Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51599 |
| ensemblid | ENSG00000105699.17 |
| hgncid | 29572 |
| symbol | LSR |
| name | lipolysis stimulated lipoprotein receptor |
| refseq_nuc | NM_205834.4 |
| refseq_prot | NP_991403.2 |
| ensembl_nuc | ENST00000605618.6 |
| ensembl_prot | ENSP00000474797.2 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 35249002 |
| end | 35267964 |
| strand | + |
| ver | v1.2 |
| region | chr19:35249002-35267964 |
| region5000 | chr19:35244002-35272964 |
| regionname0 | LSR_chr19_35249002_35267964 |
| regionname5000 | LSR_chr19_35244002_35272964 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 601 | 189 | 40 | 19 | 118 | 3 | 8 | 92 | LSR_chr19_35244002_35272964 | LSR | MALLA others(596): Show |
chr19 | 35244002 | 35272964 |
| a0002 | 0/1 | 602 | 157 | 45 | 33 | 47 | 8 | 23 | 39 | LSR_chr19_35244002_35272964 | LSR | MALLA others(597): Show |
chr19 | 35244002 | 35272964 |
| a0003 | 0/0 | 602 | 83 | 7 | 23 | 36 | 3 | 14 | 27 | LSR_chr19_35244002_35272964 | LSR | MALLA others(597): Show |
chr19 | 35244002 | 35272964 |
| a0004 | 0/0 | 601 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | MALLA others(596): Show |
chr19 | 35244002 | 35272964 |
| a0005 | 0/0 | 602 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | MALLA others(597): Show |
chr19 | 35244002 | 35272964 |
| a0006 | 0/0 | 602 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | MALLA others(597): Show |
chr19 | 35244002 | 35272964 |
| a0007 | 0/0 | 602 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | MALLA others(597): Show |
chr19 | 35244002 | 35272964 |
| a0008 | 0/0 | 601 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | MALLA others(596): Show |
chr19 | 35244002 | 35272964 |
| a0009 | 0/0 | 601 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LSR_chr19_35244002_35272964 | LSR | MALLA others(596): Show |
chr19 | 35244002 | 35272964 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 1/0 | 1803 | 112 | 31 | 5 | 69 | 2 | 4 | LSR_chr19_35244002_35272964 | LSR | ATGGC others(1798): Show |
chr19 | 35244002 | 35272964 | ||
| a0001c0004 | 0/0 | 1803 | 51 | 2 | 11 | 33 | 1 | 4 | LSR_chr19_35244002_35272964 | LSR | ATGGC others(1798): Show |
chr19 | 35244002 | 35272964 | ||
| a0001c0005 | 0/0 | 1803 | 22 | 6 | 2 | 14 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | ATGGC others(1798): Show |
chr19 | 35244002 | 35272964 | ||
| a0001c0008 | 0/0 | 1803 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | ATGGC others(1798): Show |
chr19 | 35244002 | 35272964 | ||
| a0001c0017 | 0/0 | 1803 | 1 | 0 | 1 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | ATGGC others(1798): Show |
chr19 | 35244002 | 35272964 | ||
| a0001c0020 | 0/0 | 1803 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | ATGGC others(1798): Show |
chr19 | 35244002 | 35272964 | ||
| a0001c0021 | 0/0 | 1803 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | ATGGC others(1798): Show |
chr19 | 35244002 | 35272964 | ||
| a0002c0001 | 0/1 | 1806 | 140 | 29 | 32 | 47 | 8 | 23 | LSR_chr19_35244002_35272964 | LSR | ATGGC others(1801): Show |
chr19 | 35244002 | 35272964 | ||
| a0002c0006 | 0/0 | 1806 | 15 | 15 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | ATGGC others(1801): Show |
chr19 | 35244002 | 35272964 | ||
| a0002c0013 | 0/0 | 1806 | 1 | 0 | 1 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | ATGGC others(1801): Show |
chr19 | 35244002 | 35272964 | ||
| a0002c0014 | 0/0 | 1806 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | ATGGC others(1801): Show |
chr19 | 35244002 | 35272964 | ||
| a0003c0003 | 0/0 | 1806 | 81 | 6 | 22 | 36 | 3 | 14 | LSR_chr19_35244002_35272964 | LSR | ATGGC others(1801): Show |
chr19 | 35244002 | 35272964 | ||
| a0003c0012 | 0/0 | 1806 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | ATGGC others(1801): Show |
chr19 | 35244002 | 35272964 | ||
| a0003c0018 | 0/0 | 1806 | 1 | 0 | 1 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | ATGGC others(1801): Show |
chr19 | 35244002 | 35272964 | ||
| a0004c0007 | 0/0 | 1803 | 3 | 3 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | ATGGC others(1798): Show |
chr19 | 35244002 | 35272964 | ||
| a0005c0010 | 0/0 | 1806 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | ATGGC others(1801): Show |
chr19 | 35244002 | 35272964 | ||
| a0005c0019 | 0/0 | 1806 | 1 | 0 | 1 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | ATGGC others(1801): Show |
chr19 | 35244002 | 35272964 | ||
| a0006c0015 | 0/0 | 1806 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | ATGGC others(1801): Show |
chr19 | 35244002 | 35272964 | ||
| a0007c0009 | 0/0 | 1806 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | ATGGC others(1801): Show |
