312 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(309): Show | 326 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(323): Show |
intron_variant | MODIFIER | c.486+1955T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42117045 | ||||||
| chr12:42117226
|
T | C | 1 | a0001c0001t0007g0357 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.486+1774A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42117226 | ||||||
| chr12:42117291
|
T | A | 10 | a0001c0001t0009g0003a0001c0001t0009g0254a0001c0001t0009g0255others(7): Show | 12 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.486+1709A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42117291 | ||||||
| chr12:42117292
|
A | T | 1 | a0001c0001t0002g0285 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.486+1708T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42117292 | ||||||
| chr12:42117323
|
A | T | 22 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(19): Show | 24 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(21): Show |
intron_variant | MODIFIER | c.486+1677T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42117323 | ||||||
| chr12:42117446
|
A | G | 3 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0324 | 3 | HG02896.hp1 HG02897.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.486+1554T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42117446 | ||||||
| chr12:42117469
|
G | A | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.486+1531C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42117469 | ||||||
| chr12:42117491
|
G | GT | 63 | a0001c0002t0003g0172a0001c0002t0003g0189a0001c0002t0003g0192others(60): Show | 64 | HG00323.hp1 HG00621.hp2 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.486+1508dupA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42117491 | ||||||
| chr12:42117502
|
C | T | 2 | a0001c0001t0022g0240a0001c0001t0022g0241 | 2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.486+1498G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42117502 | ||||||
| chr12:42117522
|
G | T | 1 | a0001c0001t0007g0349 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.486+1478C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42117522 | ||||||
| chr12:42117785
|
G | C | 1 | a0001c0003t0001g0130 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.486+1215C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42117785 | ||||||
| chr12:42117925
|
G | T | 1 | a0001c0003t0001g0131 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.486+1075C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42117925 | ||||||
| chr12:42118046
|
C | T | 1 | a0001c0001t0018g0263 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.486+954G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42118046 | ||||||
| chr12:42118238
|
C | T | 5 | a0001c0001t0017g0234a0001c0001t0017g0235a0001c0001t0017g0242others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.486+762G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42118238 | ||||||
| chr12:42118282
|
A | G | 1 | a0001c0003t0001g0120 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.486+718T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42118282 | ||||||
| chr12:42118322
|
A | T | 6 | a0001c0001t0007g0016a0001c0001t0007g0346a0001c0001t0007g0347others(3): Show | 7 | HG00738.hp1 HG02647.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.486+678T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42118322 | ||||||
| chr12:42118476
|
G | A | 1 | a0001c0001t0041g0333 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.486+524C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42118476 | ||||||
| chr12:42118502
|
A | G | 50 | a0001c0001t0006g0011a0001c0001t0006g0012a0001c0001t0006g0013others(47): Show | 54 | HG00423.hp1 HG00642.hp1 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.486+498T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42118502 | ||||||
| chr12:42118506
|
A | T | 2 | a0001c0003t0001g0126a0001c0003t0001g0138 | 2 | HG02040.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.486+494T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42118506 | ||||||
| chr12:42118590
|
T | C | 31 | a0001c0001t0007g0016a0001c0001t0007g0344a0001c0001t0007g0346others(28): Show | 32 | HG00642.hp1 HG00738.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.486+410A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 3/7 | chr12 | 42118590 | ||||||
| chr12:42119189
|
C | T | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.315-18G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42119189 | ||||||
| chr12:42119298
|
C | T | 6 | a0001c0001t0009g0003a0001c0001t0009g0254a0001c0001t0009g0255others(3): Show | 8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.315-127G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42119298 | ||||||
| chr12:42119325
|
G | A | 123 | a0001c0002t0003g0002a0001c0002t0003g0008a0001c0002t0003g0009others(120): Show | 129 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.315-154C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42119325 | ||||||
| chr12:42119371
|
A | G | 6 | a0001c0001t0026g0299a0001c0001t0026g0323a0001c0001t0027g0158others(3): Show | 6 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.315-200T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42119371 | ||||||
| chr12:42119444
|
GAAAGGGA others(5): Show |
G | 2 | a0001c0001t0009g0003a0001c0001t0009g0255 | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-285_315-274del others(12): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42119444 | ||||||
| chr12:42119476
|
G | A | 2 | a0001c0001t0022g0240a0001c0001t0022g0241 | 2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.315-305C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42119476 | ||||||
| chr12:42119615
|
C | A | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.315-444G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42119615 | ||||||
| chr12:42119791
|
T | G | 2 | a0001c0001t0026g0299a0001c0001t0026g0323 | 2 | HG01169.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.315-620A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42119791 | ||||||
| chr12:42119812
|
G | A | 6 | a0001c0001t0014g0228a0001c0001t0014g0229a0001c0001t0014g0233others(3): Show | 6 | HG01884.hp1 HG02280.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.315-641C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42119812 | ||||||
| chr12:42120007
|
C | T | 31 | a0001c0001t0007g0016a0001c0001t0007g0344a0001c0001t0007g0346others(28): Show | 32 | HG00642.hp1 HG00738.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.315-836G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42120007 | ||||||
| chr12:42120080
|
T | C | 17 | a0001c0001t0006g0011a0001c0001t0006g0012a0001c0001t0006g0013others(14): Show | 20 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.315-909A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42120080 | ||||||
| chr12:42120091
|
A | G | 267 | a0001c0001t0006g0011a0001c0001t0006g0012a0001c0001t0006g0013others(264): Show | 277 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.315-920T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42120091 | ||||||
| chr12:42120336
|
A | G | 1 | a0001c0001t0007g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.315-1165T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42120336 | ||||||
| chr12:42120392
|
A | G | 2 | a0001c0001t0027g0158a0001c0001t0027g0232 | 2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.315-1221T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42120392 | ||||||
| chr12:42120458
|
T | C | 310 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(307): Show | 324 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(321): Show |
intron_variant | MODIFIER | c.315-1287A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42120458 | ||||||
| chr12:42120571
|
C | G | 1 | a0001c0001t0002g0320 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.315-1400G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42120571 | ||||||
| chr12:42120747
|
G | C | 3 | a0001c0001t0014g0228a0001c0001t0014g0229a0001c0001t0014g0233 | 3 | HG01884.hp1 HG02280.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.315-1576C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42120747 | ||||||
| chr12:42120748
|
C | T | 3 | a0001c0001t0014g0228a0001c0001t0014g0229a0001c0001t0014g0233 | 3 | HG01884.hp1 HG02280.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.315-1577G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42120748 | ||||||
| chr12:42120793
|
C | T | 1 | a0001c0001t0006g0245 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.315-1622G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42120793 | ||||||
| chr12:42120945
|
A | C | 1 | a0001c0001t0006g0249 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.315-1774T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42120945 | ||||||
| chr12:42121082
|
T | C | 2 | a0001c0001t0011g0094a0001c0001t0011g0095 | 2 | HG02818.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.315-1911A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42121082 | ||||||
| chr12:42121121
|
A | C | 208 | a0001c0002t0003g0002a0001c0002t0003g0008a0001c0002t0003g0009others(205): Show | 214 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.315-1950T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42121121 | ||||||
| chr12:42121310
|
G | A | 1 | a0001c0002t0046g0182 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.315-2139C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42121310 | ||||||
| chr12:42121361
|
G | A | 2 | a0001c0001t0053g0354a0002c0004t0051g0342 | 2 | HG02809.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.315-2190C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42121361 | ||||||
| chr12:42121453
|
G | A | 7 | a0001c0001t0011g0260a0001c0001t0011g0261a0001c0001t0014g0228others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.315-2282C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42121453 | ||||||
| chr12:42121504
|
G | A | 85 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0104others(82): Show | 85 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.315-2333C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42121504 | ||||||
| chr12:42121600
|
C | G | 2 | a0001c0001t0022g0240a0001c0001t0022g0241 | 2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.315-2429G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42121600 | ||||||
| chr12:42121656
|
G | GA | 27 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(24): Show | 29 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(26): Show |
intron_variant | MODIFIER | c.315-2486dupT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42121656 | ||||||
