Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 203522 |
|---|---|
| ensemblid | ENSG00000165359.16 |
| hgncid | 27334 |
| symbol | INTS6L |
| name | integrator complex subunit 6 like |
| refseq_nuc | NM_001351601.3 |
| refseq_prot | NP_001338530.1 |
| ensembl_nuc | ENST00000639893.2 |
| ensembl_prot | ENSP00000491427.1 |
| mane_status | MANE Select |
| chr | chrX |
| start | 135520660 |
| end | 135582510 |
| strand | + |
| ver | v1.2 |
| region | chrX:135520660-135582510 |
| region5000 | chrX:135515660-135587510 |
| regionname0 | INTS6L_chrX_135520660_135582510 |
| regionname5000 | INTS6L_chrX_135515660_135587510 |
| 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 | 898 | 237 | 60 | 36 | 108 | 9 | 22 | 87 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| a0002 | 0/0 | 898 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| a0003 | 0/0 | 554 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| a0004 | 0/0 | 409 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| a0005 | 0/0 | 409 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| a0006 | 0/0 | 898 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2697 | 183 | 41 | 33 | 83 | 7 | 17 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| c0002 | 0/0 | 2697 | 32 | 15 | 0 | 15 | 0 | 2 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| c0003 | 0/0 | 2697 | 21 | 4 | 3 | 10 | 2 | 2 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| c0004 | 0/0 | 2697 | 3 | 0 | 3 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| c0005 | 0/0 | 2696 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| c0006 | 0/0 | 2699 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| c0007 | 0/0 | 2697 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| c0008 | 0/0 | 2696 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| c0009 | 0/0 | 2697 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| 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 | 1208 | 224 | 56 | 36 | 100 | 9 | 22 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| t0002 | 1/0 | 1208 | 18 | 4 | 2 | 11 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| t0003 | 0/0 | 1208 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| t0004 | 0/0 | 1208 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 5 | 1 | 0 | 4 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0007 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0016 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0042 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0201 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2697 | 183 | 41 | 33 | 83 | 7 | 17 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| a0001c0002 | 0/0 | 2697 | 32 | 15 | 0 | 15 | 0 | 2 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| a0001c0003 | 0/0 | 2697 | 21 | 4 | 3 | 10 | 2 | 2 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| a0001c0007 | 0/0 | 2697 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| a0002c0004 | 0/0 | 2697 | 3 | 0 | 3 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| a0003c0006 | 0/0 | 2699 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| a0004c0005 | 0/0 | 2696 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| a0005c0008 | 0/0 | 2696 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| a0006c0009 | 0/0 | 2697 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3904 | 164 | 37 | 30 | 72 | 7 | 17 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| a0001c0001t0002 | 1/0 | 3904 | 17 | 4 | 2 | 10 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| a0001c0001t0003 | 0/0 | 3904 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| a0001c0001t0004 | 0/0 | 3904 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| a0001c0002t0001 | 0/0 | 3904 | 32 | 15 | 0 | 15 | 0 | 2 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| a0001c0003t0001 | 0/0 | 3904 | 21 | 4 | 3 | 10 | 2 | 2 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| a0001c0007t0001 | 0/0 | 3904 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| a0002c0004t0001 | 0/0 | 3904 | 3 | 0 | 3 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| a0003c0006t0002 | 0/0 | 3906 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| a0004c0005t0001 | 0/0 | 3903 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| a0005c0008t0001 | 0/0 | 3903 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| a0006c0009t0001 | 0/0 | 3904 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | copy fasta | chrX | 135515660 | 135587510 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 1 | 0 | 4 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0201 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0002g0042 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0007 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0007t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0002c0004t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0002c0004t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0002c0004t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0003c0006t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0004c0005t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0005c0008t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0006c0009t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | GBR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0157 | EUR | GBR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0129 | EUR | GBR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | FIN | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | CHS | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | CHS | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | CHS | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01099 | hp1 | a0001 | c0003 | t0001 | g0063 | AMR | PUR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | PUR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0074 | AMR | CLM | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01346 | hp1 | a0002 | c0004 | t0001 | g0183 | AMR | CLM | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01433 | hp1 | a0002 | c0004 | t0001 | g0155 | AMR | CLM | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01496 | hp1 | a0001 | c0003 | t0001 | g0149 | AMR | CLM | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | IBS | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01516 | hp2 | a0001 | c0003 | t0001 | g0071 | EUR | IBS | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0082 | AFR | ACB | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01978 | hp1 | a0002 | c0004 | t0001 | g0112 | AMR | PEL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01978 | hp2 | a0001 | c0003 | t0001 | g0062 | AMR | PEL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02015 | hp1 | a0001 | c0003 | t0001 | g0057 | EAS | KHV | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02040 | hp1 | a0001 | c0003 | t0001 | g0070 | EAS | KHV | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | KHV | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | KHV | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | KHV | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CDX | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02257 | hp1 | a0001 | c0003 | t0001 | g0204 | AFR | ACB | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0079 | AFR | ACB | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | ACB | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0027 | SAS | PJL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0076 | AFR | GWD | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0078 | AFR | GWD | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0214 | AFR | GWD | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | ESN | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0084 | AFR | ESN | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03098 | hp1 | a0001 | c0003 | t0001 | g0203 | AFR | MSL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | ESN | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0085 | AFR | ESN | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | MSL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0072 | AFR | MSL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | MSL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | MSL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03492 | hp1 | a0001 | c0007 | t0001 | g0130 | SAS | PJL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0083 | AFR | GWD | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03654 | hp1 | a0001 | c0003 | t0001 | g0007 | SAS | PJL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | STU | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0026 | SAS | BEB | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | BEB | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG04199 | hp1 | a0001 | c0003 | t0001 | g0036 | SAS | STU | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | STU | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | STU | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | YRI | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHB | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHB | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | YRI | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0081 | AFR | YRI | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18952 | hp1 | a0001 | c0003 | t0001 | g0064 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18956 | hp1 | a0005 | c0008 | t0001 | g0029 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18956 | hp2 | a0001 | c0003 | t0001 | g0065 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18963 | hp1 | a0003 | c0006 | t0002 | g0047 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18969 | hp1 | a0001 | c0003 | t0001 | g0058 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18991 | hp1 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18994 | hp1 | a0001 | c0003 | t0001 | g0069 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19006 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | LWK | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | LWK | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | LWK | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19056 | hp1 | a0001 | c0003 | t0001 | g0215 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19058 | hp1 | a0001 | c0003 | t0001 | g0022 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19070 | hp1 | a0001 | c0003 | t0001 | g0068 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19078 | hp1 | a0006 | c0009 | t0001 | g0025 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19086 | hp1 | a0004 | c0005 | t0001 | g0133 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | YRI | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | YRI | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0086 | AFR | ASW | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | ASW | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0124 | EUR | TSI | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA20805 | hp1 | a0001 | c0003 | t0001 | g0066 | EUR | TSI | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | GIH | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0067 | AFR | ACB | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | USA | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | USA | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0201 | REF | REF | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0042 | REF | REF | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:135556253
|
A | C | 1 | a0006 | 1 | NA19078.hp1 | missense_variant | MODERATE | c.1145A>C | p.Asn382Thr | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/18 | 1478/3904 | 1145/2697 | 382/898 | chrX | 135556253 | ||
| chrX:135569362
|
TA | T | 1 | a0005 | 1 | NA18956.hp1 | frameshift_variant | HIGH | c.1220delA | p.Lys407fs | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 10/18 | 1553/3904 | 1220/2697 | 407/898 | INFO_REALIGN_3_PRIME | chrX | 135569362 | |
| chrX:135569365
|
GC | G | 1 | a0004 | 1 | NA19086.hp1 | frameshift_variant | HIGH | c.1223delC | p.Pro408fs | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 10/18 | 1556/3904 | 1223/2697 | 408/898 | INFO_REALIGN_3_PRIME | chrX | 135569365 | |
| chrX:135573977
|
T | TC | 1 | a0003 | 1 | NA18963.hp1 | frameshift_variant | HIGH | c.1660dupC | p.Arg554fs | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 13/18 | 1994/3904 | 1661/2697 | 554/898 | INFO_REALIGN_3_PRIME | chrX | 135573977 | |
| chrX:135577340
|
A | T | 1 | a0002 | 3 | HG01346.hp1 HG01433.hp1 HG01978.hp1 |
missense_variant | MODERATE | c.2032A>T | p.Thr678Ser | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 15/18 | 2365/3904 | 2032/2697 | 678/898 | chrX | 135577340 | ||
| chrX:135581535
|
A | AG | 1 | a0003 | 1 | NA18963.hp1 | frameshift_variant | HIGH | c.2597dupG | p.Arg867fs | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 18/18 | 2931/3904 | 2598/2697 | 866/898 | INFO_REALIGN_3_PRIME | chrX | 135581535 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:135575208
|
G | A | 1 | a0001c0007 | 1 | HG03492.hp1 | synonymous_variant | LOW | c.1866G>A | p.Pro622Pro | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/18 | 2199/3904 | 1866/2697 | 622/898 | chrX | 135575208 | ||
| chrX:135579930
|
G | A | 1 | a0001c0003 | 21 | HG01099.hp1 HG01496.hp1 HG01516.hp2 others(18): Show |
synonymous_variant | LOW | c.2262G>A | p.Leu754Leu | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 16/18 | 2595/3904 | 2262/2697 | 754/898 | chrX | 135579930 | ||
| chrX:135579936
|
C | T | 3 | a0001c0002a0005c0008a0006c0009 | 34 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(31): Show |
synonymous_variant | LOW | c.2268C>T | p.Asp756Asp | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 16/18 | 2601/3904 | 2268/2697 | 756/898 | chrX | 135579936 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:135520697
|
C | T | 1 | a0001c0001t0004 | 1 | HG01261.hp1 | 5_prime_UTR_variant | MODIFIER | c.-296C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 1/18 | 296 | chrX | 135520697 | |||||
| chrX:135520798
|
G | A | 1 | a0001c0001t0004 | 1 | HG01261.hp1 | 5_prime_UTR_variant | MODIFIER | c.-195G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 1/18 | 195 | chrX | 135520798 | |||||
| chrX:135520893
|
T | C | 10 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(7): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
5_prime_UTR_variant | MODIFIER | c.-100T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 1/18 | 100 | chrX | 135520893 | |||||
| chrX:135582196
|
G | A | 1 | a0001c0001t0003 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*560G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 18/18 | 560 | chrX | 135582196 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:135521335
|
TG | T | 1 | a0001c0003t0001g0022 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.189+23delG | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135521335 | |||||
| chrX:135521380
|
A | AC | 1 | a0001c0001t0001g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.189+68dupC | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135521380 | |||||
| chrX:135521415
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.189+97C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135521415 | ||||||
| chrX:135521434
|
A | AG | 1 | a0001c0001t0001g0024 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.189+121dupG | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135521434 | |||||
| chrX:135521453
|
G | A | 18 | a0001c0001t0001g0040a0001c0002t0001g0006a0001c0002t0001g0026others(15): Show | 19 | HG00621.hp1 HG00673.hp1 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.189+135G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135521453 | ||||||
| chrX:135521479
|
GGA | G | 1 | a0001c0003t0001g0022 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.189+163_189+164del others(2): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135521479 | |||||
