geneid | 55787 |
---|---|
ensemblid | ENSG00000086712.13 |
hgncid | 18578 |
symbol | TXLNG |
name | taxilin gamma |
refseq_nuc | NM_018360.3 |
refseq_prot | NP_060830.2 |
ensembl_nuc | ENST00000380122.10 |
ensembl_prot | ENSP00000369465.5 |
mane_status | MANE Select |
chr | chrX |
start | 16786466 |
end | 16844519 |
strand | + |
ver | v1.2 |
region | chrX:16786466-16844519 |
region5000 | chrX:16781466-16849519 |
regionname0 | TXLNG_chrX_16786466_16844519 |
regionname5000 | TXLNG_chrX_16781466_16849519 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 528 | 257 | 61 | 51 | 106 | 11 | 26 | 83 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0002 | 0/0 | 528 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0003 | 0/0 | 528 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0004 | 0/0 | 428 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0005 | 0/0 | 528 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0006 | 0/0 | 528 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1587 | 191 | 47 | 35 | 92 | 4 | 12 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
c0002 | 1/0 | 1587 | 59 | 7 | 16 | 14 | 7 | 14 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
c0003 | 0/0 | 1587 | 3 | 3 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
c0004 | 0/0 | 1587 | 3 | 3 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
c0005 | 0/0 | 1587 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
c0006 | 0/0 | 1587 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
c0007 | 0/0 | 1586 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
c0008 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
c0009 | 0/0 | 1587 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
c0010 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2776 | 83 | 10 | 19 | 47 | 3 | 4 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
t0002 | 1/0 | 2776 | 52 | 4 | 16 | 13 | 6 | 12 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
t0003 | 0/0 | 2775 | 49 | 12 | 8 | 25 | 1 | 3 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
t0004 | 0/0 | 2777 | 17 | 2 | 4 | 10 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
t0005 | 0/0 | 2775 | 8 | 6 | 1 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
t0006 | 0/0 | 2775 | 7 | 7 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
t0007 | 0/0 | 2778 | 5 | 0 | 0 | 3 | 0 | 2 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
t0008 | 0/0 | 2776 | 4 | 4 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
t0009 | 0/0 | 2776 | 4 | 3 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
t0010 | 0/0 | 2751 | 3 | 2 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
t0011 | 0/0 | 2779 | 2 | 0 | 0 | 1 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
t0012 | 0/0 | 2774 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
t0013 | 0/0 | 2776 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
t0014 | 0/0 | 2778 | 2 | 0 | 0 | 0 | 0 | 2 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
t0015 | 0/0 | 2775 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
t0016 | 0/0 | 2776 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
t0017 | 0/0 | 2776 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
t0018 | 0/1 | 2776 | 1 | 0 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
t0019 | 0/0 | 2776 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
t0020 | 0/0 | 2776 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
t0021 | 0/0 | 2777 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
t0022 | 0/0 | 2775 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
t0023 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
t0024 | 0/0 | 2775 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
t0025 | 0/0 | 2775 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
t0026 | 0/0 | 2775 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
t0027 | 0/0 | 2775 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
t0028 | 0/0 | 2775 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
t0029 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
t0030 | 0/0 | 2775 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
t0031 | 0/0 | 2775 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
t0032 | 0/0 | 2776 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
t0033 | 0/0 | 2799 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
t0034 | 0/0 | 2776 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
t0035 | 0/0 | 2776 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
t0036 | 0/0 | 2776 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
t0037 | 0/0 | 2776 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
t0038 | 0/0 | 2777 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0155 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0207 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1587 | 191 | 47 | 35 | 92 | 4 | 12 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0002 | 1/0 | 1587 | 59 | 7 | 16 | 14 | 7 | 14 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0004 | 0/0 | 1587 | 3 | 3 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0005 | 0/0 | 1587 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0006 | 0/0 | 1587 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0002c0003 | 0/0 | 1587 | 3 | 3 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0003c0008 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0004c0007 | 0/0 | 1586 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0005c0009 | 0/0 | 1587 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0006c0010 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4362 | 81 | 10 | 18 | 46 | 3 | 4 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0001t0003 | 0/0 | 4361 | 47 | 10 | 8 | 25 | 1 | 3 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0001t0004 | 0/0 | 4363 | 17 | 2 | 4 | 10 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0001t0005 | 0/0 | 4361 | 8 | 6 | 1 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0001t0006 | 0/0 | 4361 | 6 | 6 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0001t0007 | 0/0 | 4364 | 5 | 0 | 0 | 3 | 0 | 2 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0001t0008 | 0/0 | 4362 | 4 | 4 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0001t0010 | 0/0 | 4337 | 3 | 2 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0001t0011 | 0/0 | 4365 | 2 | 0 | 0 | 1 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0001t0012 | 0/0 | 4360 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0001t0015 | 0/0 | 4361 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0001t0016 | 0/0 | 4362 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0001t0017 | 0/0 | 4362 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0001t0018 | 0/1 | 4362 | 1 | 0 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0001t0019 | 0/0 | 4362 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0001t0020 | 0/0 | 4362 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0001t0021 | 0/0 | 4363 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0001t0022 | 0/0 | 4361 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0001t0024 | 0/0 | 4361 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0001t0025 | 0/0 | 4361 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0001t0026 | 0/0 | 4361 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0001t0027 | 0/0 | 4361 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0001t0028 | 0/0 | 4361 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0001t0029 | 0/0 | 4364 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0001t0030 | 0/0 | 4361 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0001t0031 | 0/0 | 4361 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0002t0001 | 0/0 | 4362 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0002t0002 | 1/0 | 4362 | 49 | 2 | 15 | 13 | 6 | 12 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0002t0009 | 0/0 | 4362 | 3 | 2 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0002t0013 | 0/0 | 4362 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0002t0014 | 0/0 | 4364 | 2 | 0 | 0 | 0 | 0 | 2 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0002t0036 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0002t0037 | 0/0 | 4362 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0004t0032 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0004t0033 | 0/0 | 4385 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0004t0034 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0005t0006 | 0/0 | 4361 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0005t0023 | 0/0 | 4364 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0001c0006t0002 | 0/0 | 4362 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0002c0003t0003 | 0/0 | 4361 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0002c0003t0035 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0003c0008t0009 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0004c0007t0001 | 0/0 | 4361 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0005c0009t0002 | 0/0 | 4362 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
a0006c0010t0038 | 0/0 | 4363 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | copy fasta | chrX | 16781466 | 16849519 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0004g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0004g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0004g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0004g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0005g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0005g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0005g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0006g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0006g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0006g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0006g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0006g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0007g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0007g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0007g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0007g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0007g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0008g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0008g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0008g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0008g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0010g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0010g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0010g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0011g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0011g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0012g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0012g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0015g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0016g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0017g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0018g0207 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0019g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0020g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0021g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0022g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0024g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0025g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0026g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0027g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0028g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0029g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0030g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0001t0031g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0155 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0009g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0009g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0009g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0013g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0013g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0014g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0014g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0036g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0002t0037g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0004t0032g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0004t0033g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0004t0034g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0005t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0005t0023g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0006t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0001c0006t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0002c0003t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0002c0003t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0002c0003t0035g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0003c0008t0009g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0004c0007t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0005c0009t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
a0006c0010t0038g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0002 | t0002 | g0049 | EUR | GBR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0152 | EUR | FIN | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG00323 | hp1 | a0001 | c0002 | t0002 | g0059 | EUR | FIN | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0196 | EUR | FIN | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG00438 | hp1 | a0001 | c0001 | t0005 | g0163 | EAS | CHS | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG00544 | hp1 | a0001 | c0001 | t0007 | g0097 | EAS | CHS | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0165 | EAS | CHS | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | CHS | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | CHS | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0128 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0135 | EAS | CHS | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG00733 | hp1 | a0001 | c0002 | t0002 | g0034 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0167 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG00738 | hp1 | a0001 | c0002 | t0002 | g0040 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG00741 | hp1 | a0001 | c0002 | t0002 | g0067 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG00741 | hp2 | a0005 | c0009 | t0002 | g0068 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01070 | hp1 | a0001 | c0001 | t0005 | g0020 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01070 | hp2 | a0001 | c0001 | t0004 | g0109 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01071 | hp2 | a0001 | c0001 | t0004 | g0108 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01074 | hp1 | a0001 | c0002 | t0002 | g0047 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0133 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01106 | hp1 | a0001 | c0001 | t0021 | g0114 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01109 | hp1 | a0001 | c0001 | t0010 | g0234 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01167 | hp1 | a0001 | c0002 | t0002 | g0033 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0138 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01169 | hp1 | a0001 | c0002 | t0002 | g0038 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0141 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0188 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01192 | hp1 | a0001 | c0002 | t0002 | g0259 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0209 | AMR | CLM | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | CLM | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01346 | hp2 | a0001 | c0002 | t0002 | g0066 | AMR | CLM | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01358 | hp1 | a0001 | c0001 | t0003 | g0148 | AMR | CLM | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01433 | hp1 | a0001 | c0002 | t0002 | g0026 | AMR | CLM | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0246 | EUR | IBS | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01516 | hp1 | a0001 | c0002 | t0002 | g0262 | EUR | IBS | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01516 | hp2 | a0001 | c0002 | t0002 | g0055 | EUR | IBS | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0233 | EUR | IBS | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01517 | hp2 | a0001 | c0002 | t0002 | g0261 | EUR | IBS | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01884 | hp1 | a0001 | c0004 | t0033 | g0012 | AFR | ACB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0161 | AFR | ACB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01928 | hp1 | a0001 | c0001 | t0004 | g0101 | AMR | PEL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01934 | hp1 | a0001 | c0001 | t0017 | g0221 | AMR | PEL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01943 | hp1 | a0001 | c0002 | t0002 | g0074 | AMR | PEL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01952 | hp1 | a0001 | c0001 | t0004 | g0175 | AMR | PEL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01975 | hp2 | a0001 | c0002 | t0002 | g0071 | AMR | PEL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01981 | hp2 | a0001 | c0002 | t0002 | g0042 | AMR | PEL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02004 | hp2 | a0001 | c0002 | t0002 | g0072 | AMR | PEL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02015 | hp1 | a0001 | c0001 | t0011 | g0111 | EAS | KHV | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02027 | hp1 | a0001 | c0002 | t0002 | g0057 | EAS | KHV | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | KHV | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02055 | hp1 | a0001 | c0005 | t0023 | g0025 | AFR | ACB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02071 | hp1 | a0001 | c0001 | t0004 | g0247 | EAS | KHV | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02080 | hp1 | a0001 | c0001 | t0016 | g0193 | EAS | KHV | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02080 | hp2 | a0001 | c0001 | t0004 | g0098 | EAS | KHV | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | KHV | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02129 | hp1 | a0001 | c0001 | t0004 | g0093 | EAS | KHV | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02145 | hp1 | a0001 | c0001 | t0010 | g0239 | AFR | ACB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02258 | hp1 | a0002 | c0003 | t0035 | g0160 | AFR | ACB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02280 | hp1 | a0003 | c0008 | t0009 | g0037 | AFR | ACB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0085 | AFR | ACB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02293 | hp1 | a0001 | c0001 | t0020 | g0091 | AMR | PEL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02293 | hp2 | a0001 | c0002 | t0002 | g0082 | AMR | PEL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02451 | hp1 | a0001 | c0005 | t0006 | g0024 | AFR | ACB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02451 | hp2 | a0006 | c0010 | t0038 | g0004 | AFR | ACB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | KHV | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02572 | hp1 | a0001 | c0001 | t0025 | g0088 | AFR | GWD | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02602 | hp1 | a0001 | c0002 | t0014 | g0007 | SAS | PJL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02622 | hp1 | a0001 | c0001 | t0005 | g0015 | AFR | GWD | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0134 | AFR | GWD | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02647 | hp1 | a0001 | c0001 | t0004 | g0181 | AFR | GWD | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02698 | hp1 | a0001 | c0001 | t0004 | g0102 | SAS | PJL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02717 | hp1 | a0001 | c0001 | t0008 | g0023 | AFR | GWD | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02735 | hp1 | a0001 | c0002 | t0002 | g0060 | SAS | PJL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0009 | SAS | PJL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | GWD | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0170 | AFR | GWD | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02818 | hp2 | a0001 | c0002 | t0002 | g0036 | AFR | GWD | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0086 | AFR | GWD | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02886 | hp2 | a0001 | c0002 | t0009 | g0030 | AFR | GWD | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02922 | hp1 | a0001 | c0001 | t0030 | g0169 | AFR | ESN | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02922 | hp2 | a0001 | c0001 | t0008 | g0063 | AFR | ESN | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02965 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | ESN | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02970 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | ESN | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02970 | hp2 | a0001 | c0001 | t0028 | g0130 | AFR | ESN | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02976 | hp2 | a0001 | c0001 | t0029 | g0016 | AFR | ESN | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG03017 | hp1 | a0001 | c0002 | t0002 | g0046 | SAS | PJL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG03041 | hp1 | a0001 | c0001 | t0024 | g0087 | AFR | GWD | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG03041 | hp2 | a0001 | c0006 | t0002 | g0027 | AFR | GWD | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0126 | AFR | MSL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG03195 | hp1 | a0001 | c0002 | t0009 | g0031 | AFR | ESN | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG03195 | hp2 | a0001 | c0001 | t0012 | g0173 | AFR | ESN | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0125 | AFR | MSL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG03225 | hp1 | a0001 | c0001 | t0006 | g0258 | AFR | MSL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG03239 | hp2 | a0001 | c0002 | t0002 | g0028 | SAS | PJL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG03453 | hp2 | a0001 | c0001 | t0005 | g0022 | AFR | MSL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0189 | AFR | MSL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG03486 | hp2 | a0001 | c0006 | t0002 | g0065 | AFR | MSL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG03490 | hp1 | a0001 | c0002 | t0002 | g0045 | SAS | PJL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG03491 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG03492 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0260 | AFR | ESN | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG03516 | hp2 | a0001 | c0001 | t0008 | g0080 | AFR | ESN | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG03540 | hp1 | a0001 | c0002 | t0013 | g0052 | AFR | GWD | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG03540 | hp2 | a0001 | c0001 | t0010 | g0235 | AFR | GWD | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG03579 | hp1 | a0001 | c0001 | t0012 | g0089 | AFR | MSL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG03654 | hp1 | a0001 | c0001 | t0022 | g0184 | SAS | PJL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG03688 | hp1 | a0001 | c0001 | t0007 | g0124 | SAS | STU | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG03710 | hp1 | a0001 | c0002 | t0002 | g0070 | SAS | PJL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG03831 | hp1 | a0001 | c0001 | t0011 | g0010 | SAS | BEB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG03831 | hp2 | a0001 | c0002 | t0014 | g0075 | SAS | BEB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | BEB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG03834 | hp2 | a0001 | c0002 | t0002 | g0048 | SAS | BEB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0183 | SAS | BEB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG03927 | hp2 | a0001 | c0002 | t0002 | g0076 | SAS | BEB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG03942 | hp1 | a0001 | c0002 | t0002 | g0069 | SAS | BEB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | STU | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG04199 | hp1 | a0001 | c0001 | t0007 | g0180 | SAS | STU | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0158 | SAS | STU | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG04228 | hp1 | a0001 | c0002 | t0002 | g0078 | SAS | STU | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | YRI | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | CHB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0186 | EAS | CHB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18906 | hp1 | a0001 | c0001 | t0008 | g0079 | AFR | YRI | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18906 | hp2 | a0002 | c0003 | t0003 | g0187 | AFR | YRI | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18945 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18947 | hp2 | a0001 | c0002 | t0002 | g0056 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18951 | hp1 | a0001 | c0002 | t0009 | g0084 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18951 | hp2 | a0001 | c0001 | t0031 | g0147 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18952 | hp1 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18956 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18963 | hp2 | a0001 | c0002 | t0002 | g0058 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18964 | hp1 | a0001 | c0002 | t0002 | g0083 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18968 | hp1 | a0001 | c0001 | t0004 | g0219 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18969 | hp2 | a0001 | c0001 | t0004 | g0171 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18971 | hp1 | a0001 | c0001 | t0026 | g0149 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18972 | hp1 | a0001 | c0001 | t0015 | g0192 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18972 | hp2 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18974 | hp1 | a0001 | c0001 | t0019 | g0129 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18977 | hp1 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18980 | hp1 | a0001 | c0001 | t0007 | g0176 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18988 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19002 | hp2 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19005 | hp1 | a0001 | c0001 | t0004 | g0103 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19009 | hp1 | a0001 | c0001 | t0027 | g0131 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19010 | hp1 | a0001 | c0002 | t0002 | g0073 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19012 | hp1 | a0001 | c0001 | t0004 | g0174 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19030 | hp1 | a0001 | c0004 | t0034 | g0013 | AFR | LWK | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19030 | hp2 | a0001 | c0001 | t0006 | g0081 | AFR | LWK | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19043 | hp1 | a0001 | c0002 | t0002 | g0032 | AFR | LWK | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19055 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19057 | hp2 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19060 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19066 | hp1 | a0001 | c0001 | t0004 | g0177 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19068 | hp1 | a0001 | c0001 | t0004 | g0099 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19080 | hp1 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19082 | hp1 | a0001 | c0001 | t0007 | g0105 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19083 | hp1 | a0004 | c0007 | t0001 | g0240 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19086 | hp1 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19240 | hp1 | a0001 | c0001 | t0005 | g0019 | AFR | YRI | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA19240 | hp2 | a0001 | c0001 | t0006 | g0006 | AFR | YRI | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA20129 | hp1 | a0001 | c0001 | t0004 | g0092 | AFR | ASW | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA20129 | hp2 | a0001 | c0001 | t0006 | g0257 | AFR | ASW | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA20752 | hp1 | a0001 | c0002 | t0037 | g0043 | EUR | TSI | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA20805 | hp1 | a0001 | c0002 | t0002 | g0061 | EUR | TSI | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA20905 | hp1 | a0001 | c0002 | t0002 | g0044 | SAS | GIH | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG01123 | hp2 | a0001 | c0002 | t0002 | g0054 | AMR | CLM | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02109 | hp2 | a0001 | c0001 | t0006 | g0064 | AFR | ACB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02559 | hp1 | a0001 | c0004 | t0032 | g0014 | AFR | ACB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG02559 | hp2 | a0001 | c0002 | t0013 | g0053 | AFR | ACB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0162 | AFR | MSL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | USA | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
HG06807 | hp2 | a0002 | c0003 | t0003 | g0090 | AFR | USA | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA18955 | hp1 | a0001 | c0001 | t0004 | g0106 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA21309 | hp1 | a0001 | c0001 | t0005 | g0021 | AFR | LWK | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
NA21309 | hp2 | a0001 | c0002 | t0036 | g0039 | AFR | LWK | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0018 | g0207 | REF | REF | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0155 | REF | REF | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
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:16786504
|
A | G | 1 | a0006 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.17A>G | p.Glu6Gly | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/10 | 39/4362 | 17/1587 | 6/528 | chrX | 16786504 | ||
chrX:16786510
|
C | T | 1 | a0005 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.23C>T | p.Ala8Val | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/10 | 45/4362 | 23/1587 | 8/528 | chrX | 16786510 | ||
chrX:16839875
|
TG | T | 1 | a0004 | 1 | NA19083.hp1 | frameshift_variant | HIGH | c.1210delG | p.Glu404fs | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 9/10 | 1232/4362 | 1210/1587 | 404/528 | INFO_REALIGN_3_PRIME | chrX | 16839875 | |
chrX:16841706
|
A | C | 1 | a0002 | 3 | HG02258.hp1 HG06807.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.1527A>C | p.Arg509Ser | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 1549/4362 | 1527/1587 | 509/528 | chrX | 16841706 | ||
chrX:16841744
|
C | T | 1 | a0003 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.1565C>T | p.Pro522Leu | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 1587/4362 | 1565/1587 | 522/528 | chrX | 16841744 |
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:16786538
|
A | G | 1 | a0001c0004 | 3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
synonymous_variant | LOW | c.51A>G | p.Glu17Glu | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/10 | 73/4362 | 51/1587 | 17/528 | chrX | 16786538 | ||
chrX:16841505
|
G | A | 6 | a0001c0001a0001c0004a0001c0005others(3): Show | 201 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(198): Show |
synonymous_variant | LOW | c.1326G>A | p.Gln442Gln | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 1348/4362 | 1326/1587 | 442/528 | chrX | 16841505 | ||
chrX:16841544
|
G | C | 1 | a0001c0005 | 2 | HG02055.hp1 HG02451.hp1 |
synonymous_variant | LOW | c.1365G>C | p.Leu455Leu | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 1387/4362 | 1365/1587 | 455/528 | chrX | 16841544 | ||
chrX:16841559
|
C | T | 1 | a0001c0006 | 2 | HG03041.hp2 HG03486.hp2 |
synonymous_variant | LOW | c.1380C>T | p.Ser460Ser | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 1402/4362 | 1380/1587 | 460/528 | chrX | 16841559 |
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:16842011
|
T | C | 14 | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(11): Show | 117 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*245T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 245 | chrX | 16842011 | |||||
chrX:16842079
|
G | T | 1 | a0001c0001t0021 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*313G>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 313 | chrX | 16842079 | |||||
chrX:16842130
|
A | G | 1 | a0001c0001t0020 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*364A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 364 | chrX | 16842130 | |||||
chrX:16842150
|
G | GC | 4 | a0001c0001t0004a0001c0001t0019a0001c0001t0021others(1): Show | 20 | HG01070.hp2 HG01071.hp2 HG01106.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*395dupC | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 396 | INFO_REALIGN_3_PRIME | chrX | 16842150 | ||||
chrX:16842150
|
G | GCC | 2 | a0001c0001t0007a0001c0002t0014 | 7 | HG00544.hp1 HG02602.hp1 HG03688.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*394_*395dupCC | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 396 | INFO_REALIGN_3_PRIME | chrX | 16842150 | ||||
chrX:16842150
|
G | GCCC | 1 | a0001c0001t0011 | 2 | HG02015.hp1 HG03831.hp1 |
3_prime_UTR_variant | MODIFIER | c.*393_*395dupCCC | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 396 | INFO_REALIGN_3_PRIME | chrX | 16842150 | ||||
chrX:16842150
|
GC | G | 15 | a0001c0001t0003a0001c0001t0005a0001c0001t0006others(12): Show | 74 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*395delC | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 395 | INFO_REALIGN_3_PRIME | chrX | 16842150 | ||||
chrX:16842150
|
GCC | G | 1 | a0001c0001t0012 | 2 | HG03195.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*394_*395delCC | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 394 | INFO_REALIGN_3_PRIME | chrX | 16842150 | ||||
chrX:16842373
|
C | T | 1 | a0001c0001t0031 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*607C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 607 | chrX | 16842373 | |||||
chrX:16842431
|
G | A | 1 | a0001c0001t0022 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*665G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 665 | chrX | 16842431 | |||||
chrX:16842551
|
TC | T | 1 | a0001c0001t0015 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*788delC | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 788 | INFO_REALIGN_3_PRIME | chrX | 16842551 | ||||
chrX:16842604
|
A | G | 1 | a0001c0001t0012 | 2 | HG03195.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*838A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 838 | chrX | 16842604 | |||||
chrX:16842607
|
A | C | 1 | a0001c0002t0037 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*841A>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 841 | chrX | 16842607 | |||||
chrX:16842749
|
C | T | 1 | a0001c0002t0036 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*983C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 983 | chrX | 16842749 | |||||
chrX:16842765
|
C | T | 1 | a0001c0001t0010 | 3 | HG01109.hp1 HG02145.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*999C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 999 | chrX | 16842765 | |||||
chrX:16842790
|
A | G | 28 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(25): Show | 186 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*1024A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 1024 | chrX | 16842790 | |||||
chrX:16842992
|
T | C | 1 | a0001c0004t0032 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1226T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 1226 | chrX | 16842992 | |||||
chrX:16843225
|
AG | A | 1 | a0001c0001t0019 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1462delG | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 1462 | INFO_REALIGN_3_PRIME | chrX | 16843225 | ||||
chrX:16843321
|
T | C | 2 | a0001c0001t0024a0001c0001t0025 | 2 | HG02572.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1555T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 1555 | chrX | 16843321 | |||||
chrX:16843370
|
T | C | 32 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(29): Show | 193 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*1604T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 1604 | chrX | 16843370 | |||||
chrX:16843467
|
C | A | 29 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(26): Show | 182 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*1701C>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 1701 | chrX | 16843467 | |||||
chrX:16843509
|
C | T | 1 | a0001c0001t0025 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1743C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 1743 | chrX | 16843509 | |||||
chrX:16843574
|
C | G | 1 | a0001c0001t0018 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1808C>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 1808 | chrX | 16843574 | |||||
chrX:16843701
|
A | AGAT | 1 | a0001c0005t0023 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1936_*1938dupGAT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 1939 | INFO_REALIGN_3_PRIME | chrX | 16843701 | ||||
chrX:16843783
|
C | T | 1 | a0001c0001t0017 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2017C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 2017 | chrX | 16843783 | |||||
chrX:16843833
|
A | ATTCTGTC others(16): Show |
1 | a0001c0004t0033 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2069_*2091dupTCTG others(19): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 2092 | INFO_REALIGN_3_PRIME | chrX | 16843833 | ||||
chrX:16843923
|
T | C | 1 | a0006c0010t0038 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2157T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 2157 | chrX | 16843923 | |||||
chrX:16843978
|
G | A | 30 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(27): Show | 188 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(185): Show |
3_prime_UTR_variant | MODIFIER | c.*2212G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 2212 | chrX | 16843978 | |||||
chrX:16844063
|
TTGCACCA others(18): Show |
T | 1 | a0001c0001t0010 | 3 | HG01109.hp1 HG02145.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2299_*2323delGCAC others(21): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 2299 | INFO_REALIGN_3_PRIME | chrX | 16844063 | ||||
chrX:16844104
|
C | T | 1 | a0001c0001t0027 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2338C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 2338 | chrX | 16844104 | |||||
chrX:16844332
|
A | ATCT | 1 | a0001c0001t0029 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2570_*2572dupTCT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 2573 | INFO_REALIGN_3_PRIME | chrX | 16844332 | ||||
chrX:16844392
|
T | C | 5 | a0001c0001t0006a0001c0001t0008a0001c0002t0013others(2): Show | 14 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2626T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 2626 | chrX | 16844392 | |||||
chrX:16844486
|
G | A | 1 | a0001c0001t0026 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2720G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 2720 | chrX | 16844486 |
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:16786606
|
C | T | 2 | a0001c0002t0002g0261a0001c0002t0002g0262 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.102+17C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16786606 | ||||||
chrX:16786690
|
CG | C | 1 | a0001c0001t0001g0003 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.102+104delG | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16786690 | |||||
chrX:16786705
|
G | A | 1 | a0006c0010t0038g0004 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.102+116G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16786705 | ||||||
chrX:16786744
|
T | TG | 5 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0006g0005others(2): Show | 5 | HG01099.hp1 HG02602.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.102+164dupG | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16786744 | |||||
chrX:16786744
|
TG | T | 1 | a0001c0001t0003g0260 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.102+164delG | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16786744 | |||||
chrX:16786779
|
A | AG | 1 | a0001c0001t0001g0003 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.102+193dupG | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16786779 | |||||
chrX:16786833
|
A | AG | 1 | a0001c0001t0001g0003 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.102+249dupG | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16786833 | |||||
chrX:16786922
|
C | CG | 1 | a0001c0001t0001g0003 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.102+336dupG | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16786922 | |||||
chrX:16787125
|
G | GC | 1 | a0001c0001t0011g0010 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.102+542dupC | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16787125 | |||||
chrX:16787133
|
T | TC | 1 | a0001c0001t0001g0011 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.102+549dupC | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16787133 | |||||
chrX:16787209
|
C | CG | 2 | a0001c0001t0001g0003a0001c0002t0002g0259 | 2 | HG00438.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.102+623dupG | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16787209 | |||||
chrX:16787220
|
G | GC | 1 | a0001c0002t0002g0259 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.102+636dupC | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16787220 | |||||
chrX:16787271
|
C | CG | 1 | a0001c0001t0001g0003 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.102+686dupG | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16787271 | |||||
chrX:16787313
|
C | T | 2 | a0001c0001t0006g0257a0001c0001t0006g0258 | 2 | HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.102+724C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16787313 | ||||||
chrX:16787315
|
G | A | 3 | a0001c0004t0032g0014a0001c0004t0033g0012a0001c0004t0034g0013 | 3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.102+726G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16787315 | ||||||
chrX:16787378
|
CCT | C | 66 | a0001c0001t0001g0191a0001c0001t0001g0194a0001c0001t0001g0195others(63): Show | 66 | HG00323.hp2 HG00609.hp1 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.102+792_102+793del others(2): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16787378 | |||||
chrX:16787379
|
CT | C | 1 | a0001c0001t0001g0011 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.102+791delT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16787379 | ||||||
chrX:16787380
|
T | C | 1 | a0001c0001t0001g0003 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.102+791T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16787380 | ||||||
chrX:16787381
|
C | T | 1 | a0001c0001t0001g0003 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.102+792C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16787381 | ||||||
chrX:16787481
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.102+892C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16787481 | ||||||
chrX:16787575
|
A | G | 1 | a0001c0001t0001g0256 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.102+986A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16787575 | ||||||
chrX:16787630
|
C | CG | 2 | a0001c0001t0001g0003a0001c0001t0001g0011 | 2 | HG00438.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.102+1045dupG | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16787630 | |||||
chrX:16788056
|
