Item | Value |
---|---|
geneid | 84951 |
ensemblid | ENSG00000131746.13 |
hgncid | 24352 |
symbol | TNS4 |
name | tensin 4 |
refseq_nuc | NM_032865.6 |
refseq_prot | NP_116254.4 |
ensembl_nuc | ENST00000254051.11 |
ensembl_prot | ENSP00000254051.6 |
mane_status | MANE Select |
chr | chr17 |
start | 40475834 |
end | 40501623 |
strand | - |
ver | v1.2 |
region | chr17:40475834-40501623 |
region5000 | chr17:40470834-40506623 |
regionname0 | TNS4_chr17_40475834_40501623 |
regionname5000 | TNS4_chr17_40470834_40506623 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 715 | 232 | 54 | 45 | 90 | 14 | 28 | 62 | TNS4_chr17_40470834_40506623 | TNS4 | MSQVM others(710): Show |
chr17 | 40470834 | 40506623 |
a0002 | 0/1 | 715 | 110 | 11 | 23 | 55 | 2 | 18 | 39 | TNS4_chr17_40470834_40506623 | TNS4 | MSQVM others(710): Show |
chr17 | 40470834 | 40506623 |
a0003 | 0/0 | 715 | 28 | 25 | 2 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | MSQVM others(710): Show |
chr17 | 40470834 | 40506623 |
a0004 | 0/0 | 715 | 6 | 0 | 0 | 6 | 0 | 0 | 4 | TNS4_chr17_40470834_40506623 | TNS4 | MSQVM others(710): Show |
chr17 | 40470834 | 40506623 |
a0005 | 0/0 | 715 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | MSQVM others(710): Show |
chr17 | 40470834 | 40506623 |
a0006 | 0/0 | 715 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | MSQVM others(710): Show |
chr17 | 40470834 | 40506623 |
a0007 | 0/0 | 715 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | MSQVM others(710): Show |
chr17 | 40470834 | 40506623 |
a0008 | 0/0 | 715 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | MSQVM others(710): Show |
chr17 | 40470834 | 40506623 |
a0009 | 0/0 | 715 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | MSQVM others(710): Show |
chr17 | 40470834 | 40506623 |
a0010 | 0/0 | 715 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | MSQVM others(710): Show |
chr17 | 40470834 | 40506623 |
a0011 | 0/0 | 715 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | MSQVM others(710): Show |
chr17 | 40470834 | 40506623 |
a0012 | 0/0 | 715 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | MSQVM others(710): Show |
chr17 | 40470834 | 40506623 |
a0013 | 0/0 | 715 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | MSQVM others(710): Show |
chr17 | 40470834 | 40506623 |
a0014 | 0/0 | 715 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | MSQVM others(710): Show |
chr17 | 40470834 | 40506623 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2145 | 215 | 41 | 42 | 89 | 14 | 28 | TNS4_chr17_40470834_40506623 | TNS4 | ATGTC others(2140): Show |
chr17 | 40470834 | 40506623 | ||
a0001c0004 | 0/0 | 2145 | 10 | 8 | 2 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | ATGTC others(2140): Show |
chr17 | 40470834 | 40506623 | ||
a0001c0006 | 0/0 | 2145 | 3 | 3 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | ATGTC others(2140): Show |
chr17 | 40470834 | 40506623 | ||
a0001c0008 | 0/0 | 2145 | 2 | 2 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | ATGTC others(2140): Show |
chr17 | 40470834 | 40506623 | ||
a0001c0018 | 0/0 | 2145 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | ATGTC others(2140): Show |
chr17 | 40470834 | 40506623 | ||
a0001c0021 | 0/0 | 2145 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | ATGTC others(2140): Show |
chr17 | 40470834 | 40506623 | ||
a0002c0002 | 0/1 | 2145 | 109 | 11 | 23 | 54 | 2 | 18 | TNS4_chr17_40470834_40506623 | TNS4 | ATGTC others(2140): Show |
chr17 | 40470834 | 40506623 | ||
a0002c0015 | 0/0 | 2145 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | ATGTC others(2140): Show |
chr17 | 40470834 | 40506623 | ||
a0003c0003 | 0/0 | 2145 | 28 | 25 | 2 | 0 | 1 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | ATGTC others(2140): Show |
chr17 | 40470834 | 40506623 | ||
a0004c0005 | 0/0 | 2145 | 6 | 0 | 0 | 6 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | ATGTC others(2140): Show |
chr17 | 40470834 | 40506623 | ||
a0005c0007 | 0/0 | 2145 | 3 | 3 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | ATGTC others(2140): Show |
chr17 | 40470834 | 40506623 | ||
a0005c0009 | 0/0 | 2145 | 2 | 2 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | ATGTC others(2140): Show |
chr17 | 40470834 | 40506623 | ||
a0006c0010 | 0/0 | 2145 | 2 | 0 | 2 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | ATGTC others(2140): Show |
chr17 | 40470834 | 40506623 | ||
a0007c0011 | 0/0 | 2145 | 2 | 0 | 2 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | ATGTC others(2140): Show |
chr17 | 40470834 | 40506623 | ||
a0008c0019 | 0/0 | 2145 | 1 | 0 | 0 | 0 | 1 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | ATGTC others(2140): Show |
chr17 | 40470834 | 40506623 | ||
a0009c0013 | 0/0 | 2145 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | ATGTC others(2140): Show |
chr17 | 40470834 | 40506623 | ||
a0010c0017 | 0/0 | 2145 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | ATGTC others(2140): Show |
chr17 | 40470834 | 40506623 | ||
a0011c0014 | 0/0 | 2145 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | ATGTC others(2140): Show |
chr17 | 40470834 | 40506623 | ||
a0012c0016 | 0/0 | 2145 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | ATGTC others(2140): Show |
chr17 | 40470834 | 40506623 | ||
a0013c0012 | 0/0 | 2145 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | ATGTC others(2140): Show |
chr17 | 40470834 | 40506623 | ||
a0014c0020 | 0/0 | 2145 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | ATGTC others(2140): Show |
chr17 | 40470834 | 40506623 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4083 | 26 | 3 | 3 | 12 | 3 | 5 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4078): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0002 | 1/0 | 4087 | 14 | 0 | 0 | 13 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4082): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0003 | 0/0 | 4085 | 11 | 0 | 0 | 9 | 0 | 2 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4080): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0004 | 0/0 | 4083 | 17 | 1 | 1 | 12 | 2 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4078): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0005 | 0/0 | 4070 | 6 | 6 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4065): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0006 | 0/0 | 4093 | 3 | 0 | 0 | 2 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4088): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0007 | 0/0 | 4089 | 7 | 3 | 0 | 4 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4084): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0008 | 0/0 | 4085 | 14 | 2 | 7 | 2 | 0 | 3 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4080): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0009 | 0/0 | 4081 | 7 | 2 | 0 | 4 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4076): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0010 | 0/0 | 4091 | 2 | 0 | 0 | 1 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4086): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0011 | 0/0 | 4072 | 7 | 7 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4067): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0012 | 0/0 | 4081 | 13 | 0 | 6 | 6 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4076): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0013 | 0/0 | 4084 | 12 | 2 | 3 | 0 | 4 | 3 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4079): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0014 | 0/0 | 4095 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4090): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0015 | 0/0 | 4097 | 2 | 0 | 2 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4092): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0016 | 0/0 | 4079 | 5 | 1 | 0 | 4 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4074): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0017 | 0/0 | 4077 | 3 | 0 | 0 | 2 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4072): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0018 | 0/0 | 4079 | 7 | 0 | 3 | 2 | 1 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4074): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0019 | 0/0 | 4101 | 3 | 0 | 2 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4096): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0020 | 0/0 | 4087 | 5 | 2 | 1 | 1 | 1 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4082): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0021 | 0/0 | 4080 | 5 | 0 | 2 | 0 | 1 | 2 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4075): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0022 | 0/0 | 4103 | 2 | 0 | 2 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4098): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0023 | 0/0 | 4099 | 2 | 1 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4094): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0024 | 0/0 | 4085 | 4 | 0 | 0 | 4 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4080): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0025 | 0/0 | 4082 | 4 | 1 | 2 | 0 | 1 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4077): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0027 | 0/0 | 4068 | 3 | 3 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4063): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0028 | 0/0 | 4077 | 2 | 0 | 1 | 0 | 1 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4072): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0029 | 0/0 | 4072 | 3 | 3 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4067): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0030 | 0/0 | 4105 | 2 | 0 | 2 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4100): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0031 | 0/0 | 4083 | 2 | 0 | 0 | 2 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4078): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0032 | 0/0 | 4082 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4077): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0033 | 0/0 | 4082 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4077): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0035 | 0/0 | 4074 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4069): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0037 | 0/0 | 4091 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4086): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0038 | 0/0 | 4089 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4084): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0039 | 0/0 | 4075 | 2 | 0 | 2 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4070): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0040 | 0/0 | 4082 | 2 | 0 | 0 | 2 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4077): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0047 | 0/0 | 4107 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4102): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0050 | 0/0 | 4057 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4052): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0052 | 0/0 | 4083 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4078): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0054 | 0/0 | 4076 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4071): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0056 | 0/0 | 4072 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4067): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0058 | 0/0 | 4093 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4088): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0059 | 0/0 | 4070 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4065): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0061 | 0/0 | 4066 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4061): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0062 | 0/0 | 4085 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4080): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0066 | 0/0 | 4084 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4079): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0067 | 0/0 | 4082 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4077): Show |
chr17 | 40470834 | 40506623 |
a0001c0001t0073 | 0/0 | 4085 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4080): Show |
chr17 | 40470834 | 40506623 |
a0001c0004t0002 | 0/0 | 4087 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4082): Show |
chr17 | 40470834 | 40506623 |
a0001c0004t0005 | 0/0 | 4070 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4065): Show |
chr17 | 40470834 | 40506623 |
a0001c0004t0006 | 0/0 | 4093 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4088): Show |
chr17 | 40470834 | 40506623 |
a0001c0004t0008 | 0/0 | 4085 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4080): Show |
chr17 | 40470834 | 40506623 |
a0001c0004t0041 | 0/0 | 4083 | 2 | 2 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4078): Show |
chr17 | 40470834 | 40506623 |
a0001c0004t0045 | 0/0 | 4086 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4081): Show |
chr17 | 40470834 | 40506623 |
a0001c0004t0055 | 0/0 | 4076 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4071): Show |
chr17 | 40470834 | 40506623 |
a0001c0004t0063 | 0/0 | 4092 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4087): Show |
chr17 | 40470834 | 40506623 |
a0001c0004t0065 | 0/0 | 4078 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4073): Show |
chr17 | 40470834 | 40506623 |
a0001c0006t0008 | 0/0 | 4085 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4080): Show |
chr17 | 40470834 | 40506623 |
a0001c0006t0013 | 0/0 | 4084 | 2 | 2 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4079): Show |
chr17 | 40470834 | 40506623 |
a0001c0008t0043 | 0/0 | 4087 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4082): Show |
chr17 | 40470834 | 40506623 |
a0001c0008t0044 | 0/0 | 4073 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4068): Show |
chr17 | 40470834 | 40506623 |
a0001c0018t0016 | 0/0 | 4079 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4074): Show |
chr17 | 40470834 | 40506623 |
a0001c0021t0038 | 0/0 | 4089 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4084): Show |
chr17 | 40470834 | 40506623 |
a0002c0002t0001 | 0/0 | 4083 | 3 | 0 | 0 | 1 | 0 | 2 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4078): Show |
chr17 | 40470834 | 40506623 |
a0002c0002t0002 | 0/0 | 4087 | 9 | 0 | 3 | 6 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4082): Show |
chr17 | 40470834 | 40506623 |
a0002c0002t0003 | 0/0 | 4085 | 12 | 2 | 3 | 4 | 0 | 3 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4080): Show |
chr17 | 40470834 | 40506623 |
a0002c0002t0004 | 0/0 | 4083 | 5 | 1 | 0 | 4 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4078): Show |
chr17 | 40470834 | 40506623 |
a0002c0002t0006 | 0/0 | 4093 | 14 | 0 | 1 | 8 | 2 | 3 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4088): Show |
chr17 | 40470834 | 40506623 |
a0002c0002t0007 | 0/0 | 4089 | 9 | 0 | 2 | 4 | 0 | 3 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4084): Show |
chr17 | 40470834 | 40506623 |
a0002c0002t0009 | 0/0 | 4081 | 8 | 3 | 0 | 4 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4076): Show |
chr17 | 40470834 | 40506623 |
a0002c0002t0010 | 0/0 | 4091 | 9 | 0 | 4 | 4 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4086): Show |
chr17 | 40470834 | 40506623 |
a0002c0002t0014 | 0/1 | 4095 | 10 | 0 | 2 | 6 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4090): Show |
chr17 | 40470834 | 40506623 |
a0002c0002t0015 | 0/0 | 4097 | 8 | 1 | 3 | 3 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4092): Show |
chr17 | 40470834 | 40506623 |
a0002c0002t0016 | 0/0 | 4079 | 3 | 0 | 2 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4074): Show |
chr17 | 40470834 | 40506623 |
a0002c0002t0017 | 0/0 | 4077 | 4 | 0 | 2 | 2 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4072): Show |
chr17 | 40470834 | 40506623 |
a0002c0002t0019 | 0/0 | 4101 | 3 | 0 | 0 | 3 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4096): Show |
chr17 | 40470834 | 40506623 |
a0002c0002t0020 | 0/0 | 4087 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4082): Show |
chr17 | 40470834 | 40506623 |
a0002c0002t0022 | 0/0 | 4103 | 2 | 0 | 1 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4098): Show |
chr17 | 40470834 | 40506623 |
a0002c0002t0023 | 0/0 | 4099 | 2 | 0 | 0 | 1 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4094): Show |
chr17 | 40470834 | 40506623 |
a0002c0002t0028 | 0/0 | 4077 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4072): Show |
chr17 | 40470834 | 40506623 |
a0002c0002t0032 | 0/0 | 4082 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4077): Show |
chr17 | 40470834 | 40506623 |
a0002c0002t0037 | 0/0 | 4091 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4086): Show |
chr17 | 40470834 | 40506623 |
a0002c0002t0049 | 0/0 | 4071 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4066): Show |
chr17 | 40470834 | 40506623 |
a0002c0002t0064 | 0/0 | 4078 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4073): Show |
chr17 | 40470834 | 40506623 |
a0002c0002t0069 | 0/0 | 4084 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4079): Show |
chr17 | 40470834 | 40506623 |
a0002c0002t0072 | 0/0 | 4087 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4082): Show |
chr17 | 40470834 | 40506623 |
a0002c0015t0014 | 0/0 | 4095 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4090): Show |
chr17 | 40470834 | 40506623 |
a0003c0003t0005 | 0/0 | 4070 | 12 | 11 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4065): Show |
chr17 | 40470834 | 40506623 |
a0003c0003t0008 | 0/0 | 4085 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4080): Show |
chr17 | 40470834 | 40506623 |
a0003c0003t0011 | 0/0 | 4072 | 7 | 7 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4067): Show |
chr17 | 40470834 | 40506623 |
a0003c0003t0026 | 0/0 | 4070 | 3 | 3 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4065): Show |
chr17 | 40470834 | 40506623 |
a0003c0003t0036 | 0/0 | 4074 | 2 | 2 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4069): Show |
chr17 | 40470834 | 40506623 |
a0003c0003t0051 | 0/0 | 4089 | 1 | 0 | 0 | 0 | 1 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4084): Show |
chr17 | 40470834 | 40506623 |
a0003c0003t0053 | 0/0 | 4086 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4081): Show |
chr17 | 40470834 | 40506623 |
a0003c0003t0057 | 0/0 | 4072 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4067): Show |
chr17 | 40470834 | 40506623 |
a0004c0005t0002 | 0/0 | 4087 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4082): Show |
chr17 | 40470834 | 40506623 |
a0004c0005t0003 | 0/0 | 4085 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4080): Show |
chr17 | 40470834 | 40506623 |
a0004c0005t0007 | 0/0 | 4089 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4084): Show |
chr17 | 40470834 | 40506623 |
a0004c0005t0010 | 0/0 | 4091 | 3 | 0 | 0 | 3 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4086): Show |
chr17 | 40470834 | 40506623 |
a0005c0007t0042 | 0/0 | 4080 | 2 | 2 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4075): Show |
chr17 | 40470834 | 40506623 |
a0005c0007t0070 | 0/0 | 4082 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4077): Show |
chr17 | 40470834 | 40506623 |
a0005c0009t0060 | 0/0 | 4071 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4066): Show |
chr17 | 40470834 | 40506623 |
