Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 9942 |
|---|---|
| ensemblid | ENSG00000093217.11 |
| hgncid | 12839 |
| symbol | XYLB |
| name | xylulokinase |
| refseq_nuc | NM_005108.4 |
| refseq_prot | NP_005099.2 |
| ensembl_nuc | ENST00000207870.8 |
| ensembl_prot | ENSP00000207870.3 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 38346785 |
| end | 38414985 |
| strand | + |
| ver | v1.2 |
| region | chr3:38346785-38414985 |
| region5000 | chr3:38341785-38419985 |
| regionname0 | XYLB_chr3_38346785_38414985 |
| regionname5000 | XYLB_chr3_38341785_38419985 |
| 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 | 536 | 246 | 66 | 51 | 90 | 6 | 31 | 66 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0002 | 0/0 | 536 | 79 | 6 | 16 | 43 | 4 | 10 | 29 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0003 | 0/0 | 536 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0004 | 0/0 | 536 | 7 | 5 | 2 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0005 | 0/0 | 536 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0006 | 0/0 | 536 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0007 | 0/0 | 475 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0008 | 0/0 | 536 | 2 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0009 | 0/0 | 536 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0010 | 0/0 | 536 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0011 | 0/0 | 536 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0012 | 0/0 | 449 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0013 | 0/0 | 536 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1611 | 225 | 54 | 46 | 90 | 6 | 28 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| c0002 | 0/0 | 1611 | 79 | 6 | 16 | 43 | 4 | 10 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| c0003 | 0/0 | 1611 | 17 | 10 | 4 | 0 | 0 | 3 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| c0004 | 0/0 | 1611 | 7 | 7 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| c0005 | 0/0 | 1611 | 7 | 5 | 2 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| c0006 | 0/0 | 1611 | 5 | 5 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| c0007 | 0/0 | 1611 | 3 | 0 | 0 | 3 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| c0008 | 0/0 | 1611 | 3 | 1 | 2 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| c0009 | 1/0 | 1611 | 3 | 1 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| c0010 | 0/0 | 1611 | 2 | 1 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| c0011 | 0/0 | 1611 | 2 | 2 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| c0012 | 0/0 | 1611 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| c0013 | 0/0 | 1611 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| c0014 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| c0015 | 0/0 | 1611 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| c0016 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 2057 | 97 | 12 | 18 | 42 | 7 | 17 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| t0002 | 1/0 | 2057 | 94 | 5 | 22 | 45 | 3 | 18 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| t0003 | 0/0 | 2057 | 61 | 44 | 15 | 1 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| t0004 | 0/0 | 2057 | 45 | 8 | 6 | 26 | 0 | 5 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| t0005 | 0/0 | 2054 | 29 | 0 | 8 | 20 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| t0006 | 0/0 | 2057 | 11 | 9 | 2 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| t0007 | 0/0 | 2054 | 6 | 5 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| t0008 | 0/0 | 2058 | 4 | 4 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| t0009 | 0/0 | 2057 | 2 | 2 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| t0010 | 0/0 | 2054 | 2 | 2 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| t0011 | 0/0 | 2057 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| t0012 | 0/0 | 2057 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| t0013 | 0/0 | 2057 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| t0014 | 0/0 | 2057 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| t0015 | 0/0 | 2057 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| t0016 | 0/0 | 2057 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| t0017 | 0/0 | 2057 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| 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 | 2 | 0 | 2 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0005 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0009 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0117 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1611 | 225 | 54 | 46 | 90 | 6 | 28 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0001c0003 | 0/0 | 1611 | 17 | 10 | 4 | 0 | 0 | 3 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0001c0009 | 1/0 | 1611 | 3 | 1 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0001c0014 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0002c0002 | 0/0 | 1611 | 79 | 6 | 16 | 43 | 4 | 10 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0003c0004 | 0/0 | 1611 | 7 | 7 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0004c0005 | 0/0 | 1611 | 7 | 5 | 2 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0005c0006 | 0/0 | 1611 | 5 | 5 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0006c0008 | 0/0 | 1611 | 3 | 1 | 2 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0007c0007 | 0/0 | 1611 | 3 | 0 | 0 | 3 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0008c0010 | 0/0 | 1611 | 2 | 1 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0009c0011 | 0/0 | 1611 | 2 | 2 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0010c0015 | 0/0 | 1611 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0011c0016 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0012c0013 | 0/0 | 1611 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0013c0012 | 0/0 | 1611 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3667 | 71 | 10 | 10 | 32 | 4 | 14 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0001c0001t0002 | 0/0 | 3667 | 63 | 3 | 17 | 29 | 2 | 12 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0001c0001t0003 | 0/0 | 3667 | 36 | 29 | 7 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0001c0001t0004 | 0/0 | 3667 | 19 | 0 | 6 | 12 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0001c0001t0005 | 0/0 | 3664 | 19 | 0 | 5 | 13 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0001c0001t0006 | 0/0 | 3667 | 4 | 4 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0001c0001t0007 | 0/0 | 3664 | 2 | 1 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0001c0001t0008 | 0/0 | 3668 | 3 | 3 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0001c0001t0009 | 0/0 | 3667 | 2 | 2 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0001c0001t0010 | 0/0 | 3664 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0001c0001t0011 | 0/0 | 3667 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0001c0001t0013 | 0/0 | 3667 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0001c0001t0014 | 0/0 | 3667 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0001c0001t0015 | 0/0 | 3667 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0001c0001t0017 | 0/0 | 3667 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0001c0003t0001 | 0/0 | 3667 | 2 | 0 | 0 | 0 | 0 | 2 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0001c0003t0003 | 0/0 | 3667 | 12 | 7 | 4 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0001c0003t0004 | 0/0 | 3667 | 2 | 2 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0001c0003t0008 | 0/0 | 3668 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0001c0009t0002 | 1/0 | 3667 | 1 | 0 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0001c0009t0003 | 0/0 | 3667 | 2 | 1 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0001c0014t0006 | 0/0 | 3667 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0002c0002t0001 | 0/0 | 3667 | 21 | 0 | 7 | 10 | 3 | 1 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0002c0002t0002 | 0/0 | 3667 | 25 | 1 | 5 | 13 | 1 | 5 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0002c0002t0003 | 0/0 | 3667 | 3 | 1 | 1 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0002c0002t0004 | 0/0 | 3667 | 19 | 2 | 0 | 13 | 0 | 4 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0002c0002t0005 | 0/0 | 3664 | 9 | 0 | 3 | 6 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0002c0002t0006 | 0/0 | 3667 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0002c0002t0016 | 0/0 | 3667 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0003c0004t0002 | 0/0 | 3667 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0003c0004t0003 | 0/0 | 3667 | 3 | 3 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0003c0004t0004 | 0/0 | 3667 | 3 | 3 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0004c0005t0003 | 0/0 | 3667 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0004c0005t0006 | 0/0 | 3667 | 3 | 1 | 2 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0004c0005t0007 | 0/0 | 3664 | 3 | 3 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0005c0006t0001 | 0/0 | 3667 | 2 | 2 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0005c0006t0003 | 0/0 | 3667 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0005c0006t0004 | 0/0 | 3667 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0005c0006t0007 | 0/0 | 3664 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0006c0008t0003 | 0/0 | 3667 | 3 | 1 | 2 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0007c0007t0002 | 0/0 | 3667 | 3 | 0 | 0 | 3 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0008c0010t0004 | 0/0 | 3667 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0008c0010t0010 | 0/0 | 3664 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0009c0011t0006 | 0/0 | 3667 | 2 | 2 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0010c0015t0005 | 0/0 | 3664 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0011c0016t0012 | 0/0 | 3667 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0012c0013t0001 | 0/0 | 3667 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| a0013c0012t0002 | 0/0 | 3667 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | copy fasta | chr3 | 38341785 | 38419985 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0117 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0003g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0003g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0003g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0003g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0003g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0003g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0003g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0003g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0003g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0003g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0003g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0003g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0004g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0004g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0004g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0004g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0004g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0005g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0005g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0005g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0005g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0005g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0005g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0005g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0005g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0005g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0005g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0005g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0005g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0005g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0005g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0005g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0005g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0005g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0006g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0006g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0006g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0007g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0007g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0008g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0008g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0008g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0009g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0009g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0010g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0011g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0013g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0014g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0015g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0001t0017g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0003t0003g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0003t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0003t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0003t0003g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0003t0003g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0003t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0003t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0003t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0003t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0003t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0003t0003g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0003t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0003t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0003t0008g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0009t0002g0009 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0009t0003g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0009t0003g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0001c0014t0006g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0004g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0004g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0004g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0004g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0004g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0005g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0005g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0005g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0005g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0005g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0005g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0005g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0005g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0006g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0002c0002t0016g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0003c0004t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0003c0004t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0003c0004t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0003c0004t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0003c0004t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0003c0004t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0003c0004t0004g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0004c0005t0003g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0004c0005t0006g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0004c0005t0006g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0004c0005t0007g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0004c0005t0007g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0004c0005t0007g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0005c0006t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0005c0006t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0005c0006t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0005c0006t0004g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0005c0006t0007g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0006c0008t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0006c0008t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0006c0008t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0007c0007t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0007c0007t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0007c0007t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0008c0010t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0008c0010t0010g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0009c0011t0006g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0009c0011t0006g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0010c0015t0005g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0011c0016t0012g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0012c0013t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| a0013c0012t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0002 | t0002 | g0017 | EUR | GBR | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0196 | EUR | GBR | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0227 | EUR | FIN | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0154 | EUR | FIN | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0187 | EUR | FIN | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0056 | EUR | FIN | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0087 | EAS | CHS | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0235 | EAS | CHS | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | CHS | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG00423 | hp2 | a0002 | c0002 | t0004 | g0016 | EAS | CHS | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | CHS | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0295 | EAS | CHS | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | CHS | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG00558 | hp2 | a0002 | c0002 | t0004 | g0043 | EAS | CHS | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0103 | EAS | CHS | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | CHS | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0069 | EAS | CHS | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0292 | EAS | CHS | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | CHS | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG00621 | hp2 | a0001 | c0001 | t0005 | g0293 | EAS | CHS | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG00639 | hp1 | a0002 | c0002 | t0002 | g0037 | AMR | PUR | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG00639 | hp2 | a0001 | c0001 | t0007 | g0335 | AMR | PUR | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0225 | AMR | PUR | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0226 | AMR | PUR | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG00741 | hp2 | a0001 | c0003 | t0003 | g0271 | AMR | PUR | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0240 | AMR | PUR | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0051 | AMR | PUR | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01070 | hp1 | a0001 | c0001 | t0005 | g0223 | AMR | PUR | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0158 | AMR | PUR | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | PUR | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0224 | AMR | PUR | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0247 | AMR | PUR | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01074 | hp2 | a0004 | c0005 | t0006 | g0010 | AMR | PUR | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0092 | AMR | PUR | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01081 | hp2 | a0002 | c0002 | t0002 | g0054 | AMR | PUR | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0246 | AMR | PUR | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01106 | hp1 | a0002 | c0002 | t0002 | g0083 | AMR | PUR | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0052 | AMR | PUR | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01109 | hp1 | a0006 | c0008 | t0003 | g0024 | AMR | PUR | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0237 | AMR | PUR | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0338 | AMR | PUR | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0332 | AMR | PUR | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0345 | AMR | PUR | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0339 | AMR | PUR | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0211 | AMR | PUR | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0285 | AMR | PUR | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | CLM | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01256 | hp1 | a0002 | c0002 | t0002 | g0090 | AMR | CLM | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01256 | hp2 | a0001 | c0003 | t0003 | g0007 | AMR | CLM | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0213 | AMR | CLM | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01258 | hp2 | a0001 | c0003 | t0003 | g0007 | AMR | CLM | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0027 | AMR | CLM | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01261 | hp2 | a0001 | c0003 | t0003 | g0262 | AMR | CLM | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0057 | AMR | CLM | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0281 | AMR | CLM | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0067 | AMR | CLM | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0212 | AMR | CLM | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01433 | hp1 | a0012 | c0013 | t0001 | g0080 | AMR | CLM | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | CLM | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0058 | EUR | IBS | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0050 | EUR | IBS | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0231 | EUR | IBS | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0023 | EUR | IBS | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0256 | AFR | ACB | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | ACB | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0334 | AFR | ACB | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0254 | AFR | ACB | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01928 | hp2 | a0002 | c0002 | t0003 | g0093 | AMR | PEL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0209 | AMR | PEL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01934 | hp2 | a0006 | c0008 | t0003 | g0029 | AMR | PEL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01943 | hp2 | a0001 | c0001 | t0005 | g0195 | AMR | PEL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0245 | AMR | PEL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01952 | hp2 | a0001 | c0001 | t0005 | g0307 | AMR | PEL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PEL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01975 | hp2 | a0001 | c0001 | t0005 | g0190 | AMR | PEL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01981 | hp1 | a0001 | c0001 | t0004 | g0019 | AMR | PEL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01981 | hp2 | a0004 | c0005 | t0006 | g0327 | AMR | PEL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02004 | hp1 | a0002 | c0002 | t0005 | g0073 | AMR | PEL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02004 | hp2 | a0001 | c0009 | t0003 | g0319 | AMR | PEL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0086 | EAS | KHV | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02015 | hp2 | a0002 | c0002 | t0005 | g0047 | EAS | KHV | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02027 | hp1 | a0008 | c0010 | t0004 | g0155 | EAS | KHV | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | KHV | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0347 | AFR | ACB | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | ACB | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0096 | EAS | KHV | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | KHV | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | KHV | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02080 | hp2 | a0002 | c0002 | t0005 | g0084 | EAS | KHV | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02083 | hp1 | a0002 | c0002 | t0005 | g0076 | EAS | KHV | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02083 | hp2 | a0001 | c0001 | t0005 | g0118 | EAS | KHV | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | KHV | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02129 | hp2 | a0001 | c0001 | t0004 | g0035 | EAS | KHV | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02132 | hp1 | a0002 | c0002 | t0002 | g0097 | EAS | KHV | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02132 | hp2 | a0002 | c0002 | t0005 | g0049 | EAS | KHV | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02135 | hp2 | a0001 | c0001 | t0005 | g0308 | EAS | KHV | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0346 | AFR | ACB | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | PEL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0078 | AMR | PEL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0274 | EAS | CDX | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02155 | hp2 | a0001 | c0001 | t0004 | g0191 | EAS | CDX | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02165 | hp1 | a0001 | c0001 | t0005 | g0303 | EAS | CDX | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02165 | hp2 | a0002 | c0002 | t0004 | g0048 | EAS | CDX | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02257 | hp1 | a0002 | c0002 | t0002 | g0081 | AFR | ACB | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02257 | hp2 | a0004 | c0005 | t0007 | g0326 | AFR | ACB | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02258 | hp1 | a0005 | c0006 | t0004 | g0323 | AFR | ACB | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02258 | hp2 | a0004 | c0005 | t0007 | g0348 | AFR | ACB | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PEL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0309 | AMR | PEL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02280 | hp2 | a0001 | c0001 | t0009 | g0075 | AFR | ACB | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02300 | hp1 | a0002 | c0002 | t0005 | g0011 | AMR | PEL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02300 | hp2 | a0002 | c0002 | t0005 | g0107 | AMR | PEL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02451 | hp1 | a0001 | c0003 | t0003 | g0270 | AFR | ACB | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02451 | hp2 | a0009 | c0011 | t0006 | g0324 | AFR | ACB | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02523 | hp2 | a0010 | c0015 | t0005 | g0301 | EAS | KHV | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0218 | AFR | GWD | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0143 | AFR | GWD | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02602 | hp1 | a0001 | c0003 | t0001 | g0062 | SAS | PJL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02602 | hp2 | a0002 | c0002 | t0002 | g0020 | SAS | PJL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02615 | hp1 | a0005 | c0006 | t0007 | g0321 | AFR | GWD | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02615 | hp2 | a0005 | c0006 | t0001 | g0275 | AFR | GWD | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02622 | hp1 | a0001 | c0001 | t0006 | g0199 | AFR | GWD | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0336 | AFR | GWD | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02630 | hp2 | a0003 | c0004 | t0004 | g0258 | AFR | GWD | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02647 | hp1 | a0004 | c0005 | t0003 | g0322 | AFR | GWD | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02647 | hp2 | a0001 | c0003 | t0003 | g0264 | AFR | GWD | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0342 | SAS | PJL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0284 | AFR | GWD | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0217 | AFR | GWD | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | GWD | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02723 | hp2 | a0001 | c0001 | t0007 | g0255 | AFR | GWD | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0208 | SAS | PJL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0222 | SAS | PJL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02809 | hp1 | a0001 | c0003 | t0003 | g0263 | AFR | GWD | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02809 | hp2 | a0011 | c0016 | t0012 | g0009 | AFR | GWD | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02818 | hp1 | a0005 | c0006 | t0001 | g0320 | AFR | GWD | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02818 | hp2 | a0001 | c0003 | t0003 | g0267 | AFR | GWD | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0126 | AFR | GWD | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02895 | hp2 | a0001 | c0001 | t0008 | g0169 | AFR | GWD | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0127 | AFR | GWD | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02896 | hp2 | a0001 | c0003 | t0004 | g0266 | AFR | GWD | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02897 | hp1 | a0001 | c0001 | t0008 | g0065 | AFR | GWD | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02897 | hp2 | a0001 | c0003 | t0004 | g0265 | AFR | GWD | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0253 | AFR | ESN | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ESN | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02965 | hp1 | a0003 | c0004 | t0003 | g0279 | AFR | ESN | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02965 | hp2 | a0002 | c0002 | t0016 | g0074 | AFR | ESN | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0148 | AFR | ESN | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02970 | hp2 | a0002 | c0002 | t0004 | g0042 | AFR | ESN | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02976 | hp1 | a0005 | c0006 | t0003 | g0273 | AFR | ESN | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0220 | AFR | ESN | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0180 | SAS | PJL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0330 | AFR | GWD | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0331 | AFR | GWD | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03098 | hp1 | a0001 | c0003 | t0008 | g0329 | AFR | MSL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0252 | AFR | MSL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0221 | AFR | ESN | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03130 | hp2 | a0003 | c0004 | t0003 | g0277 | AFR | ESN | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0234 | AFR | ESN | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0232 | AFR | ESN | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03195 | hp1 | a0002 | c0002 | t0003 | g0044 | AFR | ESN | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0251 | AFR | ESN | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0328 | AFR | MSL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03209 | hp2 | a0001 | c0001 | t0008 | g0064 | AFR | MSL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | MSL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0257 | AFR | MSL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03239 | hp1 | a0002 | c0002 | t0004 | g0045 | SAS | PJL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0091 | SAS | PJL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03453 | hp1 | a0001 | c0001 | t0017 | g0108 | AFR | MSL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03453 | hp2 | a0004 | c0005 | t0007 | g0325 | AFR | MSL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0202 | AFR | MSL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0344 | SAS | PJL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03490 | hp2 | a0001 | c0003 | t0003 | g0261 | SAS | PJL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03491 | hp1 | a0002 | c0002 | t0004 | g0039 | SAS | PJL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03491 | hp2 | a0002 | c0002 | t0002 | g0249 | SAS | PJL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03492 | hp1 | a0002 | c0002 | t0004 | g0028 | SAS | PJL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0341 | SAS | PJL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03516 | hp1 | a0001 | c0001 | t0010 | g0068 | AFR | ESN | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | ESN | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03540 | hp1 | a0009 | c0011 | t0006 | g0272 | AFR | GWD | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03540 | hp2 | a0002 | c0002 | t0006 | g0082 | AFR | GWD | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0161 | AFR | MSL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03579 | hp2 | a0003 | c0004 | t0004 | g0276 | AFR | MSL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0207 | SAS | PJL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | STU | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | STU | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0095 | SAS | PJL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0210 | SAS | PJL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0312 | SAS | BEB | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0300 | SAS | BEB | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0125 | SAS | BEB | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03942 | hp1 | a0002 | c0002 | t0004 | g0031 | SAS | BEB | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG04115 | hp1 | a0001 | c0003 | t0001 | g0040 | SAS | STU | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG04115 | hp2 | a0002 | c0002 | t0002 | g0055 | SAS | STU | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0036 | SAS | STU | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | STU | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0144 | SAS | STU | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0333 | SAS | STU | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0032 | SAS | STU | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | STU | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0337 | AFR | YRI | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18522 | hp2 | a0001 | c0014 | t0006 | g0268 | AFR | YRI | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18906 | hp1 | a0008 | c0010 | t0010 | g0317 | AFR | YRI | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18906 | hp2 | a0004 | c0005 | t0006 | g0010 | AFR | YRI | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18942 | hp2 | a0002 | c0002 | t0002 | g0129 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18945 | hp2 | a0001 | c0001 | t0005 | g0288 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18946 | hp1 | a0002 | c0002 | t0004 | g0059 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18948 | hp2 | a0007 | c0007 | t0002 | g0105 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18951 | hp2 | a0002 | c0002 | t0004 | g0061 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18960 | hp1 | a0001 | c0001 | t0005 | g0305 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18960 | hp2 | a0002 | c0002 | t0004 | g0104 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18962 | hp1 | a0002 | c0002 | t0005 | g0088 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0298 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18971 | hp2 | a0002 | c0002 | t0004 | g0038 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18974 | hp1 | a0001 | c0001 | t0013 | g0145 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18974 | hp2 | a0001 | c0001 | t0005 | g0171 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0130 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0100 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18985 | hp2 | a0002 | c0002 | t0004 | g0099 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18986 | hp2 | a0002 | c0002 | t0005 | g0089 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18990 | hp2 | a0002 | c0002 | t0002 | g0106 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18991 | hp1 | a0002 | c0002 | t0003 | g0094 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18993 | hp1 | a0001 | c0001 | t0011 | g0178 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18999 | hp1 | a0002 | c0002 | t0004 | g0034 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19000 | hp2 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19007 | hp1 | a0001 | c0001 | t0005 | g0290 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19009 | hp2 | a0001 | c0001 | t0004 | g0070 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19010 | hp2 | a0002 | c0002 | t0004 | g0060 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0151 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19030 | hp1 | a0001 | c0003 | t0003 | g0260 | AFR | LWK | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19030 | hp2 | a0002 | c0002 | t0004 | g0021 | AFR | LWK | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0340 | AFR | LWK | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19043 | hp2 | a0001 | c0003 | t0003 | g0066 | AFR | LWK | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19054 | hp2 | a0002 | c0002 | t0004 | g0101 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19056 | hp1 | a0002 | c0002 | t0004 | g0128 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0197 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19058 | hp1 | a0001 | c0001 | t0014 | g0160 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19064 | hp1 | a0007 | c0007 | t0002 | g0102 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19064 | hp2 | a0001 | c0001 | t0015 | g0250 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19065 | hp1 | a0001 | c0001 | t0005 | g0120 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19065 | hp2 | a0002 | c0002 | t0002 | g0063 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19066 | hp2 | a0001 | c0001 | t0005 | g0297 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19068 | hp2 | a0002 | c0002 | t0002 | g0079 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19078 | hp1 | a0002 | c0002 | t0004 | g0085 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19078 | hp2 | a0002 | c0002 | t0002 | g0025 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19079 | hp2 | a0001 | c0001 | t0005 | g0299 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19083 | hp1 | a0001 | c0001 | t0004 | g0146 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19083 | hp2 | a0001 | c0001 | t0005 | g0306 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19085 | hp2 | a0001 | c0001 | t0005 | g0302 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19086 | hp2 | a0001 | c0001 | t0004 | g0282 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0311 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA19088 | hp2 | a0007 | c0007 | t0002 | g0098 | EAS | JPT | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA20129 | hp1 | a0006 | c0008 | t0003 | g0030 | AFR | ASW | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0315 | AFR | ASW | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | GIH | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA20905 | hp2 | a0013 | c0012 | t0002 | g0248 | SAS | GIH | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0123 | AMR | CLM | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0018 | AMR | CLM | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02109 | hp1 | a0001 | c0001 | t0009 | g0201 | AFR | ACB | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02109 | hp2 | a0001 | c0009 | t0003 | g0318 | AFR | ACB | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0259 | AFR | ACB | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0203 | AFR | ACB | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG03471 | hp2 | a0003 | c0004 | t0002 | g0287 | AFR | MSL | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG06807 | hp1 | a0003 | c0004 | t0003 | g0278 | AFR | USA | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0219 | AFR | USA | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA20300 | hp1 | a0003 | c0004 | t0004 | g0316 | AFR | USA | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | USA | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA21309 | hp1 | a0001 | c0003 | t0003 | g0269 | AFR | LWK | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0343 | AFR | LWK | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0117 | REF | REF | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| homoSapiens_grch38 | hp1 | a0001 | c0009 | t0002 | g0009 | REF | REF | XYLB_chr3_38341785_38419985 | XYLB | chr3 | 38341785 | 38419985 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:38362981
|
C | A | 5 | a0002a0006a0007others(2): Show | 87 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(84): Show |
missense_variant | MODERATE | c.255C>A | p.Asp85Glu | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 4/19 | 339/3667 | 255/1611 | 85/536 | chr3 | 38362981 | ||
| chr3:38365626
|
G | A | 3 | a0004a0005a0009 | 14 | HG01074.hp2 HG01981.hp2 HG02257.hp2 others(11): Show |
missense_variant | MODERATE | c.397G>A | p.Asp133Asn | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 6/19 | 481/3667 | 397/1611 | 133/536 | chr3 | 38365626 | ||
| chr3:38365707
|
A | C | 1 | a0006 | 3 | HG01109.hp1 HG01934.hp2 NA20129.hp1 |
missense_variant | MODERATE | c.478A>C | p.Ser160Arg | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 6/19 | 562/3667 | 478/1611 | 160/536 | chr3 | 38365707 | ||
| chr3:38366860
|
A | G | 1 | a0010 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.560A>G | p.Tyr187Cys | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 7/19 | 644/3667 | 560/1611 | 187/536 | chr3 | 38366860 | ||
| chr3:38376147
|
G | T | 1 | a0011 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.1035G>T | p.Lys345Asn | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 13/19 | 1119/3667 | 1035/1611 | 345/536 | chr3 | 38376147 | ||
| chr3:38376154
|
A | G | 2 | a0003a0004 | 14 | HG01074.hp2 HG01981.hp2 HG02257.hp2 others(11): Show |
missense_variant | MODERATE | c.1042A>G | p.Asn348Asp | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 13/19 | 1126/3667 | 1042/1611 | 348/536 | chr3 | 38376154 | ||
| chr3:38379337
|
G | A | 1 | a0008 | 2 | HG02027.hp1 NA18906.hp1 |
missense_variant | MODERATE | c.1286G>A | p.Arg429Gln | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/19 | 1370/3667 | 1286/1611 | 429/536 | chr3 | 38379337 | ||
| chr3:38395561
|
C | T | 1 | a0012 | 1 | HG01433.hp1 | stop_gained&splice_region_variant | HIGH | c.1348C>T | p.Gln450* | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 16/19 | 1432/3667 | 1348/1611 | 450/536 | chr3 | 38395561 | ||
| chr3:38397147
|
C | T | 1 | a0007 | 3 | NA18948.hp2 NA19064.hp1 NA19088.hp2 |
stop_gained | HIGH | c.1426C>T | p.Arg476* | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/19 | 1510/3667 | 1426/1611 | 476/536 | chr3 | 38397147 | ||
| chr3:38400906
|
C | T | 1 | a0013 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.1454C>T | p.Thr485Ile | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/19 | 1538/3667 | 1454/1611 | 485/536 | chr3 | 38400906 | ||
| chr3:38400911
|
G | A | 1 | a0009 | 2 | HG02451.hp2 HG03540.hp1 |
missense_variant | MODERATE | c.1459G>A | p.Val487Met | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/19 | 1543/3667 | 1459/1611 | 487/536 | chr3 | 38400911 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:38360348
|
T | C | 11 | a0001c0001a0001c0003a0001c0014others(8): Show | 340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
synonymous_variant | LOW | c.150T>C | p.Gly50Gly | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/19 | 234/3667 | 150/1611 | 50/536 | chr3 | 38360348 | ||
| chr3:38365282
|
G | T | 9 | a0001c0001a0002c0002a0003c0004others(6): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
synonymous_variant | LOW | c.375G>T | p.Leu125Leu | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 5/19 | 459/3667 | 375/1611 | 125/536 | chr3 | 38365282 | ||
| chr3:38366870
|
G | A | 9 | a0001c0001a0002c0002a0003c0004others(6): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
synonymous_variant | LOW | c.570G>A | p.Thr190Thr | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 7/19 | 654/3667 | 570/1611 | 190/536 | chr3 | 38366870 | ||
| chr3:38372732
|
C | T | 1 | a0001c0014 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.843C>T | p.Asn281Asn | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 10/19 | 927/3667 | 843/1611 | 281/536 | chr3 | 38372732 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:38413105
|
A | C | 1 | a0001c0001t0017 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*92A>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 19/19 | 92 | chr3 | 38413105 | |||||
| chr3:38413241
|
T | C | 1 | a0001c0001t0011 | 1 | NA18993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*228T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 19/19 | 228 | chr3 | 38413241 | |||||
| chr3:38413245
|
C | T | 1 | a0001c0001t0011 | 1 | NA18993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*232C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 19/19 | 232 | chr3 | 38413245 | |||||
| chr3:38413250
|
C | T | 2 | a0001c0001t0017a0002c0002t0016 | 2 | HG02965.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*237C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 19/19 | 237 | chr3 | 38413250 | |||||
| chr3:38413341
|
A | G | 2 | a0001c0001t0010a0008c0010t0010 | 2 | HG03516.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*328A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 19/19 | 328 | chr3 | 38413341 | |||||
| chr3:38413364
|
A | T | 1 | a0001c0001t0011 | 1 | NA18993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*351A>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 19/19 | 351 | chr3 | 38413364 | |||||
| chr3:38413365
|
T | G | 1 | a0001c0001t0009 | 2 | HG02109.hp1 HG02280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*352T>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 19/19 | 352 | chr3 | 38413365 | |||||
| chr3:38413440
|
A | G | 38 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(35): Show | 260 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
3_prime_UTR_variant | MODIFIER | c.*427A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 19/19 | 427 | chr3 | 38413440 | |||||
| chr3:38413483
|
A | G | 1 | a0001c0001t0014 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*470A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 19/19 | 470 | chr3 | 38413483 | |||||
| chr3:38413728
|
G | A | 1 | a0001c0001t0015 | 1 | NA19064.hp2 | 3_prime_UTR_variant | MODIFIER | c.*715G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 19/19 | 715 | chr3 | 38413728 | |||||
| chr3:38413948
|
C | T | 6 | a0001c0001t0001a0001c0001t0015a0001c0003t0001others(3): Show | 98 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*935C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 19/19 | 935 | chr3 | 38413948 | |||||
| chr3:38414024
|
A | G | 5 | a0001c0001t0006a0001c0014t0006a0002c0002t0006others(2): Show | 11 | HG01074.hp2 HG01891.hp2 HG01981.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1011A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 19/19 | 1011 | chr3 | 38414024 | |||||
| chr3:38414065
|
A | T | 1 | a0001c0001t0011 | 1 | NA18993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1052A>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 19/19 | 1052 | chr3 | 38414065 | |||||
| chr3:38414158
|
C | T | 1 | a0001c0001t0013 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1145C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 19/19 | 1145 | chr3 | 38414158 | |||||
| chr3:38414159
|
G | T | 6 | a0001c0001t0001a0001c0001t0015a0001c0003t0001others(3): Show | 98 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*1146G>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 19/19 | 1146 | chr3 | 38414159 | |||||
| chr3:38414213
|
C | A | 6 | a0001c0001t0001a0001c0001t0015a0001c0003t0001others(3): Show | 98 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*1200C>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 19/19 | 1200 | chr3 | 38414213 | |||||
| chr3:38414337
|
GGAT | G | 8 | a0001c0001t0005a0001c0001t0007a0001c0001t0010others(5): Show | 37 | HG00621.hp2 HG00639.hp2 HG01070.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1327_*1329delTGA | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 19/19 | 1327 | INFO_REALIGN_3_PRIME | chr3 | 38414337 | ||||
| chr3:38414410
|
G | A | 6 | a0001c0001t0004a0001c0003t0004a0002c0002t0004others(3): Show | 45 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1397G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 19/19 | 1397 | chr3 | 38414410 | |||||
| chr3:38414435
|
T | C | 3 | a0001c0001t0007a0004c0005t0007a0005c0006t0007 | 6 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1422T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 19/19 | 1422 | chr3 | 38414435 | |||||
| chr3:38414576
|
C | T | 1 | a0011c0016t0012 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1563C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 19/19 | 1563 | chr3 | 38414576 | |||||
| chr3:38414783
|
G | GA | 2 | a0001c0001t0008a0001c0003t0008 | 4 | HG02895.hp2 HG02897.hp1 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1770_*1771insA | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 19/19 | 1771 | chr3 | 38414783 | |||||
| chr3:38414784
|
C | A | 2 | a0001c0001t0008a0001c0003t0008 | 4 | HG02895.hp2 HG02897.hp1 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1771C>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 19/19 | 1771 | chr3 | 38414784 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:38346977
|
G | A | 1 | a0002c0002t0005g0011 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.57+52G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 1/18 | chr3 | 38346977 | ||||||
| chr3:38347049
|
T | A | 4 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(1): Show | 4 | HG01255.hp1 HG01884.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.57+124T>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 1/18 | chr3 | 38347049 | ||||||
| chr3:38347061
|
C | T | 1 | a0004c0005t0007g0348 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.57+136C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 1/18 | chr3 | 38347061 | ||||||
| chr3:38347222
|
G | A | 1 | a0002c0002t0004g0016 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.57+297G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 1/18 | chr3 | 38347222 | ||||||
| chr3:38347235
|
G | C | 1 | a0002c0002t0002g0017 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.57+310G>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 1/18 | chr3 | 38347235 | ||||||
| chr3:38347334
|
A | T | 18 | a0001c0001t0001g0347a0001c0001t0002g0333a0001c0001t0002g0341others(15): Show | 18 | HG00639.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.57+409A>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 1/18 | chr3 | 38347334 | ||||||
| chr3:38347382
|
T | A | 47 | a0001c0001t0001g0053a0001c0001t0002g0041a0001c0001t0002g0057others(44): Show | 48 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.57+457T>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 1/18 | chr3 | 38347382 | ||||||
| chr3:38347397
|
C | G | 18 | a0001c0001t0001g0347a0001c0001t0002g0333a0001c0001t0002g0341others(15): Show | 18 | HG00639.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.57+472C>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 1/18 | chr3 | 38347397 | ||||||
| chr3:38347548
|
A | C | 18 | a0001c0001t0001g0347a0001c0001t0002g0333a0001c0001t0002g0341others(15): Show | 18 | HG00639.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.57+623A>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 1/18 | chr3 | 38347548 | ||||||
| chr3:38347640
|
G | C | 331 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(328): Show | 339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.57+715G>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 1/18 | chr3 | 38347640 | ||||||
| chr3:38347675
|
C | CA | 8 | a0001c0001t0008g0064a0001c0001t0008g0065a0001c0001t0010g0068others(5): Show | 8 | HG01361.hp1 HG02897.hp1 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.57+763dupA | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 38347675 | |||||
| chr3:38347713
|
C | T | 1 | a0001c0001t0003g0315 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.57+788C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 1/18 | chr3 | 38347713 | ||||||
| chr3:38347816
|
T | C | 331 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(328): Show | 339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.58-734T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 1/18 | chr3 | 38347816 | ||||||
| chr3:38347867
|
C | G | 4 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(1): Show | 4 | HG01255.hp1 HG01884.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.58-683C>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 1/18 | chr3 | 38347867 | ||||||
| chr3:38348040
|
G | A | 241 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0001g0109others(238): Show | 247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.58-510G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 1/18 | chr3 | 38348040 | ||||||
| chr3:38348326
|
T | C | 9 | a0001c0001t0003g0251a0001c0001t0003g0252a0001c0001t0003g0253others(6): Show | 9 | HG01884.hp1 HG01891.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.58-224T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 1/18 | chr3 | 38348326 | ||||||
| chr3:38348419
|
C | T | 18 | a0001c0001t0001g0347a0001c0001t0002g0333a0001c0001t0002g0341others(15): Show | 18 | HG00639.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.58-131C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 1/18 | chr3 | 38348419 | ||||||
| chr3:38348488
|
C | G | 1 | a0001c0001t0015g0250 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.58-62C>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 1/18 | chr3 | 38348488 | ||||||
| chr3:38348529
|
C | A | 331 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(328): Show | 339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.58-21C>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 1/18 | chr3 | 38348529 | ||||||
| chr3:38348543
|
C | T | 2 | a0002c0002t0002g0249a0013c0012t0002g0248 | 2 | HG03491.hp2 NA20905.hp2 |
splice_region_variant&intron_variant | LOW | c.58-7C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 1/18 | chr3 | 38348543 | ||||||
| chr3:38348782
|
T | C | 16 | a0001c0003t0003g0007a0001c0003t0003g0260a0001c0003t0003g0261others(13): Show | 17 | HG00741.hp2 HG01256.hp2 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.140+150T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38348782 | ||||||
| chr3:38348886
|
C | T | 2 | a0001c0001t0002g0246a0001c0001t0002g0247 | 2 | HG01074.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.140+254C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38348886 | ||||||
| chr3:38349007
|
A | G | 1 | a0001c0001t0004g0245 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.140+375A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38349007 | ||||||
| chr3:38349148
|
C | T | 1 | a0005c0006t0003g0273 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.140+516C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38349148 | ||||||
| chr3:38349225
|
C | A | 1 | a0004c0005t0007g0348 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.140+593C>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38349225 | ||||||
| chr3:38349249
|
A | T | 1 | a0001c0001t0002g0244 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.140+617A>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38349249 | ||||||
| chr3:38349254
|
G | A | 1 | a0002c0002t0002g0069 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.140+622G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38349254 | ||||||
| chr3:38349369
|
G | A | 1 | a0001c0001t0004g0274 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.140+737G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38349369 | ||||||
| chr3:38349393
|
T | C | 313 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(310): Show | 321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.140+761T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38349393 | ||||||
| chr3:38349410
|
T | G | 18 | a0001c0001t0001g0347a0001c0001t0002g0333a0001c0001t0002g0341others(15): Show | 18 | HG00639.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.140+778T>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38349410 | ||||||
| chr3:38349498
|
A | G | 18 | a0001c0001t0001g0347a0001c0001t0002g0333a0001c0001t0002g0341others(15): Show | 18 | HG00639.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.140+866A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38349498 | ||||||
| chr3:38349841
|
C | T | 1 | a0001c0003t0008g0329 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.140+1209C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38349841 | ||||||
| chr3:38349864
|
C | G | 345 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(342): Show | 354 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.140+1232C>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38349864 | ||||||
| chr3:38349991
|
C | A | 311 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(308): Show | 319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.140+1359C>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38349991 | ||||||
| chr3:38349992
|
C | T | 1 | a0001c0003t0001g0062 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.140+1360C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38349992 | ||||||
| chr3:38350124
|
T | C | 18 | a0001c0001t0001g0347a0001c0001t0002g0333a0001c0001t0002g0341others(15): Show | 18 | HG00639.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.140+1492T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38350124 | ||||||
| chr3:38350192
|
T | G | 1 | a0001c0001t0004g0070 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.140+1560T>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38350192 | ||||||
| chr3:38350334
|
C | T | 18 | a0001c0001t0001g0347a0001c0001t0002g0333a0001c0001t0002g0341others(15): Show | 18 | HG00639.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.140+1702C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38350334 | ||||||
| chr3:38350379
|
C | T | 18 | a0001c0001t0001g0347a0001c0001t0002g0333a0001c0001t0002g0341others(15): Show | 18 | HG00639.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.140+1747C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38350379 | ||||||
| chr3:38350567
|
A | G | 2 | a0002c0002t0004g0060a0002c0002t0004g0061 | 2 | NA18951.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.140+1935A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38350567 | ||||||
| chr3:38350644
|
C | G | 18 | a0001c0001t0001g0347a0001c0001t0002g0333a0001c0001t0002g0341others(15): Show | 18 | HG00639.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.140+2012C>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38350644 | ||||||
| chr3:38350720
|
A | G | 331 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(328): Show | 339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.140+2088A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38350720 | ||||||
| chr3:38350783
|
AT | A | 300 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(297): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.140+2159delT | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38350783 | |||||
| chr3:38350831
|
C | T | 3 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243 | 3 | HG00738.hp1 HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.140+2199C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38350831 | ||||||
| chr3:38350836
|
G | A | 18 | a0001c0001t0001g0347a0001c0001t0002g0333a0001c0001t0002g0341others(15): Show | 18 | HG00639.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.140+2204G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38350836 | ||||||
| chr3:38350932
|
C | T | 299 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(296): Show | 306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.140+2300C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38350932 | ||||||
| chr3:38351002
|
G | A | 15 | a0001c0003t0003g0007a0001c0003t0003g0066a0001c0003t0003g0260others(12): Show | 16 | HG00741.hp2 HG01256.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.140+2370G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38351002 | ||||||
| chr3:38351024
|
C | T | 5 | a0001c0001t0001g0239a0001c0001t0002g0236a0001c0001t0002g0237others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.140+2392C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38351024 | ||||||
| chr3:38351062
|
G | C | 18 | a0001c0001t0001g0347a0001c0001t0002g0333a0001c0001t0002g0341others(15): Show | 18 | HG00639.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.140+2430G>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38351062 | ||||||
| chr3:38351120
|
C | T | 1 | a0002c0002t0001g0235 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.140+2488C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38351120 | ||||||
| chr3:38351127
|
G | A | 5 | a0001c0001t0001g0239a0001c0001t0002g0236a0001c0001t0002g0237others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.140+2495G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38351127 | ||||||
| chr3:38351153
|
C | T | 1 | a0002c0002t0001g0067 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.140+2521C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38351153 | ||||||
| chr3:38351171
|
C | CA | 26 | a0001c0001t0001g0053a0001c0001t0001g0109a0001c0001t0001g0110others(23): Show | 27 | HG00741.hp1 HG01069.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.140+2567dupA | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38351171 | |||||
| chr3:38351171
|
C | CAA | 6 | a0002c0002t0005g0107a0003c0004t0003g0277a0003c0004t0003g0278others(3): Show | 6 | HG02300.hp2 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.140+2566_140+2567d others(4): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38351171 | |||||
| chr3:38351171
|
C | CAAAAAAA | 13 | a0001c0001t0003g0252a0001c0001t0003g0253a0001c0001t0003g0256others(10): Show | 13 | HG00597.hp1 HG01884.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.140+2561_140+2567d others(9): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38351171 | |||||
| chr3:38351171
|
C | CAAAAAAA others(1): Show |
6 | a0001c0001t0003g0251a0002c0002t0001g0002a0002c0002t0002g0097others(3): Show | 7 | HG02132.hp1 HG03195.hp2 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.140+2560_140+2567d others(10): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38351171 | |||||
| chr3:38351171
|
C | CAAAAAAA others(4): Show |
1 | a0008c0010t0010g0317 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.140+2557_140+2567d others(13): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38351171 | |||||
| chr3:38351171
|
C | CAAAAAAA others(5): Show |
4 | a0001c0001t0005g0095a0002c0002t0002g0096a0002c0002t0005g0011others(1): Show | 4 | HG02056.hp1 HG02300.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.140+2556_140+2567d others(14): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38351171 | |||||
| chr3:38351171
|
C | CAAAAAAA others(6): Show |
2 | a0002c0002t0003g0093a0002c0002t0003g0094 | 2 | HG01928.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.140+2555_140+2567d others(15): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38351171 | |||||
| chr3:38351171
|
C | CAAAAAAA others(13): Show |
19 | a0001c0001t0002g0041a0001c0001t0004g0035a0001c0003t0001g0040others(16): Show | 19 | HG00558.hp2 HG00639.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.140+2548_140+2567d others(22): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38351171 | |||||
| chr3:38351171
|
C | CAAAAAAA others(14): Show |
18 | a0001c0003t0001g0062a0002c0002t0001g0027a0002c0002t0001g0033others(15): Show | 18 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(15): Show |
intron_variant | MODIFIER | c.140+2547_140+2567d others(23): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38351171 | |||||
| chr3:38351171
|
C | CAAAAAAA others(15): Show |
8 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0002g0025others(5): Show | 8 | HG01106.hp1 HG01109.hp1 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.140+2546_140+2567d others(24): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38351171 | |||||
| chr3:38351171
|
C | CAAAAAAA others(16): Show |
4 | a0002c0002t0001g0235a0002c0002t0002g0022a0002c0002t0002g0063others(1): Show | 4 | HG00408.hp2 HG03540.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.140+2545_140+2567d others(25): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38351171 | |||||
| chr3:38351171
|
C | CAAAAAAA others(17): Show |
3 | a0002c0002t0001g0067a0002c0002t0002g0081a0012c0013t0001g0080 | 3 | HG01361.hp1 HG01433.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.140+2544_140+2567d others(26): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38351171 | |||||