G | A | 8 | a0001c0001t0005g0015a0001c0001t0005g0017a0001c0001t0005g0018others(5): Show | 8 | HG01070.hp1 HG02622.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.102+1467G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16788056 | ||||||
chrX:16788346
|
A | G | 1 | a0001c0001t0003g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.102+1757A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16788346 | ||||||
chrX:16788539
|
G | A | 84 | a0001c0001t0001g0029a0001c0001t0005g0015a0001c0001t0005g0017others(81): Show | 86 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.102+1950G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16788539 | ||||||
chrX:16788643
|
T | TA | 1 | a0001c0001t0011g0010 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.102+2061dupA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16788643 | |||||
chrX:16788667
|
G | GT | 24 | a0001c0001t0001g0011a0001c0001t0001g0178a0001c0001t0001g0179others(21): Show | 24 | HG01175.hp1 HG01175.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.102+2096dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16788667 | |||||
chrX:16788667
|
G | GTT | 2 | a0001c0001t0001g0003a0001c0001t0001g0255 | 2 | HG00438.hp2 HG00609.hp1 |
intron_variant | MODIFIER | c.102+2095_102+2096d others(4): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16788667 | |||||
chrX:16788667
|
G | GTTTT | 52 | a0001c0001t0001g0029a0001c0001t0005g0015a0001c0001t0006g0005others(49): Show | 53 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.102+2093_102+2096d others(6): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16788667 | |||||
chrX:16788667
|
G | GTTTTT | 25 | a0001c0001t0005g0017a0001c0001t0005g0018a0001c0001t0005g0019others(22): Show | 26 | HG00741.hp1 HG00741.hp2 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.102+2092_102+2096d others(7): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16788667 | |||||
chrX:16788667
|
G | GTTTTTT | 7 | a0001c0001t0005g0022a0001c0001t0006g0081a0001c0001t0008g0079others(4): Show | 7 | HG02293.hp2 HG03453.hp2 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.102+2091_102+2096d others(8): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16788667 | |||||
chrX:16788667
|
GT | G | 1 | a0001c0001t0001g0191 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.102+2096delT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16788667 | |||||
chrX:16788911
|
A | AC | 1 | a0001c0001t0011g0010 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.102+2325dupC | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16788911 | |||||
chrX:16788935
|
C | CG | 1 | a0001c0001t0001g0011 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.102+2349dupG | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16788935 | |||||
chrX:16788972
|
A | AT | 1 | a0001c0001t0001g0011 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.102+2390dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16788972 | |||||
chrX:16789082
|
C | CT | 1 | a0001c0001t0001g0003 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.102+2500dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16789082 | |||||
chrX:16789138
|
G | GAATTAA | 1 | a0001c0001t0011g0010 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.102+2552_102+2557d others(8): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16789138 | |||||
chrX:16789140
|
A | AT | 1 | a0001c0001t0001g0003 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.102+2553dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16789140 | |||||
chrX:16789205
|
T | C | 8 | a0001c0001t0005g0015a0001c0001t0005g0017a0001c0001t0005g0018others(5): Show | 8 | HG01070.hp1 HG02622.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.102+2616T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16789205 | ||||||
chrX:16789446
|
AT | A | 4 | a0001c0001t0008g0023a0001c0001t0008g0063a0001c0001t0008g0079others(1): Show | 4 | HG02717.hp1 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+2859delT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16789446 | |||||
chrX:16789477
|
C | G | 73 | a0001c0001t0001g0029a0001c0001t0006g0005a0001c0001t0006g0006others(70): Show | 75 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.102+2888C>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16789477 | ||||||
chrX:16789533
|
C | A | 3 | a0001c0001t0006g0064a0001c0005t0006g0024a0001c0005t0023g0025 | 3 | HG02055.hp1 HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.102+2944C>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16789533 | ||||||
chrX:16789658
|
T | TATGTAGA others(6): Show |
1 | a0001c0001t0003g0085 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.102+3070_102+3082d others(15): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16789658 | |||||
chrX:16789907
|
G | A | 1 | a0001c0001t0003g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.102+3318G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16789907 | ||||||
chrX:16790040
|
T | C | 84 | a0001c0001t0001g0029a0001c0001t0005g0015a0001c0001t0005g0017others(81): Show | 86 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.102+3451T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16790040 | ||||||
chrX:16790105
|
C | T | 1 | a0001c0002t0002g0062 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.102+3516C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16790105 | ||||||
chrX:16790108
|
AT | A | 1 | a0001c0001t0015g0192 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.102+3521delT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16790108 | |||||
chrX:16790314
|
C | T | 1 | a0001c0002t0002g0078 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.102+3725C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16790314 | ||||||
chrX:16790368
|
AT | A | 1 | a0001c0001t0001g0191 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.102+3787delT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16790368 | |||||
chrX:16790506
|
C | G | 2 | a0001c0002t0002g0060a0001c0002t0002g0061 | 2 | HG02735.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.102+3917C>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16790506 | ||||||
chrX:16790550
|
G | T | 1 | a0001c0001t0001g0248 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.102+3961G>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16790550 | ||||||
chrX:16790879
|
ATAC | A | 1 | a0001c0001t0001g0011 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.102+4294_102+4296d others(5): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16790879 | |||||
chrX:16790952
|
G | A | 2 | a0001c0001t0024g0087a0001c0001t0025g0088 | 2 | HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.102+4363G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16790952 | ||||||
chrX:16790984
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.102+4395C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16790984 | ||||||
chrX:16791212
|
TC | T | 1 | a0001c0001t0011g0010 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.102+4626delC | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16791212 | |||||
chrX:16791370
|
GAAGTA | G | 84 | a0001c0001t0001g0029a0001c0001t0005g0015a0001c0001t0005g0017others(81): Show | 86 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.102+4791_102+4795d others(7): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16791370 | |||||
chrX:16791409
|
T | A | 1 | a0001c0001t0012g0089 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.102+4820T>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16791409 | ||||||
chrX:16791423
|
C | T | 1 | a0001c0001t0004g0247 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.102+4834C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16791423 | ||||||
chrX:16791466
|
A | T | 3 | a0001c0004t0032g0014a0001c0004t0033g0012a0001c0004t0034g0013 | 3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.102+4877A>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16791466 | ||||||
chrX:16791674
|
T | C | 1 | a0001c0001t0001g0190 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.102+5085T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16791674 | ||||||
chrX:16791783
|
A | AC | 1 | a0001c0001t0011g0010 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.102+5196dupC | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16791783 | |||||
chrX:16792077
|
CA | C | 1 | a0001c0001t0011g0010 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.102+5491delA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16792077 | |||||
chrX:16792296
|
T | TAATTG | 1 | a0001c0001t0001g0011 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.102+5709_102+5713d others(7): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16792296 | |||||
chrX:16792332
|
GA | G | 1 | a0001c0001t0011g0010 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.102+5745delA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16792332 | |||||
chrX:16792372
|
C | G | 1 | a0001c0002t0002g0077 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.102+5783C>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16792372 | ||||||
chrX:16792428
|
TG | T | 3 | a0001c0002t0002g0059a0001c0002t0002g0076a0001c0002t0014g0075 | 3 | HG00323.hp1 HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.102+5840delG | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16792428 | ||||||
chrX:16792747
|
C | T | 12 | a0001c0002t0002g0002a0001c0002t0002g0056a0001c0002t0002g0057others(9): Show | 13 | HG01943.hp1 HG01975.hp2 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.102+6158C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16792747 | ||||||
chrX:16792978
|
T | TC | 1 | a0001c0001t0015g0192 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.102+6392dupC | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16792978 | |||||
chrX:16793098
|
C | CA | 3 | a0001c0001t0003g0009a0001c0001t0003g0085a0001c0002t0002g0026 | 3 | HG01433.hp1 HG02280.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.102+6523dupA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16793098 | |||||
chrX:16793098
|
CA | C | 3 | a0001c0001t0001g0191a0001c0001t0004g0171a0001c0001t0005g0022 | 3 | HG01256.hp1 HG03453.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.102+6523delA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16793098 | |||||
chrX:16793112
|
A | T | 2 | a0001c0002t0002g0054a0001c0002t0002g0055 | 2 | HG01123.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.102+6523A>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16793112 | ||||||
chrX:16793112
|
AG | A | 1 | a0001c0002t0009g0084 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.102+6524delG | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16793112 | ||||||
chrX:16793113
|
G | A | 58 | a0001c0001t0001g0029a0001c0002t0002g0001a0001c0002t0002g0002others(55): Show | 60 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.102+6524G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16793113 | ||||||
chrX:16793221
|
TG | T | 1 | a0001c0001t0015g0192 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.102+6635delG | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16793221 | |||||
chrX:16793415
|
T | TC | 1 | a0001c0001t0015g0192 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.102+6829dupC | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16793415 | |||||
chrX:16793485
|
CT | C | 4 | a0001c0001t0001g0011a0001c0001t0015g0192a0001c0006t0002g0027others(1): Show | 4 | HG02451.hp2 HG03041.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+6909delT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16793485 | |||||
chrX:16793502
|
GT | G | 1 | a0001c0001t0015g0192 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.102+6916delT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16793502 | |||||
chrX:16793647
|
C | CT | 1 | a0001c0001t0001g0246 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.102+7070dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16793647 | |||||
chrX:16793647
|
CT | C | 1 | a0001c0001t0001g0011 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.102+7070delT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16793647 | |||||
chrX:16793660
|
CT | C | 1 | a0001c0001t0015g0192 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.102+7080delT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16793660 | |||||
chrX:16793688
|
GT | G | 1 | a0001c0001t0015g0192 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.102+7101delT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16793688 | |||||
chrX:16793713
|
C | T | 1 | a0001c0001t0003g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.102+7124C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16793713 | ||||||
chrX:16793734
|
C | G | 1 | a0001c0001t0001g0191 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.102+7145C>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16793734 | ||||||
chrX:16793770
|
A | G | 81 | a0001c0001t0001g0029a0001c0001t0005g0015a0001c0001t0005g0017others(78): Show | 83 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.102+7181A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16793770 | ||||||
chrX:16793795
|
GC | G | 1 | a0001c0001t0015g0192 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.102+7208delC | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16793795 | |||||
chrX:16793801
|
A | AT | 1 | a0001c0001t0015g0192 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.102+7213dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16793801 | |||||
chrX:16793811
|
G | GT | 1 | a0001c0001t0015g0192 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.102+7230dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16793811 | |||||
chrX:16793820
|
C | CT | 1 | a0001c0001t0011g0010 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.102+7239dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16793820 | |||||
chrX:16793910
|
A | AG | 1 | a0001c0001t0015g0192 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.102+7321_102+7322i others(3): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16793910 | ||||||
chrX:16793933
|
GC | G | 1 | a0001c0001t0015g0192 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.102+7346delC | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16793933 | |||||
chrX:16793971
|
A | AT | 1 | a0001c0001t0015g0192 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.102+7384dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16793971 | |||||
chrX:16793989
|
T | G | 1 | a0001c0001t0015g0192 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.102+7400T>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16793989 | ||||||
chrX:16794043
|
C | T | 59 | a0001c0001t0001g0029a0001c0002t0002g0001a0001c0002t0002g0002others(56): Show | 61 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.102+7454C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16794043 | ||||||
chrX:16794083
|
AG | A | 1 | a0001c0001t0015g0192 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.102+7496delG | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16794083 | |||||
chrX:16794090
|
T | A | 1 | a0001c0001t0029g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.102+7501T>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16794090 | ||||||
chrX:16794131
|
T | TG | 1 | a0001c0001t0015g0192 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.102+7544dupG | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16794131 | |||||
chrX:16794185
|
T | TG | 1 | a0001c0001t0015g0192 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.102+7596_102+7597i others(3): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16794185 | ||||||
chrX:16794273
|
A | C | 1 | a0001c0001t0003g0170 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.102+7684A>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16794273 | ||||||
chrX:16794286
|
G | GT | 1 | a0001c0001t0015g0192 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.102+7702dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16794286 | |||||
chrX:16794481
|
T | G | 1 | a0002c0003t0003g0090 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.102+7892T>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16794481 | ||||||
chrX:16794536
|
ACTT | A | 73 | a0001c0001t0001g0029a0001c0001t0006g0005a0001c0001t0006g0006others(70): Show | 75 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.102+7951_102+7953d others(5): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16794536 | |||||
chrX:16794591
|
TG | T | 1 | a0001c0001t0003g0085 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.102+8006delG | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16794591 | |||||
chrX:16794659
|
T | G | 202 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0029others(199): Show | 204 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.102+8070T>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16794659 | ||||||
chrX:16794865
|
T | A | 1 | a0001c0002t0002g0028 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.102+8276T>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16794865 | ||||||
chrX:16794896
|
T | C | 1 | a0001c0001t0016g0193 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.102+8307T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16794896 | ||||||
chrX:16794979
|
A | T | 84 | a0001c0001t0001g0029a0001c0001t0005g0015a0001c0001t0005g0017others(81): Show | 86 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.102+8390A>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16794979 | ||||||
chrX:16794982
|
TA | T | 1 | a0001c0002t0002g0058 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.102+8397delA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16794982 | |||||
chrX:16795004
|
G | A | 8 | a0001c0001t0005g0015a0001c0001t0005g0017a0001c0001t0005g0018others(5): Show | 8 | HG01070.hp1 HG02622.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.102+8415G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16795004 | ||||||
chrX:16795005
|
C | T | 74 | a0001c0001t0001g0029a0001c0001t0006g0005a0001c0001t0006g0006others(71): Show | 76 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(73): Show |
intron_variant | MODIFIER | c.102+8416C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16795005 | ||||||
chrX:16795073
|
C | A | 3 | a0001c0001t0003g0125a0001c0001t0003g0126a0001c0001t0003g0189 | 3 | HG03098.hp1 HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.102+8484C>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16795073 | ||||||
chrX:16795201
|
T | C | 84 | a0001c0001t0001g0029a0001c0001t0005g0015a0001c0001t0005g0017others(81): Show | 86 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.102+8612T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16795201 | ||||||
chrX:16795208
|
C | T | 6 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(3): Show | 6 | HG02071.hp1 HG02080.hp1 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+8619C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16795208 | ||||||
chrX:16795212
|
G | A | 1 | a0001c0001t0020g0091 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.102+8623G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16795212 | ||||||
chrX:16795234
|
G | A | 1 | a0001c0001t0003g0127 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.102+8645G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16795234 | ||||||
chrX:16795276
|
C | CA | 1 | a0001c0001t0003g0085 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.102+8696dupA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16795276 | |||||
chrX:16795368
|
T | C | 1 | a0001c0001t0006g0064 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.102+8779T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16795368 | ||||||
chrX:16795538
|
C | T | 1 | a0001c0001t0001g0241 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.102+8949C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16795538 | ||||||
chrX:16795812
|
A | AT | 4 | a0001c0001t0003g0009a0001c0001t0003g0168a0001c0001t0007g0124others(1): Show | 4 | HG02572.hp1 HG02738.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+9240dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16795812 | |||||
chrX:16795812
|
AT | A | 1 | a0001c0001t0003g0128 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.102+9240delT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16795812 | |||||
chrX:16795934
|
TC | T | 1 | a0001c0002t0002g0058 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.102+9348delC | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16795934 | |||||
chrX:16796002
|
CG | C | 1 | a0001c0002t0002g0058 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.102+9417delG | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16796002 | |||||
chrX:16796094
|
A | G | 3 | a0001c0004t0032g0014a0001c0004t0033g0012a0001c0004t0034g0013 | 3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.102+9505A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16796094 | ||||||
chrX:16796116
|
A | G | 1 | a0004c0007t0001g0240 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.102+9527A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16796116 | ||||||
chrX:16796323
|
T | C | 8 | a0001c0001t0005g0015a0001c0001t0005g0017a0001c0001t0005g0018others(5): Show | 8 | HG01070.hp1 HG02622.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.102+9734T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16796323 | ||||||
chrX:16796473
|
A | G | 3 | a0001c0002t0002g0050a0001c0002t0002g0051a0001c0002t0002g0062 | 3 | NA18952.hp1 NA18977.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.102+9884A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16796473 | ||||||
chrX:16796637
|
A | AG | 1 | a0001c0001t0003g0167 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.102+10053dupG | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16796637 | |||||
chrX:16796850
|
C | T | 14 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0115others(11): Show | 14 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.102+10261C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16796850 | ||||||
chrX:16797079
|
T | A | 3 | a0001c0004t0032g0014a0001c0004t0033g0012a0001c0004t0034g0013 | 3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.102+10490T>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16797079 | ||||||
