Item | Value |
---|---|
geneid | 167838 |
ensemblid | ENSG00000164440.15 |
hgncid | 21617 |
symbol | TXLNB |
name | taxilin beta |
refseq_nuc | NM_153235.4 |
refseq_prot | NP_694967.3 |
ensembl_nuc | ENST00000358430.8 |
ensembl_prot | ENSP00000351206.3 |
mane_status | MANE Select |
chr | chr6 |
start | 139240061 |
end | 139291998 |
strand | - |
ver | v1.2 |
region | chr6:139240061-139291998 |
region5000 | chr6:139235061-139296998 |
regionname0 | TXLNB_chr6_139240061_139291998 |
regionname5000 | TXLNB_chr6_139235061_139296998 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 684 | 115 | 10 | 21 | 61 | 6 | 16 | 44 | TXLNB_chr6_139235061_139296998 | TXLNB | MEANH others(679): Show |
chr6 | 139235061 | 139296998 |
a0002 | 0/1 | 684 | 98 | 25 | 21 | 34 | 2 | 15 | 26 | TXLNB_chr6_139235061_139296998 | TXLNB | MEANH others(679): Show |
chr6 | 139235061 | 139296998 |
a0003 | 0/0 | 684 | 38 | 25 | 8 | 0 | 2 | 3 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | MEANH others(679): Show |
chr6 | 139235061 | 139296998 |
a0004 | 0/0 | 684 | 14 | 12 | 2 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | MEANH others(679): Show |
chr6 | 139235061 | 139296998 |
a0005 | 0/0 | 684 | 8 | 5 | 0 | 3 | 0 | 0 | 2 | TXLNB_chr6_139235061_139296998 | TXLNB | MEANH others(679): Show |
chr6 | 139235061 | 139296998 |
a0006 | 0/0 | 684 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | MEANH others(679): Show |
chr6 | 139235061 | 139296998 |
a0007 | 0/0 | 684 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | MEANH others(679): Show |
chr6 | 139235061 | 139296998 |
a0008 | 0/0 | 684 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TXLNB_chr6_139235061_139296998 | TXLNB | MEANH others(679): Show |
chr6 | 139235061 | 139296998 |
a0009 | 0/0 | 684 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | MEANH others(679): Show |
chr6 | 139235061 | 139296998 |
a0010 | 0/0 | 684 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | MEANH others(679): Show |
chr6 | 139235061 | 139296998 |
a0011 | 0/0 | 684 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | MEANH others(679): Show |
chr6 | 139235061 | 139296998 |
a0012 | 0/0 | 684 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | MEANH others(679): Show |
chr6 | 139235061 | 139296998 |
a0013 | 0/0 | 684 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | MEANH others(679): Show |
chr6 | 139235061 | 139296998 |
a0014 | 0/0 | 684 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | MEANH others(679): Show |
chr6 | 139235061 | 139296998 |
a0015 | 0/0 | 684 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | MEANH others(679): Show |
chr6 | 139235061 | 139296998 |
a0016 | 0/0 | 684 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | MEANH others(679): Show |
chr6 | 139235061 | 139296998 |
a0017 | 0/0 | 684 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | MEANH others(679): Show |
chr6 | 139235061 | 139296998 |
a0018 | 0/0 | 684 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | MEANH others(679): Show |
chr6 | 139235061 | 139296998 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2052 | 102 | 10 | 21 | 48 | 6 | 16 | TXLNB_chr6_139235061_139296998 | TXLNB | ATGGA others(2047): Show |
chr6 | 139235061 | 139296998 | ||
a0001c0004 | 0/0 | 2052 | 12 | 0 | 0 | 12 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | ATGGA others(2047): Show |
chr6 | 139235061 | 139296998 | ||
a0001c0028 | 0/0 | 2052 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | ATGGA others(2047): Show |
chr6 | 139235061 | 139296998 | ||
a0002c0002 | 0/1 | 2052 | 88 | 19 | 21 | 31 | 2 | 14 | TXLNB_chr6_139235061_139296998 | TXLNB | ATGGA others(2047): Show |
chr6 | 139235061 | 139296998 | ||
a0002c0009 | 0/0 | 2052 | 6 | 5 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | ATGGA others(2047): Show |
chr6 | 139235061 | 139296998 | ||
a0002c0016 | 0/0 | 2052 | 2 | 0 | 0 | 2 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | ATGGA others(2047): Show |
chr6 | 139235061 | 139296998 | ||
a0002c0025 | 0/0 | 2052 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | ATGGA others(2047): Show |
chr6 | 139235061 | 139296998 | ||
a0002c0030 | 0/0 | 2052 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | ATGGA others(2047): Show |
chr6 | 139235061 | 139296998 | ||
a0003c0003 | 0/0 | 2052 | 20 | 10 | 7 | 0 | 1 | 2 | TXLNB_chr6_139235061_139296998 | TXLNB | ATGGA others(2047): Show |
chr6 | 139235061 | 139296998 | ||
a0003c0008 | 0/0 | 2052 | 6 | 6 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | ATGGA others(2047): Show |
chr6 | 139235061 | 139296998 | ||
a0003c0011 | 0/0 | 2052 | 4 | 2 | 0 | 0 | 1 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | ATGGA others(2047): Show |
chr6 | 139235061 | 139296998 | ||
a0003c0012 | 0/0 | 2052 | 4 | 4 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | ATGGA others(2047): Show |
chr6 | 139235061 | 139296998 | ||
a0003c0014 | 0/0 | 2052 | 3 | 3 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | ATGGA others(2047): Show |
chr6 | 139235061 | 139296998 | ||
a0003c0031 | 0/0 | 2052 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | ATGGA others(2047): Show |
chr6 | 139235061 | 139296998 | ||
a0004c0005 | 0/0 | 2052 | 7 | 5 | 2 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | ATGGA others(2047): Show |
chr6 | 139235061 | 139296998 | ||
a0004c0006 | 0/0 | 2052 | 6 | 6 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | ATGGA others(2047): Show |
chr6 | 139235061 | 139296998 | ||
a0004c0017 | 0/0 | 2052 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | ATGGA others(2047): Show |
chr6 | 139235061 | 139296998 | ||
a0005c0010 | 0/0 | 2052 | 5 | 5 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | ATGGA others(2047): Show |
chr6 | 139235061 | 139296998 | ||
a0005c0013 | 0/0 | 2052 | 3 | 0 | 0 | 3 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | ATGGA others(2047): Show |
chr6 | 139235061 | 139296998 | ||
a0006c0007 | 0/0 | 2052 | 6 | 6 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | ATGGA others(2047): Show |
chr6 | 139235061 | 139296998 | ||
a0006c0018 | 0/0 | 2052 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | ATGGA others(2047): Show |
chr6 | 139235061 | 139296998 | ||
a0007c0015 | 0/0 | 2052 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | ATGGA others(2047): Show |
chr6 | 139235061 | 139296998 | ||
a0008c0023 | 0/0 | 2052 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | ATGGA others(2047): Show |
chr6 | 139235061 | 139296998 | ||
a0008c0034 | 0/0 | 2052 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | ATGGA others(2047): Show |
chr6 | 139235061 | 139296998 | ||
a0009c0021 | 0/0 | 2052 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | ATGGA others(2047): Show |
chr6 | 139235061 | 139296998 | ||
a0010c0026 | 0/0 | 2052 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | ATGGA others(2047): Show |
chr6 | 139235061 | 139296998 | ||
a0011c0033 | 0/0 | 2052 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | ATGGA others(2047): Show |
chr6 | 139235061 | 139296998 | ||
a0012c0027 | 0/0 | 2052 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | ATGGA others(2047): Show |
chr6 | 139235061 | 139296998 | ||
a0013c0020 | 0/0 | 2052 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | ATGGA others(2047): Show |
chr6 | 139235061 | 139296998 | ||
a0014c0019 | 0/0 | 2052 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | ATGGA others(2047): Show |
chr6 | 139235061 | 139296998 | ||
a0015c0022 | 0/0 | 2052 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | ATGGA others(2047): Show |
chr6 | 139235061 | 139296998 | ||
a0016c0024 | 0/0 | 2052 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | ATGGA others(2047): Show |
chr6 | 139235061 | 139296998 | ||
a0017c0032 | 0/0 | 2052 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | ATGGA others(2047): Show |
chr6 | 139235061 | 139296998 | ||
a0018c0029 | 0/0 | 2052 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | ATGGA others(2047): Show |
chr6 | 139235061 | 139296998 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 4612 | 96 | 10 | 20 | 43 | 6 | 16 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4607): Show |
chr6 | 139235061 | 139296998 |
a0001c0001t0003 | 0/0 | 4609 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0001c0001t0015 | 0/0 | 4612 | 2 | 0 | 0 | 2 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4607): Show |
chr6 | 139235061 | 139296998 |
a0001c0001t0023 | 0/0 | 4609 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0001c0001t0028 | 0/0 | 4612 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4607): Show |
chr6 | 139235061 | 139296998 |
a0001c0001t0029 | 0/0 | 4612 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4607): Show |
chr6 | 139235061 | 139296998 |
a0001c0004t0001 | 0/0 | 4612 | 12 | 0 | 0 | 12 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4607): Show |
chr6 | 139235061 | 139296998 |
a0001c0028t0001 | 0/0 | 4612 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4607): Show |
chr6 | 139235061 | 139296998 |
a0002c0002t0001 | 0/0 | 4612 | 6 | 0 | 0 | 6 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4607): Show |
chr6 | 139235061 | 139296998 |
a0002c0002t0002 | 0/0 | 4609 | 25 | 11 | 5 | 7 | 1 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0002c0002t0003 | 0/1 | 4609 | 37 | 7 | 11 | 10 | 0 | 8 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0002c0002t0006 | 0/0 | 4609 | 7 | 0 | 0 | 6 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0002c0002t0007 | 0/0 | 4609 | 6 | 0 | 2 | 0 | 1 | 3 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0002c0002t0009 | 0/0 | 4609 | 3 | 1 | 2 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0002c0002t0012 | 0/0 | 4609 | 2 | 0 | 0 | 2 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0002c0002t0022 | 0/0 | 4609 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0002c0002t0031 | 0/0 | 4609 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0002c0009t0002 | 0/0 | 4609 | 4 | 4 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0002c0009t0003 | 0/0 | 4609 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0002c0009t0005 | 0/0 | 4609 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0002c0016t0006 | 0/0 | 4609 | 2 | 0 | 0 | 2 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0002c0025t0003 | 0/0 | 4609 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0002c0030t0003 | 0/0 | 4609 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0003c0003t0004 | 0/0 | 4612 | 19 | 10 | 7 | 0 | 0 | 2 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4607): Show |
chr6 | 139235061 | 139296998 |
a0003c0003t0030 | 0/0 | 4612 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4607): Show |
chr6 | 139235061 | 139296998 |
a0003c0008t0001 | 0/0 | 4612 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4607): Show |
chr6 | 139235061 | 139296998 |
a0003c0008t0002 | 0/0 | 4609 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0003c0008t0008 | 0/0 | 4603 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4598): Show |
chr6 | 139235061 | 139296998 |
a0003c0008t0025 | 0/0 | 4609 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0003c0011t0005 | 0/0 | 4609 | 2 | 1 | 0 | 0 | 1 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0003c0011t0017 | 0/0 | 4609 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0003c0011t0018 | 0/0 | 4609 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0003c0012t0005 | 0/0 | 4609 | 3 | 3 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0003c0012t0016 | 0/0 | 4609 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0003c0014t0008 | 0/0 | 4603 | 3 | 3 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4598): Show |
chr6 | 139235061 | 139296998 |
a0003c0031t0021 | 0/0 | 4609 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0004c0005t0002 | 0/0 | 4609 | 7 | 5 | 2 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0004c0006t0005 | 0/0 | 4609 | 6 | 6 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0004c0017t0005 | 0/0 | 4609 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0005c0010t0005 | 0/0 | 4609 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0005c0010t0013 | 0/0 | 4609 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0005c0010t0014 | 0/0 | 4609 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0005c0013t0010 | 0/0 | 4612 | 3 | 0 | 0 | 3 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4607): Show |
chr6 | 139235061 | 139296998 |
a0006c0007t0002 | 0/0 | 4609 | 4 | 4 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0006c0007t0005 | 0/0 | 4609 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0006c0018t0004 | 0/0 | 4612 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4607): Show |
chr6 | 139235061 | 139296998 |
a0007c0015t0011 | 0/0 | 4609 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0008c0023t0001 | 0/0 | 4612 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4607): Show |
chr6 | 139235061 | 139296998 |
a0008c0034t0001 | 0/0 | 4612 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4607): Show |
chr6 | 139235061 | 139296998 |
a0009c0021t0001 | 0/0 | 4612 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4607): Show |
chr6 | 139235061 | 139296998 |
a0010c0026t0024 | 0/0 | 4609 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0011c0033t0019 | 0/0 | 4609 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0012c0027t0020 | 0/0 | 4609 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0013c0020t0002 | 0/0 | 4609 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0014c0019t0001 | 0/0 | 4612 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4607): Show |
chr6 | 139235061 | 139296998 |
a0015c0022t0005 | 0/0 | 4609 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0016c0024t0026 | 0/0 | 4609 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0017c0032t0027 | 0/0 | 4609 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
a0018c0029t0002 | 0/0 | 4609 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | GCTGT others(4604): Show |
chr6 | 139235061 | 139296998 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 15 | 3 | 0 | 10 | 0 | 2 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0007 | 0/0 | 3 | 2 | 0 | 0 | 1 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0008 | 1/0 | 3 | 1 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0015g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0015g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0023g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0028g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0001t0029g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0004t0001g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0004t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0004t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0004t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0001c0028t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0003 | 0/0 | 5 | 0 | 2 | 2 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0213 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0006g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0006g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0006g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0006g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0006g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0007g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0007g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0007g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0007g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0007g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0009g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0009g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0009g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0012g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0012g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0022g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0002t0031g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0009t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0009t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0009t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0009t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0009t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0009t0005g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0016t0006g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0016t0006g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0025t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0002c0030t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0003t0004g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0003t0004g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0003t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0003t0004g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0003t0004g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0003t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0003t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0003t0004g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0003t0004g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0003t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0003t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0003t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0003t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0003t0004g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0003t0004g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0003t0004g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0003t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0003t0030g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0008t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0008t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0008t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0008t0008g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0008t0008g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0008t0025g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0011t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0011t0005g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0011t0017g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0011t0018g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0012t0005g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0012t0005g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0012t0005g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0012t0016g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0014t0008g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0014t0008g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0014t0008g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0003c0031t0021g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0004c0005t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0004c0005t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0004c0005t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0004c0005t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0004c0005t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0004c0005t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0004c0006t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0004c0006t0005g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0004c0006t0005g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0004c0006t0005g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0004c0006t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0004c0006t0005g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0004c0017t0005g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0005c0010t0005g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0005c0010t0013g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0005c0010t0013g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0005c0010t0014g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0005c0010t0014g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0005c0013t0010g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0005c0013t0010g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0005c0013t0010g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0006c0007t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0006c0007t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0006c0007t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0006c0007t0005g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0006c0018t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0007c0015t0011g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0007c0015t0011g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0008c0023t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0008c0034t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0009c0021t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0010c0026t0024g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0011c0033t0019g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0012c0027t0020g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0013c0020t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0014c0019t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0015c0022t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0016c0024t0026g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0017c0032t0027g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
a0018c0029t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00323 | hp1 | a0001 | c0001 | t0001 | g0055 | EUR | FIN | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00323 | hp2 | a0003 | c0003 | t0030 | g0181 | EUR | FIN | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0201 | EAS | CHS | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00438 | hp1 | a0002 | c0002 | t0006 | g0006 | EAS | CHS | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00558 | hp1 | a0002 | c0016 | t0006 | g0136 | EAS | CHS | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00597 | hp2 | a0001 | c0001 | t0015 | g0063 | EAS | CHS | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00639 | hp1 | a0002 | c0002 | t0002 | g0218 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00642 | hp2 | a0002 | c0002 | t0003 | g0003 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00673 | hp1 | a0001 | c0004 | t0001 | g0002 | EAS | CHS | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00733 | hp1 | a0002 | c0002 | t0003 | g0032 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00733 | hp2 | a0002 | c0002 | t0007 | g0220 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00735 | hp1 | a0002 | c0002 | t0003 | g0170 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00738 | hp1 | a0002 | c0002 | t0002 | g0189 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01069 | hp1 | a0003 | c0003 | t0004 | g0019 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01070 | hp1 | a0002 | c0002 | t0003 | g0219 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01070 | hp2 | a0003 | c0003 | t0004 | g0171 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01071 | hp1 | a0003 | c0003 | t0004 | g0019 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01071 | hp2 | a0002 | c0002 | t0003 | g0003 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01081 | hp1 | a0004 | c0005 | t0002 | g0128 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01081 | hp2 | a0002 | c0002 | t0003 | g0051 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01099 | hp1 | a0002 | c0002 | t0022 | g0168 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01106 | hp2 | a0004 | c0005 | t0002 | g0130 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01109 | hp2 | a0003 | c0003 | t0004 | g0137 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01175 | hp1 | a0003 | c0003 | t0004 | g0182 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0043 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01243 | hp1 | a0003 | c0031 | t0021 | g0222 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01255 | hp1 | a0003 | c0003 | t0004 | g0053 | AMR | CLM | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01255 | hp2 | a0002 | c0002 | t0009 | g0070 | AMR | CLM | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01257 | hp2 | a0003 | c0003 | t0004 | g0183 | AMR | CLM | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01261 | hp1 | a0009 | c0021 | t0001 | g0029 | AMR | CLM | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01261 | hp2 | a0002 | c0002 | t0003 | g0009 | AMR | CLM | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01358 | hp1 | a0010 | c0026 | t0024 | g0195 | AMR | CLM | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01358 | hp2 | a0002 | c0002 | t0007 | g0011 | AMR | CLM | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01433 | hp1 | a0002 | c0002 | t0002 | g0166 | AMR | CLM | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01433 | hp2 | a0002 | c0002 | t0002 | g0207 | AMR | CLM | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01496 | hp2 | a0002 | c0002 | t0003 | g0165 | AMR | CLM | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0125 | EUR | IBS | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0078 | EUR | IBS | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01516 | hp1 | a0002 | c0002 | t0007 | g0105 | EUR | IBS | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0124 | EUR | IBS | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01884 | hp1 | a0011 | c0033 | t0019 | g0155 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01891 | hp1 | a0012 | c0027 | t0020 | g0224 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01891 | hp2 | a0003 | c0008 | t0008 | g0042 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01943 | hp2 | a0002 | c0002 | t0002 | g0109 | AMR | PEL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01975 | hp2 | a0002 | c0002 | t0003 | g0009 | AMR | PEL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01981 | hp1 | a0002 | c0002 | t0009 | g0072 | AMR | PEL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG01981 | hp2 | a0002 | c0002 | t0003 | g0169 | AMR | PEL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02015 | hp1 | a0001 | c0001 | t0028 | g0034 | EAS | KHV | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02040 | hp2 | a0001 | c0004 | t0001 | g0002 | EAS | KHV | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02055 | hp1 | a0007 | c0015 | t0011 | g0239 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02055 | hp2 | a0003 | c0012 | t0005 | g0156 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02071 | hp1 | a0002 | c0016 | t0006 | g0135 | EAS | KHV | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02071 | hp2 | a0001 | c0028 | t0001 | g0024 | EAS | KHV | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02074 | hp1 | a0001 | c0001 | t0029 | g0085 | EAS | KHV | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02074 | hp2 | a0001 | c0001 | t0015 | g0047 | EAS | KHV | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02135 | hp1 | a0005 | c0013 | t0010 | g0143 | EAS | KHV | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02145 | hp2 | a0005 | c0010 | t0013 | g0140 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02148 | hp1 | a0002 | c0002 | t0003 | g0009 | AMR | PEL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02165 | hp2 | a0002 | c0002 | t0003 | g0145 | EAS | CDX | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02257 | hp1 | a0003 | c0012 | t0016 | g0157 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02258 | hp1 | a0003 | c0008 | t0025 | g0041 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02258 | hp2 | a0004 | c0006 | t0005 | g0234 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02280 | hp2 | a0002 | c0002 | t0003 | g0217 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02451 | hp1 | a0002 | c0002 | t0003 | g0227 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02451 | hp2 | a0002 | c0002 | t0003 | g0203 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02523 | hp1 | a0002 | c0002 | t0006 | g0071 | EAS | KHV | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02523 | hp2 | a0002 | c0002 | t0003 | g0186 | EAS | KHV | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02572 | hp1 | a0004 | c0005 | t0002 | g0129 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02572 | hp2 | a0006 | c0007 | t0005 | g0017 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02615 | hp1 | a0004 | c0005 | t0002 | g0015 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02615 | hp2 | a0002 | c0002 | t0003 | g0214 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02622 | hp1 | a0005 | c0010 | t0013 | g0139 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02622 | hp2 | a0003 | c0003 | t0004 | g0179 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02630 | hp1 | a0002 | c0030 | t0003 | g0223 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02630 | hp2 | a0003 | c0011 | t0017 | g0138 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02647 | hp2 | a0002 | c0002 | t0002 | g0020 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02683 | hp1 | a0002 | c0002 | t0003 | g0202 | SAS | PJL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02683 | hp2 | a0002 | c0002 | t0007 | g0011 | SAS | PJL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02698 | hp2 | a0002 | c0002 | t0003 | g0003 | SAS | PJL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02717 | hp1 | a0014 | c0019 | t0001 | g0231 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02717 | hp2 | a0004 | c0006 | t0005 | g0232 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02723 | hp1 | a0002 | c0002 | t0002 | g0185 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02723 | hp2 | a0003 | c0011 | t0005 | g0045 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02809 | hp1 | a0015 | c0022 | t0005 | g0023 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02809 | hp2 | a0007 | c0015 | t0011 | g0238 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02886 | hp1 | a0002 | c0002 | t0002 | g0004 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02886 | hp2 | a0003 | c0008 | t0002 | g0160 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02895 | hp1 | a0003 | c0014 | t0008 | g0151 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02895 | hp2 | a0002 | c0002 | t0002 | g0187 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02897 | hp1 | a0002 | c0002 | t0002 | g0226 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02897 | hp2 | a0003 | c0014 | t0008 | g0150 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02922 | hp1 | a0004 | c0005 | t0002 | g0015 | AFR | ESN | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02922 | hp2 | a0002 | c0009 | t0005 | g0149 | AFR | ESN | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02965 | hp1 | a0002 | c0009 | t0002 | g0148 | AFR | ESN | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02965 | hp2 | a0002 | c0002 | t0002 | g0004 | AFR | ESN | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02970 | hp1 | a0002 | c0009 | t0002 | g0147 | AFR | ESN | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02970 | hp2 | a0005 | c0010 | t0014 | g0142 | AFR | ESN | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02976 | hp1 | a0002 | c0002 | t0002 | g0167 | AFR | ESN | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02976 | hp2 | a0003 | c0014 | t0008 | g0153 | AFR | ESN | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03017 | hp1 | a0002 | c0002 | t0003 | g0197 | SAS | PJL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03041 | hp1 | a0003 | c0003 | t0004 | g0176 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03098 | hp1 | a0003 | c0008 | t0002 | g0225 | AFR | MSL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03098 | hp2 | a0004 | c0006 | t0005 | g0233 | AFR | MSL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03130 | hp1 | a0002 | c0002 | t0002 | g0228 | AFR | ESN | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03139 | hp1 | a0006 | c0018 | t0004 | g0161 | AFR | ESN | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03139 | hp2 | a0016 | c0024 | t0026 | g0103 | AFR | ESN | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03195 | hp1 | a0003 | c0012 | t0005 | g0158 | AFR | ESN | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03195 | hp2 | a0005 | c0010 | t0014 | g0141 | AFR | ESN | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03209 | hp1 | a0003 | c0003 | t0004 | g0046 | AFR | MSL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03209 | hp2 | a0006 | c0007 | t0002 | g0163 | AFR | MSL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03225 | hp1 | a0005 | c0010 | t0005 | g0164 | AFR | MSL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03225 | hp2 | a0006 | c0007 | t0002 | g0022 | AFR | MSL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03239 | hp2 | a0002 | c0002 | t0002 | g0035 | SAS | PJL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03453 | hp1 | a0003 | c0008 | t0008 | g0172 | AFR | MSL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03453 | hp2 | a0003 | c0003 | t0004 | g0177 | AFR | MSL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03486 | hp1 | a0002 | c0002 | t0003 | g0208 | AFR | MSL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03486 | hp2 | a0003 | c0003 | t0004 | g0133 | AFR | MSL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03491 | hp1 | a0002 | c0002 | t0007 | g0083 | SAS | PJL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03492 | hp1 | a0002 | c0002 | t0007 | g0082 | SAS | PJL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03516 | hp1 | a0006 | c0007 | t0005 | g0017 | AFR | ESN | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03516 | hp2 | a0003 | c0008 | t0001 | g0175 | AFR | ESN | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03540 | hp1 | a0002 | c0002 | t0002 | g0004 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03579 | hp1 | a0006 | c0007 | t0002 | g0162 | AFR | MSL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03579 | hp2 | a0004 | c0006 | t0005 | g0236 | AFR | MSL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03669 | hp2 | a0003 | c0003 | t0004 | g0180 | SAS | PJL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03688 | hp1 | a0003 | c0011 | t0018 | g0117 | SAS | STU | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03688 | hp2 | a0002 | c0002 | t0003 | g0192 | SAS | STU | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03710 | hp2 | a0002 | c0002 | t0003 | g0198 | SAS | PJL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03831 | hp1 | a0002 | c0002 | t0006 | g0067 | SAS | BEB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03831 | hp2 | a0003 | c0003 | t0004 | g0054 | SAS | BEB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03834 | hp2 | a0002 | c0002 | t0003 | g0188 | SAS | BEB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | STU | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG04115 | hp2 | a0002 | c0025 | t0003 | g0229 | SAS | STU | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | STU | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG04199 | hp2 | a0002 | c0002 | t0031 | g0244 | SAS | STU | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG04204 | hp1 | a0002 | c0002 | t0003 | g0204 | SAS | STU | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | STU | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | STU | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG04228 | hp2 | a0002 | c0002 | t0003 | g0037 | SAS | STU | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18522 | hp1 | a0002 | c0002 | t0002 | g0020 | AFR | YRI | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18522 | hp2 | a0004 | c0017 | t0005 | g0235 | AFR | YRI | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18612 | hp1 | a0002 | c0002 | t0002 | g0021 | EAS | CHB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18906 | hp1 | a0018 | c0029 | t0002 | g0210 | AFR | YRI | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18944 | hp1 | a0002 | c0009 | t0003 | g0242 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18950 | hp2 | a0002 | c0002 | t0002 | g0050 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18953 | hp1 | a0002 | c0002 | t0012 | g0199 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18953 | hp2 | a0002 | c0002 | t0003 | g0209 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18954 | hp1 | a0002 | c0002 | t0003 | g0190 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18956 | hp1 | a0002 | c0002 | t0003 | g0216 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18956 | hp2 | a0001 | c0004 | t0001 | g0010 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18960 | hp1 | a0002 | c0002 | t0006 | g0006 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18961 | hp2 | a0002 | c0002 | t0001 | g0173 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18964 | hp1 | a0001 | c0004 | t0001 | g0016 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18966 | hp2 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18969 | hp1 | a0002 | c0002 | t0003 | g0221 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18970 | hp1 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18973 | hp1 | a0008 | c0023 | t0001 | g0064 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18973 | hp2 | a0001 | c0004 | t0001 | g0240 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18975 | hp2 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18978 | hp1 | a0001 | c0001 | t0023 | g0126 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18978 | hp2 | a0002 | c0002 | t0006 | g0110 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18979 | hp2 | a0002 | c0002 | t0002 | g0107 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18980 | hp2 | a0002 | c0002 | t0012 | g0193 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18983 | hp1 | a0002 | c0002 | t0006 | g0060 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18986 | hp2 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18988 | hp1 | a0002 | c0002 | t0002 | g0206 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18990 | hp2 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18992 | hp2 | a0008 | c0034 | t0001 | g0241 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18995 | hp1 | a0001 | c0004 | t0001 | g0010 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18999 | hp1 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19001 | hp1 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19001 | hp2 | a0002 | c0002 | t0002 | g0200 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19004 | hp2 | a0005 | c0013 | t0010 | g0052 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19010 | hp1 | a0001 | c0004 | t0001 | g0010 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19030 | hp1 | a0003 | c0003 | t0004 | g0178 | AFR | LWK | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19030 | hp2 | a0002 | c0009 | t0002 | g0154 | AFR | LWK | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19043 | hp1 | a0002 | c0002 | t0002 | g0004 | AFR | LWK | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19043 | hp2 | a0004 | c0005 | t0002 | g0132 | AFR | LWK | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19058 | hp2 | a0002 | c0002 | t0003 | g0243 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19059 | hp1 | a0002 | c0002 | t0001 | g0205 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19068 | hp1 | a0002 | c0002 | t0003 | g0191 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19068 | hp2 | a0001 | c0004 | t0001 | g0016 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19087 | hp1 | a0002 | c0002 | t0006 | g0006 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19087 | hp2 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19089 | hp2 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19090 | hp2 | a0005 | c0013 | t0010 | g0144 | EAS | JPT | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19240 | hp1 | a0004 | c0005 | t0002 | g0131 | AFR | YRI | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA19240 | hp2 | a0003 | c0003 | t0004 | g0018 | AFR | YRI | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA20129 | hp1 | a0002 | c0002 | t0003 | g0048 | AFR | ASW | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA20129 | hp2 | a0004 | c0006 | t0005 | g0127 | AFR | ASW | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA20752 | hp1 | a0002 | c0002 | t0002 | g0196 | EUR | TSI | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0066 | EUR | TSI | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA20805 | hp2 | a0003 | c0011 | t0005 | g0116 | EUR | TSI | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02109 | hp1 | a0003 | c0003 | t0004 | g0134 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02109 | hp2 | a0013 | c0020 | t0002 | g0230 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02486 | hp1 | a0004 | c0006 | t0005 | g0237 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02486 | hp2 | a0002 | c0002 | t0003 | g0081 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02559 | hp1 | a0006 | c0007 | t0002 | g0022 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG02559 | hp2 | a0003 | c0012 | t0005 | g0159 | AFR | ACB | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03471 | hp1 | a0003 | c0003 | t0004 | g0184 | AFR | MSL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG03471 | hp2 | a0017 | c0032 | t0027 | g0146 | AFR | MSL | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG06807 | hp1 | a0002 | c0009 | t0002 | g0152 | AFR | USA | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
HG06807 | hp2 | a0003 | c0003 | t0004 | g0018 | AFR | USA | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | USA | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
NA20300 | hp2 | a0002 | c0002 | t0009 | g0069 | AFR | USA | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
homoSapiens | chm13v2 | a0002 | c0002 | t0003 | g0213 | REF | REF | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0008 | REF | REF | TXLNB_chr6_139235061_139296998 | TXLNB | chr6 | 139235061 | 139296998 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:139242558 | C | T | 1 | a0015 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.2023G>A | p.Val675Met | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 2115/4612 | 2023/2055 | 675/684 | chr6 | 139242558 | |||
chr6:139242747 | C | T | 1 | a0011 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.1834G>A | p.Gly612Ser | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 1926/4612 | 1834/2055 | 612/684 | chr6 | 139242747 | |||
chr6:139242777 | C | G | 13 | a0002 a0003 a0004 others(10): Show |
173 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(170): Show |
missense_variant | MODERATE | c.1804G>C | p.Ala602Pro | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 1896/4612 | 1804/2055 | 602/684 | chr6 | 139242777 | |||
chr6:139242800 | G | A | 1 | a0010 | 1 | HG01358.hp1 | missense_variant | MODERATE | c.1781C>T | p.Pro594Leu | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 1873/4612 | 1781/2055 | 594/684 | chr6 | 139242800 | |||
chr6:139242980 | G | C | 5 | a0005 a0007 a0011 others(2): Show |
13 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(10): Show |
missense_variant | MODERATE | c.1601C>G | p.Ala534Gly | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 1693/4612 | 1601/2055 | 534/684 | chr6 | 139242980 | |||
chr6:139243001 | A | G | 1 | a0016 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.1580T>C | p.Ile527Thr | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 1672/4612 | 1580/2055 | 527/684 | chr6 | 139243001 | |||
chr6:139243041 | C | T | 1 | a0008 | 2 | NA18973.hp1 NA18992.hp2 |
missense_variant | MODERATE | c.1540G>A | p.Glu514Lys | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 1632/4612 | 1540/2055 | 514/684 | chr6 | 139243041 | |||
chr6:139255599 | C | T | 9 | a0003 a0004 a0005 others(6): Show |
67 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(64): Show |
missense_variant | MODERATE | c.1042G>A | p.Val348Met | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/10 | 1134/4612 | 1042/2055 | 348/684 | chr6 | 139255599 | |||
chr6:139260394 | A | G | 1 | a0018 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.926T>C | p.Leu309Pro | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/10 | 1018/4612 | 926/2055 | 309/684 | chr6 | 139260394 | |||
chr6:139288550 | C | T | 1 | a0009 | 1 | HG01261.hp1 | missense_variant | MODERATE | c.350G>A | p.Gly117Glu | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/10 | 442/4612 | 350/2055 | 117/684 | chr6 | 139288550 | |||
chr6:139288563 | G | C | 1 | a0017 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.337C>G | p.Pro113Ala | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/10 | 429/4612 | 337/2055 | 113/684 | chr6 | 139288563 | |||
chr6:139288581 | C | T | 1 | a0013 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.319G>A | p.Glu107Lys | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/10 | 411/4612 | 319/2055 | 107/684 | chr6 | 139288581 | |||
chr6:139288869 | C | T | 4 | a0004 a0006 a0007 others(1): Show |
24 | HG01081.hp1 HG01106.hp2 HG02055.hp1 others(21): Show |
missense_variant | MODERATE | c.31G>A | p.Ala11Thr | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/10 | 123/4612 | 31/2055 | 11/684 | chr6 | 139288869 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:139242667 | T | C | 1 | a0002c0025 | 1 | HG04115.hp2 | synonymous_variant | LOW | c.1914A>G | p.Glu638Glu | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 2006/4612 | 1914/2055 | 638/684 | chr6 | 139242667 | |||
chr6:139242748 | G | A | 3 | a0005c0010 a0007c0015 a0017c0032 |
8 | HG02055.hp1 HG02145.hp2 HG02622.hp1 others(5): Show |
synonymous_variant | LOW | c.1833C>T | p.Ser611Ser | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 1925/4612 | 1833/2055 | 611/684 | chr6 | 139242748 | |||
chr6:139242831 | A | G | 6 | a0005c0010 a0005c0013 a0007c0015 others(3): Show |
13 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(10): Show |
synonymous_variant | LOW | c.1750T>C | p.Leu584Leu | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 1842/4612 | 1750/2055 | 584/684 | chr6 | 139242831 | |||
chr6:139242835 | G | C | 6 | a0005c0010 a0005c0013 a0007c0015 others(3): Show |
13 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(10): Show |
synonymous_variant | LOW | c.1746C>G | p.Ala582Ala | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 1838/4612 | 1746/2055 | 582/684 | chr6 | 139242835 | |||
chr6:139242964 | C | T | 2 | a0003c0003 a0006c0018 |
21 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(18): Show |
synonymous_variant | LOW | c.1617G>A | p.Lys539Lys | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 1709/4612 | 1617/2055 | 539/684 | chr6 | 139242964 | |||
chr6:139260324 | C | T | 4 | a0003c0011 a0003c0012 a0004c0006 others(1): Show |
15 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(12): Show |
synonymous_variant | LOW | c.996G>A | p.Lys332Lys | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/10 | 1088/4612 | 996/2055 | 332/684 | chr6 | 139260324 | |||
chr6:139260405 | C | A | 2 | a0001c0028 a0002c0016 |
3 | HG00558.hp1 HG02071.hp1 HG02071.hp2 |
synonymous_variant | LOW | c.915G>T | p.Leu305Leu | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/10 | 1007/4612 | 915/2055 | 305/684 | chr6 | 139260405 | |||
chr6:139262765 | C | T | 1 | a0004c0017 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.696G>A | p.Ala232Ala | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 5/10 | 788/4612 | 696/2055 | 232/684 | chr6 | 139262765 | |||
chr6:139270582 | T | C | 6 | a0003c0008 a0003c0014 a0003c0031 others(3): Show |
19 | HG01081.hp1 HG01106.hp2 HG01243.hp1 others(16): Show |
synonymous_variant | LOW | c.561A>G | p.Gln187Gln | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/10 | 653/4612 | 561/2055 | 187/684 | chr6 | 139270582 | |||
chr6:139288561 | G | A | 2 | a0002c0030 a0003c0031 |
2 | HG01243.hp1 HG02630.hp1 |
synonymous_variant | LOW | c.339C>T | p.Pro113Pro | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/10 | 431/4612 | 339/2055 | 113/684 | chr6 | 139288561 | |||
chr6:139288618 | T | C | 6 | a0001c0004 a0002c0009 a0003c0012 others(3): Show |
27 | HG00673.hp1 HG01884.hp1 HG02040.hp2 others(24): Show |
synonymous_variant | LOW | c.282A>G | p.Ser94Ser | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/10 | 374/4612 | 282/2055 | 94/684 | chr6 | 139288618 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:139240079 | T | G | 2 | a0003c0031t0021 a0017c0032t0027 |
2 | HG01243.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2447A>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 2447 | chr6 | 139240079 | ||||||
chr6:139240097 | ATTATAG | A | 2 | a0003c0008t0008 a0003c0014t0008 |
5 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2423_*2428delCTAT others(2): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 2423 | chr6 | 139240097 | ||||||
chr6:139240101 | T | C | 2 | a0003c0003t0004 a0006c0018t0004 |
2 | HG02109.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2425A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 2425 | chr6 | 139240101 | ||||||
chr6:139240148 | G | A | 1 | a0003c0003t0030 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2378C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 2378 | chr6 | 139240148 | ||||||
chr6:139240150 | T | C | 1 | a0003c0011t0018 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2376A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 2376 | chr6 | 139240150 | ||||||
chr6:139240226 | T | C | 1 | a0002c0002t0009 | 3 | HG01255.hp2 HG01981.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2300A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 2300 | chr6 | 139240226 | ||||||
chr6:139240299 | C | T | 3 | a0002c0002t0006 a0002c0002t0012 a0002c0016t0006 |
11 | HG00438.hp1 HG00558.hp1 HG02071.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2227G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 2227 | chr6 | 139240299 | ||||||
chr6:139240312 | T | C | 3 | a0005c0010t0014 a0011c0033t0019 a0016c0024t0026 |
4 | HG01884.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2214A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 2214 | chr6 | 139240312 | ||||||
chr6:139240381 | G | A | 13 | a0001c0001t0028 a0002c0002t0002 a0002c0009t0002 others(10): Show |
54 | HG00639.hp1 HG00738.hp1 HG01081.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*2145C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 2145 | chr6 | 139240381 | ||||||