| chr3:38351171
|
C | CAAAAAAA others(18): Show |
3 | a0001c0001t0004g0001a0002c0002t0002g0079a0002c0002t0004g0021 | 4 | HG01975.hp1 HG02273.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.140+2543_140+2567d others(27): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38351171 | |||||
| chr3:38351171
|
C | CAAAAAAA others(19): Show |
2 | a0001c0001t0004g0078a0002c0002t0002g0077 | 2 | HG02148.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.140+2542_140+2567d others(28): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38351171 | |||||
| chr3:38351171
|
C | CAAAAAAA others(20): Show |
4 | a0001c0001t0004g0019a0001c0001t0004g0245a0002c0002t0001g0018others(1): Show | 4 | HG01123.hp2 HG01952.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.140+2541_140+2567d others(29): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38351171 | |||||
| chr3:38351171
|
C | CAAAAAAA others(21): Show |
4 | a0001c0001t0009g0075a0002c0002t0002g0069a0002c0002t0005g0076others(1): Show | 4 | HG00609.hp1 HG02083.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.140+2540_140+2567d others(30): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38351171 | |||||
| chr3:38351171
|
C | CAAAAAAA others(22): Show |
2 | a0002c0002t0001g0072a0002c0002t0005g0073 | 2 | HG02004.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.140+2567_140+2568i others(31): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38351171 | |||||
| chr3:38351171
|
C | CAAAAAAA others(23): Show |
1 | a0002c0002t0001g0071 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.140+2567_140+2568i others(32): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38351171 | |||||
| chr3:38351171
|
CA | C | 27 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0243others(24): Show | 28 | HG00558.hp1 HG00741.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.140+2567delA | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38351171 | |||||
| chr3:38351171
|
CAA | C | 37 | a0001c0001t0001g0008a0001c0001t0001g0286a0001c0001t0001g0291others(34): Show | 38 | HG00544.hp1 HG00609.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.140+2566_140+2567d others(4): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38351171 | |||||
| chr3:38351171
|
CAAA | C | 15 | a0001c0001t0001g0347a0001c0001t0002g0341a0001c0001t0002g0342others(12): Show | 15 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.140+2565_140+2567d others(5): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38351171 | |||||
| chr3:38351171
|
CAAAAAAA others(3): Show |
C | 1 | a0002c0002t0004g0059 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.140+2558_140+2567d others(12): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38351171 | |||||
| chr3:38351214
|
G | A | 9 | a0001c0001t0003g0251a0001c0001t0003g0252a0001c0001t0003g0253others(6): Show | 9 | HG01884.hp1 HG01891.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.140+2582G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38351214 | ||||||
| chr3:38351345
|
C | G | 1 | a0001c0003t0008g0329 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.140+2713C>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38351345 | ||||||
| chr3:38351351
|
C | T | 317 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(314): Show | 324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.140+2719C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38351351 | ||||||
| chr3:38351579
|
C | G | 15 | a0001c0003t0003g0007a0001c0003t0003g0066a0001c0003t0003g0260others(12): Show | 16 | HG00741.hp2 HG01256.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.140+2947C>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38351579 | ||||||
| chr3:38351663
|
T | C | 1 | a0001c0001t0017g0108 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.140+3031T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38351663 | ||||||
| chr3:38351672
|
G | C | 18 | a0001c0001t0001g0347a0001c0001t0002g0333a0001c0001t0002g0341others(15): Show | 18 | HG00639.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.140+3040G>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38351672 | ||||||
| chr3:38351802
|
T | C | 18 | a0001c0001t0001g0347a0001c0001t0002g0333a0001c0001t0002g0341others(15): Show | 18 | HG00639.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.140+3170T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38351802 | ||||||
| chr3:38351907
|
A | T | 15 | a0001c0003t0003g0007a0001c0003t0003g0066a0001c0003t0003g0260others(12): Show | 16 | HG00741.hp2 HG01256.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.140+3275A>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38351907 | ||||||
| chr3:38352050
|
C | T | 1 | a0001c0001t0001g0314 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.140+3418C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38352050 | ||||||
| chr3:38352060
|
C | T | 18 | a0001c0001t0001g0347a0001c0001t0002g0333a0001c0001t0002g0341others(15): Show | 18 | HG00639.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.140+3428C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38352060 | ||||||
| chr3:38352061
|
G | A | 1 | a0002c0002t0002g0097 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.140+3429G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38352061 | ||||||
| chr3:38352122
|
A | T | 18 | a0001c0001t0001g0347a0001c0001t0002g0333a0001c0001t0002g0341others(15): Show | 18 | HG00639.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.140+3490A>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38352122 | ||||||
| chr3:38352168
|
C | CA | 317 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(314): Show | 324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.140+3538dupA | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38352168 | |||||
| chr3:38352188
|
A | G | 18 | a0001c0001t0001g0347a0001c0001t0002g0333a0001c0001t0002g0341others(15): Show | 18 | HG00639.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.140+3556A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38352188 | ||||||
| chr3:38352193
|
C | CT | 35 | a0001c0001t0001g0008a0001c0001t0001g0286a0001c0001t0001g0291others(32): Show | 36 | HG00544.hp1 HG00609.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.140+3570dupT | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38352193 | |||||
| chr3:38352542
|
C | T | 15 | a0001c0003t0003g0007a0001c0003t0003g0066a0001c0003t0003g0260others(12): Show | 16 | HG00741.hp2 HG01256.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.140+3910C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38352542 | ||||||
| chr3:38352733
|
C | T | 18 | a0001c0001t0001g0347a0001c0001t0002g0333a0001c0001t0002g0341others(15): Show | 18 | HG00639.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.140+4101C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38352733 | ||||||
| chr3:38352783
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.140+4151T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38352783 | ||||||
| chr3:38352790
|
C | A | 3 | a0002c0002t0003g0093a0002c0002t0003g0094a0002c0002t0005g0011 | 3 | HG01928.hp2 HG02300.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.140+4158C>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38352790 | ||||||
| chr3:38352814
|
T | TA | 18 | a0001c0001t0001g0347a0001c0001t0002g0333a0001c0001t0002g0341others(15): Show | 18 | HG00639.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.140+4193dupA | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38352814 | |||||
| chr3:38352833
|
G | T | 1 | a0002c0002t0002g0069 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.140+4201G>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38352833 | ||||||
| chr3:38352836
|
A | G | 4 | a0003c0004t0003g0277a0003c0004t0003g0278a0003c0004t0003g0279others(1): Show | 4 | HG02965.hp1 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.140+4204A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38352836 | ||||||
| chr3:38352953
|
G | C | 299 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(296): Show | 306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.140+4321G>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38352953 | ||||||
| chr3:38353053
|
G | A | 317 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(314): Show | 324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.140+4421G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38353053 | ||||||
| chr3:38353059
|
A | G | 3 | a0001c0001t0001g0227a0001c0001t0002g0226a0002c0002t0002g0020 | 3 | HG00280.hp1 HG00738.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.140+4427A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38353059 | ||||||
| chr3:38353157
|
ACCTATGT others(2): Show |
A | 18 | a0001c0001t0001g0347a0001c0001t0002g0333a0001c0001t0002g0341others(15): Show | 18 | HG00639.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.140+4526_140+4534d others(11): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38353157 | ||||||
| chr3:38353168
|
T | A | 18 | a0001c0001t0001g0347a0001c0001t0002g0333a0001c0001t0002g0341others(15): Show | 18 | HG00639.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.140+4536T>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38353168 | ||||||
| chr3:38353229
|
C | T | 1 | a0001c0001t0002g0225 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.140+4597C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38353229 | ||||||
| chr3:38353299
|
G | A | 18 | a0001c0001t0001g0347a0001c0001t0002g0333a0001c0001t0002g0341others(15): Show | 18 | HG00639.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.140+4667G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38353299 | ||||||
| chr3:38353424
|
G | A | 1 | a0001c0001t0002g0125 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.140+4792G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38353424 | ||||||
| chr3:38353452
|
C | T | 1 | a0001c0001t0017g0108 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.140+4820C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38353452 | ||||||
| chr3:38353576
|
G | T | 17 | a0001c0001t0001g0347a0001c0001t0002g0333a0001c0001t0002g0341others(14): Show | 17 | HG01167.hp2 HG01168.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.140+4944G>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38353576 | ||||||
| chr3:38353630
|
C | T | 340 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(337): Show | 349 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.140+4998C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38353630 | ||||||
| chr3:38353662
|
G | A | 38 | a0001c0001t0001g0008a0001c0001t0001g0286a0001c0001t0001g0291others(35): Show | 39 | HG00544.hp1 HG00609.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.140+5030G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38353662 | ||||||
| chr3:38353723
|
C | T | 2 | a0001c0001t0005g0223a0001c0001t0005g0224 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.140+5091C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38353723 | ||||||
| chr3:38353732
|
C | T | 4 | a0001c0001t0002g0312a0001c0001t0002g0313a0001c0001t0004g0282others(1): Show | 4 | HG03834.hp1 NA19063.hp2 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.140+5100C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38353732 | ||||||
| chr3:38353833
|
G | A | 1 | a0001c0001t0001g0228 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.140+5201G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38353833 | ||||||
| chr3:38353873
|
T | C | 18 | a0001c0001t0001g0347a0001c0001t0002g0333a0001c0001t0002g0341others(15): Show | 18 | HG00639.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.140+5241T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38353873 | ||||||
| chr3:38353878
|
C | T | 18 | a0001c0001t0001g0347a0001c0001t0002g0333a0001c0001t0002g0341others(15): Show | 18 | HG00639.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.140+5246C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38353878 | ||||||
| chr3:38353885
|
T | A | 2 | a0001c0001t0003g0126a0001c0001t0003g0127 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.140+5253T>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38353885 | ||||||
| chr3:38353885
|
T | TA | 49 | a0001c0001t0001g0008a0001c0001t0001g0286a0001c0001t0001g0291others(46): Show | 50 | HG00544.hp1 HG00609.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.140+5270dupA | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38353885 | |||||
| chr3:38353885
|
T | TAA | 245 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0001g0109others(242): Show | 251 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.140+5269_140+5270d others(4): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38353885 | |||||
| chr3:38353885
|
TAAA | T | 18 | a0001c0001t0001g0347a0001c0001t0002g0333a0001c0001t0002g0341others(15): Show | 18 | HG00639.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.140+5268_140+5270d others(5): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38353885 | |||||
| chr3:38353939
|
G | C | 317 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(314): Show | 324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.140+5307G>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38353939 | ||||||
| chr3:38354071
|
T | C | 93 | a0001c0001t0001g0053a0001c0001t0002g0041a0001c0001t0004g0001others(90): Show | 95 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.140+5439T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38354071 | ||||||
| chr3:38354142
|
C | T | 13 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0216others(10): Show | 13 | HG00733.hp1 HG00733.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.140+5510C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38354142 | ||||||
| chr3:38354201
|
G | A | 1 | a0001c0001t0001g0131 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.140+5569G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38354201 | ||||||
| chr3:38354228
|
T | C | 4 | a0003c0004t0003g0277a0003c0004t0003g0278a0003c0004t0003g0279others(1): Show | 4 | HG02965.hp1 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.140+5596T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38354228 | ||||||
| chr3:38354420
|
T | C | 1 | a0001c0003t0003g0264 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.140+5788T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38354420 | ||||||
| chr3:38354504
|
A | AT | 15 | a0001c0001t0001g0310a0001c0001t0001g0347a0001c0001t0002g0122others(12): Show | 15 | HG00741.hp2 HG02055.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.141-5820dupT | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38354504 | |||||
| chr3:38354659
|
C | T | 1 | a0001c0001t0002g0210 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.141-5680C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38354659 | ||||||
| chr3:38354664
|
G | C | 1 | a0001c0001t0001g0132 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.141-5675G>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38354664 | ||||||
| chr3:38354674
|
T | C | 4 | a0004c0005t0007g0325a0004c0005t0007g0326a0004c0005t0007g0348others(1): Show | 4 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.141-5665T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38354674 | ||||||
| chr3:38354765
|
G | A | 18 | a0001c0001t0001g0347a0001c0001t0002g0333a0001c0001t0002g0341others(15): Show | 18 | HG00639.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.141-5574G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38354765 | ||||||
| chr3:38354778
|
ACAGGCGT others(8): Show |
A | 1 | a0002c0002t0001g0018 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.141-5560_141-5546d others(17): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38354778 | ||||||
| chr3:38354845
|
T | C | 4 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(1): Show | 4 | HG01255.hp1 HG01884.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.141-5494T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38354845 | ||||||
| chr3:38354919
|
T | G | 1 | a0002c0002t0001g0027 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.141-5420T>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38354919 | ||||||
| chr3:38355052
|
T | C | 317 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(314): Show | 324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.141-5287T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38355052 | ||||||
| chr3:38355155
|
G | A | 1 | a0002c0002t0002g0079 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.141-5184G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38355155 | ||||||
| chr3:38355269
|
C | A | 18 | a0001c0001t0001g0347a0001c0001t0002g0333a0001c0001t0002g0341others(15): Show | 18 | HG00639.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.141-5070C>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38355269 | ||||||
| chr3:38355309
|
A | G | 42 | a0001c0001t0001g0008a0001c0001t0001g0286a0001c0001t0001g0291others(39): Show | 43 | HG00544.hp1 HG00609.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.141-5030A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38355309 | ||||||
| chr3:38355325
|
T | C | 8 | a0001c0001t0003g0330a0001c0001t0003g0334a0001c0001t0003g0336others(5): Show | 8 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.141-5014T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38355325 | ||||||
| chr3:38355345
|
C | A | 18 | a0001c0001t0001g0347a0001c0001t0002g0333a0001c0001t0002g0341others(15): Show | 18 | HG00639.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.141-4994C>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38355345 | ||||||
| chr3:38355415
|
G | T | 299 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(296): Show | 306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.141-4924G>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38355415 | ||||||
| chr3:38355846
|
C | T | 18 | a0001c0001t0001g0347a0001c0001t0002g0333a0001c0001t0002g0341others(15): Show | 18 | HG00639.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.141-4493C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38355846 | ||||||
| chr3:38355867
|
A | G | 15 | a0001c0003t0003g0007a0001c0003t0003g0066a0001c0003t0003g0260others(12): Show | 16 | HG00741.hp2 HG01256.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.141-4472A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38355867 | ||||||
| chr3:38355904
|
A | T | 1 | a0001c0001t0003g0330 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.141-4435A>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38355904 | ||||||
| chr3:38355988
|
C | T | 4 | a0003c0004t0003g0277a0003c0004t0003g0278a0003c0004t0003g0279others(1): Show | 4 | HG02965.hp1 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.141-4351C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38355988 | ||||||
| chr3:38356057
|
C | CT | 35 | a0001c0001t0001g0008a0001c0001t0001g0291a0001c0001t0001g0294others(32): Show | 36 | HG00544.hp1 HG00609.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.141-4281dupT | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38356057 | |||||
| chr3:38356100
|
A | C | 4 | a0003c0004t0003g0277a0003c0004t0003g0278a0003c0004t0003g0279others(1): Show | 4 | HG02965.hp1 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.141-4239A>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38356100 | ||||||
| chr3:38356119
|
C | T | 18 | a0001c0001t0001g0347a0001c0001t0002g0333a0001c0001t0002g0341others(15): Show | 18 | HG00639.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.141-4220C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38356119 | ||||||
| chr3:38356140
|
A | G | 299 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(296): Show | 306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.141-4199A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38356140 | ||||||
| chr3:38356167
|
C | G | 299 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(296): Show | 306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.141-4172C>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38356167 | ||||||
| chr3:38356250
|
CA | C | 16 | a0001c0003t0003g0007a0001c0003t0003g0260a0001c0003t0003g0262others(13): Show | 17 | HG00741.hp2 HG01256.hp2 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.141-4073delA | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38356250 | |||||
| chr3:38356250
|
CAAA | C | 270 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0001g0109others(267): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.141-4075_141-4073d others(5): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38356250 | |||||
| chr3:38356260
|
AAAAAAAG | A | 42 | a0001c0001t0001g0008a0001c0001t0001g0286a0001c0001t0001g0291others(39): Show | 43 | HG00544.hp1 HG00609.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.141-4075_141-4069d others(9): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38356260 | |||||
| chr3:38356336
|
A | G | 1 | a0001c0001t0002g0209 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.141-4003A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38356336 | ||||||
| chr3:38356346
|
T | C | 7 | a0001c0001t0003g0251a0001c0001t0003g0252a0001c0001t0003g0253others(4): Show | 7 | HG01884.hp1 HG01891.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.141-3993T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38356346 | ||||||
| chr3:38356479
|
A | G | 2 | a0009c0011t0006g0272a0009c0011t0006g0324 | 2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.141-3860A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38356479 | ||||||
| chr3:38356572
|
C | T | 299 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(296): Show | 306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.141-3767C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38356572 | ||||||
| chr3:38356587
|
A | T | 299 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(296): Show | 306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.141-3752A>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38356587 | ||||||
| chr3:38356604
|
T | C | 299 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(296): Show | 306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.141-3735T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38356604 | ||||||
| chr3:38356607
|
A | C | 6 | a0001c0001t0001g0286a0001c0001t0003g0218a0001c0001t0003g0219others(3): Show | 6 | HG01243.hp1 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.141-3732A>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38356607 | ||||||
| chr3:38356607
|
A | G | 293 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(290): Show | 300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.141-3732A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38356607 | ||||||
| chr3:38356737
|
T | C | 1 | a0001c0001t0002g0210 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.141-3602T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38356737 | ||||||
| chr3:38356746
|
A | G | 1 | a0002c0002t0004g0059 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.141-3593A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38356746 | ||||||
| chr3:38357009
|
C | T | 3 | a0004c0005t0003g0322a0004c0005t0006g0010a0004c0005t0006g0327 | 4 | HG01074.hp2 HG01981.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.141-3330C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38357009 | ||||||
| chr3:38357206
|
T | C | 315 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(312): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.141-3133T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38357206 | ||||||
| chr3:38357263
|
T | G | 317 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(314): Show | 324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.141-3076T>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38357263 | ||||||
| chr3:38357338
|
G | A | 1 | a0001c0001t0004g0222 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.141-3001G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38357338 | ||||||
| chr3:38357363
|
G | A | 3 | a0002c0002t0001g0023a0002c0002t0001g0050a0002c0002t0002g0055 | 3 | HG01515.hp2 HG01517.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.141-2976G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38357363 | ||||||
| chr3:38357392
|
C | CT | 329 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(326): Show | 337 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.141-2935dupT | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38357392 | |||||
| chr3:38357440
|
G | A | 7 | a0001c0001t0003g0251a0001c0001t0003g0252a0001c0001t0003g0253others(4): Show | 7 | HG01884.hp1 HG01891.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.141-2899G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38357440 | ||||||
| chr3:38357455
|
C | T | 1 | a0001c0001t0003g0346 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.141-2884C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38357455 | ||||||
| chr3:38357490
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.141-2849C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38357490 | ||||||
| chr3:38357543
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.141-2796C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38357543 | ||||||
| chr3:38357544
|
G | A | 2 | a0001c0001t0002g0289a0001c0001t0005g0288 | 2 | NA18945.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.141-2795G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38357544 | ||||||
| chr3:38357632
|
C | T | 1 | a0001c0001t0002g0205 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.141-2707C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38357632 | ||||||
| chr3:38357686
|
T | C | 4 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(1): Show | 4 | HG01255.hp1 HG01884.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.141-2653T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38357686 | ||||||
| chr3:38357722
|
C | T | 1 | a0001c0003t0003g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.141-2617C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38357722 | ||||||
| chr3:38357786
|
GATA | G | 340 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(337): Show | 349 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.141-2547_141-2545d others(5): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38357786 | |||||
| chr3:38357804
|
T | G | 15 | a0001c0003t0003g0007a0001c0003t0003g0066a0001c0003t0003g0260others(12): Show | 16 | HG00741.hp2 HG01256.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.141-2535T>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38357804 | ||||||
| chr3:38357859
|
CT | C | 4 | a0003c0004t0003g0277a0003c0004t0003g0278a0003c0004t0003g0279others(1): Show | 4 | HG02965.hp1 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.141-2474delT | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38357859 | |||||
| chr3:38357865
|
TA | T | 312 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(309): Show | 319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.141-2465delA | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38357865 | |||||
| chr3:38357910
|
G | GT | 317 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(314): Show | 324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.141-2421dupT | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38357910 | |||||
| chr3:38358031
|
A | G | 299 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(296): Show | 306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.141-2308A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38358031 | ||||||
| chr3:38358087
|
C | A | 8 | a0001c0001t0003g0330a0001c0001t0003g0334a0001c0001t0003g0336others(5): Show | 8 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.141-2252C>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38358087 | ||||||
| chr3:38358206
|
T | TAAAGGTT others(286): Show |
1 | a0001c0001t0005g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.141-2130_141-2129i others(295): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358206 | |||||
| chr3:38358206
|
T | TAAAGGTT others(285): Show |
3 | a0002c0002t0002g0091a0002c0002t0002g0249a0013c0012t0002g0248 | 3 | HG03239.hp2 HG03491.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.141-2130_141-2129i others(294): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358206 | |||||
| chr3:38358206
|
T | TAAAGGTT others(285): Show |
3 | a0001c0001t0002g0284a0001c0001t0003g0234a0003c0004t0002g0287 | 3 | HG02717.hp1 HG03139.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.141-2130_141-2129i others(294): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358206 | |||||
| chr3:38358206
|
T | TAAAGGTT others(286): Show |
35 | a0001c0001t0001g0008a0001c0001t0001g0286a0001c0001t0001g0294others(32): Show | 36 | HG00544.hp1 HG00609.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.141-2130_141-2129i others(295): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358206 | |||||
| chr3:38358206
|
T | TAAAGGTT others(287): Show |
5 | a0001c0001t0001g0291a0001c0001t0002g0280a0001c0001t0003g0218others(2): Show | 5 | HG01243.hp1 HG02155.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.141-2130_141-2129i others(296): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358206 | |||||
| chr3:38358206
|
T | TAAAGGTT others(286): Show |
1 | a0001c0001t0003g0340 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.141-2130_141-2129i others(295): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358206 | |||||
| chr3:38358206
|
T | TAAAGGTT others(287): Show |
14 | a0001c0001t0002g0333a0001c0001t0002g0342a0001c0001t0002g0343others(11): Show | 14 | HG00639.hp2 HG01167.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.141-2130_141-2129i others(296): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358206 | |||||
| chr3:38358206
|
T | TAAAGGTT others(288): Show |
3 | a0001c0001t0001g0347a0001c0001t0002g0341a0001c0001t0003g0336 | 3 | HG02055.hp1 HG02622.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.141-2130_141-2129i others(297): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358206 | |||||
| chr3:38358206
|
T | TAAAGGTT others(284): Show |
4 | a0003c0004t0003g0277a0003c0004t0003g0278a0003c0004t0003g0279others(1): Show | 4 | HG02965.hp1 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.141-2130_141-2129i others(293): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358206 | |||||
| chr3:38358206
|
T | TAAAGGTT others(285): Show |
2 | a0001c0001t0003g0014a0001c0001t0003g0015 | 2 | HG01255.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.141-2130_141-2129i others(294): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358206 | |||||
| chr3:38358206
|
T | TAAAGGTT others(286): Show |
1 | a0001c0001t0003g0013 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.141-2130_141-2129i others(295): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358206 | |||||
| chr3:38358206
|
T | TAAAGGTT others(284): Show |
1 | a0002c0002t0004g0128 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.141-2130_141-2129i others(293): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358206 | |||||
| chr3:38358206
|
T | TAAAGGTT others(285): Show |
4 | a0002c0002t0003g0093a0002c0002t0003g0094a0002c0002t0004g0101others(1): Show | 4 | HG01928.hp2 HG02300.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.141-2130_141-2129i others(294): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358206 | |||||
| chr3:38358206
|
T | TAAAGGTT others(284): Show |
1 | a0002c0002t0005g0049 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.141-2130_141-2129i others(293): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358206 | |||||
| chr3:38358206
|
T | TAAAGGTT others(285): Show |
75 | a0001c0001t0001g0053a0001c0001t0001g0135a0001c0001t0001g0227others(72): Show | 77 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.141-2130_141-2129i others(294): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358206 | |||||
| chr3:38358206
|
T | TAAAGGTT others(286): Show |
15 | a0001c0001t0004g0019a0002c0002t0001g0023a0002c0002t0001g0036others(12): Show | 15 | HG01069.hp2 HG01081.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.141-2130_141-2129i others(295): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358206 | |||||
| chr3:38358206
|
T | TAAAGGTT others(285): Show |
6 | a0001c0001t0003g0253a0001c0001t0003g0256a0001c0001t0003g0257others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.141-2130_141-2129i others(294): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358206 | |||||
| chr3:38358206
|
T | TAAAGGTT others(286): Show |