| chrX:135521751
|
T | TGC | 214 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(211): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.189+433_189+434ins others(2): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135521751 | ||||||
| chrX:135521751
|
T | TGCGGC | 1 | a0001c0003t0001g0215 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.189+433_189+434ins others(5): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135521751 | ||||||
| chrX:135521752
|
C | G | 214 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(211): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.189+434C>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135521752 | ||||||
| chrX:135521755
|
C | G | 1 | a0001c0003t0001g0215 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.189+437C>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135521755 | ||||||
| chrX:135521758
|
G | C | 1 | a0001c0003t0001g0215 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.189+440G>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135521758 | ||||||
| chrX:135521758
|
G | GGC | 214 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(211): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.189+440_189+441ins others(2): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135521758 | ||||||
| chrX:135521759
|
C | G | 1 | a0001c0003t0001g0215 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.189+441C>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135521759 | ||||||
| chrX:135521767
|
C | CG | 1 | a0001c0003t0001g0057 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.189+451dupG | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135521767 | |||||
| chrX:135521770
|
A | C | 1 | a0001c0003t0001g0057 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.189+452A>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135521770 | ||||||
| chrX:135521770
|
A | G | 199 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(196): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.189+452A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135521770 | ||||||
| chrX:135521872
|
T | TC | 1 | a0006c0009t0001g0025 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.189+559dupC | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135521872 | |||||
| chrX:135522043
|
G | A | 18 | a0001c0001t0001g0061a0001c0002t0001g0059a0001c0002t0001g0060others(15): Show | 19 | HG01099.hp1 HG01516.hp2 HG01928.hp1 others(16): Show |
intron_variant | MODIFIER | c.189+725G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135522043 | ||||||
| chrX:135522422
|
T | C | 1 | a0001c0002t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.189+1104T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135522422 | ||||||
| chrX:135522447
|
G | A | 1 | a0001c0001t0001g0073 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.189+1129G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135522447 | ||||||
| chrX:135522521
|
A | AT | 1 | a0001c0002t0001g0041 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.189+1207dupT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135522521 | |||||
| chrX:135522673
|
G | C | 1 | a0001c0001t0004g0074 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.189+1355G>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135522673 | ||||||
| chrX:135522969
|
C | T | 1 | a0001c0002t0001g0214 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.189+1651C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135522969 | ||||||
| chrX:135522973
|
G | A | 1 | a0001c0003t0001g0058 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.189+1655G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135522973 | ||||||
| chrX:135523107
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.189+1789G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135523107 | ||||||
| chrX:135523173
|
T | C | 1 | a0001c0003t0001g0076 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.189+1855T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135523173 | ||||||
| chrX:135523247
|
A | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(148): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.189+1929A>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135523247 | ||||||
| chrX:135523258
|
C | T | 1 | a0001c0003t0001g0057 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.189+1940C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135523258 | ||||||
| chrX:135523269
|
G | C | 2 | a0001c0001t0001g0008a0001c0001t0001g0077 | 3 | HG01884.hp2 HG02818.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.189+1951G>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135523269 | ||||||
| chrX:135523402
|
C | CA | 13 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209others(10): Show | 13 | HG01069.hp1 HG01167.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.189+2109dupA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135523402 | |||||
| chrX:135523402
|
C | CAA | 118 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(115): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.189+2108_189+2109d others(4): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135523402 | |||||
| chrX:135523402
|
C | CAAA | 18 | a0001c0001t0001g0024a0001c0001t0001g0105a0001c0001t0001g0106others(15): Show | 18 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.189+2107_189+2109d others(5): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135523402 | |||||
| chrX:135523402
|
C | CAAAA | 6 | a0001c0001t0001g0061a0001c0001t0001g0100a0001c0001t0001g0101others(3): Show | 6 | HG01928.hp1 HG02071.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.189+2106_189+2109d others(6): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135523402 | |||||
| chrX:135523402
|
CA | C | 14 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0077others(11): Show | 16 | HG00639.hp2 HG01884.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.189+2109delA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135523402 | |||||
| chrX:135523402
|
CAAAAA | C | 1 | a0001c0001t0001g0213 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.189+2105_189+2109d others(7): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135523402 | |||||
| chrX:135523402
|
CAAAAAAA | C | 4 | a0001c0001t0001g0011a0001c0001t0001g0095a0001c0001t0001g0096others(1): Show | 5 | HG02080.hp1 HG02155.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.189+2103_189+2109d others(9): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135523402 | |||||
| chrX:135523402
|
CAAAAAAA others(1): Show |
C | 2 | a0001c0001t0001g0098a0001c0001t0001g0099 | 2 | NA18747.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.189+2102_189+2109d others(10): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135523402 | |||||
| chrX:135524039
|
T | G | 1 | a0001c0001t0001g0100 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.189+2721T>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135524039 | ||||||
| chrX:135524204
|
AATTT | A | 1 | a0001c0001t0001g0206 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.189+2887_189+2890d others(6): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135524204 | ||||||
| chrX:135524223
|
AT | A | 2 | a0001c0001t0001g0105a0001c0001t0001g0121 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.189+2914delT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135524223 | |||||
| chrX:135524450
|
G | GT | 38 | a0001c0001t0001g0011a0001c0001t0001g0095a0001c0001t0001g0096others(35): Show | 43 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(40): Show |
intron_variant | MODIFIER | c.189+3144dupT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135524450 | |||||
| chrX:135524450
|
GT | G | 4 | a0001c0001t0001g0122a0001c0002t0001g0079a0001c0002t0001g0086others(1): Show | 4 | HG02257.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+3144delT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135524450 | |||||
| chrX:135524702
|
GA | G | 1 | a0001c0003t0001g0022 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.189+3388delA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135524702 | |||||
| chrX:135524730
|
C | CT | 1 | a0001c0002t0001g0041 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.189+3413dupT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135524730 | |||||
| chrX:135524802
|
C | T | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(197): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.189+3484C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135524802 | ||||||
| chrX:135525029
|
GA | G | 1 | a0001c0003t0001g0022 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.189+3714delA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135525029 | |||||
| chrX:135525090
|
TA | T | 1 | a0001c0003t0001g0022 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.189+3776delA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135525090 | |||||
| chrX:135525130
|
GT | G | 1 | a0001c0002t0001g0041 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.189+3817delT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135525130 | |||||
| chrX:135525834
|
G | T | 3 | a0001c0001t0001g0021a0001c0001t0001g0122a0001c0001t0001g0212 | 4 | HG01167.hp1 HG02895.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+4516G>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135525834 | ||||||
| chrX:135525849
|
CA | C | 1 | a0001c0003t0001g0022 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.189+4536delA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135525849 | |||||
| chrX:135525976
|
A | AG | 1 | a0001c0002t0001g0041 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.189+4660dupG | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135525976 | |||||
| chrX:135525979
|
A | G | 46 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(43): Show | 53 | HG00621.hp1 HG00639.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.189+4661A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135525979 | ||||||
| chrX:135526117
|
AT | A | 1 | a0001c0003t0001g0022 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.189+4801delT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135526117 | |||||
| chrX:135526242
|
G | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(197): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.189+4924G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135526242 | ||||||
| chrX:135526524
|
A | T | 49 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(46): Show | 56 | HG00621.hp1 HG00639.hp2 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.189+5206A>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135526524 | ||||||
| chrX:135526791
|
A | G | 3 | a0001c0002t0001g0079a0001c0002t0001g0086a0001c0002t0001g0214 | 3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.189+5473A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135526791 | ||||||
| chrX:135527211
|
T | A | 3 | a0001c0001t0001g0012a0001c0001t0001g0106a0001c0001t0001g0123 | 4 | HG02129.hp1 NA18942.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+5893T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135527211 | ||||||
| chrX:135527258
|
A | G | 2 | a0001c0001t0002g0053a0001c0001t0002g0054 | 2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.189+5940A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135527258 | ||||||
| chrX:135527299
|
T | C | 1 | a0001c0001t0001g0106 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.189+5981T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135527299 | ||||||
| chrX:135527347
|
G | A | 1 | a0001c0001t0002g0044 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.189+6029G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135527347 | ||||||
| chrX:135527475
|
T | C | 1 | a0001c0001t0001g0124 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.189+6157T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135527475 | ||||||
| chrX:135527815
|
CT | C | 2 | a0001c0001t0001g0125a0001c0001t0001g0126 | 2 | NA18951.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.189+6501delT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135527815 | |||||
| chrX:135527843
|
G | C | 12 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0077others(9): Show | 14 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.189+6525G>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135527843 | ||||||
| chrX:135527893
|
A | AT | 1 | a0001c0002t0001g0060 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.189+6581dupT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135527893 | |||||
| chrX:135527982
|
T | C | 46 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(43): Show | 53 | HG00621.hp1 HG00639.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.189+6664T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135527982 | ||||||
| chrX:135528180
|
G | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0127a0001c0001t0001g0207 | 4 | NA18945.hp1 NA18990.hp1 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+6862G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135528180 | ||||||
| chrX:135528496
|
G | T | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(197): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.189+7178G>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135528496 | ||||||
| chrX:135528549
|
G | A | 6 | a0001c0001t0001g0011a0001c0001t0001g0095a0001c0001t0001g0096others(3): Show | 7 | HG02080.hp1 HG02155.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.189+7231G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135528549 | ||||||
| chrX:135528561
|
C | T | 3 | a0001c0003t0001g0076a0001c0003t0001g0203a0001c0003t0001g0204 | 3 | HG02257.hp1 HG02615.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.189+7243C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135528561 | ||||||
| chrX:135528809
|
C | A | 1 | a0001c0001t0001g0128 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.189+7491C>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135528809 | ||||||
| chrX:135528866
|
A | AC | 91 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(88): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.189+7559dupC | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135528866 | |||||
| chrX:135528866
|
A | ACC | 51 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(48): Show | 56 | HG00642.hp1 HG00741.hp1 HG01099.hp1 others(53): Show |
intron_variant | MODIFIER | c.189+7558_189+7559d others(4): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135528866 | |||||
| chrX:135528866
|
A | ACCC | 14 | a0001c0001t0001g0011a0001c0001t0001g0095a0001c0001t0001g0096others(11): Show | 15 | HG00140.hp1 HG01109.hp1 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.189+7557_189+7559d others(5): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135528866 | |||||
| chrX:135528873
|
C | CG | 1 | a0001c0001t0001g0199 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.189+7555_189+7556i others(3): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135528873 | ||||||
| chrX:135528873
|
C | CT | 4 | a0001c0001t0001g0120a0001c0001t0001g0200a0001c0001t0001g0201others(1): Show | 4 | HG00735.hp1 HG01074.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+7555_189+7556i others(3): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135528873 | ||||||
| chrX:135528877
|
C | G | 7 | a0001c0002t0001g0006a0001c0002t0001g0038a0001c0002t0001g0039others(4): Show | 8 | NA18943.hp1 NA18957.hp1 NA18963.hp2 others(5): Show |
intron_variant | MODIFIER | c.189+7559C>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135528877 | ||||||
| chrX:135529141
|
G | A | 1 | a0001c0002t0001g0079 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.189+7823G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135529141 | ||||||
| chrX:135529204
|
G | A | 5 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0129others(2): Show | 7 | HG00099.hp2 HG00140.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.189+7886G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135529204 | ||||||