a0005c0009t0071 | 0/0 | 4078 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4073): Show |
chr17 | 40470834 | 40506623 |
a0006c0010t0034 | 0/0 | 4078 | 2 | 0 | 2 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4073): Show |
chr17 | 40470834 | 40506623 |
a0007c0011t0033 | 0/0 | 4082 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4077): Show |
chr17 | 40470834 | 40506623 |
a0007c0011t0035 | 0/0 | 4074 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4069): Show |
chr17 | 40470834 | 40506623 |
a0008c0019t0048 | 0/0 | 4073 | 1 | 0 | 0 | 0 | 1 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4068): Show |
chr17 | 40470834 | 40506623 |
a0009c0013t0068 | 0/0 | 4080 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4075): Show |
chr17 | 40470834 | 40506623 |
a0010c0017t0012 | 0/0 | 4081 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4076): Show |
chr17 | 40470834 | 40506623 |
a0011c0014t0005 | 0/0 | 4070 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4065): Show |
chr17 | 40470834 | 40506623 |
a0012c0016t0002 | 0/0 | 4087 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4082): Show |
chr17 | 40470834 | 40506623 |
a0013c0012t0046 | 0/0 | 4087 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4082): Show |
chr17 | 40470834 | 40506623 |
a0014c0020t0002 | 0/0 | 4087 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | GCCTC others(4082): Show |
chr17 | 40470834 | 40506623 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0002g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0002g0053 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0003g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0004g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0004g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0004g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0005g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0005g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0005g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0005g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0006g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0006g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0006g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0007g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0007g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0007g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0007g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0007g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0007g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0007g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0008g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0008g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0008g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0008g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0008g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0008g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0008g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0008g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0008g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0008g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0008g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0009g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0009g0013 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0009g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0009g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0009g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0010g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0010g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0011g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0011g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0011g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0011g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0011g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0011g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0012g0001 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0012g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0012g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0012g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0012g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0012g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0013g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0013g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0013g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0013g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0013g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0013g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0013g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0013g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0013g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0013g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0014g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0015g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0016g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0016g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0016g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0016g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0017g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0017g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0017g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0018g0017 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0018g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0018g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0018g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0018g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0018g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0019g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0019g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0020g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0020g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0020g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0020g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0020g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0021g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0021g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0021g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0021g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0021g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0022g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0022g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0023g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0023g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0024g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0024g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0024g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0024g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0025g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0025g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0025g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0025g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0027g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0027g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0028g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0028g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0029g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0029g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0030g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0031g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0031g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0032g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0033g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0035g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0037g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0038g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0039g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0039g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0040g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0047g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0050g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0052g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0054g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0056g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0058g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0059g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0061g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0062g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0066g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0067g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0001t0073g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0004t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0004t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0004t0006g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0004t0008g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0004t0041g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0004t0045g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0004t0055g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0004t0063g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0004t0065g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0006t0008g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0006t0013g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0008t0043g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0008t0044g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0018t0016g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0001c0021t0038g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0003g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0003g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0004g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0006g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0006g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0006g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0006g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0006g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0006g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0006g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0006g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0006g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0006g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0006g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0006g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0006g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0006g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0007g0015 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0007g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0007g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0007g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0007g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0007g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0007g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0007g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0009g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0009g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0009g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0009g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0009g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0009g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0009g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0009g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0010g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0010g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0010g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0010g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0010g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0010g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0010g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0014g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0014g0044 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0014g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0014g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0014g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0014g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0014g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0014g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0014g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0015g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0015g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0015g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0015g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0015g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0015g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0015g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0015g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0016g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0016g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0016g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0017g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0017g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0017g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0017g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0019g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0019g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0020g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0022g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0022g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0023g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0023g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0028g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0032g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0037g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0049g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0064g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0069g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0002t0072g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0002c0015t0014g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0003c0003t0005g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0003c0003t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0003c0003t0005g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0003c0003t0005g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0003c0003t0005g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0003c0003t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0003c0003t0005g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0003c0003t0005g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0003c0003t0005g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0003c0003t0005g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0003c0003t0005g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0003c0003t0005g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0003c0003t0008g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0003c0003t0011g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0003c0003t0011g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0003c0003t0011g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0003c0003t0011g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0003c0003t0011g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0003c0003t0011g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0003c0003t0011g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0003c0003t0026g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0003c0003t0026g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0003c0003t0026g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0003c0003t0036g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0003c0003t0036g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0003c0003t0051g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0003c0003t0053g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0003c0003t0057g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0004c0005t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0004c0005t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0004c0005t0007g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0004c0005t0010g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0004c0005t0010g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0004c0005t0010g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0005c0007t0042g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0005c0007t0042g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0005c0007t0070g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0005c0009t0060g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0005c0009t0071g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0006c0010t0034g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0006c0010t0034g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0007c0011t0033g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0007c0011t0035g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0008c0019t0048g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0009c0013t0068g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0010c0017t0012g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0011c0014t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0012c0016t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0013c0012t0046g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