3 | a0001c0001t0003g0251a0001c0001t0003g0252a0001c0001t0003g0259 | 3 | HG02486.hp1 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.141-2130_141-2129i others(295): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358206 | |||||
| chr3:38358206
|
T | TAAAGGTT others(285): Show |
2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG02698.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.141-2130_141-2129i others(294): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358206 | |||||
| chr3:38358206
|
T | TAAAGGTT others(284): Show |
1 | a0001c0001t0003g0203 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.141-2130_141-2129i others(293): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358206 | |||||
| chr3:38358206
|
T | TAAAGGTT others(285): Show |
116 | a0001c0001t0001g0006a0001c0001t0001g0112a0001c0001t0001g0113others(113): Show | 120 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.141-2130_141-2129i others(294): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358206 | |||||
| chr3:38358206
|
T | TAAAGGTT others(286): Show |
19 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(16): Show | 19 | HG00621.hp1 HG00741.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.141-2130_141-2129i others(295): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358206 | |||||
| chr3:38358206
|
T | TAAAGGTT others(285): Show |
1 | a0002c0002t0002g0025 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.141-2130_141-2129i others(294): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358206 | |||||
| chr3:38358206
|
T | TAAAGGTT others(285): Show |
1 | a0001c0001t0001g0204 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.141-2130_141-2129i others(294): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358206 | |||||
| chr3:38358210
|
A | G | 317 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(314): Show | 324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.141-2129A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38358210 | ||||||
| chr3:38358309
|
T | TTG | 4 | a0001c0003t0003g0007a0001c0003t0004g0265a0001c0003t0004g0266others(1): Show | 5 | HG01256.hp2 HG01258.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.141-1982_141-1981d others(4): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358309 | |||||
| chr3:38358309
|
T | TTGTG | 6 | a0001c0003t0003g0261a0001c0003t0003g0264a0004c0005t0007g0325others(3): Show | 6 | HG02257.hp2 HG02258.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.141-1984_141-1981d others(6): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358309 | |||||
| chr3:38358309
|
T | TTGTGTG | 4 | a0001c0003t0003g0263a0001c0003t0003g0267a0001c0003t0008g0329others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.141-1986_141-1981d others(8): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358309 | |||||
| chr3:38358309
|
TTG | T | 10 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0127others(7): Show | 10 | HG02004.hp1 HG02055.hp2 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.141-1982_141-1981d others(4): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358309 | |||||
| chr3:38358309
|
TTGTG | T | 6 | a0001c0001t0002g0284a0001c0001t0003g0234a0001c0001t0003g0253others(3): Show | 7 | HG01981.hp2 HG02717.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.141-1984_141-1981d others(6): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358309 | |||||
| chr3:38358309
|
TTGTGTG | T | 10 | a0001c0001t0003g0251a0001c0001t0003g0252a0001c0001t0003g0256others(7): Show | 11 | HG01074.hp2 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.141-1986_141-1981d others(8): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358309 | |||||
| chr3:38358309
|
TTGTGTGT others(5): Show |
T | 8 | a0001c0001t0003g0218a0001c0001t0003g0219a0001c0001t0003g0220others(5): Show | 8 | HG02572.hp1 HG02965.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.141-1992_141-1981d others(14): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358309 | |||||
| chr3:38358309
|
TTGTGTGT others(7): Show |
T | 4 | a0001c0001t0001g0286a0001c0001t0003g0285a0009c0011t0006g0272others(1): Show | 4 | HG01243.hp1 HG02451.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.141-1994_141-1981d others(16): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358309 | |||||
| chr3:38358357
|
G | GTGT | 3 | a0001c0001t0001g0192a0001c0001t0001g0294a0007c0007t0002g0102 | 3 | HG02027.hp2 HG03486.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.141-1981_141-1980i others(5): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358357 | |||||
| chr3:38358357
|
G | GTGTGT | 4 | a0001c0001t0001g0133a0001c0001t0002g0237a0001c0001t0003g0346others(1): Show | 4 | HG01109.hp2 HG02145.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.141-1981_141-1980i others(7): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358357 | |||||
| chr3:38358357
|
G | GTGTGTGT others(5): Show |
3 | a0001c0001t0001g0150a0002c0002t0001g0067a0002c0002t0001g0086 | 3 | HG00544.hp2 HG01361.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.141-1981_141-1980i others(14): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358357 | |||||
| chr3:38358357
|
G | GTGTGTGT others(3): Show |
12 | a0001c0001t0001g0112a0001c0001t0001g0138a0001c0001t0001g0152others(9): Show | 12 | HG00408.hp2 HG00609.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.141-1981_141-1980i others(12): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358357 | |||||
| chr3:38358357
|
G | GTGTGTGT others(1): Show |
35 | a0001c0001t0001g0113a0001c0001t0001g0132a0001c0001t0001g0136others(32): Show | 37 | HG00280.hp2 HG00408.hp1 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.141-1981_141-1980i others(10): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358357 | |||||
| chr3:38358357
|
G | GTGTGTT | 111 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0001g0109others(108): Show | 113 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.141-1981_141-1980i others(8): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358357 | |||||
| chr3:38358357
|
G | GTGTT | 60 | a0001c0001t0001g0117a0001c0001t0001g0135a0001c0001t0001g0137others(57): Show | 61 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.141-1981_141-1980i others(6): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358357 | |||||
| chr3:38358357
|
G | GTT | 25 | a0001c0001t0001g0200a0001c0001t0001g0300a0001c0001t0002g0122others(22): Show | 25 | HG01358.hp2 HG02015.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.141-1980_141-1979d others(4): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38358357 | |||||
| chr3:38358357
|
G | T | 62 | a0001c0001t0001g0008a0001c0001t0001g0215a0001c0001t0001g0216others(59): Show | 64 | HG01069.hp1 HG01123.hp1 HG01168.hp2 others(61): Show |
intron_variant | MODIFIER | c.141-1982G>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38358357 | ||||||
| chr3:38358365
|
C | T | 2 | a0001c0001t0001g0192a0001c0001t0009g0201 | 2 | HG02109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.141-1974C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38358365 | ||||||
| chr3:38358384
|
A | G | 317 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(314): Show | 324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.141-1955A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38358384 | ||||||
| chr3:38358430
|
C | T | 18 | a0001c0001t0001g0347a0001c0001t0002g0333a0001c0001t0002g0341others(15): Show | 18 | HG00639.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.141-1909C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38358430 | ||||||
| chr3:38358496
|
C | T | 1 | a0001c0003t0003g0267 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.141-1843C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38358496 | ||||||
| chr3:38358564
|
G | T | 317 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(314): Show | 324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.141-1775G>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38358564 | ||||||
| chr3:38358577
|
C | T | 1 | a0001c0001t0013g0145 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.141-1762C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38358577 | ||||||
| chr3:38358582
|
G | T | 1 | a0005c0006t0003g0273 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.141-1757G>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38358582 | ||||||
| chr3:38358593
|
C | T | 18 | a0001c0001t0001g0347a0001c0001t0002g0333a0001c0001t0002g0341others(15): Show | 18 | HG00639.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.141-1746C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38358593 | ||||||
| chr3:38358643
|
C | T | 317 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(314): Show | 324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.141-1696C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38358643 | ||||||
| chr3:38358658
|
A | C | 1 | a0001c0001t0003g0336 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.141-1681A>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38358658 | ||||||
| chr3:38358774
|
T | C | 1 | a0005c0006t0003g0273 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.141-1565T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38358774 | ||||||
| chr3:38358937
|
C | T | 299 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(296): Show | 306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.141-1402C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38358937 | ||||||
| chr3:38358966
|
C | T | 4 | a0001c0001t0002g0003a0001c0001t0002g0209a0001c0001t0004g0191others(1): Show | 5 | HG01255.hp2 HG01928.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.141-1373C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38358966 | ||||||
| chr3:38359069
|
G | C | 4 | a0003c0004t0003g0277a0003c0004t0003g0278a0003c0004t0003g0279others(1): Show | 4 | HG02965.hp1 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.141-1270G>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38359069 | ||||||
| chr3:38359083
|
A | C | 1 | a0001c0001t0005g0118 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.141-1256A>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38359083 | ||||||
| chr3:38359167
|
T | C | 317 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(314): Show | 324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.141-1172T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38359167 | ||||||
| chr3:38359215
|
T | C | 18 | a0001c0001t0001g0347a0001c0001t0002g0333a0001c0001t0002g0341others(15): Show | 18 | HG00639.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.141-1124T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38359215 | ||||||
| chr3:38359242
|
T | A | 4 | a0005c0006t0001g0320a0005c0006t0007g0321a0009c0011t0006g0272others(1): Show | 4 | HG02451.hp2 HG02615.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.141-1097T>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38359242 | ||||||
| chr3:38359245
|
G | C | 1 | a0001c0001t0002g0213 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.141-1094G>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38359245 | ||||||
| chr3:38359275
|
G | T | 317 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(314): Show | 324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.141-1064G>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38359275 | ||||||
| chr3:38359282
|
A | T | 317 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(314): Show | 324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.141-1057A>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38359282 | ||||||
| chr3:38359430
|
AGGCCTGT others(15): Show |
A | 1 | a0005c0006t0003g0273 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.141-900_141-879del others(22): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 38359430 | |||||
| chr3:38359440
|
A | G | 299 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(296): Show | 306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.141-899A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38359440 | ||||||
| chr3:38359510
|
A | T | 1 | a0002c0002t0002g0017 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.141-829A>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38359510 | ||||||
| chr3:38359522
|
G | A | 4 | a0004c0005t0007g0325a0004c0005t0007g0326a0004c0005t0007g0348others(1): Show | 4 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.141-817G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38359522 | ||||||
| chr3:38359540
|
A | G | 3 | a0001c0001t0002g0284a0001c0001t0003g0234a0001c0001t0010g0068 | 3 | HG02717.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.141-799A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38359540 | ||||||
| chr3:38359716
|
G | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0150 | 3 | HG00438.hp1 HG00544.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.141-623G>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38359716 | ||||||
| chr3:38359750
|
G | A | 1 | a0001c0001t0006g0254 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.141-589G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38359750 | ||||||
| chr3:38359807
|
C | A | 317 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(314): Show | 324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.141-532C>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38359807 | ||||||
| chr3:38360007
|
C | T | 1 | a0002c0002t0002g0054 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.141-332C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38360007 | ||||||
| chr3:38360041
|
G | A | 1 | a0002c0002t0001g0002 | 2 | NA19007.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.141-298G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38360041 | ||||||
| chr3:38360186
|
C | T | 299 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(296): Show | 306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.141-153C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 2/18 | chr3 | 38360186 | ||||||
| chr3:38360427
|
A | G | 317 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(314): Show | 324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.210+19A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38360427 | ||||||
| chr3:38360446
|
G | A | 7 | a0004c0005t0003g0322a0004c0005t0006g0010a0004c0005t0006g0327others(4): Show | 8 | HG01074.hp2 HG01981.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.210+38G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38360446 | ||||||
| chr3:38360465
|
C | T | 1 | a0001c0003t0008g0329 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.210+57C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38360465 | ||||||
| chr3:38360506
|
G | C | 1 | a0001c0001t0001g0114 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.210+98G>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38360506 | ||||||
| chr3:38360516
|
T | A | 317 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(314): Show | 324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.210+108T>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38360516 | ||||||
| chr3:38360536
|
G | A | 332 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(329): Show | 340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.210+128G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38360536 | ||||||
| chr3:38360632
|
G | A | 1 | a0001c0001t0003g0014 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.210+224G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38360632 | ||||||
| chr3:38360797
|
G | A | 315 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(312): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.210+389G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38360797 | ||||||
| chr3:38360827
|
G | A | 315 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(312): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.210+419G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38360827 | ||||||
| chr3:38360831
|
C | T | 2 | a0002c0002t0004g0016a0002c0002t0004g0034 | 2 | HG00423.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.210+423C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38360831 | ||||||
| chr3:38360892
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.210+484G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38360892 | ||||||
| chr3:38360895
|
C | T | 1 | a0001c0001t0002g0189 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.210+487C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38360895 | ||||||
| chr3:38360919
|
C | G | 2 | a0002c0002t0001g0026a0002c0002t0001g0033 | 2 | NA18986.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.210+511C>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38360919 | ||||||
| chr3:38360958
|
T | C | 315 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(312): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.210+550T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38360958 | ||||||
| chr3:38360973
|
T | G | 1 | a0001c0001t0002g0139 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.210+565T>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38360973 | ||||||
| chr3:38360989
|
T | C | 315 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(312): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.210+581T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38360989 | ||||||
| chr3:38360990
|
G | A | 1 | a0002c0002t0002g0079 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.210+582G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38360990 | ||||||
| chr3:38361095
|
C | T | 315 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(312): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.210+687C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38361095 | ||||||
| chr3:38361227
|
G | A | 2 | a0002c0002t0002g0083a0002c0002t0002g0092 | 2 | HG01081.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.210+819G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38361227 | ||||||
| chr3:38361420
|
C | A | 315 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(312): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.210+1012C>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38361420 | ||||||
| chr3:38361536
|
G | C | 1 | a0001c0001t0002g0125 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.210+1128G>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38361536 | ||||||
| chr3:38361595
|
C | T | 18 | a0001c0001t0001g0347a0001c0001t0002g0333a0001c0001t0002g0341others(15): Show | 18 | HG00639.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.210+1187C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38361595 | ||||||
| chr3:38361673
|
C | A | 2 | a0002c0002t0005g0047a0002c0002t0005g0049 | 2 | HG02015.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.211-1264C>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38361673 | ||||||
| chr3:38361687
|
A | C | 315 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(312): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.211-1250A>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38361687 | ||||||
| chr3:38361688
|
G | A | 1 | a0001c0001t0017g0108 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.211-1249G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38361688 | ||||||
| chr3:38361695
|
G | A | 2 | a0002c0002t0005g0088a0002c0002t0005g0089 | 2 | NA18962.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.211-1242G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38361695 | ||||||
| chr3:38361712
|
C | T | 315 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(312): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.211-1225C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38361712 | ||||||
| chr3:38361795
|
G | A | 315 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(312): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.211-1142G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38361795 | ||||||
| chr3:38362090
|
C | T | 8 | a0001c0001t0003g0330a0001c0001t0003g0334a0001c0001t0003g0336others(5): Show | 8 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.211-847C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38362090 | ||||||
| chr3:38362137
|
C | T | 315 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(312): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.211-800C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38362137 | ||||||
| chr3:38362168
|
T | G | 40 | a0001c0001t0001g0008a0001c0001t0001g0286a0001c0001t0001g0291others(37): Show | 41 | HG00544.hp1 HG00609.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.211-769T>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38362168 | ||||||
| chr3:38362171
|
T | G | 315 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(312): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.211-766T>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38362171 | ||||||
| chr3:38362372
|
G | C | 2 | a0001c0001t0002g0341a0001c0001t0002g0344 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.211-565G>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38362372 | ||||||
| chr3:38362391
|
C | G | 1 | a0001c0001t0001g0134 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.211-546C>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38362391 | ||||||
| chr3:38362404
|
A | C | 1 | a0001c0001t0005g0308 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.211-533A>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38362404 | ||||||
| chr3:38362531
|
A | G | 1 | a0001c0001t0001g0113 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.211-406A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38362531 | ||||||
| chr3:38362547
|
A | C | 18 | a0001c0001t0001g0347a0001c0001t0002g0333a0001c0001t0002g0341others(15): Show | 18 | HG00639.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.211-390A>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38362547 | ||||||
| chr3:38362554
|
T | C | 315 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(312): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.211-383T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38362554 | ||||||
| chr3:38362619
|
G | A | 315 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(312): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.211-318G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38362619 | ||||||
| chr3:38362737
|
T | C | 1 | a0001c0001t0013g0145 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.211-200T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 3/18 | chr3 | 38362737 | ||||||
| chr3:38363200
|
G | A | 3 | a0001c0001t0002g0284a0001c0001t0003g0234a0001c0001t0010g0068 | 3 | HG02717.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.291+183G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 4/18 | chr3 | 38363200 | ||||||
| chr3:38363294
|
A | G | 1 | a0001c0001t0002g0144 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.291+277A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 4/18 | chr3 | 38363294 | ||||||
| chr3:38363420
|
TTAA | T | 4 | a0003c0004t0003g0277a0003c0004t0003g0278a0003c0004t0003g0279others(1): Show | 4 | HG02965.hp1 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.291+408_291+410del others(3): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr3 | 38363420 | |||||
| chr3:38363448
|
G | T | 315 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(312): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.291+431G>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 4/18 | chr3 | 38363448 | ||||||
| chr3:38363449
|
A | AGTGCAT | 315 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(312): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.291+433_291+434ins others(6): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr3 | 38363449 | |||||
| chr3:38363452
|
A | G | 315 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(312): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.291+435A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 4/18 | chr3 | 38363452 | ||||||
| chr3:38363836
|
T | C | 328 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(325): Show | 336 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.291+819T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 4/18 | chr3 | 38363836 | ||||||
| chr3:38363884
|
G | A | 315 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(312): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.291+867G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 4/18 | chr3 | 38363884 | ||||||
| chr3:38363974
|
G | A | 1 | a0001c0001t0005g0118 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.291+957G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 4/18 | chr3 | 38363974 | ||||||
| chr3:38364058
|
C | G | 95 | a0001c0001t0001g0227a0001c0001t0002g0226a0001c0001t0002g0333others(92): Show | 97 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.291+1041C>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 4/18 | chr3 | 38364058 | ||||||
| chr3:38364102
|
A | G | 315 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(312): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.291+1085A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 4/18 | chr3 | 38364102 | ||||||
| chr3:38364283
|
C | CT | 9 | a0001c0001t0001g0347a0001c0001t0002g0333a0001c0001t0002g0341others(6): Show | 9 | HG01168.hp2 HG01169.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.292-915dupT | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr3 | 38364283 | |||||
| chr3:38364285
|
C | G | 9 | a0001c0001t0001g0347a0001c0001t0002g0333a0001c0001t0002g0341others(6): Show | 9 | HG01168.hp2 HG01169.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.292-914C>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 4/18 | chr3 | 38364285 | ||||||
| chr3:38364294
|
C | T | 301 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(298): Show | 308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.292-905C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 4/18 | chr3 | 38364294 | ||||||
| chr3:38364374
|
C | T | 1 | a0001c0001t0001g0286 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.292-825C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 4/18 | chr3 | 38364374 | ||||||
| chr3:38364468
|
G | A | 9 | a0001c0001t0003g0251a0001c0001t0003g0252a0001c0001t0003g0253others(6): Show | 9 | HG01884.hp1 HG01891.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.292-731G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 4/18 | chr3 | 38364468 | ||||||
| chr3:38364583
|
G | A | 1 | a0001c0001t0007g0255 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.292-616G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 4/18 | chr3 | 38364583 | ||||||
| chr3:38364716
|
CATAGGGT others(3): Show |
C | 315 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(312): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.292-478_292-469del others(10): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr3 | 38364716 | |||||
| chr3:38364786
|
T | C | 315 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(312): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.292-413T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 4/18 | chr3 | 38364786 | ||||||
| chr3:38364949
|
T | C | 315 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(312): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.292-250T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 4/18 | chr3 | 38364949 | ||||||
| chr3:38364987
|
A | G | 149 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0001g0110others(146): Show | 153 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.292-212A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 4/18 | chr3 | 38364987 | ||||||
| chr3:38365157
|
T | C | 328 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(325): Show | 336 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.292-42T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 4/18 | chr3 | 38365157 | ||||||
| chr3:38365302
|
T | G | 258 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0001g0109others(255): Show | 264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.378+17T>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 5/18 | chr3 | 38365302 | ||||||
| chr3:38365324
|
G | A | 1 | a0001c0001t0006g0199 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.378+39G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 5/18 | chr3 | 38365324 | ||||||
| chr3:38365329
|
G | A | 4 | a0003c0004t0003g0277a0003c0004t0003g0278a0003c0004t0003g0279others(1): Show | 4 | HG02965.hp1 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.378+44G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 5/18 | chr3 | 38365329 | ||||||
| chr3:38366108
|
G | A | 314 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(311): Show | 321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.507+372G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 6/18 | chr3 | 38366108 | ||||||
| chr3:38366108
|
G | T | 1 | a0001c0001t0004g0078 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.507+372G>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 6/18 | chr3 | 38366108 | ||||||
| chr3:38366110
|
T | TA | 154 | a0001c0001t0001g0008a0001c0001t0001g0109a0001c0001t0001g0135others(151): Show | 157 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.507+390dupA | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr3 | 38366110 | |||||
| chr3:38366110
|
T | TAA | 13 | a0001c0001t0001g0227a0001c0001t0001g0291a0001c0001t0002g0289others(10): Show | 13 | HG00280.hp1 HG00544.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.507+389_507+390dup others(2): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr3 | 38366110 | |||||
| chr3:38366110
|
TA | T | 7 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(4): Show | 7 | HG00323.hp1 HG01069.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.507+390delA | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr3 | 38366110 | |||||
| chr3:38366281
|
G | A | 261 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0001g0109others(258): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.508-527G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 6/18 | chr3 | 38366281 | ||||||
| chr3:38366313
|
G | C | 315 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(312): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.508-495G>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 6/18 | chr3 | 38366313 | ||||||
| chr3:38366579
|
C | T | 4 | a0003c0004t0003g0277a0003c0004t0003g0278a0003c0004t0003g0279others(1): Show | 4 | HG02965.hp1 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.508-229C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 6/18 | chr3 | 38366579 | ||||||
| chr3:38366616
|
T | C | 315 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(312): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.508-192T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 6/18 | chr3 | 38366616 | ||||||
| chr3:38366622
|
T | C | 1 | a0002c0002t0005g0084 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.508-186T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 6/18 | chr3 | 38366622 | ||||||
| chr3:38366757
|
G | A | 315 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(312): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.508-51G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 6/18 | chr3 | 38366757 | ||||||
| chr3:38366917
|
C | A | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG02698.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.573+44C>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 7/18 | chr3 | 38366917 | ||||||
| chr3:38366962
|
G | A | 40 | a0001c0001t0001g0008a0001c0001t0001g0286a0001c0001t0001g0291others(37): Show | 41 | HG00544.hp1 HG00609.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.573+89G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 7/18 | chr3 | 38366962 | ||||||
| chr3:38366968
|
A | G | 315 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(312): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.573+95A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 7/18 | chr3 | 38366968 | ||||||
| chr3:38367038
|
A | C | 11 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015others(8): Show | 11 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.573+165A>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 7/18 | chr3 | 38367038 | ||||||
| chr3:38367045
|
G | A | 315 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(312): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.573+172G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 7/18 | chr3 | 38367045 | ||||||
| chr3:38367069
|
A | T | 250 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0001g0109others(247): Show | 256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.573+196A>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 7/18 | chr3 | 38367069 | ||||||