| chrX:135529406
|
G | A | 2 | a0001c0002t0001g0003a0001c0002t0001g0082 | 4 | HG01884.hp1 HG02970.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+8088G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135529406 | ||||||
| chrX:135529518
|
A | G | 1 | a0001c0001t0001g0206 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.189+8200A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135529518 | ||||||
| chrX:135529526
|
T | C | 5 | a0001c0001t0001g0075a0001c0001t0001g0120a0001c0001t0001g0200others(2): Show | 5 | HG00099.hp1 HG00735.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.189+8208T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135529526 | ||||||
| chrX:135529694
|
T | C | 3 | a0001c0002t0001g0079a0001c0002t0001g0086a0001c0002t0001g0214 | 3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.189+8376T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135529694 | ||||||
| chrX:135529738
|
TA | T | 1 | a0001c0001t0001g0119 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.189+8421delA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135529738 | ||||||
| chrX:135529742
|
T | A | 1 | a0001c0001t0001g0119 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.189+8424T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135529742 | ||||||
| chrX:135530131
|
ATTTATAG | A | 1 | a0001c0003t0001g0204 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.189+8814_189+8820d others(9): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135530131 | ||||||
| chrX:135530182
|
A | G | 1 | a0001c0001t0002g0054 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.189+8864A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135530182 | ||||||
| chrX:135530228
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.189+8910C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135530228 | ||||||
| chrX:135530318
|
A | AT | 1 | a0001c0002t0001g0041 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.189+9001dupT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135530318 | |||||
| chrX:135530490
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.189+9172G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135530490 | ||||||
| chrX:135530562
|
G | A | 6 | a0001c0001t0001g0011a0001c0001t0001g0095a0001c0001t0001g0096others(3): Show | 7 | HG02080.hp1 HG02155.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.189+9244G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135530562 | ||||||
| chrX:135530753
|
T | G | 40 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0077others(37): Show | 46 | HG00621.hp1 HG00639.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.189+9435T>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135530753 | ||||||
| chrX:135530902
|
A | C | 5 | a0001c0001t0001g0104a0001c0001t0001g0118a0001c0001t0001g0196others(2): Show | 5 | HG02451.hp1 HG02572.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.189+9584A>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135530902 | ||||||
| chrX:135531147
|
TG | T | 1 | a0001c0002t0001g0041 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.189+9832delG | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135531147 | |||||
| chrX:135531152
|
A | T | 1 | a0001c0002t0001g0082 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.189+9834A>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135531152 | ||||||
| chrX:135531292
|
C | A | 66 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0013others(63): Show | 74 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.189+9974C>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135531292 | ||||||
| chrX:135531320
|
G | A | 6 | a0001c0001t0001g0011a0001c0001t0001g0095a0001c0001t0001g0096others(3): Show | 7 | HG02080.hp1 HG02155.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.189+10002G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135531320 | ||||||
| chrX:135531476
|
G | GT | 1 | a0001c0002t0001g0041 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.189+10164dupT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135531476 | |||||
| chrX:135531489
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.189+10171G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135531489 | ||||||
| chrX:135531667
|
C | G | 6 | a0001c0001t0001g0011a0001c0001t0001g0095a0001c0001t0001g0096others(3): Show | 7 | HG02080.hp1 HG02155.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.189+10349C>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135531667 | ||||||
| chrX:135531692
|
GT | G | 1 | a0001c0002t0001g0041 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.189+10376delT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135531692 | |||||
| chrX:135531749
|
T | C | 1 | a0001c0001t0001g0213 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.189+10431T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135531749 | ||||||
| chrX:135531761
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.189+10443C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135531761 | ||||||
| chrX:135531911
|
G | C | 3 | a0001c0002t0001g0079a0001c0002t0001g0086a0001c0002t0001g0214 | 3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.189+10593G>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135531911 | ||||||
| chrX:135532093
|
AT | A | 1 | a0001c0002t0001g0041 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.189+10778delT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135532093 | |||||
| chrX:135532220
|
G | T | 1 | a0001c0001t0001g0174 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.189+10902G>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135532220 | ||||||
| chrX:135532469
|
A | G | 1 | a0001c0002t0001g0037 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.189+11151A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135532469 | ||||||
| chrX:135532514
|
G | A | 3 | a0001c0002t0001g0079a0001c0002t0001g0086a0001c0002t0001g0214 | 3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.189+11196G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135532514 | ||||||
| chrX:135532636
|
A | G | 1 | a0002c0004t0001g0112 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.189+11318A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135532636 | ||||||
| chrX:135532701
|
G | A | 3 | a0001c0002t0001g0079a0001c0002t0001g0086a0001c0002t0001g0214 | 3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.189+11383G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135532701 | ||||||
| chrX:135533075
|
T | TCAAAAA | 1 | a0001c0001t0002g0054 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.189+11782_189+1178 others(10): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135533075 | |||||
| chrX:135533100
|
CA | C | 4 | a0001c0001t0001g0100a0001c0001t0001g0132a0001c0001t0001g0141others(1): Show | 4 | NA18953.hp1 NA18957.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+11789delA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135533100 | |||||
| chrX:135533107
|
AC | A | 27 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0009others(24): Show | 31 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.189+11790delC | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135533107 | ||||||
| chrX:135533178
|
T | C | 1 | a0001c0002t0001g0032 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.189+11860T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135533178 | ||||||
| chrX:135533647
|
G | A | 3 | a0001c0002t0001g0079a0001c0002t0001g0086a0001c0002t0001g0214 | 3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.190-11776G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135533647 | ||||||
| chrX:135533672
|
G | C | 3 | a0001c0002t0001g0079a0001c0002t0001g0086a0001c0002t0001g0214 | 3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.190-11751G>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135533672 | ||||||
| chrX:135533755
|
T | C | 28 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0009others(25): Show | 32 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.190-11668T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135533755 | ||||||
| chrX:135533826
|
T | C | 49 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(46): Show | 56 | HG00621.hp1 HG00639.hp2 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.190-11597T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135533826 | ||||||
| chrX:135533933
|
T | G | 3 | a0001c0001t0001g0023a0001c0001t0001g0142a0001c0001t0001g0175 | 3 | HG02145.hp1 HG02647.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.190-11490T>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135533933 | ||||||
| chrX:135534039
|
G | A | 1 | a0001c0001t0001g0087 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.190-11384G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135534039 | ||||||
| chrX:135534450
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.190-10973G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135534450 | ||||||
| chrX:135534568
|
G | A | 1 | a0001c0002t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.190-10855G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135534568 | ||||||
| chrX:135534682
|
C | CT | 25 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0009others(22): Show | 29 | HG00673.hp1 HG01884.hp1 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.190-10722dupT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135534682 | |||||
| chrX:135534682
|
C | CTT | 5 | a0001c0002t0001g0031a0001c0002t0001g0041a0001c0002t0001g0079others(2): Show | 5 | HG00621.hp1 HG02257.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.190-10723_190-1072 others(6): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135534682 | |||||
| chrX:135534682
|
CT | C | 8 | a0001c0001t0001g0040a0001c0001t0001g0118a0001c0001t0001g0122others(5): Show | 8 | HG01070.hp2 HG01256.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.190-10722delT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135534682 | |||||
| chrX:135534687
|
T | C | 11 | a0001c0001t0002g0002a0001c0001t0002g0044a0001c0001t0002g0045others(8): Show | 13 | HG00741.hp2 HG01192.hp1 NA18946.hp1 others(10): Show |
intron_variant | MODIFIER | c.190-10736T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135534687 | ||||||
| chrX:135534701
|
T | A | 160 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(157): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.190-10722T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135534701 | ||||||
| chrX:135534701
|
T | TA | 3 | a0001c0001t0001g0117a0001c0002t0001g0072a0002c0004t0001g0155 | 3 | HG01433.hp1 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.190-10719dupA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135534701 | |||||
| chrX:135534708
|
A | T | 1 | a0001c0003t0001g0204 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.190-10715A>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135534708 | ||||||
| chrX:135534750
|
G | A | 13 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0077others(10): Show | 15 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.190-10673G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135534750 | ||||||
| chrX:135534895
|
G | C | 43 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0077others(40): Show | 49 | HG00621.hp1 HG00639.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.190-10528G>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135534895 | ||||||
| chrX:135535149
|
A | C | 1 | a0001c0002t0001g0030 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.190-10274A>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135535149 | ||||||
| chrX:135535284
|
A | G | 3 | a0001c0002t0001g0079a0001c0002t0001g0086a0001c0002t0001g0214 | 3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.190-10139A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135535284 | ||||||
| chrX:135535598
|
TA | T | 1 | a0001c0002t0001g0041 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.190-9823delA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135535598 | |||||
| chrX:135536297
|
A | AT | 2 | a0001c0001t0001g0194a0001c0001t0002g0053 | 2 | HG01952.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.190-9117dupT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135536297 | |||||
| chrX:135536672
|
T | A | 1 | a0001c0001t0001g0206 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.190-8751T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135536672 | ||||||
| chrX:135536756
|
A | G | 194 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(191): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.190-8667A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135536756 | ||||||
| chrX:135536821
|
A | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(148): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.190-8602A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135536821 | ||||||
| chrX:135537144
|
C | T | 1 | a0001c0003t0001g0036 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.190-8279C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135537144 | ||||||
| chrX:135537247
|
TCACTGAT others(8): Show |
T | 1 | a0001c0001t0002g0052 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.190-8174_190-8160d others(17): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135537247 | |||||
| chrX:135537437
|
G | C | 1 | a0001c0001t0001g0111 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.190-7986G>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135537437 | ||||||
| chrX:135537574
|
C | T | 4 | a0001c0002t0001g0030a0001c0002t0001g0031a0001c0002t0001g0037others(1): Show | 4 | HG00621.hp1 HG02056.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.190-7849C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135537574 | ||||||
| chrX:135537953
|
A | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(148): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.190-7470A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135537953 | ||||||
| chrX:135538040
|
AGTT | A | 1 | a0001c0001t0001g0143 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.190-7378_190-7376d others(5): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135538040 | |||||
| chrX:135538546
|
G | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(210): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.190-6877G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135538546 | ||||||
| chrX:135538563
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.190-6860C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135538563 | ||||||
| chrX:135538725
|
A | G | 194 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(191): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.190-6698A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135538725 | ||||||
| chrX:135539228
|
A | T | 1 | a0001c0001t0001g0172 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.190-6195A>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135539228 | ||||||
| chrX:135539525
|
GTTTTTCT others(3): Show |
G | 3 | a0001c0002t0001g0079a0001c0002t0001g0086a0001c0002t0001g0214 | 3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.190-5896_190-5887d others(12): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135539525 | |||||
| chrX:135539709
|
C | A | 1 | a0001c0001t0001g0095 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.190-5714C>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135539709 | ||||||
| chrX:135539939
|
C | G | 19 | a0001c0001t0001g0011a0001c0001t0001g0095a0001c0001t0001g0096others(16): Show | 22 | HG00741.hp2 HG01192.hp1 HG02080.hp1 others(19): Show |
intron_variant | MODIFIER | c.190-5484C>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135539939 | ||||||
| chrX:135540530
|
T | TC | 1 | a0001c0001t0002g0052 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.190-4891dupC | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135540530 | |||||
| chrX:135540615
|