| chr12:42121656
|
GA | G | 61 | a0001c0001t0002g0335a0001c0002t0003g0002a0001c0002t0003g0008others(58): Show | 66 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.315-2486delT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42121656 | ||||||
| chr12:42122046
|
G | A | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.315-2875C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42122046 | ||||||
| chr12:42122236
|
G | A | 1 | a0001c0001t0002g0309 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.315-3065C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42122236 | ||||||
| chr12:42122304
|
C | T | 10 | a0001c0001t0009g0003a0001c0001t0009g0254a0001c0001t0009g0255others(7): Show | 12 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.315-3133G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42122304 | ||||||
| chr12:42122341
|
G | A | 1 | a0001c0003t0001g0136 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.315-3170C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42122341 | ||||||
| chr12:42122397
|
C | T | 2 | a0001c0001t0022g0240a0001c0001t0022g0241 | 2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.315-3226G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42122397 | ||||||
| chr12:42122406
|
A | C | 1 | a0001c0002t0003g0101 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.315-3235T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42122406 | ||||||
| chr12:42122418
|
C | T | 2 | a0001c0001t0022g0240a0001c0001t0022g0241 | 2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.315-3247G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42122418 | ||||||
| chr12:42122450
|
C | T | 2 | a0001c0001t0022g0240a0001c0001t0022g0241 | 2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.315-3279G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42122450 | ||||||
| chr12:42122574
|
A | G | 60 | a0001c0002t0004g0028a0001c0002t0004g0029a0001c0002t0004g0030others(57): Show | 61 | HG00323.hp1 HG00621.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.315-3403T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42122574 | ||||||
| chr12:42122826
|
A | G | 2 | a0001c0001t0011g0265a0001c0001t0011g0266 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.315-3655T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42122826 | ||||||
| chr12:42122889
|
T | C | 22 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(19): Show | 24 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(21): Show |
intron_variant | MODIFIER | c.315-3718A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42122889 | ||||||
| chr12:42122931
|
C | G | 1 | a0001c0001t0014g0233 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.315-3760G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42122931 | ||||||
| chr12:42122967
|
G | C | 31 | a0001c0001t0007g0016a0001c0001t0007g0344a0001c0001t0007g0346others(28): Show | 32 | HG00642.hp1 HG00738.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.315-3796C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42122967 | ||||||
| chr12:42122983
|
CTAATAA | C | 6 | a0001c0001t0009g0003a0001c0001t0009g0254a0001c0001t0009g0255others(3): Show | 8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.315-3818_315-3813d others(8): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42122983 | ||||||
| chr12:42123128
|
T | C | 1 | a0001c0001t0005g0268 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.315-3957A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42123128 | ||||||
| chr12:42123153
|
G | A | 1 | a0001c0002t0004g0053 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.315-3982C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42123153 | ||||||
| chr12:42123273
|
T | C | 1 | a0001c0002t0003g0102 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.315-4102A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42123273 | ||||||
| chr12:42123347
|
C | T | 31 | a0001c0001t0007g0016a0001c0001t0007g0344a0001c0001t0007g0346others(28): Show | 32 | HG00642.hp1 HG00738.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.315-4176G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42123347 | ||||||
| chr12:42123580
|
ACTT | A | 6 | a0001c0002t0015g0183a0001c0002t0015g0184a0001c0002t0015g0200others(3): Show | 6 | HG01346.hp1 HG01433.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.315-4412_315-4410d others(5): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42123580 | ||||||
| chr12:42123617
|
CATA | C | 5 | a0001c0002t0004g0054a0001c0002t0004g0077a0001c0002t0004g0078others(2): Show | 5 | HG02083.hp1 NA18944.hp2 NA18991.hp1 others(2): Show |
intron_variant | MODIFIER | c.315-4449_315-4447d others(5): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42123617 | ||||||
| chr12:42123621
|
A | G | 1 | a0001c0002t0003g0198 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.315-4450T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42123621 | ||||||
| chr12:42123715
|
ATAAT | A | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.315-4548_315-4545d others(6): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42123715 | ||||||
| chr12:42123952
|
GA | G | 21 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(18): Show | 23 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.315-4782delT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42123952 | ||||||
| chr12:42124014
|
T | C | 2 | a0001c0001t0028g0328a0001c0001t0028g0329 | 2 | HG02109.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.315-4843A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42124014 | ||||||
| chr12:42124041
|
T | TA | 11 | a0001c0001t0006g0011a0001c0001t0006g0012a0001c0001t0006g0013others(8): Show | 14 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.315-4871dupT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42124041 | ||||||
| chr12:42124165
|
G | A | 60 | a0001c0002t0003g0002a0001c0002t0003g0008a0001c0002t0003g0009others(57): Show | 65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.315-4994C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42124165 | ||||||
| chr12:42124300
|
T | C | 60 | a0001c0002t0004g0028a0001c0002t0004g0029a0001c0002t0004g0030others(57): Show | 61 | HG00323.hp1 HG00621.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.315-5129A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42124300 | ||||||
| chr12:42124397
|
G | T | 3 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0324 | 3 | HG02896.hp1 HG02897.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.315-5226C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42124397 | ||||||
| chr12:42124461
|
T | C | 5 | a0001c0003t0013g0150a0001c0003t0013g0151a0001c0003t0013g0152others(2): Show | 5 | HG03239.hp1 HG03654.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.315-5290A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42124461 | ||||||
| chr12:42124462
|
A | G | 1 | a0001c0002t0003g0191 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.315-5291T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42124462 | ||||||
| chr12:42124485
|
A | G | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.314+5274T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42124485 | ||||||
| chr12:42124502
|
T | C | 1 | a0001c0001t0009g0257 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.314+5257A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42124502 | ||||||
| chr12:42124514
|
G | A | 2 | a0001c0003t0001g0207a0001c0003t0001g0214 | 2 | HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.314+5245C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42124514 | ||||||
| chr12:42124526
|
C | A | 311 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(308): Show | 325 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(322): Show |
intron_variant | MODIFIER | c.314+5233G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42124526 | ||||||
| chr12:42124667
|
T | A | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.314+5092A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42124667 | ||||||
| chr12:42124732
|
T | C | 6 | a0001c0001t0026g0299a0001c0001t0026g0323a0001c0001t0027g0158others(3): Show | 6 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.314+5027A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42124732 | ||||||
| chr12:42124784
|
TA | T | 3 | a0001c0001t0002g0295a0001c0001t0002g0312a0001c0001t0002g0313 | 3 | HG00408.hp1 NA18961.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.314+4974delT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42124784 | ||||||
| chr12:42124997
|
T | C | 2 | a0001c0001t0022g0240a0001c0001t0022g0241 | 2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.314+4762A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42124997 | ||||||
| chr12:42125083
|
G | A | 1 | a0001c0003t0023g0206 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.314+4676C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42125083 | ||||||
| chr12:42125098
|
T | C | 2 | a0001c0001t0021g0230a0001c0001t0021g0231 | 2 | HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.314+4661A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42125098 | ||||||
| chr12:42125138
|
T | C | 4 | a0001c0002t0004g0033a0001c0002t0004g0047a0001c0002t0004g0048others(1): Show | 4 | HG02258.hp2 HG02723.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.314+4621A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42125138 | ||||||
| chr12:42125220
|
T | C | 32 | a0001c0001t0007g0016a0001c0001t0007g0344a0001c0001t0007g0346others(29): Show | 33 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.314+4539A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42125220 | ||||||
| chr12:42125245
|
T | C | 3 | a0001c0003t0001g0130a0001c0003t0001g0219a0001c0003t0040g0111 | 3 | HG00733.hp2 HG01074.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.314+4514A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42125245 | ||||||
| chr12:42125379
|
C | G | 1 | a0001c0002t0003g0171 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.314+4380G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42125379 | ||||||
| chr12:42125394
|
G | C | 1 | a0001c0003t0001g0137 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.314+4365C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42125394 | ||||||
| chr12:42125843
|
C | T | 5 | a0001c0001t0014g0228a0001c0001t0014g0229a0001c0001t0014g0233others(2): Show | 5 | HG01884.hp1 HG02280.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+3916G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42125843 | ||||||
| chr12:42125852
|
G | A | 1 | a0001c0003t0001g0161 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.314+3907C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42125852 | ||||||