chrX:16797281
|
C | CA | 6 | a0001c0001t0001g0194a0001c0001t0004g0092a0001c0001t0004g0247others(3): Show | 6 | HG02071.hp1 HG02922.hp1 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+10708dupA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16797281 | |||||
chrX:16797281
|
CA | C | 84 | a0001c0001t0001g0029a0001c0001t0001g0123a0001c0001t0001g0245others(81): Show | 86 | HG00733.hp1 HG00738.hp1 HG00741.hp1 others(83): Show |
intron_variant | MODIFIER | c.102+10708delA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16797281 | |||||
chrX:16797281
|
CAA | C | 6 | a0001c0001t0005g0021a0001c0002t0002g0049a0001c0002t0002g0058others(3): Show | 6 | HG00140.hp1 HG00323.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+10707_102+1070 others(6): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16797281 | |||||
chrX:16797462
|
G | C | 5 | a0001c0001t0001g0029a0001c0002t0009g0030a0001c0002t0009g0031others(2): Show | 5 | HG01243.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.102+10873G>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16797462 | ||||||
chrX:16797484
|
TC | T | 1 | a0001c0002t0002g0058 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.102+10898delC | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16797484 | |||||
chrX:16797669
|
G | GA | 1 | a0001c0001t0028g0130 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.102+11083dupA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16797669 | |||||
chrX:16797845
|
T | A | 2 | a0001c0001t0012g0089a0001c0001t0012g0173 | 2 | HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.102+11256T>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16797845 | ||||||
chrX:16797845
|
TA | T | 1 | a0001c0001t0001g0191 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.102+11263delA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16797845 | |||||
chrX:16797904
|
A | G | 2 | a0001c0001t0006g0257a0001c0001t0006g0258 | 2 | HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.102+11315A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16797904 | ||||||
chrX:16798071
|
G | C | 1 | a0001c0001t0003g0183 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.102+11482G>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16798071 | ||||||
chrX:16798105
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.102+11516G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16798105 | ||||||
chrX:16798155
|
T | C | 3 | a0001c0004t0032g0014a0001c0004t0033g0012a0001c0004t0034g0013 | 3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.102+11566T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16798155 | ||||||
chrX:16798245
|
C | A | 81 | a0001c0001t0001g0029a0001c0001t0005g0015a0001c0001t0005g0017others(78): Show | 83 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.102+11656C>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16798245 | ||||||
chrX:16798383
|
T | A | 1 | a0001c0001t0028g0130 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.102+11794T>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16798383 | ||||||
chrX:16798432
|
A | G | 84 | a0001c0001t0001g0029a0001c0001t0005g0015a0001c0001t0005g0017others(81): Show | 86 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.102+11843A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16798432 | ||||||
chrX:16798536
|
T | G | 2 | a0001c0002t0002g0032a0001c0002t0002g0066 | 2 | HG01346.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.102+11947T>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16798536 | ||||||
chrX:16798583
|
G | GT | 21 | a0001c0001t0001g0110a0001c0001t0001g0122a0001c0001t0001g0190others(18): Show | 21 | HG00544.hp2 HG00609.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.102+12009dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16798583 | |||||
chrX:16798583
|
GT | G | 4 | a0001c0001t0003g0167a0001c0001t0006g0064a0001c0005t0006g0024others(1): Show | 4 | HG00735.hp2 HG02055.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+12009delT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16798583 | |||||
chrX:16798605
|
A | AG | 1 | a0001c0001t0001g0237 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.102+12017dupG | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16798605 | |||||
chrX:16798800
|
A | C | 3 | a0001c0004t0032g0014a0001c0004t0033g0012a0001c0004t0034g0013 | 3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.102+12211A>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16798800 | ||||||
chrX:16798886
|
C | CT | 1 | a0001c0001t0004g0247 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.102+12309dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16798886 | |||||
chrX:16799134
|
T | C | 84 | a0001c0001t0001g0029a0001c0001t0005g0015a0001c0001t0005g0017others(81): Show | 86 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.102+12545T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16799134 | ||||||
chrX:16799493
|
C | T | 1 | a0001c0001t0005g0163 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.102+12904C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16799493 | ||||||
chrX:16799639
|
C | T | 4 | a0001c0001t0004g0092a0001c0001t0004g0108a0001c0001t0004g0109others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+13050C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16799639 | ||||||
chrX:16799681
|
G | C | 2 | a0001c0001t0003g0127a0001c0001t0027g0131 | 2 | NA18956.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.102+13092G>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16799681 | ||||||
chrX:16799764
|
C | G | 1 | a0001c0001t0006g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.102+13175C>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16799764 | ||||||
chrX:16799793
|
G | A | 3 | a0001c0004t0032g0014a0001c0004t0033g0012a0001c0004t0034g0013 | 3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.102+13204G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16799793 | ||||||
chrX:16799973
|
A | G | 2 | a0001c0001t0006g0005a0001c0001t0006g0006 | 2 | HG02970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.102+13384A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16799973 | ||||||
chrX:16800152
|
C | T | 8 | a0001c0001t0005g0015a0001c0001t0005g0017a0001c0001t0005g0018others(5): Show | 8 | HG01070.hp1 HG02622.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.102+13563C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16800152 | ||||||
chrX:16800284
|
T | C | 1 | a0001c0001t0001g0246 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.102+13695T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16800284 | ||||||
chrX:16800539
|
A | G | 1 | a0001c0002t0009g0031 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.102+13950A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16800539 | ||||||
chrX:16800562
|
C | CT | 5 | a0001c0001t0001g0194a0001c0001t0001g0253a0001c0001t0001g0254others(2): Show | 5 | HG01175.hp1 NA18940.hp1 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.102+13993dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16800562 | |||||
chrX:16800562
|
CT | C | 11 | a0001c0001t0001g0112a0001c0001t0001g0196a0001c0001t0001g0256others(8): Show | 11 | HG00323.hp2 HG00733.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.102+13993delT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16800562 | |||||
chrX:16800648
|
T | C | 1 | a0001c0002t0002g0035 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.102+14059T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16800648 | ||||||
chrX:16800993
|
G | GC | 1 | a0001c0001t0001g0252 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.102+14408dupC | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16800993 | |||||
chrX:16801034
|
T | TG | 1 | a0001c0001t0001g0252 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.102+14447dupG | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16801034 | |||||
chrX:16801112
|
G | A | 1 | a0001c0002t0002g0054 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.102+14523G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16801112 | ||||||
chrX:16801160
|
T | TA | 1 | a0001c0001t0001g0252 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.102+14572dupA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16801160 | |||||
chrX:16801178
|
G | A | 1 | a0001c0001t0022g0184 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.102+14589G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16801178 | ||||||
chrX:16801347
|
GGCTAATT others(8151): Show |
G | 1 | a0001c0001t0001g0172 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.102+14793_103-9035 others(3): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16801347 | |||||
chrX:16801435
|
C | T | 1 | a0001c0001t0030g0169 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.102+14846C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16801435 | ||||||
chrX:16801437
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.102+14848C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16801437 | ||||||
chrX:16801619
|
A | T | 2 | a0001c0006t0002g0027a0001c0006t0002g0065 | 2 | HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.102+15030A>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16801619 | ||||||
chrX:16801628
|
CA | C | 14 | a0001c0001t0006g0005a0001c0001t0006g0006a0001c0001t0006g0064others(11): Show | 14 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.102+15041delA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16801628 | |||||
chrX:16801842
|
A | G | 215 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0029others(212): Show | 217 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.102+15253A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16801842 | ||||||
chrX:16801919
|
CT | C | 1 | a0001c0001t0001g0237 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.102+15335delT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16801919 | |||||
chrX:16801932
|
A | AT | 1 | a0001c0004t0033g0012 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.102+15352dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16801932 | |||||
chrX:16801950
|
C | CT | 1 | a0001c0001t0010g0239 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.102+15382dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16801950 | |||||
chrX:16801950
|
CT | C | 171 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0029others(168): Show | 173 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.102+15382delT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16801950 | |||||
chrX:16801950
|
CTT | C | 24 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(21): Show | 24 | HG00323.hp1 HG00544.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.102+15381_102+1538 others(6): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16801950 | |||||
chrX:16801955
|
T | C | 5 | a0001c0001t0003g0008a0001c0001t0003g0128a0001c0001t0003g0133others(2): Show | 5 | HG00639.hp2 HG01081.hp1 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.102+15366T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16801955 | ||||||
chrX:16802028
|
A | AC | 1 | a0001c0001t0001g0237 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.102+15441dupC | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16802028 | |||||
chrX:16802056
|
C | T | 4 | a0001c0001t0008g0023a0001c0001t0008g0063a0001c0001t0008g0079others(1): Show | 4 | HG02717.hp1 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+15467C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16802056 | ||||||
chrX:16802254
|
C | CT | 43 | a0001c0001t0001g0029a0001c0001t0001g0233a0001c0001t0001g0246others(40): Show | 43 | HG00140.hp1 HG00323.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.102+15680dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16802254 | |||||
chrX:16802254
|
C | CTT | 44 | a0001c0001t0006g0081a0001c0002t0002g0001a0001c0002t0002g0002others(41): Show | 46 | HG00733.hp1 HG00738.hp1 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.102+15679_102+1568 others(6): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16802254 | |||||
chrX:16802254
|
CT | C | 1 | a0001c0001t0003g0132 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.102+15680delT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16802254 | |||||
chrX:16802339
|
C | T | 1 | a0001c0002t0002g0073 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.102+15750C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16802339 | ||||||
chrX:16802407
|
T | C | 84 | a0001c0001t0001g0029a0001c0001t0005g0015a0001c0001t0005g0017others(81): Show | 86 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.102+15818T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16802407 | ||||||
chrX:16802447
|
C | T | 3 | a0001c0001t0006g0064a0001c0005t0006g0024a0001c0005t0023g0025 | 3 | HG02055.hp1 HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.102+15858C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16802447 | ||||||
chrX:16802521
|
T | C | 84 | a0001c0001t0001g0029a0001c0001t0005g0015a0001c0001t0005g0017others(81): Show | 86 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.102+15932T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16802521 | ||||||
chrX:16802547
|
C | T | 14 | a0001c0001t0006g0005a0001c0001t0006g0006a0001c0001t0006g0064others(11): Show | 14 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.102+15958C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16802547 | ||||||
chrX:16802729
|
CT | C | 1 | a0001c0001t0001g0253 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.103-15839delT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16802729 | |||||
chrX:16802815
|
TTC | T | 1 | a0001c0004t0033g0012 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.103-15757_103-1575 others(6): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16802815 | |||||
chrX:16802821
|
C | CT | 7 | a0001c0001t0001g0182a0001c0001t0001g0252a0001c0001t0001g0254others(4): Show | 7 | HG01981.hp1 HG02572.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.103-15736dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16802821 | |||||
chrX:16802821
|
CT | C | 86 | a0001c0001t0001g0029a0001c0001t0001g0197a0001c0001t0001g0242others(83): Show | 88 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.103-15736delT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16802821 | |||||
chrX:16802825
|
T | C | 1 | a0001c0001t0003g0134 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.103-15749T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16802825 | ||||||
chrX:16803008
|
T | C | 84 | a0001c0001t0001g0029a0001c0001t0005g0015a0001c0001t0005g0017others(81): Show | 86 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.103-15566T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16803008 | ||||||
chrX:16803056
|
G | T | 3 | a0001c0004t0032g0014a0001c0004t0033g0012a0001c0004t0034g0013 | 3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.103-15518G>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16803056 | ||||||
chrX:16803154
|
C | CG | 1 | a0001c0001t0001g0252 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.103-15418dupG | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16803154 | |||||
chrX:16803161
|
C | CATGG | 1 | a0001c0001t0003g0260 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.103-15413_103-1541 others(8): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16803161 | ||||||
chrX:16803162
|
C | G | 1 | a0001c0001t0003g0260 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.103-15412C>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16803162 | ||||||
chrX:16803164
|
C | T | 1 | a0001c0001t0003g0260 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.103-15410C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16803164 | ||||||
chrX:16803165
|
T | TC | 1 | a0001c0001t0003g0260 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.103-15409_103-1540 others(5): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16803165 | ||||||
chrX:16803242
|
A | G | 3 | a0001c0004t0032g0014a0001c0004t0033g0012a0001c0004t0034g0013 | 3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.103-15332A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16803242 | ||||||
chrX:16803318
|
A | G | 84 | a0001c0001t0001g0029a0001c0001t0005g0015a0001c0001t0005g0017others(81): Show | 86 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.103-15256A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16803318 | ||||||
chrX:16803354
|
A | AT | 5 | a0001c0001t0001g0232a0001c0001t0001g0254a0001c0001t0003g0085others(2): Show | 5 | HG00544.hp2 HG02280.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-15202dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16803354 | |||||
chrX:16803354
|
AT | A | 12 | a0001c0001t0001g0197a0001c0001t0003g0133a0001c0001t0005g0017others(9): Show | 12 | HG00738.hp1 HG01081.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.103-15202delT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16803354 | |||||
chrX:16803499
|
C | T | 1 | a0001c0001t0003g0159 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.103-15075C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16803499 | ||||||
chrX:16803521
|
A | AT | 1 | a0001c0001t0001g0252 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.103-15046dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16803521 | |||||
chrX:16803586
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.103-14988A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16803586 | ||||||
chrX:16803589
|
C | T | 1 | a0001c0001t0003g0158 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.103-14985C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16803589 | ||||||
chrX:16803608
|
G | C | 81 | a0001c0001t0001g0029a0001c0001t0005g0015a0001c0001t0005g0017others(78): Show | 83 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.103-14966G>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16803608 | ||||||
chrX:16803681
|
C | CG | 1 | a0001c0001t0001g0237 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.103-14891dupG | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16803681 | |||||
chrX:16803725
|
G | A | 1 | a0001c0002t0002g0041 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.103-14849G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16803725 | ||||||
chrX:16803789
|
T | TA | 1 | a0001c0001t0001g0252 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.103-14780dupA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16803789 | |||||
chrX:16803808
|
T | C | 84 | a0001c0001t0001g0029a0001c0001t0005g0015a0001c0001t0005g0017others(81): Show | 86 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.103-14766T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16803808 | ||||||
chrX:16803888
|
G | GT | 1 | a0001c0001t0001g0252 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.103-14684dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16803888 | |||||
chrX:16803901
|
G | T | 2 | a0001c0001t0003g0164a0001c0001t0003g0185 | 2 | NA18953.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.103-14673G>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16803901 | ||||||
chrX:16803951
|
C | CA | 1 | a0001c0005t0023g0025 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.103-14614dupA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16803951 | |||||
chrX:16804026
|
C | T | 1 | a0001c0001t0003g0157 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.103-14548C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804026 | ||||||
chrX:16804166
|
G | A | 84 | a0001c0001t0001g0029a0001c0001t0005g0015a0001c0001t0005g0017others(81): Show | 86 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.103-14408G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804166 | ||||||
chrX:16804196
|
T | C | 1 | a0001c0001t0008g0023 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.103-14378T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804196 | ||||||
chrX:16804331
|
T | TG | 1 | a0001c0001t0001g0253 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.103-14241dupG | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16804331 | |||||
chrX:16804502
|
A | AC | 1 | a0001c0001t0001g0252 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.103-14066dupC | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16804502 | |||||
chrX:16804562
|
C | A | 1 | a0001c0001t0025g0088 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.103-14012C>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804562 | ||||||
chrX:16804727
|
T | A | 1 | a0006c0010t0038g0004 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.103-13847T>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804727 | ||||||
chrX:16804803
|
G | A | 1 | a0005c0009t0002g0068 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.103-13771G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804803 | ||||||
chrX:16804897
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.103-13677G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804897 | ||||||
chrX:16804971
|
A | AC | 69 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0094others(66): Show | 69 | HG00438.hp2 HG00609.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.103-13591dupC | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16804971 | |||||
chrX:16804971
|
A | ACC | 16 | a0001c0001t0001g0208a0001c0001t0001g0238a0001c0001t0001g0245others(13): Show | 16 | HG00140.hp1 HG00733.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.103-13592_103-1359 others(6): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16804971 | |||||
chrX:16804971
|
A | ACCC | 3 | a0001c0001t0001g0029a0001c0001t0018g0207a0001c0002t0009g0031 | 3 | HG01243.hp1 HG03195.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.103-13593_103-1359 others(7): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16804971 | |||||
chrX:16804971
|