| chr3:38367154
|
A | G | 4 | a0003c0004t0003g0277a0003c0004t0003g0278a0003c0004t0003g0279others(1): Show | 4 | HG02965.hp1 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.573+281A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 7/18 | chr3 | 38367154 | ||||||
| chr3:38367251
|
G | A | 250 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0001g0109others(247): Show | 256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.573+378G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 7/18 | chr3 | 38367251 | ||||||
| chr3:38367332
|
A | G | 3 | a0001c0001t0002g0004a0001c0001t0002g0184a0001c0001t0002g0185 | 4 | NA18952.hp2 NA18980.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.573+459A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 7/18 | chr3 | 38367332 | ||||||
| chr3:38367801
|
C | T | 5 | a0005c0006t0001g0320a0005c0006t0004g0323a0005c0006t0007g0321others(2): Show | 5 | HG02258.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.574-384C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 7/18 | chr3 | 38367801 | ||||||
| chr3:38367882
|
C | T | 1 | a0005c0006t0003g0273 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.574-303C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 7/18 | chr3 | 38367882 | ||||||
| chr3:38368087
|
C | T | 39 | a0001c0001t0001g0008a0001c0001t0001g0286a0001c0001t0001g0291others(36): Show | 40 | HG00544.hp1 HG00609.hp2 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.574-98C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 7/18 | chr3 | 38368087 | ||||||
| chr3:38368103
|
C | T | 2 | a0001c0001t0003g0126a0001c0001t0003g0127 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.574-82C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 7/18 | chr3 | 38368103 | ||||||
| chr3:38368109
|
T | G | 315 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(312): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.574-76T>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 7/18 | chr3 | 38368109 | ||||||
| chr3:38368266
|
C | T | 3 | a0001c0001t0003g0012a0001c0001t0006g0199a0001c0001t0006g0232 | 3 | HG02622.hp1 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.646+9C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 8/18 | chr3 | 38368266 | ||||||
| chr3:38368311
|
G | C | 13 | a0004c0005t0003g0322a0004c0005t0006g0010a0004c0005t0006g0327others(10): Show | 14 | HG01074.hp2 HG01981.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.646+54G>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 8/18 | chr3 | 38368311 | ||||||
| chr3:38368450
|
C | T | 13 | a0004c0005t0003g0322a0004c0005t0006g0010a0004c0005t0006g0327others(10): Show | 14 | HG01074.hp2 HG01981.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.646+193C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 8/18 | chr3 | 38368450 | ||||||
| chr3:38368451
|
G | A | 5 | a0001c0001t0003g0217a0001c0001t0006g0161a0001c0001t0006g0199others(2): Show | 5 | HG02622.hp1 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.646+194G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 8/18 | chr3 | 38368451 | ||||||
| chr3:38368520
|
C | T | 3 | a0003c0004t0003g0277a0003c0004t0003g0278a0003c0004t0003g0279 | 3 | HG02965.hp1 HG03130.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.646+263C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 8/18 | chr3 | 38368520 | ||||||
| chr3:38368521
|
G | A | 3 | a0004c0005t0003g0322a0004c0005t0006g0010a0004c0005t0006g0327 | 4 | HG01074.hp2 HG01981.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.646+264G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 8/18 | chr3 | 38368521 | ||||||
| chr3:38368523
|
G | T | 5 | a0005c0006t0001g0320a0005c0006t0004g0323a0005c0006t0007g0321others(2): Show | 5 | HG02258.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.646+266G>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 8/18 | chr3 | 38368523 | ||||||
| chr3:38368557
|
G | A | 2 | a0001c0001t0001g0138a0001c0001t0001g0154 | 2 | HG00280.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.646+300G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 8/18 | chr3 | 38368557 | ||||||
| chr3:38368618
|
A | T | 1 | a0001c0003t0003g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.646+361A>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 8/18 | chr3 | 38368618 | ||||||
| chr3:38368767
|
C | T | 1 | a0001c0001t0002g0231 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.646+510C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 8/18 | chr3 | 38368767 | ||||||
| chr3:38368855
|
GA | G | 315 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(312): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.646+599delA | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 8/18 | chr3 | 38368855 | ||||||
| chr3:38368857
|
C | T | 1 | a0005c0006t0004g0323 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.646+600C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 8/18 | chr3 | 38368857 | ||||||
| chr3:38368863
|
T | C | 107 | a0001c0001t0001g0109a0001c0001t0001g0347a0001c0001t0002g0284others(104): Show | 109 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.646+606T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 8/18 | chr3 | 38368863 | ||||||
| chr3:38368952
|
C | T | 1 | a0001c0001t0006g0199 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.646+695C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 8/18 | chr3 | 38368952 | ||||||
| chr3:38368993
|
G | T | 2 | a0001c0001t0003g0126a0001c0001t0003g0127 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.646+736G>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 8/18 | chr3 | 38368993 | ||||||
| chr3:38369018
|
T | C | 315 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(312): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.646+761T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 8/18 | chr3 | 38369018 | ||||||
| chr3:38369057
|
T | C | 315 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(312): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.646+800T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 8/18 | chr3 | 38369057 | ||||||
| chr3:38369092
|
G | A | 315 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(312): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.646+835G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 8/18 | chr3 | 38369092 | ||||||
| chr3:38369141
|
A | G | 315 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(312): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.646+884A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 8/18 | chr3 | 38369141 | ||||||
| chr3:38369372
|
G | A | 1 | a0002c0002t0004g0042 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.647-684G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 8/18 | chr3 | 38369372 | ||||||
| chr3:38369541
|
C | T | 1 | a0005c0006t0003g0273 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.647-515C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 8/18 | chr3 | 38369541 | ||||||
| chr3:38369584
|
A | G | 328 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(325): Show | 336 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.647-472A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 8/18 | chr3 | 38369584 | ||||||
| chr3:38369703
|
C | A | 8 | a0004c0005t0003g0322a0004c0005t0006g0010a0004c0005t0006g0327others(5): Show | 9 | HG01074.hp2 HG01981.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.647-353C>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 8/18 | chr3 | 38369703 | ||||||
| chr3:38369710
|
A | G | 315 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(312): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.647-346A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 8/18 | chr3 | 38369710 | ||||||
| chr3:38369744
|
G | A | 1 | a0001c0001t0002g0225 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.647-312G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 8/18 | chr3 | 38369744 | ||||||
| chr3:38369886
|
G | A | 315 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(312): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.647-170G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 8/18 | chr3 | 38369886 | ||||||
| chr3:38370238
|
G | GCACACAC others(3): Show |
1 | a0001c0001t0009g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.765+65_765+66insAC others(8): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 38370238 | |||||
| chr3:38370240
|
G | A | 2 | a0001c0001t0009g0075a0003c0004t0004g0276 | 2 | HG02280.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.765+66G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | chr3 | 38370240 | ||||||
| chr3:38370240
|
G | GCA | 59 | a0001c0001t0001g0008a0001c0001t0001g0286a0001c0001t0001g0291others(56): Show | 61 | HG00544.hp1 HG00609.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.765+92_765+93dupAC | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 38370240 | |||||
| chr3:38370240
|
G | GCACA | 5 | a0001c0001t0003g0013a0001c0001t0004g0282a0003c0004t0003g0277others(2): Show | 5 | HG02055.hp2 HG02965.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.765+90_765+93dupAC others(2): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 38370240 | |||||
| chr3:38370240
|
G | GCACACAC others(1): Show |
12 | a0001c0001t0001g0133a0001c0001t0001g0149a0001c0001t0001g0216others(9): Show | 12 | HG01358.hp1 HG01358.hp2 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.765+86_765+93dupAC others(6): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 38370240 | |||||
| chr3:38370240
|
G | GCACACAC others(3): Show |
97 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0001g0109others(94): Show | 99 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.765+84_765+93dupAC others(8): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 38370240 | |||||
| chr3:38370240
|
G | GCACACAC others(5): Show |
97 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0117others(94): Show | 101 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.765+82_765+93dupAC others(10): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 38370240 | |||||
| chr3:38370240
|
G | GCACACAC others(7): Show |
19 | a0001c0001t0001g0111a0001c0001t0001g0124a0001c0001t0001g0134others(16): Show | 19 | HG00323.hp2 HG00741.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.765+80_765+93dupAC others(12): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 38370240 | |||||
| chr3:38370240
|
G | GCACACAC others(9): Show |
19 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0141others(16): Show | 19 | HG00597.hp2 HG02027.hp1 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.765+78_765+93dupAC others(14): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 38370240 | |||||
| chr3:38370240
|
G | GCACACAC others(11): Show |
7 | a0001c0001t0001g0132a0001c0001t0001g0140a0001c0001t0001g0162others(4): Show | 7 | HG01099.hp1 HG02056.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.765+76_765+93dupAC others(16): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 38370240 | |||||
| chr3:38370240
|
G | GCACACAC others(15): Show |
1 | a0001c0001t0001g0241 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.765+72_765+93dupAC others(20): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 38370240 | |||||
| chr3:38370240
|
G | GCGCACAC others(3): Show |
3 | a0002c0002t0001g0130a0002c0002t0002g0020a0002c0002t0002g0129 | 3 | HG02602.hp2 NA18942.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.765+67_765+68insGC others(8): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 38370240 | |||||
| chr3:38370240
|
G | GCGCGCAC others(11): Show |
2 | a0003c0004t0004g0316a0008c0010t0010g0317 | 2 | NA18906.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.765+67_765+68insGC others(16): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 38370240 | |||||
| chr3:38370369
|
C | T | 3 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015 | 3 | HG01255.hp1 HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.765+195C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | chr3 | 38370369 | ||||||
| chr3:38370785
|
G | A | 3 | a0001c0003t0003g0007a0001c0003t0003g0261a0001c0003t0003g0262 | 4 | HG01256.hp2 HG01258.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.765+611G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | chr3 | 38370785 | ||||||
| chr3:38370812
|
C | T | 41 | a0001c0001t0001g0111a0001c0001t0001g0136a0001c0001t0001g0137others(38): Show | 44 | HG00558.hp1 HG00621.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.765+638C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | chr3 | 38370812 | ||||||
| chr3:38370827
|
G | A | 2 | a0001c0001t0002g0246a0001c0001t0002g0247 | 2 | HG01074.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.765+653G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | chr3 | 38370827 | ||||||
| chr3:38371084
|
G | A | 1 | a0002c0002t0002g0103 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.765+910G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | chr3 | 38371084 | ||||||
| chr3:38371086
|
G | T | 1 | a0002c0002t0004g0059 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.765+912G>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | chr3 | 38371086 | ||||||
| chr3:38371107
|
A | G | 7 | a0004c0005t0003g0322a0004c0005t0006g0010a0004c0005t0006g0327others(4): Show | 8 | HG01074.hp2 HG01981.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.765+933A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | chr3 | 38371107 | ||||||
| chr3:38371127
|
A | G | 1 | a0001c0001t0001g0294 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.765+953A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | chr3 | 38371127 | ||||||
| chr3:38371185
|
G | T | 329 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(326): Show | 337 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.765+1011G>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | chr3 | 38371185 | ||||||
| chr3:38371275
|
AT | A | 315 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(312): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.765+1116delT | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 38371275 | |||||
| chr3:38371338
|
G | A | 315 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(312): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.765+1164G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | chr3 | 38371338 | ||||||
| chr3:38371342
|
C | T | 5 | a0005c0006t0001g0320a0005c0006t0004g0323a0005c0006t0007g0321others(2): Show | 5 | HG02258.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.765+1168C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | chr3 | 38371342 | ||||||
| chr3:38371398
|
C | T | 1 | a0001c0001t0003g0012 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.765+1224C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | chr3 | 38371398 | ||||||
| chr3:38371416
|
G | C | 2 | a0001c0001t0003g0332a0001c0001t0003g0345 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.766-1239G>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | chr3 | 38371416 | ||||||
| chr3:38371422
|
C | T | 4 | a0004c0005t0007g0325a0004c0005t0007g0326a0004c0005t0007g0348others(1): Show | 4 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.766-1233C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | chr3 | 38371422 | ||||||
| chr3:38371430
|
C | T | 6 | a0001c0001t0001g0286a0001c0001t0003g0218a0001c0001t0003g0219others(3): Show | 6 | HG01243.hp1 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.766-1225C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | chr3 | 38371430 | ||||||
| chr3:38371447
|
T | A | 2 | a0001c0001t0003g0126a0001c0001t0003g0127 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.766-1208T>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | chr3 | 38371447 | ||||||
| chr3:38371626
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.766-1029G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | chr3 | 38371626 | ||||||
| chr3:38371678
|
G | A | 1 | a0001c0001t0010g0068 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.766-977G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | chr3 | 38371678 | ||||||
| chr3:38371684
|
G | A | 2 | a0001c0001t0002g0207a0001c0001t0002g0208 | 2 | HG02735.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.766-971G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | chr3 | 38371684 | ||||||
| chr3:38371742
|
G | A | 2 | a0001c0001t0002g0115a0001c0001t0002g0174 | 2 | HG00438.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.766-913G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | chr3 | 38371742 | ||||||
| chr3:38371866
|
C | T | 2 | a0001c0001t0002g0233a0002c0002t0005g0076 | 2 | HG02083.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.766-789C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | chr3 | 38371866 | ||||||
| chr3:38371909
|
A | G | 3 | a0003c0004t0003g0277a0003c0004t0003g0278a0003c0004t0003g0279 | 3 | HG02965.hp1 HG03130.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.766-746A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | chr3 | 38371909 | ||||||
| chr3:38371981
|
G | A | 313 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(310): Show | 320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.766-674G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | chr3 | 38371981 | ||||||
| chr3:38372036
|
C | T | 257 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0001g0109others(254): Show | 263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.766-619C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | chr3 | 38372036 | ||||||
| chr3:38372074
|
C | T | 1 | a0001c0001t0002g0185 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.766-581C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | chr3 | 38372074 | ||||||
| chr3:38372120
|
C | T | 3 | a0002c0002t0001g0026a0002c0002t0001g0033a0002c0002t0001g0046 | 3 | NA18986.hp1 NA19011.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.766-535C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | chr3 | 38372120 | ||||||
| chr3:38372168
|
C | CT | 3 | a0001c0001t0001g0112a0001c0001t0001g0119a0001c0001t0001g0159 | 3 | NA18952.hp1 NA18982.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.766-486dupT | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 38372168 | |||||
| chr3:38372214
|
T | G | 6 | a0001c0001t0001g0286a0001c0001t0003g0218a0001c0001t0003g0219others(3): Show | 6 | HG01243.hp1 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.766-441T>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | chr3 | 38372214 | ||||||
| chr3:38372389
|
T | C | 328 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(325): Show | 336 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.766-266T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | chr3 | 38372389 | ||||||
| chr3:38372423
|
C | T | 2 | a0001c0001t0002g0116a0001c0001t0002g0176 | 2 | HG00423.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.766-232C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | chr3 | 38372423 | ||||||
| chr3:38372568
|
G | A | 11 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015others(8): Show | 11 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.766-87G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 9/18 | chr3 | 38372568 | ||||||
| chr3:38372743
|
A | G | 2 | a0001c0001t0008g0065a0001c0001t0008g0169 | 2 | HG02895.hp2 HG02897.hp1 |
splice_region_variant&intron_variant | LOW | c.847+7A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 10/18 | chr3 | 38372743 | ||||||
| chr3:38372877
|
T | A | 1 | a0002c0002t0002g0087 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.847+141T>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 10/18 | chr3 | 38372877 | ||||||
| chr3:38372909
|
G | A | 1 | a0001c0001t0002g0210 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.847+173G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 10/18 | chr3 | 38372909 | ||||||
| chr3:38372935
|
G | A | 1 | a0001c0001t0003g0285 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.847+199G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 10/18 | chr3 | 38372935 | ||||||
| chr3:38373091
|
C | T | 1 | a0002c0002t0004g0048 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.847+355C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 10/18 | chr3 | 38373091 | ||||||
| chr3:38373128
|
G | T | 2 | a0001c0001t0003g0259a0003c0004t0004g0258 | 2 | HG02486.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.847+392G>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 10/18 | chr3 | 38373128 | ||||||
| chr3:38373146
|
G | T | 1 | a0001c0001t0001g0137 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.847+410G>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 10/18 | chr3 | 38373146 | ||||||
| chr3:38373159
|
G | A | 7 | a0001c0001t0003g0251a0001c0001t0003g0252a0001c0001t0003g0253others(4): Show | 7 | HG01884.hp1 HG01891.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.847+423G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 10/18 | chr3 | 38373159 | ||||||
| chr3:38373183
|
C | T | 100 | a0001c0001t0001g0109a0001c0001t0001g0124a0001c0001t0001g0142others(97): Show | 101 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.847+447C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 10/18 | chr3 | 38373183 | ||||||
| chr3:38373300
|
A | C | 127 | a0001c0001t0001g0109a0001c0001t0001g0124a0001c0001t0001g0142others(124): Show | 129 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.847+564A>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 10/18 | chr3 | 38373300 | ||||||
| chr3:38373315
|
C | T | 1 | a0002c0002t0005g0076 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.847+579C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 10/18 | chr3 | 38373315 | ||||||
| chr3:38373323
|
C | T | 1 | a0002c0002t0002g0090 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.847+587C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 10/18 | chr3 | 38373323 | ||||||
| chr3:38373358
|
C | T | 1 | a0008c0010t0010g0317 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.847+622C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 10/18 | chr3 | 38373358 | ||||||
| chr3:38373392
|
C | T | 1 | a0003c0004t0004g0258 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.847+656C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 10/18 | chr3 | 38373392 | ||||||
| chr3:38373651
|
A | T | 14 | a0003c0004t0002g0287a0003c0004t0003g0277a0003c0004t0003g0278others(11): Show | 15 | HG01074.hp2 HG01981.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.848-811A>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 10/18 | chr3 | 38373651 | ||||||
| chr3:38373802
|
A | G | 1 | a0001c0001t0009g0201 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.848-660A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 10/18 | chr3 | 38373802 | ||||||
| chr3:38373886
|
G | T | 1 | a0002c0002t0003g0044 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.848-576G>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 10/18 | chr3 | 38373886 | ||||||
| chr3:38373896
|
G | A | 1 | a0002c0002t0002g0077 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.848-566G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 10/18 | chr3 | 38373896 | ||||||
| chr3:38373987
|
C | T | 3 | a0001c0001t0001g0138a0001c0001t0001g0154a0001c0001t0001g0214 | 3 | HG00280.hp2 HG00733.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.848-475C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 10/18 | chr3 | 38373987 | ||||||
| chr3:38374027
|
TA | T | 155 | a0001c0001t0001g0008a0001c0001t0001g0109a0001c0001t0001g0124others(152): Show | 158 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.848-423delA | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 38374027 | |||||
| chr3:38374298
|
T | G | 1 | a0002c0002t0004g0059 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.848-164T>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 10/18 | chr3 | 38374298 | ||||||
| chr3:38374427
|
C | T | 2 | a0001c0003t0003g0271a0002c0002t0001g0086 | 2 | HG00741.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.848-35C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 10/18 | chr3 | 38374427 | ||||||
| chr3:38374428
|
G | T | 1 | a0001c0001t0002g0237 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.848-34G>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 10/18 | chr3 | 38374428 | ||||||
| chr3:38374857
|
T | C | 1 | a0001c0001t0001g0177 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.889-287T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 11/18 | chr3 | 38374857 | ||||||
| chr3:38374873
|
T | C | 1 | a0001c0001t0001g0216 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.889-271T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 11/18 | chr3 | 38374873 | ||||||
| chr3:38375076
|
C | T | 1 | a0001c0001t0001g0117 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.889-68C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 11/18 | chr3 | 38375076 | ||||||
| chr3:38375081
|
C | T | 1 | a0003c0004t0004g0258 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.889-63C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 11/18 | chr3 | 38375081 | ||||||
| chr3:38375292
|
G | A | 4 | a0001c0001t0001g0175a0001c0001t0001g0187a0001c0001t0001g0198others(1): Show | 4 | HG00323.hp1 HG03710.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1004+33G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 12/18 | chr3 | 38375292 | ||||||
| chr3:38375394
|
A | T | 4 | a0003c0004t0003g0277a0003c0004t0003g0278a0003c0004t0003g0279others(1): Show | 4 | HG02965.hp1 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1004+135A>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 12/18 | chr3 | 38375394 | ||||||
| chr3:38375592
|
C | T | 1 | a0001c0001t0004g0019 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1004+333C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 12/18 | chr3 | 38375592 | ||||||
| chr3:38375668
|
C | G | 12 | a0003c0004t0002g0287a0003c0004t0003g0277a0003c0004t0003g0278others(9): Show | 13 | HG01074.hp2 HG01981.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1004+409C>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 12/18 | chr3 | 38375668 | ||||||
| chr3:38375675
|
C | T | 3 | a0001c0001t0001g0112a0001c0001t0001g0119a0001c0001t0001g0159 | 3 | NA18952.hp1 NA18982.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.1004+416C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 12/18 | chr3 | 38375675 | ||||||
| chr3:38375678
|
G | A | 1 | a0001c0001t0002g0283 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1004+419G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 12/18 | chr3 | 38375678 | ||||||
| chr3:38375834
|
T | C | 11 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015others(8): Show | 11 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1005-283T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 12/18 | chr3 | 38375834 | ||||||
| chr3:38375854
|
G | C | 75 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0001g0110others(72): Show | 76 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.1005-263G>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 12/18 | chr3 | 38375854 | ||||||
| chr3:38375876
|
T | C | 75 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0001g0110others(72): Show | 76 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.1005-241T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 12/18 | chr3 | 38375876 | ||||||
| chr3:38375912
|
G | A | 1 | a0001c0001t0005g0307 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1005-205G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 12/18 | chr3 | 38375912 | ||||||
| chr3:38376105
|
C | T | 13 | a0003c0004t0002g0287a0003c0004t0003g0277a0003c0004t0003g0278others(10): Show | 14 | HG01074.hp2 HG01981.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1005-12C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 12/18 | chr3 | 38376105 | ||||||
| chr3:38376253
|
C | T | 2 | a0002c0002t0004g0021a0002c0002t0004g0042 | 2 | HG02970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1120+21C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 13/18 | chr3 | 38376253 | ||||||
| chr3:38376351
|
C | T | 2 | a0001c0003t0003g0270a0001c0003t0003g0271 | 2 | HG00741.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1120+119C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 13/18 | chr3 | 38376351 | ||||||
| chr3:38376356
|
T | G | 1 | a0008c0010t0010g0317 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1120+124T>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 13/18 | chr3 | 38376356 | ||||||
| chr3:38376368
|
T | C | 1 | a0001c0001t0003g0012 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1120+136T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 13/18 | chr3 | 38376368 | ||||||
| chr3:38376445
|
C | T | 1 | a0003c0004t0004g0276 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1120+213C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 13/18 | chr3 | 38376445 | ||||||
| chr3:38376454
|
G | C | 11 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015others(8): Show | 11 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1120+222G>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 13/18 | chr3 | 38376454 | ||||||
| chr3:38376514
|
G | A | 103 | a0001c0001t0001g0109a0001c0001t0001g0124a0001c0001t0001g0136others(100): Show | 104 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1120+282G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 13/18 | chr3 | 38376514 | ||||||
| chr3:38376569
|
A | G | 8 | a0001c0001t0003g0251a0001c0001t0003g0252a0001c0001t0003g0253others(5): Show | 8 | HG01884.hp1 HG01891.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1120+337A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 13/18 | chr3 | 38376569 | ||||||
| chr3:38376623
|
C | G | 1 | a0001c0001t0003g0012 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1121-295C>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 13/18 | chr3 | 38376623 | ||||||
| chr3:38376659
|
G | A | 1 | a0001c0001t0002g0225 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1121-259G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 13/18 | chr3 | 38376659 | ||||||
| chr3:38376804
|
AGAGCCAG others(2): Show |
A | 35 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0015g0250others(32): Show | 35 | HG00423.hp2 HG00558.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.1121-111_1121-103d others(11): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 38376804 | |||||
| chr3:38377025
|
C | T | 1 | a0001c0001t0005g0306 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1194+34C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 14/18 | chr3 | 38377025 | ||||||
| chr3:38377133
|
G | A | 1 | a0003c0004t0004g0258 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1194+142G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 14/18 | chr3 | 38377133 | ||||||
| chr3:38377247
|
C | T | 1 | a0001c0001t0003g0234 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1194+256C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 14/18 | chr3 | 38377247 | ||||||
| chr3:38377442
|
C | CT | 189 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0001g0109others(186): Show | 192 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.1194+466dupT | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr3 | 38377442 | |||||
| chr3:38377442
|
C | CTT | 12 | a0001c0001t0001g0204a0001c0001t0003g0013a0001c0001t0003g0014others(9): Show | 12 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.1194+465_1194+466d others(4): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr3 | 38377442 | |||||
| chr3:38377505
|
C | T | 3 | a0004c0005t0007g0325a0004c0005t0007g0326a0004c0005t0007g0348 | 3 | HG02257.hp2 HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1194+514C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 14/18 | chr3 | 38377505 | ||||||
| chr3:38377517
|
G | A | 102 | a0001c0001t0001g0109a0001c0001t0001g0124a0001c0001t0001g0142others(99): Show | 103 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.1194+526G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 14/18 | chr3 | 38377517 | ||||||
| chr3:38377690
|
G | A | 1 | a0003c0004t0004g0258 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1194+699G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 14/18 | chr3 | 38377690 | ||||||
| chr3:38377836
|
A | ACAAG | 75 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0001g0110others(72): Show | 76 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.1194+846_1194+849d others(6): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr3 | 38377836 | |||||
| chr3:38378026
|
