Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 27075 |
| ensemblid | ENSG00000106537.8 |
| hgncid | 21643 |
| symbol | TSPAN13 |
| name | tetraspanin 13 |
| refseq_nuc | NM_014399.4 |
| refseq_prot | NP_055214.1 |
| ensembl_nuc | ENST00000262067.5 |
| ensembl_prot | ENSP00000262067.4 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 16753755 |
| end | 16784536 |
| strand | + |
| ver | v1.2 |
| region | chr7:16753755-16784536 |
| region5000 | chr7:16748755-16789536 |
| regionname0 | TSPAN13_chr7_16753755_16784536 |
| regionname5000 | TSPAN13_chr7_16748755_16789536 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 204 | 439 | 96 | 82 | 197 | 14 | 48 | 149 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | MVCGG others(199): Show |
chr7 | 16748755 | 16789536 |
| a0002 | 0/0 | 204 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | MVCGG others(199): Show |
chr7 | 16748755 | 16789536 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 612 | 203 | 32 | 28 | 120 | 5 | 17 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | ATGGT others(607): Show |
chr7 | 16748755 | 16789536 | ||
| a0001c0002 | 0/1 | 612 | 118 | 21 | 31 | 41 | 2 | 22 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | ATGGT others(607): Show |
chr7 | 16748755 | 16789536 | ||
| a0001c0003 | 0/0 | 612 | 60 | 29 | 9 | 19 | 3 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | ATGGT others(607): Show |
chr7 | 16748755 | 16789536 | ||
| a0001c0004 | 0/0 | 612 | 58 | 14 | 14 | 17 | 4 | 9 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | ATGGT others(607): Show |
chr7 | 16748755 | 16789536 | ||
| a0002c0005 | 0/0 | 612 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | ATGGT others(607): Show |
chr7 | 16748755 | 16789536 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1873 | 108 | 5 | 16 | 71 | 4 | 12 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1868): Show |
chr7 | 16748755 | 16789536 |
| a0001c0001t0002 | 0/0 | 1870 | 4 | 2 | 2 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1865): Show |
chr7 | 16748755 | 16789536 |
| a0001c0001t0003 | 1/0 | 1873 | 35 | 9 | 4 | 18 | 1 | 2 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1868): Show |
chr7 | 16748755 | 16789536 |
| a0001c0001t0004 | 0/0 | 1873 | 39 | 7 | 1 | 29 | 0 | 2 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1868): Show |
chr7 | 16748755 | 16789536 |
| a0001c0001t0005 | 0/0 | 1870 | 5 | 5 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1865): Show |
chr7 | 16748755 | 16789536 |
| a0001c0001t0007 | 0/0 | 1873 | 7 | 2 | 3 | 2 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1868): Show |
chr7 | 16748755 | 16789536 |
| a0001c0001t0011 | 0/0 | 1873 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1868): Show |
chr7 | 16748755 | 16789536 |
| a0001c0001t0013 | 0/0 | 1873 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1868): Show |
chr7 | 16748755 | 16789536 |
| a0001c0001t0017 | 0/0 | 1873 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1868): Show |
chr7 | 16748755 | 16789536 |
| a0001c0001t0018 | 0/0 | 1873 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1868): Show |
chr7 | 16748755 | 16789536 |
| a0001c0001t0024 | 0/0 | 1870 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1865): Show |
chr7 | 16748755 | 16789536 |
| a0001c0002t0001 | 0/0 | 1873 | 86 | 7 | 27 | 33 | 1 | 18 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1868): Show |
chr7 | 16748755 | 16789536 |
| a0001c0002t0002 | 0/0 | 1870 | 4 | 1 | 2 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1865): Show |
chr7 | 16748755 | 16789536 |
| a0001c0002t0003 | 0/0 | 1873 | 4 | 3 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1868): Show |
chr7 | 16748755 | 16789536 |
| a0001c0002t0005 | 0/0 | 1870 | 5 | 5 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1865): Show |
chr7 | 16748755 | 16789536 |
| a0001c0002t0006 | 0/0 | 1873 | 15 | 4 | 1 | 6 | 0 | 4 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1868): Show |
chr7 | 16748755 | 16789536 |
| a0001c0002t0008 | 0/0 | 1870 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1865): Show |
chr7 | 16748755 | 16789536 |
| a0001c0002t0016 | 0/1 | 1874 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1869): Show |
chr7 | 16748755 | 16789536 |
| a0001c0002t0019 | 0/0 | 1873 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1868): Show |
chr7 | 16748755 | 16789536 |
| a0001c0002t0026 | 0/0 | 1870 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1865): Show |
chr7 | 16748755 | 16789536 |
| a0001c0003t0001 | 0/0 | 1873 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1868): Show |
chr7 | 16748755 | 16789536 |
| a0001c0003t0002 | 0/0 | 1870 | 22 | 6 | 5 | 10 | 1 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1865): Show |
chr7 | 16748755 | 16789536 |
| a0001c0003t0003 | 0/0 | 1873 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1868): Show |
chr7 | 16748755 | 16789536 |
| a0001c0003t0005 | 0/0 | 1870 | 11 | 4 | 0 | 7 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1865): Show |
chr7 | 16748755 | 16789536 |
| a0001c0003t0006 | 0/0 | 1873 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1868): Show |
chr7 | 16748755 | 16789536 |
| a0001c0003t0007 | 0/0 | 1873 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1868): Show |
chr7 | 16748755 | 16789536 |
| a0001c0003t0008 | 0/0 | 1870 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1865): Show |
chr7 | 16748755 | 16789536 |
| a0001c0003t0009 | 0/0 | 1873 | 4 | 4 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1868): Show |
chr7 | 16748755 | 16789536 |
| a0001c0003t0010 | 0/0 | 1870 | 3 | 1 | 0 | 0 | 2 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1865): Show |
chr7 | 16748755 | 16789536 |
| a0001c0003t0011 | 0/0 | 1873 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1868): Show |
chr7 | 16748755 | 16789536 |
| a0001c0003t0012 | 0/0 | 1870 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1865): Show |
chr7 | 16748755 | 16789536 |
| a0001c0003t0014 | 0/0 | 1873 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1868): Show |
chr7 | 16748755 | 16789536 |
| a0001c0003t0015 | 0/0 | 1873 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1868): Show |
chr7 | 16748755 | 16789536 |
| a0001c0003t0020 | 0/0 | 1870 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1865): Show |
chr7 | 16748755 | 16789536 |
| a0001c0003t0022 | 0/0 | 1870 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1865): Show |
chr7 | 16748755 | 16789536 |
| a0001c0003t0023 | 0/0 | 1870 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1865): Show |
chr7 | 16748755 | 16789536 |
| a0001c0003t0025 | 0/0 | 1870 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1865): Show |
chr7 | 16748755 | 16789536 |
| a0001c0003t0027 | 0/0 | 1870 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1865): Show |
chr7 | 16748755 | 16789536 |
| a0001c0004t0001 | 0/0 | 1873 | 6 | 2 | 2 | 1 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1868): Show |
chr7 | 16748755 | 16789536 |
| a0001c0004t0002 | 0/0 | 1870 | 43 | 6 | 10 | 15 | 4 | 8 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1865): Show |
chr7 | 16748755 | 16789536 |
| a0001c0004t0003 | 0/0 | 1873 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1868): Show |
chr7 | 16748755 | 16789536 |
| a0001c0004t0005 | 0/0 | 1870 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1865): Show |
chr7 | 16748755 | 16789536 |
| a0001c0004t0006 | 0/0 | 1873 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1868): Show |
chr7 | 16748755 | 16789536 |
| a0001c0004t0008 | 0/0 | 1870 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1865): Show |
chr7 | 16748755 | 16789536 |
| a0001c0004t0021 | 0/0 | 1870 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1865): Show |
chr7 | 16748755 | 16789536 |
| a0002c0005t0001 | 0/0 | 1873 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | CCGGC others(1868): Show |
chr7 | 16748755 | 16789536 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0003g0045 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0003g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0003g0050 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0004g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0004g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0004g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0004g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0004g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0004g0047 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0004g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0004g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0004g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0005g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0005g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0005g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0005g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0005g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0007g0023 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0007g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0007g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0007g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0011g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0013g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0017g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0018g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0001t0024g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0002 | 0/0 | 9 | 0 | 4 | 5 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0004 | 0/0 | 6 | 0 | 1 | 0 | 0 | 5 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0006 | 0/0 | 5 | 1 | 0 | 0 | 0 | 4 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0042 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0043 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0049 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0059 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0060 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0003g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0005g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0005g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0005g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0005g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0005g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0006g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0006g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0006g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0006g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0006g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0006g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0006g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0006g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0006g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0006g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0006g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0006g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0008g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0016g0064 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0019g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0002t0026g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0002g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0002g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0002g0061 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0005g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0005g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0005g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0005g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0005g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0005g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0005g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0006g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0007g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0007g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0008g0062 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0009g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0010g0029 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0010g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0011g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0012g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0012g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0014g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0015g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0020g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0022g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0023g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0025g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0003t0027g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0004t0001g0058 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0004t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0004t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0004t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0004t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0004t0002g0001 | 0/0 | 12 | 2 | 3 | 5 | 1 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0004t0002g0013 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0004t0002g0027 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0004t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0004t0002g0032 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0004t0002g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0004t0002g0063 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0004t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0004t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0004t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0004t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0004t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0004t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0004t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0004t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0004t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0004t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0004t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0004t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0004t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0004t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0004t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0004t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0004t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0004t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0004t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0004t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0004t0005g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0004t0006g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0004t0006g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0004t0008g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0004t0008g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0001c0004t0021g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| a0002c0005t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0004 | t0002 | g0032 | EUR | GBR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG00099 | hp2 | a0001 | c0004 | t0002 | g0312 | EUR | GBR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0164 | EUR | FIN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG00280 | hp2 | a0001 | c0002 | t0019 | g0134 | EUR | FIN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0176 | EUR | FIN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG00323 | hp2 | a0001 | c0004 | t0002 | g0032 | EUR | FIN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | CHS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG00408 | hp2 | a0001 | c0003 | t0005 | g0104 | EAS | CHS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0057 | EAS | CHS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG00423 | hp2 | a0001 | c0001 | t0004 | g0073 | EAS | CHS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG00438 | hp2 | a0001 | c0004 | t0002 | g0107 | EAS | CHS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG00544 | hp1 | a0001 | c0003 | t0005 | g0102 | EAS | CHS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG00544 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | CHS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | CHS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG00558 | hp2 | a0001 | c0004 | t0002 | g0105 | EAS | CHS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0212 | EAS | CHS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | CHS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0171 | EAS | CHS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG00639 | hp1 | a0001 | c0002 | t0003 | g0198 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG00639 | hp2 | a0001 | c0003 | t0012 | g0293 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0051 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG00642 | hp2 | a0001 | c0004 | t0002 | g0027 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG00673 | hp1 | a0001 | c0004 | t0002 | g0087 | EAS | CHS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0235 | EAS | CHS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG00733 | hp1 | a0001 | c0004 | t0008 | g0306 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0045 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0177 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0221 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0169 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01070 | hp1 | a0001 | c0004 | t0002 | g0103 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0041 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0041 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0076 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01074 | hp2 | a0001 | c0001 | t0017 | g0236 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0303 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0043 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0049 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01109 | hp1 | a0001 | c0002 | t0006 | g0266 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01109 | hp2 | a0001 | c0004 | t0002 | g0318 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0233 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01167 | hp2 | a0001 | c0003 | t0002 | g0061 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0237 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01168 | hp2 | a0001 | c0004 | t0002 | g0001 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01169 | hp1 | a0001 | c0004 | t0002 | g0001 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01169 | hp2 | a0001 | c0003 | t0002 | g0061 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01175 | hp1 | a0001 | c0003 | t0002 | g0031 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01175 | hp2 | a0001 | c0003 | t0002 | g0110 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0223 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01243 | hp2 | a0001 | c0004 | t0006 | g0203 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01255 | hp2 | a0001 | c0003 | t0001 | g0147 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01256 | hp1 | a0001 | c0001 | t0007 | g0023 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01256 | hp2 | a0001 | c0004 | t0001 | g0058 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01257 | hp1 | a0001 | c0002 | t0002 | g0095 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0039 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0039 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01258 | hp2 | a0001 | c0004 | t0001 | g0058 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0210 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0215 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0117 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01358 | hp1 | a0001 | c0004 | t0002 | g0027 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0170 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01361 | hp2 | a0001 | c0001 | t0007 | g0023 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01433 | hp1 | a0001 | c0001 | t0018 | g0146 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0017 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0207 | EUR | IBS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01515 | hp2 | a0001 | c0003 | t0002 | g0031 | EUR | IBS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01516 | hp1 | a0001 | c0003 | t0010 | g0029 | EUR | IBS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0199 | EUR | IBS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01517 | hp1 | a0001 | c0003 | t0010 | g0029 | EUR | IBS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0232 | EUR | IBS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01884 | hp1 | a0001 | c0003 | t0002 | g0296 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0043 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01891 | hp1 | a0001 | c0004 | t0002 | g0001 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01891 | hp2 | a0001 | c0001 | t0007 | g0053 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01928 | hp1 | a0001 | c0004 | t0002 | g0317 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0051 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0050 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0217 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0017 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01978 | hp2 | a0001 | c0003 | t0002 | g0313 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01981 | hp1 | a0001 | c0004 | t0002 | g0030 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0017 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01993 | hp1 | a0001 | c0004 | t0002 | g0013 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02004 | hp1 | a0001 | c0001 | t0007 | g0023 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02004 | hp2 | a0001 | c0003 | t0006 | g0205 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02027 | hp1 | a0001 | c0003 | t0002 | g0099 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02055 | hp1 | a0001 | c0003 | t0002 | g0026 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02055 | hp2 | a0001 | c0003 | t0009 | g0011 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0047 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0016 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0281 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02083 | hp1 | a0001 | c0004 | t0002 | g0001 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0021 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0250 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02132 | hp1 | a0001 | c0004 | t0001 | g0149 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02145 | hp1 | a0001 | c0002 | t0002 | g0307 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02145 | hp2 | a0001 | c0003 | t0007 | g0126 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0175 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02165 | hp1 | a0001 | c0003 | t0002 | g0106 | EAS | CDX | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02165 | hp2 | a0001 | c0002 | t0006 | g0072 | EAS | CDX | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0174 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0050 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02258 | hp2 | a0001 | c0004 | t0001 | g0118 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02273 | hp2 | a0001 | c0002 | t0002 | g0316 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02280 | hp1 | a0001 | c0004 | t0001 | g0119 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02280 | hp2 | a0001 | c0002 | t0005 | g0311 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0131 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02300 | hp2 | a0001 | c0003 | t0020 | g0030 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02451 | hp1 | a0001 | c0003 | t0002 | g0026 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02451 | hp2 | a0001 | c0002 | t0005 | g0294 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0016 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02572 | hp1 | a0001 | c0004 | t0002 | g0108 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02572 | hp2 | a0001 | c0002 | t0003 | g0040 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0172 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0077 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0152 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0125 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02630 | hp1 | a0001 | c0003 | t0008 | g0062 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02630 | hp2 | a0001 | c0003 | t0022 | g0112 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0264 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02647 | hp2 | a0001 | c0002 | t0005 | g0310 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0216 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02683 | hp2 | a0001 | c0002 | t0006 | g0028 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02698 | hp2 | a0001 | c0004 | t0001 | g0144 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0305 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02717 | hp2 | a0001 | c0002 | t0003 | g0267 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02723 | hp1 | a0001 | c0004 | t0003 | g0197 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02723 | hp2 | a0001 | c0003 | t0005 | g0290 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0262 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0297 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0065 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02818 | hp1 | a0001 | c0003 | t0014 | g0206 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02818 | hp2 | a0001 | c0003 | t0003 | g0128 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02896 | hp1 | a0001 | c0004 | t0002 | g0063 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0231 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02897 | hp1 | a0001 | c0002 | t0006 | g0256 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0258 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02922 | hp1 | a0001 | c0003 | t0005 | g0025 | AFR | ESN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02922 | hp2 | a0001 | c0003 | t0009 | g0011 | AFR | ESN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0123 | AFR | ESN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0268 | AFR | ESN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02970 | hp1 | a0001 | c0003 | t0003 | g0121 | AFR | ESN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0053 | AFR | ESN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02976 | hp1 | a0001 | c0002 | t0006 | g0136 | AFR | ESN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02976 | hp2 | a0001 | c0003 | t0005 | g0025 | AFR | ESN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0208 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03041 | hp1 | a0001 | c0004 | t0006 | g0204 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03041 | hp2 | a0001 | c0004 | t0003 | g0154 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03098 | hp1 | a0001 | c0003 | t0008 | g0062 | AFR | MSL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03098 | hp2 | a0001 | c0002 | t0006 | g0229 | AFR | MSL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0140 | AFR | ESN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03130 | hp2 | a0001 | c0004 | t0005 | g0036 | AFR | ESN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0269 | AFR | ESN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03139 | hp2 | a0001 | c0001 | t0011 | g0122 | AFR | ESN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0302 | AFR | ESN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03195 | hp2 | a0001 | c0004 | t0005 | g0036 | AFR | ESN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0295 | AFR | MSL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03209 | hp2 | a0001 | c0002 | t0003 | g0040 | AFR | MSL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03225 | hp1 | a0001 | c0003 | t0011 | g0148 | AFR | MSL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0156 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0078 | AFR | MSL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03486 | hp1 | a0001 | c0002 | t0006 | g0124 | AFR | MSL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03486 | hp2 | a0001 | c0003 | t0002 | g0308 | AFR | MSL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03490 | hp1 | a0001 | c0004 | t0002 | g0027 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03491 | hp1 | a0001 | c0004 | t0002 | g0035 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0042 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03492 | hp1 | a0001 | c0004 | t0002 | g0035 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0020 | AFR | ESN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03516 | hp2 | a0001 | c0003 | t0009 | g0011 | AFR | ESN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03540 | hp1 | a0001 | c0003 | t0015 | g0137 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03540 | hp2 | a0001 | c0003 | t0027 | g0113 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0219 | AFR | MSL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03579 | hp2 | a0001 | c0003 | t0005 | g0025 | AFR | MSL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03654 | hp1 | a0001 | c0004 | t0002 | g0092 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03654 | hp2 | a0001 | c0001 | t0004 | g0213 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03669 | hp1 | a0001 | c0002 | t0006 | g0081 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03688 | hp1 | a0001 | c0002 | t0006 | g0028 | SAS | STU | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0006 | SAS | STU | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0006 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03704 | hp2 | a0001 | c0001 | t0013 | g0162 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03710 | hp1 | a0001 | c0004 | t0002 | g0315 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0259 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03831 | hp2 | a0001 | c0004 | t0002 | g0097 | SAS | BEB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | BEB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03834 | hp2 | a0001 | c0002 | t0006 | g0080 | SAS | BEB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0173 | SAS | BEB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | BEB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | BEB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0006 | SAS | BEB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG04115 | hp1 | a0001 | c0004 | t0002 | g0001 | SAS | STU | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0168 | SAS | STU | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0006 | SAS | BEB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | STU | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG04199 | hp2 | a0001 | c0004 | t0002 | g0093 | SAS | STU | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | STU | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | STU | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | STU | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0047 | SAS | STU | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0020 | AFR | YRI | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0138 | AFR | YRI | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18612 | hp2 | a0001 | c0003 | t0002 | g0314 | EAS | CHB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18747 | hp1 | a0001 | c0003 | t0002 | g0088 | EAS | CHB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18747 | hp2 | a0001 | c0004 | t0021 | g0001 | EAS | CHB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18906 | hp1 | a0001 | c0003 | t0002 | g0301 | AFR | YRI | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18906 | hp2 | a0001 | c0003 | t0003 | g0141 | AFR | YRI | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0263 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18940 | hp2 | a0001 | c0004 | t0002 | g0001 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18941 | hp1 | a0001 | c0003 | t0002 | g0084 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18944 | hp2 | a0001 | c0001 | t0004 | g0193 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18950 | hp2 | a0001 | c0003 | t0002 | g0033 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18952 | hp1 | a0001 | c0003 | t0002 | g0033 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18953 | hp1 | a0001 | c0004 | t0002 | g0098 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0151 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18956 | hp1 | a0001 | c0004 | t0002 | g0001 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18957 | hp2 | a0001 | c0003 | t0002 | g0101 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18959 | hp1 | a0001 | c0002 | t0006 | g0012 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0282 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18962 | hp1 | a0001 | c0004 | t0002 | g0013 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18966 | hp1 | a0001 | c0004 | t0002 | g0001 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18969 | hp1 | a0001 | c0003 | t0025 | g0086 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18971 | hp2 | a0001 | c0004 | t0002 | g0083 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18973 | hp1 | a0001 | c0002 | t0026 | g0090 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18975 | hp2 | a0001 | c0002 | t0006 | g0074 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18977 | hp1 | a0001 | c0001 | t0007 | g0278 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18979 | hp2 | a0001 | c0003 | t0005 | g0109 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18980 | hp1 | a0001 | c0001 | t0004 | g0182 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0071 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18987 | hp1 | a0001 | c0001 | t0004 | g0253 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18988 | hp1 | a0001 | c0001 | t0004 | g0184 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18988 | hp2 | a0001 | c0003 | t0002 | g0094 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18989 | hp2 | a0001 | c0003 | t0023 | g0116 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18990 | hp2 | a0001 | c0003 | t0005 | g0100 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18992 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18994 | hp2 | a0001 | c0004 | t0002 | g0001 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18997 | hp1 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18998 | hp1 | a0001 | c0001 | t0004 | g0255 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0082 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19004 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19004 | hp2 | a0001 | c0002 | t0006 | g0218 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19006 | hp1 | a0001 | c0003 | t0005 | g0034 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19030 | hp1 | a0001 | c0001 | t0024 | g0111 | AFR | LWK | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0139 | AFR | LWK | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19043 | hp1 | a0001 | c0002 | t0005 | g0309 | AFR | LWK | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19043 | hp2 | a0001 | c0004 | t0002 | g0063 | AFR | LWK | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19055 | hp1 | a0001 | c0004 | t0002 | g0085 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19055 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19057 | hp1 | a0001 | c0001 | t0004 | g0276 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19057 | hp2 | a0001 | c0003 | t0005 | g0034 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19058 | hp1 | a0001 | c0003 | t0002 | g0115 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0056 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19062 | hp2 | a0001 | c0004 | t0002 | g0013 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19064 | hp2 | a0001 | c0003 | t0005 | g0089 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0272 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19072 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19072 | hp2 | a0001 | c0002 | t0001 | g0271 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19077 | hp1 | a0001 | c0004 | t0002 | g0091 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19078 | hp1 | a0001 | c0002 | t0006 | g0012 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19078 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19079 | hp1 | a0001 | c0004 | t0002 | g0114 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19080 | hp1 | a0001 | c0001 | t0004 | g0056 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0283 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19082 | hp2 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0070 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19086 | hp2 | a0001 | c0001 | t0007 | g0251 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0057 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19089 | hp2 | a0002 | c0005 | t0001 | g0133 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0265 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19240 | hp1 | a0001 | c0003 | t0010 | g0292 | AFR | YRI | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA19240 | hp2 | a0001 | c0003 | t0012 | g0289 | AFR | YRI | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA20129 | hp1 | a0001 | c0003 | t0002 | g0026 | AFR | ASW | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA20129 | hp2 | a0001 | c0004 | t0008 | g0300 | AFR | ASW | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA20752 | hp1 | a0001 | c0004 | t0002 | g0001 | EUR | TSI | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0209 | EUR | TSI | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0165 | SAS | GIH | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0220 | SAS | GIH | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG01123 | hp2 | a0001 | c0004 | t0002 | g0001 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02109 | hp2 | a0001 | c0003 | t0001 | g0135 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0298 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02486 | hp2 | a0001 | c0003 | t0009 | g0011 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0299 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0287 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03471 | hp1 | a0001 | c0004 | t0002 | g0291 | AFR | MSL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG03471 | hp2 | a0001 | c0002 | t0005 | g0288 | AFR | MSL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0049 | AFR | USA | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| HG06807 | hp2 | a0001 | c0003 | t0007 | g0127 | AFR | USA | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA18955 | hp2 | a0001 | c0002 | t0006 | g0012 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA20300 | hp1 | a0001 | c0002 | t0008 | g0304 | AFR | USA | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | USA | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | LWK | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| NA21309 | hp2 | a0001 | c0004 | t0002 | g0001 | AFR | LWK | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0016 | g0064 | REF | REF | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0045 | REF | REF | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:16779091 | T | A | 1 | a0002 | 1 | NA19089.hp2 | missense_variant | MODERATE | c.515T>A | p.Ile172Asn | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/6 | 728/1873 | 515/615 | 172/204 | chr7 | 16779091 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:16776375 | T | C | 2 | a0001c0003 a0001c0004 |
118 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(115): Show |
synonymous_variant | LOW | c.228T>C | p.Phe76Phe | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 2/6 | 441/1873 | 228/615 | 76/204 | chr7 | 16776375 | |||
| chr7:16783470 | G | A | 3 | a0001c0002 a0001c0004 a0002c0005 |
176 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(173): Show |
synonymous_variant | LOW | c.594G>A | p.Ala198Ala | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 6/6 | 807/1873 | 594/615 | 198/204 | chr7 | 16783470 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:16753796 | AGCC | A | 21 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0024 others(18): Show |
114 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(111): Show |
5_prime_UTR_variant | MODIFIER | c.-163_-161delCGC | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/6 | 161 | INFO_REALIGN_3_PRIME | chr7 | 16753796 | |||||
| chr7:16753801 | C | T | 1 | a0001c0003t0027 | 1 | HG03540.hp2 | 5_prime_UTR_variant | MODIFIER | c.-167C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/6 | 167 | chr7 | 16753801 | ||||||
| chr7:16753846 | C | A | 1 | a0001c0003t0020 | 1 | HG02300.hp2 | 5_prime_UTR_variant | MODIFIER | c.-122C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/6 | 122 | chr7 | 16753846 | ||||||
| chr7:16753874 | G | A | 1 | a0001c0004t0021 | 1 | NA18747.hp2 | 5_prime_UTR_variant | MODIFIER | c.-94G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/6 | 94 | chr7 | 16753874 | ||||||
| chr7:16753879 | A | G | 23 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0018 others(20): Show |
116 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(113): Show |
5_prime_UTR_variant | MODIFIER | c.-89A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/6 | 89 | chr7 | 16753879 | ||||||
| chr7:16753930 | G | C | 1 | a0001c0003t0022 | 1 | HG02630.hp2 | 5_prime_UTR_variant | MODIFIER | c.-38G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/6 | 38 | chr7 | 16753930 | ||||||
| chr7:16783492 | T | G | 4 | a0001c0001t0004 a0001c0001t0013 a0001c0003t0010 others(1): Show |
44 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1T>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 6/6 | 1 | chr7 | 16783492 | ||||||
| chr7:16783544 | A | C | 8 | a0001c0001t0004 a0001c0001t0007 a0001c0002t0026 others(5): Show |
56 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*53A>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 6/6 | 53 | chr7 | 16783544 | ||||||
| chr7:16783552 | G | A | 1 | a0001c0003t0023 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*61G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 6/6 | 61 | chr7 | 16783552 | ||||||
| chr7:16783693 | C | T | 1 | a0001c0001t0017 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*202C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 6/6 | 202 | chr7 | 16783693 | ||||||
| chr7:16783703 | C | T | 10 | a0001c0001t0011 a0001c0002t0006 a0001c0002t0008 others(7): Show |
27 | HG00280.hp2 HG00733.hp1 HG01109.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*212C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 6/6 | 212 | chr7 | 16783703 | ||||||
| chr7:16783861 | T | C | 1 | a0001c0003t0009 | 4 | HG02055.hp2 HG02486.hp2 HG02922.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*370T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 6/6 | 370 | chr7 | 16783861 | ||||||
| chr7:16783928 | G | C | 2 | a0001c0001t0024 a0001c0003t0015 |
2 | HG03540.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*437G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 6/6 | 437 | chr7 | 16783928 | ||||||
| chr7:16783982 | T | TG | 38 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0007 others(35): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(337): Show |
3_prime_UTR_variant | MODIFIER | c.*491_*492insG | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 6/6 | 492 | chr7 | 16783982 | ||||||
| chr7:16784251 | T | C | 1 | a0001c0003t0025 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*760T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 6/6 | 760 | chr7 | 16784251 | ||||||
| chr7:16784288 | G | A | 2 | a0001c0001t0011 a0001c0003t0011 |
2 | HG03139.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*797G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 6/6 | 797 | chr7 | 16784288 | ||||||
| chr7:16784353 | T | G | 21 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0007 others(18): Show |
299 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(296): Show |
3_prime_UTR_variant | MODIFIER | c.*862T>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 6/6 | 862 | chr7 | 16784353 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:16754043 | A | G | 8 | a0001c0002t0002g0316 a0001c0003t0002g0313 a0001c0003t0002g0314 others(5): Show |
10 | HG00099.hp2 HG00642.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.63+13A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16754043 | |||||||
| chr7:16754052 | C | T | 15 | a0001c0001t0002g0299 a0001c0001t0002g0303 a0001c0001t0002g0305 others(12): Show |
16 | HG00733.hp1 HG01081.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.63+22C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16754052 | |||||||
| chr7:16754389 | C | T | 15 | a0001c0001t0005g0287 a0001c0001t0005g0295 a0001c0001t0005g0297 others(12): Show |
21 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.63+359C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16754389 | |||||||
| chr7:16754473 | G | C | 2 | a0001c0001t0001g0066 a0001c0001t0003g0065 |
2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.63+443G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16754473 | |||||||
| chr7:16754509 | G | C | 102 | a0001c0001t0001g0075 a0001c0001t0001g0079 a0001c0001t0002g0096 others(99): Show |
134 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.63+479G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16754509 | |||||||
| chr7:16754632 | A | C | 74 | a0001c0001t0001g0286 a0001c0001t0002g0096 a0001c0001t0005g0287 others(71): Show |
102 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.63+602A>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16754632 | |||||||
| chr7:16754639 | G | C | 2 | a0001c0001t0001g0037 a0001c0002t0001g0117 |
3 | HG01255.hp1 HG01346.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.63+609G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16754639 | |||||||
| chr7:16754691 | A | T | 73 | a0001c0001t0002g0096 a0001c0001t0005g0287 a0001c0001t0005g0295 others(70): Show |
101 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.63+661A>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16754691 | |||||||
| chr7:16754860 | A | G | 1 | a0001c0001t0001g0285 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.63+830A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16754860 | |||||||
| chr7:16754895 | C | A | 2 | a0001c0004t0001g0118 a0001c0004t0001g0119 |
2 | HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.63+865C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16754895 | |||||||
| chr7:16754928 | A | G | 1 | a0001c0002t0001g0060 | 2 | NA18962.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.63+898A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16754928 | |||||||
| chr7:16754957 | G | C | 17 | a0001c0001t0001g0038 a0001c0001t0001g0120 a0001c0001t0002g0299 others(14): Show |
19 | HG00733.hp1 HG01081.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.63+927G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16754957 | |||||||
| chr7:16754972 | A | C | 17 | a0001c0001t0001g0024 a0001c0001t0001g0273 a0001c0001t0001g0274 others(14): Show |
22 | HG00609.hp1 HG01256.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.63+942A>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16754972 | |||||||
| chr7:16755037 | TTCCACAG others(5828): Show |
T | 3 | a0001c0003t0002g0115 a0001c0003t0023g0116 a0001c0004t0002g0114 |
3 | NA18989.hp2 NA19058.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.63+1011_63+6845del | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16755037 | ||||||
| chr7:16755045 | G | A | 1 | a0001c0004t0002g0083 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.63+1015G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16755045 | |||||||
| chr7:16755115 | A | G | 4 | a0001c0002t0002g0316 a0001c0003t0002g0313 a0001c0004t0002g0027 others(1): Show |
4 | HG01358.hp1 HG01928.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+1085A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16755115 | |||||||
| chr7:16755489 | T | C | 99 | a0001c0001t0001g0038 a0001c0001t0001g0066 a0001c0001t0001g0120 others(96): Show |
132 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.63+1459T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16755489 | |||||||
| chr7:16755541 | G | GT | 6 | a0001c0001t0001g0222 a0001c0001t0001g0279 a0001c0003t0002g0084 others(3): Show |
6 | HG00639.hp2 NA18941.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+1528dupT | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16755541 | ||||||
| chr7:16755541 | G | GTT | 78 | a0001c0001t0001g0286 a0001c0001t0002g0096 a0001c0001t0002g0303 others(75): Show |
108 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.63+1527_63+1528dup others(2): Show |
TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16755541 | ||||||
| chr7:16755541 | G | GTTT | 7 | a0001c0001t0001g0038 a0001c0001t0001g0120 a0001c0001t0002g0299 others(4): Show |
7 | HG00438.hp2 HG01175.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+1526_63+1528dup others(3): Show |
TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16755541 | ||||||
| chr7:16755541 | GT | G | 82 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0052 others(79): Show |
110 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.63+1528delT | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16755541 | ||||||
| chr7:16755578 | G | T | 1 | a0001c0002t0001g0006 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.63+1548G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16755578 | |||||||
| chr7:16755636 | A | G | 3 | a0001c0003t0002g0084 a0001c0004t0002g0001 a0001c0004t0002g0013 |
4 | NA18941.hp1 NA18962.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+1606A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16755636 | |||||||
| chr7:16755658 | C | G | 2 | a0001c0001t0001g0200 a0001c0002t0001g0199 |
2 | HG01433.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.63+1628C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16755658 | |||||||
| chr7:16755701 | C | T | 8 | a0001c0001t0003g0123 a0001c0001t0004g0125 a0001c0001t0011g0122 others(5): Show |
8 | HG02145.hp2 HG02622.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+1671C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16755701 | |||||||
| chr7:16755745 | C | A | 93 | a0001c0001t0002g0096 a0001c0001t0002g0299 a0001c0001t0002g0303 others(90): Show |
125 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.63+1715C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16755745 | |||||||
| chr7:16755797 | T | A | 1 | a0001c0001t0001g0075 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.63+1767T>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16755797 | |||||||
| chr7:16755837 | C | T | 1 | a0001c0002t0001g0142 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.63+1807C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16755837 | |||||||
| chr7:16755939 | A | G | 34 | a0001c0001t0002g0299 a0001c0001t0003g0123 a0001c0001t0003g0268 others(31): Show |
44 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(41): Show |
intron_variant | MODIFIER | c.63+1909A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16755939 | |||||||
| chr7:16755961 | A | G | 30 | a0001c0001t0001g0024 a0001c0001t0001g0052 a0001c0001t0001g0230 others(27): Show |
47 | HG00609.hp1 HG00642.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.63+1931A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16755961 | |||||||
| chr7:16756246 | A | T | 17 | a0001c0001t0001g0079 a0001c0001t0003g0067 a0001c0001t0003g0068 others(14): Show |
20 | HG00423.hp2 HG01074.hp1 HG02165.hp2 others(17): Show |
intron_variant | MODIFIER | c.63+2216A>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16756246 | |||||||
| chr7:16756267 | T | G | 1 | a0001c0001t0003g0067 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.63+2237T>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16756267 | |||||||
| chr7:16756412 | G | T | 7 | a0001c0001t0001g0066 a0001c0001t0003g0065 a0001c0001t0018g0146 others(4): Show |
8 | HG00280.hp2 HG01433.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+2382G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16756412 | |||||||
| chr7:16756658 | G | A | 31 | a0001c0001t0002g0299 a0001c0001t0003g0123 a0001c0001t0004g0125 others(28): Show |
38 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(35): Show |
intron_variant | MODIFIER | c.63+2628G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16756658 | |||||||
| chr7:16756867 | T | C | 1 | a0001c0003t0002g0301 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.63+2837T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16756867 | |||||||
| chr7:16756907 | G | T | 300 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(297): Show |
415 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(412): Show |
intron_variant | MODIFIER | c.63+2877G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16756907 | |||||||
| chr7:16756971 | A | G | 3 | a0001c0001t0003g0268 a0001c0001t0003g0269 a0001c0003t0009g0011 |
6 | HG02055.hp2 HG02486.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+2941A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16756971 | |||||||
| chr7:16757246 | T | G | 1 | a0001c0004t0003g0197 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.63+3216T>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16757246 | |||||||
| chr7:16757371 | A | T | 3 | a0001c0001t0003g0268 a0001c0001t0003g0269 a0001c0003t0009g0011 |
6 | HG02055.hp2 HG02486.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+3341A>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16757371 | |||||||
| chr7:16757491 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.63+3461A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16757491 | |||||||
| chr7:16757507 | CA | C | 53 | a0001c0001t0002g0096 a0001c0002t0002g0095 a0001c0002t0002g0316 others(50): Show |
75 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.63+3485delA | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16757507 | ||||||
| chr7:16757578 | AC | A | 3 | a0001c0003t0002g0088 a0001c0004t0002g0087 a0001c0004t0002g0097 |
3 | HG00673.hp1 HG03831.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.63+3549delC | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16757578 | |||||||
| chr7:16757651 | T | C | 1 | a0001c0002t0001g0165 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.63+3621T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16757651 | |||||||
| chr7:16757765 | T | C | 1 | a0001c0001t0001g0179 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.63+3735T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16757765 | |||||||
| chr7:16757815 | G | A | 11 | a0001c0001t0002g0299 a0001c0001t0003g0123 a0001c0001t0004g0125 others(8): Show |
11 | HG02145.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.63+3785G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16757815 | |||||||