A | ACCCC | 3 | a0001c0001t0001g0195a0001c0001t0004g0098a0001c0002t0009g0030 | 3 | HG00735.hp1 HG02080.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.103-13594_103-1359 others(8): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16804971 | |||||
chrX:16804971
|
AC | A | 22 | a0001c0002t0002g0001a0001c0002t0002g0026a0001c0002t0002g0028others(19): Show | 23 | HG01074.hp1 HG01123.hp2 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.103-13591delC | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16804971 | |||||
chrX:16804973
|
C | CG | 2 | a0001c0001t0003g0158a0001c0001t0003g0162 | 2 | HG03471.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.103-13601_103-1360 others(5): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804973 | ||||||
chrX:16804974
|
C | G | 1 | a0001c0001t0007g0097 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.103-13600C>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804974 | ||||||
chrX:16804975
|
C | CA | 1 | a0001c0001t0001g0206 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.103-13599_103-1359 others(5): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804975 | ||||||
chrX:16804975
|
C | G | 1 | a0001c0002t0002g0072 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.103-13599C>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804975 | ||||||
chrX:16804976
|
C | A | 1 | a0001c0001t0001g0198 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.103-13598C>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804976 | ||||||
chrX:16804977
|
C | CG | 1 | a0001c0001t0001g0123 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.103-13597_103-1359 others(5): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804977 | ||||||
chrX:16804978
|
C | G | 1 | a0001c0001t0003g0156 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.103-13596C>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804978 | ||||||
chrX:16804979
|
C | G | 1 | a0001c0002t0002g0048 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.103-13595C>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804979 | ||||||
chrX:16804982
|
C | G | 1 | a0001c0002t0002g0061 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.103-13592C>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804982 | ||||||
chrX:16804983
|
CG | C | 13 | a0001c0001t0001g0113a0001c0001t0001g0119a0001c0001t0001g0120others(10): Show | 13 | HG00733.hp2 HG01071.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.103-13590delG | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804983 | ||||||
chrX:16804984
|
G | C | 156 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0094others(153): Show | 156 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.103-13590G>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804984 | ||||||
chrX:16804984
|
G | T | 1 | a0001c0002t0002g0061 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.103-13590G>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804984 | ||||||
chrX:16804985
|
C | CCCCGCTT others(1): Show |
1 | a0001c0001t0005g0018 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.103-13589_103-1358 others(12): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804985 | ||||||
chrX:16804985
|
C | CCCG | 1 | a0001c0001t0001g0253 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.103-13589_103-1358 others(7): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804985 | ||||||
chrX:16804985
|
C | CCCGCTTT | 1 | a0001c0001t0029g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.103-13589_103-1358 others(11): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804985 | ||||||
chrX:16804985
|
C | CCG | 5 | a0001c0001t0001g0179a0001c0001t0001g0224a0001c0001t0001g0256others(2): Show | 5 | HG00673.hp1 HG01175.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-13589_103-1358 others(6): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804985 | ||||||
chrX:16804985
|
C | CCGCTT | 1 | a0001c0001t0005g0017 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.103-13589_103-1358 others(9): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804985 | ||||||
chrX:16804985
|
C | CCGCTTT | 3 | a0001c0001t0005g0015a0001c0001t0005g0019a0001c0001t0005g0022 | 3 | HG02622.hp1 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.103-13589_103-1358 others(10): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804985 | ||||||
chrX:16804985
|
C | CG | 12 | a0001c0001t0003g0008a0001c0001t0003g0127a0001c0001t0003g0133others(9): Show | 12 | HG00544.hp2 HG01081.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.103-13589_103-1358 others(5): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804985 | ||||||
chrX:16804985
|
C | CGCT | 3 | a0001c0001t0006g0005a0001c0001t0006g0257a0001c0002t0013g0052 | 3 | HG02970.hp1 HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.103-13589_103-1358 others(7): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804985 | ||||||
chrX:16804985
|
C | CGCTT | 1 | a0001c0001t0005g0020 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.103-13589_103-1358 others(8): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804985 | ||||||
chrX:16804985
|
C | CGCTTT | 1 | a0001c0001t0005g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.103-13589_103-1358 others(9): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804985 | ||||||
chrX:16804985
|
C | CT | 9 | a0001c0001t0006g0006a0001c0001t0006g0064a0001c0001t0006g0258others(6): Show | 9 | HG02109.hp2 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.103-13567dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16804985 | |||||
chrX:16804985
|
C | CTT | 5 | a0001c0001t0006g0081a0001c0004t0032g0014a0001c0004t0033g0012others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-13568_103-1356 others(6): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16804985 | |||||
chrX:16804985
|
C | G | 29 | a0001c0001t0001g0145a0001c0001t0003g0009a0001c0001t0003g0085others(26): Show | 29 | HG00438.hp1 HG00621.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.103-13589C>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804985 | ||||||
chrX:16804985
|
C | T | 1 | a0001c0002t0002g0061 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.103-13589C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804985 | ||||||
chrX:16804985
|
CT | C | 15 | a0001c0001t0001g0153a0001c0001t0003g0152a0001c0001t0003g0154others(12): Show | 15 | HG00280.hp1 HG00735.hp2 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.103-13567delT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16804985 | |||||
chrX:16804985
|
CTT | C | 2 | a0001c0001t0001g0123a0001c0001t0004g0109 | 2 | HG01070.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.103-13568_103-1356 others(6): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16804985 | |||||
chrX:16804986
|
T | C | 50 | a0001c0001t0001g0145a0001c0001t0001g0179a0001c0001t0001g0202others(47): Show | 50 | HG00438.hp1 HG00544.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.103-13588T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804986 | ||||||
chrX:16804986
|
T | G | 108 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0094others(105): Show | 108 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.103-13588T>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804986 | ||||||
chrX:16804987
|
T | C | 108 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0094others(105): Show | 108 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.103-13587T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804987 | ||||||
chrX:16804987
|
T | G | 3 | a0001c0001t0001g0202a0001c0001t0001g0225a0001c0001t0016g0193 | 3 | HG02080.hp1 NA18959.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.103-13587T>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804987 | ||||||
chrX:16804988
|
T | C | 3 | a0001c0001t0001g0202a0001c0001t0001g0225a0001c0001t0016g0193 | 3 | HG02080.hp1 NA18959.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.103-13586T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804988 | ||||||
chrX:16804989
|
T | G | 1 | a0001c0001t0004g0101 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.103-13585T>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804989 | ||||||
chrX:16805007
|
T | TTTTTG | 8 | a0001c0001t0001g0029a0001c0002t0002g0036a0001c0002t0002g0076others(5): Show | 8 | HG01243.hp1 HG02451.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.103-13567_103-1356 others(9): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16805007 | ||||||
chrX:16805007
|
T | TTTTTTG | 8 | a0001c0002t0002g0033a0001c0002t0002g0038a0001c0002t0002g0049others(5): Show | 8 | HG00140.hp1 HG00323.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.103-13567_103-1356 others(10): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16805007 | ||||||
chrX:16805007
|
T | TTTTTTTG | 4 | a0001c0002t0002g0028a0001c0002t0002g0055a0001c0002t0002g0071others(1): Show | 4 | HG01516.hp1 HG01516.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.103-13567_103-1356 others(11): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16805007 | ||||||
chrX:16805007
|
T | TTTTTTTT others(1): Show |
28 | a0001c0002t0002g0002a0001c0002t0002g0032a0001c0002t0002g0034others(25): Show | 29 | HG00733.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.103-13567_103-1356 others(12): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16805007 | ||||||
chrX:16805007
|
T | TTTTTTTT others(2): Show |
6 | a0001c0002t0002g0047a0001c0002t0002g0050a0001c0002t0002g0057others(3): Show | 6 | HG01074.hp1 HG02027.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.103-13567_103-1356 others(13): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16805007 | ||||||
chrX:16805007
|
T | TTTTTTTT others(3): Show |
2 | a0001c0002t0002g0026a0001c0002t0002g0051 | 2 | HG01433.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.103-13567_103-1356 others(14): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16805007 | ||||||
chrX:16805007
|
T | TTTTTTTT others(4): Show |
1 | a0001c0002t0002g0259 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.103-13567_103-1356 others(15): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16805007 | ||||||
chrX:16805007
|
T | TTTTTTTT others(5): Show |
1 | a0001c0002t0002g0070 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.103-13567_103-1356 others(16): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16805007 | ||||||
chrX:16805007
|
T | TTTTTTTT others(6): Show |
1 | a0001c0002t0002g0001 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.103-13567_103-1356 others(17): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16805007 | ||||||
chrX:16805010
|
G | C | 84 | a0001c0001t0001g0029a0001c0001t0005g0015a0001c0001t0005g0017others(81): Show | 86 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.103-13564G>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16805010 | ||||||
chrX:16805059
|
A | G | 3 | a0001c0001t0001g0118a0001c0001t0001g0121a0001c0001t0001g0122 | 3 | HG02109.hp1 HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.103-13515A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16805059 | ||||||
chrX:16805152
|
T | G | 1 | a0001c0001t0001g0003 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.103-13422T>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16805152 | ||||||
chrX:16805261
|
GCGT | G | 1 | a0001c0001t0001g0253 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.103-13312_103-1331 others(7): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16805261 | ||||||
chrX:16805390
|
A | G | 2 | a0001c0001t0006g0005a0001c0001t0006g0006 | 2 | HG02970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.103-13184A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16805390 | ||||||
chrX:16805417
|
T | TA | 1 | a0001c0001t0001g0252 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.103-13150dupA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16805417 | |||||
chrX:16805451
|
CCTT | C | 84 | a0001c0001t0001g0029a0001c0001t0005g0015a0001c0001t0005g0017others(81): Show | 86 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.103-13118_103-1311 others(7): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16805451 | |||||
chrX:16805473
|
GA | G | 1 | a0001c0001t0001g0253 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.103-13094delA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16805473 | |||||
chrX:16805676
|
T | TG | 1 | a0001c0001t0001g0253 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.103-12896dupG | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16805676 | |||||
chrX:16805703
|
T | TA | 1 | a0001c0001t0001g0253 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.103-12869dupA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16805703 | |||||
chrX:16805755
|
TA | T | 1 | a0001c0001t0001g0253 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.103-12817delA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16805755 | |||||
chrX:16805906
|
T | TC | 1 | a0001c0001t0001g0253 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.103-12667dupC | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16805906 | |||||
chrX:16805965
|
CA | C | 2 | a0001c0002t0002g0032a0001c0002t0002g0066 | 2 | HG01346.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.103-12608delA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16805965 | ||||||
chrX:16806106
|
TA | T | 1 | a0001c0001t0001g0253 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.103-12465delA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16806106 | |||||
chrX:16806231
|
C | G | 81 | a0001c0001t0001g0029a0001c0001t0005g0015a0001c0001t0005g0017others(78): Show | 83 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.103-12343C>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16806231 | ||||||
chrX:16806299
|
G | A | 1 | a0001c0001t0011g0111 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.103-12275G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16806299 | ||||||
chrX:16806395
|
G | A | 3 | a0001c0004t0032g0014a0001c0004t0033g0012a0001c0004t0034g0013 | 3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.103-12179G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16806395 | ||||||
chrX:16806615
|
C | T | 1 | a0001c0001t0016g0193 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.103-11959C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16806615 | ||||||
chrX:16806619
|
TA | T | 1 | a0001c0001t0003g0260 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.103-11949delA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16806619 | |||||
chrX:16806639
|
C | CCG | 1 | a0001c0001t0001g0252 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.103-11935_103-1193 others(6): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16806639 | ||||||
chrX:16806733
|
C | T | 1 | a0001c0002t0009g0031 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.103-11841C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16806733 | ||||||
chrX:16806788
|
G | A | 2 | a0001c0001t0004g0101a0001c0001t0004g0175 | 2 | HG01928.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.103-11786G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16806788 | ||||||
chrX:16806916
|
C | CA | 31 | a0001c0001t0001g0011a0001c0001t0001g0194a0001c0001t0001g0208others(28): Show | 31 | HG00280.hp1 HG01123.hp1 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.103-11636dupA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16806916 | |||||
chrX:16806916
|
C | CAA | 1 | a0001c0006t0002g0065 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.103-11637_103-1163 others(6): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16806916 | |||||
chrX:16806916
|
CA | C | 7 | a0001c0001t0001g0225a0001c0001t0003g0008a0001c0001t0003g0151others(4): Show | 7 | HG01099.hp1 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.103-11636delA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16806916 | |||||
chrX:16806916
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0202 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.103-11645_103-1163 others(14): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16806916 | |||||
chrX:16806945
|
G | A | 81 | a0001c0001t0001g0029a0001c0001t0005g0015a0001c0001t0005g0017others(78): Show | 83 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.103-11629G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16806945 | ||||||
chrX:16806998
|
C | T | 2 | a0002c0003t0003g0187a0002c0003t0035g0160 | 2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.103-11576C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16806998 | ||||||
chrX:16807690
|
A | G | 1 | a0001c0002t0002g0066 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.103-10884A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16807690 | ||||||
chrX:16807710
|
A | G | 1 | a0001c0001t0005g0019 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.103-10864A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16807710 | ||||||
chrX:16807752
|
C | A | 81 | a0001c0001t0001g0029a0001c0001t0005g0015a0001c0001t0005g0017others(78): Show | 83 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.103-10822C>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16807752 | ||||||
chrX:16807883
|
GA | G | 1 | a0001c0001t0011g0010 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.103-10688delA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16807883 | |||||
chrX:16807889
|
T | TA | 1 | a0001c0001t0001g0252 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.103-10680dupA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16807889 | |||||
chrX:16807911
|
G | GT | 1 | a0001c0001t0001g0252 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.103-10659dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16807911 | |||||
chrX:16808056
|
A | G | 8 | a0001c0001t0005g0015a0001c0001t0005g0017a0001c0001t0005g0018others(5): Show | 8 | HG01070.hp1 HG02622.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.103-10518A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16808056 | ||||||
chrX:16808129
|
TG | T | 1 | a0001c0001t0011g0010 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.103-10443delG | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16808129 | |||||
chrX:16808131
|
G | A | 2 | a0001c0002t0002g0056a0001c0002t0002g0058 | 2 | NA18947.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.103-10443G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16808131 | ||||||
chrX:16808161
|
C | T | 14 | a0001c0001t0006g0005a0001c0001t0006g0006a0001c0001t0006g0064others(11): Show | 14 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.103-10413C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16808161 | ||||||
chrX:16808194
|
T | A | 1 | a0001c0001t0008g0023 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.103-10380T>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16808194 | ||||||
chrX:16808226
|
C | T | 2 | a0001c0001t0006g0005a0001c0001t0006g0006 | 2 | HG02970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.103-10348C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16808226 | ||||||
chrX:16808307
|
AG | A | 1 | a0001c0001t0001g0253 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.103-10264delG | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16808307 | |||||
chrX:16808340
|
C | CG | 1 | a0001c0001t0001g0252 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.103-10234_103-1023 others(5): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16808340 | ||||||
chrX:16808389
|
A | AT | 8 | a0001c0001t0005g0015a0001c0001t0005g0017a0001c0001t0005g0018others(5): Show | 8 | HG01070.hp1 HG02622.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.103-10182dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16808389 | |||||
chrX:16808503
|
G | T | 1 | a0001c0002t0036g0039 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.103-10071G>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16808503 | ||||||
chrX:16808661
|
A | G | 2 | a0001c0001t0006g0257a0001c0001t0006g0258 | 2 | HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.103-9913A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16808661 | ||||||
chrX:16808667
|
C | CT | 1 | a0001c0001t0001g0252 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.103-9902dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16808667 | |||||
chrX:16808684
|
G | A | 3 | a0001c0001t0010g0234a0001c0001t0010g0235a0001c0001t0010g0239 | 3 | HG01109.hp1 HG02145.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.103-9890G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16808684 | ||||||
chrX:16808990
|
T | C | 1 | a0001c0001t0029g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.103-9584T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16808990 | ||||||
chrX:16809345
|
G | GT | 16 | a0001c0001t0001g0201a0001c0001t0001g0223a0001c0001t0001g0241others(13): Show | 16 | HG01070.hp1 HG01884.hp1 HG02523.hp2 others(13): Show |
intron_variant | MODIFIER | c.103-9213dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16809345 | |||||
chrX:16809345
|
G | GTT | 65 | a0001c0001t0001g0029a0001c0001t0006g0005a0001c0001t0006g0006others(62): Show | 67 | HG00323.hp1 HG00733.hp1 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.103-9214_103-9213d others(4): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16809345 | |||||
chrX:16809345
|
G | GTTT | 8 | a0001c0001t0008g0023a0001c0001t0008g0063a0001c0001t0008g0079others(5): Show | 8 | HG00140.hp1 HG01192.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.103-9215_103-9213d others(5): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16809345 | |||||
chrX:16809345
|
GT | G | 1 | a0001c0001t0007g0097 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.103-9213delT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16809345 | |||||
chrX:16809518
|
A | G | 1 | a0001c0004t0033g0012 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.103-9056A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16809518 | ||||||
chrX:16809589
|
C | G | 1 | a0001c0001t0001g0222 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.103-8985C>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16809589 | ||||||
chrX:16809637
|