a0014c0020t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0018 | g0017 | EUR | GBR | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG00099 | hp2 | a0001 | c0001 | t0021 | g0058 | EUR | GBR | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG00140 | hp1 | a0008 | c0019 | t0048 | g0147 | EUR | GBR | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG00140 | hp2 | a0001 | c0001 | t0004 | g0220 | EUR | GBR | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG00280 | hp1 | a0001 | c0001 | t0028 | g0090 | EUR | FIN | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0155 | EUR | FIN | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG00323 | hp1 | a0001 | c0001 | t0025 | g0109 | EUR | FIN | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0252 | EUR | FIN | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG00408 | hp1 | a0002 | c0002 | t0006 | g0331 | EAS | CHS | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | CHS | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0267 | EAS | CHS | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | CHS | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG00438 | hp1 | a0001 | c0001 | t0008 | g0134 | EAS | CHS | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG00438 | hp2 | a0001 | c0001 | t0050 | g0270 | EAS | CHS | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG00544 | hp1 | a0001 | c0001 | t0004 | g0153 | EAS | CHS | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG00544 | hp2 | a0001 | c0001 | t0052 | g0163 | EAS | CHS | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG00558 | hp1 | a0001 | c0001 | t0009 | g0010 | EAS | CHS | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG00558 | hp2 | a0002 | c0002 | t0002 | g0204 | EAS | CHS | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG00597 | hp1 | a0001 | c0018 | t0016 | g0168 | EAS | CHS | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG00597 | hp2 | a0002 | c0002 | t0006 | g0261 | EAS | CHS | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | CHS | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG00609 | hp2 | a0002 | c0002 | t0006 | g0182 | EAS | CHS | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG00621 | hp1 | a0001 | c0001 | t0018 | g0337 | EAS | CHS | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG00621 | hp2 | a0002 | c0002 | t0009 | g0327 | EAS | CHS | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG00639 | hp1 | a0002 | c0002 | t0003 | g0212 | AMR | PUR | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG00639 | hp2 | a0001 | c0001 | t0012 | g0322 | AMR | PUR | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG00642 | hp1 | a0001 | c0001 | t0018 | g0259 | AMR | PUR | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG00642 | hp2 | a0002 | c0002 | t0010 | g0096 | AMR | PUR | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG00673 | hp1 | a0001 | c0001 | t0004 | g0106 | EAS | CHS | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG00673 | hp2 | a0002 | c0002 | t0014 | g0014 | EAS | CHS | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG00735 | hp1 | a0001 | c0001 | t0038 | g0047 | AMR | PUR | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG00735 | hp2 | a0001 | c0021 | t0038 | g0236 | AMR | PUR | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG00738 | hp1 | a0001 | c0001 | t0047 | g0228 | AMR | PUR | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG00738 | hp2 | a0002 | c0002 | t0022 | g0206 | AMR | PUR | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG00741 | hp1 | a0001 | c0001 | t0025 | g0293 | AMR | PUR | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG00741 | hp2 | a0001 | c0001 | t0021 | g0098 | AMR | PUR | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01069 | hp1 | a0001 | c0001 | t0012 | g0006 | AMR | PUR | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01069 | hp2 | a0006 | c0010 | t0034 | g0318 | AMR | PUR | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01070 | hp1 | a0001 | c0001 | t0023 | g0235 | AMR | PUR | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01070 | hp2 | a0001 | c0001 | t0039 | g0226 | AMR | PUR | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01071 | hp1 | a0006 | c0010 | t0034 | g0319 | AMR | PUR | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01071 | hp2 | a0001 | c0001 | t0039 | g0224 | AMR | PUR | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01074 | hp1 | a0002 | c0002 | t0016 | g0241 | AMR | PUR | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01074 | hp2 | a0001 | c0001 | t0008 | g0321 | AMR | PUR | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01081 | hp1 | a0009 | c0013 | t0068 | g0347 | AMR | PUR | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01081 | hp2 | a0002 | c0002 | t0003 | g0016 | AMR | PUR | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01099 | hp1 | a0002 | c0002 | t0016 | g0202 | AMR | PUR | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01099 | hp2 | a0001 | c0001 | t0008 | g0132 | AMR | PUR | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01109 | hp1 | a0007 | c0011 | t0035 | g0135 | AMR | PUR | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01109 | hp2 | a0001 | c0004 | t0063 | g0348 | AMR | PUR | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01168 | hp1 | a0001 | c0001 | t0012 | g0006 | AMR | PUR | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01168 | hp2 | a0002 | c0002 | t0002 | g0045 | AMR | PUR | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01169 | hp1 | a0002 | c0002 | t0015 | g0183 | AMR | PUR | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01169 | hp2 | a0001 | c0001 | t0012 | g0006 | AMR | PUR | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01175 | hp1 | a0007 | c0011 | t0033 | g0320 | AMR | PUR | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01175 | hp2 | a0001 | c0001 | t0018 | g0335 | AMR | PUR | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01192 | hp1 | a0002 | c0002 | t0017 | g0203 | AMR | PUR | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01192 | hp2 | a0001 | c0001 | t0013 | g0219 | AMR | PUR | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01243 | hp1 | a0001 | c0001 | t0008 | g0011 | AMR | PUR | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01243 | hp2 | a0003 | c0003 | t0005 | g0323 | AMR | PUR | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01256 | hp1 | a0001 | c0001 | t0018 | g0243 | AMR | CLM | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01256 | hp2 | a0002 | c0002 | t0010 | g0003 | AMR | CLM | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01257 | hp1 | a0001 | c0001 | t0013 | g0008 | AMR | CLM | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01257 | hp2 | a0002 | c0002 | t0010 | g0003 | AMR | CLM | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01258 | hp1 | a0002 | c0002 | t0010 | g0003 | AMR | CLM | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01258 | hp2 | a0001 | c0001 | t0013 | g0008 | AMR | CLM | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01261 | hp2 | a0003 | c0003 | t0008 | g0187 | AMR | CLM | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01346 | hp1 | a0001 | c0001 | t0022 | g0221 | AMR | CLM | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01346 | hp2 | a0002 | c0002 | t0002 | g0188 | AMR | CLM | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01358 | hp1 | a0001 | c0001 | t0008 | g0317 | AMR | CLM | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01358 | hp2 | a0002 | c0002 | t0007 | g0333 | AMR | CLM | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01361 | hp1 | a0002 | c0002 | t0014 | g0216 | AMR | CLM | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01361 | hp2 | a0001 | c0004 | t0008 | g0174 | AMR | CLM | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01433 | hp1 | a0010 | c0017 | t0012 | g0294 | AMR | CLM | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01433 | hp2 | a0002 | c0002 | t0007 | g0097 | AMR | CLM | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01496 | hp1 | a0002 | c0002 | t0015 | g0207 | AMR | CLM | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01496 | hp2 | a0001 | c0001 | t0020 | g0222 | AMR | CLM | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0169 | EUR | IBS | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01515 | hp2 | a0001 | c0001 | t0013 | g0025 | EUR | IBS | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01516 | hp1 | a0001 | c0001 | t0013 | g0093 | EUR | IBS | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01516 | hp2 | a0003 | c0003 | t0051 | g0211 | EUR | IBS | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01517 | hp1 | a0001 | c0001 | t0013 | g0094 | EUR | IBS | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01517 | hp2 | a0001 | c0001 | t0013 | g0025 | EUR | IBS | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01884 | hp1 | a0002 | c0002 | t0015 | g0287 | AFR | ACB | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01884 | hp2 | a0003 | c0003 | t0005 | g0117 | AFR | ACB | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01891 | hp1 | a0001 | c0001 | t0005 | g0035 | AFR | ACB | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01891 | hp2 | a0005 | c0007 | t0042 | g0238 | AFR | ACB | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01934 | hp1 | a0001 | c0001 | t0012 | g0125 | AMR | PEL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01934 | hp2 | a0001 | c0001 | t0028 | g0218 | AMR | PEL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01943 | hp2 | a0001 | c0001 | t0030 | g0019 | AMR | PEL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01952 | hp1 | a0001 | c0001 | t0012 | g0001 | AMR | PEL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01952 | hp2 | a0001 | c0001 | t0019 | g0020 | AMR | PEL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01975 | hp1 | a0001 | c0001 | t0008 | g0004 | AMR | PEL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01975 | hp2 | a0001 | c0001 | t0019 | g0020 | AMR | PEL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01978 | hp1 | a0001 | c0001 | t0022 | g0234 | AMR | PEL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01981 | hp1 | a0002 | c0002 | t0003 | g0080 | AMR | PEL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01981 | hp2 | a0001 | c0001 | t0008 | g0004 | AMR | PEL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01993 | hp1 | a0002 | c0002 | t0002 | g0092 | AMR | PEL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01993 | hp2 | a0001 | c0001 | t0025 | g0067 | AMR | PEL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02004 | hp1 | a0001 | c0001 | t0015 | g0021 | AMR | PEL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02004 | hp2 | a0002 | c0002 | t0015 | g0084 | AMR | PEL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02015 | hp2 | a0002 | c0002 | t0017 | g0194 | EAS | KHV | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02027 | hp1 | a0001 | c0001 | t0062 | g0274 | EAS | KHV | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | KHV | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02040 | hp1 | a0002 | c0002 | t0002 | g0195 | EAS | KHV | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02040 | hp2 | a0001 | c0001 | t0024 | g0156 | EAS | KHV | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02055 | hp1 | a0003 | c0003 | t0005 | g0074 | AFR | ACB | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02055 | hp2 | a0003 | c0003 | t0011 | g0342 | AFR | ACB | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02056 | hp1 | a0002 | c0002 | t0014 | g0205 | EAS | KHV | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02056 | hp2 | a0002 | c0002 | t0002 | g0197 | EAS | KHV | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02071 | hp1 | a0002 | c0002 | t0010 | g0338 | EAS | KHV | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02071 | hp2 | a0004 | c0005 | t0010 | g0208 | EAS | KHV | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02074 | hp1 | a0001 | c0001 | t0024 | g0130 | EAS | KHV | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02074 | hp2 | a0001 | c0001 | t0017 | g0316 | EAS | KHV | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02080 | hp1 | a0001 | c0001 | t0031 | g0256 | EAS | KHV | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02129 | hp1 | a0001 | c0001 | t0004 | g0213 | EAS | KHV | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02129 | hp2 | a0002 | c0002 | t0019 | g0190 | EAS | KHV | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02132 | hp1 | a0002 | c0002 | t0023 | g0191 | EAS | KHV | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02132 | hp2 | a0001 | c0001 | t0024 | g0276 | EAS | KHV | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02135 | hp2 | a0004 | c0005 | t0010 | g0315 | EAS | KHV | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02145 | hp1 | a0001 | c0004 | t0041 | g0027 | AFR | ACB | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02145 | hp2 | a0003 | c0003 | t0011 | g0300 | AFR | ACB | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02148 | hp1 | a0002 | c0002 | t0017 | g0184 | AMR | PEL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02148 | hp2 | a0001 | c0001 | t0021 | g0056 | AMR | PEL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02155 | hp1 | a0002 | c0002 | t0016 | g0142 | EAS | CDX | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | CDX | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02165 | hp1 | a0001 | c0001 | t0007 | g0277 | EAS | CDX | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02165 | hp2 | a0002 | c0002 | t0007 | g0141 | EAS | CDX | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02257 | hp1 | a0001 | c0001 | t0009 | g0013 | AFR | ACB | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02257 | hp2 | a0002 | c0002 | t0009 | g0314 | AFR | ACB | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02258 | hp1 | a0003 | c0003 | t0036 | g0284 | AFR | ACB | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02258 | hp2 | a0003 | c0003 | t0036 | g0180 | AFR | ACB | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02273 | hp1 | a0001 | c0001 | t0015 | g0021 | AMR | PEL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02273 | hp2 | a0002 | c0002 | t0014 | g0014 | AMR | PEL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02280 | hp1 | a0001 | c0001 | t0011 | g0071 | AFR | ACB | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02280 | hp2 | a0001 | c0001 | t0020 | g0051 | AFR | ACB | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02293 | hp1 | a0001 | c0001 | t0030 | g0019 | AMR | PEL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02293 | hp2 | a0001 | c0001 | t0008 | g0004 | AMR | PEL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02451 | hp1 | a0011 | c0014 | t0005 | g0046 | AFR | ACB | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02451 | hp2 | a0002 | c0002 | t0009 | g0286 | AFR | ACB | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02572 | hp1 | a0003 | c0003 | t0026 | g0299 | AFR | GWD | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02572 | hp2 | a0001 | c0001 | t0008 | g0033 | AFR | GWD | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02602 | hp1 | a0002 | c0002 | t0007 | g0015 | SAS | PJL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02602 | hp2 | a0002 | c0002 | t0028 | g0215 | SAS | PJL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02615 | hp1 | a0001 | c0008 | t0043 | g0030 | AFR | GWD | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02615 | hp2 | a0001 | c0001 | t0020 | g0344 | AFR | GWD | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02630 | hp1 | a0001 | c0001 | t0008 | g0039 | AFR | GWD | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02630 | hp2 | a0003 | c0003 | t0005 | g0076 | AFR | GWD | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02647 | hp1 | a0001 | c0001 | t0005 | g0036 | AFR | GWD | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02647 | hp2 | a0005 | c0009 | t0071 | g0070 | AFR | GWD | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0255 | SAS | PJL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02683 | hp2 | a0001 | c0001 | t0059 | g0246 | SAS | PJL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02698 | hp1 | a0001 | c0001 | t0008 | g0325 | SAS | PJL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02698 | hp2 | a0001 | c0001 | t0054 | g0101 | SAS | PJL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02717 | hp1 | a0005 | c0007 | t0042 | g0345 | AFR | GWD | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02717 | hp2 | a0001 | c0001 | t0011 | g0172 | AFR | GWD | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02723 | hp1 | a0002 | c0002 | t0009 | g0285 | AFR | GWD | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02723 | hp2 | a0001 | c0001 | t0027 | g0024 | AFR | GWD | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02735 | hp1 | a0002 | c0002 | t0006 | g0083 | SAS | PJL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02735 | hp2 | a0001 | c0001 | t0004 | g0065 | SAS | PJL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02738 | hp1 | a0002 | c0002 | t0007 | g0091 | SAS | PJL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02738 | hp2 | a0001 | c0001 | t0013 | g0257 | SAS | PJL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02809 | hp1 | a0002 | c0002 | t0069 | g0038 | AFR | GWD | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02809 | hp2 | a0005 | c0009 | t0060 | g0043 | AFR | GWD | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02818 | hp1 | a0003 | c0003 | t0026 | g0301 | AFR | GWD | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02818 | hp2 | a0001 | c0001 | t0066 | g0307 | AFR | GWD | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02886 | hp1 | a0001 | c0001 | t0005 | g0305 | AFR | GWD | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02886 | hp2 | a0003 | c0003 | t0005 | g0330 | AFR | GWD | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02895 | hp1 | a0001 | c0008 | t0044 | g0031 | AFR | GWD | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02895 | hp2 | a0001 | c0001 | t0011 | g0028 | AFR | GWD | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02896 | hp1 | a0001 | c0006 | t0008 | g0349 | AFR | GWD | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02896 | hp2 | a0001 | c0001 | t0011 | g0028 | AFR | GWD | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02922 | hp2 | a0003 | c0003 | t0057 | g0329 | AFR | ESN | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02965 | hp1 | a0001 | c0004 | t0041 | g0027 | AFR | ESN | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02965 | hp2 | a0001 | c0001 | t0013 | g0068 | AFR | ESN | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02970 | hp1 | a0001 | c0004 | t0065 | g0306 | AFR | ESN | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02970 | hp2 | a0002 | c0002 | t0037 | g0077 | AFR | ESN | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02976 | hp1 | a0001 | c0004 | t0002 | g0124 | AFR | ESN | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02976 | hp2 | a0001 | c0001 | t0058 | g0049 | AFR | ESN | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03017 | hp2 | a0001 | c0001 | t0012 | g0081 | SAS | PJL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03041 | hp1 | a0003 | c0003 | t0005 | g0061 | AFR | GWD | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03041 | hp2 | a0001 | c0001 | t0027 | g0024 | AFR | GWD | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03098 | hp1 | a0001 | c0001 | t0005 | g0339 | AFR | MSL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03130 | hp1 | a0002 | c0002 | t0003 | g0281 | AFR | ESN | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03130 | hp2 | a0001 | c0001 | t0073 | g0309 | AFR | ESN | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03139 | hp1 | a0003 | c0003 | t0011 | g0302 | AFR | ESN | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03139 | hp2 | a0001 | c0001 | t0011 | g0034 | AFR | ESN | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03195 | hp1 | a0002 | c0002 | t0049 | g0245 | AFR | ESN | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03195 | hp2 | a0002 | c0002 | t0064 | g0346 | AFR | ESN | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03209 | hp1 | a0001 | c0001 | t0004 | g0283 | AFR | MSL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03209 | hp2 | a0002 | c0002 | t0003 | g0282 | AFR | MSL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03225 | hp1 | a0002 | c0002 | t0004 | g0069 | AFR | MSL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03225 | hp2 | a0001 | c0001 | t0007 | g0054 | AFR | MSL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03239 | hp1 | a0001 | c0001 | t0008 | g0011 | SAS | PJL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03239 | hp2 | a0001 | c0001 | t0035 | g0060 | SAS | PJL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03453 | hp1 | a0003 | c0003 | t0011 | g0113 | AFR | MSL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03453 | hp2 | a0005 | c0007 | t0070 | g0313 | AFR | MSL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03486 | hp1 | a0001 | c0001 | t0027 | g0341 | AFR | MSL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03486 | hp2 | a0001 | c0006 | t0013 | g0029 | AFR | MSL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03491 | hp2 | a0001 | c0001 | t0006 | g0225 | SAS | PJL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03516 | hp1 | a0001 | c0001 | t0005 | g0340 | AFR | ESN | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03516 | hp2 | a0001 | c0006 | t0013 | g0029 | AFR | ESN | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03540 | hp1 | a0001 | c0001 | t0067 | g0164 | AFR | GWD | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03540 | hp2 | a0003 | c0003 | t0026 | g0303 | AFR | GWD | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03579 | hp1 | a0003 | c0003 | t0005 | g0181 | AFR | MSL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | MSL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03654 | hp1 | a0001 | c0001 | t0013 | g0217 | SAS | PJL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03654 | hp2 | a0001 | c0001 | t0008 | g0227 | SAS | PJL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03669 | hp1 | a0001 | c0001 | t0018 | g0248 | SAS | PJL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03669 | hp2 | a0002 | c0002 | t0006 | g0291 | SAS | PJL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03688 | hp1 | a0001 | c0001 | t0056 | g0059 | SAS | STU | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03688 | hp2 | a0002 | c0002 | t0003 | g0201 | SAS | STU | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03704 | hp1 | a0002 | c0002 | t0020 | g0214 | SAS | PJL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03704 | hp2 | a0002 | c0002 | t0007 | g0289 | SAS | PJL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03710 | hp1 | a0002 | c0002 | t0010 | g0292 | SAS | PJL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03831 | hp1 | a0002 | c0002 | t0006 | g0324 | SAS | BEB | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03831 | hp2 | a0002 | c0002 | t0003 | g0260 | SAS | BEB | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03834 | hp1 | a0001 | c0001 | t0017 | g0055 | SAS | BEB | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03834 | hp2 | a0002 | c0002 | t0003 | g0016 | SAS | BEB | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03927 | hp1 | a0001 | c0001 | t0013 | g0085 | SAS | BEB | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0254 | SAS | BEB | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG04115 | hp1 | a0002 | c0002 | t0014 | g0082 | SAS | STU | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0242 | SAS | STU | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0265 | SAS | BEB | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG04184 | hp2 | a0001 | c0001 | t0021 | g0099 | SAS | BEB | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG04199 | hp1 | a0002 | c0002 | t0015 | g0290 | SAS | STU | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG04199 | hp2 | a0001 | c0001 | t0009 | g0078 | SAS | STU | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG04204 | hp1 | a0001 | c0001 | t0033 | g0057 | SAS | STU | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG04204 | hp2 | a0002 | c0002 | t0023 | g0079 | SAS | STU | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG04228 | hp1 | a0002 | c0002 | t0009 | g0041 | SAS | STU | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG04228 | hp2 | a0001 | c0001 | t0037 | g0173 | SAS | STU | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18522 | hp1 | a0003 | c0003 | t0011 | g0062 | AFR | YRI | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18522 | hp2 | a0001 | c0001 | t0007 | g0295 | AFR | YRI | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18612 | hp1 | a0001 | c0001 | t0004 | g0178 | EAS | CHB | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18612 | hp2 | a0002 | c0002 | t0072 | g0123 | EAS | CHB | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18747 | hp1 | a0001 | c0001 | t0004 | g0152 | EAS | CHB | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18747 | hp2 | a0001 | c0001 | t0017 | g0167 | EAS | CHB | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18906 | hp1 | a0003 | c0003 | t0005 | g0165 | AFR | YRI | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18906 | hp2 | a0001 | c0004 | t0006 | g0048 | AFR | YRI | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18940 | hp1 | a0001 | c0001 | t0012 | g0001 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18940 | hp2 | a0001 | c0001 | t0007 | g0334 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18941 | hp2 | a0001 | c0001 | t0012 | g0264 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18944 | hp1 | a0002 | c0002 | t0002 | g0161 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18945 | hp1 | a0001 | c0001 | t0009 | g0010 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18945 | hp2 | a0001 | c0001 | t0012 | g0001 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18947 | hp1 | a0001 | c0001 | t0018 | g0017 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18947 | hp2 | a0001 | c0001 | t0009 | g0013 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18948 | hp1 | a0002 | c0002 | t0014 | g0138 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18948 | hp2 | a0001 | c0001 | t0007 | g0129 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18950 | hp2 | a0002 | c0002 | t0002 | g0042 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18951 | hp1 | a0002 | c0002 | t0010 | g0200 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18951 | hp2 | a0001 | c0001 | t0007 | g0151 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18952 | hp1 | a0001 | c0001 | t0010 | g0148 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18952 | hp2 | a0002 | c0002 | t0010 | g0159 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18954 | hp1 | a0002 | c0002 | t0006 | g0185 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18954 | hp2 | a0001 | c0001 | t0016 | g0012 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18957 | hp2 | a0002 | c0002 | t0002 | g0108 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18960 | hp1 | a0002 | c0002 | t0009 | g0193 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18963 | hp1 | a0002 | c0002 | t0003 | g0139 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18963 | hp2 | a0002 | c0002 | t0003 | g0198 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18964 | hp1 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18964 | hp2 | a0002 | c0002 | t0004 | g0007 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18965 | hp1 | a0001 | c0001 | t0004 | g0269 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18966 | hp1 | a0002 | c0002 | t0004 | g0007 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18971 | hp1 | a0002 | c0002 | t0015 | g0275 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18971 | hp2 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18973 | hp1 | a0002 | c0002 | t0014 | g0310 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18973 | hp2 | a0001 | c0001 | t0012 | g0001 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18975 | hp1 | a0002 | c0002 | t0019 | g0009 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18975 | hp2 | a0001 | c0001 | t0019 | g0114 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18979 | hp1 | a0002 | c0002 | t0010 | g0140 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18979 | hp2 | a0002 | c0002 | t0006 | g0158 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18980 | hp1 | a0001 | c0001 | t0032 | g0232 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18980 | hp2 | a0012 | c0016 | t0002 | g0143 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18981 | hp2 | a0002 | c0002 | t0014 | g0249 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18984 | hp1 | a0002 | c0002 | t0007 | g0015 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18984 | hp2 | a0001 | c0001 | t0016 | g0012 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18985 | hp1 | a0001 | c0001 | t0006 | g0328 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18985 | hp2 | a0001 | c0001 | t0014 | g0311 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18990 | hp1 | a0001 | c0001 | t0006 | g0175 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18990 | hp2 | a0001 | c0001 | t0040 | g0018 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18991 | hp1 | a0002 | c0002 | t0006 | g0199 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18991 | hp2 | a0004 | c0005 | t0007 | g0040 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18992 | hp1 | a0001 | c0001 | t0020 | g0128 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0189 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18994 | hp2 | a0002 | c0002 | t0003 | g0119 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18997 | hp1 | a0001 | c0001 | t0061 | g0237 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18997 | hp2 | a0002 | c0002 | t0006 | g0332 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18999 | hp1 | a0001 | c0001 | t0008 | g0223 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18999 | hp2 | a0004 | c0005 | t0002 | g0209 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19000 | hp1 | a0001 | c0001 | t0016 | g0146 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19000 | hp2 | a0002 | c0002 | t0003 | g0118 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19001 | hp1 | a0002 | c0002 | t0032 | g0122 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19002 | hp1 | a0002 | c0002 | t0007 | g0162 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19002 | hp2 | a0004 | c0005 | t0003 | g0210 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19003 | hp1 | a0002 | c0015 | t0014 | g0103 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19003 | hp2 | a0001 | c0001 | t0004 | g0273 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19004 | hp1 | a0002 | c0002 | t0015 | g0244 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19009 | hp1 | a0001 | c0001 | t0004 | g0154 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19009 | hp2 | a0001 | c0001 | t0009 | g0262 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19010 | hp2 | a0002 | c0002 | t0009 | g0121 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19011 | hp1 | a0001 | c0001 | t0012 | g0001 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19011 | hp2 | a0002 | c0002 | t0007 | g0160 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19030 | hp1 | a0001 | c0001 | t0009 | g0304 | AFR | LWK | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19030 | hp2 | a0001 | c0004 | t0005 | g0032 | AFR | LWK | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19043 | hp1 | a0003 | c0003 | t0005 | g0308 | AFR | LWK | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19043 | hp2 | a0001 | c0001 | t0011 | g0037 | AFR | LWK | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19055 | hp1 | a0002 | c0002 | t0015 | g0111 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19055 | hp2 | a0001 | c0001 | t0024 | g0133 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19062 | hp1 | a0002 | c0002 | t0022 | g0110 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19063 | hp1 | a0013 | c0012 | t0046 | g0088 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19063 | hp2 | a0002 | c0002 | t0019 | g0009 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19065 | hp1 | a0002 | c0002 | t0009 | g0253 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19065 | hp2 | a0001 | c0001 | t0040 | g0018 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19066 | hp1 | a0004 | c0005 | t0010 | g0278 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19066 | hp2 | a0002 | c0002 | t0006 | g0137 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19070 | hp1 | a0002 | c0002 | t0014 | g0196 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19074 | hp1 | a0002 | c0002 | t0017 | g0107 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19074 | hp2 | a0001 | c0001 | t0031 | g0131 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19079 | hp1 | a0001 | c0001 | t0004 | g0127 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19079 | hp2 | a0001 | c0001 | t0004 | g0231 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19085 | hp2 | a0014 | c0020 | t0002 | g0272 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19087 | hp1 | a0002 | c0002 | t0004 | g0120 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19087 | hp2 | a0001 | c0001 | t0012 | g0001 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19240 | hp1 | a0003 | c0003 | t0011 | g0075 | AFR | YRI | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA19240 | hp2 | a0003 | c0003 | t0053 | g0288 | AFR | YRI | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA20129 | hp1 | a0003 | c0003 | t0005 | g0052 | AFR | ASW | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA20129 | hp2 | a0001 | c0001 | t0023 | g0229 | AFR | ASW | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA20752 | hp1 | a0001 | c0001 | t0004 | g0233 | EUR | TSI | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA20752 | hp2 | a0002 | c0002 | t0006 | g0100 | EUR | TSI | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA20805 | hp1 | a0002 | c0002 | t0006 | g0157 | EUR | TSI | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA20805 | hp2 | a0001 | c0001 | t0020 | g0296 | EUR | TSI | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA20905 | hp1 | a0001 | c0001 | t0021 | g0250 | SAS | GIH | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA20905 | hp2 | a0001 | c0001 | t0010 | g0089 | SAS | GIH | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01123 | hp1 | a0002 | c0002 | t0006 | g0192 | AMR | CLM | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG01123 | hp2 | a0001 | c0001 | t0004 | g0166 | AMR | CLM | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02109 | hp1 | a0001 | c0001 | t0013 | g0136 | AFR | ACB | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02109 | hp2 | a0003 | c0003 | t0005 | g0112 | AFR | ACB | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02486 | hp1 | a0003 | c0003 | t0005 | g0350 | AFR | ACB | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02486 | hp2 | a0001 | c0001 | t0029 | g0343 | AFR | ACB | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02559 | hp1 | a0003 | c0003 | t0011 | g0073 | AFR | ACB | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG02559 | hp2 | a0001 | c0004 | t0045 | g0312 | AFR | ACB | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03471 | hp1 | a0001 | c0001 | t0016 | g0297 | AFR | MSL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG03471 | hp2 | a0001 | c0001 | t0029 | g0026 | AFR | MSL | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG06807 | hp1 | a0001 | c0001 | t0005 | g0280 | AFR | USA | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
HG06807 | hp2 | a0001 | c0001 | t0029 | g0026 | AFR | USA | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18955 | hp1 | a0002 | c0002 | t0004 | g0007 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA18955 | hp2 | a0001 | c0001 | t0016 | g0263 | EAS | JPT | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA20300 | hp1 | a0001 | c0001 | t0007 | g0230 | AFR | USA | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA20300 | hp2 | a0001 | c0001 | t0025 | g0186 | AFR | USA | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA21309 | hp1 | a0001 | c0004 | t0055 | g0072 | AFR | LWK | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
NA21309 | hp2 | a0001 | c0001 | t0011 | g0298 | AFR | LWK | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
homoSapiens | chm13v2 | a0002 | c0002 | t0014 | g0044 | REF | REF | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0053 | REF | REF | TNS4_chr17_40470834_40506623 | TNS4 | chr17 | 40470834 | 40506623 |
view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:40477591 | C | T | 1 | a0006 | 2 | HG01069.hp2 HG01071.hp1 |
missense_variant | MODERATE | c.2145G>A | p.Met715Ile | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 2330/4087 | 2145/2148 | 715/715 | chr17 | 40477591 | |||
chr17:40477629 | C | T | 1 | a0014 | 1 | NA19085.hp2 | missense_variant | MODERATE | c.2107G>A | p.Gly703Ser | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 2292/4087 | 2107/2148 | 703/715 | chr17 | 40477629 | |||
chr17:40479729 | C | T | 1 | a0008 | 1 | HG00140.hp1 | missense_variant | MODERATE | c.1855G>A | p.Val619Met | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 10/13 | 2040/4087 | 1855/2148 | 619/715 | chr17 | 40479729 | |||
chr17:40484492 | C | T | 4 | a0002 a0004 a0011 others(1): Show |
117 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(114): Show |
missense_variant | MODERATE | c.1493G>A | p.Ser498Asn | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 6/13 | 1678/4087 | 1493/2148 | 498/715 | chr17 | 40484492 | |||
chr17:40484950 | C | G | 1 | a0010 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.1346G>C | p.Trp449Ser | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 5/13 | 1531/4087 | 1346/2148 | 449/715 | chr17 | 40484950 | |||
chr17:40487132 | C | A | 1 | a0004 | 6 | HG02071.hp2 HG02135.hp2 NA18991.hp2 others(3): Show |
missense_variant | MODERATE | c.1192G>T | p.Val398Phe | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 4/13 | 1377/4087 | 1192/2148 | 398/715 | chr17 | 40487132 | |||
chr17:40487189 | C | T | 2 | a0006 a0007 |
4 | HG01069.hp2 HG01071.hp1 HG01109.hp1 others(1): Show |
missense_variant | MODERATE | c.1135G>A | p.Gly379Ser | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 4/13 | 1320/4087 | 1135/2148 | 379/715 | chr17 | 40487189 | |||
chr17:40487344 | G | T | 1 | a0005 | 5 | HG01891.hp2 HG02647.hp2 HG02717.hp1 others(2): Show |
missense_variant | MODERATE | c.980C>A | p.Thr327Lys | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 4/13 | 1165/4087 | 980/2148 | 327/715 | chr17 | 40487344 | |||
chr17:40488687 | G | A | 1 | a0012 | 1 | NA18980.hp2 | missense_variant | MODERATE | c.722C>T | p.Ser241Leu | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 3/13 | 907/4087 | 722/2148 | 241/715 | chr17 | 40488687 | |||
chr17:40488870 | C | T | 1 | a0011 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.539G>A | p.Arg180His | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 3/13 | 724/4087 | 539/2148 | 180/715 | chr17 | 40488870 | |||
chr17:40488873 | A | G | 5 | a0002 a0003 a0004 others(2): Show |
145 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(142): Show |
missense_variant | MODERATE | c.536T>C | p.Leu179Pro | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 3/13 | 721/4087 | 536/2148 | 179/715 | chr17 | 40488873 | |||
chr17:40488910 | A | G | 1 | a0009 | 1 | HG01081.hp1 | missense_variant | MODERATE | c.499T>C | p.Cys167Arg | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 3/13 | 684/4087 | 499/2148 | 167/715 | chr17 | 40488910 | |||
chr17:40496089 | C | T | 1 | a0013 | 1 | NA19063.hp1 | missense_variant | MODERATE | c.337G>A | p.Asp113Asn | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/13 | 522/4087 | 337/2148 | 113/715 | chr17 | 40496089 |
view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:40478621 | G | C | 1 | a0005c0009 | 2 | HG02647.hp2 HG02809.hp2 |
synonymous_variant | LOW | c.1938C>G | p.Leu646Leu | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 11/13 | 2123/4087 | 1938/2148 | 646/715 | chr17 | 40478621 | |||
chr17:40479832 | G | T | 1 | a0001c0018 | 1 | HG00597.hp1 | synonymous_variant | LOW | c.1752C>A | p.Thr584Thr | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 10/13 | 1937/4087 | 1752/2148 | 584/715 | chr17 | 40479832 | |||
chr17:40480737 | A | G | 1 | a0002c0015 | 1 | NA19003.hp1 | synonymous_variant | LOW | c.1704T>C | p.Ser568Ser | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 9/13 | 1889/4087 | 1704/2148 | 568/715 | chr17 | 40480737 | |||