chr19 | 35244002 | 35272964 | ||
| a0008c0016 | 0/0 | 1803 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | ATGGC others(1798): Show |
chr19 | 35244002 | 35272964 | ||
| a0009c0011 | 0/0 | 1803 | 1 | 0 | 0 | 0 | 0 | 1 | LSR_chr19_35244002_35272964 | LSR | ATGGC others(1798): Show |
chr19 | 35244002 | 35272964 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 1/0 | 1932 | 112 | 31 | 5 | 69 | 2 | 4 | LSR_chr19_35244002_35272964 | LSR | AGACG others(1927): Show |
chr19 | 35244002 | 35272964 |
| a0001c0004t0001 | 0/0 | 1932 | 51 | 2 | 11 | 33 | 1 | 4 | LSR_chr19_35244002_35272964 | LSR | AGACG others(1927): Show |
chr19 | 35244002 | 35272964 |
| a0001c0005t0001 | 0/0 | 1932 | 20 | 6 | 2 | 12 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | AGACG others(1927): Show |
chr19 | 35244002 | 35272964 |
| a0001c0005t0002 | 0/0 | 1932 | 2 | 0 | 0 | 2 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | AGACG others(1927): Show |
chr19 | 35244002 | 35272964 |
| a0001c0008t0001 | 0/0 | 1932 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | AGACG others(1927): Show |
chr19 | 35244002 | 35272964 |
| a0001c0017t0001 | 0/0 | 1932 | 1 | 0 | 1 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | AGACG others(1927): Show |
chr19 | 35244002 | 35272964 |
| a0001c0020t0001 | 0/0 | 1932 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | AGACG others(1927): Show |
chr19 | 35244002 | 35272964 |
| a0001c0021t0001 | 0/0 | 1932 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | AGACG others(1927): Show |
chr19 | 35244002 | 35272964 |
| a0002c0001t0001 | 0/1 | 1935 | 140 | 29 | 32 | 47 | 8 | 23 | LSR_chr19_35244002_35272964 | LSR | AGACG others(1930): Show |
chr19 | 35244002 | 35272964 |
| a0002c0006t0001 | 0/0 | 1935 | 15 | 15 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | AGACG others(1930): Show |
chr19 | 35244002 | 35272964 |
| a0002c0013t0001 | 0/0 | 1935 | 1 | 0 | 1 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | AGACG others(1930): Show |
chr19 | 35244002 | 35272964 |
| a0002c0014t0001 | 0/0 | 1935 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | AGACG others(1930): Show |
chr19 | 35244002 | 35272964 |
| a0003c0003t0001 | 0/0 | 1935 | 80 | 6 | 22 | 35 | 3 | 14 | LSR_chr19_35244002_35272964 | LSR | AGACG others(1930): Show |
chr19 | 35244002 | 35272964 |
| a0003c0003t0003 | 0/0 | 1935 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | AGACG others(1930): Show |
chr19 | 35244002 | 35272964 |
| a0003c0012t0001 | 0/0 | 1935 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | AGACG others(1930): Show |
chr19 | 35244002 | 35272964 |
| a0003c0018t0001 | 0/0 | 1935 | 1 | 0 | 1 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | AGACG others(1930): Show |
chr19 | 35244002 | 35272964 |
| a0004c0007t0001 | 0/0 | 1932 | 3 | 3 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | AGACG others(1927): Show |
chr19 | 35244002 | 35272964 |
| a0005c0010t0001 | 0/0 | 1935 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | AGACG others(1930): Show |
chr19 | 35244002 | 35272964 |
| a0005c0019t0001 | 0/0 | 1935 | 1 | 0 | 1 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | AGACG others(1930): Show |
chr19 | 35244002 | 35272964 |
| a0006c0015t0001 | 0/0 | 1935 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | AGACG others(1930): Show |
chr19 | 35244002 | 35272964 |
| a0007c0009t0001 | 0/0 | 1935 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | AGACG others(1930): Show |
chr19 | 35244002 | 35272964 |
| a0008c0016t0001 | 0/0 | 1932 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | AGACG others(1927): Show |
chr19 | 35244002 | 35272964 |
| a0009c0011t0001 | 0/0 | 1932 | 1 | 0 | 0 | 0 | 0 | 1 | LSR_chr19_35244002_35272964 | LSR | AGACG others(1927): Show |
chr19 | 35244002 | 35272964 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0003 | 1/0 | 22 | 0 | 1 | 18 | 0 | 2 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0004 | 0/0 | 21 | 7 | 1 | 13 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0015 | 0/0 | 4 | 1 | 0 | 2 | 0 | 1 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0004t0001g0002 | 0/0 | 26 | 0 | 5 | 18 | 1 | 2 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0004t0001g0010 | 0/0 | 9 | 0 | 3 | 5 | 0 | 1 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0004t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0004t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0004t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0004t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0004t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0004t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0004t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0004t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0004t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0004t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0004t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0004t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0004t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0004t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0004t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0005t0001g0008 