C | G | 2 | a0001c0001t0001g0201a0001c0001t0001g0223 | 2 | HG02523.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.103-8937C>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16809637 | ||||||
chrX:16809919
|
G | A | 4 | a0001c0001t0008g0023a0001c0001t0008g0063a0001c0001t0008g0079others(1): Show | 4 | HG02717.hp1 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.103-8655G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16809919 | ||||||
chrX:16809947
|
G | A | 3 | a0001c0004t0032g0014a0001c0004t0033g0012a0001c0004t0034g0013 | 3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.103-8627G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16809947 | ||||||
chrX:16810510
|
A | C | 1 | a0001c0001t0001g0226 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.103-8064A>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16810510 | ||||||
chrX:16810584
|
C | CA | 1 | a0001c0001t0001g0252 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.103-7987dupA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16810584 | |||||
chrX:16810933
|
G | T | 2 | a0001c0002t0002g0032a0001c0002t0002g0066 | 2 | HG01346.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.103-7641G>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16810933 | ||||||
chrX:16810934
|
G | GC | 1 | a0001c0001t0001g0178 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.103-7634dupC | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16810934 | |||||
chrX:16810934
|
GC | G | 1 | a0001c0001t0001g0202 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.103-7634delC | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16810934 | |||||
chrX:16810940
|
C | CCCA | 1 | a0001c0001t0001g0252 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.103-7634_103-7633i others(5): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16810940 | ||||||
chrX:16810948
|
T | TG | 1 | a0001c0001t0001g0252 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.103-7623dupG | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16810948 | |||||
chrX:16810996
|
A | G | 2 | a0001c0001t0003g0150a0001c0001t0005g0163 | 2 | HG00438.hp1 HG00621.hp1 |
intron_variant | MODIFIER | c.103-7578A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16810996 | ||||||
chrX:16811048
|
A | AT | 1 | a0001c0001t0001g0252 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.103-7521dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16811048 | |||||
chrX:16811105
|
A | T | 1 | a0001c0001t0001g0107 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.103-7469A>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16811105 | ||||||
chrX:16811194
|
C | CA | 1 | a0001c0001t0001g0252 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.103-7373dupA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16811194 | |||||
chrX:16811336
|
T | TA | 1 | a0001c0001t0001g0252 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.103-7237dupA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16811336 | |||||
chrX:16811362
|
AT | A | 1 | a0001c0002t0002g0041 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.103-7202delT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16811362 | |||||
chrX:16811381
|
G | GT | 1 | a0001c0001t0001g0252 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.103-7189dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16811381 | |||||
chrX:16811423
|
C | CT | 1 | a0001c0001t0001g0252 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.103-7150dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16811423 | |||||
chrX:16811480
|
C | A | 4 | a0001c0001t0008g0023a0001c0001t0008g0063a0001c0001t0008g0079others(1): Show | 4 | HG02717.hp1 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.103-7094C>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16811480 | ||||||
chrX:16811576
|
G | C | 1 | a0001c0002t0002g0042 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.103-6998G>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16811576 | ||||||
chrX:16811646
|
C | CT | 8 | a0001c0001t0001g0179a0001c0001t0001g0230a0001c0001t0001g0231others(5): Show | 8 | HG00741.hp1 HG01175.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.103-6914dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16811646 | |||||
chrX:16811762
|
A | G | 84 | a0001c0001t0001g0029a0001c0001t0005g0015a0001c0001t0005g0017others(81): Show | 86 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.103-6812A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16811762 | ||||||
chrX:16811827
|
C | T | 2 | a0001c0001t0006g0257a0001c0001t0006g0258 | 2 | HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.103-6747C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16811827 | ||||||
chrX:16812005
|
C | CT | 1 | a0001c0001t0001g0252 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.103-6566dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16812005 | |||||
chrX:16812009
|
C | CT | 1 | a0001c0002t0002g0001 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.103-6553dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16812009 | |||||
chrX:16812078
|
A | T | 1 | a0001c0001t0003g0159 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.103-6496A>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16812078 | ||||||
chrX:16812099
|
G | GT | 1 | a0001c0001t0001g0252 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.103-6473dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16812099 | |||||
chrX:16812177
|
C | CT | 2 | a0001c0001t0024g0087a0001c0001t0025g0088 | 2 | HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.103-6386dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16812177 | |||||
chrX:16812177
|
CT | C | 196 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0029others(193): Show | 198 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.103-6386delT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16812177 | |||||
chrX:16812229
|
GA | G | 1 | a0001c0001t0001g0252 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.103-6343delA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16812229 | |||||
chrX:16812396
|
C | CT | 3 | a0001c0001t0012g0173a0001c0002t0014g0075a0001c0005t0023g0025 | 3 | HG02055.hp1 HG03195.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.103-6163dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16812396 | |||||
chrX:16812396
|
CT | C | 173 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0094others(170): Show | 173 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.103-6163delT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16812396 | |||||
chrX:16812433
|
T | TC | 1 | a0001c0001t0001g0252 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.103-6138dupC | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16812433 | |||||
chrX:16812456
|
C | T | 1 | a0003c0008t0009g0037 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.103-6118C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16812456 | ||||||
chrX:16812550
|
T | C | 188 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0094others(185): Show | 188 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.103-6024T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16812550 | ||||||
chrX:16812691
|
C | CT | 18 | a0001c0001t0001g0029a0001c0001t0001g0252a0001c0001t0003g0162others(15): Show | 18 | HG00741.hp1 HG00741.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.103-5855dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16812691 | |||||
chrX:16812691
|
C | CTT | 2 | a0001c0004t0033g0012a0001c0004t0034g0013 | 2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.103-5856_103-5855d others(4): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16812691 | |||||
chrX:16812691
|
CT | C | 93 | a0001c0001t0001g0003a0001c0001t0001g0095a0001c0001t0001g0107others(90): Show | 93 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.103-5855delT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16812691 | |||||
chrX:16812691
|
CTT | C | 80 | a0001c0001t0001g0011a0001c0001t0001g0094a0001c0001t0001g0096others(77): Show | 80 | HG00323.hp2 HG00544.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.103-5856_103-5855d others(4): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16812691 | |||||
chrX:16812691
|
CTTT | C | 3 | a0001c0001t0001g0210a0001c0001t0001g0256a0001c0001t0020g0091 | 3 | HG02293.hp1 NA18970.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.103-5857_103-5855d others(5): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16812691 | |||||
chrX:16812797
|
G | GT | 1 | a0001c0001t0001g0252 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.103-5775dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16812797 | |||||
chrX:16812843
|
A | AGGCTT | 1 | a0001c0001t0001g0252 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.103-5729_103-5725d others(7): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16812843 | |||||
chrX:16812892
|
T | G | 188 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0094others(185): Show | 188 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.103-5682T>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16812892 | ||||||
chrX:16813365
|
C | T | 1 | a0001c0004t0034g0013 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.103-5209C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16813365 | ||||||
chrX:16813384
|
G | A | 2 | a0001c0001t0006g0257a0001c0001t0006g0258 | 2 | HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.103-5190G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16813384 | ||||||
chrX:16813414
|
A | G | 177 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0094others(174): Show | 177 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.103-5160A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16813414 | ||||||
chrX:16813485
|
TA | T | 4 | a0001c0001t0001g0178a0001c0002t0002g0032a0001c0002t0002g0036others(1): Show | 4 | HG01943.hp1 HG02818.hp2 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.103-5076delA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16813485 | |||||
chrX:16813601
|
T | C | 1 | a0001c0001t0003g0162 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.103-4973T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16813601 | ||||||
chrX:16813637
|
C | CA | 10 | a0001c0001t0001g0190a0001c0001t0001g0230a0001c0001t0001g0231others(7): Show | 10 | HG02027.hp1 HG02056.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.103-4920dupA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16813637 | |||||
chrX:16813637
|
CA | C | 10 | a0001c0001t0001g0178a0001c0001t0001g0200a0001c0001t0004g0219others(7): Show | 10 | HG01070.hp1 HG02622.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.103-4920delA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16813637 | |||||
chrX:16813637
|
CAA | C | 1 | a0001c0001t0005g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.103-4921_103-4920d others(4): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16813637 | |||||
chrX:16813722
|
A | G | 8 | a0001c0001t0005g0015a0001c0001t0005g0017a0001c0001t0005g0018others(5): Show | 8 | HG01070.hp1 HG02622.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.103-4852A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16813722 | ||||||
chrX:16813808
|
C | T | 3 | a0001c0004t0032g0014a0001c0004t0033g0012a0001c0004t0034g0013 | 3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.103-4766C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16813808 | ||||||
chrX:16813816
|
G | A | 11 | a0001c0001t0001g0110a0001c0001t0004g0093a0001c0001t0004g0099others(8): Show | 11 | HG00544.hp1 HG01928.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.103-4758G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16813816 | ||||||
chrX:16813838
|
G | A | 10 | a0001c0001t0005g0015a0001c0001t0005g0017a0001c0001t0005g0018others(7): Show | 10 | HG01070.hp1 HG02559.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.103-4736G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16813838 | ||||||
chrX:16814010
|
C | T | 1 | a0001c0001t0005g0022 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.103-4564C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16814010 | ||||||
chrX:16814064
|
C | T | 2 | a0001c0001t0001g0199a0001c0001t0001g0230 | 2 | NA18967.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.103-4510C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16814064 | ||||||
chrX:16814085
|
CA | C | 1 | a0001c0001t0001g0178 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.103-4481delA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16814085 | |||||
chrX:16814173
|
CA | C | 1 | a0001c0001t0001g0252 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.103-4396delA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16814173 | |||||
chrX:16814540
|
G | A | 3 | a0001c0004t0032g0014a0001c0004t0033g0012a0001c0004t0034g0013 | 3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.103-4034G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16814540 | ||||||
chrX:16814650
|
T | A | 177 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0094others(174): Show | 177 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.103-3924T>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16814650 | ||||||
chrX:16814658
|
C | CT | 1 | a0001c0001t0001g0252 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.103-3915dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16814658 | |||||
chrX:16814710
|
T | C | 8 | a0001c0001t0005g0015a0001c0001t0005g0017a0001c0001t0005g0018others(5): Show | 8 | HG01070.hp1 HG02622.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.103-3864T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16814710 | ||||||
chrX:16814711
|
A | T | 8 | a0001c0001t0005g0015a0001c0001t0005g0017a0001c0001t0005g0018others(5): Show | 8 | HG01070.hp1 HG02622.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.103-3863A>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16814711 | ||||||
chrX:16814792
|
G | A | 3 | a0001c0001t0003g0125a0001c0001t0003g0126a0001c0001t0003g0189 | 3 | HG03098.hp1 HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.103-3782G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16814792 | ||||||
chrX:16814806
|
G | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0172 | 2 | HG01168.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.103-3768G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16814806 | ||||||
chrX:16814977
|
AGCCTCAG others(11): Show |
A | 1 | a0001c0001t0011g0111 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.103-3585_103-3568d others(20): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16814977 | |||||
chrX:16815531
|
A | AT | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.103-3035dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16815531 | |||||
chrX:16815637
|
C | T | 1 | a0001c0001t0028g0130 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.103-2937C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16815637 | ||||||
chrX:16815790
|
G | A | 2 | a0001c0002t0002g0034a0001c0002t0002g0067 | 2 | HG00733.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.103-2784G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16815790 | ||||||
chrX:16815828
|
AT | A | 1 | a0001c0002t0002g0045 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.103-2734delT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16815828 | |||||
chrX:16815832
|
T | G | 1 | a0001c0002t0002g0044 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.103-2742T>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16815832 | ||||||
chrX:16815940
|
C | T | 8 | a0001c0001t0005g0015a0001c0001t0005g0017a0001c0001t0005g0018others(5): Show | 8 | HG01070.hp1 HG02622.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.103-2634C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16815940 | ||||||
chrX:16816064
|
A | AT | 3 | a0001c0001t0001g0096a0001c0002t0013g0052a0001c0002t0013g0053 | 3 | HG01168.hp2 HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.103-2501dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16816064 | |||||
chrX:16816074
|
C | CT | 1 | a0001c0001t0001g0197 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.103-2490dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16816074 | |||||
chrX:16816134
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.103-2440T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16816134 | ||||||
chrX:16816142
|
G | C | 177 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0094others(174): Show | 177 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.103-2432G>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16816142 | ||||||
chrX:16816292
|
G | A | 3 | a0001c0001t0001g0153a0001c0001t0001g0249a0001c0001t0001g0256 | 3 | NA18982.hp1 NA19010.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.103-2282G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16816292 | ||||||
chrX:16816293
|
GC | G | 1 | a0001c0001t0001g0200 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.103-2279delC | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16816293 | |||||
chrX:16816580
|
A | C | 1 | a0001c0001t0018g0207 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.103-1994A>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16816580 | ||||||
chrX:16816777
|
T | C | 2 | a0001c0001t0012g0089a0001c0001t0012g0173 | 2 | HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.103-1797T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16816777 | ||||||
chrX:16816973
|
A | G | 1 | a0002c0003t0003g0187 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.103-1601A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16816973 | ||||||
chrX:16817385
|
A | C | 1 | a0001c0001t0001g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.103-1189A>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16817385 | ||||||
chrX:16817623
|
C | T | 1 | a0001c0001t0003g0170 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.103-951C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16817623 | ||||||
chrX:16817719
|
A | G | 2 | a0001c0002t0002g0028a0001c0002t0014g0007 | 2 | HG02602.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.103-855A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16817719 | ||||||
chrX:16818027
|
T | G | 1 | a0001c0004t0033g0012 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.103-547T>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16818027 | ||||||
chrX:16818144
|
A | C | 1 | a0001c0001t0001g0197 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.103-430A>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16818144 | ||||||
chrX:16818337
|
T | TG | 1 | a0004c0007t0001g0240 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.103-234dupG | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16818337 | |||||
chrX:16818524
|
A | G | 11 | a0001c0002t0002g0002a0001c0002t0002g0056a0001c0002t0002g0058others(8): Show | 12 | HG01943.hp1 HG01975.hp2 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.103-50A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16818524 | ||||||
chrX:16819105
|
TA | T | 1 | a0001c0002t0002g0058 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.406+234delA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 16819105 | |||||
chrX:16819505
|
T | TA | 1 | a0001c0001t0001g0237 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.406+632dupA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 16819505 | |||||
chrX:16819623
|
T | C | 1 | a0001c0005t0006g0024 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.407-541T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 2/9 | chrX | 16819623 | ||||||
chrX:16819821
|
TA | T | 1 | a0001c0001t0001g0246 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.407-335delA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 16819821 | |||||
chrX:16820396
|
GT | G | 1 | a0001c0002t0002g0058 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.498+145delT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 16820396 | |||||
chrX:16820415
|
T | C | 12 | a0001c0001t0003g0085a0001c0001t0003g0125a0001c0001t0003g0126others(9): Show | 12 | HG01884.hp2 HG02258.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.498+160T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16820415 | ||||||
chrX:16820719
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.498+464C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16820719 | ||||||
chrX:16820803
|
C | G | 8 | a0001c0001t0001g0178a0001c0001t0001g0208a0001c0001t0001g0218others(5): Show | 8 | HG02074.hp1 NA18950.hp1 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.498+548C>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16820803 | ||||||
chrX:16821054
|
T | C | 177 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0094others(174): Show | 177 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.498+799T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16821054 | ||||||
chrX:16821136
|
CTTTCTTT | C | 1 | a0001c0001t0016g0193 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.498+885_498+891del others(7): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 16821136 | |||||
chrX:16821137
|
TTTC | T | 3 | a0001c0001t0001g0191a0001c0001t0001g0232a0001c0001t0003g0162 | 3 | HG01256.hp1 HG03471.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.498+885_498+887del others(3): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 16821137 | |||||
chrX:16821138
|
T | C | 1 | a0001c0001t0006g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.498+883T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16821138 | ||||||
chrX:16821138
|
TTC | T | 167 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0094others(164): Show | 167 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.498+885_498+886del others(2): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 16821138 | |||||
chrX:16821139
|
TC | T | 73 | a0001c0001t0001g0228a0001c0001t0001g0230a0001c0001t0001g0237others(70): Show | 75 | HG00733.hp1 HG00738.hp1 HG00741.hp1 others(72): Show |
intron_variant | MODIFIER | c.498+885delC | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16821139 | ||||||