A | G | 1 | a0001c0001t0002g0051 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.190-4808A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135540615 | ||||||
| chrX:135540680
|
TC | T | 1 | a0001c0001t0001g0176 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.190-4739delC | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135540680 | |||||
| chrX:135540704
|
A | C | 3 | a0001c0002t0001g0079a0001c0002t0001g0086a0001c0002t0001g0214 | 3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.190-4719A>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135540704 | ||||||
| chrX:135540716
|
G | GCTC | 189 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(186): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.190-4685_190-4683d others(5): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135540716 | |||||
| chrX:135540716
|
G | GCTCCTC | 1 | a0001c0002t0001g0082 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.190-4688_190-4683d others(8): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135540716 | |||||
| chrX:135540716
|
GCTC | G | 1 | a0001c0001t0001g0154 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.190-4685_190-4683d others(5): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135540716 | |||||
| chrX:135540883
|
T | TC | 1 | a0001c0001t0001g0100 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.190-4537dupC | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135540883 | |||||
| chrX:135540932
|
AC | A | 1 | a0001c0001t0002g0052 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.190-4488delC | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135540932 | |||||
| chrX:135541115
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.190-4308A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135541115 | ||||||
| chrX:135541149
|
G | C | 2 | a0001c0001t0001g0145a0001c0001t0001g0210 | 2 | HG01256.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.190-4274G>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135541149 | ||||||
| chrX:135541178
|
G | T | 1 | a0001c0001t0001g0171 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.190-4245G>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135541178 | ||||||
| chrX:135541900
|
C | A | 3 | a0001c0002t0001g0079a0001c0002t0001g0086a0001c0002t0001g0214 | 3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.190-3523C>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135541900 | ||||||
| chrX:135542303
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.190-3120C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135542303 | ||||||
| chrX:135542308
|
G | A | 3 | a0001c0002t0001g0079a0001c0002t0001g0086a0001c0002t0001g0214 | 3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.190-3115G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135542308 | ||||||
| chrX:135542373
|
T | C | 191 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(188): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.190-3050T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135542373 | ||||||
| chrX:135542395
|
G | A | 28 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0009others(25): Show | 32 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.190-3028G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135542395 | ||||||
| chrX:135542553
|
GGGAA | G | 13 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0077others(10): Show | 15 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.190-2849_190-2846d others(6): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135542553 | |||||
| chrX:135543066
|
C | G | 1 | a0001c0001t0001g0093 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.190-2357C>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135543066 | ||||||
| chrX:135543098
|
A | G | 1 | a0001c0001t0001g0170 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.190-2325A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135543098 | ||||||
| chrX:135543150
|
T | C | 1 | a0001c0001t0002g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.190-2273T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135543150 | ||||||
| chrX:135543533
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.190-1890A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135543533 | ||||||
| chrX:135543602
|
C | T | 3 | a0001c0001t0001g0103a0001c0001t0001g0143a0001c0001t0001g0152 | 3 | NA18951.hp1 NA19001.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.190-1821C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135543602 | ||||||
| chrX:135543766
|
T | A | 1 | a0001c0001t0001g0177 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.190-1657T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135543766 | ||||||
| chrX:135543940
|
C | T | 1 | a0001c0002t0001g0078 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.190-1483C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135543940 | ||||||
| chrX:135544292
|
C | T | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.190-1131C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135544292 | ||||||
| chrX:135544322
|
C | A | 1 | a0001c0002t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.190-1101C>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135544322 | ||||||
| chrX:135544338
|
G | A | 27 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0009others(24): Show | 31 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.190-1085G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135544338 | ||||||
| chrX:135544353
|
A | C | 2 | a0001c0001t0001g0104a0001c0001t0001g0118 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.190-1070A>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135544353 | ||||||
| chrX:135544363
|
T | A | 5 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0160others(2): Show | 6 | HG03017.hp1 NA18948.hp1 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.190-1060T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135544363 | ||||||
| chrX:135544742
|
A | G | 1 | a0001c0002t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.190-681A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135544742 | ||||||
| chrX:135544925
|
C | G | 163 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(160): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.190-498C>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135544925 | ||||||
| chrX:135545583
|
T | A | 5 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0178others(2): Show | 5 | HG02280.hp1 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.339+11T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 3/17 | chrX | 135545583 | ||||||
| chrX:135545844
|
A | T | 1 | a0001c0001t0001g0151 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.339+272A>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 3/17 | chrX | 135545844 | ||||||
| chrX:135545932
|
T | A | 28 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0009others(25): Show | 32 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.339+360T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 3/17 | chrX | 135545932 | ||||||
| chrX:135546032
|
GT | G | 1 | a0001c0001t0002g0052 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.340-347delT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 3/17 | chrX | 135546032 | ||||||
| chrX:135546136
|
G | A | 1 | a0001c0001t0001g0170 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.340-244G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 3/17 | chrX | 135546136 | ||||||
| chrX:135546480
|
AT | A | 1 | a0001c0001t0002g0045 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.429+21delT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chrX | 135546480 | |||||
| chrX:135546607
|
T | C | 1 | a0001c0001t0001g0136 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.430-95T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 4/17 | chrX | 135546607 | ||||||
| chrX:135546616
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.430-86A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 4/17 | chrX | 135546616 | ||||||
| chrX:135546893
|
C | T | 3 | a0001c0002t0001g0079a0001c0002t0001g0086a0001c0002t0001g0214 | 3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
splice_region_variant&intron_variant | LOW | c.613+8C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 5/17 | chrX | 135546893 | ||||||
| chrX:135547314
|
G | A | 1 | a0001c0001t0001g0181 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.742+49G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 6/17 | chrX | 135547314 | ||||||
| chrX:135547587
|
C | T | 3 | a0001c0002t0001g0079a0001c0002t0001g0086a0001c0002t0001g0214 | 3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.742+322C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 6/17 | chrX | 135547587 | ||||||
| chrX:135548039
|
G | T | 151 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(148): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.742+774G>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 6/17 | chrX | 135548039 | ||||||
| chrX:135548047
|
G | GTATA | 2 | a0001c0002t0001g0003a0001c0002t0001g0082 | 4 | HG01884.hp1 HG02970.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.742+799_742+802dup others(4): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chrX | 135548047 | |||||
| chrX:135548047
|
G | GTATATA | 3 | a0001c0002t0001g0081a0001c0002t0001g0084a0001c0002t0001g0085 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.742+797_742+802dup others(6): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chrX | 135548047 | |||||
| chrX:135548047
|
GTA | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(127): Show | 147 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(144): Show |
intron_variant | MODIFIER | c.742+801_742+802del others(2): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chrX | 135548047 | |||||
| chrX:135548161
|
T | C | 1 | a0001c0001t0001g0103 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.742+896T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 6/17 | chrX | 135548161 | ||||||
| chrX:135548367
|
G | A | 3 | a0001c0002t0001g0079a0001c0002t0001g0086a0001c0002t0001g0214 | 3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.742+1102G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 6/17 | chrX | 135548367 | ||||||
| chrX:135548505
|
C | A | 1 | a0001c0002t0001g0083 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.743-1137C>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 6/17 | chrX | 135548505 | ||||||
| chrX:135548639
|
A | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(151): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.743-1003A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 6/17 | chrX | 135548639 | ||||||
| chrX:135548721
|
C | T | 3 | a0001c0002t0001g0079a0001c0002t0001g0086a0001c0002t0001g0214 | 3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.743-921C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 6/17 | chrX | 135548721 | ||||||
| chrX:135548783
|
A | G | 1 | a0001c0001t0001g0136 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.743-859A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 6/17 | chrX | 135548783 | ||||||
| chrX:135549218
|
A | G | 28 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0009others(25): Show | 32 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.743-424A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 6/17 | chrX | 135549218 | ||||||
| chrX:135549224
|
A | G | 213 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(210): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.743-418A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 6/17 | chrX | 135549224 | ||||||
| chrX:135549939
|
A | G | 163 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(160): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.906+134A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 7/17 | chrX | 135549939 | ||||||
| chrX:135550026
|
G | A | 1 | a0001c0002t0001g0031 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.906+221G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 7/17 | chrX | 135550026 | ||||||
| chrX:135550127
|
G | T | 26 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0009others(23): Show | 30 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.906+322G>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 7/17 | chrX | 135550127 | ||||||
| chrX:135550370
|
C | T | 1 | a0001c0001t0001g0168 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.906+565C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 7/17 | chrX | 135550370 | ||||||
| chrX:135550430
|
C | CT | 159 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(156): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.906+641dupT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chrX | 135550430 | |||||
| chrX:135550430
|
C | CTT | 4 | a0001c0001t0001g0023a0001c0001t0001g0120a0001c0001t0001g0190others(1): Show | 4 | HG00735.hp1 HG02145.hp1 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.906+640_906+641dup others(2): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chrX | 135550430 | |||||
| chrX:135550430
|
CT | C | 27 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0009others(24): Show | 31 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.906+641delT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chrX | 135550430 | |||||
| chrX:135550584
|
C | G | 3 | a0001c0002t0001g0079a0001c0002t0001g0086a0001c0002t0001g0214 | 3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.906+779C>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 7/17 | chrX | 135550584 | ||||||
| chrX:135550779
|
C | CG | 1 | a0001c0001t0002g0052 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.906+975dupG | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chrX | 135550779 | |||||
| chrX:135550844
|
G | A | 1 | a0001c0003t0001g0064 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.906+1039G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 7/17 | chrX | 135550844 | ||||||
| chrX:135550949
|
T | TC | 1 | a0001c0001t0002g0052 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.907-1045_907-1044i others(3): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 7/17 | chrX | 135550949 | ||||||
| chrX:135550950
|
T | A | 1 | a0001c0001t0002g0052 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.907-1044T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 7/17 | chrX | 135550950 | ||||||
| chrX:135550951
|
C | T | 1 | a0001c0001t0002g0052 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.907-1043C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 7/17 | chrX | 135550951 | ||||||
| chrX:135550976
|
G | GA | 1 | a0001c0002t0001g0041 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.907-1012dupA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chrX | 135550976 | |||||
| chrX:135551899
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.907-95A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 7/17 | chrX | 135551899 | ||||||
| chrX:135551977
|
TA | T | 1 | a0001c0001t0002g0052 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.907-11delA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chrX | 135551977 | |||||
| chrX:135551983
|
A | T | 12 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0077others(9): Show | 14 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.907-11A>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 7/17 | chrX | 135551983 | ||||||
| chrX:135551983
|
AT | A | 1 | a0006c0009t0001g0025 | 1 | NA19078.hp1 | splice_region_variant&intron_variant | LOW | c.907-3delT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chrX | 135551983 | |||||
| chrX:135552298
|
G | A | 27 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0009others(24): Show | 31 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.1059+152G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135552298 | ||||||
| chrX:135552527
|
A | G | 1 | a0001c0001t0001g0189 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1059+381A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135552527 | ||||||