chr17:40484503 | C | A | 2 | a0005c0007 a0005c0009 |
5 | HG01891.hp2 HG02647.hp2 HG02717.hp1 others(2): Show |
synonymous_variant | LOW | c.1482G>T | p.Ala494Ala | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 6/13 | 1667/4087 | 1482/2148 | 494/715 | chr17 | 40484503 | |||
chr17:40487133 | G | A | 3 | a0001c0004 a0005c0007 a0005c0009 |
15 | HG01109.hp2 HG01361.hp2 HG01891.hp2 others(12): Show |
synonymous_variant | LOW | c.1191C>T | p.Ser397Ser | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 4/13 | 1376/4087 | 1191/2148 | 397/715 | chr17 | 40487133 | |||
chr17:40487355 | C | T | 1 | a0001c0006 | 3 | HG02896.hp1 HG03486.hp2 HG03516.hp2 |
synonymous_variant | LOW | c.969G>A | p.Val323Val | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 4/13 | 1154/4087 | 969/2148 | 323/715 | chr17 | 40487355 | |||
chr17:40488944 | G | A | 1 | a0001c0021 | 1 | HG00735.hp2 | synonymous_variant | LOW | c.465C>T | p.Ser155Ser | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 3/13 | 650/4087 | 465/2148 | 155/715 | chr17 | 40488944 | |||
chr17:40496291 | C | T | 1 | a0001c0008 | 2 | HG02615.hp1 HG02895.hp1 |
synonymous_variant | LOW | c.135G>A | p.Thr45Thr | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/13 | 320/4087 | 135/2148 | 45/715 | chr17 | 40496291 |
view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:40475911 | C | T | 2 | a0001c0001t0024 a0001c0001t0031 |
6 | HG02040.hp2 HG02074.hp1 HG02080.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1677G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 1677 | chr17 | 40475911 | ||||||
chr17:40475952 | T | C | 1 | a0005c0009t0071 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1636A>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 1636 | chr17 | 40475952 | ||||||
chr17:40475997 | G | A | 1 | a0003c0003t0026 | 3 | HG02572.hp1 HG02818.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1591C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 1591 | chr17 | 40475997 | ||||||
chr17:40476251 | T | G | 3 | a0002c0002t0069 a0005c0007t0042 a0005c0007t0070 |
4 | HG01891.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1337A>C | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 1337 | chr17 | 40476251 | ||||||
chr17:40476264 | C | T | 1 | a0003c0003t0057 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1324G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 1324 | chr17 | 40476264 | ||||||
chr17:40476325 | C | T | 1 | a0002c0002t0064 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1263G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 1263 | chr17 | 40476325 | ||||||
chr17:40476334 | G | T | 23 | a0001c0001t0013 a0001c0001t0021 a0001c0001t0025 others(20): Show |
47 | HG00099.hp2 HG00323.hp1 HG00741.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1254C>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 1254 | chr17 | 40476334 | ||||||
chr17:40476369 | C | CGT | 6 | a0001c0001t0007 a0001c0001t0038 a0001c0021t0038 others(3): Show |
20 | HG00735.hp1 HG00735.hp2 HG01358.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1217_*1218dupAC | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 1218 | chr17 | 40476369 | ||||||
chr17:40476369 | C | CGTGT | 5 | a0001c0001t0010 a0001c0001t0037 a0002c0002t0010 others(2): Show |
16 | HG00642.hp2 HG01256.hp2 HG01257.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1215_*1218dupACAC | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 1218 | chr17 | 40476369 | ||||||
chr17:40476369 | C | CGTGTGT | 5 | a0001c0001t0006 a0001c0001t0058 a0001c0004t0006 others(2): Show |
20 | HG00408.hp1 HG00597.hp2 HG00609.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1213_*1218dupACAC others(2): Show |
TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 1218 | chr17 | 40476369 | ||||||
chr17:40476369 | C | CGTGTGTG others(1): Show |
3 | a0001c0001t0014 a0002c0002t0014 a0002c0015t0014 |
11 | HG00673.hp2 HG01361.hp1 HG02056.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1211_*1218dupACAC others(4): Show |
TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 1218 | chr17 | 40476369 | ||||||
chr17:40476369 | C | CGTGTGTG others(3): Show |
2 | a0001c0001t0015 a0002c0002t0015 |
10 | HG01169.hp1 HG01496.hp1 HG01884.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1209_*1218dupACAC others(6): Show |
TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 1218 | chr17 | 40476369 | ||||||
chr17:40476369 | C | CGTGTGTG others(5): Show |
2 | a0001c0001t0023 a0002c0002t0023 |
4 | HG01070.hp1 HG02132.hp1 HG04204.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1207_*1218dupACAC others(8): Show |
TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 1218 | chr17 | 40476369 | ||||||
chr17:40476369 | C | CGTGTGTG others(7): Show |
2 | a0001c0001t0019 a0002c0002t0019 |
6 | HG01952.hp2 HG01975.hp2 HG02129.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1205_*1218dupACAC others(10): Show |
TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 1218 | chr17 | 40476369 | ||||||
chr17:40476369 | C | CGTGTGTG others(9): Show |
2 | a0001c0001t0022 a0002c0002t0022 |
4 | HG00738.hp2 HG01346.hp1 HG01978.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1203_*1218dupACAC others(12): Show |
TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 1218 | chr17 | 40476369 | ||||||
chr17:40476369 | C | CGTGTGTG others(11): Show |
1 | a0001c0001t0030 | 2 | HG01943.hp2 HG02293.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1201_*1218dupACAC others(14): Show |
TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 1218 | chr17 | 40476369 | ||||||
chr17:40476369 | C | CGTGTGTG others(13): Show |
1 | a0001c0001t0047 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1199_*1218dupACAC others(16): Show |
TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 1218 | chr17 | 40476369 | ||||||
chr17:40476369 | CGT | C | 14 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0013 others(11): Show |
63 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*1217_*1218delAC | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 1217 | chr17 | 40476369 | ||||||
chr17:40476369 | CGTGT | C | 12 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0025 others(9): Show |
64 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*1215_*1218delACAC | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 1215 | chr17 | 40476369 | ||||||
chr17:40476369 | CGTGTGT | C | 8 | a0001c0001t0009 a0001c0001t0012 a0001c0001t0021 others(5): Show |
38 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*1213_*1218delACAC others(2): Show |
TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 1213 | chr17 | 40476369 | ||||||
chr17:40476369 | CGTGTGTG others(1): Show |
C | 8 | a0001c0001t0016 a0001c0001t0018 a0001c0004t0065 others(5): Show |
21 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1211_*1218delACAC others(4): Show |
TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 1211 | chr17 | 40476369 | ||||||
chr17:40476369 | CGTGTGTG others(3): Show |
C | 6 | a0001c0001t0017 a0001c0001t0028 a0001c0001t0054 others(3): Show |
12 | HG00280.hp1 HG01192.hp1 HG01934.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1209_*1218delACAC others(6): Show |
TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 1209 | chr17 | 40476369 | ||||||
chr17:40476369 | CGTGTGTG others(5): Show |
C | 4 | a0001c0001t0035 a0001c0001t0039 a0003c0003t0036 others(1): Show |
6 | HG01070.hp2 HG01071.hp2 HG01109.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1207_*1218delACAC others(8): Show |
TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 1207 | chr17 | 40476369 | ||||||
chr17:40476369 | CGTGTGTG others(7): Show |
C | 7 | a0001c0001t0011 a0001c0001t0029 a0001c0001t0056 others(4): Show |
21 | HG00140.hp1 HG02055.hp2 HG02145.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1205_*1218delACAC others(10): Show |
TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 1205 | chr17 | 40476369 | ||||||
chr17:40476369 | CGTGTGTG others(9): Show |
C | 7 | a0001c0001t0005 a0001c0004t0005 a0002c0002t0049 others(4): Show |
25 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1203_*1218delACAC others(12): Show |
TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 1203 | chr17 | 40476369 | ||||||
chr17:40476369 | CGTGTGTG others(11): Show |
C | 1 | a0001c0001t0027 | 3 | HG02723.hp2 HG03041.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1201_*1218delACAC others(14): Show |
TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 1201 | chr17 | 40476369 | ||||||
chr17:40476369 | CGTGTGTG others(23): Show |
C | 1 | a0001c0001t0050 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1189_*1218delACAC others(26): Show |
TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 1189 | chr17 | 40476369 | ||||||
chr17:40476406 | GTGTGTGT others(10): Show |
G | 1 | a0001c0001t0059 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1165_*1181delACAC others(13): Show |
TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 1165 | chr17 | 40476406 | ||||||
chr17:40476419 | T | C | 1 | a0001c0001t0001 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1169A>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 1169 | chr17 | 40476419 | ||||||
chr17:40476424 | GTGTGT | G | 3 | a0001c0001t0032 a0001c0001t0040 a0002c0002t0032 |
4 | NA18980.hp1 NA18990.hp2 NA19001.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1159_*1163delACAC others(1): Show |
TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 1159 | chr17 | 40476424 | ||||||
chr17:40476426 | GTGT | G | 3 | a0001c0001t0002 a0012c0016t0002 a0014c0020t0002 |
3 | NA18957.hp1 NA18980.hp2 NA19085.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1159_*1161delACA | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 1159 | chr17 | 40476426 | ||||||
chr17:40476430 | T | G | 1 | a0013c0012t0046 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1158A>C | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 1158 | chr17 | 40476430 | ||||||
chr17:40476431 | G | T | 1 | a0013c0012t0046 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1157C>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 1157 | chr17 | 40476431 | ||||||
chr17:40476465 | G | A | 1 | a0001c0001t0066 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1123C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 1123 | chr17 | 40476465 | ||||||
chr17:40476508 | C | T | 2 | a0001c0001t0067 a0009c0013t0068 |
2 | HG01081.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1080G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 1080 | chr17 | 40476508 | ||||||
chr17:40476509 | C | G | 34 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0013 others(31): Show |
90 | HG00099.hp2 HG00323.hp1 HG00741.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*1079G>C | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 1079 | chr17 | 40476509 | ||||||
chr17:40476600 | T | C | 37 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0013 others(34): Show |
94 | HG00099.hp2 HG00323.hp1 HG00741.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*988A>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 988 | chr17 | 40476600 | ||||||
chr17:40476630 | C | T | 7 | a0001c0001t0013 a0001c0001t0025 a0001c0001t0066 others(4): Show |
22 | HG00323.hp1 HG00741.hp1 HG01109.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*958G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 958 | chr17 | 40476630 | ||||||
chr17:40476691 | C | A | 1 | a0001c0001t0052 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*897G>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 897 | chr17 | 40476691 | ||||||
chr17:40476811 | CTAGATCA others(8): Show |
C | 1 | a0001c0001t0061 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*762_*776delCAGTGG others(9): Show |
TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 762 | chr17 | 40476811 | ||||||
chr17:40476860 | CA | C | 35 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0013 others(32): Show |
91 | HG00099.hp2 HG00323.hp1 HG00741.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*727delT | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 727 | chr17 | 40476860 | ||||||
chr17:40476882 | C | A | 60 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0008 others(57): Show |
182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*706G>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 706 | chr17 | 40476882 | ||||||
chr17:40477076 | T | C | 1 | a0001c0001t0062 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*512A>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 512 | chr17 | 40477076 | ||||||
chr17:40477077 | G | A | 14 | a0001c0001t0013 a0001c0001t0025 a0001c0001t0029 others(11): Show |
32 | HG00323.hp1 HG00741.hp1 HG01081.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*511C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 511 | chr17 | 40477077 | ||||||
chr17:40477242 | T | C | 1 | a0005c0009t0071 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*346A>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 346 | chr17 | 40477242 | ||||||
chr17:40477282 | T | A | 1 | a0002c0002t0072 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*306A>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 306 | chr17 | 40477282 | ||||||
chr17:40477311 | T | C | 1 | a0001c0001t0073 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*277A>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 277 | chr17 | 40477311 | ||||||
chr17:40477342 | C | T | 1 | a0001c0004t0045 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*246G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 13/13 | 246 | chr17 | 40477342 | ||||||
chr17:40501590 | C | T | 2 | a0001c0008t0043 a0001c0008t0044 |
2 | HG02615.hp1 HG02895.hp1 |
5_prime_UTR_variant | MODIFIER | c.-152G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/13 | 5165 | chr17 | 40501590 |
view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:40477932 | A | G | 1 | a0005c0009t0071g0070 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2007-203T>C | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 12/12 | chr17 | 40477932 | |||||||
chr17:40478115 | G | C | 82 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0280 others(79): Show |
88 | HG00099.hp2 HG00323.hp1 HG00741.hp1 others(85): Show |
intron_variant | MODIFIER | c.2006+192C>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 12/12 | chr17 | 40478115 | |||||||
chr17:40478131 | A | T | 84 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0280 others(81): Show |
90 | HG00099.hp2 HG00323.hp1 HG00741.hp1 others(87): Show |
intron_variant | MODIFIER | c.2006+176T>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 12/12 | chr17 | 40478131 | |||||||
chr17:40478214 | C | A | 2 | a0001c0004t0065g0306 a0002c0002t0064g0346 |
2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2006+93G>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 12/12 | chr17 | 40478214 | |||||||
chr17:40478353 | T | C | 13 | a0001c0001t0021g0056 a0001c0001t0021g0058 a0001c0001t0021g0098 others(10): Show |
13 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.1980-20A>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 11/12 | chr17 | 40478353 | |||||||
chr17:40478380 | C | T | 1 | a0001c0004t0041g0027 | 2 | HG02145.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1980-47G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 11/12 | chr17 | 40478380 | |||||||
chr17:40478511 | C | T | 3 | a0001c0001t0004g0065 a0001c0001t0004g0166 a0001c0001t0009g0078 |
3 | HG01123.hp2 HG02735.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1979+69G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 11/12 | chr17 | 40478511 | |||||||
chr17:40478677 | C | T | 83 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0280 others(80): Show |
89 | HG00099.hp2 HG00323.hp1 HG00741.hp1 others(86): Show |
intron_variant | MODIFIER | c.1911-29G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 10/12 | chr17 | 40478677 | |||||||
chr17:40478812 | C | T | 84 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0280 others(81): Show |
90 | HG00099.hp2 HG00323.hp1 HG00741.hp1 others(87): Show |
intron_variant | MODIFIER | c.1911-164G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 10/12 | chr17 | 40478812 | |||||||
chr17:40478855 | C | G | 84 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0280 others(81): Show |
89 | HG00099.hp2 HG00323.hp1 HG00741.hp1 others(86): Show |
intron_variant | MODIFIER | c.1911-207G>C | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 10/12 | chr17 | 40478855 | |||||||
chr17:40478894 | C | T | 2 | a0001c0001t0001g0145 a0005c0009t0060g0043 |
2 | HG02809.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1911-246G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 10/12 | chr17 | 40478894 | |||||||
chr17:40478967 | T | C | 2 | a0001c0001t0029g0026 a0001c0001t0029g0343 |
3 | HG02486.hp2 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1911-319A>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 10/12 | chr17 | 40478967 | |||||||
chr17:40479075 | G | T | 1 | a0003c0003t0051g0211 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1911-427C>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 10/12 | chr17 | 40479075 | |||||||
chr17:40479194 | T | A | 4 | a0006c0010t0034g0318 a0006c0010t0034g0319 a0007c0011t0033g0320 others(1): Show |
4 | HG01069.hp2 HG01071.hp1 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1910+480A>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 10/12 | chr17 | 40479194 | |||||||
chr17:40479389 | C | T | 1 | a0004c0005t0010g0315 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1910+285G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 10/12 | chr17 | 40479389 | |||||||
chr17:40479391 | C | T | 1 | a0001c0001t0010g0089 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1910+283G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 10/12 | chr17 | 40479391 | |||||||
chr17:40479394 | G | A | 4 | a0006c0010t0034g0318 a0006c0010t0034g0319 a0007c0011t0033g0320 others(1): Show |
4 | HG01069.hp2 HG01071.hp1 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1910+280C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 10/12 | chr17 | 40479394 | |||||||
chr17:40479396 | C | T | 1 | a0002c0002t0015g0287 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1910+278G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 10/12 | chr17 | 40479396 | |||||||
chr17:40479399 | G | A | 1 | a0002c0002t0007g0162 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1910+275C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 10/12 | chr17 | 40479399 | |||||||
chr17:40479420 | T | G | 6 | a0001c0001t0006g0225 a0002c0002t0003g0260 a0002c0002t0006g0291 others(3): Show |
6 | HG03491.hp2 HG03669.hp2 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.1910+254A>C | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 10/12 | chr17 | 40479420 | |||||||
chr17:40479472 | A | G | 2 | a0001c0001t0005g0305 a0001c0001t0011g0071 |
2 | HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1910+202T>C | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 10/12 | chr17 | 40479472 | |||||||
chr17:40479491 | G | A | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1910+183C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 10/12 | chr17 | 40479491 | |||||||
chr17:40479557 | G | A | 2 | a0001c0001t0067g0164 a0009c0013t0068g0347 |
2 | HG01081.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1910+117C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 10/12 | chr17 | 40479557 | |||||||