| chr7:16757850 | T | C | 1 | a0001c0003t0002g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.63+3820T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16757850 | |||||||
| chr7:16757982 | C | T | 1 | a0001c0001t0004g0016 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.63+3952C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16757982 | |||||||
| chr7:16758054 | T | G | 1 | a0001c0001t0001g0188 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.63+4024T>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16758054 | |||||||
| chr7:16758087 | G | A | 2 | a0001c0001t0003g0268 a0001c0001t0003g0269 |
2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.63+4057G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16758087 | |||||||
| chr7:16758236 | T | A | 8 | a0001c0001t0001g0066 a0001c0001t0003g0065 a0001c0001t0018g0146 others(5): Show |
9 | HG00280.hp2 HG01433.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+4206T>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16758236 | |||||||
| chr7:16758390 | T | A | 8 | a0001c0001t0001g0066 a0001c0001t0003g0065 a0001c0001t0018g0146 others(5): Show |
9 | HG00280.hp2 HG01433.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+4360T>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16758390 | |||||||
| chr7:16758731 | C | A | 1 | a0001c0003t0002g0026 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.63+4701C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16758731 | |||||||
| chr7:16758751 | C | CT | 78 | a0001c0001t0001g0038 a0001c0001t0001g0120 a0001c0001t0001g0279 others(75): Show |
108 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.63+4733dupT | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16758751 | ||||||
| chr7:16758861 | G | T | 3 | a0001c0001t0003g0268 a0001c0001t0003g0269 a0001c0001t0005g0297 |
3 | HG02809.hp1 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.63+4831G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16758861 | |||||||
| chr7:16759009 | G | C | 1 | a0001c0001t0001g0279 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.63+4979G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16759009 | |||||||
| chr7:16759014 | C | G | 3 | a0001c0001t0001g0066 a0001c0001t0003g0065 a0001c0003t0009g0011 |
6 | HG02055.hp2 HG02109.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+4984C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16759014 | |||||||
| chr7:16759085 | C | T | 3 | a0001c0001t0003g0078 a0001c0002t0001g0076 a0001c0002t0001g0077 |
3 | HG01074.hp1 HG02615.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.63+5055C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16759085 | |||||||
| chr7:16759149 | C | T | 1 | a0001c0003t0002g0308 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.63+5119C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16759149 | |||||||
| chr7:16759177 | G | T | 5 | a0001c0003t0001g0147 a0001c0003t0006g0205 a0001c0003t0014g0206 others(2): Show |
5 | HG01243.hp2 HG01255.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+5147G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16759177 | |||||||
| chr7:16759292 | T | A | 1 | a0001c0001t0001g0188 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.63+5262T>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16759292 | |||||||
| chr7:16759397 | C | T | 4 | a0001c0001t0003g0175 a0001c0002t0001g0017 a0001c0002t0001g0177 others(1): Show |
6 | HG00741.hp1 HG01192.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+5367C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16759397 | |||||||
| chr7:16759429 | A | C | 9 | a0001c0001t0003g0123 a0001c0001t0004g0125 a0001c0001t0005g0287 others(6): Show |
9 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+5399A>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16759429 | |||||||
| chr7:16759487 | C | T | 1 | a0001c0002t0005g0294 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.63+5457C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16759487 | |||||||
| chr7:16759506 | T | A | 9 | a0001c0001t0003g0123 a0001c0001t0004g0125 a0001c0001t0005g0287 others(6): Show |
9 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+5476T>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16759506 | |||||||
| chr7:16759510 | G | T | 3 | a0001c0003t0002g0088 a0001c0004t0002g0087 a0001c0004t0002g0097 |
3 | HG00673.hp1 HG03831.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.63+5480G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16759510 | |||||||
| chr7:16759513 | C | G | 3 | a0001c0003t0022g0112 a0001c0003t0027g0113 a0001c0004t0005g0036 |
4 | HG02630.hp2 HG03130.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+5483C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16759513 | |||||||
| chr7:16759607 | G | A | 9 | a0001c0001t0003g0123 a0001c0001t0004g0125 a0001c0001t0005g0287 others(6): Show |
9 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+5577G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16759607 | |||||||
| chr7:16759641 | C | G | 215 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0038 others(212): Show |
285 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(282): Show |
intron_variant | MODIFIER | c.63+5611C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16759641 | |||||||
| chr7:16759677 | C | CT | 9 | a0001c0001t0003g0123 a0001c0001t0004g0125 a0001c0001t0005g0287 others(6): Show |
9 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+5655dupT | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16759677 | ||||||
| chr7:16759695 | CTTTCTTT others(3): Show |
C | 9 | a0001c0001t0003g0123 a0001c0001t0004g0125 a0001c0001t0005g0287 others(6): Show |
9 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+5669_63+5678del others(10): Show |
TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16759695 | ||||||
| chr7:16759699 | C | CT | 17 | a0001c0001t0001g0007 a0001c0001t0001g0257 a0001c0001t0003g0216 others(14): Show |
18 | HG00280.hp2 HG00738.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.63+5686dupT | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16759699 | ||||||
| chr7:16759699 | CT | C | 9 | a0001c0001t0001g0008 a0001c0001t0001g0183 a0001c0001t0017g0236 others(6): Show |
9 | HG01074.hp2 HG01243.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+5686delT | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16759699 | ||||||
| chr7:16759699 | CTT | C | 64 | a0001c0001t0001g0038 a0001c0001t0001g0120 a0001c0001t0002g0096 others(61): Show |
88 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.63+5685_63+5686del others(2): Show |
TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16759699 | ||||||
| chr7:16759745 | G | C | 84 | a0001c0001t0001g0038 a0001c0001t0001g0120 a0001c0001t0002g0096 others(81): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.63+5715G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16759745 | |||||||
| chr7:16759780 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.63+5750C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16759780 | |||||||
| chr7:16759979 | G | C | 84 | a0001c0001t0001g0038 a0001c0001t0001g0120 a0001c0001t0002g0096 others(81): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.63+5949G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16759979 | |||||||
| chr7:16760023 | A | G | 4 | a0001c0001t0003g0150 a0001c0001t0003g0214 a0001c0002t0001g0151 others(1): Show |
4 | NA18953.hp2 NA19065.hp2 NA19087.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+5993A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760023 | |||||||
| chr7:16760074 | G | T | 15 | a0001c0001t0005g0295 a0001c0001t0024g0111 a0001c0002t0003g0267 others(12): Show |
21 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.63+6044G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760074 | |||||||
| chr7:16760151 | A | G | 9 | a0001c0001t0003g0123 a0001c0001t0004g0125 a0001c0001t0005g0287 others(6): Show |
9 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+6121A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760151 | |||||||
| chr7:16760183 | C | A | 1 | a0001c0001t0001g0075 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.63+6153C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760183 | |||||||
| chr7:16760183 | C | T | 1 | a0001c0001t0024g0111 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.63+6153C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760183 | |||||||
| chr7:16760207 | T | A | 85 | a0001c0001t0001g0038 a0001c0001t0001g0120 a0001c0001t0001g0286 others(82): Show |
116 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.63+6177T>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760207 | |||||||
| chr7:16760408 | A | G | 9 | a0001c0001t0003g0123 a0001c0001t0004g0125 a0001c0001t0005g0287 others(6): Show |
9 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+6378A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760408 | |||||||
| chr7:16760418 | G | C | 1 | a0001c0002t0001g0051 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.63+6388G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760418 | |||||||
| chr7:16760580 | T | C | 96 | a0001c0001t0001g0038 a0001c0001t0001g0120 a0001c0001t0001g0286 others(93): Show |
127 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.63+6550T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760580 | |||||||
| chr7:16760581 | A | T | 87 | a0001c0001t0001g0038 a0001c0001t0001g0120 a0001c0001t0001g0286 others(84): Show |
118 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.63+6551A>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760581 | |||||||
| chr7:16760623 | G | A | 9 | a0001c0001t0003g0123 a0001c0001t0004g0125 a0001c0001t0005g0287 others(6): Show |
9 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+6593G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760623 | |||||||
| chr7:16760633 | A | G | 9 | a0001c0001t0003g0123 a0001c0001t0004g0125 a0001c0001t0005g0287 others(6): Show |
9 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+6603A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760633 | |||||||
| chr7:16760654 | G | T | 1 | a0001c0004t0003g0197 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.63+6624G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760654 | |||||||
| chr7:16760688 | G | A | 1 | a0001c0003t0027g0113 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.63+6658G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760688 | |||||||
| chr7:16760689 | G | T | 1 | a0001c0003t0027g0113 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.63+6659G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760689 | |||||||
| chr7:16760760 | C | G | 1 | a0001c0002t0001g0129 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.63+6730C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760760 | |||||||
| chr7:16760771 | A | G | 2 | a0001c0001t0001g0066 a0001c0001t0003g0065 |
2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.63+6741A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760771 | |||||||
| chr7:16760808 | G | T | 54 | a0001c0001t0002g0096 a0001c0002t0002g0095 a0001c0002t0002g0316 others(51): Show |
77 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.63+6778G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760808 | |||||||
| chr7:16760836 | G | A | 214 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0038 others(211): Show |
284 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.63+6806G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760836 | |||||||
| chr7:16760898 | G | C | 9 | a0001c0001t0003g0123 a0001c0001t0004g0125 a0001c0001t0005g0287 others(6): Show |
9 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+6868G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760898 | |||||||
| chr7:16760900 | A | C | 1 | a0001c0001t0001g0270 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.63+6870A>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760900 | |||||||
| chr7:16760907 | C | G | 9 | a0001c0001t0003g0123 a0001c0001t0004g0125 a0001c0001t0005g0287 others(6): Show |
9 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+6877C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760907 | |||||||
| chr7:16761007 | C | A | 1 | a0001c0002t0001g0129 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.63+6977C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761007 | |||||||
| chr7:16761062 | G | T | 1 | a0001c0004t0002g0318 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.63+7032G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761062 | |||||||
| chr7:16761187 | A | G | 4 | a0001c0001t0003g0268 a0001c0001t0003g0269 a0001c0001t0005g0297 others(1): Show |
7 | HG02055.hp2 HG02486.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+7157A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761187 | |||||||
| chr7:16761254 | T | C | 3 | a0001c0001t0001g0007 a0001c0001t0001g0130 a0001c0002t0001g0131 |
6 | HG01975.hp2 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+7224T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761254 | |||||||
| chr7:16761334 | G | C | 9 | a0001c0001t0003g0123 a0001c0001t0004g0125 a0001c0001t0005g0287 others(6): Show |
9 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+7304G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761334 | |||||||
| chr7:16761358 | A | G | 19 | a0001c0001t0005g0295 a0001c0001t0024g0111 a0001c0002t0002g0307 others(16): Show |
26 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.63+7328A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761358 | |||||||
| chr7:16761381 | C | T | 87 | a0001c0001t0001g0038 a0001c0001t0001g0120 a0001c0001t0002g0096 others(84): Show |
118 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.63+7351C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761381 | |||||||
| chr7:16761391 | T | C | 9 | a0001c0001t0003g0123 a0001c0001t0004g0125 a0001c0001t0005g0287 others(6): Show |
9 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+7361T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761391 | |||||||
| chr7:16761454 | T | C | 9 | a0001c0001t0003g0123 a0001c0001t0004g0125 a0001c0001t0005g0287 others(6): Show |
9 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+7424T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761454 | |||||||
| chr7:16761536 | A | T | 4 | a0001c0001t0003g0268 a0001c0001t0003g0269 a0001c0001t0005g0297 others(1): Show |
7 | HG02055.hp2 HG02486.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+7506A>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761536 | |||||||
| chr7:16761550 | A | C | 9 | a0001c0001t0003g0123 a0001c0001t0004g0125 a0001c0001t0005g0287 others(6): Show |
9 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+7520A>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761550 | |||||||
| chr7:16761560 | T | C | 101 | a0001c0001t0001g0038 a0001c0001t0001g0120 a0001c0001t0001g0286 others(98): Show |
135 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.63+7530T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761560 | |||||||
| chr7:16761565 | C | G | 1 | a0001c0001t0003g0265 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.63+7535C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761565 | |||||||
| chr7:16761573 | C | T | 1 | a0001c0003t0002g0110 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.63+7543C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761573 | |||||||
| chr7:16761589 | C | T | 1 | a0001c0003t0027g0113 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.63+7559C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761589 | |||||||
| chr7:16761602 | T | C | 28 | a0001c0001t0003g0123 a0001c0001t0004g0125 a0001c0001t0005g0287 others(25): Show |
35 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.63+7572T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761602 | |||||||
| chr7:16761603 | G | A | 9 | a0001c0001t0003g0123 a0001c0001t0004g0125 a0001c0001t0005g0287 others(6): Show |
9 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+7573G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761603 | |||||||
| chr7:16761690 | A | AT | 70 | a0001c0001t0001g0024 a0001c0001t0001g0052 a0001c0001t0001g0079 others(67): Show |
98 | HG00597.hp1 HG00609.hp1 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.63+7684dupT | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16761690 | ||||||
| chr7:16761690 | A | ATT | 37 | a0001c0001t0001g0009 a0001c0001t0001g0054 a0001c0001t0001g0055 others(34): Show |
49 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.63+7683_63+7684dup others(2): Show |
TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16761690 | ||||||
| chr7:16761690 | A | ATTT | 7 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0284 others(4): Show |
7 | HG02027.hp2 HG02647.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+7682_63+7684dup others(3): Show |
TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16761690 | ||||||
| chr7:16761690 | AT | A | 77 | a0001c0001t0001g0038 a0001c0001t0001g0120 a0001c0001t0001g0130 others(74): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.63+7684delT | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16761690 | ||||||
| chr7:16761690 | ATT | A | 7 | a0001c0001t0003g0268 a0001c0001t0003g0269 a0001c0001t0005g0297 others(4): Show |
10 | HG02055.hp2 HG02486.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.63+7683_63+7684del others(2): Show |
TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16761690 | ||||||
| chr7:16761690 | ATTTTTT | A | 11 | a0001c0001t0001g0075 a0001c0001t0003g0123 a0001c0001t0004g0125 others(8): Show |
11 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.63+7679_63+7684del others(6): Show |
TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16761690 | ||||||
| chr7:16761690 | ATTTTTTT others(3): Show |
A | 10 | a0001c0001t0003g0067 a0001c0001t0003g0068 a0001c0001t0004g0070 others(7): Show |
12 | HG00423.hp2 HG02165.hp2 NA18955.hp2 others(9): Show |
intron_variant | MODIFIER | c.63+7675_63+7684del others(10): Show |
TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16761690 | ||||||
| chr7:16761711 | T | C | 4 | a0001c0001t0003g0268 a0001c0001t0003g0269 a0001c0001t0005g0297 others(1): Show |
7 | HG02055.hp2 HG02486.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+7681T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761711 | |||||||
| chr7:16761810 | C | G | 3 | a0001c0001t0005g0295 a0001c0002t0003g0267 a0001c0002t0005g0294 |
3 | HG02451.hp2 HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.63+7780C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761810 | |||||||