chr6:139240419 | T | A | 1 | a0002c0002t0022 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2107A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 2107 | chr6 | 139240419 | ||||||
chr6:139240467 | G | C | 14 | a0001c0001t0015 a0001c0001t0023 a0002c0002t0002 others(11): Show |
56 | HG00597.hp2 HG00639.hp1 HG00738.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*2059C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 2059 | chr6 | 139240467 | ||||||
chr6:139240594 | T | C | 1 | a0010c0026t0024 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1932A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 1932 | chr6 | 139240594 | ||||||
chr6:139240660 | G | T | 1 | a0003c0011t0017 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1866C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 1866 | chr6 | 139240660 | ||||||
chr6:139241137 | T | G | 2 | a0012c0027t0020 a0016c0024t0026 |
2 | HG01891.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1389A>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 1389 | chr6 | 139241137 | ||||||
chr6:139241199 | T | C | 2 | a0012c0027t0020 a0016c0024t0026 |
2 | HG01891.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1327A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 1327 | chr6 | 139241199 | ||||||
chr6:139241277 | C | T | 1 | a0003c0012t0016 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1249G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 1249 | chr6 | 139241277 | ||||||
chr6:139241303 | G | C | 26 | a0001c0001t0003 a0001c0001t0023 a0002c0002t0002 others(23): Show |
116 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*1223C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 1223 | chr6 | 139241303 | ||||||
chr6:139241383 | T | G | 4 | a0003c0008t0008 a0003c0008t0025 a0003c0014t0008 others(1): Show |
7 | HG01891.hp2 HG02258.hp1 HG02895.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1143A>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 1143 | chr6 | 139241383 | ||||||
chr6:139241727 | T | C | 4 | a0002c0002t0006 a0002c0002t0009 a0002c0016t0006 others(1): Show |
15 | HG00438.hp1 HG00558.hp1 HG01255.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*799A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 799 | chr6 | 139241727 | ||||||
chr6:139241774 | T | C | 8 | a0002c0002t0006 a0002c0002t0009 a0002c0016t0006 others(5): Show |
22 | HG00438.hp1 HG00558.hp1 HG01255.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*752A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 752 | chr6 | 139241774 | ||||||
chr6:139241890 | T | A | 1 | a0002c0002t0007 | 6 | HG00733.hp2 HG01358.hp2 HG01516.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*636A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 636 | chr6 | 139241890 | ||||||
chr6:139241923 | T | C | 1 | a0001c0001t0029 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*603A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 603 | chr6 | 139241923 | ||||||
chr6:139241992 | C | T | 1 | a0007c0015t0011 | 2 | HG02055.hp1 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*534G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 534 | chr6 | 139241992 | ||||||
chr6:139242037 | G | A | 1 | a0005c0013t0010 | 3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
3_prime_UTR_variant | MODIFIER | c.*489C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 489 | chr6 | 139242037 | ||||||
chr6:139242050 | TATA | T | 43 | a0001c0001t0003 a0001c0001t0023 a0002c0002t0002 others(40): Show |
145 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*473_*475delTAT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 473 | chr6 | 139242050 | ||||||
chr6:139242485 | T | C | 3 | a0003c0003t0004 a0003c0003t0030 a0006c0018t0004 |
21 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*41A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 41 | chr6 | 139242485 | ||||||
chr6:139242518 | G | A | 3 | a0003c0003t0004 a0003c0003t0030 a0006c0018t0004 |
21 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*8C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 10/10 | 8 | chr6 | 139242518 | ||||||
chr6:139291939 | G | C | 1 | a0002c0002t0031 | 1 | HG04199.hp2 | 5_prime_UTR_variant | MODIFIER | c.-33C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/10 | 3040 | chr6 | 139291939 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:139243453 | T | C | 1 | a0018c0029t0002g0210 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1267-139A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 9/9 | chr6 | 139243453 | |||||||
chr6:139243492 | C | CT | 111 | a0001c0001t0001g0040 a0001c0001t0001g0099 a0001c0001t0023g0126 others(108): Show |
126 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(123): Show |
intron_variant | MODIFIER | c.1267-179dupA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 9/9 | chr6 | 139243492 | |||||||
chr6:139243492 | C | CTT | 8 | a0002c0002t0002g0166 a0002c0009t0002g0152 a0003c0008t0008g0042 others(5): Show |
8 | HG01243.hp1 HG01433.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1267-180_1267-179d others(4): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 9/9 | chr6 | 139243492 | |||||||
chr6:139243492 | CT | C | 6 | a0001c0001t0001g0055 a0001c0001t0001g0062 a0001c0001t0001g0076 others(3): Show |
6 | HG00323.hp1 HG01175.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.1267-179delA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 9/9 | chr6 | 139243492 | |||||||
chr6:139243668 | G | A | 2 | a0006c0007t0005g0017 a0011c0033t0019g0155 |
3 | HG01884.hp1 HG02572.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1267-354C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 9/9 | chr6 | 139243668 | |||||||
chr6:139243851 | C | T | 120 | a0001c0001t0023g0126 a0002c0002t0001g0173 a0002c0002t0001g0174 others(117): Show |
135 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(132): Show |
intron_variant | MODIFIER | c.1267-537G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 9/9 | chr6 | 139243851 | |||||||
chr6:139243886 | C | T | 2 | a0005c0010t0014g0141 a0005c0010t0014g0142 |
2 | HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1267-572G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 9/9 | chr6 | 139243886 | |||||||
chr6:139243967 | G | A | 1 | a0012c0027t0020g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1266+628C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 9/9 | chr6 | 139243967 | |||||||
chr6:139243968 | C | T | 1 | a0002c0002t0009g0069 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1266+627G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 9/9 | chr6 | 139243968 | |||||||
chr6:139243992 | T | C | 1 | a0015c0022t0005g0023 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1266+603A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 9/9 | chr6 | 139243992 | |||||||
chr6:139243994 | TC | T | 20 | a0002c0002t0001g0205 a0003c0003t0004g0018 a0003c0003t0004g0019 others(17): Show |
22 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.1266+600delG | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 9/9 | chr6 | 139243994 | |||||||
chr6:139244001 | C | A | 19 | a0003c0003t0004g0018 a0003c0003t0004g0019 a0003c0003t0004g0046 others(16): Show |
21 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.1266+594G>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 9/9 | chr6 | 139244001 | |||||||
chr6:139244002 | T | A | 3 | a0005c0013t0010g0052 a0005c0013t0010g0143 a0005c0013t0010g0144 |
3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1266+593A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 9/9 | chr6 | 139244002 | |||||||
chr6:139244143 | A | T | 5 | a0003c0008t0002g0225 a0004c0005t0002g0015 a0004c0005t0002g0128 others(2): Show |
6 | HG01081.hp1 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1266+452T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 9/9 | chr6 | 139244143 | |||||||
chr6:139244261 | A | G | 1 | a0002c0002t0003g0214 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1266+334T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 9/9 | chr6 | 139244261 | |||||||
chr6:139244535 | G | A | 1 | a0005c0010t0005g0164 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1266+60C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 9/9 | chr6 | 139244535 | |||||||
chr6:139244832 | T | C | 3 | a0002c0016t0006g0135 a0002c0016t0006g0136 a0018c0029t0002g0210 |
3 | HG00558.hp1 HG02071.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1171-142A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139244832 | |||||||
chr6:139244847 | A | G | 3 | a0005c0013t0010g0052 a0005c0013t0010g0143 a0005c0013t0010g0144 |
3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1171-157T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139244847 | |||||||
chr6:139244952 | T | C | 1 | a0003c0008t0001g0175 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1171-262A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139244952 | |||||||
chr6:139245238 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1171-548T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139245238 | |||||||
chr6:139245313 | C | T | 3 | a0005c0013t0010g0052 a0005c0013t0010g0143 a0005c0013t0010g0144 |
3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1171-623G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139245313 | |||||||
chr6:139245338 | C | T | 3 | a0005c0013t0010g0052 a0005c0013t0010g0143 a0005c0013t0010g0144 |
3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1171-648G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139245338 | |||||||
chr6:139245665 | A | T | 3 | a0005c0013t0010g0052 a0005c0013t0010g0143 a0005c0013t0010g0144 |
3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1171-975T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139245665 | |||||||
chr6:139245725 | C | T | 1 | a0012c0027t0020g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1171-1035G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139245725 | |||||||
chr6:139245762 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1171-1072C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139245762 | |||||||
chr6:139245778 | T | C | 1 | a0002c0002t0002g0189 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1171-1088A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139245778 | |||||||
chr6:139245793 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1171-1103T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139245793 | |||||||
chr6:139245807 | C | T | 1 | a0004c0017t0005g0235 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1171-1117G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139245807 | |||||||
chr6:139245859 | AT | A | 22 | a0003c0003t0004g0018 a0003c0003t0004g0019 a0003c0003t0004g0046 others(19): Show |
24 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.1171-1170delA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139245859 | |||||||
chr6:139245883 | AGT | A | 3 | a0005c0013t0010g0052 a0005c0013t0010g0143 a0005c0013t0010g0144 |
3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1171-1195_1171-119 others(6): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139245883 | |||||||
chr6:139245917 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1171-1227A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139245917 | |||||||
chr6:139245939 | C | T | 1 | a0002c0002t0006g0060 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1171-1249G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139245939 | |||||||
chr6:139246030 | G | A | 19 | a0003c0003t0004g0018 a0003c0003t0004g0019 a0003c0003t0004g0046 others(16): Show |
21 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.1171-1340C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139246030 | |||||||
chr6:139246084 | AT | A | 142 | a0001c0001t0023g0126 a0002c0002t0001g0173 a0002c0002t0001g0174 others(139): Show |
159 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(156): Show |
intron_variant | MODIFIER | c.1171-1395delA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139246084 | |||||||
chr6:139246128 | T | A | 3 | a0005c0013t0010g0052 a0005c0013t0010g0143 a0005c0013t0010g0144 |
3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1171-1438A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139246128 | |||||||
chr6:139246230 | A | T | 3 | a0005c0013t0010g0052 a0005c0013t0010g0143 a0005c0013t0010g0144 |
3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1171-1540T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139246230 | |||||||
chr6:139246271 | C | A | 142 | a0001c0001t0023g0126 a0002c0002t0001g0173 a0002c0002t0001g0174 others(139): Show |
159 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(156): Show |
intron_variant | MODIFIER | c.1170+1546G>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139246271 | |||||||
chr6:139246386 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1170+1431C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139246386 | |||||||
chr6:139246390 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1170+1427A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139246390 | |||||||
chr6:139246428 | C | T | 19 | a0003c0003t0004g0018 a0003c0003t0004g0019 a0003c0003t0004g0046 others(16): Show |
21 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.1170+1389G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139246428 | |||||||
chr6:139246512 | C | T | 1 | a0003c0008t0002g0160 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1170+1305G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139246512 | |||||||
chr6:139246531 | A | G | 143 | a0001c0001t0001g0120 a0001c0001t0023g0126 a0002c0002t0001g0173 others(140): Show |
160 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(157): Show |
intron_variant | MODIFIER | c.1170+1286T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139246531 | |||||||
chr6:139246577 | C | A | 1 | a0016c0024t0026g0103 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1170+1240G>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139246577 | |||||||
chr6:139246639 | G | T | 19 | a0003c0003t0004g0018 a0003c0003t0004g0019 a0003c0003t0004g0046 others(16): Show |
21 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.1170+1178C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139246639 | |||||||
chr6:139246783 | G | A | 3 | a0005c0013t0010g0052 a0005c0013t0010g0143 a0005c0013t0010g0144 |
3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1170+1034C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139246783 | |||||||
chr6:139246907 | T | C | 120 | a0001c0001t0023g0126 a0002c0002t0001g0173 a0002c0002t0001g0174 others(117): Show |
135 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(132): Show |
intron_variant | MODIFIER | c.1170+910A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139246907 | |||||||
chr6:139246914 | C | CA | 20 | a0002c0002t0003g0165 a0003c0003t0004g0018 a0003c0003t0004g0019 others(17): Show |
22 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.1170+902dupT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139246914 | |||||||
chr6:139246914 | CA | C | 12 | a0001c0001t0001g0112 a0001c0001t0001g0124 a0002c0002t0001g0173 others(9): Show |
12 | HG00639.hp1 HG01169.hp1 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.1170+902delT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139246914 | |||||||
chr6:139246985 | C | T | 6 | a0003c0008t0002g0225 a0004c0005t0002g0015 a0004c0005t0002g0128 others(3): Show |
7 | HG01081.hp1 HG01106.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1170+832G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139246985 | |||||||
chr6:139247170 | T | G | 3 | a0005c0013t0010g0052 a0005c0013t0010g0143 a0005c0013t0010g0144 |
3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1170+647A>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139247170 | |||||||
chr6:139247174 | G | A | 1 | a0005c0010t0005g0164 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1170+643C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139247174 | |||||||
chr6:139247203 | C | T | 1 | a0003c0008t0002g0160 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1170+614G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139247203 | |||||||
chr6:139247227 | T | C | 3 | a0005c0013t0010g0052 a0005c0013t0010g0143 a0005c0013t0010g0144 |
3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1170+590A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139247227 | |||||||
chr6:139247244 | C | T | 19 | a0003c0003t0004g0018 a0003c0003t0004g0019 a0003c0003t0004g0046 others(16): Show |
21 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.1170+573G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139247244 | |||||||
chr6:139247299 | G | A | 2 | a0001c0001t0001g0118 a0007c0015t0011g0239 |
2 | HG01169.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1170+518C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139247299 | |||||||
chr6:139247383 | T | A | 3 | a0005c0013t0010g0052 a0005c0013t0010g0143 a0005c0013t0010g0144 |
3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1170+434A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139247383 | |||||||
chr6:139247529 | CTTCTTTT others(36): Show |
C | 1 | a0005c0010t0005g0164 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1170+245_1170+287d others(45): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139247529 | |||||||
chr6:139247532 | C | CT | 15 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(12): Show |
16 | HG00558.hp2 HG01243.hp2 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.1170+284dupA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139247532 | |||||||
chr6:139247532 | CT | C | 58 | a0001c0001t0001g0001 a0001c0001t0001g0044 a0001c0001t0001g0066 others(55): Show |
61 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.1170+284delA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139247532 | |||||||
chr6:139247532 | CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0001g0077 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1170+269_1170+284d others(18): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139247532 | |||||||
chr6:139247618 | T | A | 1 | a0016c0024t0026g0103 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1170+199A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 8/9 | chr6 | 139247618 | |||||||
chr6:139247945 | C | T | 1 | a0017c0032t0027g0146 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1078-36G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139247945 | |||||||
chr6:139248049 | G | C | 2 | a0006c0007t0005g0017 a0011c0033t0019g0155 |
3 | HG01884.hp1 HG02572.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1078-140C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139248049 | |||||||
chr6:139248056 | T | C | 1 | a0016c0024t0026g0103 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1078-147A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139248056 | |||||||
chr6:139248186 | T | C | 3 | a0005c0013t0010g0052 a0005c0013t0010g0143 a0005c0013t0010g0144 |
3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1078-277A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139248186 | |||||||
chr6:139248222 | G | A | 3 | a0001c0001t0001g0044 a0001c0001t0001g0073 a0009c0021t0001g0029 |
3 | HG01257.hp1 HG01261.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1078-313C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139248222 | |||||||
chr6:139248237 | T | C | 3 | a0005c0013t0010g0052 a0005c0013t0010g0143 a0005c0013t0010g0144 |
3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1078-328A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139248237 | |||||||
chr6:139248272 | C | CA | 11 | a0001c0001t0001g0113 a0001c0001t0003g0043 a0001c0001t0015g0047 others(8): Show |
12 | HG01175.hp2 HG02074.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1078-364dupT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139248272 | |||||||
chr6:139248272 | CA | C | 19 | a0002c0002t0001g0205 a0003c0003t0004g0018 a0003c0003t0004g0019 others(16): Show |
21 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.1078-364delT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139248272 | |||||||
chr6:139248303 | C | G | 5 | a0005c0010t0013g0139 a0005c0010t0013g0140 a0005c0010t0014g0141 others(2): Show |
5 | HG02145.hp2 HG02622.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1078-394G>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139248303 | |||||||
chr6:139248324 | C | T | 2 | a0002c0016t0006g0135 a0002c0016t0006g0136 |
2 | HG00558.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.1078-415G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139248324 | |||||||
chr6:139248371 | C | T | 2 | a0007c0015t0011g0238 a0007c0015t0011g0239 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1078-462G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139248371 | |||||||
chr6:139248387 | T | C | 113 | a0001c0001t0023g0126 a0002c0002t0001g0173 a0002c0002t0001g0174 others(110): Show |
128 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(125): Show |
intron_variant | MODIFIER | c.1078-478A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139248387 | |||||||
chr6:139248497 | C | A | 1 | a0012c0027t0020g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1078-588G>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139248497 | |||||||
chr6:139248530 | T | C | 19 | a0003c0003t0004g0018 a0003c0003t0004g0019 a0003c0003t0004g0046 others(16): Show |
21 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.1078-621A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139248530 | |||||||
chr6:139248632 | G | T | 1 | a0002c0002t0003g0209 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1078-723C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139248632 | |||||||
chr6:139248696 | G | A | 78 | a0001c0001t0023g0126 a0002c0002t0001g0173 a0002c0002t0001g0174 others(75): Show |
91 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(88): Show |
intron_variant | MODIFIER | c.1078-787C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139248696 | |||||||
chr6:139248724 | C | T | 1 | a0001c0001t0001g0057 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1078-815G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139248724 | |||||||
chr6:139249024 | G | C | 19 | a0003c0003t0004g0018 a0003c0003t0004g0019 a0003c0003t0004g0046 others(16): Show |
21 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.1078-1115C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139249024 | |||||||
chr6:139249127 | G | C | 1 | a0001c0001t0001g0121 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1078-1218C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139249127 | |||||||
chr6:139249159 | A | C | 148 | a0001c0001t0001g0120 a0001c0001t0023g0126 a0002c0002t0001g0173 others(145): Show |
165 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(162): Show |
intron_variant | MODIFIER | c.1078-1250T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139249159 | |||||||
chr6:139249428 | T | G | 3 | a0005c0013t0010g0052 a0005c0013t0010g0143 a0005c0013t0010g0144 |
3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1078-1519A>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139249428 | |||||||
chr6:139249455 | C | T | 1 | a0002c0002t0003g0170 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1078-1546G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139249455 | |||||||
chr6:139249565 | C | G | 1 | a0001c0001t0001g0068 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1078-1656G>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139249565 | |||||||
chr6:139249619 | G | A | 1 | a0005c0010t0005g0164 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1078-1710C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139249619 | |||||||
chr6:139249639 | G | A | 16 | a0003c0008t0001g0175 a0003c0008t0002g0160 a0003c0008t0002g0225 others(13): Show |
17 | HG01081.hp1 HG01106.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.1078-1730C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139249639 | |||||||
chr6:139249949 | G | A | 113 | a0001c0001t0023g0126 a0002c0002t0001g0173 a0002c0002t0001g0174 others(110): Show |
128 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(125): Show |
intron_variant | MODIFIER | c.1078-2040C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139249949 | |||||||
chr6:139249983 | C | T | 7 | a0005c0010t0013g0139 a0005c0010t0013g0140 a0005c0010t0014g0141 others(4): Show |
7 | HG02055.hp1 HG02145.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1078-2074G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139249983 | |||||||
chr6:139250003 | G | A | 146 | a0001c0001t0023g0126 a0002c0002t0001g0173 a0002c0002t0001g0174 others(143): Show |
163 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(160): Show |
intron_variant | MODIFIER | c.1078-2094C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139250003 | |||||||
chr6:139250084 | A | C | 1 | a0002c0009t0002g0148 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1078-2175T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139250084 | |||||||
chr6:139250177 | C | CT | 6 | a0002c0002t0006g0067 a0003c0011t0005g0116 a0003c0011t0018g0117 others(3): Show |