| chrX:135552599
|
T | C | 11 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0077others(8): Show | 13 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1059+453T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135552599 | ||||||
| chrX:135552601
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1059+455G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135552601 | ||||||
| chrX:135552613
|
A | C | 5 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0129others(2): Show | 7 | HG00099.hp2 HG00140.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.1059+467A>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135552613 | ||||||
| chrX:135552682
|
A | G | 1 | a0001c0001t0002g0054 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1059+536A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135552682 | ||||||
| chrX:135553168
|
C | CAG | 28 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0009others(25): Show | 32 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1059+1030_1059+103 others(6): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chrX | 135553168 | |||||
| chrX:135553168
|
CAGAG | C | 1 | a0001c0001t0001g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1059+1028_1059+103 others(8): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chrX | 135553168 | |||||
| chrX:135553222
|
TG | T | 1 | a0001c0001t0001g0141 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1059+1082delG | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chrX | 135553222 | |||||
| chrX:135553280
|
CT | C | 1 | a0006c0009t0001g0025 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1059+1137delT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chrX | 135553280 | |||||
| chrX:135553427
|
C | G | 2 | a0001c0001t0001g0113a0001c0001t0001g0135 | 2 | HG03669.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1059+1281C>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135553427 | ||||||
| chrX:135553481
|
A | AT | 2 | a0001c0001t0001g0096a0001c0002t0001g0035 | 2 | NA18991.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1059+1358dupT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chrX | 135553481 | |||||
| chrX:135553481
|
A | ATCTTT | 1 | a0001c0001t0001g0168 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1059+1336_1059+133 others(9): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chrX | 135553481 | |||||
| chrX:135553481
|
AT | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0176a0001c0001t0001g0188others(1): Show | 6 | NA18954.hp2 NA18974.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1059+1358delT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chrX | 135553481 | |||||
| chrX:135553481
|
ATT | A | 1 | a0001c0001t0001g0182 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1059+1357_1059+135 others(6): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chrX | 135553481 | |||||
| chrX:135553482
|
T | TC | 9 | a0001c0001t0001g0107a0001c0001t0001g0123a0001c0001t0001g0135others(6): Show | 9 | HG01099.hp1 HG02040.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1059+1336_1059+133 others(5): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135553482 | ||||||
| chrX:135553483
|
T | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0012others(137): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.1059+1337T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135553483 | ||||||
| chrX:135553485
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1059+1339T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135553485 | ||||||
| chrX:135553512
|
C | T | 1 | a0001c0002t0001g0026 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1059+1366C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135553512 | ||||||
| chrX:135553619
|
G | A | 1 | a0001c0001t0001g0143 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1059+1473G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135553619 | ||||||
| chrX:135553647
|
C | A | 1 | a0001c0001t0001g0161 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1059+1501C>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135553647 | ||||||
| chrX:135553919
|
T | C | 166 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(163): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.1059+1773T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135553919 | ||||||
| chrX:135554118
|
C | T | 14 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0024others(11): Show | 16 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.1059+1972C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135554118 | ||||||
| chrX:135554310
|
A | T | 1 | a0001c0001t0001g0061 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1060-1858A>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135554310 | ||||||
| chrX:135554409
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1060-1759A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135554409 | ||||||
| chrX:135554575
|
G | C | 1 | a0002c0004t0001g0183 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1060-1593G>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135554575 | ||||||
| chrX:135554640
|
G | A | 166 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(163): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.1060-1528G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135554640 | ||||||
| chrX:135554883
|
C | CT | 46 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(43): Show | 53 | HG00621.hp1 HG00639.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.1060-1260dupT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chrX | 135554883 | |||||
| chrX:135554883
|
C | CTT | 17 | a0001c0001t0001g0113a0001c0001t0001g0153a0001c0001t0001g0159others(14): Show | 19 | HG00741.hp2 HG01070.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.1060-1261_1060-126 others(6): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chrX | 135554883 | |||||
| chrX:135554883
|
C | CTTT | 126 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(123): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.1060-1262_1060-126 others(7): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chrX | 135554883 | |||||
| chrX:135554883
|
C | CTTTT | 20 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0061others(17): Show | 22 | HG00609.hp1 HG01358.hp1 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.1060-1263_1060-126 others(8): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chrX | 135554883 | |||||
| chrX:135554977
|
A | T | 14 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0024others(11): Show | 16 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.1060-1191A>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135554977 | ||||||
| chrX:135555312
|
G | GA | 1 | a0001c0001t0001g0136 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1060-847dupA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chrX | 135555312 | |||||
| chrX:135555720
|
G | A | 1 | a0001c0007t0001g0130 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1060-448G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135555720 | ||||||
| chrX:135555732
|
AG | A | 1 | a0006c0009t0001g0025 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1060-433delG | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chrX | 135555732 | |||||
| chrX:135555764
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1060-404C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135555764 | ||||||
| chrX:135556031
|
T | C | 5 | a0001c0001t0002g0002a0001c0001t0002g0044a0001c0001t0002g0052others(2): Show | 7 | NA18946.hp1 NA18947.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.1060-137T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135556031 | ||||||
| chrX:135556390
|
G | A | 3 | a0001c0002t0001g0079a0001c0002t0001g0086a0001c0002t0001g0214 | 3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1192+90G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135556390 | ||||||
| chrX:135556549
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1192+249C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135556549 | ||||||
| chrX:135556574
|
TG | T | 1 | a0006c0009t0001g0025 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1192+276delG | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135556574 | |||||
| chrX:135556655
|
C | G | 1 | a0001c0003t0001g0069 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1192+355C>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135556655 | ||||||
| chrX:135556830
|
TG | T | 1 | a0006c0009t0001g0025 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1192+532delG | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135556830 | |||||
| chrX:135556902
|
A | G | 28 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0009others(25): Show | 32 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1192+602A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135556902 | ||||||
| chrX:135556903
|
G | T | 1 | a0001c0002t0001g0083 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1192+603G>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135556903 | ||||||
| chrX:135557114
|
AT | A | 1 | a0006c0009t0001g0025 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1192+818delT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135557114 | |||||
| chrX:135557266
|
T | G | 1 | a0001c0001t0001g0175 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1192+966T>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135557266 | ||||||
| chrX:135557349
|
A | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(151): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.1192+1049A>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135557349 | ||||||
| chrX:135557426
|
A | C | 1 | a0006c0009t0001g0025 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1192+1126A>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135557426 | ||||||
| chrX:135557526
|
A | G | 11 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0077others(8): Show | 13 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1192+1226A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135557526 | ||||||
| chrX:135558178
|
A | AT | 1 | a0006c0009t0001g0025 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1192+1879dupT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135558178 | |||||
| chrX:135558180
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1192+1880C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135558180 | ||||||
| chrX:135558226
|
T | A | 1 | a0001c0001t0001g0216 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1192+1926T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135558226 | ||||||
| chrX:135558281
|
C | A | 28 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0009others(25): Show | 32 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1192+1981C>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135558281 | ||||||
| chrX:135558390
|
A | G | 3 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0198 | 3 | HG02451.hp1 HG02572.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1192+2090A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135558390 | ||||||
| chrX:135558552
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1192+2252A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135558552 | ||||||
| chrX:135558584
|
A | G | 1 | a0001c0001t0004g0074 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1192+2284A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135558584 | ||||||
| chrX:135558785
|
TTC | T | 1 | a0006c0009t0001g0025 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1192+2487_1192+248 others(6): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135558785 | |||||
| chrX:135558787
|
C | CT | 7 | a0001c0001t0001g0021a0001c0001t0001g0105a0001c0001t0001g0121others(4): Show | 8 | HG01167.hp1 HG02055.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1192+2503dupT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135558787 | |||||
| chrX:135558787
|
CT | C | 3 | a0001c0001t0001g0172a0001c0002t0001g0009a0001c0002t0001g0083 | 4 | HG02258.hp1 HG03540.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.1192+2503delT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135558787 | |||||
| chrX:135558788
|
T | C | 1 | a0006c0009t0001g0025 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1192+2488T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135558788 | ||||||
| chrX:135558933
|
G | A | 14 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0024others(11): Show | 16 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.1192+2633G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135558933 | ||||||
| chrX:135559003
|
G | A | 28 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0009others(25): Show | 32 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1192+2703G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135559003 | ||||||
| chrX:135559108
|
TA | T | 1 | a0006c0009t0001g0025 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1192+2814delA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135559108 | |||||
| chrX:135559181
|
A | G | 28 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0009others(25): Show | 32 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1192+2881A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135559181 | ||||||
| chrX:135559244
|
A | AC | 1 | a0006c0009t0001g0025 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1192+2946dupC | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135559244 | |||||
| chrX:135559252
|
G | A | 28 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0009others(25): Show | 32 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1192+2952G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135559252 | ||||||
| chrX:135559308
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1192+3008T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135559308 | ||||||
| chrX:135559327
|
A | AC | 1 | a0006c0009t0001g0025 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1192+3028dupC | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135559327 | |||||
| chrX:135559604
|
AT | A | 1 | a0006c0009t0001g0025 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1192+3307delT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135559604 | |||||
| chrX:135559686
|
TG | T | 1 | a0001c0002t0001g0027 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1192+3387delG | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135559686 | ||||||
| chrX:135559749
|
T | G | 1 | a0001c0001t0002g0045 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1192+3449T>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135559749 | ||||||
| chrX:135559819
|
T | TA | 1 | a0006c0009t0001g0025 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1192+3523dupA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135559819 | |||||
| chrX:135559905
|
A | AT | 1 | a0006c0009t0001g0025 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1192+3606dupT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135559905 | |||||
| chrX:135560057
|
G | A | 28 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0009others(25): Show | 32 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1192+3757G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135560057 | ||||||
| chrX:135560065
|
C | A | 2 | a0001c0001t0002g0053a0001c0001t0002g0054 | 2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1192+3765C>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135560065 | ||||||
| chrX:135560214
|
G | T | 12 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0077others(9): Show | 14 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1192+3914G>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135560214 | ||||||
| chrX:135560375
|
T | C | 153 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(150): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.1192+4075T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135560375 | ||||||
| chrX:135560395