T | A | 24 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015others(21): Show | 25 | HG00639.hp2 HG01074.hp2 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.1194+1035T>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 14/18 | chr3 | 38378026 | ||||||
| chr3:38378091
|
T | C | 75 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0001g0110others(72): Show | 76 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.1194+1100T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 14/18 | chr3 | 38378091 | ||||||
| chr3:38378208
|
T | C | 11 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015others(8): Show | 11 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1195-1038T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 14/18 | chr3 | 38378208 | ||||||
| chr3:38378385
|
G | C | 1 | a0008c0010t0010g0317 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1195-861G>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 14/18 | chr3 | 38378385 | ||||||
| chr3:38378424
|
T | C | 212 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0001g0109others(209): Show | 215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.1195-822T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 14/18 | chr3 | 38378424 | ||||||
| chr3:38378457
|
T | G | 345 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(342): Show | 354 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.1195-789T>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 14/18 | chr3 | 38378457 | ||||||
| chr3:38378558
|
T | C | 1 | a0001c0001t0005g0120 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1195-688T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 14/18 | chr3 | 38378558 | ||||||
| chr3:38378775
|
A | G | 1 | a0008c0010t0010g0317 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1195-471A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 14/18 | chr3 | 38378775 | ||||||
| chr3:38378846
|
C | T | 1 | a0008c0010t0010g0317 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1195-400C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 14/18 | chr3 | 38378846 | ||||||
| chr3:38378891
|
G | A | 107 | a0001c0001t0001g0109a0001c0001t0001g0124a0001c0001t0001g0136others(104): Show | 108 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1195-355G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 14/18 | chr3 | 38378891 | ||||||
| chr3:38378905
|
T | C | 108 | a0001c0001t0001g0109a0001c0001t0001g0124a0001c0001t0001g0136others(105): Show | 109 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.1195-341T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 14/18 | chr3 | 38378905 | ||||||
| chr3:38378979
|
A | G | 1 | a0010c0015t0005g0301 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1195-267A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 14/18 | chr3 | 38378979 | ||||||
| chr3:38379217
|
A | C | 25 | a0001c0001t0001g0300a0001c0001t0002g0041a0001c0001t0002g0147others(22): Show | 25 | HG00621.hp1 HG00621.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.1195-29A>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 14/18 | chr3 | 38379217 | ||||||
| chr3:38379381
|
G | A | 3 | a0001c0001t0001g0296a0001c0001t0001g0304a0001c0001t0001g0314 | 3 | NA18980.hp1 NA18998.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.1291+39G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38379381 | ||||||
| chr3:38379457
|
T | C | 66 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0227others(63): Show | 67 | HG00280.hp1 HG00423.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.1291+115T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38379457 | ||||||
| chr3:38379607
|
C | G | 281 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(278): Show | 287 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.1291+265C>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38379607 | ||||||
| chr3:38379839
|
T | C | 1 | a0001c0003t0003g0066 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1291+497T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38379839 | ||||||
| chr3:38379878
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1291+536A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38379878 | ||||||
| chr3:38379977
|
G | T | 1 | a0001c0001t0002g0181 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1291+635G>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38379977 | ||||||
| chr3:38380159
|
A | G | 1 | a0002c0002t0001g0067 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1291+817A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38380159 | ||||||
| chr3:38380301
|
A | G | 173 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(170): Show | 176 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.1291+959A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38380301 | ||||||
| chr3:38380422
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1291+1080G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38380422 | ||||||
| chr3:38380481
|
T | C | 1 | a0001c0003t0008g0329 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1291+1139T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38380481 | ||||||
| chr3:38380490
|
T | C | 8 | a0002c0002t0002g0069a0002c0002t0002g0077a0002c0002t0003g0093others(5): Show | 8 | HG00609.hp1 HG01928.hp2 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.1291+1148T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38380490 | ||||||
| chr3:38380535
|
G | A | 4 | a0002c0002t0001g0235a0002c0002t0002g0025a0002c0002t0002g0063others(1): Show | 4 | HG00408.hp1 HG00408.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.1291+1193G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38380535 | ||||||
| chr3:38380631
|
C | T | 17 | a0001c0001t0001g0124a0001c0001t0001g0142a0001c0001t0001g0347others(14): Show | 17 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.1291+1289C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38380631 | ||||||
| chr3:38380708
|
G | A | 2 | a0001c0001t0001g0124a0001c0001t0001g0142 | 2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1291+1366G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38380708 | ||||||
| chr3:38380784
|
G | A | 1 | a0001c0001t0005g0288 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1291+1442G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38380784 | ||||||
| chr3:38380832
|
C | T | 17 | a0001c0001t0001g0124a0001c0001t0001g0142a0001c0001t0001g0347others(14): Show | 17 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.1291+1490C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38380832 | ||||||
| chr3:38380836
|
A | G | 2 | a0003c0004t0004g0258a0003c0004t0004g0276 | 2 | HG02630.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1291+1494A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38380836 | ||||||
| chr3:38380874
|
C | A | 302 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(299): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.1291+1532C>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38380874 | ||||||
| chr3:38380981
|
G | A | 17 | a0001c0001t0001g0124a0001c0001t0001g0142a0001c0001t0001g0347others(14): Show | 17 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.1291+1639G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38380981 | ||||||
| chr3:38381205
|
A | G | 1 | a0001c0001t0001g0186 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1291+1863A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38381205 | ||||||
| chr3:38381233
|
A | G | 24 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015others(21): Show | 25 | HG00741.hp2 HG01168.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.1291+1891A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38381233 | ||||||
| chr3:38381356
|
C | T | 2 | a0001c0001t0002g0005a0001c0001t0002g0180 | 3 | HG01243.hp2 HG03017.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1291+2014C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38381356 | ||||||
| chr3:38381406
|
G | A | 24 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015others(21): Show | 25 | HG00741.hp2 HG01168.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.1291+2064G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38381406 | ||||||
| chr3:38381416
|
G | A | 24 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015others(21): Show | 25 | HG00741.hp2 HG01168.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.1291+2074G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38381416 | ||||||
| chr3:38381428
|
G | A | 86 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(83): Show | 88 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.1291+2086G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38381428 | ||||||
| chr3:38381596
|
C | G | 2 | a0001c0001t0002g0115a0001c0001t0002g0174 | 2 | HG00438.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.1291+2254C>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38381596 | ||||||
| chr3:38381621
|
G | A | 1 | a0001c0001t0002g0174 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1291+2279G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38381621 | ||||||
| chr3:38381657
|
T | A | 1 | a0001c0001t0001g0192 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1291+2315T>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38381657 | ||||||
| chr3:38381750
|
A | C | 115 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(112): Show | 117 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.1291+2408A>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38381750 | ||||||
| chr3:38381780
|
C | G | 27 | a0001c0001t0002g0233a0001c0001t0002g0283a0001c0001t0002g0289others(24): Show | 27 | HG00544.hp1 HG00621.hp2 HG01943.hp2 others(24): Show |
intron_variant | MODIFIER | c.1291+2438C>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38381780 | ||||||
| chr3:38381819
|
C | T | 1 | a0001c0001t0015g0250 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1291+2477C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38381819 | ||||||
| chr3:38381850
|
C | G | 17 | a0001c0001t0001g0124a0001c0001t0001g0142a0001c0001t0001g0347others(14): Show | 17 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.1291+2508C>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38381850 | ||||||
| chr3:38381938
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1291+2596A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38381938 | ||||||
| chr3:38382007
|
G | A | 2 | a0001c0001t0002g0057a0001c0001t0002g0058 | 2 | HG01346.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1291+2665G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38382007 | ||||||
| chr3:38382095
|
C | T | 3 | a0001c0001t0008g0064a0001c0001t0008g0065a0001c0001t0008g0169 | 3 | HG02895.hp2 HG02897.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1291+2753C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38382095 | ||||||
| chr3:38382141
|
A | G | 4 | a0002c0002t0003g0093a0002c0002t0003g0094a0002c0002t0004g0101others(1): Show | 4 | HG01928.hp2 NA18991.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.1291+2799A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38382141 | ||||||
| chr3:38382158
|
G | A | 4 | a0002c0002t0001g0002a0002c0002t0004g0099a0002c0002t0005g0073others(1): Show | 5 | HG02004.hp1 HG02300.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.1291+2816G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38382158 | ||||||
| chr3:38382179
|
C | T | 3 | a0001c0001t0001g0296a0001c0001t0001g0304a0001c0001t0001g0314 | 3 | NA18980.hp1 NA18998.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.1291+2837C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38382179 | ||||||
| chr3:38382694
|
G | A | 117 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(114): Show | 119 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.1291+3352G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38382694 | ||||||
| chr3:38382946
|
A | G | 137 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0136others(134): Show | 142 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.1291+3604A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38382946 | ||||||
| chr3:38382948
|
G | T | 1 | a0001c0001t0003g0336 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1291+3606G>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38382948 | ||||||
| chr3:38382949
|
C | T | 1 | a0001c0001t0004g0070 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1291+3607C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38382949 | ||||||
| chr3:38382951
|
C | T | 136 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0136others(133): Show | 141 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.1291+3609C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38382951 | ||||||
| chr3:38383117
|
G | C | 1 | a0002c0002t0002g0091 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1291+3775G>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38383117 | ||||||
| chr3:38383178
|
G | A | 1 | a0005c0006t0003g0273 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1291+3836G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38383178 | ||||||
| chr3:38383276
|
C | G | 109 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0136others(106): Show | 114 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.1291+3934C>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38383276 | ||||||
| chr3:38383426
|
A | C | 1 | a0001c0003t0008g0329 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1291+4084A>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38383426 | ||||||
| chr3:38383554
|
A | G | 1 | a0001c0001t0009g0201 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1291+4212A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38383554 | ||||||
| chr3:38383698
|
C | T | 1 | a0001c0001t0003g0328 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1291+4356C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38383698 | ||||||
| chr3:38383960
|
C | T | 24 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015others(21): Show | 25 | HG00741.hp2 HG01168.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.1291+4618C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38383960 | ||||||
| chr3:38383970
|
C | A | 27 | a0001c0001t0002g0233a0001c0001t0002g0283a0001c0001t0002g0289others(24): Show | 27 | HG00544.hp1 HG00621.hp2 HG01943.hp2 others(24): Show |
intron_variant | MODIFIER | c.1291+4628C>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38383970 | ||||||
| chr3:38384126
|
G | A | 27 | a0001c0001t0002g0233a0001c0001t0002g0283a0001c0001t0002g0289others(24): Show | 27 | HG00544.hp1 HG00621.hp2 HG01943.hp2 others(24): Show |
intron_variant | MODIFIER | c.1291+4784G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38384126 | ||||||
| chr3:38384255
|
G | A | 24 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015others(21): Show | 25 | HG00741.hp2 HG01168.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.1291+4913G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38384255 | ||||||
| chr3:38384290
|
T | A | 1 | a0002c0002t0001g0033 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1291+4948T>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38384290 | ||||||
| chr3:38384317
|
C | T | 24 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015others(21): Show | 25 | HG00741.hp2 HG01168.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.1291+4975C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38384317 | ||||||
| chr3:38384326
|
A | G | 1 | a0006c0008t0003g0024 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1291+4984A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38384326 | ||||||
| chr3:38384355
|
C | T | 15 | a0001c0001t0001g0286a0001c0001t0003g0126a0001c0001t0003g0127others(12): Show | 15 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.1291+5013C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38384355 | ||||||
| chr3:38384449
|
C | G | 1 | a0002c0002t0002g0087 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1291+5107C>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38384449 | ||||||
| chr3:38384473
|
C | G | 12 | a0001c0001t0007g0255a0001c0001t0007g0335a0003c0004t0002g0287others(9): Show | 12 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1291+5131C>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38384473 | ||||||
| chr3:38384625
|
T | G | 144 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0136others(141): Show | 149 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.1291+5283T>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38384625 | ||||||
| chr3:38384672
|
T | A | 294 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(291): Show | 302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.1291+5330T>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38384672 | ||||||
| chr3:38384686
|
CCTTTCCT others(1): Show |
C | 83 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(80): Show | 85 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.1291+5351_1291+535 others(12): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 38384686 | |||||
| chr3:38384738
|
T | C | 3 | a0003c0004t0003g0277a0003c0004t0003g0278a0003c0004t0003g0279 | 3 | HG02965.hp1 HG03130.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1291+5396T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38384738 | ||||||
| chr3:38385032
|
A | G | 3 | a0001c0001t0001g0114a0001c0001t0001g0135a0001c0001t0001g0206 | 3 | HG02738.hp1 HG03688.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1291+5690A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38385032 | ||||||
| chr3:38385147
|
C | T | 7 | a0001c0001t0003g0251a0001c0001t0003g0253a0001c0001t0003g0256others(4): Show | 7 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1291+5805C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38385147 | ||||||
| chr3:38385148
|
G | A | 1 | a0001c0001t0001g0117 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1291+5806G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38385148 | ||||||
| chr3:38385149
|
C | T | 5 | a0001c0001t0001g0192a0001c0001t0008g0064a0001c0001t0008g0065others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1291+5807C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38385149 | ||||||
| chr3:38385267
|
G | A | 1 | a0001c0001t0002g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1291+5925G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38385267 | ||||||
| chr3:38385353
|
T | C | 3 | a0001c0003t0003g0007a0001c0003t0003g0261a0001c0003t0003g0262 | 4 | HG01256.hp2 HG01258.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1291+6011T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38385353 | ||||||
| chr3:38385359
|
A | T | 17 | a0001c0001t0001g0124a0001c0001t0001g0142a0001c0001t0001g0347others(14): Show | 17 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.1291+6017A>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38385359 | ||||||
| chr3:38385401
|
A | G | 1 | a0001c0001t0002g0342 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1291+6059A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38385401 | ||||||
| chr3:38385444
|
T | C | 1 | a0001c0001t0002g0230 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1291+6102T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38385444 | ||||||
| chr3:38385594
|
A | G | 1 | a0001c0001t0002g0004 | 2 | NA18952.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.1291+6252A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38385594 | ||||||
| chr3:38385947
|
A | G | 2 | a0002c0002t0003g0093a0002c0002t0003g0094 | 2 | HG01928.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1291+6605A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38385947 | ||||||
| chr3:38386005
|
T | C | 1 | a0001c0001t0013g0145 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1291+6663T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38386005 | ||||||
| chr3:38386082
|
G | A | 17 | a0001c0001t0001g0124a0001c0001t0001g0142a0001c0001t0001g0347others(14): Show | 17 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.1291+6740G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38386082 | ||||||
| chr3:38386184
|
A | T | 1 | a0001c0001t0002g0179 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1291+6842A>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38386184 | ||||||
| chr3:38386235
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1291+6893G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38386235 | ||||||
| chr3:38386266
|
C | G | 1 | a0001c0001t0001g0192 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1291+6924C>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38386266 | ||||||
| chr3:38386435
|
T | C | 1 | a0001c0001t0003g0259 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1291+7093T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38386435 | ||||||
| chr3:38386516
|
T | A | 1 | a0001c0001t0003g0123 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1291+7174T>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38386516 | ||||||
| chr3:38386714
|
C | T | 1 | a0002c0002t0004g0042 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1291+7372C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38386714 | ||||||
| chr3:38386727
|
A | T | 1 | a0002c0002t0002g0055 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1291+7385A>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38386727 | ||||||
| chr3:38386735
|
A | C | 1 | a0001c0001t0001g0134 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1291+7393A>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38386735 | ||||||
| chr3:38386766
|
G | A | 1 | a0001c0001t0001g0314 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1291+7424G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38386766 | ||||||
| chr3:38386807
|
T | C | 4 | a0005c0006t0001g0275a0005c0006t0001g0320a0009c0011t0006g0272others(1): Show | 4 | HG02451.hp2 HG02615.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+7465T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38386807 | ||||||
| chr3:38387000
|
C | G | 1 | a0001c0001t0002g0180 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1291+7658C>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38387000 | ||||||
| chr3:38387096
|
T | C | 7 | a0001c0001t0003g0251a0001c0001t0003g0253a0001c0001t0003g0256others(4): Show | 7 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1291+7754T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38387096 | ||||||
| chr3:38387170
|
G | C | 1 | a0001c0003t0008g0329 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1291+7828G>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38387170 | ||||||
| chr3:38387237
|
T | C | 7 | a0001c0001t0003g0251a0001c0001t0003g0253a0001c0001t0003g0256others(4): Show | 7 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1291+7895T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38387237 | ||||||
| chr3:38387381
|
G | A | 3 | a0002c0002t0002g0083a0002c0002t0002g0090a0002c0002t0002g0092 | 3 | HG01081.hp1 HG01106.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.1291+8039G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38387381 | ||||||
| chr3:38387403
|
C | T | 5 | a0001c0001t0001g0192a0001c0001t0008g0064a0001c0001t0008g0065others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1291+8061C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38387403 | ||||||
| chr3:38387483
|
G | T | 7 | a0001c0001t0003g0251a0001c0001t0003g0253a0001c0001t0003g0256others(4): Show | 7 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1292-8022G>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38387483 | ||||||
| chr3:38387546
|
A | AT | 17 | a0001c0001t0001g0124a0001c0001t0001g0142a0001c0001t0001g0347others(14): Show | 17 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.1292-7954dupT | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 38387546 | |||||
| chr3:38387546
|
A | G | 90 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(87): Show | 92 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.1292-7959A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38387546 | ||||||
| chr3:38387614
|
C | T | 1 | a0002c0002t0016g0074 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1292-7891C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38387614 | ||||||
| chr3:38387628
|
TCC | T | 5 | a0001c0001t0001g0286a0001c0001t0003g0218a0001c0001t0003g0219others(2): Show | 5 | HG02572.hp1 HG02723.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1292-7875_1292-787 others(6): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 38387628 | |||||
| chr3:38387743
|
A | T | 1 | a0001c0001t0002g0180 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1292-7762A>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38387743 | ||||||
| chr3:38387989
|
TTGAA | T | 8 | a0001c0001t0001g0192a0001c0001t0008g0064a0001c0001t0008g0065others(5): Show | 9 | HG01074.hp2 HG01981.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1292-7513_1292-751 others(8): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 38387989 | |||||
| chr3:38388169
|
GT | G | 150 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(147): Show | 153 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.1292-7314delT | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 38388169 | |||||
| chr3:38388171
|
T | TTTG | 143 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0136others(140): Show | 148 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.1292-7332_1292-733 others(7): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 38388171 | |||||
| chr3:38388174
|
T | G | 6 | a0001c0001t0002g0139a0001c0001t0002g0333a0005c0006t0001g0275others(3): Show | 6 | HG02451.hp2 HG02615.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1292-7331T>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38388174 | ||||||
| chr3:38388175
|
T | G | 149 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(146): Show | 152 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.1292-7330T>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38388175 | ||||||
| chr3:38388176
|
T | G | 143 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0136others(140): Show | 148 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.1292-7329T>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38388176 | ||||||
| chr3:38388177
|
T | G | 1 | a0001c0001t0004g0019 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1292-7328T>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38388177 | ||||||
| chr3:38388179
|
T | G | 1 | a0001c0001t0003g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1292-7326T>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38388179 | ||||||
| chr3:38388180
|
T | G | 2 | a0001c0001t0001g0134a0001c0001t0004g0274 | 2 | HG02155.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.1292-7325T>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38388180 | ||||||
| chr3:38388181
|
T | G | 6 | a0001c0001t0002g0058a0001c0001t0002g0246a0001c0001t0002g0247others(3): Show | 6 | HG01074.hp1 HG01099.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.1292-7324T>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38388181 | ||||||
| chr3:38388182
|
T | G | 1 | a0003c0004t0004g0258 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1292-7323T>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38388182 | ||||||
| chr3:38388248
|
C | T | 17 | a0001c0001t0001g0124a0001c0001t0001g0142a0001c0001t0001g0347others(14): Show | 17 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.1292-7257C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38388248 | ||||||
| chr3:38388356
|
G | A | 17 | a0001c0001t0001g0124a0001c0001t0001g0142a0001c0001t0001g0347others(14): Show | 17 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.1292-7149G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38388356 | ||||||
| chr3:38388416
|
G | A | 1 | a0001c0001t0003g0334 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1292-7089G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38388416 | ||||||
| chr3:38388418
|
A | G | 17 | a0001c0001t0001g0124a0001c0001t0001g0142a0001c0001t0001g0347others(14): Show | 17 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.1292-7087A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38388418 | ||||||
| chr3:38388525
|
A | G | 12 | a0001c0001t0007g0255a0001c0001t0007g0335a0003c0004t0002g0287others(9): Show | 12 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1292-6980A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38388525 | ||||||
| chr3:38388898
|
C | A | 155 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(152): Show | 158 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.1292-6607C>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38388898 | ||||||
| chr3:38388914
|
AAAG | A | 24 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015others(21): Show | 25 | HG00741.hp2 HG01168.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.1292-6588_1292-658 others(7): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 38388914 | |||||
| chr3:38388951
|
CT | C | 24 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015others(21): Show | 25 | HG00741.hp2 HG01168.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.1292-6542delT | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 38388951 | |||||
| chr3:38389058
|
G | A | 1 | a0001c0001t0002g0342 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1292-6447G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38389058 | ||||||
| chr3:38389097
|
C | T | 2 | a0001c0001t0001g0124a0001c0001t0001g0142 | 2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1292-6408C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38389097 | ||||||
| chr3:38389158
|
G | T | 136 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0136others(133): Show | 141 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.1292-6347G>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38389158 | ||||||
| chr3:38389163
|
C | T | 1 | a0002c0002t0001g0026 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1292-6342C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38389163 | ||||||
| chr3:38389191
|
C | G | 17 | a0001c0001t0001g0124a0001c0001t0001g0142a0001c0001t0001g0347others(14): Show | 17 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.1292-6314C>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38389191 | ||||||
| chr3:38389551
|
AGACGGGG others(40): Show |
A | 5 | a0001c0001t0003g0234a0001c0001t0003g0330a0001c0001t0003g0336others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1292-5934_1292-588 others(51): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 38389551 | |||||
| chr3:38389554
|
C | T | 24 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015others(21): Show | 25 | HG00741.hp2 HG01168.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.1292-5951C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38389554 | ||||||
| chr3:38389583
|
C | T | 1 | a0002c0002t0002g0081 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1292-5922C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38389583 | ||||||
| chr3:38389617
|
G | GT | 7 | a0001c0001t0002g0139a0001c0001t0002g0168a0001c0001t0003g0221others(4): Show | 7 | HG00597.hp2 HG03130.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.1292-5879dupT | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 38389617 | |||||
| chr3:38390072
|
T | C | 1 | a0001c0001t0001g0134 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1292-5433T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38390072 | ||||||
| chr3:38390078
|
GGTT | G | 4 | a0001c0001t0006g0161a0001c0001t0006g0199a0001c0001t0006g0232others(1): Show | 4 | HG02622.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1292-5417_1292-541 others(7): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 38390078 | |||||
| chr3:38390308
|
G | T | 5 | a0001c0001t0003g0234a0001c0001t0003g0330a0001c0001t0003g0336others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1292-5197G>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38390308 | ||||||
| chr3:38390381
|
G | T | 17 | a0001c0001t0001g0124a0001c0001t0001g0142a0001c0001t0001g0347others(14): Show | 17 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.1292-5124G>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38390381 | ||||||
| chr3:38390402
|
C | T | 1 | a0002c0002t0001g0033 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1292-5103C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38390402 | ||||||
| chr3:38390491
|
G | A | 1 | a0002c0002t0001g0036 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1292-5014G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38390491 | ||||||
| chr3:38390592
|
G | A | 114 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(111): Show | 116 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1292-4913G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38390592 | ||||||