6 | HG02809.hp1 HG03139.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1078-2269dupA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139250177 | |||||||
chr6:139250177 | C | CTT | 25 | a0002c0016t0006g0135 a0002c0016t0006g0136 a0003c0003t0004g0018 others(22): Show |
27 | HG00323.hp2 HG00558.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.1078-2270_1078-226 others(6): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139250177 | |||||||
chr6:139250177 | CT | C | 81 | a0001c0001t0001g0044 a0001c0001t0001g0088 a0001c0001t0023g0126 others(78): Show |
95 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.1078-2269delA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139250177 | |||||||
chr6:139250177 | CTT | C | 9 | a0002c0002t0003g0192 a0003c0008t0008g0042 a0003c0008t0008g0172 others(6): Show |
9 | HG01106.hp2 HG01243.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1078-2270_1078-226 others(6): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139250177 | |||||||
chr6:139250177 | CTTT | C | 5 | a0003c0008t0002g0225 a0004c0005t0002g0015 a0004c0005t0002g0128 others(2): Show |
6 | HG01081.hp1 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1078-2271_1078-226 others(7): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139250177 | |||||||
chr6:139250217 | C | T | 1 | a0002c0002t0003g0197 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1078-2308G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139250217 | |||||||
chr6:139250218 | G | A | 1 | a0011c0033t0019g0155 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1078-2309C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139250218 | |||||||
chr6:139250357 | C | CT | 25 | a0001c0001t0001g0079 a0001c0001t0001g0111 a0001c0001t0001g0115 others(22): Show |
26 | HG00323.hp2 HG00423.hp1 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.1078-2449dupA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139250357 | |||||||
chr6:139250357 | CT | C | 78 | a0001c0001t0001g0013 a0001c0001t0001g0088 a0001c0001t0001g0104 others(75): Show |
90 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(87): Show |
intron_variant | MODIFIER | c.1078-2449delA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139250357 | |||||||
chr6:139250358 | T | TTTC | 7 | a0005c0010t0013g0139 a0005c0010t0013g0140 a0005c0010t0014g0141 others(4): Show |
7 | HG02055.hp1 HG02145.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1078-2450_1078-244 others(7): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139250358 | |||||||
chr6:139250523 | G | T | 4 | a0003c0003t0004g0018 a0003c0003t0004g0133 a0003c0003t0004g0134 others(1): Show |
5 | HG01109.hp2 HG02109.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1078-2614C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139250523 | |||||||
chr6:139250529 | A | C | 1 | a0010c0026t0024g0195 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1078-2620T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139250529 | |||||||
chr6:139250577 | T | C | 1 | a0016c0024t0026g0103 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1078-2668A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139250577 | |||||||
chr6:139250871 | G | A | 1 | a0002c0002t0007g0083 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1078-2962C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139250871 | |||||||
chr6:139251283 | G | A | 80 | a0001c0001t0023g0126 a0002c0002t0001g0173 a0002c0002t0001g0174 others(77): Show |
94 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(91): Show |
intron_variant | MODIFIER | c.1078-3374C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139251283 | |||||||
chr6:139251397 | G | C | 1 | a0005c0010t0005g0164 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1078-3488C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139251397 | |||||||
chr6:139251508 | C | T | 1 | a0016c0024t0026g0103 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1078-3599G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139251508 | |||||||
chr6:139251532 | A | G | 1 | a0001c0001t0001g0031 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1078-3623T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139251532 | |||||||
chr6:139251568 | T | C | 16 | a0003c0008t0001g0175 a0003c0008t0002g0160 a0003c0008t0002g0225 others(13): Show |
17 | HG01081.hp1 HG01106.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.1078-3659A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139251568 | |||||||
chr6:139251587 | G | C | 3 | a0005c0013t0010g0052 a0005c0013t0010g0143 a0005c0013t0010g0144 |
3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1078-3678C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139251587 | |||||||
chr6:139251771 | G | A | 1 | a0011c0033t0019g0155 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1077+3793C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139251771 | |||||||
chr6:139251877 | G | C | 1 | a0018c0029t0002g0210 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1077+3687C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139251877 | |||||||
chr6:139251977 | A | C | 14 | a0003c0008t0001g0175 a0003c0008t0002g0225 a0003c0008t0008g0042 others(11): Show |
15 | HG01081.hp1 HG01106.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1077+3587T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139251977 | |||||||
chr6:139252033 | C | T | 5 | a0003c0008t0002g0225 a0004c0005t0002g0015 a0004c0005t0002g0128 others(2): Show |
6 | HG01081.hp1 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1077+3531G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139252033 | |||||||
chr6:139252039 | A | AT | 7 | a0005c0010t0013g0139 a0005c0010t0013g0140 a0005c0010t0014g0141 others(4): Show |
7 | HG02055.hp1 HG02145.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1077+3524dupA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139252039 | |||||||
chr6:139252162 | G | A | 1 | a0016c0024t0026g0103 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1077+3402C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139252162 | |||||||
chr6:139252292 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1077+3272G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139252292 | |||||||
chr6:139252355 | A | C | 1 | a0001c0001t0001g0061 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1077+3209T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139252355 | |||||||
chr6:139252501 | A | C | 1 | a0001c0001t0001g0104 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1077+3063T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139252501 | |||||||
chr6:139252774 | G | A | 1 | a0002c0002t0002g0189 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1077+2790C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139252774 | |||||||
chr6:139252916 | C | T | 113 | a0001c0001t0023g0126 a0002c0002t0001g0173 a0002c0002t0001g0174 others(110): Show |
128 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(125): Show |
intron_variant | MODIFIER | c.1077+2648G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139252916 | |||||||
chr6:139252951 | C | A | 2 | a0001c0001t0015g0047 a0001c0001t0015g0063 |
2 | HG00597.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.1077+2613G>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139252951 | |||||||
chr6:139252982 | A | T | 1 | a0001c0004t0001g0010 | 3 | NA18956.hp2 NA18995.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1077+2582T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139252982 | |||||||
chr6:139252997 | C | T | 7 | a0005c0010t0013g0139 a0005c0010t0013g0140 a0005c0010t0014g0141 others(4): Show |
7 | HG02055.hp1 HG02145.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1077+2567G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139252997 | |||||||
chr6:139253077 | A | C | 1 | a0003c0003t0004g0133 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1077+2487T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139253077 | |||||||
chr6:139253233 | G | A | 1 | a0016c0024t0026g0103 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1077+2331C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139253233 | |||||||
chr6:139253246 | G | C | 18 | a0003c0003t0004g0018 a0003c0003t0004g0019 a0003c0003t0004g0046 others(15): Show |
20 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.1077+2318C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139253246 | |||||||
chr6:139253317 | A | G | 3 | a0004c0006t0005g0236 a0004c0006t0005g0237 a0004c0017t0005g0235 |
3 | HG02486.hp1 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1077+2247T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139253317 | |||||||
chr6:139253365 | C | T | 3 | a0003c0008t0002g0160 a0003c0031t0021g0222 a0013c0020t0002g0230 |
3 | HG01243.hp1 HG02109.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1077+2199G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139253365 | |||||||
chr6:139253421 | A | G | 18 | a0003c0003t0004g0018 a0003c0003t0004g0019 a0003c0003t0004g0046 others(15): Show |
20 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.1077+2143T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139253421 | |||||||
chr6:139253456 | C | T | 1 | a0004c0005t0002g0128 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1077+2108G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139253456 | |||||||
chr6:139253457 | G | A | 3 | a0005c0010t0005g0164 a0005c0013t0010g0052 a0005c0013t0010g0144 |
3 | HG03225.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1077+2107C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139253457 | |||||||
chr6:139253524 | T | C | 1 | a0015c0022t0005g0023 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1077+2040A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139253524 | |||||||
chr6:139253563 | C | T | 18 | a0003c0003t0004g0018 a0003c0003t0004g0019 a0003c0003t0004g0046 others(15): Show |
20 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.1077+2001G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139253563 | |||||||
chr6:139253627 | A | G | 1 | a0011c0033t0019g0155 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1077+1937T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139253627 | |||||||
chr6:139253685 | A | G | 1 | a0003c0008t0002g0160 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1077+1879T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139253685 | |||||||
chr6:139253734 | T | A | 1 | a0011c0033t0019g0155 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1077+1830A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139253734 | |||||||
chr6:139253773 | A | G | 7 | a0001c0001t0001g0033 a0001c0001t0001g0065 a0001c0004t0001g0002 others(4): Show |
15 | HG00673.hp1 HG02040.hp2 NA18956.hp2 others(12): Show |
intron_variant | MODIFIER | c.1077+1791T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139253773 | |||||||
chr6:139253804 | G | A | 1 | a0016c0024t0026g0103 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1077+1760C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139253804 | |||||||
chr6:139253887 | C | G | 18 | a0003c0003t0004g0018 a0003c0003t0004g0019 a0003c0003t0004g0046 others(15): Show |
20 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.1077+1677G>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139253887 | |||||||
chr6:139253927 | T | G | 18 | a0003c0003t0004g0018 a0003c0003t0004g0019 a0003c0003t0004g0046 others(15): Show |
20 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.1077+1637A>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139253927 | |||||||
chr6:139254026 | G | A | 1 | a0011c0033t0019g0155 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1077+1538C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254026 | |||||||
chr6:139254026 | G | T | 6 | a0003c0012t0005g0156 a0003c0012t0005g0158 a0003c0012t0005g0159 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1077+1538C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254026 | |||||||
chr6:139254192 | A | G | 1 | a0003c0003t0004g0133 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1077+1372T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254192 | |||||||
chr6:139254223 | A | G | 1 | a0003c0014t0008g0153 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1077+1341T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254223 | |||||||
chr6:139254311 | C | T | 1 | a0003c0003t0004g0018 | 2 | HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1077+1253G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254311 | |||||||
chr6:139254315 | T | G | 1 | a0002c0002t0003g0203 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1077+1249A>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254315 | |||||||
chr6:139254315 | T | TTG | 14 | a0001c0001t0001g0005 a0003c0003t0004g0133 a0003c0003t0004g0137 others(11): Show |
16 | HG01109.hp2 HG01978.hp1 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.1077+1247_1077+124 others(6): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254315 | |||||||
chr6:139254315 | T | TTGTG | 7 | a0002c0002t0002g0167 a0002c0002t0002g0185 a0002c0002t0002g0207 others(4): Show |
7 | HG01433.hp2 HG02280.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1077+1245_1077+124 others(8): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254315 | |||||||
chr6:139254315 | T | TTGTGTG | 3 | a0002c0002t0002g0196 a0002c0002t0002g0218 a0015c0022t0005g0023 |
3 | HG00639.hp1 HG02809.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1077+1243_1077+124 others(10): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254315 | |||||||
chr6:139254315 | T | TTGTGTGT others(1): Show |
72 | a0001c0001t0001g0120 a0001c0001t0023g0126 a0002c0002t0001g0173 others(69): Show |
85 | HG00423.hp2 HG00642.hp2 HG00733.hp2 others(82): Show |
intron_variant | MODIFIER | c.1077+1241_1077+124 others(12): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254315 | |||||||
chr6:139254315 | T | TTGTGTGT others(3): Show |
20 | a0002c0002t0002g0206 a0002c0002t0003g0170 a0002c0002t0003g0202 others(17): Show |
21 | HG00735.hp1 HG01106.hp2 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.1077+1239_1077+124 others(14): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254315 | |||||||
chr6:139254315 | T | TTGTGTGT others(5): Show |
8 | a0002c0002t0003g0032 a0003c0008t0002g0225 a0003c0031t0021g0222 others(5): Show |
9 | HG00733.hp1 HG01081.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1077+1237_1077+124 others(16): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254315 | |||||||
chr6:139254315 | T | TTGTGTGT others(9): Show |
1 | a0005c0010t0005g0164 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1077+1233_1077+124 others(20): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254315 | |||||||
chr6:139254315 | T | TTGTGTGT others(11): Show |
1 | a0013c0020t0002g0230 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1077+1231_1077+124 others(22): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254315 | |||||||
chr6:139254315 | TTG | T | 2 | a0003c0003t0004g0018 a0003c0003t0004g0134 |
3 | HG02109.hp1 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1077+1247_1077+124 others(6): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254315 | |||||||
chr6:139254715 | C | T | 146 | a0001c0001t0023g0126 a0002c0002t0001g0173 a0002c0002t0001g0174 others(143): Show |
163 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(160): Show |
intron_variant | MODIFIER | c.1077+849G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254715 | |||||||
chr6:139254747 | A | AT | 3 | a0005c0013t0010g0052 a0005c0013t0010g0143 a0005c0013t0010g0144 |
3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1077+816dupA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254747 | |||||||
chr6:139254781 | G | T | 1 | a0001c0001t0001g0030 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1077+783C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254781 | |||||||
chr6:139254784 | T | A | 1 | a0002c0002t0001g0059 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1077+780A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254784 | |||||||
chr6:139254827 | T | G | 1 | a0002c0009t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1077+737A>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254827 | |||||||
chr6:139254878 | A | G | 148 | a0001c0001t0001g0120 a0001c0001t0023g0126 a0002c0002t0001g0173 others(145): Show |
165 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(162): Show |
intron_variant | MODIFIER | c.1077+686T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254878 | |||||||
chr6:139254975 | C | T | 1 | a0002c0002t0003g0243 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1077+589G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139254975 | |||||||
chr6:139255041 | C | T | 15 | a0003c0011t0005g0045 a0003c0011t0005g0116 a0003c0011t0017g0138 others(12): Show |
15 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1077+523G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139255041 | |||||||
chr6:139255060 | G | A | 1 | a0010c0026t0024g0195 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1077+504C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139255060 | |||||||
chr6:139255118 | G | A | 1 | a0016c0024t0026g0103 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1077+446C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139255118 | |||||||
chr6:139255356 | C | T | 1 | a0018c0029t0002g0210 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1077+208G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139255356 | |||||||
chr6:139255357 | G | A | 1 | a0003c0011t0018g0117 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1077+207C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139255357 | |||||||
chr6:139255407 | G | A | 64 | a0003c0003t0004g0018 a0003c0003t0004g0019 a0003c0003t0004g0046 others(61): Show |
67 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(64): Show |
intron_variant | MODIFIER | c.1077+157C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139255407 | |||||||
chr6:139255513 | A | T | 1 | a0001c0001t0001g0084 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1077+51T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 7/9 | chr6 | 139255513 | |||||||
chr6:139255642 | T | G | 1 | a0001c0001t0001g0026 | 1 | NA18988.hp2 | splice_region_variant&intron_variant | LOW | c.1003-4A>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139255642 | |||||||
chr6:139255669 | G | T | 1 | a0018c0029t0002g0210 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1003-31C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139255669 | |||||||
chr6:139255898 | G | A | 2 | a0002c0009t0002g0147 a0002c0009t0002g0154 |
2 | HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1003-260C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139255898 | |||||||
chr6:139255912 | G | GA | 13 | a0001c0001t0003g0043 a0002c0002t0001g0205 a0002c0002t0003g0204 others(10): Show |
13 | HG01175.hp1 HG01175.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1003-275dupT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139255912 | |||||||
chr6:139255927 | C | A | 12 | a0001c0001t0001g0031 a0001c0001t0001g0074 a0002c0002t0003g0037 others(9): Show |
12 | HG00642.hp1 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1003-289G>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139255927 | |||||||
chr6:139256063 | T | C | 1 | a0012c0027t0020g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1003-425A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139256063 | |||||||
chr6:139256207 | A | T | 2 | a0002c0002t0006g0006 a0002c0002t0006g0060 |
4 | HG00438.hp1 NA18960.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.1003-569T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139256207 | |||||||
chr6:139256569 | C | G | 1 | a0018c0029t0002g0210 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1003-931G>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139256569 | |||||||
chr6:139256603 | T | C | 1 | a0018c0029t0002g0210 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1003-965A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139256603 | |||||||
chr6:139256618 | G | A | 8 | a0005c0010t0013g0139 a0005c0010t0013g0140 a0005c0010t0014g0141 others(5): Show |
8 | HG02055.hp1 HG02145.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1003-980C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139256618 | |||||||
chr6:139256623 | C | A | 3 | a0001c0028t0001g0024 a0002c0016t0006g0135 a0002c0016t0006g0136 |
3 | HG00558.hp1 HG02071.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.1003-985G>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139256623 | |||||||
chr6:139256703 | A | G | 3 | a0001c0028t0001g0024 a0002c0016t0006g0135 a0002c0016t0006g0136 |
3 | HG00558.hp1 HG02071.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.1003-1065T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139256703 | |||||||
chr6:139256850 | A | G | 1 | a0004c0006t0005g0127 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1003-1212T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139256850 | |||||||
chr6:139257243 | T | C | 3 | a0005c0013t0010g0052 a0005c0013t0010g0143 a0005c0013t0010g0144 |
3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1003-1605A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139257243 | |||||||
chr6:139257477 | G | A | 8 | a0005c0010t0013g0139 a0005c0010t0013g0140 a0005c0010t0014g0141 others(5): Show |
8 | HG02055.hp1 HG02145.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1003-1839C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139257477 | |||||||
chr6:139257477 | G | T | 1 | a0016c0024t0026g0103 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1003-1839C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139257477 | |||||||
chr6:139257560 | T | C | 1 | a0005c0010t0005g0164 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1003-1922A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139257560 | |||||||
chr6:139257572 | T | C | 78 | a0001c0001t0023g0126 a0002c0002t0001g0173 a0002c0002t0001g0174 others(75): Show |
92 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(89): Show |
intron_variant | MODIFIER | c.1003-1934A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139257572 | |||||||
chr6:139257645 | G | A | 1 | a0016c0024t0026g0103 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1003-2007C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139257645 | |||||||
chr6:139257724 | T | TA | 18 | a0003c0003t0004g0018 a0003c0003t0004g0019 a0003c0003t0004g0046 others(15): Show |
20 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.1003-2087dupT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139257724 | |||||||
chr6:139257789 | T | C | 1 | a0002c0002t0003g0221 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1003-2151A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139257789 | |||||||
chr6:139257872 | G | T | 78 | a0001c0001t0023g0126 a0002c0002t0001g0173 a0002c0002t0001g0174 others(75): Show |
92 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(89): Show |
intron_variant | MODIFIER | c.1003-2234C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139257872 | |||||||
chr6:139258263 | G | A | 5 | a0002c0002t0003g0032 a0002c0002t0007g0011 a0002c0002t0007g0082 others(2): Show |
6 | HG00733.hp1 HG01358.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1002+2055C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139258263 | |||||||
chr6:139258327 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1002+1991T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139258327 | |||||||
chr6:139258362 | A | G | 1 | a0015c0022t0005g0023 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1002+1956T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139258362 | |||||||
chr6:139258412 | C | T | 18 | a0003c0003t0004g0018 a0003c0003t0004g0019 a0003c0003t0004g0046 others(15): Show |
20 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.1002+1906G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139258412 | |||||||
chr6:139258414 | A | G | 1 | a0005c0010t0005g0164 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1002+1904T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139258414 | |||||||
chr6:139258622 | C | T | 146 | a0001c0001t0023g0126 a0001c0028t0001g0024 a0002c0002t0001g0173 others(143): Show |
163 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(160): Show |
intron_variant | MODIFIER | c.1002+1696G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139258622 | |||||||
chr6:139258742 | A | C | 1 | a0016c0024t0026g0103 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1002+1576T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139258742 | |||||||
chr6:139258749 | C | T | 1 | a0010c0026t0024g0195 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1002+1569G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139258749 | |||||||
chr6:139258750 | G | A | 3 | a0002c0002t0003g0009 a0002c0002t0003g0165 a0002c0002t0003g0188 |
5 | HG01261.hp2 HG01496.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1002+1568C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139258750 | |||||||
chr6:139258798 | A | C | 1 | a0003c0003t0004g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1002+1520T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139258798 | |||||||