| chr12:42125886
|
C | G | 317 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(314): Show | 331 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(328): Show |
intron_variant | MODIFIER | c.314+3873G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42125886 | ||||||
| chr12:42126032
|
C | A | 60 | a0001c0002t0003g0002a0001c0002t0003g0008a0001c0002t0003g0009others(57): Show | 65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.314+3727G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42126032 | ||||||
| chr12:42126037
|
A | C | 26 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(23): Show | 28 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(25): Show |
intron_variant | MODIFIER | c.314+3722T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42126037 | ||||||
| chr12:42126073
|
C | CT | 39 | a0001c0001t0002g0286a0001c0001t0002g0287a0001c0001t0006g0011others(36): Show | 44 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.314+3685dupA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42126073 | ||||||
| chr12:42126073
|
C | CTT | 39 | a0001c0001t0006g0244a0001c0001t0007g0016a0001c0001t0007g0344others(36): Show | 40 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.314+3684_314+3685d others(4): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42126073 | ||||||
| chr12:42126096
|
C | T | 208 | a0001c0002t0003g0002a0001c0002t0003g0008a0001c0002t0003g0009others(205): Show | 214 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.314+3663G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42126096 | ||||||
| chr12:42126123
|
G | A | 5 | a0001c0001t0017g0234a0001c0001t0017g0235a0001c0001t0017g0242others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+3636C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42126123 | ||||||
| chr12:42126186
|
G | A | 1 | a0001c0001t0053g0354 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.314+3573C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42126186 | ||||||
| chr12:42126221
|
G | A | 1 | a0001c0001t0002g0310 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.314+3538C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42126221 | ||||||
| chr12:42126255
|
G | T | 32 | a0001c0001t0007g0016a0001c0001t0007g0344a0001c0001t0007g0346others(29): Show | 33 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.314+3504C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42126255 | ||||||
| chr12:42126320
|
A | G | 1 | a0001c0003t0001g0112 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.314+3439T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42126320 | ||||||
| chr12:42126450
|
T | C | 209 | a0001c0001t0002g0123a0001c0002t0003g0002a0001c0002t0003g0008others(206): Show | 215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.314+3309A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42126450 | ||||||
| chr12:42126721
|
C | A | 1 | a0001c0003t0001g0125 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.314+3038G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42126721 | ||||||
| chr12:42126765
|
C | T | 209 | a0001c0001t0002g0123a0001c0002t0003g0002a0001c0002t0003g0008others(206): Show | 215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.314+2994G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42126765 | ||||||
| chr12:42126880
|
G | GA | 9 | a0001c0001t0002g0293a0001c0001t0002g0311a0001c0002t0003g0237others(6): Show | 9 | HG00621.hp2 HG02572.hp2 NA18949.hp1 others(6): Show |
intron_variant | MODIFIER | c.314+2878dupT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42126880 | ||||||
| chr12:42126880
|
GA | G | 21 | a0001c0001t0006g0011a0001c0001t0006g0012a0001c0001t0006g0013others(18): Show | 24 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.314+2878delT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42126880 | ||||||
| chr12:42126948
|
G | GT | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.314+2810_314+2811i others(3): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42126948 | ||||||
| chr12:42126959
|
T | C | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.314+2800A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42126959 | ||||||
| chr12:42126998
|
T | G | 2 | a0001c0002t0020g0027a0001c0002t0034g0025 | 2 | HG02055.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.314+2761A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42126998 | ||||||
| chr12:42127287
|
G | C | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.314+2472C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42127287 | ||||||
| chr12:42127352
|
C | CT | 28 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(25): Show | 30 | HG00544.hp1 HG00597.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.314+2406dupA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42127352 | ||||||
| chr12:42127359
|
T | TA | 209 | a0001c0001t0002g0123a0001c0002t0003g0002a0001c0002t0003g0008others(206): Show | 215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.314+2399dupT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42127359 | ||||||
| chr12:42127600
|
C | T | 1 | a0001c0001t0027g0158 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.314+2159G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42127600 | ||||||
| chr12:42127756
|
T | C | 6 | a0001c0001t0026g0299a0001c0001t0026g0323a0001c0001t0027g0158others(3): Show | 6 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.314+2003A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42127756 | ||||||
| chr12:42127764
|
C | A | 6 | a0001c0001t0026g0299a0001c0001t0026g0323a0001c0001t0027g0158others(3): Show | 6 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.314+1995G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42127764 | ||||||
| chr12:42127786
|
G | A | 6 | a0001c0001t0014g0228a0001c0001t0014g0229a0001c0001t0014g0233others(3): Show | 6 | HG01884.hp1 HG02280.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.314+1973C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42127786 | ||||||
| chr12:42127991
|
A | C | 1 | a0001c0002t0004g0077 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.314+1768T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42127991 | ||||||
| chr12:42128071
|
T | C | 1 | a0001c0006t0056g0375 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.314+1688A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42128071 | ||||||
| chr12:42128135
|
A | G | 1 | a0001c0002t0003g0190 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.314+1624T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42128135 | ||||||
| chr12:42128156
|
C | A | 1 | a0001c0002t0020g0026 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.314+1603G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42128156 | ||||||
| chr12:42128244
|
G | T | 1 | a0001c0001t0002g0297 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.314+1515C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42128244 | ||||||
| chr12:42128329
|
T | A | 17 | a0001c0001t0006g0011a0001c0001t0006g0012a0001c0001t0006g0013others(14): Show | 20 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.314+1430A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42128329 | ||||||
| chr12:42128397
|
T | G | 1 | a0001c0001t0053g0354 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.314+1362A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42128397 | ||||||
| chr12:42128429
|
T | C | 3 | a0001c0001t0017g0234a0001c0001t0017g0235a0001c0001t0017g0242 | 3 | HG02451.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.314+1330A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42128429 | ||||||
| chr12:42128599
|
C | T | 2 | a0001c0001t0011g0094a0001c0001t0011g0095 | 2 | HG02818.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.314+1160G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42128599 | ||||||
| chr12:42128803
|
C | A | 1 | a0001c0001t0002g0314 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.314+956G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42128803 | ||||||
| chr12:42128809
|
C | T | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.314+950G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42128809 | ||||||
| chr12:42128810
|
A | G | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.314+949T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42128810 | ||||||
| chr12:42128853
|
T | A | 1 | a0001c0003t0001g0212 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.314+906A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42128853 | ||||||
| chr12:42128955
|
C | T | 3 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0139 | 3 | NA19007.hp2 NA19079.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.314+804G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42128955 | ||||||
| chr12:42129083
|
G | A | 311 | a0001c0001t0002g0123a0001c0001t0005g0004a0001c0001t0005g0267others(308): Show | 325 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(322): Show |
intron_variant | MODIFIER | c.314+676C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42129083 | ||||||
| chr12:42129131
|
A | G | 209 | a0001c0001t0002g0123a0001c0002t0003g0002a0001c0002t0003g0008others(206): Show | 215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.314+628T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42129131 | ||||||
| chr12:42129147
|
T | C | 1 | a0001c0003t0001g0224 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.314+612A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42129147 | ||||||
| chr12:42129213
|
T | C | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.314+546A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42129213 | ||||||
| chr12:42129358
|
G | T | 212 | a0001c0001t0002g0123a0001c0001t0016g0084a0001c0001t0016g0085others(209): Show | 218 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.314+401C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42129358 | ||||||
| chr12:42129443
|
C | A | 1 | a0001c0001t0005g0274 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.314+316G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42129443 | ||||||
| chr12:42129525
|
T | C | 2 | a0001c0001t0011g0265a0001c0001t0011g0266 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.314+234A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42129525 | ||||||
| chr12:42129533
|
G | C | 6 | a0001c0001t0010g0019a0001c0001t0010g0020a0001c0001t0010g0021others(3): Show | 6 | HG03704.hp1 HG03831.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.314+226C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42129533 | ||||||
| chr12:42129564
|
T | C | 209 | a0001c0001t0002g0123a0001c0002t0003g0002a0001c0002t0003g0008others(206): Show | 215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.314+195A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42129564 | ||||||