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1192+4095T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135560395 | ||||||
| chrX:135560458
|
T | C | 4 | a0001c0001t0001g0120a0001c0001t0001g0200a0001c0001t0001g0201others(1): Show | 4 | HG00735.hp1 HG01074.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.1192+4158T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135560458 | ||||||
| chrX:135560558
|
T | C | 1 | a0001c0003t0001g0071 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1192+4258T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135560558 | ||||||
| chrX:135560667
|
AC | A | 1 | a0006c0009t0001g0025 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1192+4370delC | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135560667 | |||||
| chrX:135560759
|
A | G | 193 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(190): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1192+4459A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135560759 | ||||||
| chrX:135560769
|
G | A | 4 | a0001c0001t0001g0147a0001c0001t0001g0151a0001c0001t0001g0184others(1): Show | 4 | HG01496.hp2 HG01943.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1192+4469G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135560769 | ||||||
| chrX:135560801
|
GC | G | 1 | a0006c0009t0001g0025 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1192+4503delC | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135560801 | |||||
| chrX:135560937
|
C | CT | 3 | a0001c0001t0001g0159a0001c0001t0001g0165a0001c0001t0001g0191 | 3 | HG00639.hp1 HG01070.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.1192+4649dupT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135560937 | |||||
| chrX:135560958
|
T | C | 1 | a0006c0009t0001g0025 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1192+4658T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135560958 | ||||||
| chrX:135560959
|
C | CT | 168 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(165): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.1192+4670dupT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135560959 | |||||
| chrX:135560959
|
C | CTT | 3 | a0001c0001t0001g0127a0001c0001t0001g0177a0001c0001t0001g0207 | 3 | NA19030.hp1 NA19079.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1192+4669_1192+467 others(6): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135560959 | |||||
| chrX:135560959
|
C | T | 1 | a0006c0009t0001g0025 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1192+4659C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135560959 | ||||||
| chrX:135561065
|
G | GC | 1 | a0006c0009t0001g0025 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1192+4767dupC | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135561065 | |||||
| chrX:135561363
|
TC | T | 1 | a0006c0009t0001g0025 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1192+5066delC | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135561363 | |||||
| chrX:135561392
|
C | T | 11 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0077others(8): Show | 13 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1192+5092C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135561392 | ||||||
| chrX:135561582
|
GA | G | 1 | a0006c0009t0001g0025 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1192+5286delA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135561582 | |||||
| chrX:135561657
|
TA | T | 1 | a0006c0009t0001g0025 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1192+5360delA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135561657 | |||||
| chrX:135561821
|
A | G | 193 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(190): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1192+5521A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135561821 | ||||||
| chrX:135561891
|
C | G | 1 | a0001c0001t0001g0212 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1192+5591C>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135561891 | ||||||
| chrX:135562012
|
TA | T | 1 | a0001c0003t0001g0204 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1192+5716delA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135562012 | |||||
| chrX:135562013
|
A | T | 152 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(149): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.1192+5713A>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135562013 | ||||||
| chrX:135562066
|
CTTTTT | C | 28 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0009others(25): Show | 32 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1192+5768_1192+577 others(9): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135562066 | |||||
| chrX:135562140
|
T | C | 153 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(150): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.1192+5840T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135562140 | ||||||
| chrX:135562196
|
T | C | 28 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0009others(25): Show | 32 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1192+5896T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135562196 | ||||||
| chrX:135562316
|
C | CT | 1 | a0006c0009t0001g0025 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1192+6021dupT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135562316 | |||||
| chrX:135562328
|
A | G | 12 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0077others(9): Show | 14 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1192+6028A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135562328 | ||||||
| chrX:135562486
|
G | A | 12 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0077others(9): Show | 14 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1192+6186G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135562486 | ||||||
| chrX:135562777
|
T | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(162): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.1192+6477T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135562777 | ||||||
| chrX:135562955
|
T | G | 1 | a0001c0003t0001g0065 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1193-6382T>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135562955 | ||||||
| chrX:135563341
|
C | T | 1 | a0001c0001t0002g0051 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1193-5996C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135563341 | ||||||
| chrX:135563584
|
C | CAT | 152 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(149): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.1193-5744_1193-574 others(6): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135563584 | |||||
| chrX:135563619
|
A | ATGTG | 3 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0094 | 3 | HG01123.hp1 HG02615.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1193-5706_1193-570 others(8): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135563619 | |||||
| chrX:135563619
|
A | ATGTGTG | 5 | a0001c0001t0001g0010a0001c0001t0001g0077a0001c0001t0001g0088others(2): Show | 6 | HG02280.hp2 HG02717.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1193-5708_1193-570 others(10): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135563619 | |||||
| chrX:135563619
|
A | ATGTGTGT others(1): Show |
2 | a0001c0001t0001g0008a0001c0001t0001g0087 | 3 | HG01884.hp2 HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1193-5710_1193-570 others(12): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135563619 | |||||
| chrX:135563619
|
A | G | 3 | a0001c0002t0001g0079a0001c0002t0001g0086a0001c0002t0001g0214 | 3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1193-5718A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135563619 | ||||||
| chrX:135563619
|
ATGTG | A | 7 | a0001c0002t0001g0027a0001c0002t0001g0032a0001c0002t0001g0034others(4): Show | 7 | HG00673.hp1 HG02602.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1193-5706_1193-570 others(8): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135563619 | |||||
| chrX:135563629
|
G | GTA | 2 | a0001c0002t0001g0030a0001c0003t0001g0036 | 2 | HG02056.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1193-5707_1193-570 others(6): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135563629 | |||||
| chrX:135563631
|
G | A | 19 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0026others(16): Show | 22 | HG00621.hp1 HG01884.hp1 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.1193-5706G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135563631 | ||||||
| chrX:135563631
|
G | GTATA | 11 | a0001c0001t0001g0011a0001c0001t0001g0061a0001c0001t0001g0096others(8): Show | 12 | HG00741.hp2 HG01928.hp1 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.1193-5705_1193-570 others(8): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135563631 | |||||
| chrX:135563631
|
G | GTATATA | 2 | a0001c0001t0001g0095a0001c0001t0002g0045 | 2 | HG01192.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.1193-5705_1193-570 others(10): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135563631 | |||||
| chrX:135563631
|
G | GTATATAT others(1): Show |
5 | a0001c0001t0002g0002a0001c0001t0002g0044a0001c0001t0002g0052others(2): Show | 7 | NA18946.hp1 NA18947.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.1193-5705_1193-570 others(12): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135563631 | |||||
| chrX:135563633
|
G | A | 39 | a0001c0001t0001g0011a0001c0001t0001g0061a0001c0001t0001g0095others(36): Show | 45 | HG00621.hp1 HG00741.hp2 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.1193-5704G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135563633 | ||||||
| chrX:135563633
|
G | GTGTGTGT others(3): Show |
2 | a0001c0001t0001g0089a0001c0001t0001g0091 | 2 | HG00639.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1193-5703_1193-570 others(14): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135563633 | |||||
| chrX:135563635
|
A | G | 161 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(158): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.1193-5702A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135563635 | ||||||
| chrX:135563637
|
A | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(148): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.1193-5700A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135563637 | ||||||
| chrX:135563639
|
A | G | 5 | a0001c0001t0001g0092a0001c0001t0001g0157a0001c0001t0001g0169others(2): Show | 5 | HG00099.hp2 HG01261.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1193-5698A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135563639 | ||||||
| chrX:135563645
|
ATATATAT others(19): Show |
A | 147 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(144): Show | 166 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1193-5681_1193-565 others(30): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135563645 | |||||
| chrX:135563647
|
ATATATAT others(17): Show |
A | 3 | a0001c0001t0001g0157a0001c0001t0001g0169a0001c0001t0001g0213 | 3 | HG00099.hp2 HG02523.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1193-5675_1193-565 others(28): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135563647 | |||||
| chrX:135563655
|
ATAGCTAT others(9): Show |
A | 2 | a0001c0002t0001g0028a0001c0002t0001g0033 | 2 | HG02074.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.1193-5679_1193-566 others(20): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135563655 | |||||
| chrX:135563657
|
AGC | A | 25 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0009others(22): Show | 29 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.1193-5679_1193-567 others(6): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135563657 | ||||||
| chrX:135563658
|
G | T | 16 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0077others(13): Show | 18 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1193-5679G>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135563658 | ||||||
| chrX:135563659
|
C | A | 16 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0077others(13): Show | 18 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1193-5678C>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135563659 | ||||||
| chrX:135563669
|
AGC | A | 12 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0026others(9): Show | 15 | HG00621.hp1 HG02602.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.1193-5667_1193-566 others(6): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135563669 | ||||||
| chrX:135563670
|
G | T | 29 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0077others(26): Show | 32 | HG00639.hp2 HG00673.hp1 HG01123.hp1 others(29): Show |
intron_variant | MODIFIER | c.1193-5667G>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135563670 | ||||||
| chrX:135563671
|
C | A | 29 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0077others(26): Show | 32 | HG00639.hp2 HG00673.hp1 HG01123.hp1 others(29): Show |
intron_variant | MODIFIER | c.1193-5666C>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135563671 | ||||||
| chrX:135563734
|
T | TG | 1 | a0001c0002t0001g0041 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1193-5602dupG | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135563734 | |||||
| chrX:135564004
|
C | CA | 1 | a0001c0002t0001g0041 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1193-5332dupA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135564004 | |||||
| chrX:135564145
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1193-5192T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135564145 | ||||||
| chrX:135564181
|
T | TC | 1 | a0001c0002t0001g0041 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1193-5152dupC | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135564181 | |||||
| chrX:135564244
|
A | G | 2 | a0001c0001t0001g0119a0001c0001t0001g0168 | 2 | HG02083.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1193-5093A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135564244 | ||||||
| chrX:135564307
|
TG | T | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-5029delG | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135564307 | ||||||
| chrX:135564347
|
G | GA | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-4987dupA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135564347 | |||||
| chrX:135564367
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1193-4970C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135564367 | ||||||
| chrX:135564372
|
TA | T | 1 | a0001c0002t0001g0041 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1193-4962delA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135564372 | |||||
| chrX:135564376
|
T | C | 12 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0077others(9): Show | 14 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1193-4961T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135564376 | ||||||
| chrX:135564453
|
C | CA | 1 | a0001c0002t0001g0041 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1193-4883dupA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135564453 | |||||
| chrX:135564584
|
T | C | 12 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0077others(9): Show | 14 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1193-4753T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135564584 | ||||||
| chrX:135564624
|
CG | C | 1 | a0001c0002t0001g0041 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1193-4710delG | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135564624 | |||||
| chrX:135564719
|
G | GGATGA | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-4618_1193-461 others(9): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135564719 | ||||||
| chrX:135564721
|
T | A | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-4616T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135564721 | ||||||
| chrX:135564722
|
A | C | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-4615A>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135564722 | ||||||