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0005t0001g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0005t0001g0027 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0005t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0005t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0005t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0005t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0005t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0005t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0005t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0005t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0008t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0017t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0020t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0001c0021t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0001 | 0/0 | 33 | 3 | 6 | 21 | 1 | 2 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0006 | 0/0 | 11 | 2 | 1 | 3 | 1 | 4 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0007 | 0/0 | 10 | 3 | 4 | 3 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0013 | 0/0 | 5 | 0 | 2 | 0 | 1 | 2 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0016 | 0/0 | 4 | 1 | 2 | 0 | 0 | 1 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0018 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0019 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0025 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0035 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0042 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0196 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0006t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0006t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0006t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0006t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0006t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0006t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0006t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0006t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0006t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0006t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0013t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0002c0014t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0005 | 0/0 | 13 | 0 | 6 | 4 | 0 | 3 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0009 | 0/0 | 10 | 0 | 4 | 6 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0014 | 0/0 | 5 | 0 | 2 | 0 | 2 | 1 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0024 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0046 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0003t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0012t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0003c0018t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0004c0007t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0004c0007t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0004c0007t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0005c0010t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0005c0019t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0006c0015t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0007c0009t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0008c0016t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| a0009c0011t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0003 | t0001 | g0014 | EUR | GBR | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG00099 | hp2 | a0002 | c0001 | t0001 | g0006 | EUR | GBR | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG00140 | hp1 | a0001 | c0004 | t0001 | g0002 | EUR | GBR | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0034 | EUR | GBR | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG00280 | hp1 | a0002 | c0001 | t0001 | g0001 | EUR | FIN | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0091 | EUR | FIN | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG00408 | hp1 | a0003 | c0003 | t0001 | g0012 | EAS | CHS | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | CHS | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG00423 