| chr12:42129640
|
G | A | 1 | a0001c0002t0003g0251 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.314+119C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 2/7 | chr12 | 42129640 | ||||||
| chr12:42130073
|
T | G | 2 | a0001c0001t0022g0240a0001c0001t0022g0241 | 2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.222-222A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42130073 | ||||||
| chr12:42130090
|
T | C | 1 | a0001c0001t0002g0318 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.222-239A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42130090 | ||||||
| chr12:42130095
|
G | A | 17 | a0001c0001t0006g0011a0001c0001t0006g0012a0001c0001t0006g0013others(14): Show | 20 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.222-244C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42130095 | ||||||
| chr12:42130133
|
C | T | 209 | a0001c0001t0002g0123a0001c0002t0003g0002a0001c0002t0003g0008others(206): Show | 215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.222-282G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42130133 | ||||||
| chr12:42130204
|
G | A | 1 | a0001c0001t0014g0236 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.222-353C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42130204 | ||||||
| chr12:42130249
|
C | T | 2 | a0001c0001t0016g0085a0001c0001t0016g0086 | 2 | HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.222-398G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42130249 | ||||||
| chr12:42130277
|
T | C | 1 | a0001c0001t0002g0293 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.222-426A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42130277 | ||||||
| chr12:42130359
|
A | C | 1 | a0001c0001t0002g0298 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.222-508T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42130359 | ||||||
| chr12:42130360
|
T | C | 6 | a0001c0001t0026g0299a0001c0001t0026g0323a0001c0001t0027g0158others(3): Show | 6 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.222-509A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42130360 | ||||||
| chr12:42130444
|
T | C | 1 | a0001c0001t0002g0294 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.222-593A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42130444 | ||||||
| chr12:42130529
|
A | C | 11 | a0001c0001t0006g0011a0001c0001t0006g0012a0001c0001t0006g0013others(8): Show | 14 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.222-678T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42130529 | ||||||
| chr12:42130564
|
T | C | 1 | a0001c0002t0049g0186 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.222-713A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42130564 | ||||||
| chr12:42130570
|
T | G | 85 | a0001c0001t0002g0123a0001c0003t0001g0099a0001c0003t0001g0100others(82): Show | 85 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.222-719A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42130570 | ||||||
| chr12:42130713
|
G | A | 3 | a0001c0001t0002g0295a0001c0001t0002g0312a0001c0001t0002g0313 | 3 | HG00408.hp1 NA18961.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.222-862C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42130713 | ||||||
| chr12:42130779
|
C | T | 2 | a0001c0001t0011g0094a0001c0001t0011g0095 | 2 | HG02818.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.222-928G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42130779 | ||||||
| chr12:42130898
|
G | C | 2 | a0001c0001t0022g0240a0001c0001t0022g0241 | 2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.222-1047C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42130898 | ||||||
| chr12:42131037
|
T | C | 1 | a0001c0001t0002g0319 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.222-1186A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42131037 | ||||||
| chr12:42131173
|
T | C | 4 | a0001c0001t0011g0094a0001c0001t0011g0095a0001c0001t0037g0096others(1): Show | 4 | HG02717.hp1 HG02818.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.222-1322A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42131173 | ||||||
| chr12:42131406
|
T | C | 209 | a0001c0001t0002g0123a0001c0002t0003g0002a0001c0002t0003g0008others(206): Show | 215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.222-1555A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42131406 | ||||||
| chr12:42131606
|
T | C | 2 | a0001c0002t0004g0038a0001c0002t0004g0040 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.222-1755A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42131606 | ||||||
| chr12:42131657
|
G | T | 2 | a0001c0002t0003g0008a0001c0002t0003g0168 | 3 | HG01943.hp2 HG02132.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.222-1806C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42131657 | ||||||
| chr12:42131899
|
G | A | 1 | a0001c0002t0003g0187 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.222-2048C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42131899 | ||||||
| chr12:42132046
|
A | T | 7 | a0001c0001t0012g0345a0001c0001t0012g0350a0001c0001t0012g0352others(4): Show | 7 | NA18946.hp1 NA18957.hp1 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.222-2195T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132046 | ||||||
| chr12:42132071
|
A | C | 6 | a0001c0001t0009g0003a0001c0001t0009g0254a0001c0001t0009g0255others(3): Show | 8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.222-2220T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132071 | ||||||
| chr12:42132182
|
T | A | 2 | a0001c0001t0016g0085a0001c0001t0016g0086 | 2 | HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.222-2331A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132182 | ||||||
| chr12:42132197
|
T | C | 17 | a0001c0001t0006g0011a0001c0001t0006g0012a0001c0001t0006g0013others(14): Show | 20 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.222-2346A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132197 | ||||||
| chr12:42132275
|
G | C | 313 | a0001c0001t0002g0123a0001c0001t0005g0004a0001c0001t0005g0267others(310): Show | 327 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(324): Show |
intron_variant | MODIFIER | c.222-2424C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132275 | ||||||
| chr12:42132343
|
G | T | 2 | a0001c0001t0024g0226a0001c0001t0024g0227 | 2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.222-2492C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132343 | ||||||
| chr12:42132386
|
C | T | 1 | a0001c0003t0001g0142 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.222-2535G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132386 | ||||||
| chr12:42132447
|
A | G | 3 | a0001c0001t0018g0262a0001c0001t0018g0263a0001c0001t0018g0264 | 3 | HG02922.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.222-2596T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132447 | ||||||
| chr12:42132591
|
G | A | 1 | a0001c0002t0034g0025 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.222-2740C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132591 | ||||||
| chr12:42132593
|
G | A | 1 | a0001c0002t0004g0060 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.222-2742C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132593 | ||||||
| chr12:42132635
|
T | C | 2 | a0001c0003t0001g0117a0001c0003t0001g0149 | 2 | NA19012.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.222-2784A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132635 | ||||||
| chr12:42132688
|
C | G | 3 | a0001c0001t0018g0262a0001c0001t0018g0263a0001c0001t0018g0264 | 3 | HG02922.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.222-2837G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132688 | ||||||
| chr12:42132784
|
G | GT | 6 | a0001c0001t0021g0230a0001c0001t0021g0231a0001c0002t0004g0043others(3): Show | 6 | HG00621.hp2 HG01192.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.222-2934dupA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132784 | ||||||
| chr12:42132784
|
G | T | 1 | a0001c0003t0001g0208 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.222-2933C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132784 | ||||||
| chr12:42132826
|
A | G | 1 | a0001c0001t0037g0096 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.222-2975T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132826 | ||||||
| chr12:42132856
|
T | C | 1 | a0001c0002t0020g0026 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.222-3005A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132856 | ||||||
| chr12:42132873
|
G | A | 4 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086others(1): Show | 4 | HG00099.hp2 HG02630.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.222-3022C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132873 | ||||||
| chr12:42132875
|
G | C | 1 | a0001c0001t0027g0158 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.222-3024C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132875 | ||||||
| chr12:42132938
|
G | C | 1 | a0001c0005t0004g0006 | 2 | HG01106.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.222-3087C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132938 | ||||||
| chr12:42132971
|
C | T | 1 | a0001c0002t0003g0167 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.222-3120G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42132971 | ||||||
| chr12:42133035
|
C | T | 1 | a0001c0001t0009g0258 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.222-3184G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42133035 | ||||||
| chr12:42133041
|
G | C | 1 | a0001c0002t0004g0061 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.222-3190C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42133041 | ||||||
| chr12:42133135
|
A | C | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.222-3284T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42133135 | ||||||
| chr12:42133147
|
G | A | 6 | a0001c0001t0026g0299a0001c0001t0026g0323a0001c0001t0027g0158others(3): Show | 6 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.222-3296C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42133147 | ||||||
| chr12:42133192
|
C | T | 2 | a0001c0001t0011g0260a0001c0001t0011g0261 | 2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.222-3341G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42133192 | ||||||
| chr12:42133193
|
G | A | 1 | a0001c0003t0001g0203 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.222-3342C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42133193 | ||||||
| chr12:42133300
|
C | A | 6 | a0001c0001t0009g0003a0001c0001t0009g0254a0001c0001t0009g0255others(3): Show | 8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.222-3449G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42133300 | ||||||