| chr7:16761955 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.63+7925C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761955 | |||||||
| chr7:16761985 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.63+7955T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761985 | |||||||
| chr7:16762067 | G | A | 6 | a0001c0001t0003g0123 a0001c0001t0004g0125 a0001c0001t0005g0287 others(3): Show |
6 | HG02559.hp2 HG02622.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+8037G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16762067 | |||||||
| chr7:16762070 | C | G | 6 | a0001c0001t0003g0123 a0001c0001t0004g0125 a0001c0001t0005g0287 others(3): Show |
6 | HG02559.hp2 HG02622.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+8040C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16762070 | |||||||
| chr7:16762164 | A | C | 1 | a0001c0001t0001g0201 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.63+8134A>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16762164 | |||||||
| chr7:16762197 | G | C | 1 | a0001c0002t0006g0266 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.63+8167G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16762197 | |||||||
| chr7:16762243 | G | A | 9 | a0001c0003t0002g0026 a0001c0003t0002g0061 a0001c0003t0005g0025 others(6): Show |
15 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.63+8213G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16762243 | |||||||
| chr7:16762436 | G | A | 4 | a0001c0001t0003g0268 a0001c0001t0003g0269 a0001c0001t0005g0297 others(1): Show |
7 | HG02055.hp2 HG02486.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+8406G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16762436 | |||||||
| chr7:16762452 | C | T | 2 | a0001c0001t0002g0299 a0001c0001t0005g0298 |
2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.63+8422C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16762452 | |||||||
| chr7:16762474 | C | A | 6 | a0001c0001t0003g0123 a0001c0001t0004g0125 a0001c0001t0005g0287 others(3): Show |
6 | HG02559.hp2 HG02622.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+8444C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16762474 | |||||||
| chr7:16762511 | T | A | 9 | a0001c0001t0003g0123 a0001c0001t0004g0125 a0001c0001t0005g0287 others(6): Show |
9 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+8481T>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16762511 | |||||||
| chr7:16762523 | G | C | 9 | a0001c0001t0003g0123 a0001c0001t0004g0125 a0001c0001t0005g0287 others(6): Show |
9 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+8493G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16762523 | |||||||
| chr7:16762553 | C | T | 4 | a0001c0001t0003g0268 a0001c0001t0003g0269 a0001c0001t0005g0297 others(1): Show |
7 | HG02055.hp2 HG02486.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+8523C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16762553 | |||||||
| chr7:16762575 | C | A | 100 | a0001c0001t0001g0038 a0001c0001t0001g0120 a0001c0001t0002g0096 others(97): Show |
134 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.63+8545C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16762575 | |||||||
| chr7:16762622 | C | G | 1 | a0001c0004t0008g0306 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.63+8592C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16762622 | |||||||
| chr7:16762623 | C | T | 2 | a0001c0001t0001g0200 a0001c0002t0001g0199 |
2 | HG01433.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.63+8593C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16762623 | |||||||
| chr7:16762755 | A | C | 2 | a0001c0002t0006g0080 a0001c0002t0006g0081 |
2 | HG03669.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.63+8725A>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16762755 | |||||||
| chr7:16762796 | G | T | 5 | a0001c0001t0007g0053 a0001c0002t0001g0231 a0001c0002t0001g0258 others(2): Show |
6 | HG00639.hp1 HG01891.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+8766G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16762796 | |||||||
| chr7:16762867 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.63+8837G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16762867 | |||||||
| chr7:16762870 | G | A | 1 | a0001c0002t0019g0134 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.63+8840G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16762870 | |||||||
| chr7:16762964 | A | G | 90 | a0001c0001t0001g0038 a0001c0001t0001g0120 a0001c0001t0002g0096 others(87): Show |
121 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.63+8934A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16762964 | |||||||
| chr7:16763036 | C | G | 1 | a0001c0004t0003g0197 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.63+9006C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763036 | |||||||
| chr7:16763066 | C | T | 6 | a0001c0001t0003g0123 a0001c0001t0004g0125 a0001c0001t0005g0287 others(3): Show |
6 | HG02559.hp2 HG02622.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+9036C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763066 | |||||||
| chr7:16763166 | T | G | 2 | a0001c0002t0006g0080 a0001c0002t0006g0081 |
2 | HG03669.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.63+9136T>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763166 | |||||||
| chr7:16763232 | T | C | 7 | a0001c0001t0003g0123 a0001c0001t0004g0125 a0001c0001t0005g0287 others(4): Show |
7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+9202T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763232 | |||||||
| chr7:16763284 | G | A | 3 | a0001c0001t0003g0268 a0001c0001t0003g0269 a0001c0001t0005g0297 |
3 | HG02809.hp1 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.63+9254G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763284 | |||||||
| chr7:16763285 | A | G | 7 | a0001c0001t0003g0123 a0001c0001t0004g0125 a0001c0001t0005g0287 others(4): Show |
7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+9255A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763285 | |||||||
| chr7:16763319 | T | A | 7 | a0001c0001t0003g0123 a0001c0001t0004g0125 a0001c0001t0005g0287 others(4): Show |
7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+9289T>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763319 | |||||||
| chr7:16763321 | T | C | 1 | a0001c0004t0003g0197 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.63+9291T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763321 | |||||||
| chr7:16763365 | G | A | 107 | a0001c0001t0001g0038 a0001c0001t0001g0120 a0001c0001t0001g0286 others(104): Show |
141 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.63+9335G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763365 | |||||||
| chr7:16763421 | A | G | 1 | a0001c0002t0001g0129 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.63+9391A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763421 | |||||||
| chr7:16763436 | A | T | 14 | a0001c0001t0005g0295 a0001c0002t0003g0267 a0001c0002t0005g0294 others(11): Show |
20 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.63+9406A>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763436 | |||||||
| chr7:16763475 | G | C | 91 | a0001c0001t0001g0038 a0001c0001t0001g0120 a0001c0001t0001g0286 others(88): Show |
122 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.63+9445G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763475 | |||||||
| chr7:16763497 | C | T | 6 | a0001c0003t0001g0147 a0001c0003t0006g0205 a0001c0003t0014g0206 others(3): Show |
6 | HG01243.hp2 HG01255.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+9467C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763497 | |||||||
| chr7:16763536 | C | T | 1 | a0001c0002t0006g0081 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.63+9506C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763536 | |||||||
| chr7:16763572 | C | G | 9 | a0001c0001t0002g0303 a0001c0001t0002g0305 a0001c0001t0005g0302 others(6): Show |
9 | HG01081.hp1 HG01109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+9542C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763572 | |||||||
| chr7:16763580 | A | G | 3 | a0001c0001t0001g0196 a0001c0001t0003g0048 a0001c0001t0003g0265 |
4 | NA18966.hp2 NA18979.hp1 NA19076.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+9550A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763580 | |||||||
| chr7:16763645 | C | T | 1 | a0001c0002t0001g0129 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.63+9615C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763645 | |||||||
| chr7:16763654 | A | G | 54 | a0001c0001t0001g0286 a0001c0001t0002g0096 a0001c0002t0002g0095 others(51): Show |
76 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.63+9624A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763654 | |||||||
| chr7:16763690 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.63+9660A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763690 | |||||||
| chr7:16763691 | TC | T | 6 | a0001c0003t0001g0147 a0001c0003t0006g0205 a0001c0003t0014g0206 others(3): Show |
6 | HG01243.hp2 HG01255.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+9664delC | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16763691 | ||||||
| chr7:16763837 | T | C | 106 | a0001c0001t0001g0038 a0001c0001t0001g0120 a0001c0001t0001g0286 others(103): Show |
137 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.63+9807T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763837 | |||||||
| chr7:16764050 | G | A | 4 | a0001c0001t0003g0268 a0001c0001t0003g0269 a0001c0001t0005g0297 others(1): Show |
7 | HG02055.hp2 HG02486.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+10020G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16764050 | |||||||
| chr7:16764092 | A | G | 11 | a0001c0003t0001g0147 a0001c0003t0002g0026 a0001c0003t0002g0061 others(8): Show |
17 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.63+10062A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16764092 | |||||||
| chr7:16764095 | G | A | 1 | a0001c0002t0006g0266 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.63+10065G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16764095 | |||||||
| chr7:16764111 | G | A | 2 | a0001c0001t0001g0207 a0001c0001t0001g0232 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.63+10081G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16764111 | |||||||
| chr7:16764184 | A | AT | 6 | a0001c0001t0018g0146 a0001c0002t0001g0228 a0001c0002t0001g0262 others(3): Show |
6 | HG01433.hp1 HG02738.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+10170dupT | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16764184 | ||||||
| chr7:16764184 | ATTT | A | 108 | a0001c0001t0001g0038 a0001c0001t0001g0286 a0001c0001t0002g0096 others(105): Show |
142 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.63+10168_63+10170d others(5): Show |
TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16764184 | ||||||
| chr7:16764317 | G | A | 1 | a0001c0001t0004g0014 | 3 | NA18959.hp2 NA19055.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.63+10287G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16764317 | |||||||
| chr7:16764365 | T | C | 188 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0038 others(185): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.63+10335T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16764365 | |||||||
| chr7:16764384 | T | C | 109 | a0001c0001t0001g0038 a0001c0001t0001g0286 a0001c0001t0002g0096 others(106): Show |
143 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.63+10354T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16764384 | |||||||
| chr7:16764452 | G | A | 9 | a0001c0003t0002g0026 a0001c0003t0002g0061 a0001c0003t0005g0025 others(6): Show |
15 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.63+10422G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16764452 | |||||||
| chr7:16764455 | G | C | 1 | a0001c0001t0003g0152 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.63+10425G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16764455 | |||||||
| chr7:16764495 | T | C | 9 | a0001c0003t0002g0026 a0001c0003t0002g0061 a0001c0003t0005g0025 others(6): Show |
15 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.63+10465T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16764495 | |||||||
| chr7:16764541 | A | G | 1 | a0001c0004t0002g0035 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.63+10511A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16764541 | |||||||
| chr7:16764934 | G | GT | 112 | a0001c0001t0001g0038 a0001c0001t0001g0257 a0001c0001t0001g0286 others(109): Show |
146 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.63+10914dupT | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16764934 | ||||||
| chr7:16764953 | G | A | 101 | a0001c0001t0001g0038 a0001c0001t0001g0286 a0001c0001t0002g0096 others(98): Show |
132 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.63+10923G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16764953 | |||||||
| chr7:16765047 | C | G | 1 | a0001c0001t0003g0219 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.63+11017C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16765047 | |||||||
| chr7:16765062 | G | T | 1 | a0001c0002t0003g0198 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.63+11032G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16765062 | |||||||
| chr7:16765107 | C | A | 2 | a0001c0001t0001g0153 a0001c0002t0006g0229 |
2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.63+11077C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16765107 | |||||||
| chr7:16765167 | A | C | 1 | a0001c0001t0003g0219 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.64-11044A>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16765167 | |||||||
| chr7:16765266 | AT | A | 109 | a0001c0001t0001g0038 a0001c0001t0001g0286 a0001c0001t0002g0096 others(106): Show |
143 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.64-10937delT | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16765266 | ||||||
| chr7:16765363 | C | G | 21 | a0001c0001t0005g0295 a0001c0001t0024g0111 a0001c0002t0003g0267 others(18): Show |
28 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.64-10848C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16765363 | |||||||
| chr7:16765369 | G | A | 1 | a0001c0001t0003g0067 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-10842G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16765369 | |||||||
| chr7:16765451 | C | A | 7 | a0001c0001t0001g0052 a0001c0001t0003g0211 a0001c0001t0004g0021 others(4): Show |
18 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.64-10760C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16765451 | |||||||
| chr7:16765515 | G | A | 1 | a0001c0001t0003g0208 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.64-10696G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16765515 | |||||||
| chr7:16765610 | T | C | 1 | a0001c0004t0003g0154 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.64-10601T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16765610 | |||||||
| chr7:16765707 | A | G | 1 | a0001c0002t0001g0132 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.64-10504A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16765707 | |||||||
| chr7:16765912 | C | G | 1 | a0001c0001t0001g0075 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.64-10299C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16765912 | |||||||
| chr7:16765963 | C | T | 18 | a0001c0001t0001g0195 a0001c0001t0001g0243 a0001c0001t0001g0244 others(15): Show |
22 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.64-10248C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16765963 | |||||||
| chr7:16765978 | A | G | 22 | a0001c0001t0005g0295 a0001c0001t0024g0111 a0001c0002t0003g0267 others(19): Show |
29 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.64-10233A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16765978 | |||||||
| chr7:16766071 | A | G | 2 | a0001c0001t0017g0236 a0001c0002t0001g0237 |
2 | HG01074.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.64-10140A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16766071 | |||||||
| chr7:16766136 | T | A | 1 | a0001c0001t0001g0273 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.64-10075T>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16766136 | |||||||
| chr7:16766201 | C | G | 4 | a0001c0001t0004g0138 a0001c0001t0004g0139 a0001c0001t0004g0140 others(1): Show |
4 | HG03130.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-10010C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16766201 | |||||||
| chr7:16766346 | T | A | 104 | a0001c0001t0001g0038 a0001c0001t0002g0096 a0001c0001t0002g0299 others(101): Show |
135 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.64-9865T>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16766346 | |||||||
| chr7:16766348 | C | G | 4 | a0001c0001t0003g0268 a0001c0001t0003g0269 a0001c0001t0005g0297 others(1): Show |
7 | HG02055.hp2 HG02486.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-9863C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16766348 | |||||||
| chr7:16766403 | G | T | 16 | a0001c0001t0001g0079 a0001c0001t0003g0067 a0001c0001t0003g0078 others(13): Show |
19 | HG00423.hp2 HG01074.hp1 HG02165.hp2 others(16): Show |
intron_variant | MODIFIER | c.64-9808G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16766403 | |||||||
| chr7:16766436 | T | C | 4 | a0001c0003t0006g0205 a0001c0003t0014g0206 a0001c0004t0003g0197 others(1): Show |
4 | HG02004.hp2 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-9775T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16766436 | |||||||
| chr7:16766517 | T | G | 1 | a0001c0001t0001g0155 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.64-9694T>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16766517 | |||||||
| chr7:16766655 | A | T | 1 | a0001c0002t0001g0242 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.64-9556A>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16766655 | |||||||
| chr7:16766676 | C | T | 41 | a0001c0001t0002g0299 a0001c0001t0002g0303 a0001c0001t0002g0305 others(38): Show |
48 | HG00639.hp2 HG01081.hp1 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.64-9535C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16766676 | |||||||
| chr7:16766726 | A | G | 4 | a0001c0003t0006g0205 a0001c0003t0014g0206 a0001c0004t0003g0197 others(1): Show |
4 | HG02004.hp2 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-9485A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16766726 | |||||||