chrX:16821140
|
C | CT | 1 | a0001c0001t0006g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.498+903dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 16821140 | |||||
chrX:16821140
|
C | T | 1 | a0001c0001t0006g0258 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.498+885C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16821140 | ||||||
chrX:16821140
|
CT | C | 1 | a0001c0002t0002g0059 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.498+903delT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 16821140 | |||||
chrX:16821268
|
G | A | 3 | a0001c0001t0003g0009a0001c0001t0003g0158a0001c0001t0003g0183 | 3 | HG02738.hp1 HG03927.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.498+1013G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16821268 | ||||||
chrX:16821326
|
G | C | 6 | a0001c0001t0003g0085a0001c0001t0003g0125a0001c0001t0003g0126others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.498+1071G>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16821326 | ||||||
chrX:16821341
|
G | A | 1 | a0001c0001t0030g0169 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.498+1086G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16821341 | ||||||
chrX:16821377
|
G | T | 2 | a0001c0001t0006g0257a0001c0001t0006g0258 | 2 | HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.498+1122G>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16821377 | ||||||
chrX:16821382
|
G | A | 2 | a0001c0001t0001g0113a0001c0001t0021g0114 | 2 | HG01106.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.498+1127G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16821382 | ||||||
chrX:16821404
|
T | G | 1 | a0001c0001t0011g0010 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.498+1149T>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16821404 | ||||||
chrX:16821718
|
C | T | 4 | a0001c0001t0001g0199a0001c0001t0001g0230a0001c0002t0002g0059others(1): Show | 4 | HG00323.hp1 HG03927.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.498+1463C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16821718 | ||||||
chrX:16821726
|
C | T | 5 | a0001c0001t0003g0127a0001c0001t0003g0136a0001c0001t0003g0139others(2): Show | 5 | NA18956.hp1 NA18956.hp2 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.498+1471C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16821726 | ||||||
chrX:16821792
|
C | T | 200 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0094others(197): Show | 200 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(197): Show |
intron_variant | MODIFIER | c.498+1537C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16821792 | ||||||
chrX:16821807
|
G | A | 1 | a0001c0001t0001g0241 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.498+1552G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16821807 | ||||||
chrX:16821817
|
T | C | 5 | a0001c0001t0001g0241a0001c0001t0003g0086a0001c0002t0002g0050others(2): Show | 5 | HG02886.hp1 NA18952.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.498+1562T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16821817 | ||||||
chrX:16821834
|
CA | C | 3 | a0001c0001t0001g0153a0001c0001t0001g0249a0001c0001t0001g0256 | 3 | NA18982.hp1 NA19010.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.498+1589delA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 16821834 | |||||
chrX:16821867
|
G | A | 9 | a0001c0001t0001g0112a0001c0001t0001g0115a0001c0001t0001g0118others(6): Show | 9 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.498+1612G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16821867 | ||||||
chrX:16821886
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.498+1631C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16821886 | ||||||
chrX:16821926
|
A | G | 1 | a0001c0001t0003g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.498+1671A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16821926 | ||||||
chrX:16822182
|
C | CA | 3 | a0001c0001t0001g0230a0001c0001t0006g0005a0001c0001t0006g0006 | 3 | HG02970.hp1 NA18967.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.498+1936dupA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 16822182 | |||||
chrX:16822319
|
C | T | 176 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0094others(173): Show | 176 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.498+2064C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16822319 | ||||||
chrX:16822340
|
CA | C | 3 | a0001c0004t0032g0014a0001c0004t0033g0012a0001c0004t0034g0013 | 3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.498+2099delA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 16822340 | |||||
chrX:16822478
|
C | G | 1 | a0001c0002t0002g0066 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.498+2223C>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16822478 | ||||||
chrX:16822840
|
C | T | 2 | a0001c0002t0002g0055a0001c0002t0002g0261 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.498+2585C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16822840 | ||||||
chrX:16822846
|
G | A | 12 | a0001c0001t0006g0005a0001c0001t0006g0006a0001c0001t0006g0064others(9): Show | 12 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.498+2591G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16822846 | ||||||
chrX:16822864
|
G | A | 46 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0100others(43): Show | 46 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.498+2609G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16822864 | ||||||
chrX:16823301
|
A | T | 2 | a0001c0001t0024g0087a0001c0001t0025g0088 | 2 | HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.498+3046A>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16823301 | ||||||
chrX:16823458
|
C | CA | 5 | a0001c0001t0005g0017a0001c0001t0005g0019a0001c0001t0005g0020others(2): Show | 5 | HG01070.hp1 HG02965.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.498+3229dupA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 16823458 | |||||
chrX:16823458
|
C | CAA | 1 | a0001c0001t0005g0015 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.498+3228_498+3229d others(4): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 16823458 | |||||
chrX:16823458
|
CA | C | 227 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0029others(224): Show | 227 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.498+3229delA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 16823458 | |||||
chrX:16823458
|
CAA | C | 6 | a0001c0001t0001g0117a0001c0001t0003g0151a0001c0002t0002g0002others(3): Show | 7 | HG00733.hp1 NA18522.hp1 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.498+3228_498+3229d others(4): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 16823458 | |||||
chrX:16823600
|
C | T | 3 | a0001c0004t0032g0014a0001c0004t0033g0012a0001c0004t0034g0013 | 3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.498+3345C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16823600 | ||||||
chrX:16823816
|
C | A | 2 | a0001c0001t0004g0106a0001c0001t0007g0105 | 2 | NA18955.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.498+3561C>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16823816 | ||||||
chrX:16823936
|
ACT | A | 43 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0026others(40): Show | 45 | HG00733.hp1 HG00738.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.498+3686_498+3687d others(4): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 16823936 | |||||
chrX:16824186
|
G | A | 1 | a0001c0001t0003g0157 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.499-3908G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16824186 | ||||||
chrX:16824200
|
A | G | 2 | a0001c0001t0003g0100a0001c0001t0003g0144 | 2 | NA19062.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.499-3894A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16824200 | ||||||
chrX:16824344
|
C | CA | 1 | a0001c0001t0003g0140 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.499-3736dupA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 16824344 | |||||
chrX:16824344
|
CA | C | 1 | a0001c0001t0001g0237 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.499-3736delA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 16824344 | |||||
chrX:16824762
|
TA | T | 199 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0094others(196): Show | 199 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.499-3319delA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 16824762 | |||||
chrX:16824762
|
TAA | T | 2 | a0001c0001t0003g0151a0001c0001t0031g0147 | 2 | NA18951.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.499-3320_499-3319d others(4): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 16824762 | |||||
chrX:16824882
|
C | T | 3 | a0001c0004t0032g0014a0001c0004t0033g0012a0001c0004t0034g0013 | 3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.499-3212C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16824882 | ||||||
chrX:16825552
|
G | GT | 1 | a0001c0001t0012g0089 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.499-2539dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 16825552 | |||||
chrX:16826102
|
C | A | 21 | a0001c0001t0001g0107a0001c0001t0001g0110a0001c0001t0004g0093others(18): Show | 21 | HG00544.hp1 HG01928.hp1 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.499-1992C>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16826102 | ||||||
chrX:16826274
|
A | G | 3 | a0001c0004t0032g0014a0001c0004t0033g0012a0001c0004t0034g0013 | 3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.499-1820A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16826274 | ||||||
chrX:16826696
|
G | T | 1 | a0001c0004t0033g0012 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.499-1398G>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16826696 | ||||||
chrX:16826708
|
G | A | 176 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0094others(173): Show | 176 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.499-1386G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16826708 | ||||||
chrX:16826946
|
C | A | 2 | a0001c0001t0006g0005a0001c0001t0006g0006 | 2 | HG02970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.499-1148C>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16826946 | ||||||
chrX:16827148
|
G | A | 2 | a0001c0001t0003g0138a0001c0001t0003g0141 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.499-946G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16827148 | ||||||
chrX:16827208
|
A | T | 1 | a0001c0001t0020g0091 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.499-886A>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16827208 | ||||||
chrX:16827285
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.499-809C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16827285 | ||||||
chrX:16827318
|
A | G | 2 | a0001c0001t0006g0257a0001c0001t0006g0258 | 2 | HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.499-776A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16827318 | ||||||
chrX:16827392
|
G | A | 1 | a0001c0001t0030g0169 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.499-702G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16827392 | ||||||
chrX:16827845
|
A | AT | 1 | a0001c0001t0001g0230 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.499-240dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 16827845 | |||||
chrX:16827867
|
G | A | 1 | a0001c0004t0033g0012 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.499-227G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16827867 | ||||||
chrX:16827869
|
T | A | 1 | a0001c0004t0033g0012 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.499-225T>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16827869 | ||||||
chrX:16829029
|
A | AT | 1 | a0001c0001t0003g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.670-537dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chrX | 16829029 | |||||
chrX:16829029
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.670-547A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 4/9 | chrX | 16829029 | ||||||
chrX:16829050
|
A | G | 1 | a0001c0001t0003g0134 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.670-526A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 4/9 | chrX | 16829050 | ||||||
chrX:16829083
|
A | G | 1 | a0001c0001t0030g0169 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.670-493A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 4/9 | chrX | 16829083 | ||||||
chrX:16829203
|
G | A | 3 | a0001c0002t0002g0026a0001c0002t0002g0042a0001c0002t0002g0259 | 3 | HG01192.hp1 HG01433.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.670-373G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 4/9 | chrX | 16829203 | ||||||
chrX:16829855
|
G | C | 2 | a0001c0001t0012g0089a0001c0001t0012g0173 | 2 | HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.864+85G>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | chrX | 16829855 | ||||||
chrX:16829954
|
A | ACT | 8 | a0001c0001t0005g0015a0001c0001t0005g0017a0001c0001t0005g0018others(5): Show | 8 | HG01070.hp1 HG02622.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.864+185_864+186dup others(2): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16829954 | |||||
chrX:16830182
|
A | AT | 175 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0094others(172): Show | 175 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.864+424dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830182 | |||||
chrX:16830195
|
A | T | 1 | a0001c0001t0020g0091 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.864+425A>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | chrX | 16830195 | ||||||
chrX:16830204
|
C | T | 8 | a0001c0001t0005g0015a0001c0001t0005g0017a0001c0001t0005g0018others(5): Show | 8 | HG01070.hp1 HG02622.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.864+434C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | chrX | 16830204 | ||||||
chrX:16830247
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.864+477A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | chrX | 16830247 | ||||||
chrX:16830373
|
A | AGG | 1 | a0001c0001t0001g0229 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.864+604_864+605dup others(2): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830373 | |||||
chrX:16830395
|
C | T | 201 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0094others(198): Show | 201 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(198): Show |
intron_variant | MODIFIER | c.864+625C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | chrX | 16830395 | ||||||
chrX:16830475
|
G | T | 176 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0094others(173): Show | 176 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.864+705G>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | chrX | 16830475 | ||||||
chrX:16830593
|
C | G | 8 | a0001c0001t0005g0015a0001c0001t0005g0017a0001c0001t0005g0018others(5): Show | 8 | HG01070.hp1 HG02622.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.864+823C>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | chrX | 16830593 | ||||||
chrX:16830604
|
T | TA | 3 | a0001c0004t0032g0014a0001c0004t0033g0012a0001c0004t0034g0013 | 3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.864+847dupA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830604 | |||||
chrX:16830604
|
TA | T | 2 | a0001c0001t0001g0217a0001c0001t0001g0237 | 2 | HG03491.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.864+847delA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830604 | |||||
chrX:16830664
|
T | C | 2 | a0001c0001t0003g0127a0001c0001t0027g0131 | 2 | NA18956.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.864+894T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | chrX | 16830664 | ||||||
chrX:16830697
|
A | AT | 6 | a0001c0001t0003g0085a0001c0001t0003g0125a0001c0001t0003g0126others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.864+937dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830697 | |||||
chrX:16830697
|
AT | A | 2 | a0001c0001t0003g0086a0005c0009t0002g0068 | 2 | HG00741.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.864+937delT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830697 | |||||
chrX:16830745
|
A | T | 176 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0094others(173): Show | 176 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.864+975A>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | chrX | 16830745 | ||||||
chrX:16830804
|
G | GGCTTCA | 1 | a0001c0001t0006g0064 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.864+1037_864+1042d others(8): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830804 | |||||
chrX:16830830
|
C | CGT | 5 | a0001c0001t0001g0029a0001c0001t0003g0151a0001c0001t0004g0247others(2): Show | 5 | HG00140.hp1 HG01243.hp1 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.864+1115_864+1116d others(4): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGT | 6 | a0001c0001t0003g0104a0001c0001t0003g0154a0001c0001t0005g0022others(3): Show | 6 | HG02040.hp1 HG02818.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.864+1113_864+1116d others(6): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGT | 9 | a0001c0001t0001g0245a0001c0001t0003g0143a0001c0001t0003g0150others(6): Show | 9 | HG00621.hp1 HG02083.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.864+1111_864+1116d others(8): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGTG others(1): Show |
10 | a0001c0001t0001g0118a0001c0001t0003g0132a0001c0001t0003g0137others(7): Show | 10 | HG00280.hp1 HG00438.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.864+1109_864+1116d others(10): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGTG others(3): Show |
8 | a0001c0001t0003g0009a0001c0001t0003g0100a0001c0001t0003g0138others(5): Show | 8 | HG01168.hp1 HG01169.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.864+1107_864+1116d others(12): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGTG others(5): Show |
7 | a0001c0001t0001g0121a0001c0001t0001g0253a0001c0001t0003g0156others(4): Show | 7 | HG00735.hp2 HG03453.hp1 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.864+1105_864+1116d others(14): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGTG others(7): Show |
8 | a0001c0001t0001g0107a0001c0001t0001g0182a0001c0001t0001g0228others(5): Show | 8 | HG01081.hp2 HG01109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.864+1103_864+1116d others(16): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGTG others(9): Show |
4 | a0001c0001t0003g0085a0001c0001t0003g0161a0001c0001t0003g0185others(1): Show | 4 | HG01884.hp2 HG02280.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.864+1101_864+1116d others(18): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGTG others(11): Show |
9 | a0001c0001t0001g0116a0001c0001t0001g0203a0001c0001t0003g0086others(6): Show | 9 | HG00673.hp1 HG02015.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.864+1099_864+1116d others(20): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGTG others(13): Show |
11 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0190others(8): Show | 11 | HG00639.hp2 HG01069.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.864+1097_864+1116d others(22): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGTG others(15): Show |
8 | a0001c0001t0001g0119a0001c0001t0001g0205a0001c0001t0001g0222others(5): Show | 8 | HG00544.hp2 HG01071.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.864+1095_864+1116d others(24): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGTG others(17): Show |
11 | a0001c0001t0001g0120a0001c0001t0001g0191a0001c0001t0001g0201others(8): Show | 11 | HG00733.hp2 HG01175.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.864+1093_864+1116d others(26): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGTG others(19): Show |
6 | a0001c0001t0001g0179a0001c0001t0001g0202a0001c0001t0004g0177others(3): Show | 6 | HG01175.hp2 HG01258.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.864+1091_864+1116d others(28): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGTG others(21): Show |
7 | a0001c0001t0001g0123a0001c0001t0001g0197a0001c0001t0003g0139others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.864+1089_864+1116d others(30): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGTG others(23): Show |
8 | a0001c0001t0001g0226a0001c0001t0001g0232a0001c0001t0001g0233others(5): Show | 8 | HG01123.hp1 HG01515.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.864+1087_864+1116d others(32): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGTG others(25): Show |
8 | a0001c0001t0001g0094a0001c0001t0001g0117a0001c0001t0001g0241others(5): Show | 8 | HG00639.hp1 HG03540.hp1 HG03540.hp2 others(5): Show |
intron_variant | MODIFIER | c.864+1085_864+1116d others(34): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGTG others(27): Show |
3 | a0001c0001t0001g0196a0001c0001t0008g0063a0001c0001t0019g0129 | 3 | HG00323.hp2 HG02922.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.864+1083_864+1116d others(36): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGTG others(29): Show |
4 | a0001c0001t0001g0210a0001c0001t0001g0230a0001c0001t0025g0088others(1): Show | 4 | HG02055.hp1 HG02572.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.864+1081_864+1116d others(38): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGTG others(31): Show |
2 | a0001c0001t0001g0212a0001c0001t0001g0236 | 2 | HG01346.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.864+1079_864+1116d others(40): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGTG others(35): Show |
3 | a0001c0001t0001g0112a0001c0001t0001g0178a0001c0001t0021g0114 | 3 | HG01106.hp1 HG02976.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.864+1075_864+1116d others(44): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGTG others(37): Show |