| chr12:42133459
|
T | G | 1 | a0001c0001t0002g0340 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.222-3608A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42133459 | ||||||
| chr12:42133608
|
T | C | 4 | a0001c0001t0011g0094a0001c0001t0011g0095a0001c0001t0037g0096others(1): Show | 4 | HG02717.hp1 HG02818.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.222-3757A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42133608 | ||||||
| chr12:42133609
|
C | G | 2 | a0001c0001t0053g0354a0002c0004t0051g0342 | 2 | HG02809.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.222-3758G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42133609 | ||||||
| chr12:42133690
|
T | C | 1 | a0001c0001t0007g0347 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.222-3839A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42133690 | ||||||
| chr12:42133751
|
T | A | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.222-3900A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42133751 | ||||||
| chr12:42133837
|
C | A | 6 | a0001c0001t0026g0299a0001c0001t0026g0323a0001c0001t0027g0158others(3): Show | 6 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.222-3986G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42133837 | ||||||
| chr12:42133900
|
A | C | 6 | a0001c0001t0026g0299a0001c0001t0026g0323a0001c0001t0027g0158others(3): Show | 6 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.222-4049T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42133900 | ||||||
| chr12:42133919
|
G | A | 1 | a0001c0002t0003g0188 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.222-4068C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42133919 | ||||||
| chr12:42133963
|
G | A | 1 | a0001c0001t0005g0279 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.222-4112C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42133963 | ||||||
| chr12:42134028
|
C | T | 1 | a0001c0002t0003g0196 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.222-4177G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42134028 | ||||||
| chr12:42134062
|
T | C | 3 | a0001c0002t0003g0102a0001c0002t0003g0164a0001c0002t0003g0199 | 3 | HG00639.hp2 HG00738.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.222-4211A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42134062 | ||||||
| chr12:42134066
|
GGT | G | 4 | a0001c0001t0011g0094a0001c0001t0011g0095a0001c0001t0037g0096others(1): Show | 4 | HG02717.hp1 HG02818.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.222-4217_222-4216d others(4): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42134066 | ||||||
| chr12:42134105
|
TAGG | T | 59 | a0001c0002t0003g0002a0001c0002t0003g0008a0001c0002t0003g0009others(56): Show | 64 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.222-4257_222-4255d others(5): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42134105 | ||||||
| chr12:42134143
|
T | A | 7 | a0001c0001t0009g0003a0001c0001t0009g0254a0001c0001t0009g0255others(4): Show | 9 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.222-4292A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42134143 | ||||||
| chr12:42134215
|
AAG | A | 5 | a0001c0003t0013g0150a0001c0003t0013g0151a0001c0003t0013g0152others(2): Show | 5 | HG03239.hp1 HG03654.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.222-4366_222-4365d others(4): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42134215 | ||||||
| chr12:42134329
|
T | C | 1 | a0001c0002t0003g0189 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.222-4478A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42134329 | ||||||
| chr12:42134472
|
A | C | 3 | a0001c0001t0017g0234a0001c0001t0017g0235a0001c0001t0017g0242 | 3 | HG02451.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.222-4621T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42134472 | ||||||
| chr12:42134485
|
T | A | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.222-4634A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42134485 | ||||||
| chr12:42134546
|
G | A | 3 | a0001c0001t0014g0228a0001c0001t0014g0229a0001c0001t0014g0233 | 3 | HG01884.hp1 HG02280.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.222-4695C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42134546 | ||||||
| chr12:42134599
|
G | T | 3 | a0001c0001t0017g0234a0001c0001t0017g0235a0001c0001t0017g0242 | 3 | HG02451.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.222-4748C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42134599 | ||||||
| chr12:42134600
|
C | T | 3 | a0001c0001t0017g0234a0001c0001t0017g0235a0001c0001t0017g0242 | 3 | HG02451.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.222-4749G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42134600 | ||||||
| chr12:42134604
|
A | G | 1 | a0001c0001t0017g0234 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.222-4753T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42134604 | ||||||
| chr12:42134728
|
G | A | 1 | a0001c0001t0002g0298 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.222-4877C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42134728 | ||||||
| chr12:42134811
|
T | A | 1 | a0001c0001t0014g0236 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.222-4960A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42134811 | ||||||
| chr12:42134896
|
T | G | 118 | a0001c0001t0002g0123a0001c0001t0007g0016a0001c0001t0007g0344others(115): Show | 119 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.222-5045A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42134896 | ||||||
| chr12:42134982
|
C | G | 85 | a0001c0001t0002g0123a0001c0003t0001g0099a0001c0003t0001g0100others(82): Show | 85 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.222-5131G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42134982 | ||||||
| chr12:42135081
|
G | C | 1 | a0001c0001t0054g0358 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.222-5230C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42135081 | ||||||
| chr12:42135088
|
T | C | 1 | a0001c0002t0004g0062 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.222-5237A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42135088 | ||||||
| chr12:42135349
|
G | A | 1 | a0001c0001t0041g0333 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.222-5498C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42135349 | ||||||
| chr12:42135350
|
T | C | 1 | a0001c0001t0007g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.222-5499A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42135350 | ||||||
| chr12:42135400
|
T | G | 1 | a0001c0001t0002g0314 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.222-5549A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42135400 | ||||||
| chr12:42135434
|
T | A | 32 | a0001c0001t0007g0016a0001c0001t0007g0344a0001c0001t0007g0346others(29): Show | 33 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.222-5583A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42135434 | ||||||
| chr12:42135568
|
G | A | 3 | a0001c0001t0011g0094a0001c0001t0011g0095a0001c0001t0043g0093 | 3 | HG02818.hp2 HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.222-5717C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42135568 | ||||||
| chr12:42135575
|
AAAT | A | 58 | a0001c0002t0003g0202a0001c0002t0004g0028a0001c0002t0004g0029others(55): Show | 59 | HG00323.hp1 HG00621.hp2 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.222-5727_222-5725d others(5): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42135575 | ||||||
| chr12:42135642
|
A | G | 4 | a0001c0001t0026g0299a0001c0001t0026g0323a0001c0001t0028g0328others(1): Show | 4 | HG01169.hp1 HG02109.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.222-5791T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42135642 | ||||||
| chr12:42135670
|
C | T | 209 | a0001c0001t0002g0123a0001c0002t0003g0002a0001c0002t0003g0008others(206): Show | 215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.222-5819G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42135670 | ||||||
| chr12:42135692
|
A | C | 3 | a0001c0001t0018g0262a0001c0001t0018g0263a0001c0001t0018g0264 | 3 | HG02922.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.222-5841T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42135692 | ||||||
| chr12:42135727
|
C | G | 1 | a0001c0001t0041g0333 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.222-5876G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42135727 | ||||||
| chr12:42135775
|
T | C | 11 | a0001c0001t0009g0003a0001c0001t0009g0254a0001c0001t0009g0255others(8): Show | 13 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.222-5924A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42135775 | ||||||
| chr12:42135919
|
T | C | 2 | a0001c0001t0022g0240a0001c0001t0022g0241 | 2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.222-6068A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42135919 | ||||||
| chr12:42135966
|
T | C | 3 | a0001c0001t0014g0228a0001c0001t0014g0229a0001c0001t0014g0233 | 3 | HG01884.hp1 HG02280.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.222-6115A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42135966 | ||||||
| chr12:42135986
|
A | G | 1 | a0001c0002t0003g0170 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.222-6135T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42135986 | ||||||
| chr12:42136003
|
C | T | 1 | a0001c0002t0004g0072 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.222-6152G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136003 | ||||||
| chr12:42136017
|
T | C | 1 | a0001c0001t0028g0328 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.222-6166A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136017 | ||||||
| chr12:42136126
|
A | C | 1 | a0001c0001t0014g0236 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.222-6275T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136126 | ||||||
| chr12:42136134
|
G | T | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.222-6283C>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136134 | ||||||
| chr12:42136299
|
G | A | 2 | a0001c0001t0027g0158a0001c0001t0027g0232 | 2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.222-6448C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136299 | ||||||
| chr12:42136380
|
C | T | 2 | a0001c0003t0001g0207a0001c0003t0001g0214 | 2 | HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.222-6529G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136380 | ||||||
| chr12:42136604
|
A | G | 2 | a0001c0001t0022g0240a0001c0001t0022g0241 | 2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.222-6753T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136604 | ||||||
| chr12:42136683
|