| chr7:16766849 | A | G | 4 | a0001c0001t0004g0138 a0001c0001t0004g0139 a0001c0001t0004g0140 others(1): Show |
4 | HG03130.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-9362A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16766849 | |||||||
| chr7:16766918 | A | T | 1 | a0001c0003t0012g0289 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.64-9293A>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16766918 | |||||||
| chr7:16766973 | C | A | 1 | a0001c0002t0002g0307 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.64-9238C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16766973 | |||||||
| chr7:16767049 | C | T | 1 | a0001c0003t0015g0137 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.64-9162C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16767049 | |||||||
| chr7:16767055 | C | T | 5 | a0001c0003t0003g0128 a0001c0003t0007g0126 a0001c0003t0007g0127 others(2): Show |
6 | HG02145.hp2 HG02818.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-9156C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16767055 | |||||||
| chr7:16767087 | A | G | 82 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0024 others(79): Show |
115 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.64-9124A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16767087 | |||||||
| chr7:16767438 | G | C | 1 | a0001c0002t0003g0040 | 2 | HG02572.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.64-8773G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16767438 | |||||||
| chr7:16767541 | T | C | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | NA18942.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.64-8670T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16767541 | |||||||
| chr7:16767600 | A | G | 1 | a0001c0004t0002g0317 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.64-8611A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16767600 | |||||||
| chr7:16767640 | C | G | 2 | a0001c0001t0001g0018 a0001c0001t0003g0191 |
4 | NA18978.hp1 NA18994.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-8571C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16767640 | |||||||
| chr7:16767661 | C | T | 63 | a0001c0001t0001g0038 a0001c0001t0002g0096 a0001c0002t0002g0095 others(60): Show |
87 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.64-8550C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16767661 | |||||||
| chr7:16767666 | A | G | 3 | a0001c0001t0001g0066 a0001c0001t0003g0065 a0001c0003t0009g0011 |
6 | HG02055.hp2 HG02109.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-8545A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16767666 | |||||||
| chr7:16767671 | A | G | 3 | a0001c0001t0001g0066 a0001c0001t0003g0065 a0001c0003t0009g0011 |
6 | HG02055.hp2 HG02109.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-8540A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16767671 | |||||||
| chr7:16767729 | A | G | 63 | a0001c0001t0001g0038 a0001c0001t0002g0096 a0001c0002t0002g0095 others(60): Show |
87 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.64-8482A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16767729 | |||||||
| chr7:16767813 | T | C | 1 | a0001c0002t0002g0307 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.64-8398T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16767813 | |||||||
| chr7:16767943 | G | A | 63 | a0001c0001t0001g0038 a0001c0001t0002g0096 a0001c0002t0002g0095 others(60): Show |
87 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.64-8268G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16767943 | |||||||
| chr7:16767974 | A | G | 1 | a0001c0004t0002g0103 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.64-8237A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16767974 | |||||||
| chr7:16768015 | C | T | 4 | a0001c0001t0002g0299 a0001c0001t0002g0305 a0001c0001t0005g0298 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-8196C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16768015 | |||||||
| chr7:16768033 | C | T | 1 | a0001c0003t0002g0301 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.64-8178C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16768033 | |||||||
| chr7:16768036 | C | T | 44 | a0001c0001t0001g0024 a0001c0001t0001g0052 a0001c0001t0001g0054 others(41): Show |
65 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.64-8175C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16768036 | |||||||
| chr7:16768156 | C | T | 17 | a0001c0001t0002g0299 a0001c0001t0002g0303 a0001c0001t0002g0305 others(14): Show |
17 | HG01081.hp1 HG01109.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.64-8055C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16768156 | |||||||
| chr7:16768157 | G | A | 1 | a0001c0002t0001g0156 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.64-8054G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16768157 | |||||||
| chr7:16768180 | C | T | 1 | a0001c0001t0003g0190 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.64-8031C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16768180 | |||||||
| chr7:16768198 | G | A | 1 | a0001c0004t0002g0312 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.64-8013G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16768198 | |||||||
| chr7:16768259 | C | T | 3 | a0001c0003t0002g0101 a0001c0003t0005g0100 a0001c0003t0005g0102 |
3 | HG00544.hp1 NA18957.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.64-7952C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16768259 | |||||||
| chr7:16768265 | T | C | 177 | a0001c0001t0001g0024 a0001c0001t0001g0038 a0001c0001t0001g0052 others(174): Show |
235 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.64-7946T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16768265 | |||||||
| chr7:16768397 | C | A | 3 | a0001c0003t0006g0205 a0001c0003t0014g0206 a0001c0004t0006g0204 |
3 | HG02004.hp2 HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.64-7814C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16768397 | |||||||
| chr7:16768486 | A | G | 1 | a0001c0002t0006g0218 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.64-7725A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16768486 | |||||||
| chr7:16768689 | G | A | 63 | a0001c0001t0001g0038 a0001c0001t0002g0096 a0001c0002t0002g0095 others(60): Show |
87 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.64-7522G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16768689 | |||||||
| chr7:16768746 | A | T | 1 | a0001c0004t0002g0085 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.64-7465A>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16768746 | |||||||
| chr7:16768752 | G | T | 1 | a0001c0001t0001g0257 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.64-7459G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16768752 | |||||||
| chr7:16768842 | C | T | 1 | a0001c0001t0003g0189 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.64-7369C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16768842 | |||||||
| chr7:16768847 | G | A | 21 | a0001c0001t0005g0295 a0001c0001t0024g0111 a0001c0002t0003g0267 others(18): Show |
28 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.64-7364G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16768847 | |||||||
| chr7:16768878 | CTTATT | C | 4 | a0001c0003t0006g0205 a0001c0003t0014g0206 a0001c0004t0003g0197 others(1): Show |
4 | HG02004.hp2 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-7325_64-7321del others(5): Show |
TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16768878 | ||||||
| chr7:16768937 | C | T | 1 | a0001c0002t0005g0311 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.64-7274C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16768937 | |||||||
| chr7:16768938 | G | A | 2 | a0001c0004t0006g0203 a0001c0004t0008g0300 |
2 | HG01243.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.64-7273G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16768938 | |||||||
| chr7:16769228 | A | G | 4 | a0001c0003t0006g0205 a0001c0003t0014g0206 a0001c0004t0003g0197 others(1): Show |
4 | HG02004.hp2 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-6983A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16769228 | |||||||
| chr7:16769280 | A | G | 4 | a0001c0001t0003g0268 a0001c0001t0003g0269 a0001c0001t0005g0297 others(1): Show |
7 | HG02055.hp2 HG02486.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-6931A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16769280 | |||||||
| chr7:16769286 | G | A | 7 | a0001c0001t0001g0066 a0001c0001t0003g0065 a0001c0001t0003g0268 others(4): Show |
10 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-6925G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16769286 | |||||||
| chr7:16769447 | T | G | 4 | a0001c0003t0006g0205 a0001c0003t0014g0206 a0001c0004t0003g0197 others(1): Show |
4 | HG02004.hp2 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-6764T>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16769447 | |||||||
| chr7:16769537 | T | TGG | 65 | a0001c0001t0001g0038 a0001c0001t0001g0286 a0001c0001t0002g0096 others(62): Show |
89 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.64-6670_64-6669dup others(2): Show |
TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16769537 | ||||||
| chr7:16769545 | T | A | 20 | a0001c0001t0002g0299 a0001c0001t0002g0303 a0001c0001t0002g0305 others(17): Show |
20 | HG01081.hp1 HG01109.hp1 HG02004.hp2 others(17): Show |
intron_variant | MODIFIER | c.64-6666T>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16769545 | |||||||
| chr7:16769571 | T | C | 220 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0038 others(217): Show |
287 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.64-6640T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16769571 | |||||||
| chr7:16769572 | G | A | 20 | a0001c0001t0002g0299 a0001c0001t0002g0303 a0001c0001t0002g0305 others(17): Show |
20 | HG01081.hp1 HG01109.hp1 HG02004.hp2 others(17): Show |
intron_variant | MODIFIER | c.64-6639G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16769572 | |||||||
| chr7:16769807 | T | C | 1 | a0001c0001t0001g0245 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.64-6404T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16769807 | |||||||
| chr7:16770066 | C | T | 2 | a0001c0001t0007g0053 a0001c0002t0003g0198 |
3 | HG00639.hp1 HG01891.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.64-6145C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16770066 | |||||||
| chr7:16770123 | T | A | 1 | a0001c0001t0003g0211 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.64-6088T>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16770123 | |||||||
| chr7:16770124 | A | T | 3 | a0001c0003t0006g0205 a0001c0003t0014g0206 a0001c0004t0006g0204 |
3 | HG02004.hp2 HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.64-6087A>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16770124 | |||||||
| chr7:16770191 | TTA | T | 4 | a0001c0001t0003g0268 a0001c0001t0003g0269 a0001c0001t0005g0297 others(1): Show |
7 | HG02055.hp2 HG02486.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-6018_64-6017del others(2): Show |
TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16770191 | ||||||
| chr7:16770198 | A | T | 129 | a0001c0001t0001g0024 a0001c0001t0001g0038 a0001c0001t0001g0052 others(126): Show |
183 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.64-6013A>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16770198 | |||||||
| chr7:16770457 | G | C | 49 | a0001c0001t0001g0024 a0001c0001t0001g0052 a0001c0001t0001g0054 others(46): Show |
70 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.64-5754G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16770457 | |||||||
| chr7:16770510 | C | G | 4 | a0001c0001t0003g0268 a0001c0001t0003g0269 a0001c0001t0005g0297 others(1): Show |
7 | HG02055.hp2 HG02486.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-5701C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16770510 | |||||||
| chr7:16770697 | G | A | 16 | a0001c0001t0002g0299 a0001c0001t0002g0303 a0001c0001t0002g0305 others(13): Show |
16 | HG01081.hp1 HG01109.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.64-5514G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16770697 | |||||||
| chr7:16770902 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.64-5309G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16770902 | |||||||
| chr7:16770980 | C | G | 1 | a0001c0003t0012g0293 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.64-5231C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16770980 | |||||||
| chr7:16770994 | A | G | 1 | a0001c0001t0001g0188 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.64-5217A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16770994 | |||||||
| chr7:16771062 | T | C | 122 | a0001c0001t0001g0024 a0001c0001t0001g0038 a0001c0001t0001g0052 others(119): Show |
170 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.64-5149T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16771062 | |||||||
| chr7:16771252 | C | G | 54 | a0001c0001t0001g0024 a0001c0001t0001g0052 a0001c0001t0001g0054 others(51): Show |
78 | HG00280.hp2 HG00609.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.64-4959C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16771252 | |||||||
| chr7:16771294 | G | A | 10 | a0001c0003t0001g0147 a0001c0003t0002g0026 a0001c0003t0002g0061 others(7): Show |
16 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.64-4917G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16771294 | |||||||
| chr7:16771366 | C | A | 2 | a0001c0004t0002g0063 a0001c0004t0003g0154 |
3 | HG02896.hp1 HG03041.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.64-4845C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16771366 | |||||||
| chr7:16771459 | G | C | 8 | a0001c0003t0002g0026 a0001c0003t0002g0061 a0001c0003t0005g0025 others(5): Show |
14 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.64-4752G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16771459 | |||||||
| chr7:16771514 | G | A | 13 | a0001c0001t0001g0075 a0001c0001t0001g0153 a0001c0001t0004g0138 others(10): Show |
14 | HG00280.hp2 HG01433.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.64-4697G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16771514 | |||||||
| chr7:16771542 | T | C | 122 | a0001c0001t0001g0024 a0001c0001t0001g0038 a0001c0001t0001g0052 others(119): Show |
170 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.64-4669T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16771542 | |||||||
| chr7:16771685 | T | C | 3 | a0001c0003t0003g0128 a0001c0003t0007g0126 a0001c0003t0007g0127 |
3 | HG02145.hp2 HG02818.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.64-4526T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16771685 | |||||||
| chr7:16771767 | A | T | 1 | a0001c0001t0001g0187 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.64-4444A>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16771767 | |||||||
| chr7:16771775 | C | G | 1 | a0001c0004t0002g0108 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.64-4436C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16771775 | |||||||
| chr7:16771887 | G | C | 1 | a0001c0001t0004g0138 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.64-4324G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16771887 | |||||||
| chr7:16771928 | C | T | 63 | a0001c0001t0001g0038 a0001c0001t0001g0286 a0001c0001t0002g0096 others(60): Show |
87 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.64-4283C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16771928 | |||||||
| chr7:16771948 | A | C | 16 | a0001c0001t0002g0299 a0001c0001t0002g0303 a0001c0001t0002g0305 others(13): Show |
16 | HG01081.hp1 HG01109.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.64-4263A>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16771948 | |||||||
| chr7:16772040 | T | G | 1 | a0001c0001t0001g0227 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.64-4171T>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772040 | |||||||
| chr7:16772113 | G | T | 23 | a0001c0001t0001g0008 a0001c0001t0001g0183 a0001c0001t0001g0185 others(20): Show |
35 | HG02015.hp2 HG02056.hp1 HG02135.hp1 others(32): Show |
intron_variant | MODIFIER | c.64-4098G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772113 | |||||||
| chr7:16772139 | C | T | 2 | a0001c0001t0001g0079 a0001c0002t0006g0028 |
3 | HG02683.hp2 HG03688.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.64-4072C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772139 | |||||||
| chr7:16772151 | G | A | 113 | a0001c0001t0001g0024 a0001c0001t0001g0038 a0001c0001t0001g0052 others(110): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.64-4060G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772151 | |||||||
| chr7:16772161 | T | C | 1 | a0001c0003t0011g0148 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.64-4050T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772161 | |||||||
| chr7:16772183 | C | T | 51 | a0001c0001t0001g0024 a0001c0001t0001g0052 a0001c0001t0001g0066 others(48): Show |
71 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.64-4028C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772183 | |||||||
| chr7:16772304 | C | A | 6 | a0001c0003t0003g0128 a0001c0003t0007g0126 a0001c0003t0007g0127 others(3): Show |
7 | HG02145.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-3907C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772304 | |||||||
| chr7:16772369 | G | A | 1 | a0001c0001t0004g0212 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.64-3842G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772369 | |||||||
| chr7:16772457 | G | C | 1 | a0001c0001t0001g0157 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.64-3754G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772457 | |||||||
| chr7:16772482 | G | A | 4 | a0001c0001t0003g0268 a0001c0001t0003g0269 a0001c0001t0005g0297 others(1): Show |
7 | HG02055.hp2 HG02486.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-3729G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772482 | |||||||
| chr7:16772508 | C | G | 1 | a0001c0001t0001g0201 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.64-3703C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772508 | |||||||
| chr7:16772604 | G | C | 16 | a0001c0001t0001g0079 a0001c0001t0003g0067 a0001c0001t0003g0078 others(13): Show |
19 | HG00423.hp2 HG01074.hp1 HG02165.hp2 others(16): Show |
intron_variant | MODIFIER | c.64-3607G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772604 | |||||||
| chr7:16772610 | C | A | 2 | a0001c0001t0007g0053 a0001c0002t0003g0198 |