| chr3:38390608
|
G | A | 4 | a0001c0001t0003g0218a0001c0001t0003g0219a0001c0001t0003g0220others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1292-4897G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38390608 | ||||||
| chr3:38390814
|
T | A | 1 | a0001c0001t0002g0139 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1292-4691T>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38390814 | ||||||
| chr3:38390865
|
A | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0167 | 2 | NA19079.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1292-4640A>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38390865 | ||||||
| chr3:38390894
|
T | C | 17 | a0001c0001t0001g0124a0001c0001t0001g0142a0001c0001t0001g0347others(14): Show | 17 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.1292-4611T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38390894 | ||||||
| chr3:38390954
|
T | G | 1 | a0002c0002t0001g0026 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1292-4551T>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38390954 | ||||||
| chr3:38390995
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1292-4510G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38390995 | ||||||
| chr3:38391119
|
C | T | 1 | a0001c0001t0005g0305 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1292-4386C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38391119 | ||||||
| chr3:38391219
|
C | A | 17 | a0001c0001t0001g0124a0001c0001t0001g0142a0001c0001t0001g0347others(14): Show | 17 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.1292-4286C>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38391219 | ||||||
| chr3:38391235
|
A | C | 136 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0136others(133): Show | 141 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.1292-4270A>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38391235 | ||||||
| chr3:38391236
|
AC | A | 31 | a0001c0001t0001g0286a0001c0001t0003g0012a0001c0001t0003g0013others(28): Show | 32 | HG01168.hp2 HG01169.hp1 HG01256.hp2 others(29): Show |
intron_variant | MODIFIER | c.1292-4268delC | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38391236 | ||||||
| chr3:38391237
|
CA | C | 314 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(311): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.1292-4259delA | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 38391237 | |||||
| chr3:38391241
|
A | C | 117 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(114): Show | 119 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.1292-4264A>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38391241 | ||||||
| chr3:38391431
|
T | C | 2 | a0002c0002t0001g0071a0002c0002t0001g0072 | 2 | NA18964.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1292-4074T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38391431 | ||||||
| chr3:38391454
|
A | G | 27 | a0001c0001t0002g0233a0001c0001t0002g0283a0001c0001t0002g0289others(24): Show | 27 | HG00544.hp1 HG00621.hp2 HG01943.hp2 others(24): Show |
intron_variant | MODIFIER | c.1292-4051A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38391454 | ||||||
| chr3:38391483
|
T | C | 17 | a0001c0001t0001g0124a0001c0001t0001g0142a0001c0001t0001g0347others(14): Show | 17 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.1292-4022T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38391483 | ||||||
| chr3:38391609
|
A | G | 330 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(327): Show | 339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.1292-3896A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38391609 | ||||||
| chr3:38391639
|
TA | T | 137 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0136others(134): Show | 142 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.1292-3861delA | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 38391639 | |||||
| chr3:38391702
|
T | C | 1 | a0001c0001t0003g0336 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1292-3803T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38391702 | ||||||
| chr3:38391922
|
G | A | 1 | a0001c0001t0001g0117 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1292-3583G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38391922 | ||||||
| chr3:38392027
|
T | G | 1 | a0001c0001t0002g0139 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1292-3478T>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38392027 | ||||||
| chr3:38392076
|
T | A | 1 | a0001c0001t0002g0139 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1292-3429T>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38392076 | ||||||
| chr3:38392378
|
A | G | 1 | a0002c0002t0002g0081 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1292-3127A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38392378 | ||||||
| chr3:38392549
|
G | A | 2 | a0001c0001t0005g0290a0001c0001t0005g0302 | 2 | NA19007.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1292-2956G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38392549 | ||||||
| chr3:38392576
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1292-2929C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38392576 | ||||||
| chr3:38392587
|
G | A | 1 | a0002c0002t0002g0079 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1292-2918G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38392587 | ||||||
| chr3:38392832
|
A | C | 8 | a0001c0001t0003g0012a0001c0001t0006g0161a0001c0001t0006g0199others(5): Show | 9 | HG01074.hp2 HG01981.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1292-2673A>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38392832 | ||||||
| chr3:38393061
|
G | T | 1 | a0001c0001t0001g0177 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1292-2444G>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38393061 | ||||||
| chr3:38393070
|
A | G | 3 | a0001c0001t0001g0192a0001c0003t0008g0329a0003c0004t0004g0316 | 3 | HG03098.hp1 HG03486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1292-2435A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38393070 | ||||||
| chr3:38393119
|
T | C | 2 | a0001c0001t0002g0341a0001c0001t0002g0344 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1292-2386T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38393119 | ||||||
| chr3:38393122
|
A | G | 2 | a0001c0001t0003g0259a0003c0004t0004g0276 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1292-2383A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38393122 | ||||||
| chr3:38393148
|
A | AT | 9 | a0001c0001t0001g0124a0001c0001t0001g0142a0001c0001t0001g0291others(6): Show | 9 | HG01167.hp2 HG01169.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1292-2347dupT | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 38393148 | |||||
| chr3:38393165
|
T | C | 1 | a0001c0001t0001g0347 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1292-2340T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38393165 | ||||||
| chr3:38393190
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1292-2315G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38393190 | ||||||
| chr3:38393201
|
A | T | 1 | a0001c0001t0002g0139 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1292-2304A>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38393201 | ||||||
| chr3:38393212
|
G | A | 1 | a0001c0001t0010g0068 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1292-2293G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38393212 | ||||||
| chr3:38393250
|
C | T | 4 | a0001c0001t0017g0108a0003c0004t0004g0316a0004c0005t0006g0010others(1): Show | 5 | HG01074.hp2 HG01981.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1292-2255C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38393250 | ||||||
| chr3:38393532
|
A | T | 93 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(90): Show | 95 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.1292-1973A>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38393532 | ||||||
| chr3:38393533
|
G | A | 1 | a0005c0006t0003g0273 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1292-1972G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38393533 | ||||||
| chr3:38393566
|
C | T | 1 | a0001c0001t0003g0259 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1292-1939C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38393566 | ||||||
| chr3:38393666
|
G | A | 1 | a0001c0003t0003g0264 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1292-1839G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38393666 | ||||||
| chr3:38393876
|
A | T | 345 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(342): Show | 354 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.1292-1629A>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38393876 | ||||||
| chr3:38394338
|
TTGA | T | 4 | a0005c0006t0001g0275a0005c0006t0001g0320a0009c0011t0006g0272others(1): Show | 4 | HG02451.hp2 HG02615.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1292-1165_1292-116 others(7): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 38394338 | |||||
| chr3:38394684
|
T | C | 26 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0057others(23): Show | 28 | HG00140.hp1 HG01069.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.1292-821T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38394684 | ||||||
| chr3:38394736
|
T | C | 1 | a0001c0001t0001g0286 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1292-769T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38394736 | ||||||
| chr3:38394809
|
G | C | 1 | a0001c0001t0003g0328 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1292-696G>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38394809 | ||||||
| chr3:38395175
|
A | G | 1 | a0002c0002t0005g0089 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1292-330A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38395175 | ||||||
| chr3:38395409
|
C | G | 1 | a0001c0009t0003g0319 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1292-96C>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 15/18 | chr3 | 38395409 | ||||||
| chr3:38395668
|
G | A | 2 | a0001c0001t0003g0013a0001c0001t0003g0014 | 2 | HG01255.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1350+105G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 16/18 | chr3 | 38395668 | ||||||
| chr3:38395717
|
C | G | 1 | a0001c0001t0001g0206 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1350+154C>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 16/18 | chr3 | 38395717 | ||||||
| chr3:38395781
|
C | G | 2 | a0002c0002t0003g0093a0002c0002t0003g0094 | 2 | HG01928.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1350+218C>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 16/18 | chr3 | 38395781 | ||||||
| chr3:38395891
|
G | A | 2 | a0001c0001t0002g0230a0001c0001t0011g0178 | 2 | HG00558.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.1350+328G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 16/18 | chr3 | 38395891 | ||||||
| chr3:38395980
|
G | A | 98 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(95): Show | 101 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1350+417G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 16/18 | chr3 | 38395980 | ||||||
| chr3:38396016
|
A | G | 1 | a0002c0002t0005g0011 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1350+453A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 16/18 | chr3 | 38396016 | ||||||
| chr3:38396043
|
G | A | 5 | a0001c0001t0003g0234a0001c0001t0003g0330a0001c0001t0003g0336others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1350+480G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 16/18 | chr3 | 38396043 | ||||||
| chr3:38396175
|
C | T | 2 | a0002c0002t0003g0093a0002c0002t0003g0094 | 2 | HG01928.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1350+612C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 16/18 | chr3 | 38396175 | ||||||
| chr3:38396344
|
A | G | 136 | a0001c0001t0001g0177a0001c0001t0001g0227a0001c0001t0002g0003others(133): Show | 140 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.1351-728A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 16/18 | chr3 | 38396344 | ||||||
| chr3:38396433
|
T | C | 22 | a0001c0001t0002g0004a0001c0001t0002g0115a0001c0001t0002g0157others(19): Show | 23 | HG00423.hp1 HG00558.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.1351-639T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 16/18 | chr3 | 38396433 | ||||||
| chr3:38396477
|
G | A | 41 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015others(38): Show | 42 | HG00741.hp2 HG01109.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.1351-595G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 16/18 | chr3 | 38396477 | ||||||
| chr3:38396565
|
T | G | 42 | a0001c0001t0001g0192a0001c0001t0001g0286a0001c0001t0002g0233others(39): Show | 42 | HG00544.hp1 HG00621.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.1351-507T>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 16/18 | chr3 | 38396565 | ||||||
| chr3:38396608
|
A | G | 34 | a0001c0001t0001g0177a0001c0001t0001g0227a0001c0001t0002g0226others(31): Show | 35 | HG00280.hp1 HG00423.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.1351-464A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 16/18 | chr3 | 38396608 | ||||||
| chr3:38396691
|
G | C | 108 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(105): Show | 111 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.1351-381G>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 16/18 | chr3 | 38396691 | ||||||
| chr3:38396756
|
G | C | 1 | a0001c0001t0002g0176 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1351-316G>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 16/18 | chr3 | 38396756 | ||||||
| chr3:38396816
|
G | C | 1 | a0001c0001t0003g0148 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1351-256G>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 16/18 | chr3 | 38396816 | ||||||
| chr3:38396875
|
A | G | 12 | a0001c0001t0003g0012a0001c0001t0003g0219a0001c0001t0003g0251others(9): Show | 13 | HG01074.hp2 HG01243.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1351-197A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 16/18 | chr3 | 38396875 | ||||||
| chr3:38396881
|
T | C | 102 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(99): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.1351-191T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 16/18 | chr3 | 38396881 | ||||||
| chr3:38396966
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1351-106G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 16/18 | chr3 | 38396966 | ||||||
| chr3:38397209
|
G | A | 6 | a0001c0003t0003g0007a0001c0003t0003g0261a0001c0003t0003g0262others(3): Show | 7 | HG01109.hp1 HG01256.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1438+50G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | chr3 | 38397209 | ||||||
| chr3:38397389
|
G | T | 13 | a0001c0001t0003g0012a0001c0001t0003g0251a0001c0001t0003g0253others(10): Show | 14 | HG01074.hp2 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1438+230G>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | chr3 | 38397389 | ||||||
| chr3:38397445
|
T | C | 2 | a0009c0011t0006g0272a0009c0011t0006g0324 | 2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1438+286T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | chr3 | 38397445 | ||||||
| chr3:38397598
|
T | G | 1 | a0001c0001t0003g0259 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1438+439T>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | chr3 | 38397598 | ||||||
| chr3:38397642
|
G | A | 1 | a0002c0002t0002g0022 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1438+483G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | chr3 | 38397642 | ||||||
| chr3:38397649
|
G | A | 43 | a0001c0001t0001g0192a0001c0001t0001g0286a0001c0001t0002g0233others(40): Show | 43 | HG00544.hp1 HG00621.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.1438+490G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | chr3 | 38397649 | ||||||
| chr3:38397822
|
T | C | 1 | a0001c0001t0005g0171 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1438+663T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | chr3 | 38397822 | ||||||
| chr3:38397823
|
C | CT | 90 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(87): Show | 93 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.1438+678dupT | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr3 | 38397823 | |||||
| chr3:38397823
|
C | T | 1 | a0001c0001t0005g0171 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1438+664C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | chr3 | 38397823 | ||||||
| chr3:38397878
|
G | T | 1 | a0001c0001t0001g0111 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1438+719G>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | chr3 | 38397878 | ||||||
| chr3:38397950
|
G | C | 1 | a0002c0002t0002g0077 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1438+791G>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | chr3 | 38397950 | ||||||
| chr3:38397967
|
T | C | 2 | a0001c0001t0001g0132a0001c0003t0008g0329 | 2 | HG03098.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1438+808T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | chr3 | 38397967 | ||||||
| chr3:38398007
|
G | A | 1 | a0008c0010t0010g0317 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1438+848G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | chr3 | 38398007 | ||||||
| chr3:38398008
|
A | T | 1 | a0008c0010t0010g0317 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1438+849A>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | chr3 | 38398008 | ||||||
| chr3:38398067
|
C | G | 1 | a0001c0001t0001g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1438+908C>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | chr3 | 38398067 | ||||||
| chr3:38398071
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1438+912G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | chr3 | 38398071 | ||||||
| chr3:38398095
|
G | C | 37 | a0001c0001t0001g0177a0001c0001t0004g0001a0001c0001t0004g0019others(34): Show | 38 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.1438+936G>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | chr3 | 38398095 | ||||||
| chr3:38398097
|
C | T | 37 | a0001c0001t0001g0177a0001c0001t0004g0001a0001c0001t0004g0019others(34): Show | 38 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.1438+938C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | chr3 | 38398097 | ||||||
| chr3:38398110
|
A | G | 92 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(89): Show | 95 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.1438+951A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | chr3 | 38398110 | ||||||
| chr3:38398184
|
C | A | 4 | a0001c0001t0005g0120a0001c0001t0005g0223a0001c0001t0005g0224others(1): Show | 4 | HG01070.hp1 HG01071.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.1438+1025C>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | chr3 | 38398184 | ||||||
| chr3:38398192
|
G | A | 1 | a0001c0001t0005g0307 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1438+1033G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | chr3 | 38398192 | ||||||
| chr3:38398241
|
G | A | 34 | a0001c0001t0001g0177a0001c0001t0004g0001a0001c0001t0004g0019others(31): Show | 35 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.1438+1082G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | chr3 | 38398241 | ||||||
| chr3:38398603
|
T | C | 4 | a0001c0001t0003g0330a0001c0001t0003g0336a0001c0001t0003g0338others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1438+1444T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | chr3 | 38398603 | ||||||
| chr3:38398641
|
T | TCTGC | 52 | a0001c0001t0002g0003a0001c0001t0002g0209a0001c0001t0003g0012others(49): Show | 54 | HG00423.hp2 HG00609.hp2 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.1438+1517_1438+152 others(8): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr3 | 38398641 | |||||
| chr3:38398641
|
T | TCTGCCTG others(1): Show |
3 | a0001c0001t0004g0274a0002c0002t0004g0038a0002c0002t0004g0043 | 3 | HG00558.hp2 HG02155.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1438+1513_1438+152 others(12): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr3 | 38398641 | |||||
| chr3:38398641
|
TCTGC | T | 15 | a0001c0001t0001g0132a0001c0001t0001g0192a0001c0001t0001g0286others(12): Show | 15 | HG01081.hp1 HG01106.hp1 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.1438+1517_1438+152 others(8): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr3 | 38398641 | |||||
| chr3:38398712
|
CT | C | 98 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(95): Show | 101 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.1438+1567delT | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr3 | 38398712 | |||||
| chr3:38398743
|
G | A | 1 | a0001c0001t0001g0186 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1438+1584G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | chr3 | 38398743 | ||||||
| chr3:38398746
|
T | C | 154 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(151): Show | 158 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.1438+1587T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | chr3 | 38398746 | ||||||
| chr3:38398763
|
G | A | 1 | a0005c0006t0003g0273 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1438+1604G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | chr3 | 38398763 | ||||||
| chr3:38398867
|
CA | C | 35 | a0001c0001t0005g0095a0001c0001t0005g0118a0001c0001t0005g0120others(32): Show | 35 | HG00621.hp2 HG00639.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.1438+1719delA | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr3 | 38398867 | |||||
| chr3:38398903
|
A | G | 95 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(92): Show | 98 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.1438+1744A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | chr3 | 38398903 | ||||||
| chr3:38398966
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1438+1807A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | chr3 | 38398966 | ||||||
| chr3:38398999
|
C | T | 1 | a0001c0001t0002g0343 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1438+1840C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | chr3 | 38398999 | ||||||
| chr3:38399204
|
A | T | 4 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0219others(1): Show | 4 | HG01255.hp1 HG02055.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1439-1687A>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | chr3 | 38399204 | ||||||
| chr3:38399285
|
T | C | 6 | a0001c0001t0007g0255a0001c0001t0007g0335a0004c0005t0007g0325others(3): Show | 6 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1439-1606T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | chr3 | 38399285 | ||||||
| chr3:38399462
|
G | GA | 96 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(93): Show | 99 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.1439-1427dupA | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr3 | 38399462 | |||||
| chr3:38399625
|
A | T | 1 | a0001c0001t0002g0173 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1439-1266A>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | chr3 | 38399625 | ||||||
| chr3:38399826
|
A | T | 4 | a0004c0005t0006g0010a0004c0005t0006g0327a0009c0011t0006g0272others(1): Show | 5 | HG01074.hp2 HG01981.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1439-1065A>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | chr3 | 38399826 | ||||||
| chr3:38399838
|
C | A | 4 | a0001c0001t0008g0064a0001c0001t0008g0065a0001c0001t0008g0169others(1): Show | 4 | HG02895.hp2 HG02897.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1439-1053C>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | chr3 | 38399838 | ||||||
| chr3:38399910
|
T | G | 4 | a0001c0001t0004g0282a0001c0001t0004g0292a0001c0001t0004g0311others(1): Show | 4 | HG00609.hp2 HG02027.hp1 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.1439-981T>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | chr3 | 38399910 | ||||||
| chr3:38399948
|
C | T | 95 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(92): Show | 98 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.1439-943C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | chr3 | 38399948 | ||||||
| chr3:38400038
|
C | T | 1 | a0003c0004t0004g0316 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1439-853C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | chr3 | 38400038 | ||||||
| chr3:38400052
|
C | A | 45 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015others(42): Show | 46 | HG00741.hp2 HG01109.hp1 HG01123.hp1 others(43): Show |
intron_variant | MODIFIER | c.1439-839C>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | chr3 | 38400052 | ||||||
| chr3:38400265
|
C | T | 2 | a0001c0001t0001g0242a0001c0001t0001g0243 | 2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1439-626C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | chr3 | 38400265 | ||||||
| chr3:38400313
|
T | C | 1 | a0004c0005t0007g0348 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1439-578T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 17/18 | chr3 | 38400313 | ||||||
| chr3:38400999
|
G | A | 101 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(98): Show | 104 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.1533+14G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38400999 | ||||||
| chr3:38401013
|
G | A | 44 | a0001c0001t0004g0001a0001c0001t0004g0019a0001c0001t0004g0035others(41): Show | 45 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.1533+28G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38401013 | ||||||
| chr3:38401235
|
C | T | 2 | a0001c0001t0002g0341a0001c0001t0002g0344 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1533+250C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38401235 | ||||||
| chr3:38401239
|
G | A | 2 | a0001c0001t0001g0140a0001c0001t0001g0162 | 2 | HG01099.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.1533+254G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38401239 | ||||||
| chr3:38401352
|
G | GCAGT | 3 | a0001c0003t0003g0007a0001c0003t0003g0261a0001c0003t0003g0262 | 4 | HG01256.hp2 HG01258.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1533+370_1533+373d others(6): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr3 | 38401352 | |||||
| chr3:38401689
|
G | C | 95 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(92): Show | 98 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.1533+704G>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38401689 | ||||||
| chr3:38401748
|
C | G | 11 | a0001c0001t0002g0115a0001c0001t0002g0157a0001c0001t0002g0176others(8): Show | 11 | HG00423.hp1 HG01074.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.1533+763C>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38401748 | ||||||
| chr3:38401821
|
T | C | 101 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(98): Show | 104 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.1533+836T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38401821 | ||||||
| chr3:38401829
|
G | A | 84 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(81): Show | 87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.1533+844G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38401829 | ||||||
| chr3:38401908
|
G | A | 1 | a0009c0011t0006g0324 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1533+923G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38401908 | ||||||
| chr3:38401922
|
C | A | 1 | a0001c0001t0002g0184 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1533+937C>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38401922 | ||||||
| chr3:38402237
|
A | T | 1 | a0001c0001t0001g0114 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1533+1252A>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38402237 | ||||||
| chr3:38402782
|
G | A | 95 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(92): Show | 98 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.1533+1797G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38402782 | ||||||
| chr3:38402807
|
C | G | 189 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(186): Show | 193 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.1533+1822C>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38402807 | ||||||
| chr3:38402882
|
G | A | 3 | a0001c0001t0008g0064a0001c0001t0008g0065a0001c0001t0008g0169 | 3 | HG02895.hp2 HG02897.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1533+1897G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38402882 | ||||||
| chr3:38402945
|
C | G | 2 | a0009c0011t0006g0272a0009c0011t0006g0324 | 2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1533+1960C>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38402945 | ||||||
| chr3:38402998
|
T | A | 142 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(139): Show | 146 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.1533+2013T>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38402998 | ||||||
| chr3:38403094
|
C | T | 2 | a0001c0001t0009g0075a0001c0001t0009g0201 | 2 | HG02109.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1533+2109C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38403094 | ||||||
| chr3:38403217
|
C | T | 2 | a0005c0006t0001g0275a0005c0006t0001g0320 | 2 | HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1533+2232C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38403217 | ||||||
| chr3:38403289
|
C | CA | 94 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(91): Show | 97 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.1533+2321dupA | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr3 | 38403289 | |||||
| chr3:38403289
|
CA | C | 36 | a0001c0001t0001g0164a0001c0001t0005g0118a0001c0001t0005g0120others(33): Show | 36 | HG00621.hp2 HG00639.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.1533+2321delA | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr3 | 38403289 | |||||
| chr3:38403441
|
G | T | 95 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(92): Show | 98 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.1533+2456G>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38403441 | ||||||
| chr3:38403519
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1533+2534G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38403519 | ||||||
| chr3:38403674
|
T | G | 95 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(92): Show | 98 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.1533+2689T>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38403674 | ||||||
| chr3:38403735
|
C | T | 107 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(104): Show | 110 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1533+2750C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38403735 | ||||||
| chr3:38403878
|
T | C | 47 | a0001c0001t0003g0012a0001c0001t0004g0001a0001c0001t0004g0019others(44): Show | 48 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.1533+2893T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38403878 | ||||||
| chr3:38403909
|
C | G | 4 | a0001c0001t0008g0064a0001c0001t0008g0065a0001c0001t0008g0169others(1): Show | 4 | HG02895.hp2 HG02897.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1533+2924C>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38403909 | ||||||
| chr3:38403951
|
C | T | 4 | a0001c0001t0008g0064a0001c0001t0008g0065a0001c0001t0008g0169others(1): Show | 4 | HG02895.hp2 HG02897.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1533+2966C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38403951 | ||||||
| chr3:38404028
|
C | G | 4 | a0001c0001t0008g0064a0001c0001t0008g0065a0001c0001t0008g0169others(1): Show | 4 | HG02895.hp2 HG02897.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1533+3043C>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38404028 | ||||||
| chr3:38404079
|
A | G | 2 | a0001c0001t0002g0207a0001c0001t0002g0208 | 2 | HG02735.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1533+3094A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38404079 | ||||||
| chr3:38404184
|
T | C | 2 | a0001c0001t0001g0124a0001c0001t0001g0142 | 2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1533+3199T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38404184 | ||||||
| chr3:38404299
|
C | T | 2 | a0001c0001t0005g0290a0001c0001t0005g0302 | 2 | NA19007.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1533+3314C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38404299 | ||||||
| chr3:38404415
|