chr6:139259018 | T | C | 1 | a0015c0022t0005g0023 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1002+1300A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139259018 | |||||||
chr6:139259101 | C | T | 1 | a0011c0033t0019g0155 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1002+1217G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139259101 | |||||||
chr6:139259102 | A | G | 1 | a0003c0003t0004g0180 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1002+1216T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139259102 | |||||||
chr6:139259176 | G | A | 1 | a0012c0027t0020g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1002+1142C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139259176 | |||||||
chr6:139259348 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1002+970C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139259348 | |||||||
chr6:139259459 | C | T | 1 | a0005c0010t0005g0164 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1002+859G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139259459 | |||||||
chr6:139259488 | G | A | 1 | a0011c0033t0019g0155 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1002+830C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139259488 | |||||||
chr6:139259655 | C | T | 200 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(197): Show |
235 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.1002+663G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139259655 | |||||||
chr6:139259860 | T | C | 36 | a0001c0001t0001g0120 a0003c0008t0001g0175 a0003c0008t0002g0160 others(33): Show |
37 | HG01081.hp1 HG01106.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.1002+458A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139259860 | |||||||
chr6:139259957 | T | A | 2 | a0002c0002t0002g0185 a0002c0002t0002g0207 |
2 | HG01433.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1002+361A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139259957 | |||||||
chr6:139259979 | T | C | 1 | a0003c0031t0021g0222 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1002+339A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139259979 | |||||||
chr6:139259998 | G | A | 7 | a0005c0010t0013g0139 a0005c0010t0013g0140 a0005c0010t0014g0141 others(4): Show |
7 | HG02055.hp1 HG02145.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1002+320C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139259998 | |||||||
chr6:139260122 | A | T | 16 | a0001c0001t0001g0120 a0003c0011t0005g0045 a0003c0011t0005g0116 others(13): Show |
16 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1002+196T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139260122 | |||||||
chr6:139260136 | C | T | 1 | a0002c0025t0003g0229 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1002+182G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139260136 | |||||||
chr6:139260219 | C | CAAAT | 15 | a0001c0028t0001g0024 a0002c0002t0003g0145 a0002c0016t0006g0135 others(12): Show |
15 | HG00558.hp1 HG02055.hp1 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1002+95_1002+98dup others(4): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139260219 | |||||||
chr6:139260267 | C | G | 1 | a0003c0011t0005g0045 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1002+51G>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 6/9 | chr6 | 139260267 | |||||||
chr6:139260670 | A | T | 1 | a0012c0027t0020g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.883-233T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 5/9 | chr6 | 139260670 | |||||||
chr6:139260967 | C | G | 1 | a0002c0009t0002g0148 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.883-530G>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 5/9 | chr6 | 139260967 | |||||||
chr6:139261289 | T | C | 1 | a0004c0005t0002g0130 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.883-852A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 5/9 | chr6 | 139261289 | |||||||
chr6:139261329 | A | AGATAAAA others(2): Show |
3 | a0005c0013t0010g0052 a0005c0013t0010g0143 a0005c0013t0010g0144 |
3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.883-901_883-893dup others(9): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 5/9 | chr6 | 139261329 | |||||||
chr6:139261348 | C | T | 2 | a0002c0002t0001g0194 a0002c0002t0001g0205 |
2 | NA19059.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.883-911G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 5/9 | chr6 | 139261348 | |||||||
chr6:139261828 | G | T | 13 | a0003c0008t0002g0225 a0003c0008t0008g0042 a0003c0008t0008g0172 others(10): Show |
14 | HG01081.hp1 HG01106.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.882+751C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 5/9 | chr6 | 139261828 | |||||||
chr6:139261901 | C | CT | 107 | a0001c0001t0001g0027 a0001c0001t0001g0120 a0001c0001t0003g0043 others(104): Show |
122 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(119): Show |
intron_variant | MODIFIER | c.882+677dupA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 5/9 | chr6 | 139261901 | |||||||
chr6:139261901 | C | CTT | 13 | a0001c0001t0023g0126 a0002c0002t0002g0206 a0002c0002t0003g0051 others(10): Show |
13 | HG01081.hp2 HG01243.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.882+676_882+677dup others(2): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 5/9 | chr6 | 139261901 | |||||||
chr6:139261901 | CT | C | 12 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0114 others(9): Show |
12 | HG01257.hp2 HG01975.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.882+677delA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 5/9 | chr6 | 139261901 | |||||||
chr6:139262049 | G | A | 3 | a0005c0013t0010g0052 a0005c0013t0010g0143 a0005c0013t0010g0144 |
3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.882+530C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 5/9 | chr6 | 139262049 | |||||||
chr6:139262070 | A | AT | 18 | a0003c0003t0004g0018 a0003c0003t0004g0019 a0003c0003t0004g0046 others(15): Show |
20 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.882+508dupA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 5/9 | chr6 | 139262070 | |||||||
chr6:139262088 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.882+491T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 5/9 | chr6 | 139262088 | |||||||
chr6:139262257 | G | A | 1 | a0003c0003t0004g0137 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.882+322C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 5/9 | chr6 | 139262257 | |||||||
chr6:139262330 | C | T | 2 | a0005c0010t0005g0164 a0011c0033t0019g0155 |
2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.882+249G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 5/9 | chr6 | 139262330 | |||||||
chr6:139262446 | G | A | 1 | a0003c0003t0004g0133 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.882+133C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 5/9 | chr6 | 139262446 | |||||||
chr6:139262452 | G | A | 1 | a0003c0011t0017g0138 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.882+127C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 5/9 | chr6 | 139262452 | |||||||
chr6:139262777 | C | A | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | HG01099.hp2 HG01515.hp2 |
splice_region_variant&intron_variant | LOW | c.688-4G>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139262777 | |||||||
chr6:139262821 | T | C | 7 | a0005c0010t0013g0139 a0005c0010t0013g0140 a0005c0010t0014g0141 others(4): Show |
7 | HG02055.hp1 HG02145.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.688-48A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139262821 | |||||||
chr6:139262853 | A | T | 147 | a0001c0001t0001g0120 a0001c0001t0023g0126 a0001c0028t0001g0024 others(144): Show |
164 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(161): Show |
intron_variant | MODIFIER | c.688-80T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139262853 | |||||||
chr6:139262911 | C | T | 7 | a0005c0010t0013g0139 a0005c0010t0013g0140 a0005c0010t0014g0141 others(4): Show |
7 | HG02055.hp1 HG02145.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.688-138G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139262911 | |||||||
chr6:139263029 | C | T | 3 | a0005c0013t0010g0052 a0005c0013t0010g0143 a0005c0013t0010g0144 |
3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.688-256G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139263029 | |||||||
chr6:139263121 | A | C | 7 | a0005c0010t0013g0139 a0005c0010t0013g0140 a0005c0010t0014g0141 others(4): Show |
7 | HG02055.hp1 HG02145.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.688-348T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139263121 | |||||||
chr6:139263280 | A | C | 7 | a0005c0010t0013g0139 a0005c0010t0013g0140 a0005c0010t0014g0141 others(4): Show |
7 | HG02055.hp1 HG02145.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.688-507T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139263280 | |||||||
chr6:139263414 | A | C | 1 | a0002c0002t0002g0109 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.688-641T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139263414 | |||||||
chr6:139263477 | A | G | 2 | a0003c0011t0005g0116 a0003c0011t0018g0117 |
2 | HG03688.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.688-704T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139263477 | |||||||
chr6:139263511 | G | A | 9 | a0003c0011t0005g0045 a0003c0012t0005g0156 a0003c0012t0005g0158 others(6): Show |
9 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.688-738C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139263511 | |||||||
chr6:139263535 | G | C | 1 | a0001c0001t0001g0092 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.688-762C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139263535 | |||||||
chr6:139263681 | G | GTTATTC | 147 | a0001c0001t0023g0126 a0001c0028t0001g0024 a0002c0002t0001g0173 others(144): Show |
164 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(161): Show |
intron_variant | MODIFIER | c.688-914_688-909dup others(6): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139263681 | |||||||
chr6:139263696 | TA | T | 7 | a0005c0010t0013g0139 a0005c0010t0013g0140 a0005c0010t0014g0141 others(4): Show |
7 | HG02055.hp1 HG02145.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.688-924delT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139263696 | |||||||
chr6:139264000 | A | G | 1 | a0012c0027t0020g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.688-1227T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139264000 | |||||||
chr6:139264244 | G | A | 2 | a0003c0008t0002g0160 a0003c0031t0021g0222 |
2 | HG01243.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.688-1471C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139264244 | |||||||
chr6:139264336 | T | C | 3 | a0005c0013t0010g0052 a0005c0013t0010g0143 a0005c0013t0010g0144 |
3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.688-1563A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139264336 | |||||||
chr6:139264413 | T | C | 2 | a0001c0001t0001g0079 a0001c0001t0001g0115 |
2 | NA19010.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.688-1640A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139264413 | |||||||
chr6:139264478 | T | A | 2 | a0003c0003t0004g0018 a0011c0033t0019g0155 |
3 | HG01884.hp1 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.688-1705A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139264478 | |||||||
chr6:139264541 | A | T | 1 | a0016c0024t0026g0103 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.688-1768T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139264541 | |||||||
chr6:139264543 | T | A | 1 | a0003c0011t0017g0138 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.688-1770A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139264543 | |||||||
chr6:139264543 | T | TTTTTG | 59 | a0001c0001t0001g0120 a0001c0001t0023g0126 a0002c0002t0001g0173 others(56): Show |
69 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.688-1775_688-1771d others(7): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139264543 | |||||||
chr6:139264543 | T | TTTTTGTT others(3): Show |
3 | a0002c0002t0002g0035 a0002c0002t0002g0166 a0006c0018t0004g0161 |
3 | HG01433.hp1 HG03139.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.688-1780_688-1771d others(12): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139264543 | |||||||
chr6:139264548 | G | GTT | 8 | a0005c0010t0013g0139 a0005c0010t0013g0140 a0005c0010t0014g0141 others(5): Show |
8 | HG02055.hp1 HG02145.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.688-1777_688-1776d others(4): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139264548 | |||||||
chr6:139264707 | G | A | 1 | a0012c0027t0020g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.688-1934C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139264707 | |||||||
chr6:139264748 | C | T | 1 | a0002c0002t0003g0190 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.688-1975G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139264748 | |||||||
chr6:139264815 | C | T | 7 | a0002c0002t0003g0145 a0002c0002t0003g0190 a0002c0002t0003g0191 others(4): Show |
7 | HG02165.hp2 HG03688.hp2 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.688-2042G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139264815 | |||||||
chr6:139265066 | G | A | 2 | a0002c0002t0002g0167 a0002c0009t0005g0149 |
2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.688-2293C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139265066 | |||||||
chr6:139265143 | A | G | 1 | a0016c0024t0026g0103 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.688-2370T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139265143 | |||||||
chr6:139265426 | A | ATG | 18 | a0003c0008t0002g0225 a0003c0008t0008g0042 a0003c0008t0008g0172 others(15): Show |
19 | HG01081.hp1 HG01106.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.688-2655_688-2654d others(4): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139265426 | |||||||
chr6:139265446 | C | CTG | 6 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0212 others(3): Show |
6 | HG02135.hp1 HG02698.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.688-2675_688-2674d others(4): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139265446 | |||||||
chr6:139265456 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.688-2683C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139265456 | |||||||
chr6:139265483 | C | T | 7 | a0005c0010t0013g0139 a0005c0010t0013g0140 a0005c0010t0014g0141 others(4): Show |
7 | HG02055.hp1 HG02145.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.688-2710G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139265483 | |||||||
chr6:139265517 | G | A | 14 | a0002c0002t0003g0009 a0002c0002t0003g0032 a0002c0002t0003g0037 others(11): Show |
17 | HG00733.hp1 HG00735.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.688-2744C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139265517 | |||||||
chr6:139265578 | T | C | 17 | a0003c0003t0004g0019 a0003c0003t0004g0046 a0003c0003t0004g0053 others(14): Show |
18 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.688-2805A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139265578 | |||||||
chr6:139265632 | T | G | 6 | a0002c0002t0003g0214 a0002c0009t0002g0152 a0004c0006t0005g0236 others(3): Show |
7 | HG02486.hp1 HG02559.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.688-2859A>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139265632 | |||||||
chr6:139265742 | T | C | 8 | a0005c0010t0013g0139 a0005c0010t0013g0140 a0005c0010t0014g0141 others(5): Show |
8 | HG02055.hp1 HG02145.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.688-2969A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139265742 | |||||||
chr6:139266288 | T | A | 2 | a0003c0011t0005g0116 a0003c0011t0018g0117 |
2 | HG03688.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.688-3515A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139266288 | |||||||
chr6:139266340 | A | C | 1 | a0002c0025t0003g0229 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.688-3567T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139266340 | |||||||
chr6:139266590 | C | T | 3 | a0002c0002t0003g0214 a0002c0009t0002g0152 a0006c0007t0002g0022 |
4 | HG02559.hp1 HG02615.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.688-3817G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139266590 | |||||||
chr6:139266623 | A | G | 1 | a0002c0002t0006g0060 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.687+3833T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139266623 | |||||||
chr6:139266656 | A | G | 1 | a0002c0002t0031g0244 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.687+3800T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139266656 | |||||||
chr6:139266824 | C | T | 1 | a0003c0003t0004g0177 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.687+3632G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139266824 | |||||||
chr6:139266880 | G | C | 1 | a0001c0001t0001g0095 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.687+3576C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139266880 | |||||||
chr6:139266951 | T | C | 1 | a0005c0010t0005g0164 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.687+3505A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139266951 | |||||||
chr6:139266965 | G | GA | 77 | a0001c0001t0001g0026 a0001c0001t0001g0038 a0001c0001t0001g0056 others(74): Show |
91 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(88): Show |
intron_variant | MODIFIER | c.687+3490dupT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139266965 | |||||||
chr6:139266965 | G | GAA | 47 | a0001c0001t0001g0120 a0001c0028t0001g0024 a0002c0002t0002g0050 others(44): Show |
49 | HG00558.hp1 HG01081.hp1 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.687+3489_687+3490d others(4): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139266965 | |||||||
chr6:139266965 | G | GAAA | 10 | a0003c0008t0001g0175 a0003c0008t0008g0042 a0003c0008t0008g0172 others(7): Show |
10 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.687+3488_687+3490d others(5): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139266965 | |||||||
chr6:139267039 | TA | T | 13 | a0003c0008t0002g0225 a0003c0008t0008g0042 a0003c0008t0008g0172 others(10): Show |
14 | HG01081.hp1 HG01106.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.687+3416delT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139267039 | |||||||
chr6:139267073 | G | A | 18 | a0003c0008t0001g0175 a0003c0008t0002g0160 a0003c0008t0002g0225 others(15): Show |
19 | HG01081.hp1 HG01106.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.687+3383C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139267073 | |||||||
chr6:139267207 | A | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(4): Show |
9 | HG00673.hp2 HG01978.hp1 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.687+3249T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139267207 | |||||||
chr6:139267223 | G | C | 18 | a0003c0008t0001g0175 a0003c0008t0002g0160 a0003c0008t0002g0225 others(15): Show |
19 | HG01081.hp1 HG01106.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.687+3233C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139267223 | |||||||
chr6:139267616 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.687+2840G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139267616 | |||||||
chr6:139267626 | A | G | 1 | a0003c0008t0001g0175 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.687+2830T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139267626 | |||||||
chr6:139267814 | A | G | 1 | a0005c0010t0005g0164 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.687+2642T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139267814 | |||||||
chr6:139267878 | C | A | 13 | a0003c0008t0002g0225 a0003c0008t0008g0042 a0003c0008t0008g0172 others(10): Show |
14 | HG01081.hp1 HG01106.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.687+2578G>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139267878 | |||||||
chr6:139267923 | C | T | 1 | a0012c0027t0020g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.687+2533G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139267923 | |||||||
chr6:139268075 | G | A | 18 | a0003c0003t0004g0018 a0003c0003t0004g0019 a0003c0003t0004g0046 others(15): Show |
20 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.687+2381C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139268075 | |||||||
chr6:139268109 | C | T | 1 | a0002c0002t0002g0189 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.687+2347G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139268109 | |||||||
chr6:139268151 | C | CA | 33 | a0001c0001t0001g0038 a0001c0001t0001g0084 a0001c0001t0001g0086 others(30): Show |
34 | HG00558.hp1 HG00673.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.687+2304dupT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139268151 | |||||||
chr6:139268151 | C | CAA | 19 | a0001c0001t0001g0120 a0002c0002t0003g0214 a0002c0009t0002g0152 others(16): Show |
20 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.687+2303_687+2304d others(4): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139268151 | |||||||
chr6:139268151 | CA | C | 16 | a0003c0003t0004g0019 a0003c0003t0004g0046 a0003c0003t0004g0053 others(13): Show |
17 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.687+2304delT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139268151 | |||||||
chr6:139268261 | G | C | 2 | a0007c0015t0011g0238 a0007c0015t0011g0239 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.687+2195C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139268261 | |||||||
chr6:139268322 | T | C | 1 | a0001c0001t0001g0093 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.687+2134A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139268322 | |||||||
chr6:139268444 | T | C | 18 | a0003c0008t0001g0175 a0003c0008t0002g0160 a0003c0008t0002g0225 others(15): Show |
19 | HG01081.hp1 HG01106.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.687+2012A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139268444 | |||||||
chr6:139268563 | A | T | 18 | a0003c0003t0004g0018 a0003c0003t0004g0019 a0003c0003t0004g0046 others(15): Show |
20 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.687+1893T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139268563 | |||||||
chr6:139268822 | G | A | 1 | a0002c0002t0003g0051 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.687+1634C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139268822 | |||||||
chr6:139268846 | T | C | 1 | a0003c0011t0018g0117 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.687+1610A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139268846 | |||||||
chr6:139268897 | T | C | 1 | a0016c0024t0026g0103 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.687+1559A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139268897 | |||||||
chr6:139268908 | C | T | 138 | a0001c0001t0023g0126 a0001c0028t0001g0024 a0002c0002t0001g0173 others(135): Show |
154 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.687+1548G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139268908 | |||||||
chr6:139268970 | A | T | 3 | a0001c0028t0001g0024 a0002c0016t0006g0135 a0002c0016t0006g0136 |
3 | HG00558.hp1 HG02071.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.687+1486T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139268970 | |||||||
chr6:139268996 | C | T | 18 | a0003c0003t0004g0018 a0003c0003t0004g0019 a0003c0003t0004g0046 others(15): Show |
20 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.687+1460G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139268996 | |||||||
chr6:139269031 | C | T | 13 | a0002c0002t0003g0214 a0002c0009t0002g0152 a0004c0006t0005g0236 others(10): Show |
14 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.687+1425G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139269031 | |||||||
chr6:139269089 | T | C | 65 | a0002c0002t0003g0214 a0002c0009t0002g0152 a0003c0003t0004g0018 others(62): Show |
69 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.687+1367A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139269089 | |||||||
chr6:139269125 | G | A | 13 | a0003c0008t0002g0225 a0003c0008t0008g0042 a0003c0008t0008g0172 others(10): Show |
14 | HG01081.hp1 HG01106.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.687+1331C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139269125 | |||||||
chr6:139269295 | C | T | 3 | a0005c0013t0010g0052 a0005c0013t0010g0143 a0005c0013t0010g0144 |
3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.687+1161G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139269295 | |||||||
chr6:139269318 | T | G | 2 | a0003c0011t0005g0116 a0003c0011t0018g0117 |
2 | HG03688.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.687+1138A>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139269318 | |||||||
chr6:139269403 | C | T | 1 | a0015c0022t0005g0023 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.687+1053G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139269403 | |||||||