3 | HG00639.hp1 HG01891.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.64-3601C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772610 | |||||||
| chr7:16772678 | T | G | 1 | a0001c0003t0002g0110 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.64-3533T>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772678 | |||||||
| chr7:16772717 | C | T | 6 | a0001c0001t0001g0273 a0001c0001t0001g0277 a0001c0001t0004g0276 others(3): Show |
8 | HG01256.hp1 HG01361.hp2 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-3494C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772717 | |||||||
| chr7:16772722 | G | A | 2 | a0001c0001t0002g0303 a0001c0001t0005g0302 |
2 | HG01081.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.64-3489G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772722 | |||||||
| chr7:16772724 | G | A | 5 | a0001c0001t0003g0123 a0001c0001t0004g0125 a0001c0001t0005g0287 others(2): Show |
5 | HG02559.hp2 HG02622.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-3487G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772724 | |||||||
| chr7:16772824 | C | T | 1 | a0001c0001t0001g0270 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.64-3387C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772824 | |||||||
| chr7:16772857 | G | C | 1 | a0001c0002t0003g0198 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.64-3354G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772857 | |||||||
| chr7:16772921 | G | C | 1 | a0001c0003t0012g0293 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.64-3290G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772921 | |||||||
| chr7:16772952 | C | T | 1 | a0001c0002t0002g0307 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.64-3259C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772952 | |||||||
| chr7:16772994 | T | C | 16 | a0001c0001t0002g0299 a0001c0001t0002g0303 a0001c0001t0002g0305 others(13): Show |
16 | HG01081.hp1 HG01109.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.64-3217T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772994 | |||||||
| chr7:16772995 | C | A | 6 | a0001c0003t0002g0026 a0001c0003t0002g0061 a0001c0003t0005g0025 others(3): Show |
12 | HG01167.hp2 HG01169.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-3216C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772995 | |||||||
| chr7:16773075 | G | T | 6 | a0001c0003t0003g0128 a0001c0003t0007g0126 a0001c0003t0007g0127 others(3): Show |
7 | HG02145.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-3136G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16773075 | |||||||
| chr7:16773087 | A | T | 2 | a0001c0001t0001g0180 a0001c0001t0001g0224 |
2 | NA19058.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.64-3124A>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16773087 | |||||||
| chr7:16773116 | CA | C | 3 | a0001c0001t0001g0046 a0001c0001t0001g0179 a0001c0001t0001g0275 |
4 | HG02080.hp1 NA18986.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-3094delA | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16773116 | |||||||
| chr7:16773152 | T | C | 5 | a0001c0001t0003g0123 a0001c0001t0004g0125 a0001c0001t0005g0287 others(2): Show |
5 | HG02559.hp2 HG02622.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-3059T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16773152 | |||||||
| chr7:16773164 | T | TG | 38 | a0001c0001t0001g0038 a0001c0001t0001g0052 a0001c0001t0001g0075 others(35): Show |
51 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.64-3038dupG | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16773164 | ||||||
| chr7:16773168 | G | C | 3 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0001t0001g0232 |
3 | HG01515.hp1 HG01517.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.64-3043G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16773168 | |||||||
| chr7:16773206 | G | T | 1 | a0001c0001t0003g0214 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.64-3005G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16773206 | |||||||
| chr7:16773239 | G | A | 1 | a0001c0001t0003g0268 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.64-2972G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16773239 | |||||||
| chr7:16773290 | T | G | 62 | a0001c0001t0001g0286 a0001c0002t0026g0090 a0001c0003t0002g0031 others(59): Show |
85 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.64-2921T>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16773290 | |||||||
| chr7:16773337 | T | TA | 51 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0054 others(48): Show |
65 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.64-2859dupA | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16773337 | ||||||
| chr7:16773337 | TAA | T | 61 | a0001c0001t0001g0286 a0001c0002t0026g0090 a0001c0003t0002g0031 others(58): Show |
84 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.64-2860_64-2859del others(2): Show |
TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16773337 | ||||||
| chr7:16773351 | AAGG | A | 4 | a0001c0001t0003g0067 a0001c0001t0004g0070 a0001c0002t0001g0069 others(1): Show |
6 | NA18955.hp2 NA18959.hp1 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-2855_64-2853del others(3): Show |
TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16773351 | ||||||
| chr7:16773552 | G | C | 1 | a0001c0001t0024g0111 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.64-2659G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16773552 | |||||||
| chr7:16773665 | A | T | 17 | a0001c0001t0003g0123 a0001c0001t0004g0125 a0001c0001t0005g0287 others(14): Show |
20 | HG01255.hp2 HG01884.hp1 HG02004.hp2 others(17): Show |
intron_variant | MODIFIER | c.64-2546A>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16773665 | |||||||
| chr7:16773733 | A | T | 2 | a0001c0001t0001g0252 a0001c0001t0007g0251 |
2 | NA18963.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.64-2478A>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16773733 | |||||||
| chr7:16773802 | T | C | 174 | a0001c0001t0001g0024 a0001c0001t0001g0038 a0001c0001t0001g0052 others(171): Show |
232 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.64-2409T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16773802 | |||||||
| chr7:16773820 | T | C | 1 | a0001c0001t0004g0020 | 3 | HG02257.hp2 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.64-2391T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16773820 | |||||||
| chr7:16773863 | T | C | 94 | a0001c0001t0001g0024 a0001c0001t0001g0038 a0001c0001t0001g0052 others(91): Show |
119 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.64-2348T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16773863 | |||||||
| chr7:16773892 | C | G | 2 | a0001c0001t0001g0200 a0001c0002t0001g0199 |
2 | HG01433.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.64-2319C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16773892 | |||||||
| chr7:16773902 | A | G | 1 | a0001c0002t0006g0266 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.64-2309A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16773902 | |||||||
| chr7:16773951 | G | T | 1 | a0001c0003t0014g0206 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.64-2260G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16773951 | |||||||
| chr7:16773970 | T | G | 92 | a0001c0001t0001g0024 a0001c0001t0001g0038 a0001c0001t0001g0052 others(89): Show |
117 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.64-2241T>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16773970 | |||||||
| chr7:16774011 | T | A | 92 | a0001c0001t0001g0024 a0001c0001t0001g0038 a0001c0001t0001g0052 others(89): Show |
117 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.64-2200T>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16774011 | |||||||
| chr7:16774166 | G | A | 3 | a0001c0003t0002g0088 a0001c0004t0002g0087 a0001c0004t0002g0097 |
3 | HG00673.hp1 HG03831.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.64-2045G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16774166 | |||||||
| chr7:16774421 | C | T | 83 | a0001c0002t0026g0090 a0001c0003t0001g0135 a0001c0003t0001g0147 others(80): Show |
116 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.64-1790C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16774421 | |||||||
| chr7:16774449 | G | A | 3 | a0001c0001t0003g0123 a0001c0001t0011g0122 a0001c0002t0006g0124 |
3 | HG02965.hp1 HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.64-1762G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16774449 | |||||||
| chr7:16774647 | A | T | 1 | a0001c0002t0001g0250 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.64-1564A>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16774647 | |||||||
| chr7:16774663 | A | G | 2 | a0001c0002t0005g0288 a0001c0002t0005g0310 |
2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64-1548A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16774663 | |||||||
| chr7:16774709 | C | T | 84 | a0001c0002t0026g0090 a0001c0003t0001g0135 a0001c0003t0001g0147 others(81): Show |
117 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.64-1502C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16774709 | |||||||
| chr7:16774774 | T | C | 308 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(305): Show |
424 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(421): Show |
intron_variant | MODIFIER | c.64-1437T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16774774 | |||||||
| chr7:16774778 | A | G | 1 | a0001c0002t0006g0136 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.64-1433A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16774778 | |||||||
| chr7:16774831 | GT | G | 11 | a0001c0001t0001g0038 a0001c0001t0001g0075 a0001c0001t0001g0153 others(8): Show |
13 | HG00280.hp2 HG01433.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.64-1376delT | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16774831 | ||||||
| chr7:16774857 | A | C | 1 | a0001c0003t0023g0116 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.64-1354A>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16774857 | |||||||
| chr7:16774865 | A | G | 1 | a0001c0003t0023g0116 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.64-1346A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16774865 | |||||||
| chr7:16774881 | A | G | 1 | a0001c0001t0003g0268 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.64-1330A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16774881 | |||||||
| chr7:16774982 | G | A | 7 | a0001c0001t0003g0268 a0001c0001t0003g0269 a0001c0001t0005g0297 others(4): Show |
7 | HG02280.hp2 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-1229G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16774982 | |||||||
| chr7:16775185 | G | T | 1 | a0001c0003t0002g0301 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.64-1026G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16775185 | |||||||
| chr7:16775477 | A | ATGATCTC others(15): Show |
1 | a0002c0005t0001g0133 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.64-732_64-711dupGA others(20): Show |
TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16775477 | ||||||
| chr7:16775495 | A | G | 1 | a0001c0002t0001g0129 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.64-716A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16775495 | |||||||
| chr7:16775502 | A | G | 1 | a0001c0002t0001g0177 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.64-709A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16775502 | |||||||
| chr7:16775505 | A | C | 1 | a0001c0002t0001g0171 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.64-706A>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16775505 | |||||||
| chr7:16775585 | C | T | 2 | a0001c0002t0001g0043 a0001c0002t0001g0170 |
3 | HG01081.hp2 HG01361.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.64-626C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16775585 | |||||||
| chr7:16775720 | T | G | 103 | a0001c0001t0001g0079 a0001c0001t0003g0067 a0001c0001t0003g0078 others(100): Show |
139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.64-491T>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16775720 | |||||||
| chr7:16775735 | C | T | 1 | a0001c0004t0002g0315 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.64-476C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16775735 | |||||||
| chr7:16775741 | C | T | 1 | a0001c0003t0002g0308 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.64-470C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16775741 | |||||||
| chr7:16775752 | C | G | 1 | a0001c0003t0002g0094 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.64-459C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16775752 | |||||||
| chr7:16775769 | C | G | 13 | a0001c0001t0001g0066 a0001c0001t0002g0299 a0001c0001t0002g0303 others(10): Show |
13 | HG01081.hp1 HG01109.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.64-442C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16775769 | |||||||
| chr7:16775917 | G | A | 55 | a0001c0001t0001g0024 a0001c0001t0001g0038 a0001c0001t0001g0052 others(52): Show |
76 | HG00280.hp2 HG00609.hp1 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.64-294G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16775917 | |||||||
| chr7:16775919 | A | G | 1 | a0001c0003t0022g0112 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.64-292A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16775919 | |||||||
| chr7:16776156 | C | G | 1 | a0001c0002t0001g0170 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.64-55C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16776156 | |||||||
| chr7:16776161 | C | G | 83 | a0001c0003t0001g0147 a0001c0003t0002g0026 a0001c0003t0002g0031 others(80): Show |
116 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.64-50C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16776161 | |||||||
| chr7:16776175 | T | G | 3 | a0001c0003t0006g0205 a0001c0003t0014g0206 a0001c0004t0006g0204 |
3 | HG02004.hp2 HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.64-36T>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16776175 | |||||||
| chr7:16776441 | A | G | 3 | a0001c0001t0003g0169 a0001c0002t0001g0168 a0001c0002t0001g0210 |
3 | HG01069.hp1 HG01261.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.231+63A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 2/5 | chr7 | 16776441 | |||||||
| chr7:16776465 | G | A | 10 | a0001c0001t0002g0303 a0001c0001t0002g0305 a0001c0001t0005g0298 others(7): Show |
10 | HG01081.hp1 HG01109.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.231+87G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 2/5 | chr7 | 16776465 | |||||||
| chr7:16776610 | G | A | 1 | a0001c0002t0001g0220 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.231+232G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 2/5 | chr7 | 16776610 | |||||||
| chr7:16776716 | A | G | 1 | a0001c0002t0001g0129 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.232-326A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 2/5 | chr7 | 16776716 | |||||||
| chr7:16776952 | T | C | 3 | a0001c0001t0003g0268 a0001c0001t0003g0269 a0001c0001t0005g0297 |
3 | HG02809.hp1 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.232-90T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 2/5 | chr7 | 16776952 | |||||||
| chr7:16776967 | T | G | 1 | a0001c0003t0012g0293 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.232-75T>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 2/5 | chr7 | 16776967 | |||||||
| chr7:16777156 | A | G | 1 | a0001c0001t0024g0111 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.312+34A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 3/5 | chr7 | 16777156 | |||||||
| chr7:16777292 | C | T | 1 | a0001c0001t0004g0020 | 3 | HG02257.hp2 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.312+170C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 3/5 | chr7 | 16777292 | |||||||
| chr7:16777318 | C | A | 17 | a0001c0001t0001g0079 a0001c0001t0003g0067 a0001c0001t0003g0078 others(14): Show |
20 | HG00423.hp2 HG01074.hp1 HG02165.hp2 others(17): Show |
intron_variant | MODIFIER | c.312+196C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 3/5 | chr7 | 16777318 | |||||||
| chr7:16777324 | C | CT | 11 | a0001c0001t0001g0052 a0001c0001t0001g0285 a0001c0001t0003g0208 others(8): Show |
23 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.312+206dupT | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 16777324 | ||||||
| chr7:16777376 | A | C | 1 | a0001c0003t0012g0293 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.312+254A>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 3/5 | chr7 | 16777376 | |||||||
| chr7:16777383 | C | A | 1 | a0002c0005t0001g0133 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.312+261C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 3/5 | chr7 | 16777383 | |||||||
| chr7:16777387 | A | G | 1 | a0001c0001t0003g0048 | 2 | NA18966.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.312+265A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 3/5 | chr7 | 16777387 | |||||||
| chr7:16777658 | A | C | 13 | a0001c0001t0001g0066 a0001c0001t0002g0299 a0001c0001t0002g0303 others(10): Show |
13 | HG01081.hp1 HG01109.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.313-140A>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 3/5 | chr7 | 16777658 | |||||||
| chr7:16778020 | T | C | 1 | a0001c0001t0003g0048 | 2 | NA18966.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.426+109T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 4/5 | chr7 | 16778020 | |||||||
| chr7:16778148 | C | G | 3 | a0001c0001t0001g0277 a0001c0001t0007g0023 a0001c0001t0007g0278 |
5 | HG01256.hp1 HG01361.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.426+237C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 4/5 | chr7 | 16778148 | |||||||
| chr7:16778185 | G | T | 1 | a0001c0001t0001g0194 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.426+274G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 4/5 | chr7 | 16778185 | |||||||
| chr7:16778186 | T | C | 17 | a0001c0001t0001g0079 a0001c0001t0003g0067 a0001c0001t0003g0078 others(14): Show |
20 | HG00423.hp2 HG01074.hp1 HG02165.hp2 others(17): Show |
intron_variant | MODIFIER | c.426+275T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 4/5 | chr7 | 16778186 | |||||||
| chr7:16778420 | C | T | 3 | a0001c0001t0001g0066 a0001c0001t0002g0299 a0001c0001t0003g0065 |
3 | HG02109.hp1 HG02559.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.426+509C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 4/5 | chr7 | 16778420 | |||||||