A | C | 6 | a0001c0001t0010g0019a0001c0001t0010g0020a0001c0001t0010g0021others(3): Show | 6 | HG03704.hp1 HG03831.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.222-6832T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136683 | ||||||
| chr12:42136751
|
T | TATAC | 9 | a0001c0001t0002g0334a0001c0001t0005g0341a0001c0001t0007g0361others(6): Show | 9 | HG01255.hp1 HG02886.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.222-6904_222-6901d others(6): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136751 | ||||||
| chr12:42136751
|
T | TATACATA others(1): Show |
44 | a0001c0001t0002g0285a0001c0001t0002g0335a0001c0001t0005g0267others(41): Show | 46 | HG00733.hp2 HG00738.hp1 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.222-6908_222-6901d others(10): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136751 | ||||||
| chr12:42136751
|
T | TATACATA others(5): Show |
205 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0014others(202): Show | 222 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.222-6912_222-6901d others(14): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136751 | ||||||
| chr12:42136751
|
T | TATACATA others(9): Show |
91 | a0001c0001t0002g0015a0001c0001t0002g0296a0001c0001t0002g0315others(88): Show | 92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.222-6916_222-6901d others(18): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136751 | ||||||
| chr12:42136751
|
T | TATACATA others(13): Show |
10 | a0001c0001t0002g0320a0001c0001t0002g0321a0001c0001t0016g0084others(7): Show | 10 | HG00642.hp2 HG01517.hp2 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.222-6920_222-6901d others(22): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136751 | ||||||
| chr12:42136751
|
T | TTATACAT others(6): Show |
1 | a0001c0003t0001g0203 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.222-6901_222-6900i others(15): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136751 | ||||||
| chr12:42136751
|
TATACATA others(9): Show |
T | 3 | a0001c0001t0009g0254a0001c0001t0009g0256a0001c0001t0009g0257 | 3 | HG02055.hp1 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.222-6916_222-6901d others(18): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136751 | ||||||
| chr12:42136785
|
T | TACATACA others(9): Show |
2 | a0001c0001t0002g0297a0002c0004t0002g0007 | 3 | HG00423.hp2 HG02015.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.222-6935_222-6934i others(18): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136785 | ||||||
| chr12:42136789
|
A | T | 6 | a0001c0001t0002g0302a0001c0001t0011g0260a0001c0001t0011g0261others(3): Show | 6 | HG01891.hp1 HG02630.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.222-6938T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136789 | ||||||
| chr12:42136793
|
A | C | 3 | a0001c0001t0022g0240a0001c0001t0022g0241a0001c0002t0019g0046 | 3 | HG02258.hp1 HG03225.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.222-6942T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136793 | ||||||
| chr12:42136797
|
C | A | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.222-6946G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136797 | ||||||
| chr12:42136837
|
G | A | 10 | a0001c0001t0009g0003a0001c0001t0009g0254a0001c0001t0009g0255others(7): Show | 12 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.222-6986C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42136837 | ||||||
| chr12:42137028
|
T | C | 1 | a0001c0001t0016g0084 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.222-7177A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137028 | ||||||
| chr12:42137132
|
G | C | 5 | a0001c0001t0017g0234a0001c0001t0017g0235a0001c0001t0017g0242others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.222-7281C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137132 | ||||||
| chr12:42137209
|
C | T | 1 | a0001c0002t0004g0045 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.221+7217G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137209 | ||||||
| chr12:42137235
|
G | A | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.221+7191C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137235 | ||||||
| chr12:42137236
|
C | T | 1 | a0001c0002t0004g0044 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.221+7190G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137236 | ||||||
| chr12:42137335
|
T | C | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.221+7091A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137335 | ||||||
| chr12:42137344
|
T | C | 2 | a0001c0002t0020g0026a0001c0002t0020g0027 | 2 | HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.221+7082A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137344 | ||||||
| chr12:42137503
|
C | CA | 127 | a0001c0001t0002g0322a0001c0001t0005g0280a0001c0001t0005g0282others(124): Show | 133 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.221+6922dupT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137503 | ||||||
| chr12:42137503
|
C | CAA | 21 | a0001c0001t0024g0226a0001c0001t0024g0227a0001c0002t0003g0091others(18): Show | 21 | HG00140.hp1 HG00609.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.221+6921_221+6922d others(4): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137503 | ||||||
| chr12:42137503
|
C | CAAA | 66 | a0001c0001t0002g0123a0001c0002t0003g0198a0001c0002t0025g0098others(63): Show | 66 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.221+6920_221+6922d others(5): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137503 | ||||||
| chr12:42137503
|
C | CAAAA | 9 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0139others(6): Show | 9 | HG01255.hp2 HG01934.hp1 HG03540.hp2 others(6): Show |
intron_variant | MODIFIER | c.221+6919_221+6922d others(6): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137503 | ||||||
| chr12:42137503
|
CA | C | 7 | a0001c0001t0002g0284a0001c0001t0005g0272a0001c0001t0007g0344others(4): Show | 7 | HG02922.hp1 HG02922.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.221+6922delT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137503 | ||||||
| chr12:42137529
|
G | A | 1 | a0001c0001t0024g0227 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.221+6897C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137529 | ||||||
| chr12:42137549
|
G | A | 1 | a0001c0006t0056g0375 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.221+6877C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137549 | ||||||
| chr12:42137574
|
G | A | 2 | a0001c0003t0001g0124a0001c0003t0001g0144 | 2 | HG00544.hp2 HG00597.hp2 |
intron_variant | MODIFIER | c.221+6852C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137574 | ||||||
| chr12:42137617
|
C | G | 1 | a0001c0001t0027g0158 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.221+6809G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137617 | ||||||
| chr12:42137705
|
C | A | 1 | a0001c0001t0043g0093 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.221+6721G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137705 | ||||||
| chr12:42137749
|
T | C | 3 | a0001c0002t0003g0102a0001c0002t0003g0164a0001c0002t0003g0199 | 3 | HG00639.hp2 HG00738.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.221+6677A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137749 | ||||||
| chr12:42137750
|
C | T | 4 | a0001c0003t0001g0204a0001c0003t0001g0215a0001c0003t0001g0216others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.221+6676G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137750 | ||||||
| chr12:42137751
|
C | A | 3 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0324 | 3 | HG02896.hp1 HG02897.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.221+6675G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137751 | ||||||
| chr12:42137762
|
G | GAAAAA | 19 | a0001c0001t0005g0331a0001c0001t0007g0351a0001c0001t0009g0254others(16): Show | 19 | HG01243.hp1 HG01255.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.221+6659_221+6663d others(7): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137762 | ||||||
| chr12:42137762
|
G | GAAAAAA | 279 | a0001c0001t0002g0123a0001c0001t0002g0298a0001c0001t0005g0004others(276): Show | 293 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.221+6658_221+6663d others(8): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137762 | ||||||
| chr12:42137762
|
G | GAAAAAAA | 8 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0324others(5): Show | 8 | HG02896.hp1 HG02897.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.221+6657_221+6663d others(9): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137762 | ||||||
| chr12:42137762
|
G | GGAAAAAA | 10 | a0001c0001t0007g0360a0001c0001t0008g0363a0001c0001t0008g0364others(7): Show | 10 | HG00642.hp1 HG01069.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.221+6663_221+6664i others(9): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137762 | ||||||
| chr12:42137821
|
G | A | 2 | a0001c0002t0004g0072a0001c0002t0004g0073 | 2 | HG00323.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.221+6605C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137821 | ||||||
| chr12:42137852
|
T | C | 17 | a0001c0001t0006g0011a0001c0001t0006g0012a0001c0001t0006g0013others(14): Show | 20 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.221+6574A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137852 | ||||||
| chr12:42137864
|
G | A | 123 | a0001c0002t0003g0002a0001c0002t0003g0008a0001c0002t0003g0009others(120): Show | 129 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.221+6562C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137864 | ||||||
| chr12:42137872
|
A | T | 1 | a0001c0002t0004g0074 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.221+6554T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137872 | ||||||
| chr12:42137976
|
A | G | 1 | a0001c0001t0014g0236 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.221+6450T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137976 | ||||||
| chr12:42137990
|
G | A | 1 | a0001c0002t0004g0074 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.221+6436C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42137990 | ||||||
| chr12:42138136
|
A | G | 1 | a0001c0002t0020g0026 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.221+6290T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42138136 | ||||||
| chr12:42138218
|
G | A | 2 | a0001c0003t0001g0099a0001c0003t0001g0120 | 2 | NA18990.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.221+6208C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42138218 | ||||||
| chr12:42138306
|
C | T | 1 | a0001c0002t0003g0165 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.221+6120G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42138306 | ||||||