chr17:40479624 | C | T | 13 | a0001c0001t0021g0056 a0001c0001t0021g0058 a0001c0001t0021g0098 others(10): Show |
13 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.1910+50G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 10/12 | chr17 | 40479624 | |||||||
chr17:40479645 | G | A | 83 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0280 others(80): Show |
88 | HG00099.hp2 HG00323.hp1 HG00741.hp1 others(85): Show |
intron_variant | MODIFIER | c.1910+29C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 10/12 | chr17 | 40479645 | |||||||
chr17:40479863 | G | T | 5 | a0002c0002t0002g0197 a0002c0002t0003g0198 a0002c0002t0004g0007 others(2): Show |
7 | HG02056.hp2 NA18955.hp1 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.1742-21C>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 9/12 | chr17 | 40479863 | |||||||
chr17:40479875 | G | A | 2 | a0002c0002t0004g0007 a0002c0002t0009g0253 |
4 | NA18955.hp1 NA18964.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.1742-33C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 9/12 | chr17 | 40479875 | |||||||
chr17:40479894 | C | T | 1 | a0005c0009t0071g0070 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1742-52G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 9/12 | chr17 | 40479894 | |||||||
chr17:40479964 | G | A | 1 | a0001c0001t0002g0271 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1742-122C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 9/12 | chr17 | 40479964 | |||||||
chr17:40479983 | G | A | 41 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0280 others(38): Show |
43 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.1742-141C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 9/12 | chr17 | 40479983 | |||||||
chr17:40480111 | G | A | 2 | a0001c0001t0067g0164 a0009c0013t0068g0347 |
2 | HG01081.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1742-269C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 9/12 | chr17 | 40480111 | |||||||
chr17:40480112 | C | T | 2 | a0001c0004t0065g0306 a0002c0002t0064g0346 |
2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1742-270G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 9/12 | chr17 | 40480112 | |||||||
chr17:40480148 | G | C | 2 | a0001c0001t0067g0164 a0009c0013t0068g0347 |
2 | HG01081.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1742-306C>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 9/12 | chr17 | 40480148 | |||||||
chr17:40480300 | T | C | 1 | a0002c0002t0002g0195 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1741+400A>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 9/12 | chr17 | 40480300 | |||||||
chr17:40480301 | G | C | 1 | a0002c0002t0002g0195 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1741+399C>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 9/12 | chr17 | 40480301 | |||||||
chr17:40480421 | C | T | 1 | a0001c0001t0020g0296 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1741+279G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 9/12 | chr17 | 40480421 | |||||||
chr17:40480422 | G | A | 1 | a0001c0004t0045g0312 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1741+278C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 9/12 | chr17 | 40480422 | |||||||
chr17:40480493 | C | T | 1 | a0001c0001t0008g0223 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1741+207G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 9/12 | chr17 | 40480493 | |||||||
chr17:40480573 | C | A | 75 | a0001c0001t0001g0002 a0001c0001t0001g0050 a0001c0001t0001g0066 others(72): Show |
93 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.1741+127G>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 9/12 | chr17 | 40480573 | |||||||
chr17:40481022 | T | C | 1 | a0003c0003t0026g0299 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1673-254A>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 8/12 | chr17 | 40481022 | |||||||
chr17:40481185 | C | T | 1 | a0001c0001t0067g0164 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1673-417G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 8/12 | chr17 | 40481185 | |||||||
chr17:40481299 | C | T | 1 | a0002c0002t0037g0077 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1673-531G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 8/12 | chr17 | 40481299 | |||||||
chr17:40481300 | G | A | 1 | a0001c0004t0041g0027 | 2 | HG02145.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1673-532C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 8/12 | chr17 | 40481300 | |||||||
chr17:40481387 | T | C | 168 | a0001c0001t0001g0002 a0001c0001t0001g0050 a0001c0001t0001g0066 others(165): Show |
193 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.1673-619A>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 8/12 | chr17 | 40481387 | |||||||
chr17:40481509 | C | T | 1 | a0001c0001t0038g0047 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1672+620G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 8/12 | chr17 | 40481509 | |||||||
chr17:40481538 | G | A | 42 | a0001c0001t0005g0305 a0001c0001t0011g0071 a0001c0001t0013g0008 others(39): Show |
44 | HG00099.hp2 HG00323.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.1672+591C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 8/12 | chr17 | 40481538 | |||||||
chr17:40481662 | A | G | 19 | a0001c0001t0013g0008 a0001c0001t0013g0068 a0001c0001t0013g0085 others(16): Show |
21 | HG00323.hp1 HG00741.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.1672+467T>C | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 8/12 | chr17 | 40481662 | |||||||
chr17:40481869 | G | C | 2 | a0001c0001t0005g0305 a0001c0001t0011g0071 |
2 | HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1672+260C>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 8/12 | chr17 | 40481869 | |||||||
chr17:40481895 | T | A | 46 | a0001c0001t0005g0305 a0001c0001t0011g0071 a0001c0001t0013g0008 others(43): Show |
50 | HG00099.hp2 HG00323.hp1 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.1672+234A>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 8/12 | chr17 | 40481895 | |||||||
chr17:40481898 | C | T | 1 | a0003c0003t0057g0329 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1672+231G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 8/12 | chr17 | 40481898 | |||||||
chr17:40481951 | G | A | 16 | a0001c0001t0013g0008 a0001c0001t0013g0068 a0001c0001t0013g0085 others(13): Show |
18 | HG00323.hp1 HG00741.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.1672+178C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 8/12 | chr17 | 40481951 | |||||||
chr17:40481999 | C | T | 78 | a0001c0001t0001g0002 a0001c0001t0001g0050 a0001c0001t0001g0066 others(75): Show |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.1672+130G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 8/12 | chr17 | 40481999 | |||||||
chr17:40482008 | T | C | 13 | a0001c0001t0021g0056 a0001c0001t0021g0058 a0001c0001t0021g0098 others(10): Show |
13 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.1672+121A>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 8/12 | chr17 | 40482008 | |||||||
chr17:40482047 | A | T | 1 | a0005c0009t0071g0070 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1672+82T>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 8/12 | chr17 | 40482047 | |||||||
chr17:40482240 | G | A | 1 | a0005c0009t0060g0043 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1595-34C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 7/12 | chr17 | 40482240 | |||||||
chr17:40482481 | C | T | 2 | a0001c0001t0002g0271 a0013c0012t0046g0088 |
2 | NA18944.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1502-65G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 6/12 | chr17 | 40482481 | |||||||
chr17:40482585 | G | GAC | 71 | a0001c0001t0001g0002 a0001c0001t0001g0050 a0001c0001t0001g0066 others(68): Show |
88 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1502-171_1502-170d others(4): Show |
TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 6/12 | chr17 | 40482585 | |||||||
chr17:40482585 | G | GACAC | 12 | a0001c0001t0001g0104 a0001c0001t0001g0336 a0001c0001t0005g0036 others(9): Show |
12 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(9): Show |
intron_variant | MODIFIER | c.1502-173_1502-170d others(6): Show |
TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 6/12 | chr17 | 40482585 | |||||||
chr17:40482585 | G | GACACACA others(1): Show |
10 | a0001c0001t0001g0155 a0001c0001t0001g0251 a0001c0001t0008g0004 others(7): Show |
13 | HG00280.hp2 HG00735.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1502-177_1502-170d others(10): Show |
TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 6/12 | chr17 | 40482585 | |||||||
chr17:40482585 | GAC | G | 95 | a0001c0001t0002g0149 a0001c0001t0002g0258 a0001c0001t0003g0150 others(92): Show |
102 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.1502-171_1502-170d others(4): Show |
TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 6/12 | chr17 | 40482585 | |||||||
chr17:40482585 | GACAC | G | 7 | a0001c0001t0013g0219 a0001c0001t0067g0164 a0002c0002t0069g0038 others(4): Show |
7 | HG01081.hp1 HG01192.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1502-173_1502-170d others(6): Show |
TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 6/12 | chr17 | 40482585 | |||||||
chr17:40482661 | C | T | 1 | a0001c0001t0011g0071 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1502-245G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 6/12 | chr17 | 40482661 | |||||||
chr17:40482737 | T | C | 169 | a0001c0001t0001g0002 a0001c0001t0001g0050 a0001c0001t0001g0066 others(166): Show |
194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.1502-321A>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 6/12 | chr17 | 40482737 | |||||||
chr17:40482757 | G | C | 2 | a0001c0001t0067g0164 a0009c0013t0068g0347 |
2 | HG01081.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1502-341C>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 6/12 | chr17 | 40482757 | |||||||
chr17:40482782 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1502-366C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 6/12 | chr17 | 40482782 | |||||||
chr17:40482782 | G | GA | 7 | a0001c0001t0004g0154 a0001c0001t0017g0316 a0001c0001t0020g0128 others(4): Show |
7 | HG01496.hp2 HG02056.hp1 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.1502-367dupT | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 6/12 | chr17 | 40482782 | |||||||
chr17:40482818 | C | T | 6 | a0001c0001t0013g0008 a0001c0001t0013g0085 a0001c0001t0013g0093 others(3): Show |
7 | HG00323.hp1 HG00741.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1502-402G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 6/12 | chr17 | 40482818 | |||||||
chr17:40482858 | T | C | 1 | a0005c0009t0060g0043 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1502-442A>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 6/12 | chr17 | 40482858 | |||||||
chr17:40482953 | A | AT | 25 | a0001c0001t0001g0086 a0001c0001t0006g0328 a0001c0001t0012g0125 others(22): Show |
27 | HG00323.hp1 HG00597.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.1502-538dupA | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 6/12 | chr17 | 40482953 | |||||||
chr17:40482953 | AT | A | 12 | a0001c0001t0021g0056 a0001c0001t0021g0058 a0001c0001t0021g0098 others(9): Show |
12 | HG00099.hp2 HG00738.hp2 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.1502-538delA | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 6/12 | chr17 | 40482953 | |||||||
chr17:40483003 | G | A | 4 | a0002c0002t0069g0038 a0005c0007t0042g0238 a0005c0007t0042g0345 others(1): Show |
4 | HG01891.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1502-587C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 6/12 | chr17 | 40483003 | |||||||
chr17:40483165 | A | G | 110 | a0001c0001t0001g0002 a0001c0001t0001g0050 a0001c0001t0001g0066 others(107): Show |
132 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.1502-749T>C | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 6/12 | chr17 | 40483165 | |||||||
chr17:40483166 | C | T | 2 | a0001c0001t0005g0305 a0001c0001t0011g0071 |
2 | HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1502-750G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 6/12 | chr17 | 40483166 | |||||||
chr17:40483386 | C | T | 1 | a0002c0002t0003g0139 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1502-970G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 6/12 | chr17 | 40483386 | |||||||
chr17:40483470 | G | T | 2 | a0001c0001t0005g0305 a0001c0001t0011g0071 |
2 | HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1501+1014C>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 6/12 | chr17 | 40483470 | |||||||
chr17:40483485 | G | A | 1 | a0001c0001t0021g0056 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1501+999C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 6/12 | chr17 | 40483485 | |||||||
chr17:40483512 | T | C | 12 | a0001c0001t0001g0155 a0001c0001t0001g0251 a0001c0001t0008g0004 others(9): Show |
15 | HG00280.hp2 HG00735.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.1501+972A>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 6/12 | chr17 | 40483512 | |||||||
chr17:40483531 | C | T | 1 | a0001c0004t0055g0072 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1501+953G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 6/12 | chr17 | 40483531 | |||||||
chr17:40483563 | C | T | 1 | a0001c0001t0008g0227 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1501+921G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 6/12 | chr17 | 40483563 | |||||||
chr17:40483590 | C | T | 8 | a0001c0001t0021g0056 a0001c0001t0021g0058 a0001c0001t0021g0099 others(5): Show |
8 | HG00099.hp2 HG02148.hp2 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.1501+894G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 6/12 | chr17 | 40483590 | |||||||
chr17:40483678 | C | G | 2 | a0001c0004t0002g0124 a0005c0009t0060g0043 |
2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1501+806G>C | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 6/12 | chr17 | 40483678 | |||||||
chr17:40483750 | T | C | 2 | a0002c0002t0015g0111 a0002c0002t0022g0110 |
2 | NA19055.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1501+734A>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 6/12 | chr17 | 40483750 | |||||||
chr17:40483797 | T | C | 4 | a0001c0001t0006g0225 a0002c0002t0003g0260 a0002c0002t0006g0291 others(1): Show |
4 | HG03491.hp2 HG03669.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1501+687A>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 6/12 | chr17 | 40483797 | |||||||
chr17:40483833 | G | A | 2 | a0001c0001t0002g0279 a0001c0001t0014g0311 |
2 | NA18970.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.1501+651C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 6/12 | chr17 | 40483833 | |||||||
chr17:40483844 | C | G | 17 | a0001c0004t0005g0032 a0003c0003t0005g0052 a0003c0003t0005g0061 others(14): Show |
17 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1501+640G>C | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 6/12 | chr17 | 40483844 | |||||||
chr17:40483937 | T | C | 4 | a0006c0010t0034g0318 a0006c0010t0034g0319 a0007c0011t0033g0320 others(1): Show |
4 | HG01069.hp2 HG01071.hp1 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1501+547A>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 6/12 | chr17 | 40483937 | |||||||
chr17:40484299 | C | T | 2 | a0001c0001t0005g0305 a0001c0001t0011g0071 |
2 | HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1501+185G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 6/12 | chr17 | 40484299 | |||||||
chr17:40484353 | C | T | 77 | a0001c0001t0001g0145 a0001c0001t0001g0155 a0001c0001t0002g0005 others(74): Show |
87 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.1501+131G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 6/12 | chr17 | 40484353 | |||||||
chr17:40484438 | C | T | 4 | a0006c0010t0034g0318 a0006c0010t0034g0319 a0007c0011t0033g0320 others(1): Show |
4 | HG01069.hp2 HG01071.hp1 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1501+46G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 6/12 | chr17 | 40484438 | |||||||
chr17:40484474 | A | G | 1 | a0002c0002t0001g0242 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1501+10T>C | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 6/12 | chr17 | 40484474 | |||||||
chr17:40484478 | G | A | 1 | a0005c0009t0071g0070 | 1 | HG02647.hp2 | splice_region_variant&intron_variant | LOW | c.1501+6C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 6/12 | chr17 | 40484478 | |||||||
chr17:40484740 | A | G | 107 | a0002c0002t0001g0189 a0002c0002t0001g0265 a0002c0002t0002g0042 others(104): Show |
115 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.1376-131T>C | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 5/12 | chr17 | 40484740 | |||||||
chr17:40484868 | T | A | 2 | a0002c0002t0007g0333 a0002c0002t0015g0207 |
2 | HG01358.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1375+53A>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 5/12 | chr17 | 40484868 | |||||||
chr17:40485130 | C | T | 108 | a0002c0002t0001g0189 a0002c0002t0001g0265 a0002c0002t0002g0042 others(105): Show |
116 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.1289-123G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 4/12 | chr17 | 40485130 | |||||||
chr17:40485160 | C | G | 104 | a0001c0001t0001g0145 a0001c0001t0001g0155 a0001c0001t0002g0005 others(101): Show |
114 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.1289-153G>C | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 4/12 | chr17 | 40485160 | |||||||
chr17:40485167 | C | T | 107 | a0002c0002t0001g0189 a0002c0002t0001g0265 a0002c0002t0002g0042 others(104): Show |
115 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.1289-160G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 4/12 | chr17 | 40485167 | |||||||
chr17:40485253 | G | A | 261 | a0001c0001t0001g0145 a0001c0001t0001g0155 a0001c0001t0002g0005 others(258): Show |
282 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.1289-246C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 4/12 | chr17 | 40485253 | |||||||
chr17:40485347 | A | G | 8 | a0001c0001t0001g0251 a0001c0001t0008g0004 a0001c0001t0012g0125 others(5): Show |
10 | HG00735.hp2 HG01261.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.1289-340T>C | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 4/12 | chr17 | 40485347 | |||||||
chr17:40485607 | A | G | 1 | a0001c0001t0004g0127 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1289-600T>C | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 4/12 | chr17 | 40485607 | |||||||
chr17:40486038 | T | TG | 9 | a0001c0001t0021g0056 a0001c0001t0021g0058 a0001c0001t0021g0098 others(6): Show |
9 | HG00099.hp2 HG00741.hp2 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.1288+997dupC | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 4/12 | chr17 | 40486038 | |||||||
chr17:40486168 | C | T | 1 | a0002c0002t0007g0091 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1288+868G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 4/12 | chr17 | 40486168 | |||||||
chr17:40486174 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1288+862G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 4/12 | chr17 | 40486174 | |||||||
chr17:40486254 | C | T | 1 | a0002c0002t0022g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1288+782G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 4/12 | chr17 | 40486254 | |||||||