chr6:139269404 | G | A | 1 | a0005c0010t0005g0164 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.687+1052C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139269404 | |||||||
chr6:139269780 | G | A | 1 | a0011c0033t0019g0155 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.687+676C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139269780 | |||||||
chr6:139269902 | T | C | 1 | a0001c0001t0001g0089 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.687+554A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139269902 | |||||||
chr6:139269988 | G | T | 1 | a0016c0024t0026g0103 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.687+468C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139269988 | |||||||
chr6:139270018 | C | T | 1 | a0003c0031t0021g0222 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.687+438G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139270018 | |||||||
chr6:139270065 | CAAAAATG others(3): Show |
C | 1 | a0001c0001t0001g0090 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.687+381_687+390del others(10): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139270065 | |||||||
chr6:139270088 | T | C | 18 | a0003c0003t0004g0018 a0003c0003t0004g0019 a0003c0003t0004g0046 others(15): Show |
20 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.687+368A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139270088 | |||||||
chr6:139270201 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.687+255C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139270201 | |||||||
chr6:139270368 | TA | T | 74 | a0001c0001t0001g0211 a0001c0001t0023g0126 a0001c0028t0001g0024 others(71): Show |
86 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.687+87delT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 4/9 | chr6 | 139270368 | |||||||
chr6:139270709 | A | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-83T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270709 | |||||||
chr6:139270710 | C | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-84G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270710 | |||||||
chr6:139270712 | C | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-86G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270712 | |||||||
chr6:139270714 | G | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-88C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270714 | |||||||
chr6:139270715 | T | A | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-89A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270715 | |||||||
chr6:139270716 | G | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-90C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270716 | |||||||
chr6:139270717 | G | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-91C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270717 | |||||||
chr6:139270720 | G | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-94C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270720 | |||||||
chr6:139270724 | G | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-98C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270724 | |||||||
chr6:139270725 | G | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-99C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270725 | |||||||
chr6:139270726 | A | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-100T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270726 | |||||||
chr6:139270727 | A | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-101T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270727 | |||||||
chr6:139270729 | C | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-103G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270729 | |||||||
chr6:139270737 | G | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-111C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270737 | |||||||
chr6:139270738 | C | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-112G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270738 | |||||||
chr6:139270740 | A | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-114T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270740 | |||||||
chr6:139270741 | T | A | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-115A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270741 | |||||||
chr6:139270743 | A | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-117T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270743 | |||||||
chr6:139270745 | C | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-119G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270745 | |||||||
chr6:139270747 | C | T | 2 | a0002c0009t0002g0154 a0015c0022t0005g0023 |
2 | HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.517-121G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270747 | |||||||
chr6:139270750 | C | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-124G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270750 | |||||||
chr6:139270751 | C | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-125G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270751 | |||||||
chr6:139270753 | C | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-127G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270753 | |||||||
chr6:139270754 | T | C | 8 | a0002c0002t0003g0009 a0002c0002t0003g0037 a0002c0002t0003g0051 others(5): Show |
10 | HG00735.hp1 HG01081.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.517-128A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270754 | |||||||
chr6:139270755 | G | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-129C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270755 | |||||||
chr6:139270756 | G | C | 1 | a0002c0002t0003g0209 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.517-130C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270756 | |||||||
chr6:139270756 | G | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-130C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270756 | |||||||
chr6:139270757 | A | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-131T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270757 | |||||||
chr6:139270758 | A | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-132T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270758 | |||||||
chr6:139270759 | G | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-133C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270759 | |||||||
chr6:139270761 | A | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-135T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270761 | |||||||
chr6:139270762 | A | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-136T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270762 | |||||||
chr6:139270763 | A | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-137T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270763 | |||||||
chr6:139270765 | G | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-139C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270765 | |||||||
chr6:139270766 | A | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-140T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270766 | |||||||
chr6:139270767 | A | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-141T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270767 | |||||||
chr6:139270768 | A | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-142T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270768 | |||||||
chr6:139270771 | C | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-145G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270771 | |||||||
chr6:139270772 | A | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-146T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270772 | |||||||
chr6:139270773 | C | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-147G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270773 | |||||||
chr6:139270774 | A | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-148T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270774 | |||||||
chr6:139270775 | A | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-149T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270775 | |||||||
chr6:139270776 | A | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-150T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270776 | |||||||
chr6:139270777 | C | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-151G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270777 | |||||||
chr6:139270778 | G | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0100 |
3 | HG01243.hp2 NA18966.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.517-152C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270778 | |||||||
chr6:139270778 | G | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-152C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270778 | |||||||
chr6:139270780 | C | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-154G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270780 | |||||||
chr6:139270781 | A | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-155T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270781 | |||||||
chr6:139270782 | C | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-156G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270782 | |||||||
chr6:139270783 | C | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-157G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270783 | |||||||
chr6:139270787 | G | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-161C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270787 | |||||||
chr6:139270789 | A | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-163T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270789 | |||||||
chr6:139270790 | G | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-164C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270790 | |||||||
chr6:139270792 | A | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-166T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270792 | |||||||
chr6:139270793 | C | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-167G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270793 | |||||||
chr6:139270796 | G | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-170C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270796 | |||||||
chr6:139270797 | A | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-171T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270797 | |||||||
chr6:139270798 | A | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-172T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270798 | |||||||
chr6:139270799 | G | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-173C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270799 | |||||||
chr6:139270800 | G | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-174C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270800 | |||||||
chr6:139270802 | A | T | 1 | a0002c0009t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517-176T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270802 | |||||||
chr6:139270979 | G | A | 1 | a0002c0002t0002g0185 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.517-353C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139270979 | |||||||
chr6:139271004 | T | A | 13 | a0002c0002t0003g0214 a0002c0009t0002g0152 a0004c0006t0005g0236 others(10): Show |
14 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.517-378A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139271004 | |||||||
chr6:139271055 | C | G | 13 | a0002c0002t0003g0214 a0002c0009t0002g0152 a0004c0006t0005g0236 others(10): Show |
14 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.517-429G>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139271055 | |||||||
chr6:139271066 | C | T | 18 | a0003c0003t0004g0018 a0003c0003t0004g0019 a0003c0003t0004g0046 others(15): Show |
20 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.517-440G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139271066 | |||||||
chr6:139271139 | G | T | 18 | a0003c0003t0004g0018 a0003c0003t0004g0019 a0003c0003t0004g0046 others(15): Show |
20 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.517-513C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139271139 | |||||||
chr6:139271276 | T | A | 1 | a0015c0022t0005g0023 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.517-650A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139271276 | |||||||
chr6:139271444 | C | T | 1 | a0004c0005t0002g0130 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.517-818G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139271444 | |||||||
chr6:139271527 | A | G | 3 | a0001c0028t0001g0024 a0002c0016t0006g0135 a0002c0016t0006g0136 |
3 | HG00558.hp1 HG02071.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.517-901T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139271527 | |||||||
chr6:139271675 | T | C | 1 | a0001c0001t0001g0100 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.517-1049A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139271675 | |||||||
chr6:139271734 | G | T | 59 | a0001c0001t0001g0211 a0001c0001t0023g0126 a0002c0002t0001g0173 others(56): Show |
68 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.517-1108C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139271734 | |||||||
chr6:139271745 | T | C | 1 | a0001c0001t0001g0096 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.517-1119A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139271745 | |||||||
chr6:139271991 | C | T | 13 | a0003c0008t0002g0225 a0003c0008t0008g0042 a0003c0008t0008g0172 others(10): Show |
14 | HG01081.hp1 HG01106.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.517-1365G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139271991 | |||||||
chr6:139272029 | C | T | 1 | a0004c0017t0005g0235 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.517-1403G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139272029 | |||||||
chr6:139272188 | T | A | 1 | a0002c0002t0003g0227 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.517-1562A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139272188 | |||||||
chr6:139272271 | C | T | 1 | a0001c0001t0001g0025 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.517-1645G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139272271 | |||||||
chr6:139272272 | G | A | 16 | a0002c0002t0003g0214 a0002c0009t0002g0152 a0004c0006t0005g0236 others(13): Show |
18 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.517-1646C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139272272 | |||||||
chr6:139272384 | G | A | 13 | a0002c0002t0003g0214 a0002c0009t0002g0152 a0004c0006t0005g0236 others(10): Show |
14 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.517-1758C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139272384 | |||||||
chr6:139272617 | C | A | 5 | a0005c0010t0013g0139 a0005c0010t0013g0140 a0005c0010t0014g0141 others(2): Show |
5 | HG02145.hp2 HG02622.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.517-1991G>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139272617 | |||||||
chr6:139272635 | T | C | 71 | a0001c0001t0001g0094 a0001c0001t0001g0211 a0001c0001t0023g0126 others(68): Show |
83 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.517-2009A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139272635 | |||||||
chr6:139272902 | C | T | 13 | a0002c0002t0003g0214 a0002c0009t0002g0152 a0004c0006t0005g0236 others(10): Show |
14 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.517-2276G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139272902 | |||||||
chr6:139272903 | G | A | 18 | a0003c0008t0001g0175 a0003c0008t0002g0160 a0003c0008t0002g0225 others(15): Show |
19 | HG01081.hp1 HG01106.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.517-2277C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139272903 | |||||||
chr6:139273012 | T | C | 13 | a0002c0002t0003g0214 a0002c0009t0002g0152 a0004c0006t0005g0236 others(10): Show |
14 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.517-2386A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139273012 | |||||||
chr6:139273013 | G | A | 13 | a0002c0002t0003g0214 a0002c0009t0002g0152 a0004c0006t0005g0236 others(10): Show |
14 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.517-2387C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139273013 | |||||||
chr6:139273216 | C | G | 14 | a0002c0002t0003g0214 a0002c0009t0002g0152 a0004c0006t0005g0236 others(11): Show |
15 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.517-2590G>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139273216 | |||||||
chr6:139273309 | C | T | 3 | a0002c0002t0003g0214 a0002c0009t0002g0152 a0006c0007t0002g0022 |
4 | HG02559.hp1 HG02615.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-2683G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139273309 | |||||||
chr6:139273353 | T | C | 1 | a0005c0013t0010g0052 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.517-2727A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139273353 | |||||||
chr6:139273403 | A | T | 1 | a0001c0001t0001g0056 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.517-2777T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139273403 | |||||||
chr6:139273454 | T | C | 1 | a0003c0011t0017g0138 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.517-2828A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139273454 | |||||||
chr6:139273554 | C | T | 13 | a0002c0002t0003g0214 a0002c0009t0002g0152 a0004c0006t0005g0236 others(10): Show |
14 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.517-2928G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139273554 | |||||||
chr6:139273595 | GCTGGGA | G | 3 | a0002c0002t0003g0009 a0002c0002t0003g0165 a0002c0002t0003g0188 |
5 | HG01261.hp2 HG01496.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.517-2975_517-2970d others(8): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139273595 | |||||||
chr6:139273626 | A | G | 1 | a0001c0001t0001g0012 | 2 | HG01192.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.517-3000T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139273626 | |||||||
chr6:139274502 | G | T | 1 | a0001c0001t0001g0108 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.516+2328C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139274502 | |||||||
chr6:139274586 | T | A | 1 | a0018c0029t0002g0210 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.516+2244A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139274586 | |||||||
chr6:139274659 | C | G | 10 | a0003c0011t0005g0045 a0003c0011t0017g0138 a0003c0012t0005g0156 others(7): Show |
10 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.516+2171G>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139274659 | |||||||
chr6:139274685 | G | A | 3 | a0005c0013t0010g0052 a0005c0013t0010g0143 a0005c0013t0010g0144 |
3 | HG02135.hp1 NA19004.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.516+2145C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139274685 | |||||||
chr6:139274718 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.516+2112G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139274718 | |||||||
chr6:139274775 | C | T | 14 | a0003c0008t0001g0175 a0003c0008t0002g0225 a0003c0008t0008g0042 others(11): Show |
15 | HG01081.hp1 HG01106.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.516+2055G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139274775 | |||||||
chr6:139274834 | T | C | 1 | a0003c0008t0002g0160 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.516+1996A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139274834 | |||||||
chr6:139274913 | C | T | 23 | a0003c0008t0002g0225 a0003c0008t0008g0042 a0003c0008t0008g0172 others(20): Show |
24 | HG01081.hp1 HG01106.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.516+1917G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139274913 | |||||||
chr6:139275156 | T | C | 1 | a0003c0008t0002g0160 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.516+1674A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139275156 | |||||||
chr6:139275249 | T | A | 1 | a0003c0014t0008g0153 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.516+1581A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139275249 | |||||||
chr6:139275299 | C | A | 1 | a0015c0022t0005g0023 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.516+1531G>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139275299 | |||||||
chr6:139275482 | T | C | 3 | a0001c0001t0001g0013 a0001c0001t0001g0095 a0001c0001t0001g0096 |
4 | NA18960.hp2 NA18995.hp2 NA19059.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+1348A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139275482 | |||||||
chr6:139275547 | T | A | 6 | a0003c0008t0001g0175 a0003c0008t0002g0160 a0003c0031t0021g0222 others(3): Show |
6 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.516+1283A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139275547 | |||||||
chr6:139275644 | G | A | 24 | a0002c0009t0005g0149 a0003c0008t0002g0225 a0003c0008t0008g0042 others(21): Show |
25 | HG01081.hp1 HG01106.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.516+1186C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139275644 | |||||||
chr6:139275872 | C | T | 13 | a0002c0002t0003g0214 a0002c0009t0002g0152 a0004c0006t0005g0236 others(10): Show |
14 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.516+958G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139275872 | |||||||
chr6:139275891 | A | G | 13 | a0002c0002t0003g0214 a0002c0009t0002g0152 a0004c0006t0005g0236 others(10): Show |
14 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.516+939T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139275891 | |||||||
chr6:139276075 | T | C | 1 | a0016c0024t0026g0103 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.516+755A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139276075 | |||||||
chr6:139276127 | A | G | 1 | a0015c0022t0005g0023 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.516+703T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139276127 | |||||||
chr6:139276256 | C | T | 1 | a0002c0009t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.516+574G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139276256 | |||||||
chr6:139276378 | G | A | 34 | a0002c0002t0003g0214 a0002c0009t0002g0152 a0003c0003t0004g0018 others(31): Show |
37 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.516+452C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139276378 | |||||||
chr6:139276455 | T | G | 1 | a0001c0004t0001g0016 | 2 | NA18964.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.516+375A>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139276455 | |||||||
chr6:139276457 | C | T | 3 | a0005c0010t0013g0139 a0005c0010t0013g0140 a0017c0032t0027g0146 |
3 | HG02145.hp2 HG02622.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.516+373G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139276457 | |||||||
chr6:139276460 | G | A | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | HG01496.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.516+370C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139276460 | |||||||
chr6:139276529 | T | C | 18 | a0003c0003t0004g0018 a0003c0003t0004g0019 a0003c0003t0004g0046 others(15): Show |
20 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.516+301A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139276529 | |||||||
chr6:139276654 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.516+176A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139276654 | |||||||
chr6:139276697 | G | A | 3 | a0003c0011t0005g0045 a0004c0006t0005g0233 a0004c0006t0005g0234 |
3 | HG02258.hp2 HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.516+133C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139276697 | |||||||
chr6:139276743 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.516+87C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139276743 | |||||||
chr6:139276752 | G | C | 1 | a0015c0022t0005g0023 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.516+78C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139276752 | |||||||
chr6:139276789 | C | T | 1 | a0002c0002t0002g0187 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.516+41G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139276789 | |||||||
chr6:139276797 | G | A | 1 | a0015c0022t0005g0023 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.516+33C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 3/9 | chr6 | 139276797 | |||||||
chr6:139276924 | TA | T | 140 | a0001c0001t0001g0211 a0001c0001t0023g0126 a0001c0028t0001g0024 others(137): Show |
156 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(153): Show |
splice_region_variant&intron_variant | LOW | c.425-4delT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139276924 | |||||||
chr6:139277182 | A | C | 69 | a0001c0001t0001g0211 a0001c0001t0023g0126 a0002c0002t0001g0173 others(66): Show |
81 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.425-261T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139277182 | |||||||