| chr7:16778474 | A | T | 1 | a0002c0005t0001g0133 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.427-529A>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 4/5 | chr7 | 16778474 | |||||||
| chr7:16778549 | T | C | 87 | a0001c0001t0001g0038 a0001c0001t0001g0079 a0001c0001t0001g0286 others(84): Show |
118 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.427-454T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 4/5 | chr7 | 16778549 | |||||||
| chr7:16778637 | C | T | 15 | a0001c0003t0001g0135 a0001c0003t0002g0026 a0001c0003t0002g0061 others(12): Show |
21 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.427-366C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 4/5 | chr7 | 16778637 | |||||||
| chr7:16778779 | C | G | 2 | a0001c0001t0001g0153 a0001c0002t0006g0229 |
2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.427-224C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 4/5 | chr7 | 16778779 | |||||||
| chr7:16778851 | T | G | 58 | a0001c0001t0001g0038 a0001c0001t0004g0255 a0001c0003t0002g0031 others(55): Show |
81 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.427-152T>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 4/5 | chr7 | 16778851 | |||||||
| chr7:16778933 | G | A | 27 | a0001c0001t0001g0153 a0001c0001t0002g0303 a0001c0001t0002g0305 others(24): Show |
28 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.427-70G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 4/5 | chr7 | 16778933 | |||||||
| chr7:16779174 | A | G | 87 | a0001c0001t0001g0038 a0001c0001t0001g0079 a0001c0001t0003g0067 others(84): Show |
118 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.540+58A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16779174 | |||||||
| chr7:16779182 | C | A | 3 | a0001c0001t0001g0066 a0001c0001t0002g0299 a0001c0001t0003g0065 |
3 | HG02109.hp1 HG02559.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.540+66C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16779182 | |||||||
| chr7:16779298 | G | C | 1 | a0001c0004t0008g0300 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.540+182G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16779298 | |||||||
| chr7:16779327 | T | C | 3 | a0001c0001t0003g0268 a0001c0001t0003g0269 a0001c0001t0005g0297 |
3 | HG02809.hp1 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.540+211T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16779327 | |||||||
| chr7:16779632 | A | G | 18 | a0001c0001t0001g0079 a0001c0001t0003g0067 a0001c0001t0003g0078 others(15): Show |
21 | HG00423.hp2 HG01074.hp1 HG02165.hp2 others(18): Show |
intron_variant | MODIFIER | c.540+516A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16779632 | |||||||
| chr7:16779670 | C | G | 66 | a0001c0001t0001g0038 a0001c0001t0001g0286 a0001c0003t0002g0031 others(63): Show |
94 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.540+554C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16779670 | |||||||
| chr7:16779771 | A | G | 1 | a0001c0002t0005g0288 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.540+655A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16779771 | |||||||
| chr7:16779772 | T | C | 1 | a0001c0001t0001g0046 | 2 | HG02080.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.540+656T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16779772 | |||||||
| chr7:16779776 | C | CT | 69 | a0001c0001t0001g0038 a0001c0001t0001g0176 a0001c0001t0001g0249 others(66): Show |
97 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.540+673dupT | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 16779776 | ||||||
| chr7:16779776 | C | CTT | 18 | a0001c0001t0001g0079 a0001c0001t0003g0067 a0001c0001t0003g0078 others(15): Show |
21 | HG00423.hp2 HG01074.hp1 HG02165.hp2 others(18): Show |
intron_variant | MODIFIER | c.540+672_540+673dup others(2): Show |
TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 16779776 | ||||||
| chr7:16779803 | G | A | 17 | a0001c0001t0001g0075 a0001c0003t0001g0135 a0001c0003t0002g0026 others(14): Show |
23 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.540+687G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16779803 | |||||||
| chr7:16779811 | A | G | 103 | a0001c0001t0001g0038 a0001c0001t0001g0075 a0001c0001t0001g0079 others(100): Show |
140 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.540+695A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16779811 | |||||||
| chr7:16779860 | C | A | 1 | a0002c0005t0001g0133 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.540+744C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16779860 | |||||||
| chr7:16779870 | C | G | 2 | a0001c0004t0001g0118 a0001c0004t0001g0119 |
2 | HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.540+754C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16779870 | |||||||
| chr7:16779881 | C | T | 24 | a0001c0001t0001g0153 a0001c0001t0002g0303 a0001c0001t0002g0305 others(21): Show |
25 | HG00280.hp2 HG01081.hp1 HG01433.hp1 others(22): Show |
intron_variant | MODIFIER | c.540+765C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16779881 | |||||||
| chr7:16779920 | C | A | 3 | a0001c0002t0001g0129 a0001c0002t0001g0238 a0001c0002t0001g0263 |
3 | NA18940.hp1 NA18957.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.540+804C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16779920 | |||||||
| chr7:16779927 | A | G | 3 | a0001c0002t0001g0129 a0001c0002t0001g0238 a0001c0002t0001g0263 |
3 | NA18940.hp1 NA18957.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.540+811A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16779927 | |||||||
| chr7:16779932 | C | T | 3 | a0001c0002t0001g0129 a0001c0002t0001g0238 a0001c0002t0001g0263 |
3 | NA18940.hp1 NA18957.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.540+816C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16779932 | |||||||
| chr7:16779933 | A | G | 3 | a0001c0002t0001g0129 a0001c0002t0001g0238 a0001c0002t0001g0263 |
3 | NA18940.hp1 NA18957.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.540+817A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16779933 | |||||||
| chr7:16780032 | A | G | 18 | a0001c0001t0001g0075 a0001c0001t0003g0078 a0001c0003t0001g0135 others(15): Show |
24 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.540+916A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16780032 | |||||||
| chr7:16780074 | T | C | 18 | a0001c0001t0001g0075 a0001c0001t0003g0078 a0001c0003t0001g0135 others(15): Show |
24 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.540+958T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16780074 | |||||||
| chr7:16780203 | G | A | 1 | a0001c0003t0010g0029 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.540+1087G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16780203 | |||||||
| chr7:16780425 | T | A | 1 | a0001c0001t0001g0279 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.540+1309T>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16780425 | |||||||
| chr7:16780434 | C | G | 1 | a0001c0001t0001g0279 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.540+1318C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16780434 | |||||||
| chr7:16780434 | C | T | 24 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0037 others(21): Show |
39 | HG00544.hp2 HG00621.hp2 HG01123.hp1 others(36): Show |
intron_variant | MODIFIER | c.540+1318C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16780434 | |||||||
| chr7:16780437 | C | G | 1 | a0001c0001t0001g0279 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.540+1321C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16780437 | |||||||
| chr7:16780439 | T | G | 1 | a0001c0001t0001g0279 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.540+1323T>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16780439 | |||||||
| chr7:16780441 | A | T | 1 | a0001c0001t0001g0279 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.540+1325A>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16780441 | |||||||
| chr7:16780463 | A | G | 1 | a0001c0002t0001g0165 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.540+1347A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16780463 | |||||||
| chr7:16780534 | G | A | 1 | a0001c0003t0007g0126 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.540+1418G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16780534 | |||||||
| chr7:16780761 | A | C | 1 | a0001c0002t0001g0142 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.540+1645A>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16780761 | |||||||
| chr7:16781170 | C | T | 1 | a0001c0001t0003g0164 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.540+2054C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16781170 | |||||||
| chr7:16781274 | G | A | 8 | a0001c0001t0001g0153 a0001c0001t0003g0123 a0001c0001t0011g0122 others(5): Show |
9 | HG00280.hp2 HG01433.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.541-2143G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16781274 | |||||||
| chr7:16781279 | A | G | 21 | a0001c0001t0001g0075 a0001c0001t0003g0078 a0001c0001t0005g0295 others(18): Show |
27 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.541-2138A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16781279 | |||||||
| chr7:16781372 | G | C | 71 | a0001c0001t0001g0038 a0001c0001t0004g0071 a0001c0002t0001g0059 others(68): Show |
100 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.541-2045G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16781372 | |||||||
| chr7:16781379 | T | A | 1 | a0001c0002t0006g0074 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.541-2038T>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16781379 | |||||||
| chr7:16781458 | T | C | 56 | a0001c0001t0001g0024 a0001c0001t0001g0052 a0001c0001t0001g0054 others(53): Show |
78 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.541-1959T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16781458 | |||||||
| chr7:16781539 | A | G | 4 | a0001c0001t0001g0153 a0001c0001t0018g0146 a0001c0002t0006g0229 others(1): Show |
4 | HG00280.hp2 HG01433.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.541-1878A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16781539 | |||||||
| chr7:16781591 | G | A | 67 | a0001c0001t0001g0038 a0001c0001t0001g0178 a0001c0001t0004g0071 others(64): Show |
91 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.541-1826G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16781591 | |||||||
| chr7:16781730 | G | A | 195 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0038 others(192): Show |
260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.541-1687G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16781730 | |||||||
| chr7:16781746 | A | G | 1 | a0001c0003t0002g0088 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.541-1671A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16781746 | |||||||
| chr7:16781811 | G | A | 2 | a0001c0001t0001g0185 a0001c0001t0001g0225 |
2 | HG03239.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.541-1606G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16781811 | |||||||
| chr7:16781931 | G | T | 1 | a0001c0001t0001g0160 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.541-1486G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16781931 | |||||||
| chr7:16781963 | G | A | 1 | a0001c0001t0007g0053 | 2 | HG01891.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.541-1454G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16781963 | |||||||
| chr7:16781987 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.541-1430A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16781987 | |||||||
| chr7:16782012 | T | C | 294 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(291): Show |
407 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(404): Show |
intron_variant | MODIFIER | c.541-1405T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16782012 | |||||||
| chr7:16782021 | C | T | 1 | a0001c0004t0002g0092 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.541-1396C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16782021 | |||||||
| chr7:16782100 | T | C | 1 | a0001c0001t0001g0280 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.541-1317T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16782100 | |||||||
| chr7:16782245 | A | G | 2 | a0001c0004t0003g0197 a0001c0004t0005g0036 |
3 | HG02723.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.541-1172A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16782245 | |||||||
| chr7:16782255 | C | T | 3 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0017g0236 |
3 | HG01074.hp2 HG02698.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.541-1162C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16782255 | |||||||
| chr7:16782350 | ACT | A | 22 | a0001c0001t0001g0230 a0001c0001t0003g0065 a0001c0001t0003g0078 others(19): Show |
25 | HG00408.hp2 HG00544.hp1 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.541-1062_541-1061d others(4): Show |
TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 16782350 | ||||||
| chr7:16782429 | G | A | 26 | a0001c0001t0007g0053 a0001c0001t0011g0122 a0001c0002t0006g0012 others(23): Show |
31 | HG00280.hp2 HG00733.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.541-988G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16782429 | |||||||
| chr7:16782440 | G | T | 2 | a0001c0001t0003g0050 a0001c0001t0003g0164 |
3 | HG00280.hp1 HG01934.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.541-977G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16782440 | |||||||
| chr7:16782452 | A | T | 1 | a0002c0005t0001g0133 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.541-965A>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16782452 | |||||||
| chr7:16782597 | G | A | 104 | a0001c0001t0001g0019 a0001c0001t0001g0046 a0001c0001t0001g0055 others(101): Show |
157 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.541-820G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16782597 | |||||||
| chr7:16782691 | T | G | 2 | a0001c0001t0004g0138 a0001c0001t0004g0140 |
2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.541-726T>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16782691 | |||||||
| chr7:16782799 | T | A | 1 | a0001c0003t0022g0112 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.541-618T>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16782799 | |||||||
| chr7:16782813 | A | G | 3 | a0001c0002t0001g0005 a0001c0002t0001g0132 a0001c0002t0001g0220 |
7 | HG00558.hp1 NA18942.hp1 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.541-604A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16782813 | |||||||
| chr7:16782818 | T | C | 2 | a0001c0004t0003g0197 a0001c0004t0005g0036 |
3 | HG02723.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.541-599T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16782818 | |||||||
| chr7:16782841 | A | G | 3 | a0001c0001t0004g0138 a0001c0001t0004g0139 a0001c0001t0004g0140 |
3 | HG03130.hp1 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.541-576A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16782841 | |||||||
| chr7:16782883 | G | A | 5 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0002g0303 others(2): Show |
5 | HG01074.hp2 HG01081.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.541-534G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16782883 | |||||||
| chr7:16782946 | A | G | 1 | a0001c0001t0003g0078 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.541-471A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16782946 | |||||||
| chr7:16782980 | C | A | 3 | a0001c0002t0008g0304 a0001c0004t0006g0203 a0001c0004t0008g0300 |
3 | HG01243.hp2 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.541-437C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16782980 | |||||||
| chr7:16783048 | C | T | 3 | a0001c0001t0004g0138 a0001c0001t0004g0139 a0001c0001t0004g0140 |
3 | HG03130.hp1 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.541-369C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16783048 | |||||||
| chr7:16783062 | CCCTGTGA others(6): Show |
C | 1 | a0002c0005t0001g0133 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.541-353_541-341del others(13): Show |
TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 16783062 | ||||||
| chr7:16783124 | A | C | 1 | a0001c0001t0001g0226 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.541-293A>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16783124 | |||||||
| chr7:16783128 | C | T | 106 | a0001c0001t0001g0163 a0001c0001t0001g0178 a0001c0001t0001g0240 others(103): Show |
160 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.541-289C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16783128 | |||||||
| chr7:16783133 | A | C | 1 | a0001c0001t0001g0226 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.541-284A>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16783133 | |||||||
| chr7:16783191 | C | T | 95 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(92): Show |
129 | HG00438.hp1 HG00609.hp1 HG00609.hp2 others(126): Show |
intron_variant | MODIFIER | c.541-226C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16783191 | |||||||
| chr7:16783213 | A | G | 1 | a0001c0001t0001g0226 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.541-204A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16783213 | |||||||
| chr7:16783214 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.541-203G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16783214 | |||||||
| chr7:16783250 | C | G | 104 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(101): Show |
142 | HG00438.hp1 HG00609.hp1 HG00609.hp2 others(139): Show |
intron_variant | MODIFIER | c.541-167C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16783250 | |||||||
| chr7:16783252 | C | A | 1 | a0001c0003t0001g0147 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.541-165C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16783252 | |||||||
| chr7:16783311 | TG | T | 19 | a0001c0001t0011g0122 a0001c0002t0006g0012 a0001c0002t0006g0028 others(16): Show |
23 | HG00280.hp2 HG00733.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.541-105delG | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16783311 | |||||||
| chr7:16783396 | AT | A | 27 | a0001c0001t0004g0010 a0001c0001t0004g0014 a0001c0001t0004g0016 others(24): Show |
42 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.541-12delT | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 16783396 |