| chrX:135564731
|
C | CA | 7 | a0001c0001t0001g0040a0001c0001t0001g0116a0001c0001t0001g0180others(4): Show | 7 | HG02257.hp2 HG02723.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1193-4592dupA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135564731 | |||||
| chrX:135564731
|
C | CAA | 137 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(134): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.1193-4593_1193-459 others(6): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135564731 | |||||
| chrX:135564731
|
C | CAAA | 10 | a0001c0001t0001g0021a0001c0001t0001g0105a0001c0001t0001g0108others(7): Show | 11 | HG01167.hp1 HG02055.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1193-4594_1193-459 others(7): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135564731 | |||||
| chrX:135564731
|
CA | C | 13 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0077others(10): Show | 15 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1193-4592delA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135564731 | |||||
| chrX:135564806
|
A | G | 1 | a0001c0003t0001g0149 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1193-4531A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135564806 | ||||||
| chrX:135564851
|
T | TTA | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-4486_1193-448 others(6): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135564851 | ||||||
| chrX:135564920
|
TC | T | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-4415delC | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135564920 | |||||
| chrX:135565030
|
G | GGA | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-4306_1193-430 others(6): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135565030 | |||||
| chrX:135565226
|
G | GA | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-4111_1193-411 others(5): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135565226 | ||||||
| chrX:135565226
|
G | GC | 1 | a0001c0002t0001g0041 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1193-4110dupC | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135565226 | |||||
| chrX:135565251
|
T | TG | 1 | a0001c0002t0001g0041 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1193-4085dupG | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135565251 | |||||
| chrX:135565295
|
C | CT | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-4039dupT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135565295 | |||||
| chrX:135565303
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1193-4034G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135565303 | ||||||
| chrX:135565316
|
TG | T | 1 | a0001c0002t0001g0041 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1193-4019delG | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135565316 | |||||
| chrX:135565369
|
A | AT | 1 | a0001c0002t0001g0041 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1193-3967dupT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135565369 | |||||
| chrX:135565396
|
A | G | 3 | a0001c0002t0001g0079a0001c0002t0001g0086a0001c0002t0001g0214 | 3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1193-3941A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135565396 | ||||||
| chrX:135565423
|
T | TG | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-3912dupG | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135565423 | |||||
| chrX:135565474
|
T | TG | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-3862dupG | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135565474 | |||||
| chrX:135565622
|
GC | G | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-3713delC | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135565622 | |||||
| chrX:135565655
|
G | GC | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-3679dupC | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135565655 | |||||
| chrX:135565696
|
A | G | 12 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0077others(9): Show | 14 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1193-3641A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135565696 | ||||||
| chrX:135565710
|
C | G | 12 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0077others(9): Show | 14 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1193-3627C>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135565710 | ||||||
| chrX:135565750
|
TG | T | 1 | a0001c0002t0001g0041 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1193-3585delG | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135565750 | |||||
| chrX:135565774
|
A | C | 1 | a0001c0001t0001g0092 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1193-3563A>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135565774 | ||||||
| chrX:135565785
|
G | GA | 1 | a0001c0002t0001g0041 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1193-3549dupA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135565785 | |||||
| chrX:135565875
|
C | CCTG | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-3462_1193-346 others(7): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135565875 | ||||||
| chrX:135565877
|
G | C | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-3460G>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135565877 | ||||||
| chrX:135565939
|
A | AG | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-3395dupG | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135565939 | |||||
| chrX:135566041
|
A | G | 28 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0009others(25): Show | 32 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1193-3296A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135566041 | ||||||
| chrX:135566072
|
T | TG | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-3265_1193-326 others(5): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135566072 | ||||||
| chrX:135566078
|
G | A | 1 | a0001c0001t0001g0138 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1193-3259G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135566078 | ||||||
| chrX:135566116
|
G | GT | 1 | a0001c0002t0001g0041 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1193-3220dupT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135566116 | |||||
| chrX:135566213
|
T | TG | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-3123dupG | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135566213 | |||||
| chrX:135566436
|
G | GT | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-2900dupT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135566436 | |||||
| chrX:135566505
|
GT | G | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-2831delT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135566505 | ||||||
| chrX:135566600
|
A | AC | 1 | a0001c0002t0001g0041 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1193-2736dupC | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135566600 | |||||
| chrX:135566670
|
A | AC | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-2665dupC | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135566670 | |||||
| chrX:135566758
|
AC | A | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-2577delC | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135566758 | |||||
| chrX:135566783
|
A | AT | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-2551dupT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135566783 | |||||
| chrX:135566794
|
C | CT | 1 | a0001c0002t0001g0041 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1193-2534dupT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135566794 | |||||
| chrX:135566805
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1193-2532G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135566805 | ||||||
| chrX:135566842
|
T | C | 1 | a0001c0002t0001g0027 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1193-2495T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135566842 | ||||||
| chrX:135566893
|
TA | T | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-2440delA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135566893 | |||||
| chrX:135566910
|
AG | A | 1 | a0001c0001t0001g0136 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1193-2425delG | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135566910 | |||||
| chrX:135566926
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1193-2411G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135566926 | ||||||
| chrX:135566934
|
A | AG | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-2402dupG | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135566934 | |||||
| chrX:135566950
|
G | A | 1 | a0001c0001t0001g0188 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1193-2387G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135566950 | ||||||
| chrX:135566951
|
C | A | 1 | a0001c0001t0001g0188 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1193-2386C>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135566951 | ||||||
| chrX:135566999
|
C | CT | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-2336dupT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135566999 | |||||
| chrX:135567101
|
AT | A | 1 | a0001c0001t0001g0136 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1193-2232delT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135567101 | |||||
| chrX:135567113
|
A | AG | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-2224_1193-222 others(5): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135567113 | ||||||
| chrX:135567122
|
C | G | 3 | a0001c0001t0001g0103a0001c0001t0001g0143a0001c0001t0001g0152 | 3 | NA18951.hp1 NA19001.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1193-2215C>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135567122 | ||||||
| chrX:135567193
|
T | TC | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-2141dupC | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135567193 | |||||
| chrX:135567215
|
T | TG | 1 | a0001c0001t0001g0136 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1193-2118dupG | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135567215 | |||||
| chrX:135567221
|
G | GA | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-2113dupA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135567221 | |||||
| chrX:135567230
|
TG | T | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-2105delG | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135567230 | |||||
| chrX:135567257
|
A | AG | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-2078dupG | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135567257 | |||||
| chrX:135567272
|
C | T | 3 | a0001c0001t0001g0103a0001c0001t0001g0143a0001c0001t0001g0152 | 3 | NA18951.hp1 NA19001.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1193-2065C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135567272 | ||||||
| chrX:135567301
|
T | C | 165 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(162): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.1193-2036T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135567301 | ||||||
| chrX:135567429
|
AG | A | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-1906delG | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135567429 | |||||
| chrX:135567434
|
G | GA | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-1903_1193-190 others(5): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135567434 | ||||||
| chrX:135567498
|
TC | T | 1 | a0001c0001t0001g0136 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1193-1836delC | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135567498 | |||||
| chrX:135567551
|
GA | G | 1 | a0001c0001t0001g0136 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1193-1784delA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135567551 | |||||
| chrX:135567644
|
G | GT | 1 | a0001c0001t0001g0136 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1193-1690dupT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135567644 | |||||
| chrX:135567687
|
A | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(162): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.1193-1650A>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135567687 | ||||||
| chrX:135567689
|
A | C | 165 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(162): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.1193-1648A>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135567689 | ||||||
| chrX:135567810
|
CA | C | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-1523delA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135567810 | |||||
| chrX:135567822
|
A | AT | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-1511dupT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135567822 | |||||
| chrX:135567822
|
AT | A | 1 | a0001c0001t0001g0136 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1193-1511delT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135567822 | |||||
| chrX:135567894
|
AG | A | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-1441delG | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135567894 | |||||
| chrX:135568010
|
A | AT | 1 | a0001c0001t0001g0144 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1193-1319dupT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135568010 | |||||
| chrX:135568010
|
AT | A | 1 | a0005c0008t0001g0029 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1193-1319delT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135568010 | |||||
| chrX:135568018
|
T | A | 3 | a0001c0001t0001g0139a0001c0001t0001g0185a0001c0003t0001g0058 | 3 | HG02148.hp2 HG02523.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.1193-1319T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135568018 | ||||||
| chrX:135568019
|
A | T | 4 | a0001c0001t0001g0147a0001c0002t0001g0079a0001c0002t0001g0086others(1): Show | 4 | HG02257.hp2 HG02300.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1193-1318A>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135568019 | ||||||
| chrX:135568160
|
G | GT | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-1170dupT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135568160 | |||||
| chrX:135568175
|
T | C | 1 | a0001c0001t0001g0161 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1193-1162T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135568175 | ||||||
| chrX:135568247
|
T | TA | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-1087dupA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135568247 | |||||
| chrX:135568291
|
AT | A | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-1041delT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135568291 | |||||
| chrX:135568469
|
T | TA | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-858dupA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135568469 | |||||
| chrX:135568555
|
AT | A | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-780delT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135568555 | |||||
| chrX:135568582
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1193-755C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135568582 | ||||||
| chrX:135568589
|
A | AC | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-745dupC | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135568589 | |||||
| chrX:135568671
|
T | TC | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-662dupC | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135568671 | |||||
| chrX:135568790
|
T | G | 162 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(159): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.1193-547T>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135568790 | ||||||
| chrX:135568864
|
C | CT | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-471dupT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135568864 | |||||
| chrX:135568885
|
A | T | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-452A>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135568885 | ||||||