| chr12:42138337
|
C | T | 309 | a0001c0001t0002g0123a0001c0001t0005g0004a0001c0001t0005g0267others(306): Show | 323 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.221+6089G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42138337 | ||||||
| chr12:42138399
|
T | C | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.221+6027A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42138399 | ||||||
| chr12:42138442
|
T | G | 28 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(25): Show | 30 | HG00544.hp1 HG00597.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.221+5984A>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42138442 | ||||||
| chr12:42138482
|
C | G | 2 | a0001c0001t0011g0094a0001c0001t0011g0095 | 2 | HG02818.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.221+5944G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42138482 | ||||||
| chr12:42138546
|
G | GA | 305 | a0001c0001t0002g0123a0001c0001t0005g0004a0001c0001t0005g0267others(302): Show | 319 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(316): Show |
intron_variant | MODIFIER | c.221+5879dupT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42138546 | ||||||
| chr12:42138557
|
G | A | 2 | a0001c0001t0021g0230a0001c0001t0021g0231 | 2 | HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.221+5869C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42138557 | ||||||
| chr12:42138584
|
G | A | 2 | a0001c0001t0027g0158a0001c0001t0027g0232 | 2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.221+5842C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42138584 | ||||||
| chr12:42138660
|
C | A | 1 | a0001c0003t0001g0121 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.221+5766G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42138660 | ||||||
| chr12:42138673
|
T | A | 6 | a0001c0002t0003g0087a0001c0002t0003g0088a0001c0002t0003g0089others(3): Show | 6 | HG01175.hp2 HG01884.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.221+5753A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42138673 | ||||||
| chr12:42138819
|
A | C | 86 | a0001c0001t0002g0123a0001c0003t0001g0099a0001c0003t0001g0100others(83): Show | 86 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.221+5607T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42138819 | ||||||
| chr12:42138913
|
C | G | 17 | a0001c0001t0006g0011a0001c0001t0006g0012a0001c0001t0006g0013others(14): Show | 20 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.221+5513G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42138913 | ||||||
| chr12:42138986
|
C | T | 3 | a0001c0002t0004g0038a0001c0002t0004g0039a0001c0002t0004g0040 | 3 | HG01081.hp1 HG01243.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.221+5440G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42138986 | ||||||
| chr12:42139037
|
C | CA | 79 | a0001c0001t0011g0260a0001c0001t0011g0261a0001c0003t0001g0099others(76): Show | 79 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.221+5388dupT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42139037 | ||||||
| chr12:42139037
|
C | CAA | 8 | a0001c0001t0002g0123a0001c0003t0001g0122a0001c0003t0001g0140others(5): Show | 8 | NA18962.hp1 NA18969.hp1 NA18977.hp2 others(5): Show |
intron_variant | MODIFIER | c.221+5387_221+5388d others(4): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42139037 | ||||||
| chr12:42139121
|
A | G | 3 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0157 | 3 | NA18953.hp1 NA18972.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.221+5305T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42139121 | ||||||
| chr12:42139203
|
T | TA | 7 | a0001c0001t0011g0260a0001c0001t0011g0261a0001c0001t0016g0084others(4): Show | 7 | HG01891.hp1 HG02630.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.221+5222dupT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42139203 | ||||||
| chr12:42139262
|
T | TTTCTCCT others(11): Show |
3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.221+5146_221+5163d others(20): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42139262 | ||||||
| chr12:42139348
|
T | A | 1 | a0001c0001t0014g0236 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.221+5078A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42139348 | ||||||
| chr12:42139442
|
G | C | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.221+4984C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42139442 | ||||||
| chr12:42139552
|
A | T | 1 | a0001c0001t0043g0093 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.221+4874T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42139552 | ||||||
| chr12:42139594
|
T | C | 6 | a0001c0001t0010g0019a0001c0001t0010g0020a0001c0001t0010g0021others(3): Show | 6 | HG03704.hp1 HG03831.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.221+4832A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42139594 | ||||||
| chr12:42139617
|
G | C | 1 | a0001c0001t0038g0271 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.221+4809C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42139617 | ||||||
| chr12:42139696
|
C | A | 1 | a0001c0001t0014g0236 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.221+4730G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42139696 | ||||||
| chr12:42139789
|
C | T | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.221+4637G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42139789 | ||||||
| chr12:42139877
|
C | A | 1 | a0001c0002t0015g0200 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.221+4549G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42139877 | ||||||
| chr12:42139892
|
G | A | 1 | a0001c0002t0004g0030 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.221+4534C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42139892 | ||||||
| chr12:42139895
|
A | G | 2 | a0001c0002t0004g0036a0001c0002t0004g0037 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.221+4531T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42139895 | ||||||
| chr12:42140063
|
C | A | 2 | a0001c0002t0004g0075a0001c0002t0004g0076 | 2 | HG01975.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.221+4363G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140063 | ||||||
| chr12:42140163
|
A | C | 1 | a0001c0002t0004g0035 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.221+4263T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140163 | ||||||
| chr12:42140180
|
C | CA | 84 | a0001c0001t0002g0301a0001c0001t0005g0004a0001c0001t0005g0268others(81): Show | 92 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.221+4245dupT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140180 | ||||||
| chr12:42140197
|
A | C | 1 | a0001c0001t0016g0086 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.221+4229T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140197 | ||||||
| chr12:42140197
|
A | G | 2 | a0001c0001t0016g0084a0001c0001t0016g0085 | 2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.221+4229T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140197 | ||||||
| chr12:42140198
|
G | A | 60 | a0001c0001t0005g0282a0001c0001t0007g0361a0001c0001t0027g0232others(57): Show | 61 | HG00323.hp1 HG00621.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.221+4228C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140198 | ||||||
| chr12:42140199
|
GC | G | 5 | a0001c0002t0003g0202a0001c0002t0004g0077a0001c0002t0004g0078others(2): Show | 5 | NA18944.hp2 NA18991.hp1 NA19058.hp1 others(2): Show |
intron_variant | MODIFIER | c.221+4226delG | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140199 | ||||||
| chr12:42140200
|
C | CG | 95 | a0001c0001t0002g0001a0001c0001t0002g0015a0001c0001t0002g0302others(92): Show | 103 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.221+4225dupC | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140200 | ||||||
| chr12:42140200
|
C | CGG | 73 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0123others(70): Show | 77 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.221+4224_221+4225d others(4): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140200 | ||||||
| chr12:42140200
|
C | G | 62 | a0001c0001t0005g0282a0001c0001t0007g0361a0001c0001t0010g0019others(59): Show | 63 | HG00323.hp1 HG00621.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.221+4226G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140200 | ||||||
| chr12:42140200
|
CG | C | 62 | a0001c0001t0008g0370a0001c0001t0011g0260a0001c0001t0011g0261others(59): Show | 67 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.221+4225delC | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140200 | ||||||
| chr12:42140201
|
G | C | 55 | a0001c0001t0005g0282a0001c0001t0007g0361a0001c0001t0027g0232others(52): Show | 56 | HG00323.hp1 HG00621.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.221+4225C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140201 | ||||||
| chr12:42140202
|
G | C | 5 | a0001c0002t0003g0202a0001c0002t0004g0077a0001c0002t0004g0078others(2): Show | 5 | NA18944.hp2 NA18991.hp1 NA19058.hp1 others(2): Show |
intron_variant | MODIFIER | c.221+4224C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140202 | ||||||
| chr12:42140261
|
T | C | 1 | a0001c0001t0014g0233 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.221+4165A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140261 | ||||||
| chr12:42140272
|
A | G | 1 | a0001c0002t0003g0160 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.221+4154T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140272 | ||||||
| chr12:42140283
|
G | C | 85 | a0001c0001t0002g0123a0001c0003t0001g0099a0001c0003t0001g0100others(82): Show | 85 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.221+4143C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140283 | ||||||
| chr12:42140296
|
A | C | 1 | a0001c0002t0050g0159 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.221+4130T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140296 | ||||||
| chr12:42140437
|
A | G | 1 | a0001c0001t0043g0093 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.221+3989T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140437 | ||||||
| chr12:42140569
|
A | ACAGT | 212 | a0001c0001t0002g0123a0001c0001t0016g0084a0001c0001t0016g0085others(209): Show | 218 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.221+3853_221+3856d others(6): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140569 | ||||||
| chr12:42140580
|
C | T | 209 | a0001c0001t0002g0123a0001c0002t0003g0002a0001c0002t0003g0008others(206): Show | 215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.221+3846G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140580 | ||||||
| chr12:42140640