chr6:139277336 | G | A | 1 | a0002c0002t0003g0209 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.425-415C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139277336 | |||||||
chr6:139277412 | G | A | 30 | a0002c0009t0005g0149 a0003c0008t0001g0175 a0003c0008t0002g0160 others(27): Show |
31 | HG01081.hp1 HG01106.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.425-491C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139277412 | |||||||
chr6:139277434 | T | A | 32 | a0002c0009t0005g0149 a0003c0008t0001g0175 a0003c0008t0002g0160 others(29): Show |
33 | HG01081.hp1 HG01106.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.425-513A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139277434 | |||||||
chr6:139277455 | C | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0104 |
2 | NA19085.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.425-534G>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139277455 | |||||||
chr6:139277548 | T | G | 1 | a0004c0005t0002g0130 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.425-627A>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139277548 | |||||||
chr6:139277723 | TA | T | 26 | a0002c0009t0005g0149 a0003c0008t0002g0225 a0003c0008t0008g0042 others(23): Show |
27 | HG01081.hp1 HG01106.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.425-803delT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139277723 | |||||||
chr6:139277816 | T | C | 3 | a0001c0001t0001g0014 a0001c0001t0001g0124 a0001c0001t0001g0125 |
4 | HG01109.hp1 HG01515.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.425-895A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139277816 | |||||||
chr6:139277909 | C | T | 1 | a0013c0020t0002g0230 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.425-988G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139277909 | |||||||
chr6:139278072 | C | T | 70 | a0001c0001t0001g0211 a0001c0001t0023g0126 a0002c0002t0001g0173 others(67): Show |
82 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.425-1151G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278072 | |||||||
chr6:139278117 | A | G | 47 | a0002c0002t0003g0214 a0002c0009t0002g0152 a0002c0009t0005g0149 others(44): Show |
49 | HG01081.hp1 HG01106.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.425-1196T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278117 | |||||||
chr6:139278193 | A | T | 1 | a0001c0001t0015g0047 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.425-1272T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278193 | |||||||
chr6:139278194 | T | C | 1 | a0004c0005t0002g0131 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.425-1273A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278194 | |||||||
chr6:139278197 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.425-1276A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278197 | |||||||
chr6:139278335 | A | G | 5 | a0001c0028t0001g0024 a0002c0016t0006g0135 a0002c0016t0006g0136 others(2): Show |
5 | HG00558.hp1 HG01243.hp1 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.425-1414T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278335 | |||||||
chr6:139278629 | C | CTG | 60 | a0001c0028t0001g0024 a0002c0002t0003g0214 a0002c0009t0002g0152 others(57): Show |
64 | HG00323.hp2 HG00558.hp1 HG01069.hp1 others(61): Show |
intron_variant | MODIFIER | c.425-1709_425-1708i others(4): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278629 | |||||||
chr6:139278702 | A | G | 1 | a0005c0010t0005g0164 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.425-1781T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278702 | |||||||
chr6:139278713 | A | G | 67 | a0001c0001t0001g0044 a0001c0001t0001g0106 a0001c0001t0001g0118 others(64): Show |
79 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.425-1792T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278713 | |||||||
chr6:139278732 | A | G | 1 | a0003c0008t0001g0175 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.425-1811T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278732 | |||||||
chr6:139278768 | G | A | 2 | a0015c0022t0005g0023 a0016c0024t0026g0103 |
2 | HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.425-1847C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278768 | |||||||
chr6:139278776 | C | T | 1 | a0002c0030t0003g0223 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.425-1855G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278776 | |||||||
chr6:139278780 | C | T | 8 | a0001c0001t0003g0043 a0002c0002t0002g0004 a0002c0002t0002g0226 others(5): Show |
11 | HG01175.hp2 HG01891.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.425-1859G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278780 | |||||||
chr6:139278781 | G | A | 8 | a0003c0008t0008g0042 a0003c0008t0025g0041 a0003c0012t0005g0156 others(5): Show |
8 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.425-1860C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278781 | |||||||
chr6:139278787 | C | T | 8 | a0003c0008t0008g0042 a0003c0008t0025g0041 a0003c0012t0005g0156 others(5): Show |
8 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.425-1866G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278787 | |||||||
chr6:139278816 | C | T | 3 | a0001c0001t0001g0040 a0001c0004t0001g0240 a0008c0034t0001g0241 |
3 | HG01106.hp1 NA18973.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.425-1895G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278816 | |||||||
chr6:139278833 | A | G | 3 | a0001c0001t0001g0039 a0009c0021t0001g0029 a0014c0019t0001g0231 |
3 | HG01261.hp1 HG02717.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.425-1912T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278833 | |||||||
chr6:139278873 | A | G | 8 | a0001c0001t0001g0038 a0001c0028t0001g0024 a0002c0002t0003g0032 others(5): Show |
9 | HG00558.hp1 HG00733.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.425-1952T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278873 | |||||||
chr6:139278884 | G | A | 2 | a0002c0002t0003g0169 a0002c0002t0003g0170 |
2 | HG00735.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.425-1963C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278884 | |||||||
chr6:139278990 | G | A | 73 | a0001c0001t0001g0091 a0001c0001t0001g0211 a0001c0001t0001g0215 others(70): Show |
83 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.425-2069C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139278990 | |||||||
chr6:139279099 | T | C | 3 | a0001c0028t0001g0024 a0002c0016t0006g0135 a0002c0016t0006g0136 |
3 | HG00558.hp1 HG02071.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.425-2178A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139279099 | |||||||
chr6:139279190 | T | C | 66 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0211 others(63): Show |
75 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.425-2269A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139279190 | |||||||
chr6:139279246 | C | T | 1 | a0002c0002t0002g0185 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.425-2325G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139279246 | |||||||
chr6:139279280 | G | A | 24 | a0002c0002t0003g0214 a0002c0009t0002g0147 a0002c0009t0002g0148 others(21): Show |
26 | HG01081.hp1 HG01106.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.425-2359C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139279280 | |||||||
chr6:139279335 | C | G | 74 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(71): Show |
83 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.425-2414G>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139279335 | |||||||
chr6:139279489 | A | T | 19 | a0001c0001t0001g0033 a0001c0001t0001g0120 a0001c0004t0001g0002 others(16): Show |
28 | HG00673.hp1 HG01109.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.425-2568T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139279489 | |||||||
chr6:139279513 | T | A | 1 | a0003c0011t0017g0138 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.425-2592A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139279513 | |||||||
chr6:139279627 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.425-2706G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139279627 | |||||||
chr6:139279743 | C | CA | 29 | a0002c0009t0002g0147 a0002c0009t0002g0148 a0002c0009t0002g0152 others(26): Show |
31 | HG01081.hp1 HG01106.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.425-2823dupT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139279743 | |||||||
chr6:139279849 | G | A | 3 | a0001c0028t0001g0024 a0002c0016t0006g0135 a0002c0016t0006g0136 |
3 | HG00558.hp1 HG02071.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.425-2928C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139279849 | |||||||
chr6:139279878 | T | G | 1 | a0003c0014t0008g0153 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.425-2957A>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139279878 | |||||||
chr6:139279911 | G | A | 1 | a0002c0002t0003g0217 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.425-2990C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139279911 | |||||||
chr6:139279978 | A | G | 11 | a0003c0003t0004g0019 a0003c0003t0004g0171 a0003c0003t0004g0176 others(8): Show |
12 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.425-3057T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139279978 | |||||||
chr6:139279997 | C | T | 1 | a0012c0027t0020g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.425-3076G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139279997 | |||||||
chr6:139279999 | A | G | 94 | a0001c0001t0001g0033 a0001c0001t0001g0120 a0001c0001t0001g0121 others(91): Show |
112 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.425-3078T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139279999 | |||||||
chr6:139280002 | G | A | 2 | a0003c0008t0002g0160 a0005c0010t0005g0164 |
2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.425-3081C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139280002 | |||||||
chr6:139280013 | T | C | 2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | HG01515.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.425-3092A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139280013 | |||||||
chr6:139280068 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.425-3147G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139280068 | |||||||
chr6:139280088 | T | A | 125 | a0001c0001t0001g0033 a0001c0001t0001g0120 a0001c0001t0001g0121 others(122): Show |
146 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(143): Show |
intron_variant | MODIFIER | c.425-3167A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139280088 | |||||||
chr6:139280251 | TA | T | 116 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(113): Show |
144 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.425-3331delT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139280251 | |||||||
chr6:139280266 | A | G | 93 | a0001c0001t0001g0033 a0001c0001t0001g0120 a0001c0001t0001g0121 others(90): Show |
112 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.425-3345T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139280266 | |||||||
chr6:139280268 | A | G | 2 | a0012c0027t0020g0224 a0014c0019t0001g0231 |
2 | HG01891.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.425-3347T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139280268 | |||||||
chr6:139280272 | A | G | 32 | a0001c0028t0001g0024 a0002c0009t0002g0147 a0002c0009t0002g0148 others(29): Show |
34 | HG00558.hp1 HG01081.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.425-3351T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139280272 | |||||||
chr6:139280283 | A | G | 3 | a0002c0002t0003g0145 a0005c0013t0010g0143 a0005c0013t0010g0144 |
3 | HG02135.hp1 HG02165.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.425-3362T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139280283 | |||||||
chr6:139280297 | A | C | 1 | a0003c0011t0017g0138 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.425-3376T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139280297 | |||||||
chr6:139280471 | G | A | 83 | a0001c0001t0001g0033 a0001c0001t0001g0121 a0001c0001t0001g0122 others(80): Show |
100 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.425-3550C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139280471 | |||||||
chr6:139280495 | A | T | 94 | a0001c0001t0001g0033 a0001c0001t0001g0121 a0001c0001t0001g0122 others(91): Show |
112 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.425-3574T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139280495 | |||||||
chr6:139280505 | C | A | 11 | a0001c0001t0001g0120 a0002c0002t0003g0145 a0003c0003t0004g0137 others(8): Show |
12 | HG01109.hp2 HG02135.hp1 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.425-3584G>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139280505 | |||||||
chr6:139280547 | A | AG | 94 | a0001c0001t0001g0033 a0001c0001t0001g0121 a0001c0001t0001g0122 others(91): Show |
112 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.425-3627dupC | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139280547 | |||||||
chr6:139280676 | A | AT | 88 | a0001c0001t0001g0033 a0001c0001t0001g0121 a0001c0001t0001g0122 others(85): Show |
106 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.425-3756dupA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139280676 | |||||||
chr6:139280719 | G | A | 93 | a0001c0001t0001g0033 a0001c0001t0001g0121 a0001c0001t0001g0122 others(90): Show |
111 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.425-3798C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139280719 | |||||||
chr6:139281041 | GATTTATT others(1): Show |
G | 6 | a0003c0011t0017g0138 a0005c0010t0013g0139 a0005c0010t0013g0140 others(3): Show |
6 | HG02145.hp2 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.425-4128_425-4121d others(10): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139281041 | |||||||
chr6:139281058 | T | A | 20 | a0001c0001t0001g0120 a0001c0001t0001g0215 a0002c0002t0002g0004 others(17): Show |
25 | HG00323.hp2 HG00738.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.425-4137A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139281058 | |||||||
chr6:139281066 | T | A | 2 | a0003c0008t0002g0160 a0005c0010t0005g0164 |
2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.425-4145A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139281066 | |||||||
chr6:139281084 | G | T | 2 | a0002c0030t0003g0223 a0003c0031t0021g0222 |
2 | HG01243.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.425-4163C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139281084 | |||||||
chr6:139281180 | T | C | 93 | a0001c0001t0001g0033 a0001c0001t0001g0121 a0001c0001t0001g0122 others(90): Show |
111 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.425-4259A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139281180 | |||||||
chr6:139281198 | A | T | 93 | a0001c0001t0001g0033 a0001c0001t0001g0121 a0001c0001t0001g0122 others(90): Show |
111 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.425-4277T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139281198 | |||||||
chr6:139281251 | C | T | 1 | a0001c0001t0028g0034 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.425-4330G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139281251 | |||||||
chr6:139281302 | T | A | 132 | a0001c0001t0001g0033 a0001c0001t0001g0120 a0001c0001t0001g0121 others(129): Show |
156 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(153): Show |
intron_variant | MODIFIER | c.425-4381A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139281302 | |||||||
chr6:139281330 | C | T | 93 | a0001c0001t0001g0033 a0001c0001t0001g0121 a0001c0001t0001g0122 others(90): Show |
111 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.425-4409G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139281330 | |||||||
chr6:139281398 | G | A | 2 | a0002c0030t0003g0223 a0003c0031t0021g0222 |
2 | HG01243.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.425-4477C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139281398 | |||||||
chr6:139281461 | CTCTTATC others(4543): Show |
C | 62 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(59): Show |
70 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.424+2465_425-4541d others(2): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139281461 | |||||||
chr6:139281495 | G | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0095 a0001c0001t0001g0096 |
4 | NA18960.hp2 NA18995.hp2 NA19059.hp2 others(1): Show |
intron_variant | MODIFIER | c.425-4574C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139281495 | |||||||
chr6:139281530 | TCTGGAGT others(310): Show |
T | 72 | a0001c0001t0001g0120 a0001c0004t0001g0002 a0001c0004t0001g0010 others(69): Show |
88 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.425-4926_425-4610d others(2): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139281530 | |||||||
chr6:139281538 | T | TC | 7 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(4): Show |
7 | HG01255.hp2 NA18959.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.425-4618dupG | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139281538 | |||||||
chr6:139281539 | C | CT | 33 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(30): Show |
34 | HG00597.hp2 HG00738.hp2 HG01358.hp2 others(31): Show |
intron_variant | MODIFIER | c.425-4619dupA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139281539 | |||||||
chr6:139281611 | C | G | 1 | a0001c0001t0028g0034 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.425-4690G>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139281611 | |||||||
chr6:139281999 | C | T | 3 | a0002c0002t0003g0145 a0005c0013t0010g0143 a0005c0013t0010g0144 |
3 | HG02135.hp1 HG02165.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.425-5078G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139281999 | |||||||
chr6:139282053 | T | G | 25 | a0003c0003t0004g0046 a0003c0003t0004g0133 a0003c0003t0004g0134 others(22): Show |
27 | HG01081.hp1 HG01106.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.425-5132A>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139282053 | |||||||
chr6:139282120 | T | C | 54 | a0001c0001t0001g0120 a0001c0004t0001g0002 a0001c0004t0001g0010 others(51): Show |
68 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.425-5199A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139282120 | |||||||
chr6:139282256 | A | G | 54 | a0001c0001t0001g0120 a0001c0004t0001g0002 a0001c0004t0001g0010 others(51): Show |
68 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.425-5335T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139282256 | |||||||
chr6:139282272 | G | A | 6 | a0003c0011t0017g0138 a0005c0010t0013g0139 a0005c0010t0013g0140 others(3): Show |
6 | HG02145.hp2 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.425-5351C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139282272 | |||||||
chr6:139282277 | G | A | 54 | a0001c0001t0001g0120 a0001c0004t0001g0002 a0001c0004t0001g0010 others(51): Show |
68 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.425-5356C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139282277 | |||||||
chr6:139282305 | G | A | 1 | a0002c0002t0007g0011 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.425-5384C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139282305 | |||||||
chr6:139282335 | G | A | 20 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0016 others(17): Show |
28 | HG00673.hp1 HG01884.hp1 HG02040.hp2 others(25): Show |
intron_variant | MODIFIER | c.425-5414C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139282335 | |||||||
chr6:139282337 | G | A | 1 | a0001c0001t0001g0013 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.425-5416C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139282337 | |||||||
chr6:139282502 | G | A | 54 | a0001c0001t0001g0120 a0001c0004t0001g0002 a0001c0004t0001g0010 others(51): Show |
68 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.425-5581C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139282502 | |||||||
chr6:139282607 | G | A | 10 | a0002c0002t0002g0004 a0002c0002t0002g0226 a0002c0002t0002g0228 others(7): Show |
14 | HG01109.hp2 HG02451.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.425-5686C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139282607 | |||||||
chr6:139282766 | G | A | 3 | a0001c0028t0001g0024 a0002c0016t0006g0135 a0002c0016t0006g0136 |
3 | HG00558.hp1 HG02071.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.424+5710C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139282766 | |||||||
chr6:139282787 | A | C | 10 | a0001c0028t0001g0024 a0002c0016t0006g0135 a0002c0016t0006g0136 others(7): Show |
10 | HG00558.hp1 HG01891.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+5689T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139282787 | |||||||
chr6:139282996 | A | G | 1 | a0001c0001t0001g0001 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.424+5480T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139282996 | |||||||
chr6:139283065 | C | T | 54 | a0001c0001t0001g0120 a0001c0004t0001g0002 a0001c0004t0001g0010 others(51): Show |
68 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.424+5411G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139283065 | |||||||
chr6:139283178 | G | A | 2 | a0007c0015t0011g0238 a0007c0015t0011g0239 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.424+5298C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139283178 | |||||||
chr6:139283271 | T | TA | 8 | a0001c0001t0001g0008 a0001c0001t0001g0066 a0001c0001t0001g0086 others(5): Show |
8 | HG00639.hp2 HG00738.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+5204dupT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139283271 | |||||||
chr6:139283271 | TA | T | 28 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0016 others(25): Show |
40 | HG00673.hp1 HG01109.hp2 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.424+5204delT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139283271 | |||||||
chr6:139283271 | TAA | T | 23 | a0001c0001t0001g0120 a0001c0028t0001g0024 a0002c0002t0002g0166 others(20): Show |
25 | HG00558.hp1 HG00735.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.424+5203_424+5204d others(4): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139283271 | |||||||
chr6:139283345 | C | G | 72 | a0001c0001t0001g0120 a0001c0004t0001g0002 a0001c0004t0001g0010 others(69): Show |
88 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.424+5131G>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139283345 | |||||||
chr6:139283367 | G | A | 1 | a0013c0020t0002g0230 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.424+5109C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139283367 | |||||||
chr6:139283490 | C | T | 54 | a0001c0001t0001g0120 a0001c0004t0001g0002 a0001c0004t0001g0010 others(51): Show |
68 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.424+4986G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139283490 | |||||||
chr6:139283525 | G | A | 54 | a0001c0001t0001g0120 a0001c0004t0001g0002 a0001c0004t0001g0010 others(51): Show |
68 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.424+4951C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139283525 | |||||||
chr6:139283528 | A | T | 3 | a0001c0028t0001g0024 a0002c0016t0006g0135 a0002c0016t0006g0136 |
3 | HG00558.hp1 HG02071.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.424+4948T>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139283528 | |||||||
chr6:139283563 | C | T | 14 | a0001c0001t0001g0120 a0002c0002t0002g0004 a0002c0002t0002g0226 others(11): Show |
18 | HG01109.hp2 HG02135.hp1 HG02165.hp2 others(15): Show |
intron_variant | MODIFIER | c.424+4913G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139283563 | |||||||
chr6:139283576 | C | CA | 26 | a0001c0001t0001g0001 a0001c0001t0001g0098 a0001c0001t0001g0119 others(23): Show |
34 | HG00673.hp1 HG01261.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.424+4899dupT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139283576 | |||||||
chr6:139283576 | CA | C | 21 | a0001c0001t0001g0001 a0001c0001t0001g0096 a0001c0001t0001g0114 others(18): Show |
25 | HG01109.hp2 HG01891.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.424+4899delT | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139283576 | |||||||
chr6:139283848 | A | G | 8 | a0002c0002t0002g0166 a0002c0002t0002g0167 a0002c0002t0003g0009 others(5): Show |
10 | HG00735.hp1 HG01070.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+4628T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139283848 | |||||||
chr6:139283967 | A | C | 2 | a0001c0001t0001g0098 a0002c0002t0003g0081 |
2 | HG01943.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.424+4509T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139283967 | |||||||
chr6:139284098 | C | G | 54 | a0001c0001t0001g0120 a0001c0004t0001g0002 a0001c0004t0001g0010 others(51): Show |
68 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.424+4378G>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139284098 | |||||||
chr6:139284119 | A | G | 4 | a0001c0028t0001g0024 a0002c0016t0006g0135 a0002c0016t0006g0136 others(1): Show |