| chrX:135568886
|
T | A | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-451T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135568886 | ||||||
| chrX:135568891
|
G | T | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-446G>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135568891 | ||||||
| chrX:135569135
|
TA | T | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-200delA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135569135 | |||||
| chrX:135569183
|
T | G | 162 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(159): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.1193-154T>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135569183 | ||||||
| chrX:135569229
|
AT | A | 2 | a0001c0001t0001g0196a0001c0001t0001g0198 | 2 | HG02572.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1193-107delT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135569229 | ||||||
| chrX:135569265
|
A | C | 4 | a0001c0001t0002g0046a0001c0001t0002g0048a0001c0001t0002g0049others(1): Show | 4 | HG00741.hp2 NA18964.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1193-72A>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135569265 | ||||||
| chrX:135569275
|
T | TC | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-62_1193-61ins others(1): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135569275 | ||||||
| chrX:135569443
|
T | TG | 1 | a0004c0005t0001g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1287+13dupG | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chrX | 135569443 | |||||
| chrX:135570032
|
C | T | 3 | a0001c0002t0001g0079a0001c0002t0001g0086a0001c0002t0001g0214 | 3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1288-404C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 10/17 | chrX | 135570032 | ||||||
| chrX:135571110
|
C | A | 1 | a0001c0001t0001g0148 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1398+564C>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 11/17 | chrX | 135571110 | ||||||
| chrX:135571731
|
T | A | 1 | a0001c0002t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1399-1084T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 11/17 | chrX | 135571731 | ||||||
| chrX:135571934
|
T | A | 1 | a0001c0001t0001g0089 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1399-881T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 11/17 | chrX | 135571934 | ||||||
| chrX:135571963
|
A | G | 1 | a0001c0001t0002g0046 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1399-852A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 11/17 | chrX | 135571963 | ||||||
| chrX:135572344
|
G | T | 26 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0009others(23): Show | 30 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.1399-471G>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 11/17 | chrX | 135572344 | ||||||
| chrX:135572586
|
T | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(151): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.1399-229T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 11/17 | chrX | 135572586 | ||||||
| chrX:135572605
|
GAAAA | G | 1 | a0001c0001t0001g0121 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1399-204_1399-201d others(6): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chrX | 135572605 | |||||
| chrX:135572671
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1399-144G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 11/17 | chrX | 135572671 | ||||||
| chrX:135572678
|
G | A | 27 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0009others(24): Show | 31 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.1399-137G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 11/17 | chrX | 135572678 | ||||||
| chrX:135573523
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1618-416G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 12/17 | chrX | 135573523 | ||||||
| chrX:135573526
|
T | G | 1 | a0001c0001t0001g0186 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1618-413T>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 12/17 | chrX | 135573526 | ||||||
| chrX:135573698
|
CG | C | 1 | a0003c0006t0002g0047 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1618-238delG | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chrX | 135573698 | |||||
| chrX:135573839
|
G | A | 1 | a0001c0001t0001g0103 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1618-100G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 12/17 | chrX | 135573839 | ||||||
| chrX:135573843
|
T | C | 2 | a0001c0001t0001g0163a0001c0001t0001g0213 | 2 | HG02735.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1618-96T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 12/17 | chrX | 135573843 | ||||||
| chrX:135574082
|
C | CT | 15 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0077others(12): Show | 17 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1741+35dupT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chrX | 135574082 | |||||
| chrX:135574082
|
CT | C | 6 | a0001c0001t0001g0123a0001c0001t0001g0164a0001c0001t0001g0166others(3): Show | 6 | HG01167.hp1 NA18956.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.1741+35delT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chrX | 135574082 | |||||
| chrX:135574166
|
T | C | 12 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0077others(9): Show | 14 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1741+104T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 13/17 | chrX | 135574166 | ||||||
| chrX:135574219
|
A | AT | 1 | a0001c0002t0001g0030 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1741+167dupT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chrX | 135574219 | |||||
| chrX:135574704
|
T | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(190): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1742-380T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 13/17 | chrX | 135574704 | ||||||
| chrX:135574792
|
G | C | 1 | a0005c0008t0001g0029 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1742-292G>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 13/17 | chrX | 135574792 | ||||||
| chrX:135574818
|
A | AG | 1 | a0003c0006t0002g0047 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1742-263dupG | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chrX | 135574818 | |||||
| chrX:135574915
|
T | G | 1 | a0001c0001t0001g0206 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1742-169T>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 13/17 | chrX | 135574915 | ||||||
| chrX:135574919
|
TG | T | 1 | a0003c0006t0002g0047 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1742-162delG | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chrX | 135574919 | |||||
| chrX:135575390
|
G | T | 1 | a0001c0002t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1884+164G>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/17 | chrX | 135575390 | ||||||
| chrX:135575644
|
G | A | 163 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(160): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.1884+418G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/17 | chrX | 135575644 | ||||||
| chrX:135575785
|
A | AGT | 156 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(153): Show | 177 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.1884+582_1884+583d others(4): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chrX | 135575785 | |||||
| chrX:135575785
|
A | AGTGT | 4 | a0001c0001t0001g0075a0001c0001t0001g0087a0001c0001t0001g0089others(1): Show | 4 | HG00099.hp1 HG00639.hp2 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.1884+580_1884+583d others(6): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chrX | 135575785 | |||||
| chrX:135575785
|
A | AGTGTGT | 1 | a0001c0001t0001g0216 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1884+578_1884+583d others(8): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chrX | 135575785 | |||||
| chrX:135575785
|
AGT | A | 49 | a0001c0001t0001g0011a0001c0001t0001g0061a0001c0001t0001g0095others(46): Show | 56 | HG00621.hp1 HG00673.hp1 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.1884+582_1884+583d others(4): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chrX | 135575785 | |||||
| chrX:135575808
|
G | GTGTGTA | 1 | a0001c0003t0001g0036 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1884+583_1884+584i others(8): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chrX | 135575808 | |||||
| chrX:135575810
|
A | G | 1 | a0001c0003t0001g0036 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1884+584A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/17 | chrX | 135575810 | ||||||
| chrX:135575992
|
A | G | 6 | a0001c0001t0001g0004a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 8 | HG00609.hp1 NA18947.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.1884+766A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/17 | chrX | 135575992 | ||||||
| chrX:135576024
|
G | A | 163 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(160): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.1884+798G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/17 | chrX | 135576024 | ||||||
| chrX:135576083
|
C | T | 213 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(210): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.1884+857C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/17 | chrX | 135576083 | ||||||
| chrX:135576327
|
C | CA | 21 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0077others(18): Show | 23 | HG00639.hp2 HG01123.hp1 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.1885-848dupA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chrX | 135576327 | |||||
| chrX:135576327
|
C | CAA | 136 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(133): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1885-849_1885-848d others(4): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chrX | 135576327 | |||||
| chrX:135576327
|
C | CAAA | 7 | a0001c0001t0001g0123a0001c0001t0001g0129a0001c0001t0001g0139others(4): Show | 7 | HG00140.hp1 HG02148.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.1885-850_1885-848d others(5): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chrX | 135576327 | |||||
| chrX:135576391
|
A | C | 1 | a0001c0001t0001g0135 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1885-802A>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/17 | chrX | 135576391 | ||||||
| chrX:135576396
|
C | T | 193 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(190): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1885-797C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/17 | chrX | 135576396 | ||||||
| chrX:135576685
|
G | GA | 213 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(210): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.1885-507dupA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chrX | 135576685 | |||||
| chrX:135576688
|
G | T | 213 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(210): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.1885-505G>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/17 | chrX | 135576688 | ||||||
| chrX:135576690
|
G | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(210): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.1885-503G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/17 | chrX | 135576690 | ||||||
| chrX:135577053
|
AT | A | 12 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0077others(9): Show | 14 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1885-137delT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chrX | 135577053 | |||||
| chrX:135577862
|
C | T | 2 | a0001c0001t0002g0053a0001c0001t0002g0054 | 2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2119+435C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 15/17 | chrX | 135577862 | ||||||
| chrX:135578011
|
G | A | 3 | a0001c0002t0001g0079a0001c0002t0001g0086a0001c0002t0001g0214 | 3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2119+584G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 15/17 | chrX | 135578011 | ||||||
| chrX:135578041
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2119+614C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 15/17 | chrX | 135578041 | ||||||
| chrX:135578074
|
T | A | 193 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(190): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.2119+647T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 15/17 | chrX | 135578074 | ||||||
| chrX:135578165
|
G | A | 4 | a0001c0001t0001g0107a0001c0001t0001g0131a0001c0001t0001g0156others(1): Show | 4 | HG03490.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.2119+738G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 15/17 | chrX | 135578165 | ||||||
| chrX:135578169
|
T | A | 1 | a0001c0001t0001g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2119+742T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 15/17 | chrX | 135578169 | ||||||
| chrX:135578531
|
G | GT | 1 | a0001c0001t0001g0100 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2119+1105dupT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chrX | 135578531 | |||||
| chrX:135578616
|
T | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(151): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.2120-1172T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 15/17 | chrX | 135578616 | ||||||
| chrX:135579271
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2120-517A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 15/17 | chrX | 135579271 | ||||||
| chrX:135579480
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2120-308C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 15/17 | chrX | 135579480 | ||||||
| chrX:135579498
|
T | A | 193 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(190): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.2120-290T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 15/17 | chrX | 135579498 | ||||||
| chrX:135580243
|
C | G | 4 | a0001c0002t0001g0030a0001c0002t0001g0031a0001c0002t0001g0037others(1): Show | 4 | HG00621.hp1 HG02056.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.2494+81C>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 16/17 | chrX | 135580243 | ||||||
| chrX:135580358
|
A | T | 1 | a0001c0001t0002g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2494+196A>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 16/17 | chrX | 135580358 | ||||||
| chrX:135580609
|
CT | C | 1 | a0001c0001t0001g0206 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2495-436delT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chrX | 135580609 | |||||
| chrX:135580671
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2495-379C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 16/17 | chrX | 135580671 | ||||||
| chrX:135580973
|
C | G | 1 | a0001c0002t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2495-77C>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 16/17 | chrX | 135580973 | ||||||
| chrX:135581037
|
T | A | 27 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0009others(24): Show | 31 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.2495-13T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 16/17 | chrX | 135581037 | ||||||
| chrX:135581349
|
G | A | 73 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0013others(70): Show | 81 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.2589-179G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 17/17 | chrX | 135581349 | ||||||
| chrX:135581367
|
A | G | 3 | a0001c0002t0001g0079a0001c0002t0001g0086a0001c0002t0001g0214 | 3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2589-161A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 17/17 | chrX | 135581367 | ||||||
| chrX:135581485
|
CT | C | 1 | a0001c0001t0004g0074 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2589-40delT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chrX | 135581485 |