chr17:40486519 | A | T | 5 | a0001c0001t0008g0039 a0001c0001t0038g0047 a0001c0001t0058g0049 others(2): Show |
5 | HG00735.hp1 HG01081.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1288+517T>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 4/12 | chr17 | 40486519 | |||||||
chr17:40486522 | G | A | 1 | a0001c0004t0045g0312 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1288+514C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 4/12 | chr17 | 40486522 | |||||||
chr17:40486532 | A | AT | 11 | a0001c0001t0005g0280 a0001c0001t0005g0340 a0001c0001t0006g0175 others(8): Show |
12 | HG01346.hp2 HG02145.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1288+503dupA | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 4/12 | chr17 | 40486532 | |||||||
chr17:40486532 | AT | A | 34 | a0001c0001t0001g0086 a0001c0001t0001g0239 a0001c0001t0008g0325 others(31): Show |
36 | HG00323.hp1 HG00741.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.1288+503delA | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 4/12 | chr17 | 40486532 | |||||||
chr17:40486532 | ATT | A | 7 | a0001c0001t0008g0039 a0001c0001t0013g0094 a0001c0001t0038g0047 others(4): Show |
7 | HG00735.hp1 HG01071.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1288+502_1288+503d others(4): Show |
TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 4/12 | chr17 | 40486532 | |||||||
chr17:40486646 | C | T | 9 | a0001c0001t0021g0056 a0001c0001t0021g0058 a0001c0001t0021g0098 others(6): Show |
9 | HG00099.hp2 HG00741.hp2 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.1288+390G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 4/12 | chr17 | 40486646 | |||||||
chr17:40486689 | T | A | 1 | a0001c0001t0008g0227 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1288+347A>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 4/12 | chr17 | 40486689 | |||||||
chr17:40486764 | C | A | 1 | a0001c0001t0002g0179 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1288+272G>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 4/12 | chr17 | 40486764 | |||||||
chr17:40486778 | C | T | 1 | a0001c0004t0055g0072 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1288+258G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 4/12 | chr17 | 40486778 | |||||||
chr17:40487528 | G | A | 77 | a0001c0001t0001g0145 a0001c0001t0001g0155 a0001c0001t0002g0005 others(74): Show |
87 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.864-68C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 3/12 | chr17 | 40487528 | |||||||
chr17:40487580 | T | C | 2 | a0001c0001t0067g0164 a0009c0013t0068g0347 |
2 | HG01081.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.864-120A>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 3/12 | chr17 | 40487580 | |||||||
chr17:40487590 | C | T | 108 | a0002c0002t0001g0189 a0002c0002t0001g0265 a0002c0002t0002g0042 others(105): Show |
116 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.864-130G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 3/12 | chr17 | 40487590 | |||||||
chr17:40487776 | C | T | 1 | a0002c0002t0037g0077 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.864-316G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 3/12 | chr17 | 40487776 | |||||||
chr17:40487909 | A | G | 1 | a0002c0002t0037g0077 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.864-449T>C | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 3/12 | chr17 | 40487909 | |||||||
chr17:40487962 | C | T | 15 | a0001c0001t0013g0008 a0001c0001t0013g0068 a0001c0001t0013g0085 others(12): Show |
17 | HG00323.hp1 HG00741.hp1 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.864-502G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 3/12 | chr17 | 40487962 | |||||||
chr17:40488028 | T | C | 1 | a0002c0002t0037g0077 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.863+518A>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 3/12 | chr17 | 40488028 | |||||||
chr17:40488311 | C | T | 2 | a0002c0002t0009g0285 a0002c0002t0009g0286 |
2 | HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.863+235G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 3/12 | chr17 | 40488311 | |||||||
chr17:40488500 | G | A | 136 | a0002c0002t0001g0189 a0002c0002t0001g0242 a0002c0002t0001g0265 others(133): Show |
144 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(141): Show |
intron_variant | MODIFIER | c.863+46C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 3/12 | chr17 | 40488500 | |||||||
chr17:40489020 | T | C | 1 | a0001c0004t0045g0312 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.440-51A>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40489020 | |||||||
chr17:40489079 | C | T | 108 | a0002c0002t0001g0189 a0002c0002t0001g0265 a0002c0002t0002g0042 others(105): Show |
116 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.440-110G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40489079 | |||||||
chr17:40489181 | G | A | 2 | a0001c0001t0067g0164 a0009c0013t0068g0347 |
2 | HG01081.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.440-212C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40489181 | |||||||
chr17:40489307 | G | T | 136 | a0002c0002t0001g0189 a0002c0002t0001g0242 a0002c0002t0001g0265 others(133): Show |
144 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(141): Show |
intron_variant | MODIFIER | c.440-338C>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40489307 | |||||||
chr17:40489388 | A | C | 3 | a0001c0001t0007g0295 a0001c0001t0029g0026 a0001c0001t0029g0343 |
4 | HG02486.hp2 HG03471.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.440-419T>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40489388 | |||||||
chr17:40489533 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.440-564G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40489533 | |||||||
chr17:40489535 | C | T | 3 | a0001c0001t0005g0305 a0001c0001t0011g0071 a0001c0001t0021g0098 |
3 | HG00741.hp2 HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.440-566G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40489535 | |||||||
chr17:40489536 | G | A | 1 | a0002c0002t0015g0084 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.440-567C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40489536 | |||||||
chr17:40489543 | C | T | 3 | a0001c0001t0004g0220 a0001c0001t0013g0219 a0010c0017t0012g0294 |
3 | HG00140.hp2 HG01192.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.440-574G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40489543 | |||||||
chr17:40489570 | G | T | 4 | a0001c0004t0002g0124 a0001c0004t0006g0048 a0001c0004t0041g0027 others(1): Show |
5 | HG01109.hp2 HG02145.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.440-601C>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40489570 | |||||||
chr17:40489796 | C | CA | 49 | a0001c0001t0005g0305 a0001c0001t0007g0334 a0001c0001t0008g0039 others(46): Show |
53 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.440-828dupT | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40489796 | |||||||
chr17:40489796 | C | CAAAAAAA others(1): Show |
101 | a0002c0002t0001g0189 a0002c0002t0001g0265 a0002c0002t0002g0042 others(98): Show |
109 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.440-835_440-828dup others(8): Show |
TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40489796 | |||||||
chr17:40489796 | C | CAAAAAAA others(3): Show |
2 | a0003c0003t0005g0061 a0003c0003t0036g0180 |
2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.440-837_440-828dup others(10): Show |
TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40489796 | |||||||
chr17:40489796 | C | CAAAAAAA others(4): Show |
18 | a0002c0002t0001g0242 a0003c0003t0005g0052 a0003c0003t0005g0074 others(15): Show |
18 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.440-838_440-828dup others(11): Show |
TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40489796 | |||||||
chr17:40489796 | C | CAAAAAAA others(5): Show |
7 | a0003c0003t0005g0076 a0003c0003t0005g0330 a0003c0003t0011g0073 others(4): Show |
7 | HG02055.hp2 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.440-839_440-828dup others(12): Show |
TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40489796 | |||||||
chr17:40489895 | T | C | 186 | a0001c0001t0005g0305 a0001c0001t0008g0039 a0001c0001t0011g0071 others(183): Show |
198 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.440-926A>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40489895 | |||||||
chr17:40489934 | G | T | 1 | a0003c0003t0026g0299 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.440-965C>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40489934 | |||||||
chr17:40490128 | T | C | 3 | a0001c0001t0008g0039 a0001c0001t0038g0047 a0001c0001t0058g0049 |
3 | HG00735.hp1 HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.440-1159A>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40490128 | |||||||
chr17:40490207 | C | T | 1 | a0001c0001t0028g0218 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.440-1238G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40490207 | |||||||
chr17:40490237 | C | T | 1 | a0003c0003t0005g0074 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.440-1268G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40490237 | |||||||
chr17:40490289 | G | A | 1 | a0002c0002t0049g0245 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.440-1320C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40490289 | |||||||
chr17:40490488 | C | T | 26 | a0003c0003t0005g0052 a0003c0003t0005g0061 a0003c0003t0005g0074 others(23): Show |
26 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.440-1519G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40490488 | |||||||
chr17:40490650 | G | T | 1 | a0001c0001t0021g0098 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.440-1681C>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40490650 | |||||||
chr17:40490980 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.440-2011G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40490980 | |||||||
chr17:40491020 | C | G | 1 | a0001c0001t0017g0167 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.440-2051G>C | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40491020 | |||||||
chr17:40491042 | C | T | 4 | a0002c0002t0006g0137 a0002c0002t0006g0182 a0002c0002t0014g0138 others(1): Show |
5 | HG00609.hp2 NA18948.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.440-2073G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40491042 | |||||||
chr17:40491131 | C | T | 1 | a0002c0002t0007g0289 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.440-2162G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40491131 | |||||||
chr17:40491221 | A | G | 185 | a0001c0001t0005g0305 a0001c0001t0008g0039 a0001c0001t0011g0071 others(182): Show |
196 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.440-2252T>C | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40491221 | |||||||
chr17:40491331 | TA | T | 142 | a0001c0001t0005g0305 a0001c0001t0011g0071 a0001c0001t0013g0068 others(139): Show |
150 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(147): Show |
intron_variant | MODIFIER | c.440-2363delT | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40491331 | |||||||
chr17:40491533 | C | G | 1 | a0001c0001t0012g0125 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.440-2564G>C | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40491533 | |||||||
chr17:40491546 | A | T | 1 | a0003c0003t0011g0073 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.440-2577T>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40491546 | |||||||
chr17:40491703 | G | T | 1 | a0001c0001t0009g0078 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.440-2734C>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40491703 | |||||||
chr17:40491739 | T | C | 175 | a0001c0001t0001g0002 a0001c0001t0001g0239 a0001c0001t0003g0063 others(172): Show |
191 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.440-2770A>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40491739 | |||||||
chr17:40491740 | G | T | 27 | a0002c0002t0001g0242 a0003c0003t0005g0052 a0003c0003t0005g0061 others(24): Show |
27 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.440-2771C>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40491740 | |||||||
chr17:40491778 | G | C | 5 | a0001c0001t0001g0240 a0001c0001t0012g0006 a0001c0001t0012g0322 others(2): Show |
7 | HG00639.hp2 HG00642.hp1 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.440-2809C>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40491778 | |||||||
chr17:40491805 | C | T | 3 | a0001c0001t0004g0065 a0001c0001t0004g0166 a0001c0001t0009g0078 |
3 | HG01123.hp2 HG02735.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.440-2836G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40491805 | |||||||
chr17:40491811 | C | T | 2 | a0001c0001t0067g0164 a0009c0013t0068g0347 |
2 | HG01081.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.440-2842G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40491811 | |||||||
chr17:40491945 | G | T | 3 | a0003c0003t0005g0052 a0003c0003t0005g0165 a0003c0003t0036g0284 |
3 | HG02258.hp1 NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.440-2976C>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40491945 | |||||||
chr17:40492094 | A | G | 143 | a0001c0001t0003g0063 a0001c0001t0010g0089 a0001c0001t0013g0068 others(140): Show |
150 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(147): Show |
intron_variant | MODIFIER | c.440-3125T>C | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40492094 | |||||||
chr17:40492108 | G | A | 20 | a0002c0002t0001g0242 a0003c0003t0005g0052 a0003c0003t0005g0074 others(17): Show |
20 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.440-3139C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40492108 | |||||||
chr17:40492153 | C | T | 2 | a0001c0001t0027g0024 a0001c0001t0027g0341 |
3 | HG02723.hp2 HG03041.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.440-3184G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40492153 | |||||||
chr17:40492185 | T | C | 3 | a0002c0002t0001g0265 a0002c0002t0020g0214 a0002c0002t0028g0215 |
3 | HG02602.hp2 HG03704.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.440-3216A>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40492185 | |||||||
chr17:40492223 | G | A | 184 | a0001c0001t0002g0144 a0001c0001t0003g0063 a0001c0001t0004g0213 others(181): Show |
194 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.440-3254C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40492223 | |||||||
chr17:40492375 | C | CT | 172 | a0001c0001t0001g0268 a0001c0001t0001g0336 a0001c0001t0002g0064 others(169): Show |
180 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.440-3407dupA | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40492375 | |||||||
chr17:40492595 | GT | G | 29 | a0001c0001t0005g0305 a0001c0001t0008g0039 a0001c0001t0008g0317 others(26): Show |
32 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.439+3391delA | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40492595 | |||||||
chr17:40492595 | GTT | G | 7 | a0001c0001t0001g0050 a0001c0001t0008g0033 a0001c0001t0020g0051 others(4): Show |
7 | HG02280.hp2 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.439+3390_439+3391d others(4): Show |
TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40492595 | |||||||
chr17:40492610 | T | G | 2 | a0001c0001t0025g0109 a0002c0002t0006g0157 |
2 | HG00323.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.439+3377A>C | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40492610 | |||||||
chr17:40492613 | TG | T | 96 | a0001c0001t0001g0095 a0001c0001t0001g0268 a0001c0001t0001g0336 others(93): Show |
101 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.439+3373delC | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40492613 | |||||||
chr17:40492614 | G | T | 5 | a0001c0001t0002g0115 a0001c0001t0008g0004 a0001c0001t0019g0114 others(2): Show |
5 | HG02293.hp2 HG02738.hp1 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.439+3373C>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40492614 | |||||||
chr17:40492671 | G | T | 4 | a0001c0001t0001g0050 a0001c0001t0008g0033 a0001c0001t0020g0051 others(1): Show |
4 | HG02280.hp2 HG02572.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.439+3316C>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40492671 | |||||||
chr17:40492718 | C | T | 1 | a0011c0014t0005g0046 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.439+3269G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40492718 | |||||||
chr17:40492731 | A | C | 3 | a0001c0004t0055g0072 a0001c0008t0044g0031 a0005c0009t0071g0070 |
3 | HG02647.hp2 HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.439+3256T>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40492731 | |||||||
chr17:40492764 | T | C | 17 | a0001c0001t0005g0305 a0001c0001t0011g0037 a0001c0001t0013g0136 others(14): Show |
18 | HG01168.hp2 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.439+3223A>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40492764 | |||||||
chr17:40492767 | T | C | 10 | a0001c0001t0001g0050 a0001c0001t0007g0054 a0001c0001t0008g0033 others(7): Show |
10 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.439+3220A>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40492767 | |||||||
chr17:40492826 | G | A | 1 | a0001c0004t0063g0348 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.439+3161C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40492826 | |||||||
chr17:40492836 | A | G | 135 | a0001c0001t0001g0050 a0001c0001t0001g0104 a0001c0001t0001g0145 others(132): Show |
141 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.439+3151T>C | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40492836 | |||||||
chr17:40492840 | T | A | 55 | a0001c0001t0001g0145 a0001c0001t0001g0155 a0001c0001t0001g0247 others(52): Show |
58 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.439+3147A>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40492840 | |||||||
chr17:40492843 | A | G | 2 | a0003c0003t0005g0330 a0003c0003t0057g0329 |
2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.439+3144T>C | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40492843 | |||||||
chr17:40492850 | G | T | 7 | a0001c0001t0002g0064 a0001c0001t0025g0109 a0001c0004t0005g0032 others(4): Show |
7 | HG00323.hp1 HG02886.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.439+3137C>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40492850 | |||||||
chr17:40492890 | C | CA | 10 | a0001c0001t0001g0050 a0001c0001t0008g0033 a0001c0001t0020g0051 others(7): Show |
12 | HG02027.hp1 HG02280.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.439+3096dupT | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40492890 | |||||||
chr17:40492951 | C | G | 117 | a0001c0001t0001g0050 a0001c0001t0001g0104 a0001c0001t0001g0126 others(114): Show |
123 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.439+3036G>C | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40492951 | |||||||
chr17:40493065 | G | A | 2 | a0001c0001t0003g0254 a0001c0001t0003g0255 |
2 | HG02683.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.439+2922C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40493065 | |||||||
chr17:40493313 | A | G | 1 | a0001c0001t0001g0326 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.439+2674T>C | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40493313 | |||||||
chr17:40493337 | A | T | 1 | a0001c0001t0004g0106 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.439+2650T>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40493337 | |||||||