2 | a0001c0001t0001g0251a0001c0001t0007g0097 | 2 | HG00544.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.864+1073_864+1116d others(46): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGTG others(39): Show |
7 | a0001c0001t0001g0199a0001c0001t0001g0217a0001c0001t0001g0242others(4): Show | 7 | HG02293.hp1 HG02970.hp1 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.864+1071_864+1116d others(48): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGTG others(41): Show |
4 | a0001c0001t0001g0110a0001c0001t0001g0194a0001c0001t0004g0171others(1): Show | 4 | HG02922.hp1 NA18940.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.864+1069_864+1116d others(50): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGTG others(43): Show |
3 | a0001c0001t0001g0218a0001c0001t0004g0093a0001c0001t0004g0219 | 3 | HG02129.hp1 NA18966.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.864+1067_864+1116d others(52): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGTG others(45): Show |
1 | a0001c0001t0001g0213 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.864+1065_864+1116d others(54): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGTG others(47): Show |
3 | a0001c0001t0001g0003a0001c0001t0001g0208a0004c0007t0001g0240 | 3 | HG00438.hp2 NA19067.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.864+1063_864+1116d others(56): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGTG others(49): Show |
1 | a0001c0001t0001g0250 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.864+1061_864+1116d others(58): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGTG others(51): Show |
5 | a0001c0001t0001g0145a0001c0001t0004g0101a0001c0001t0004g0106others(2): Show | 5 | HG01928.hp1 NA18955.hp1 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.864+1116_864+1117i others(60): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGTG others(53): Show |
3 | a0001c0001t0001g0195a0001c0001t0001g0200a0001c0001t0006g0258 | 3 | HG00735.hp1 HG03225.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.864+1116_864+1117i others(62): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGTG others(55): Show |
4 | a0001c0001t0001g0095a0001c0001t0001g0227a0001c0001t0001g0252others(1): Show | 4 | HG01981.hp1 NA19011.hp2 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.864+1116_864+1117i others(64): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGTG others(57): Show |
4 | a0001c0001t0001g0096a0001c0001t0001g0214a0001c0001t0001g0248others(1): Show | 4 | HG01168.hp2 HG02004.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.864+1116_864+1117i others(66): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGTG others(59): Show |
4 | a0001c0001t0001g0198a0001c0001t0001g0224a0001c0001t0001g0244others(1): Show | 4 | HG01934.hp1 HG01975.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.864+1116_864+1117i others(68): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGTG others(61): Show |
3 | a0001c0001t0001g0206a0001c0001t0001g0229a0001c0001t0001g0256 | 3 | HG00642.hp1 NA18950.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.864+1116_864+1117i others(70): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGTG others(63): Show |
4 | a0001c0001t0001g0172a0001c0001t0001g0237a0001c0001t0004g0174others(1): Show | 4 | HG01255.hp1 HG02970.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.864+1116_864+1117i others(72): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGTG others(65): Show |
1 | a0001c0001t0001g0011 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.864+1116_864+1117i others(74): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGTG others(67): Show |
3 | a0001c0001t0001g0153a0001c0001t0001g0238a0001c0001t0003g0159 | 3 | HG02074.hp1 NA18980.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.864+1116_864+1117i others(76): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGTG others(69): Show |
3 | a0001c0001t0001g0215a0001c0001t0001g0220a0001c0001t0001g0249 | 3 | HG02135.hp1 NA18986.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.864+1116_864+1117i others(78): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGTG others(71): Show |
2 | a0001c0001t0001g0216a0001c0001t0001g0255 | 2 | HG00609.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.864+1116_864+1117i others(80): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGTG others(73): Show |
1 | a0001c0001t0001g0231 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.864+1116_864+1117i others(82): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGTG others(75): Show |
1 | a0001c0002t0013g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.864+1116_864+1117i others(84): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGTG others(79): Show |
1 | a0001c0001t0001g0225 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.864+1116_864+1117i others(88): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
C | CGTGTGTG others(93): Show |
1 | a0001c0001t0004g0175 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.864+1116_864+1117i others(102): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
CGT | C | 5 | a0001c0001t0003g0125a0001c0002t0002g0033a0001c0002t0002g0038others(2): Show | 5 | HG01123.hp2 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.864+1115_864+1116d others(4): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
CGTGT | C | 10 | a0001c0001t0001g0122a0001c0002t0002g0035a0001c0002t0002g0040others(7): Show | 10 | HG00738.hp1 HG02109.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.864+1113_864+1116d others(6): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
CGTGTGT | C | 17 | a0001c0001t0003g0189a0001c0001t0005g0020a0001c0002t0002g0001others(14): Show | 18 | HG00733.hp1 HG00741.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.864+1111_864+1116d others(8): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
CGTGTGTG others(1): Show |
C | 6 | a0001c0002t0002g0047a0001c0002t0002g0057a0001c0002t0002g0067others(3): Show | 6 | HG00741.hp1 HG01074.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.864+1109_864+1116d others(10): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
CGTGTGTG others(3): Show |
C | 9 | a0001c0001t0016g0193a0001c0002t0002g0002a0001c0002t0002g0056others(6): Show | 10 | HG01943.hp1 HG02080.hp1 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.864+1107_864+1116d others(12): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
CGTGTGTG others(5): Show |
C | 4 | a0001c0001t0003g0142a0001c0002t0002g0026a0001c0002t0002g0042others(1): Show | 4 | HG01192.hp1 HG01433.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.864+1105_864+1116d others(14): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
CGTGTGTG others(7): Show |
C | 1 | a0001c0002t0002g0059 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.864+1103_864+1116d others(16): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830830
|
CGTGTGTG others(9): Show |
C | 1 | a0001c0002t0002g0078 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.864+1101_864+1116d others(18): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | |||||
chrX:16830887
|
A | G | 17 | a0001c0001t0001g0211a0001c0001t0003g0188a0001c0001t0006g0005others(14): Show | 17 | HG01175.hp1 HG02055.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.864+1117A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | chrX | 16830887 | ||||||
chrX:16830915
|
A | C | 12 | a0001c0001t0001g0112a0001c0001t0001g0115a0001c0001t0001g0116others(9): Show | 12 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.864+1145A>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | chrX | 16830915 | ||||||
chrX:16830915
|
A | T | 12 | a0001c0001t0006g0005a0001c0001t0006g0006a0001c0001t0006g0064others(9): Show | 12 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.864+1145A>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | chrX | 16830915 | ||||||
chrX:16831184
|
A | C | 1 | a0001c0005t0023g0025 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.864+1414A>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | chrX | 16831184 | ||||||
chrX:16831878
|
G | T | 1 | a0001c0001t0003g0260 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.865-745G>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | chrX | 16831878 | ||||||
chrX:16832000
|
A | T | 1 | a0003c0008t0009g0037 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.865-623A>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | chrX | 16832000 | ||||||
chrX:16832231
|
G | GA | 1 | a0001c0001t0019g0129 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.865-386dupA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16832231 | |||||
chrX:16832463
|
C | A | 175 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0094others(172): Show | 175 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.865-160C>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | chrX | 16832463 | ||||||
chrX:16832467
|
G | A | 1 | a0001c0002t0002g0067 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.865-156G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | chrX | 16832467 | ||||||
chrX:16832808
|
T | G | 1 | a0001c0001t0007g0105 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.984+66T>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 6/9 | chrX | 16832808 | ||||||
chrX:16832915
|
GGT | G | 3 | a0001c0001t0003g0125a0001c0001t0003g0126a0001c0001t0003g0189 | 3 | HG03098.hp1 HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.984+184_984+185del others(2): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chrX | 16832915 | |||||
chrX:16833419
|
T | G | 1 | a0001c0001t0005g0022 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.984+677T>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 6/9 | chrX | 16833419 | ||||||
chrX:16833433
|
C | T | 4 | a0001c0001t0030g0169a0002c0003t0003g0090a0002c0003t0003g0187others(1): Show | 4 | HG02258.hp1 HG02922.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.984+691C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 6/9 | chrX | 16833433 | ||||||
chrX:16833442
|
G | C | 1 | a0001c0001t0007g0105 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.984+700G>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 6/9 | chrX | 16833442 | ||||||
chrX:16833485
|
C | T | 2 | a0001c0002t0002g0054a0001c0002t0002g0262 | 2 | HG01123.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.984+743C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 6/9 | chrX | 16833485 | ||||||
chrX:16833486
|
G | A | 1 | a0001c0005t0006g0024 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.984+744G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 6/9 | chrX | 16833486 | ||||||
chrX:16833624
|
T | TAC | 8 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0204others(5): Show | 8 | HG02451.hp1 HG02970.hp1 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.985-640_985-639dup others(2): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chrX | 16833624 | |||||
chrX:16833624
|
T | TACAC | 3 | a0001c0004t0032g0014a0001c0004t0033g0012a0001c0004t0034g0013 | 3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.985-642_985-639dup others(4): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chrX | 16833624 | |||||
chrX:16833624
|
TAC | T | 16 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0115others(13): Show | 16 | HG00642.hp1 HG00733.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.985-640_985-639del others(2): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chrX | 16833624 | |||||
chrX:16833946
|
A | G | 1 | a0001c0006t0002g0065 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.985-337A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 6/9 | chrX | 16833946 | ||||||
chrX:16834168
|
T | A | 8 | a0001c0001t0005g0015a0001c0001t0005g0017a0001c0001t0005g0018others(5): Show | 8 | HG01070.hp1 HG02622.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.985-115T>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 6/9 | chrX | 16834168 | ||||||
chrX:16834186
|
G | C | 1 | a0001c0005t0006g0024 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.985-97G>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 6/9 | chrX | 16834186 | ||||||
chrX:16834204
|
A | C | 116 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0094others(113): Show | 116 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.985-79A>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 6/9 | chrX | 16834204 | ||||||
chrX:16834218
|
C | A | 2 | a0001c0001t0001g0213a0001c0001t0015g0192 | 2 | NA18972.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.985-65C>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 6/9 | chrX | 16834218 | ||||||
chrX:16834780
|
AACAAG | A | 1 | a0001c0002t0001g0209 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1059+430_1059+434d others(7): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chrX | 16834780 | |||||
chrX:16834806
|
T | TA | 1 | a0001c0001t0003g0136 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1059+456dupA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chrX | 16834806 | |||||
chrX:16834819
|
A | G | 3 | a0001c0004t0032g0014a0001c0004t0033g0012a0001c0004t0034g0013 | 3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1059+462A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 7/9 | chrX | 16834819 | ||||||
chrX:16834984
|
C | T | 3 | a0001c0002t0002g0047a0001c0002t0002g0060a0001c0002t0002g0061 | 3 | HG01074.hp1 HG02735.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1059+627C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 7/9 | chrX | 16834984 | ||||||
chrX:16835006
|
G | C | 1 | a0001c0002t0002g0032 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1059+649G>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 7/9 | chrX | 16835006 | ||||||
chrX:16835058
|
TGTA | T | 1 | a0001c0001t0001g0204 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1059+703_1059+705d others(5): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chrX | 16835058 | |||||
chrX:16835078
|
T | TA | 3 | a0001c0001t0006g0005a0001c0001t0006g0006a0004c0007t0001g0240 | 3 | HG02970.hp1 NA19083.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1059+734dupA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chrX | 16835078 | |||||
chrX:16835153
|
A | G | 1 | a0001c0001t0003g0167 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1059+796A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 7/9 | chrX | 16835153 | ||||||
chrX:16835667
|
G | A | 2 | a0001c0002t0002g0055a0001c0002t0002g0261 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1059+1310G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 7/9 | chrX | 16835667 | ||||||
chrX:16835732
|
CTT | C | 3 | a0001c0002t0002g0050a0001c0002t0002g0051a0001c0002t0002g0062 | 3 | NA18952.hp1 NA18977.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1059+1376_1059+137 others(6): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 7/9 | chrX | 16835732 | ||||||
chrX:16835902
|
T | C | 1 | a0001c0001t0004g0106 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1059+1545T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 7/9 | chrX | 16835902 | ||||||
chrX:16835995
|
C | T | 176 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0094others(173): Show | 176 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.1060-1598C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 7/9 | chrX | 16835995 | ||||||
chrX:16836248
|
T | A | 1 | a0001c0001t0004g0247 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1060-1345T>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 7/9 | chrX | 16836248 | ||||||
chrX:16836494
|
C | T | 1 | a0001c0001t0004g0102 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1060-1099C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 7/9 | chrX | 16836494 | ||||||
chrX:16836992
|
AG | A | 1 | a0001c0001t0019g0129 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1060-596delG | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chrX | 16836992 | |||||
chrX:16837207
|
G | T | 1 | a0001c0002t0002g0078 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1060-386G>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 7/9 | chrX | 16837207 | ||||||
chrX:16837295
|
G | C | 2 | a0001c0001t0006g0257a0001c0001t0006g0258 | 2 | HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1060-298G>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 7/9 | chrX | 16837295 | ||||||
chrX:16837315
|
C | T | 2 | a0001c0001t0001g0199a0001c0001t0001g0230 | 2 | NA18967.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1060-278C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 7/9 | chrX | 16837315 | ||||||
chrX:16837534
|
T | C | 2 | a0001c0002t0002g0034a0001c0002t0002g0067 | 2 | HG00733.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.1060-59T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 7/9 | chrX | 16837534 | ||||||
chrX:16837842
|
A | G | 3 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0224 | 3 | HG03139.hp1 NA18522.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1152+157A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 8/9 | chrX | 16837842 | ||||||
chrX:16837941
|
G | T | 1 | a0001c0001t0003g0161 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1152+256G>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 8/9 | chrX | 16837941 | ||||||
chrX:16838026
|
G | A | 1 | a0001c0001t0003g0134 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1152+341G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 8/9 | chrX | 16838026 | ||||||
chrX:16838719
|
G | A | 1 | a0001c0002t0002g0259 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1152+1034G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 8/9 | chrX | 16838719 | ||||||
chrX:16839348
|
C | CT | 1 | a0001c0001t0022g0184 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1153-471dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 16839348 | |||||
chrX:16839479
|
C | T | 1 | a0001c0001t0003g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1153-342C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 8/9 | chrX | 16839479 | ||||||
chrX:16840042
|
TG | T | 1 | a0001c0001t0019g0129 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1248+130delG | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 16840042 | |||||
chrX:16840181
|
T | TA | 1 | a0004c0007t0001g0240 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1248+269dupA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 16840181 | |||||
chrX:16840331
|
C | CT | 1 | a0001c0002t0002g0036 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1248+416dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 16840331 | |||||
chrX:16840397
|
C | CA | 1 | a0004c0007t0001g0240 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1248+488dupA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 16840397 | |||||
chrX:16840552
|
T | A | 1 | a0001c0001t0001g0190 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1248+636T>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 9/9 | chrX | 16840552 | ||||||
chrX:16840642
|
C | T | 1 | a0001c0001t0028g0130 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1248+726C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 9/9 | chrX | 16840642 | ||||||
chrX:16840653
|
T | C | 178 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0029others(175): Show | 178 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.1248+737T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 9/9 | chrX | 16840653 | ||||||
chrX:16840703
|
C | T | 1 | a0001c0001t0020g0091 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1249-725C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 9/9 | chrX | 16840703 | ||||||
chrX:16840842
|
A | G | 1 | a0001c0002t0002g0262 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1249-586A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 9/9 | chrX | 16840842 | ||||||
chrX:16840950
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1249-478G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 9/9 | chrX | 16840950 | ||||||
chrX:16840963
|
A | G | 1 | a0001c0001t0016g0193 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1249-465A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 9/9 | chrX | 16840963 | ||||||
chrX:16841012
|
T | C | 1 | a0001c0001t0007g0180 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1249-416T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 9/9 | chrX | 16841012 | ||||||
chrX:16841021
|
T | C | 3 | a0001c0001t0004g0219a0001c0001t0007g0176a0001c0001t0019g0129 | 3 | NA18968.hp1 NA18974.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.1249-407T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 9/9 | chrX | 16841021 | ||||||
chrX:16841022
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1249-406C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 9/9 | chrX | 16841022 | ||||||
chrX:16841032
|
TA | T | 1 | a0001c0002t0013g0052 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1249-391delA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 16841032 | |||||
chrX:16841054
|
G | A | 2 | a0001c0001t0003g0009a0001c0001t0003g0183 | 2 | HG02738.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1249-374G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 9/9 | chrX | 16841054 | ||||||
chrX:16841092
|
T | G | 1 | a0001c0001t0003g0104 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1249-336T>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 9/9 | chrX | 16841092 | ||||||
chrX:16841156
|
T | C | 177 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0029others(174): Show | 177 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.1249-272T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 9/9 | chrX | 16841156 | ||||||
chrX:16841193
|
C | CA | 40 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0095others(37): Show | 40 | HG00438.hp2 HG00642.hp1 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.1249-222dupA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 16841193 | |||||
chrX:16841193
|
C | CAA | 1 | a0001c0001t0015g0192 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1249-223_1249-222d others(4): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 16841193 |