C | T | 1 | a0002c0002t0005g0107 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1533+3430C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38404415 | ||||||
| chr3:38404576
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1533+3591G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38404576 | ||||||
| chr3:38404582
|
C | T | 94 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(91): Show | 97 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.1533+3597C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38404582 | ||||||
| chr3:38404602
|
A | T | 1 | a0001c0001t0002g0312 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1533+3617A>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38404602 | ||||||
| chr3:38404632
|
C | T | 3 | a0003c0004t0003g0277a0003c0004t0003g0278a0003c0004t0003g0279 | 3 | HG02965.hp1 HG03130.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1533+3647C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38404632 | ||||||
| chr3:38404671
|
C | G | 1 | a0001c0001t0002g0284 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1533+3686C>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38404671 | ||||||
| chr3:38404818
|
C | A | 91 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(88): Show | 94 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.1533+3833C>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38404818 | ||||||
| chr3:38404937
|
G | A | 1 | a0001c0001t0001g0132 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1533+3952G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38404937 | ||||||
| chr3:38404967
|
A | G | 2 | a0002c0002t0003g0093a0002c0002t0003g0094 | 2 | HG01928.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1533+3982A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38404967 | ||||||
| chr3:38404971
|
C | T | 1 | a0002c0002t0002g0103 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1533+3986C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38404971 | ||||||
| chr3:38405067
|
G | A | 1 | a0002c0002t0001g0018 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1533+4082G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38405067 | ||||||
| chr3:38405197
|
T | A | 4 | a0001c0001t0003g0330a0001c0001t0003g0336a0001c0001t0003g0338others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1533+4212T>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38405197 | ||||||
| chr3:38405251
|
G | A | 93 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(90): Show | 96 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1533+4266G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38405251 | ||||||
| chr3:38405264
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1533+4279C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38405264 | ||||||
| chr3:38405265
|
G | A | 2 | a0001c0001t0001g0124a0001c0001t0001g0142 | 2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1533+4280G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38405265 | ||||||
| chr3:38405371
|
T | TA | 62 | a0001c0001t0001g0149a0001c0001t0001g0206a0001c0001t0001g0294others(59): Show | 63 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.1533+4409dupA | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr3 | 38405371 | |||||
| chr3:38405371
|
TA | T | 41 | a0001c0001t0001g0136a0001c0001t0001g0188a0001c0001t0001g0216others(38): Show | 41 | HG00621.hp2 HG01069.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.1533+4409delA | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr3 | 38405371 | |||||
| chr3:38405429
|
G | C | 140 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(137): Show | 144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1533+4444G>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38405429 | ||||||
| chr3:38405455
|
C | T | 1 | a0001c0003t0008g0329 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1533+4470C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38405455 | ||||||
| chr3:38405464
|
C | T | 93 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(90): Show | 96 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1533+4479C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38405464 | ||||||
| chr3:38405550
|
T | C | 140 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(137): Show | 144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1533+4565T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38405550 | ||||||
| chr3:38405566
|
C | T | 4 | a0001c0001t0003g0330a0001c0001t0003g0336a0001c0001t0003g0338others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1533+4581C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38405566 | ||||||
| chr3:38405568
|
A | T | 1 | a0001c0001t0003g0340 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1533+4583A>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38405568 | ||||||
| chr3:38405608
|
G | A | 8 | a0001c0001t0002g0170a0001c0001t0002g0289a0001c0001t0002g0312others(5): Show | 8 | HG00408.hp1 HG03834.hp1 NA18956.hp2 others(5): Show |
intron_variant | MODIFIER | c.1533+4623G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38405608 | ||||||
| chr3:38405697
|
C | T | 7 | a0001c0001t0002g0157a0001c0001t0007g0255a0001c0001t0007g0335others(4): Show | 7 | HG00639.hp2 HG02071.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1533+4712C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38405697 | ||||||
| chr3:38405741
|
C | A | 93 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(90): Show | 96 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1533+4756C>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38405741 | ||||||
| chr3:38405759
|
C | T | 1 | a0002c0002t0002g0092 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1533+4774C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38405759 | ||||||
| chr3:38405766
|
G | A | 1 | a0001c0003t0003g0264 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1533+4781G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38405766 | ||||||
| chr3:38405793
|
G | A | 1 | a0001c0003t0003g0066 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1533+4808G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38405793 | ||||||
| chr3:38405827
|
G | A | 1 | a0001c0003t0008g0329 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1533+4842G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38405827 | ||||||
| chr3:38405912
|
T | C | 15 | a0001c0001t0002g0057a0001c0001t0002g0058a0001c0001t0002g0144others(12): Show | 15 | HG00140.hp1 HG00639.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.1533+4927T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38405912 | ||||||
| chr3:38405952
|
G | C | 1 | a0001c0001t0002g0157 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1533+4967G>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38405952 | ||||||
| chr3:38406054
|
G | A | 1 | a0002c0002t0005g0076 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1533+5069G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38406054 | ||||||
| chr3:38406302
|
T | C | 21 | a0001c0001t0003g0123a0001c0001t0003g0217a0001c0001t0003g0328others(18): Show | 22 | HG00741.hp2 HG01109.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.1533+5317T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38406302 | ||||||
| chr3:38406306
|
A | G | 1 | a0002c0002t0006g0082 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1533+5321A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38406306 | ||||||
| chr3:38406377
|
C | T | 1 | a0001c0001t0005g0171 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1533+5392C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38406377 | ||||||
| chr3:38406397
|
A | G | 2 | a0001c0001t0003g0331a0001c0001t0003g0346 | 2 | HG02145.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1533+5412A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38406397 | ||||||
| chr3:38406498
|
C | T | 1 | a0001c0003t0003g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1533+5513C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38406498 | ||||||
| chr3:38406499
|
G | A | 8 | a0001c0001t0005g0095a0001c0001t0005g0120a0001c0001t0005g0223others(5): Show | 8 | HG01070.hp1 HG01071.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.1533+5514G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38406499 | ||||||
| chr3:38406668
|
C | T | 44 | a0001c0001t0004g0001a0001c0001t0004g0019a0001c0001t0004g0035others(41): Show | 45 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.1533+5683C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38406668 | ||||||
| chr3:38406676
|
A | G | 1 | a0001c0001t0004g0298 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1533+5691A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38406676 | ||||||
| chr3:38406759
|
G | A | 2 | a0001c0001t0001g0188a0001c0001t0001g0291 | 2 | HG02523.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.1533+5774G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38406759 | ||||||
| chr3:38406796
|
A | C | 2 | a0001c0001t0010g0068a0008c0010t0010g0317 | 2 | HG03516.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1533+5811A>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38406796 | ||||||
| chr3:38406925
|
A | T | 44 | a0001c0001t0004g0001a0001c0001t0004g0019a0001c0001t0004g0035others(41): Show | 45 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.1533+5940A>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38406925 | ||||||
| chr3:38406959
|
G | T | 2 | a0001c0001t0001g0124a0001c0001t0001g0142 | 2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1533+5974G>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38406959 | ||||||
| chr3:38406973
|
A | T | 1 | a0001c0001t0003g0253 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1534-5963A>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38406973 | ||||||
| chr3:38406990
|
C | G | 1 | a0002c0002t0004g0060 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1534-5946C>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38406990 | ||||||
| chr3:38407033
|
C | T | 2 | a0001c0001t0001g0124a0001c0001t0001g0142 | 2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1534-5903C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38407033 | ||||||
| chr3:38407138
|
G | A | 3 | a0001c0003t0003g0264a0002c0002t0003g0093a0002c0002t0003g0094 | 3 | HG01928.hp2 HG02647.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1534-5798G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38407138 | ||||||
| chr3:38407140
|
C | T | 3 | a0001c0003t0003g0264a0002c0002t0003g0093a0002c0002t0003g0094 | 3 | HG01928.hp2 HG02647.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1534-5796C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38407140 | ||||||
| chr3:38407141
|
G | A | 1 | a0005c0006t0004g0323 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1534-5795G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38407141 | ||||||
| chr3:38407178
|
G | A | 6 | a0001c0001t0001g0124a0001c0001t0001g0142a0001c0001t0003g0330others(3): Show | 6 | HG01167.hp2 HG01169.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1534-5758G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38407178 | ||||||
| chr3:38407180
|
A | C | 4 | a0001c0001t0008g0064a0001c0001t0008g0065a0001c0001t0008g0169others(1): Show | 4 | HG02895.hp2 HG02897.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1534-5756A>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38407180 | ||||||
| chr3:38407186
|
C | T | 5 | a0001c0001t0001g0053a0001c0001t0001g0216a0002c0002t0001g0051others(2): Show | 5 | HG00323.hp2 HG01069.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.1534-5750C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38407186 | ||||||
| chr3:38407406
|
C | T | 6 | a0001c0001t0007g0255a0001c0001t0007g0335a0004c0005t0007g0325others(3): Show | 6 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1534-5530C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38407406 | ||||||
| chr3:38407426
|
A | G | 1 | a0001c0001t0001g0294 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1534-5510A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38407426 | ||||||
| chr3:38407537
|
T | C | 143 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(140): Show | 147 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1534-5399T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38407537 | ||||||
| chr3:38407705
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1534-5231G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38407705 | ||||||
| chr3:38407758
|
A | G | 6 | a0001c0001t0007g0255a0001c0001t0007g0335a0004c0005t0007g0325others(3): Show | 6 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1534-5178A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38407758 | ||||||
| chr3:38407775
|
A | C | 1 | a0001c0001t0003g0259 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1534-5161A>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38407775 | ||||||
| chr3:38407833
|
A | C | 10 | a0001c0001t0006g0161a0001c0001t0006g0199a0001c0001t0006g0232others(7): Show | 11 | HG01074.hp2 HG01981.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1534-5103A>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38407833 | ||||||
| chr3:38407836
|
G | A | 149 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(146): Show | 153 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1534-5100G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38407836 | ||||||
| chr3:38407971
|
A | T | 2 | a0002c0002t0003g0093a0002c0002t0003g0094 | 2 | HG01928.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1534-4965A>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38407971 | ||||||
| chr3:38408030
|
G | A | 2 | a0001c0003t0004g0265a0001c0003t0004g0266 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1534-4906G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38408030 | ||||||
| chr3:38408033
|
C | T | 4 | a0001c0001t0008g0064a0001c0001t0008g0065a0001c0001t0008g0169others(1): Show | 4 | HG02895.hp2 HG02897.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1534-4903C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38408033 | ||||||
| chr3:38408165
|
A | G | 94 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(91): Show | 97 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.1534-4771A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38408165 | ||||||
| chr3:38408184
|
C | T | 1 | a0002c0002t0005g0011 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1534-4752C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38408184 | ||||||
| chr3:38408242
|
A | G | 141 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(138): Show | 145 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1534-4694A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38408242 | ||||||
| chr3:38408242
|
A | T | 2 | a0005c0006t0001g0275a0005c0006t0001g0320 | 2 | HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1534-4694A>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38408242 | ||||||
| chr3:38408278
|
A | G | 3 | a0001c0001t0003g0340a0005c0006t0001g0275a0005c0006t0001g0320 | 3 | HG02615.hp2 HG02818.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1534-4658A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38408278 | ||||||
| chr3:38408328
|
G | T | 1 | a0001c0001t0011g0178 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1534-4608G>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38408328 | ||||||
| chr3:38408329
|
A | G | 1 | a0001c0001t0011g0178 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1534-4607A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38408329 | ||||||
| chr3:38408332
|
C | A | 1 | a0001c0001t0011g0178 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1534-4604C>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38408332 | ||||||
| chr3:38408360
|
G | T | 1 | a0003c0004t0004g0258 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1534-4576G>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38408360 | ||||||
| chr3:38408371
|
A | T | 2 | a0001c0001t0001g0242a0001c0001t0001g0243 | 2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1534-4565A>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38408371 | ||||||
| chr3:38408463
|
C | T | 37 | a0001c0001t0005g0095a0001c0001t0005g0118a0001c0001t0005g0120others(34): Show | 37 | HG00621.hp2 HG00639.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.1534-4473C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38408463 | ||||||
| chr3:38408472
|
G | C | 2 | a0001c0001t0003g0148a0001c0001t0003g0203 | 2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1534-4464G>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38408472 | ||||||
| chr3:38408523
|
A | G | 4 | a0001c0001t0008g0064a0001c0001t0008g0065a0001c0001t0008g0169others(1): Show | 4 | HG02895.hp2 HG02897.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1534-4413A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38408523 | ||||||
| chr3:38408539
|
A | C | 143 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(140): Show | 147 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1534-4397A>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38408539 | ||||||
| chr3:38408575
|
CA | C | 4 | a0001c0001t0008g0064a0001c0001t0008g0065a0001c0001t0008g0169others(1): Show | 4 | HG02895.hp2 HG02897.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1534-4355delA | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr3 | 38408575 | |||||
| chr3:38408576
|
A | C | 29 | a0001c0001t0005g0095a0001c0001t0005g0118a0001c0001t0005g0120others(26): Show | 29 | HG00621.hp2 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1534-4360A>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38408576 | ||||||
| chr3:38408583
|
T | A | 1 | a0001c0001t0003g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1534-4353T>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38408583 | ||||||
| chr3:38408591
|
T | C | 1 | a0001c0001t0003g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1534-4345T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38408591 | ||||||
| chr3:38408680
|
G | C | 1 | a0003c0004t0003g0277 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1534-4256G>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38408680 | ||||||
| chr3:38408690
|
AT | A | 85 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(82): Show | 88 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.1534-4245delT | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38408690 | ||||||
| chr3:38408690
|
ATG | A | 3 | a0002c0002t0001g0051a0002c0002t0001g0052a0002c0002t0001g0056 | 3 | HG00323.hp2 HG01069.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.1534-4245_1534-424 others(6): Show |
XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38408690 | ||||||
| chr3:38408692
|
G | A | 93 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(90): Show | 96 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1534-4244G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38408692 | ||||||
| chr3:38408694
|
T | A | 3 | a0002c0002t0001g0051a0002c0002t0001g0052a0002c0002t0001g0056 | 3 | HG00323.hp2 HG01069.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.1534-4242T>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38408694 | ||||||
| chr3:38408715
|
G | T | 47 | a0001c0001t0003g0012a0001c0001t0004g0001a0001c0001t0004g0019others(44): Show | 48 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.1534-4221G>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38408715 | ||||||
| chr3:38408763
|
C | T | 1 | a0002c0002t0005g0107 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1534-4173C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38408763 | ||||||
| chr3:38408767
|
A | T | 1 | a0001c0001t0011g0178 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1534-4169A>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38408767 | ||||||
| chr3:38408805
|
C | T | 1 | a0008c0010t0010g0317 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1534-4131C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38408805 | ||||||
| chr3:38409066
|
G | A | 1 | a0002c0002t0002g0054 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1534-3870G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38409066 | ||||||
| chr3:38409085
|
A | G | 47 | a0001c0001t0003g0012a0001c0001t0004g0001a0001c0001t0004g0019others(44): Show | 48 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.1534-3851A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38409085 | ||||||
| chr3:38409168
|
C | T | 4 | a0001c0001t0003g0330a0001c0001t0003g0336a0001c0001t0003g0338others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1534-3768C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38409168 | ||||||
| chr3:38409244
|
A | G | 6 | a0001c0001t0001g0008a0001c0001t0001g0294a0001c0001t0001g0296others(3): Show | 7 | HG02027.hp2 NA18942.hp1 NA18980.hp1 others(4): Show |
intron_variant | MODIFIER | c.1534-3692A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38409244 | ||||||
| chr3:38409342
|
C | T | 45 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015others(42): Show | 46 | HG00741.hp2 HG01109.hp1 HG01123.hp1 others(43): Show |
intron_variant | MODIFIER | c.1534-3594C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38409342 | ||||||
| chr3:38409461
|
C | A | 2 | a0001c0001t0001g0124a0001c0001t0001g0142 | 2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1534-3475C>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38409461 | ||||||
| chr3:38409480
|
A | T | 37 | a0001c0001t0005g0095a0001c0001t0005g0118a0001c0001t0005g0120others(34): Show | 37 | HG00621.hp2 HG00639.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.1534-3456A>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38409480 | ||||||
| chr3:38409514
|
G | A | 190 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(187): Show | 194 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.1534-3422G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38409514 | ||||||
| chr3:38409543
|
T | C | 1 | a0001c0001t0002g0313 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1534-3393T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38409543 | ||||||
| chr3:38409679
|
T | G | 2 | a0001c0003t0004g0265a0001c0003t0004g0266 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1534-3257T>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38409679 | ||||||
| chr3:38409808
|
T | C | 1 | a0001c0001t0001g0228 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1534-3128T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38409808 | ||||||
| chr3:38409847
|
A | C | 1 | a0001c0001t0001g0153 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1534-3089A>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38409847 | ||||||
| chr3:38409949
|
C | A | 4 | a0001c0001t0003g0330a0001c0001t0003g0336a0001c0001t0003g0338others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1534-2987C>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38409949 | ||||||
| chr3:38409967
|
T | G | 1 | a0001c0001t0002g0179 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1534-2969T>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38409967 | ||||||
| chr3:38410029
|
A | G | 143 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(140): Show | 147 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1534-2907A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38410029 | ||||||
| chr3:38410132
|
T | G | 1 | a0001c0003t0003g0066 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1534-2804T>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38410132 | ||||||
| chr3:38410202
|
C | T | 1 | a0008c0010t0010g0317 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1534-2734C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38410202 | ||||||
| chr3:38410265
|
G | C | 1 | a0002c0002t0002g0087 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1534-2671G>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38410265 | ||||||
| chr3:38410314
|
G | A | 1 | a0001c0001t0011g0178 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1534-2622G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38410314 | ||||||
| chr3:38410319
|
C | T | 1 | a0001c0001t0002g0179 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1534-2617C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38410319 | ||||||
| chr3:38410465
|
G | T | 144 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(141): Show | 148 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.1534-2471G>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38410465 | ||||||
| chr3:38410500
|
A | C | 3 | a0001c0003t0003g0264a0002c0002t0003g0093a0002c0002t0003g0094 | 3 | HG01928.hp2 HG02647.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1534-2436A>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38410500 | ||||||
| chr3:38410611
|
G | C | 2 | a0001c0001t0001g0124a0001c0001t0001g0142 | 2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1534-2325G>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38410611 | ||||||
| chr3:38410636
|
C | T | 1 | a0005c0006t0001g0320 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1534-2300C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38410636 | ||||||
| chr3:38410686
|
A | G | 4 | a0001c0001t0003g0012a0001c0001t0017g0108a0002c0002t0016g0074others(1): Show | 4 | HG02965.hp2 HG03453.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1534-2250A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38410686 | ||||||
| chr3:38410771
|
C | T | 96 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(93): Show | 99 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.1534-2165C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38410771 | ||||||
| chr3:38410787
|
C | T | 143 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(140): Show | 147 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1534-2149C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38410787 | ||||||
| chr3:38410826
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1534-2110A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38410826 | ||||||
| chr3:38410855
|
G | A | 8 | a0001c0001t0003g0251a0001c0001t0003g0253a0001c0001t0003g0256others(5): Show | 8 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1534-2081G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38410855 | ||||||
| chr3:38410925
|
T | G | 140 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(137): Show | 144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1534-2011T>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38410925 | ||||||
| chr3:38410983
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1534-1953A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38410983 | ||||||
| chr3:38410991
|
G | A | 4 | a0001c0001t0003g0330a0001c0001t0003g0336a0001c0001t0003g0338others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1534-1945G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38410991 | ||||||
| chr3:38411027
|
C | G | 2 | a0001c0001t0010g0068a0008c0010t0010g0317 | 2 | HG03516.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1534-1909C>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38411027 | ||||||
| chr3:38411029
|
A | G | 1 | a0002c0002t0002g0020 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1534-1907A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38411029 | ||||||
| chr3:38411030
|
G | A | 4 | a0001c0001t0008g0064a0001c0001t0008g0065a0001c0001t0008g0169others(1): Show | 4 | HG02895.hp2 HG02897.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1534-1906G>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38411030 | ||||||
| chr3:38411077
|
C | A | 3 | a0001c0001t0002g0057a0001c0001t0002g0058a0001c0001t0002g0231 | 3 | HG01346.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1534-1859C>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38411077 | ||||||
| chr3:38411159
|
A | T | 1 | a0001c0001t0011g0178 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1534-1777A>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38411159 | ||||||
| chr3:38411208
|
G | T | 1 | a0001c0001t0001g0227 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1534-1728G>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38411208 | ||||||
| chr3:38411273
|
C | T | 29 | a0001c0001t0005g0095a0001c0001t0005g0118a0001c0001t0005g0120others(26): Show | 29 | HG00621.hp2 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1534-1663C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38411273 | ||||||
| chr3:38411384
|
G | T | 1 | a0001c0001t0011g0178 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1534-1552G>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38411384 | ||||||
| chr3:38411386
|
G | T | 143 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(140): Show | 147 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1534-1550G>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38411386 | ||||||
| chr3:38411520
|
T | G | 47 | a0001c0001t0003g0012a0001c0001t0004g0001a0001c0001t0004g0019others(44): Show | 48 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.1534-1416T>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38411520 | ||||||
| chr3:38411527
|
TA | T | 8 | a0001c0001t0002g0233a0001c0001t0007g0255a0001c0001t0007g0335others(5): Show | 8 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1534-1398delA | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr3 | 38411527 | |||||
| chr3:38411647
|
T | TA | 57 | a0001c0001t0001g0053a0001c0001t0001g0121a0001c0001t0002g0115others(54): Show | 58 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.1534-1275dupA | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr3 | 38411647 | |||||
| chr3:38411693
|
T | G | 2 | a0001c0001t0005g0303a0002c0002t0005g0084 | 2 | HG02080.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.1534-1243T>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38411693 | ||||||
| chr3:38411756
|
C | G | 2 | a0001c0001t0010g0068a0008c0010t0010g0317 | 2 | HG03516.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1534-1180C>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38411756 | ||||||
| chr3:38411817
|
A | G | 1 | a0001c0001t0002g0116 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1534-1119A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38411817 | ||||||
| chr3:38411895
|
A | G | 47 | a0001c0001t0003g0012a0001c0001t0004g0001a0001c0001t0004g0019others(44): Show | 48 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.1534-1041A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38411895 | ||||||
| chr3:38411967
|
T | G | 1 | a0001c0001t0011g0178 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1534-969T>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38411967 | ||||||
| chr3:38411984
|
CT | C | 107 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0053others(104): Show | 110 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1534-937delT | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr3 | 38411984 | |||||
| chr3:38411999
|
T | C | 1 | a0001c0001t0008g0065 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1534-937T>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38411999 | ||||||
| chr3:38412000
|
C | T | 1 | a0001c0001t0008g0065 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1534-936C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38412000 | ||||||
| chr3:38412303
|
T | A | 7 | a0001c0001t0003g0251a0001c0001t0003g0253a0001c0001t0003g0256others(4): Show | 7 | HG01243.hp1 HG01884.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1534-633T>A | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38412303 | ||||||
| chr3:38412305
|
T | G | 7 | a0001c0001t0003g0251a0001c0001t0003g0253a0001c0001t0003g0256others(4): Show | 7 | HG01243.hp1 HG01884.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1534-631T>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38412305 | ||||||
| chr3:38412324
|
G | C | 1 | a0001c0001t0001g0286 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1534-612G>C | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38412324 | ||||||
| chr3:38412357
|
C | T | 3 | a0001c0003t0003g0264a0002c0002t0003g0093a0002c0002t0003g0094 | 3 | HG01928.hp2 HG02647.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1534-579C>T | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38412357 | ||||||
| chr3:38412571
|
A | G | 1 | a0001c0001t0013g0145 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1534-365A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38412571 | ||||||
| chr3:38412824
|
A | G | 3 | a0001c0001t0006g0161a0001c0001t0006g0199a0001c0001t0006g0232 | 3 | HG02622.hp1 HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1534-112A>G | XYLB | ENSG00000093217.11 | transcript | ENST00000207870.8 | protein_coding | 18/18 | chr3 | 38412824 |