4 | HG00558.hp1 HG01891.hp1 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+4357T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139284119 | |||||||
chr6:139284142 | C | T | 54 | a0001c0001t0001g0120 a0001c0004t0001g0002 a0001c0004t0001g0010 others(51): Show |
68 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.424+4334G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139284142 | |||||||
chr6:139284267 | C | A | 1 | a0001c0001t0001g0007 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.424+4209G>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139284267 | |||||||
chr6:139284444 | C | T | 54 | a0001c0001t0001g0120 a0001c0004t0001g0002 a0001c0004t0001g0010 others(51): Show |
68 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.424+4032G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139284444 | |||||||
chr6:139284459 | T | A | 1 | a0001c0004t0001g0002 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.424+4017A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139284459 | |||||||
chr6:139284485 | G | A | 2 | a0004c0005t0002g0015 a0004c0005t0002g0131 |
2 | HG02615.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.424+3991C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139284485 | |||||||
chr6:139284579 | G | T | 72 | a0001c0001t0001g0120 a0001c0004t0001g0002 a0001c0004t0001g0010 others(69): Show |
88 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.424+3897C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139284579 | |||||||
chr6:139284643 | C | A | 54 | a0001c0001t0001g0120 a0001c0004t0001g0002 a0001c0004t0001g0010 others(51): Show |
68 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.424+3833G>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139284643 | |||||||
chr6:139284762 | C | A | 7 | a0004c0006t0005g0232 a0004c0006t0005g0233 a0004c0006t0005g0234 others(4): Show |
8 | HG02258.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.424+3714G>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139284762 | |||||||
chr6:139284777 | G | A | 1 | a0015c0022t0005g0023 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.424+3699C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139284777 | |||||||
chr6:139284814 | A | G | 1 | a0004c0006t0005g0232 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.424+3662T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139284814 | |||||||
chr6:139284840 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.424+3636G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139284840 | |||||||
chr6:139284922 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.424+3554T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139284922 | |||||||
chr6:139285010 | T | C | 54 | a0001c0001t0001g0120 a0001c0004t0001g0002 a0001c0004t0001g0010 others(51): Show |
68 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.424+3466A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285010 | |||||||
chr6:139285036 | G | A | 74 | a0001c0001t0001g0120 a0001c0004t0001g0002 a0001c0004t0001g0010 others(71): Show |
90 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(87): Show |
intron_variant | MODIFIER | c.424+3440C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285036 | |||||||
chr6:139285093 | C | T | 54 | a0001c0001t0001g0120 a0001c0004t0001g0002 a0001c0004t0001g0010 others(51): Show |
68 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.424+3383G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285093 | |||||||
chr6:139285094 | G | A | 1 | a0001c0001t0001g0008 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.424+3382C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285094 | |||||||
chr6:139285246 | T | A | 1 | a0004c0005t0002g0129 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.424+3230A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285246 | |||||||
chr6:139285257 | A | AAC | 10 | a0001c0001t0001g0001 a0001c0001t0001g0119 a0002c0002t0002g0004 others(7): Show |
10 | HG02055.hp1 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+3217_424+3218d others(4): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285257 | |||||||
chr6:139285257 | A | AACAC | 3 | a0003c0008t0002g0225 a0004c0006t0005g0237 a0004c0017t0005g0235 |
3 | HG02486.hp1 HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.424+3215_424+3218d others(6): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285257 | |||||||
chr6:139285257 | A | AACACAC | 4 | a0002c0002t0003g0145 a0004c0006t0005g0236 a0005c0013t0010g0143 others(1): Show |
4 | HG02109.hp2 HG02135.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+3213_424+3218d others(8): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285257 | |||||||
chr6:139285257 | AAC | A | 19 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0031 others(16): Show |
19 | HG00639.hp2 HG00642.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.424+3217_424+3218d others(4): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285257 | |||||||
chr6:139285257 | AACAC | A | 34 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(31): Show |
36 | HG00558.hp1 HG00673.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.424+3215_424+3218d others(6): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285257 | |||||||
chr6:139285257 | AACACAC | A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(69): Show |
90 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.424+3213_424+3218d others(8): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285257 | |||||||
chr6:139285257 | AACACACA others(1): Show |
A | 14 | a0001c0001t0001g0005 a0001c0001t0001g0040 a0001c0001t0001g0079 others(11): Show |
16 | HG00735.hp1 HG01070.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.424+3211_424+3218d others(10): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285257 | |||||||
chr6:139285257 | AACACACA others(3): Show |
A | 5 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0002c0002t0002g0167 others(2): Show |
5 | HG01884.hp1 HG02976.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+3209_424+3218d others(12): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285257 | |||||||
chr6:139285257 | AACACACA others(5): Show |
A | 17 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0240 others(14): Show |
24 | HG00673.hp1 HG02040.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.424+3207_424+3218d others(14): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285257 | |||||||
chr6:139285257 | AACACACA others(7): Show |
A | 3 | a0001c0001t0001g0120 a0001c0004t0001g0016 a0002c0009t0002g0147 |
4 | HG02647.hp1 HG02970.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+3205_424+3218d others(16): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285257 | |||||||
chr6:139285416 | C | T | 17 | a0004c0005t0002g0015 a0004c0005t0002g0128 a0004c0005t0002g0129 others(14): Show |
19 | HG01081.hp1 HG01106.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.424+3060G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285416 | |||||||
chr6:139285594 | T | C | 54 | a0001c0001t0001g0120 a0001c0004t0001g0002 a0001c0004t0001g0010 others(51): Show |
68 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.424+2882A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285594 | |||||||
chr6:139285706 | C | G | 1 | a0013c0020t0002g0230 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.424+2770G>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285706 | |||||||
chr6:139285717 | G | A | 1 | a0012c0027t0020g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+2759C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285717 | |||||||
chr6:139285809 | C | G | 1 | a0014c0019t0001g0231 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.424+2667G>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285809 | |||||||
chr6:139285818 | C | T | 2 | a0003c0003t0004g0133 a0003c0003t0004g0134 |
2 | HG02109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.424+2658G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285818 | |||||||
chr6:139285833 | C | A | 1 | a0012c0027t0020g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+2643G>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285833 | |||||||
chr6:139285927 | C | T | 5 | a0001c0001t0001g0055 a0001c0001t0001g0076 a0002c0002t0003g0037 others(2): Show |
5 | HG00323.hp1 HG01975.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+2549G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285927 | |||||||
chr6:139285947 | C | T | 17 | a0004c0005t0002g0015 a0004c0005t0002g0128 a0004c0005t0002g0129 others(14): Show |
19 | HG01081.hp1 HG01106.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.424+2529G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285947 | |||||||
chr6:139285999 | T | G | 72 | a0001c0001t0001g0120 a0001c0004t0001g0002 a0001c0004t0001g0010 others(69): Show |
88 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.424+2477A>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139285999 | |||||||
chr6:139286011 | T | C | 14 | a0002c0002t0002g0166 a0002c0002t0003g0009 a0002c0002t0003g0165 others(11): Show |
17 | HG00735.hp1 HG01070.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.424+2465A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139286011 | |||||||
chr6:139286201 | G | C | 1 | a0002c0025t0003g0229 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.424+2275C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139286201 | |||||||
chr6:139286225 | T | C | 116 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(113): Show |
138 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.424+2251A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139286225 | |||||||
chr6:139286264 | C | G | 1 | a0003c0031t0021g0222 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.424+2212G>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139286264 | |||||||
chr6:139286328 | C | T | 4 | a0006c0007t0002g0162 a0006c0007t0002g0163 a0006c0007t0005g0017 others(1): Show |
5 | HG02572.hp2 HG03139.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+2148G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139286328 | |||||||
chr6:139286353 | T | C | 105 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(102): Show |
127 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(124): Show |
intron_variant | MODIFIER | c.424+2123A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139286353 | |||||||
chr6:139286438 | A | G | 2 | a0002c0002t0001g0173 a0002c0002t0001g0174 |
2 | NA18961.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.424+2038T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139286438 | |||||||
chr6:139286489 | A | G | 113 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(110): Show |
135 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.424+1987T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139286489 | |||||||
chr6:139286504 | C | T | 1 | a0002c0002t0003g0032 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.424+1972G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139286504 | |||||||
chr6:139286510 | G | A | 113 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(110): Show |
135 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.424+1966C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139286510 | |||||||
chr6:139286538 | A | G | 114 | a0001c0001t0001g0031 a0001c0001t0001g0120 a0001c0001t0001g0121 others(111): Show |
136 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.424+1938T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139286538 | |||||||
chr6:139286588 | C | A | 62 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(59): Show |
70 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.424+1888G>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139286588 | |||||||
chr6:139286635 | C | T | 1 | a0001c0001t0001g0030 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.424+1841G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139286635 | |||||||
chr6:139286636 | G | A | 20 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0016 others(17): Show |
28 | HG00673.hp1 HG01884.hp1 HG02040.hp2 others(25): Show |
intron_variant | MODIFIER | c.424+1840C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139286636 | |||||||
chr6:139286685 | T | C | 60 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(57): Show |
68 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.424+1791A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139286685 | |||||||
chr6:139286768 | T | A | 1 | a0013c0020t0002g0230 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.424+1708A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139286768 | |||||||
chr6:139286861 | A | G | 113 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(110): Show |
135 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.424+1615T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139286861 | |||||||
chr6:139286932 | T | C | 3 | a0002c0002t0003g0145 a0005c0013t0010g0143 a0005c0013t0010g0144 |
3 | HG02135.hp1 HG02165.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.424+1544A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139286932 | |||||||
chr6:139286992 | G | A | 28 | a0001c0001t0001g0120 a0002c0002t0002g0004 a0002c0002t0002g0226 others(25): Show |
34 | HG01081.hp1 HG01106.hp2 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.424+1484C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139286992 | |||||||
chr6:139287029 | C | T | 30 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0016 others(27): Show |
40 | HG00673.hp1 HG00735.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.424+1447G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139287029 | |||||||
chr6:139287050 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.424+1426G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139287050 | |||||||
chr6:139287742 | T | C | 3 | a0001c0028t0001g0024 a0002c0016t0006g0135 a0002c0016t0006g0136 |
3 | HG00558.hp1 HG02071.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.424+734A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139287742 | |||||||
chr6:139287834 | G | A | 8 | a0001c0028t0001g0024 a0002c0016t0006g0135 a0002c0016t0006g0136 others(5): Show |
8 | HG00558.hp1 HG02071.hp1 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+642C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139287834 | |||||||
chr6:139287875 | G | GT | 113 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(110): Show |
135 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.424+600dupA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139287875 | |||||||
chr6:139287916 | T | C | 134 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(131): Show |
158 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(155): Show |
intron_variant | MODIFIER | c.424+560A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139287916 | |||||||
chr6:139288087 | A | C | 134 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(131): Show |
158 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(155): Show |
intron_variant | MODIFIER | c.424+389T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139288087 | |||||||
chr6:139288258 | G | A | 18 | a0004c0005t0002g0015 a0004c0005t0002g0128 a0004c0005t0002g0129 others(15): Show |
20 | HG01081.hp1 HG01106.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.424+218C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 2/9 | chr6 | 139288258 | |||||||
chr6:139288932 | AGGCTTTA others(43): Show |
A | 1 | a0004c0005t0002g0132 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-14-69_-14-20delCA others(48): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139288932 | |||||||
chr6:139288987 | G | T | 71 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(68): Show |
81 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.-14-74C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139288987 | |||||||
chr6:139289032 | GAGAA | G | 134 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(131): Show |
158 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(155): Show |
intron_variant | MODIFIER | c.-14-123_-14-120del others(4): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139289032 | |||||||
chr6:139289039 | G | T | 134 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(131): Show |
158 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(155): Show |
intron_variant | MODIFIER | c.-14-126C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139289039 | |||||||
chr6:139289040 | C | G | 134 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(131): Show |
158 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(155): Show |
intron_variant | MODIFIER | c.-14-127G>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139289040 | |||||||
chr6:139289334 | CT | C | 71 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(68): Show |
81 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.-14-422delA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139289334 | |||||||
chr6:139289462 | C | T | 1 | a0015c0022t0005g0023 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-14-549G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139289462 | |||||||
chr6:139289525 | G | A | 134 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(131): Show |
158 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(155): Show |
intron_variant | MODIFIER | c.-14-612C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139289525 | |||||||
chr6:139289537 | T | G | 120 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(117): Show |
144 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(141): Show |
intron_variant | MODIFIER | c.-14-624A>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139289537 | |||||||
chr6:139289561 | G | GT | 19 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0016 others(16): Show |
27 | HG00673.hp1 HG01884.hp1 HG02040.hp2 others(24): Show |
intron_variant | MODIFIER | c.-14-649dupA | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139289561 | |||||||
chr6:139289791 | A | C | 120 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(117): Show |
144 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(141): Show |
intron_variant | MODIFIER | c.-14-878T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139289791 | |||||||
chr6:139289811 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-14-898A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139289811 | |||||||
chr6:139289859 | A | G | 134 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(131): Show |
158 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(155): Show |
intron_variant | MODIFIER | c.-14-946T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139289859 | |||||||
chr6:139289966 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-14-1053A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139289966 | |||||||
chr6:139290211 | C | T | 121 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(118): Show |
145 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(142): Show |
intron_variant | MODIFIER | c.-14-1298G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139290211 | |||||||
chr6:139290255 | C | T | 3 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0013c0020t0002g0230 |
3 | HG02109.hp2 NA18939.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.-14-1342G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139290255 | |||||||
chr6:139290317 | C | T | 121 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(118): Show |
145 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(142): Show |
intron_variant | MODIFIER | c.-14-1404G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139290317 | |||||||
chr6:139290337 | G | GCCCCCCC others(40): Show |
1 | a0004c0005t0002g0132 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-14-1425_-14-1424i others(49): Show |
TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139290337 | |||||||
chr6:139290340 | A | G | 1 | a0004c0005t0002g0132 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-14-1427T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139290340 | |||||||
chr6:139290342 | T | C | 1 | a0004c0005t0002g0132 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-14-1429A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139290342 | |||||||
chr6:139290343 | G | C | 1 | a0004c0005t0002g0132 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-14-1430C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139290343 | |||||||
chr6:139290482 | G | C | 5 | a0002c0002t0002g0004 a0002c0002t0002g0226 a0002c0002t0002g0228 others(2): Show |
8 | HG02451.hp1 HG02886.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15+1439C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139290482 | |||||||
chr6:139290500 | T | A | 1 | a0002c0025t0003g0229 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-15+1421A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139290500 | |||||||
chr6:139290552 | G | T | 1 | a0003c0008t0002g0160 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-15+1369C>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139290552 | |||||||
chr6:139290554 | A | G | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | NA18939.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.-15+1367T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139290554 | |||||||
chr6:139290562 | A | G | 13 | a0001c0028t0001g0024 a0002c0002t0003g0145 a0002c0016t0006g0135 others(10): Show |
13 | HG00558.hp1 HG01109.hp2 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.-15+1359T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139290562 | |||||||
chr6:139290606 | A | G | 19 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0016 others(16): Show |
27 | HG00673.hp1 HG01884.hp1 HG02040.hp2 others(24): Show |
intron_variant | MODIFIER | c.-15+1315T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139290606 | |||||||
chr6:139290618 | G | A | 103 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(100): Show |
125 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.-15+1303C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139290618 | |||||||
chr6:139290625 | T | A | 18 | a0004c0005t0002g0015 a0004c0005t0002g0128 a0004c0005t0002g0129 others(15): Show |
20 | HG01081.hp1 HG01106.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-15+1296A>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139290625 | |||||||
chr6:139290633 | G | A | 6 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0016 others(3): Show |
14 | HG00673.hp1 HG02040.hp2 NA18944.hp1 others(11): Show |
intron_variant | MODIFIER | c.-15+1288C>T | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139290633 | |||||||
chr6:139290669 | A | C | 1 | a0001c0004t0001g0016 | 2 | NA18964.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.-15+1252T>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139290669 | |||||||
chr6:139290906 | A | G | 121 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(118): Show |
145 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(142): Show |
intron_variant | MODIFIER | c.-15+1015T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139290906 | |||||||
chr6:139291130 | C | G | 3 | a0001c0028t0001g0024 a0002c0016t0006g0135 a0002c0016t0006g0136 |
3 | HG00558.hp1 HG02071.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.-15+791G>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139291130 | |||||||
chr6:139291184 | G | C | 1 | a0002c0002t0003g0243 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-15+737C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139291184 | |||||||
chr6:139291231 | C | T | 1 | a0015c0022t0005g0023 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-15+690G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139291231 | |||||||
chr6:139291275 | G | C | 121 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(118): Show |
145 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(142): Show |
intron_variant | MODIFIER | c.-15+646C>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139291275 | |||||||
chr6:139291317 | T | C | 2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | HG01515.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.-15+604A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139291317 | |||||||
chr6:139291334 | A | G | 2 | a0003c0003t0004g0133 a0003c0003t0004g0134 |
2 | HG02109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-15+587T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139291334 | |||||||
chr6:139291801 | A | G | 7 | a0004c0005t0002g0015 a0004c0005t0002g0128 a0004c0005t0002g0129 others(4): Show |
8 | HG01081.hp1 HG01106.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15+120T>C | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139291801 | |||||||
chr6:139291871 | C | T | 1 | a0001c0001t0023g0126 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-15+50G>A | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139291871 | |||||||
chr6:139291880 | T | C | 131 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0215 others(128): Show |
155 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(152): Show |
intron_variant | MODIFIER | c.-15+41A>G | TXLNB | ENSG00000164440.15 | transcript | ENST00000358430.8 | protein_coding | 1/9 | chr6 | 139291880 |