|
A | C | 1 | a0001c0001t0007g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.221+3786T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140640 | ||||||
| chr12:42140689
|
C | T | 209 | a0001c0001t0002g0123a0001c0002t0003g0002a0001c0002t0003g0008others(206): Show | 215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.221+3737G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140689 | ||||||
| chr12:42140704
|
A | G | 1 | a0001c0001t0027g0158 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.221+3722T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140704 | ||||||
| chr12:42140827
|
T | A | 3 | a0001c0001t0017g0234a0001c0001t0017g0235a0001c0001t0017g0242 | 3 | HG02451.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.221+3599A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140827 | ||||||
| chr12:42140941
|
T | C | 17 | a0001c0001t0006g0011a0001c0001t0006g0012a0001c0001t0006g0013others(14): Show | 20 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.221+3485A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42140941 | ||||||
| chr12:42141017
|
T | C | 1 | a0001c0001t0014g0236 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.221+3409A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42141017 | ||||||
| chr12:42141047
|
C | A | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.221+3379G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42141047 | ||||||
| chr12:42141403
|
T | C | 1 | a0001c0001t0005g0283 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.221+3023A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42141403 | ||||||
| chr12:42141498
|
C | T | 1 | a0001c0003t0001g0100 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.221+2928G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42141498 | ||||||
| chr12:42141547
|
C | CA | 11 | a0001c0001t0002g0330a0001c0001t0002g0332a0001c0001t0009g0003others(8): Show | 13 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.221+2878dupT | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42141547 | ||||||
| chr12:42141578
|
A | G | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.221+2848T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42141578 | ||||||
| chr12:42141601
|
T | C | 1 | a0001c0002t0015g0238 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.221+2825A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42141601 | ||||||
| chr12:42141672
|
T | C | 1 | a0001c0002t0048g0239 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.221+2754A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42141672 | ||||||
| chr12:42141798
|
G | A | 4 | a0001c0001t0011g0094a0001c0001t0011g0095a0001c0001t0037g0096others(1): Show | 4 | HG02717.hp1 HG02818.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.221+2628C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42141798 | ||||||
| chr12:42141870
|
G | A | 20 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(17): Show | 22 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(19): Show |
intron_variant | MODIFIER | c.221+2556C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42141870 | ||||||
| chr12:42141895
|
GTTCCT | G | 6 | a0001c0001t0010g0019a0001c0001t0010g0020a0001c0001t0010g0021others(3): Show | 6 | HG03704.hp1 HG03831.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.221+2526_221+2530d others(7): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42141895 | ||||||
| chr12:42141975
|
A | G | 32 | a0001c0001t0007g0016a0001c0001t0007g0344a0001c0001t0007g0346others(29): Show | 33 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.221+2451T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42141975 | ||||||
| chr12:42142019
|
C | T | 22 | a0001c0001t0005g0004a0001c0001t0005g0267a0001c0001t0005g0268others(19): Show | 24 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(21): Show |
intron_variant | MODIFIER | c.221+2407G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42142019 | ||||||
| chr12:42142254
|
T | C | 2 | a0001c0001t0022g0240a0001c0001t0022g0241 | 2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.221+2172A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42142254 | ||||||
| chr12:42142262
|
G | A | 51 | a0001c0001t0006g0011a0001c0001t0006g0012a0001c0001t0006g0013others(48): Show | 55 | HG00423.hp1 HG00639.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.221+2164C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42142262 | ||||||
| chr12:42142320
|
G | A | 2 | a0001c0001t0022g0240a0001c0001t0022g0241 | 2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.221+2106C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42142320 | ||||||
| chr12:42142337
|
A | AT | 75 | a0001c0001t0002g0123a0001c0001t0008g0363a0001c0001t0008g0364others(72): Show | 75 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.221+2088dupA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42142337 | ||||||
| chr12:42142337
|
A | ATT | 8 | a0001c0001t0011g0094a0001c0001t0011g0095a0001c0001t0011g0260others(5): Show | 8 | HG01891.hp1 HG02717.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.221+2087_221+2088d others(4): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42142337 | ||||||
| chr12:42142337
|
AT | A | 21 | a0001c0001t0005g0331a0001c0001t0006g0011a0001c0001t0006g0012others(18): Show | 24 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.221+2088delA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42142337 | ||||||
| chr12:42142381
|
G | C | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.221+2045C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42142381 | ||||||
| chr12:42142395
|
G | A | 10 | a0001c0001t0009g0003a0001c0001t0009g0254a0001c0001t0009g0255others(7): Show | 12 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.221+2031C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42142395 | ||||||
| chr12:42142462
|
A | C | 1 | a0001c0002t0034g0025 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.221+1964T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42142462 | ||||||
| chr12:42142504
|
T | A | 1 | a0001c0002t0003g0251 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.221+1922A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42142504 | ||||||
| chr12:42142507
|
T | C | 1 | a0001c0001t0002g0332 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.221+1919A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42142507 | ||||||
| chr12:42142522
|
A | AT | 62 | a0001c0002t0004g0028a0001c0002t0004g0029a0001c0002t0004g0030others(59): Show | 63 | HG00323.hp1 HG00621.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.221+1903dupA | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42142522 | ||||||
| chr12:42142695
|
T | C | 1 | a0001c0001t0016g0086 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.221+1731A>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42142695 | ||||||
| chr12:42142711
|
C | T | 3 | a0001c0001t0018g0262a0001c0001t0018g0263a0001c0001t0018g0264 | 3 | HG02922.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.221+1715G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42142711 | ||||||
| chr12:42142805
|
C | T | 4 | a0001c0001t0011g0094a0001c0001t0011g0095a0001c0001t0037g0096others(1): Show | 4 | HG02717.hp1 HG02818.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.221+1621G>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42142805 | ||||||
| chr12:42142825
|
G | A | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.221+1601C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42142825 | ||||||
| chr12:42142882
|
A | T | 32 | a0001c0001t0007g0016a0001c0001t0007g0344a0001c0001t0007g0346others(29): Show | 33 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.221+1544T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42142882 | ||||||
| chr12:42143217
|
C | A | 2 | a0001c0003t0001g0253a0001c0003t0039g0252 | 2 | HG00323.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.221+1209G>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42143217 | ||||||
| chr12:42143254
|
A | G | 6 | a0001c0002t0003g0087a0001c0002t0003g0088a0001c0002t0003g0089others(3): Show | 6 | HG01175.hp2 HG01884.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.221+1172T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42143254 | ||||||
| chr12:42143335
|
A | C | 3 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086 | 3 | HG02630.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.221+1091T>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42143335 | ||||||
| chr12:42143582
|
G | C | 6 | a0001c0001t0009g0003a0001c0001t0009g0254a0001c0001t0009g0255others(3): Show | 8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.221+844C>G | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42143582 | ||||||
| chr12:42143748
|
C | G | 2 | a0001c0001t0008g0363a0001c0001t0008g0364 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.221+678G>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42143748 | ||||||
| chr12:42143816
|
G | A | 1 | a0001c0003t0013g0259 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.221+610C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42143816 | ||||||
| chr12:42143869
|
T | A | 1 | a0001c0001t0041g0333 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.221+557A>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42143869 | ||||||
| chr12:42143870
|
G | A | 2 | a0001c0002t0004g0082a0001c0002t0004g0083 | 2 | HG02300.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.221+556C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42143870 | ||||||
| chr12:42143952
|
G | A | 1 | a0001c0001t0008g0372 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.221+474C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42143952 | ||||||
| chr12:42144004
|
A | T | 2 | a0001c0001t0011g0260a0001c0001t0011g0261 | 2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.221+422T>A | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42144004 | ||||||
| chr12:42144260
|
A | G | 286 | a0001c0001t0002g0123a0001c0001t0006g0011a0001c0001t0006g0012others(283): Show | 298 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.221+166T>C | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42144260 | ||||||
| chr12:42144317
|
G | A | 7 | a0001c0001t0002g0334a0001c0001t0002g0335a0001c0001t0002g0336others(4): Show | 7 | HG00099.hp1 HG00140.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.221+109C>T | GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42144317 | ||||||
| chr12:42144351
|
G | GCAGCCCG others(9): Show |
1 | a0001c0001t0005g0341 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.221+59_221+74dupGG others(14): Show |
GXYLT1 | ENSG00000151233.11 | transcript | ENST00000398675.8 | protein_coding | 1/7 | chr12 | 42144351 |