chr17:40493350 | C | T | 1 | a0001c0001t0021g0056 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.439+2637G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40493350 | |||||||
chr17:40493370 | C | T | 2 | a0005c0007t0042g0345 a0005c0007t0070g0313 |
2 | HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.439+2617G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40493370 | |||||||
chr17:40493607 | C | T | 3 | a0001c0004t0041g0027 a0001c0004t0045g0312 a0001c0004t0063g0348 |
4 | HG01109.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.439+2380G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40493607 | |||||||
chr17:40493678 | C | T | 1 | a0001c0001t0008g0033 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.439+2309G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40493678 | |||||||
chr17:40493782 | C | T | 5 | a0001c0001t0021g0056 a0001c0001t0021g0058 a0001c0001t0033g0057 others(2): Show |
5 | HG00099.hp2 HG02148.hp2 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.439+2205G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40493782 | |||||||
chr17:40493814 | A | C | 1 | a0001c0001t0002g0105 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.439+2173T>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40493814 | |||||||
chr17:40493815 | C | T | 25 | a0001c0001t0001g0050 a0001c0001t0008g0033 a0001c0001t0011g0028 others(22): Show |
27 | HG00735.hp1 HG01081.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.439+2172G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40493815 | |||||||
chr17:40493980 | T | C | 2 | a0005c0007t0042g0345 a0005c0007t0070g0313 |
2 | HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.439+2007A>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40493980 | |||||||
chr17:40494332 | G | A | 1 | a0001c0001t0054g0101 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.439+1655C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40494332 | |||||||
chr17:40494368 | C | T | 1 | a0002c0002t0009g0285 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.439+1619G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40494368 | |||||||
chr17:40494589 | G | T | 1 | a0001c0001t0001g0104 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.439+1398C>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40494589 | |||||||
chr17:40494729 | CA | C | 11 | a0001c0001t0001g0268 a0001c0001t0001g0326 a0001c0001t0008g0033 others(8): Show |
11 | HG00099.hp2 HG02148.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.439+1257delT | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40494729 | |||||||
chr17:40494729 | CAA | C | 24 | a0001c0001t0001g0266 a0001c0001t0001g0336 a0001c0001t0002g0258 others(21): Show |
24 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.439+1256_439+1257d others(4): Show |
TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40494729 | |||||||
chr17:40494729 | CAAA | C | 264 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0086 others(261): Show |
303 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.439+1255_439+1257d others(5): Show |
TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40494729 | |||||||
chr17:40494729 | CAAAA | C | 6 | a0001c0001t0002g0279 a0001c0001t0066g0307 a0001c0004t0065g0306 others(3): Show |
6 | HG02258.hp1 HG02818.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.439+1254_439+1257d others(6): Show |
TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40494729 | |||||||
chr17:40494857 | T | C | 1 | a0003c0003t0005g0074 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.439+1130A>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40494857 | |||||||
chr17:40495195 | G | A | 303 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0086 others(300): Show |
342 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.439+792C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40495195 | |||||||
chr17:40495493 | G | A | 4 | a0001c0004t0045g0312 a0002c0002t0004g0069 a0005c0007t0042g0345 others(1): Show |
4 | HG02559.hp2 HG02717.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.439+494C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40495493 | |||||||
chr17:40495577 | A | G | 1 | a0001c0001t0003g0102 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.439+410T>C | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40495577 | |||||||
chr17:40495580 | T | C | 305 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0086 others(302): Show |
344 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(341): Show |
intron_variant | MODIFIER | c.439+407A>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40495580 | |||||||
chr17:40495637 | A | G | 10 | a0001c0004t0041g0027 a0001c0004t0045g0312 a0001c0004t0055g0072 others(7): Show |
11 | HG01081.hp1 HG01109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.439+350T>C | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40495637 | |||||||
chr17:40495747 | C | T | 1 | a0001c0001t0008g0033 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.439+240G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40495747 | |||||||
chr17:40495836 | G | A | 5 | a0001c0001t0021g0056 a0001c0001t0021g0058 a0001c0001t0033g0057 others(2): Show |
5 | HG00099.hp2 HG02148.hp2 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.439+151C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40495836 | |||||||
chr17:40495850 | G | A | 7 | a0001c0001t0002g0271 a0001c0001t0004g0269 a0001c0001t0004g0273 others(4): Show |
7 | HG00438.hp2 HG02027.hp1 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.439+137C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40495850 | |||||||
chr17:40495916 | T | C | 3 | a0001c0001t0013g0068 a0001c0001t0025g0067 a0002c0002t0064g0346 |
3 | HG01993.hp2 HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.439+71A>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40495916 | |||||||
chr17:40495968 | C | T | 19 | a0001c0001t0001g0095 a0001c0001t0010g0089 a0001c0001t0013g0008 others(16): Show |
22 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.439+19G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 2/12 | chr17 | 40495968 | |||||||
chr17:40496582 | C | G | 1 | a0001c0001t0003g0087 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-95-62G>C | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40496582 | |||||||
chr17:40496592 | A | G | 305 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0086 others(302): Show |
344 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(341): Show |
intron_variant | MODIFIER | c.-95-72T>C | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40496592 | |||||||
chr17:40496724 | C | T | 334 | a0001c0001t0001g0002 a0001c0001t0001g0050 a0001c0001t0001g0066 others(331): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.-95-204G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40496724 | |||||||
chr17:40496876 | C | T | 1 | a0001c0004t0045g0312 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-95-356G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40496876 | |||||||
chr17:40497014 | G | A | 311 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0086 others(308): Show |
353 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(350): Show |
intron_variant | MODIFIER | c.-95-494C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40497014 | |||||||
chr17:40497102 | C | G | 294 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0086 others(291): Show |
333 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.-95-582G>C | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40497102 | |||||||
chr17:40497203 | G | A | 5 | a0001c0001t0001g0050 a0001c0001t0020g0051 a0001c0001t0020g0344 others(2): Show |
5 | HG02280.hp2 HG02615.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-95-683C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40497203 | |||||||
chr17:40497280 | G | A | 1 | a0001c0004t0065g0306 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-95-760C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40497280 | |||||||
chr17:40497505 | G | A | 4 | a0001c0004t0045g0312 a0002c0002t0004g0069 a0005c0007t0042g0345 others(1): Show |
4 | HG02559.hp2 HG02717.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-95-985C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40497505 | |||||||
chr17:40497551 | C | T | 2 | a0002c0002t0003g0281 a0002c0002t0003g0282 |
2 | HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-95-1031G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40497551 | |||||||
chr17:40497683 | A | G | 1 | a0001c0001t0001g0326 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-95-1163T>C | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40497683 | |||||||
chr17:40497687 | C | A | 335 | a0001c0001t0001g0002 a0001c0001t0001g0050 a0001c0001t0001g0066 others(332): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.-95-1167G>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40497687 | |||||||
chr17:40497765 | G | T | 2 | a0001c0001t0005g0280 a0001c0001t0005g0339 |
2 | HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-95-1245C>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40497765 | |||||||
chr17:40497818 | G | A | 4 | a0001c0001t0007g0277 a0001c0001t0024g0276 a0002c0002t0010g0338 others(1): Show |
4 | HG02071.hp1 HG02132.hp2 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.-95-1298C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40497818 | |||||||
chr17:40497921 | T | C | 1 | a0004c0005t0010g0278 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-95-1401A>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40497921 | |||||||
chr17:40498098 | A | C | 2 | a0001c0001t0001g0086 a0001c0001t0013g0085 |
2 | HG01261.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-95-1578T>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40498098 | |||||||
chr17:40498115 | C | G | 3 | a0002c0002t0006g0083 a0002c0002t0014g0082 a0002c0002t0015g0084 |
3 | HG02004.hp2 HG02735.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-95-1595G>C | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40498115 | |||||||
chr17:40498133 | C | A | 1 | a0001c0001t0002g0279 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-95-1613G>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40498133 | |||||||
chr17:40498331 | T | C | 1 | a0001c0001t0066g0307 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-95-1811A>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40498331 | |||||||
chr17:40498540 | G | A | 305 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0086 others(302): Show |
344 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(341): Show |
intron_variant | MODIFIER | c.-95-2020C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40498540 | |||||||
chr17:40498669 | C | T | 1 | a0002c0002t0009g0314 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-95-2149G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40498669 | |||||||
chr17:40498694 | A | G | 1 | a0001c0004t0055g0072 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-95-2174T>C | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40498694 | |||||||
chr17:40498903 | C | T | 254 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0086 others(251): Show |
290 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.-95-2383G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40498903 | |||||||
chr17:40498922 | G | A | 1 | a0001c0001t0058g0049 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-95-2402C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40498922 | |||||||
chr17:40499049 | A | G | 1 | a0001c0001t0012g0081 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-96+2485T>C | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40499049 | |||||||
chr17:40499348 | G | C | 1 | a0001c0004t0055g0072 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-96+2186C>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40499348 | |||||||
chr17:40499441 | G | T | 7 | a0001c0001t0011g0028 a0001c0004t0041g0027 a0001c0004t0063g0348 others(4): Show |
10 | HG01081.hp1 HG01109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.-96+2093C>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40499441 | |||||||
chr17:40499463 | C | T | 295 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0086 others(292): Show |
334 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.-96+2071G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40499463 | |||||||
chr17:40499586 | C | T | 1 | a0002c0002t0003g0080 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-96+1948G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40499586 | |||||||
chr17:40499651 | C | T | 1 | a0005c0007t0042g0345 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-96+1883G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40499651 | |||||||
chr17:40499924 | G | A | 1 | a0003c0003t0005g0308 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-96+1610C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40499924 | |||||||
chr17:40499967 | C | T | 294 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0086 others(291): Show |
333 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.-96+1567G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40499967 | |||||||
chr17:40500044 | A | G | 1 | a0001c0001t0001g0326 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-96+1490T>C | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40500044 | |||||||
chr17:40500158 | C | T | 2 | a0001c0008t0043g0030 a0001c0008t0044g0031 |
2 | HG02615.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-96+1376G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40500158 | |||||||
chr17:40500239 | C | T | 1 | a0002c0002t0023g0079 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-96+1295G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40500239 | |||||||
chr17:40500323 | G | A | 2 | a0001c0008t0043g0030 a0001c0008t0044g0031 |
2 | HG02615.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-96+1211C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40500323 | |||||||
chr17:40500376 | T | C | 1 | a0002c0002t0009g0314 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-96+1158A>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40500376 | |||||||
chr17:40500386 | T | C | 1 | a0004c0005t0010g0315 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-96+1148A>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40500386 | |||||||
chr17:40500514 | C | T | 1 | a0001c0001t0009g0078 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-96+1020G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40500514 | |||||||
chr17:40500633 | T | A | 1 | a0001c0001t0017g0316 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-96+901A>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40500633 | |||||||
chr17:40500720 | C | G | 1 | a0001c0001t0013g0008 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-96+814G>C | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40500720 | |||||||
chr17:40500755 | C | A | 4 | a0001c0001t0001g0050 a0001c0001t0020g0051 a0001c0004t0005g0032 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-96+779G>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40500755 | |||||||
chr17:40500872 | C | T | 1 | a0001c0001t0008g0325 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-96+662G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40500872 | |||||||
chr17:40500883 | G | C | 6 | a0001c0001t0017g0055 a0001c0001t0021g0056 a0001c0001t0021g0058 others(3): Show |
6 | HG00099.hp2 HG02148.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.-96+651C>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40500883 | |||||||
chr17:40500883 | G | T | 341 | a0001c0001t0001g0002 a0001c0001t0001g0050 a0001c0001t0001g0066 others(338): Show |
383 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(380): Show |
intron_variant | MODIFIER | c.-96+651C>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40500883 | |||||||
chr17:40500894 | C | T | 1 | a0002c0002t0006g0324 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-96+640G>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40500894 | |||||||
chr17:40500949 | G | C | 5 | a0001c0001t0008g0317 a0001c0001t0008g0321 a0006c0010t0034g0318 others(2): Show |
5 | HG01069.hp2 HG01071.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.-96+585C>G | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40500949 | |||||||
chr17:40501020 | G | A | 1 | a0001c0001t0012g0322 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-96+514C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40501020 | |||||||
chr17:40501105 | C | G | 1 | a0001c0004t0005g0032 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-96+429G>C | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40501105 | |||||||
chr17:40501223 | G | A | 2 | a0001c0001t0011g0071 a0001c0004t0055g0072 |
2 | HG02280.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-96+311C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40501223 | |||||||
chr17:40501223 | G | T | 6 | a0002c0002t0037g0077 a0003c0003t0005g0061 a0003c0003t0005g0076 others(3): Show |
6 | HG01243.hp2 HG02630.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-96+311C>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40501223 | |||||||
chr17:40501263 | A | T | 2 | a0003c0003t0005g0074 a0003c0003t0011g0073 |
2 | HG02055.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-96+271T>A | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40501263 | |||||||
chr17:40501276 | G | A | 6 | a0001c0001t0017g0055 a0001c0001t0021g0056 a0001c0001t0021g0058 others(3): Show |
6 | HG00099.hp2 HG02148.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.-96+258C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40501276 | |||||||
chr17:40501405 | G | A | 2 | a0001c0008t0043g0030 a0001c0008t0044g0031 |
2 | HG02615.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-96+129C>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40501405 | |||||||
chr17:40501447 | C | CA | 13 | a0001c0001t0011g0028 a0001c0001t0017g0055 a0001c0001t0021g0056 others(10): Show |
16 | HG00099.hp2 HG01081.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.-96+86dupT | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40501447 | |||||||
chr17:40501447 | C | CAAAA | 12 | a0001c0001t0001g0066 a0001c0001t0002g0064 a0001c0001t0003g0063 others(9): Show |
12 | HG01993.hp2 HG02280.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.-96+83_-96+86dupTT others(2): Show |
TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40501447 | |||||||
chr17:40501447 | C | CAAAAA | 275 | a0001c0001t0001g0002 a0001c0001t0001g0086 a0001c0001t0001g0095 others(272): Show |
313 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.-96+82_-96+86dupTT others(3): Show |
TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40501447 | |||||||
chr17:40501447 | C | CAAAAAA | 24 | a0001c0001t0001g0326 a0001c0001t0001g0336 a0001c0001t0005g0339 others(21): Show |
25 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.-96+81_-96+86dupTT others(4): Show |
TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40501447 | |||||||
chr17:40501465 | T | A | 1 | a0002c0002t0064g0346 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-96+69A>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40501465 | |||||||
chr17:40501484 | C | A | 7 | a0001c0001t0011g0028 a0001c0004t0041g0027 a0001c0004t0063g0348 others(4): Show |
10 | HG01081.hp1 HG01109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.-96+50G>T | TNS4 | ENSG00000131746.13 | transcript | ENST00000254051.11 | protein_coding | 1/12 | chr17 | 40501484 |