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | CHS | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG00423 | hp2 | a0001 | c0005 | t0001 | g0008 | EAS | CHS | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG00438 | hp1 | a0002 | c0001 | t0001 | g0036 | EAS | CHS | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | CHS | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG00544 | hp1 | a0002 | c0001 | t0001 | g0054 | EAS | CHS | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG00544 | hp2 | a0003 | c0003 | t0001 | g0023 | EAS | CHS | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG00558 | hp1 | a0001 | c0005 | t0001 | g0008 | EAS | CHS | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG00558 | hp2 | a0001 | c0004 | t0001 | g0002 | EAS | CHS | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG00621 | hp1 | a0003 | c0003 | t0001 | g0147 | EAS | CHS | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG00621 | hp2 | a0002 | c0001 | t0001 | g0100 | EAS | CHS | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG00639 | hp1 | a0003 | c0003 | t0001 | g0014 | AMR | PUR | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG00639 | hp2 | a0002 | c0001 | t0001 | g0042 | AMR | PUR | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG00642 | hp1 | a0002 | c0001 | t0001 | g0131 | AMR | PUR | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG00642 | hp2 | a0001 | c0005 | t0001 | g0026 | AMR | PUR | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG00673 | hp1 | a0001 | c0005 | t0001 | g0187 | EAS | CHS | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG00673 | hp2 | a0001 | c0004 | t0001 | g0002 | EAS | CHS | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG00733 | hp1 | a0002 | c0001 | t0001 | g0037 | AMR | PUR | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG00733 | hp2 | a0001 | c0004 | t0001 | g0002 | AMR | PUR | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG00735 | hp1 | a0001 | c0005 | t0001 | g0027 | AMR | PUR | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG00735 | hp2 | a0003 | c0003 | t0001 | g0206 | AMR | PUR | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG00738 | hp1 | a0002 | c0001 | t0001 | g0007 | AMR | PUR | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG00738 | hp2 | a0002 | c0013 | t0001 | g0019 | AMR | PUR | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG00741 | hp1 | a0002 | c0001 | t0001 | g0106 | AMR | PUR | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG00741 | hp2 | a0002 | c0001 | t0001 | g0001 | AMR | PUR | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01070 | hp1 | a0001 | c0004 | t0001 | g0163 | AMR | PUR | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01070 | hp2 | a0003 | c0003 | t0001 | g0140 | AMR | PUR | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01081 | hp1 | a0003 | c0003 | t0001 | g0024 | AMR | PUR | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01081 | hp2 | a0003 | c0003 | t0001 | g0145 | AMR | PUR | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01099 | hp1 | a0002 | c0001 | t0001 | g0016 | AMR | PUR | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01099 | hp2 | a0002 | c0001 | t0001 | g0112 | AMR | PUR | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01106 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | PUR | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01106 | hp2 | a0002 | c0001 | t0001 | g0006 | AMR | PUR | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0125 | AMR | PUR | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01109 | hp2 | a0002 | c0001 | t0001 | g0103 | AMR | PUR | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01167 | hp1 | a0003 | c0003 | t0001 | g0005 | AMR | PUR | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01167 | hp2 | a0002 | c0001 | t0001 | g0013 | AMR | PUR | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01169 | hp1 | a0002 | c0001 | t0001 | g0102 | AMR | PUR | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01169 | hp2 | a0003 | c0003 | t0001 | g0005 | AMR | PUR | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01175 | hp1 | a0001 | c0017 | t0001 | g0073 | AMR | PUR | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01175 | hp2 | a0002 | c0001 | t0001 | g0178 | AMR | PUR | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01192 | hp1 | a0003 | c0003 | t0001 | g0014 | AMR | PUR | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01192 | hp2 | a0002 | c0001 | t0001 | g0118 | AMR | PUR | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01243 | hp2 | a0002 | c0001 | t0001 | g0098 | AMR | PUR | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01256 | hp1 | a0003 | c0003 | t0001 | g0024 | AMR | CLM | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01256 | hp2 | a0003 | c0003 | t0001 | g0009 | AMR | CLM | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0097 | AMR | CLM | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01257 | hp2 | a0001 | c0004 | t0001 | g0010 | AMR | CLM | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01258 | hp1 | a0003 | c0003 | t0001 | g0024 | AMR | CLM | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01258 | hp2 | a0001 | c0004 | t0001 | g0010 | AMR | CLM | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01261 | hp1 | a0003 | c0003 | t0001 | g0005 | AMR | CLM | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01261 | hp2 | a0001 | c0004 | t0001 | g0002 | AMR | CLM | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01346 | hp1 | a0003 | c0003 | t0001 | g0005 | AMR | CLM | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01346 | hp2 | a0002 | c0001 | t0001 | g0057 | AMR | CLM | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01358 | hp1 | a0003 | c0003 | t0001 | g0009 | AMR | CLM | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01358 | hp2 | a0002 | c0001 | t0001 | g0013 | AMR | CLM | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01361 | hp1 | a0002 | c0001 | t0001 | g0025 | AMR | CLM | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01361 | hp2 | a0003 | c0018 | t0001 | g0136 | AMR | CLM | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01433 | hp1 | a0002 | c0001 | t0001 | g0115 | AMR | CLM | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01433 | hp2 | a0002 | c0001 | t0001 | g0007 | AMR | CLM | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0034 | AMR | CLM | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01496 | hp2 | a0002 | c0001 | t0001 | g0001 | AMR | CLM | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01516 | hp1 | a0003 | c0003 | t0001 | g0157 | EUR | IBS | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01516 | hp2 | a0002 | c0001 | t0001 | g0038 | EUR | IBS | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01517 | hp1 | a0002 | c0001 | t0001 | g0038 | EUR | IBS | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01517 | hp2 | a0002 | c0001 | t0001 | g0108 | EUR | IBS | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01884 | hp1 | a0002 | c0001 | t0001 | g0052 | AFR | ACB | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01884 | hp2 | a0002 | c0006 | t0001 | g0096 | AFR | ACB | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01891 | hp1 | a0002 | c0006 | t0001 | g0077 | AFR | ACB | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0032 | AFR | ACB | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01928 | hp1 | a0003 | c0003 | t0001 | g0150 | AMR | PEL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01928 | hp2 | a0003 | c0003 | t0001 | g0160 | AMR | PEL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01934 | hp1 | a0003 | c0003 | t0001 | g0009 | AMR | PEL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01934 | hp2 | a0001 | c0004 | t0001 | g0002 | AMR | PEL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01943 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | PEL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01943 | hp2 | a0001 | c0004 | t0001 | g0002 | AMR | PEL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01952 | hp1 | a0003 | c0003 | t0001 | g0009 | AMR | PEL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01952 | hp2 | a0001 | c0004 | t0001 | g0166 | AMR | PEL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01975 | hp1 | a0003 | c0003 | t0001 | g0005 | AMR | PEL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01975 | hp2 | a0002 | c0001 | t0001 | g0001 | AMR | PEL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01978 | hp1 | a0002 | c0001 | t0001 | g0018 | AMR | PEL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01978 | hp2 | a0002 | c0001 | t0001 | g0192 | AMR | PEL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01981 | hp1 | a0002 | c0001 | t0001 | g0007 | AMR | PEL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01981 | hp2 | a0003 | c0003 | t0001 | g0155 | AMR | PEL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01993 | hp1 | a0003 | c0003 | t0001 | g0005 | AMR | PEL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01993 | hp2 | a0002 | c0001 | t0001 | g0001 | AMR | PEL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02004 | hp1 | a0005 | c0019 | t0001 | g0007 | AMR | PEL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02004 | hp2 | a0001 | c0004 | t0001 | g0002 | AMR | PEL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02015 | hp1 | a0003 | c0003 | t0001 | g0009 | EAS | KHV | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02015 | hp2 | a0003 | c0003 | t0001 | g0137 | EAS | KHV | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | KHV | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02027 | hp2 | a0001 | c0004 | t0001 | g0002 | EAS | KHV | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02040 | hp2 | a0002 | c0001 | t0001 | g0109 | EAS | KHV | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0041 | AFR | ACB | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0031 | AFR | ACB | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02056 | hp1 | a0001 | c0008 | t0001 | g0011 | EAS | KHV | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02056 | hp2 | a0003 | c0003 | t0001 | g0045 | EAS | KHV | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02071 | hp1 | a0001 | c0004 | t0001 | g0164 | EAS | KHV | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02080 | hp1 | a0002 | c0001 | t0001 | g0036 | EAS | KHV | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02080 | hp2 | a0001 | c0004 | t0001 | g0175 | EAS | KHV | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02083 | hp1 | a0002 | c0001 | t0001 | g0201 | EAS | KHV | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | KHV | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | KHV | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02129 | hp2 | a0002 | c0001 | t0001 | g0054 | EAS | KHV | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02132 | hp2 | a0001 | c0005 | t0001 | g0182 | EAS | KHV | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02135 | hp1 | a0006 | c0015 | t0001 | g0012 | EAS | KHV | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | ACB | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02145 | hp2 | a0003 | c0003 | t0001 | g0047 | AFR | ACB | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02148 | hp1 | a0002 | c0001 | t0001 | g0110 | AMR | PEL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02148 | hp2 | a0001 | c0004 | t0001 | g0010 | AMR | PEL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | CDX | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02155 | hp2 | a0003 | c0003 | t0001 | g0009 | EAS | CDX | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | CDX | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | CDX | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02257 | hp1 | a0007 | c0009 | t0001 | g0060 | AFR | ACB | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02257 | hp2 | a0003 | c0003 | t0001 | g0148 | AFR | ACB | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02258 | hp1 | a0002 | c0001 | t0001 | g0107 | AFR | ACB | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02258 | hp2 | a0002 | c0001 | t0001 | g0051 | AFR | ACB | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | ACB | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0126 | AFR | ACB | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02293 | hp1 | a0002 | c0001 | t0001 | g0007 | AMR | PEL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02293 | hp2 | a0003 | c0003 | t0001 | g0046 | AMR | PEL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02300 | hp1 | a0001 | c0004 | t0001 | g0168 | AMR | PEL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02300 | hp2 | a0002 | c0001 | t0001 | g0193 | AMR | PEL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02451 | hp1 | a0004 | c0007 | t0001 | g0061 | AFR | ACB | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02451 | hp2 | a0002 | c0006 | t0001 | g0064 | AFR | ACB | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02523 | hp1 | a0001 | c0004 | t0001 | g0173 | EAS | KHV | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02523 | hp2 | a0003 | c0003 | t0001 | g0161 | EAS | KHV | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | GWD | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02572 | hp2 | a0003 | c0003 | t0001 | g0129 | AFR | GWD | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02602 | hp1 | a0002 | c0001 | t0001 | g0001 | SAS | PJL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02602 | hp2 | a0003 | c0003 | t0001 | g0014 | SAS | PJL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02615 | hp1 | a0002 | c0001 | t0001 | g0165 | AFR | GWD | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0022 | AFR | GWD | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02622 | hp1 | a0002 | c0001 | t0001 | g0181 | AFR | GWD | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02622 | hp2 | a0002 | c0006 | t0001 | g0121 | AFR | GWD | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | GWD | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0022 | AFR | GWD | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0003 | SAS | PJL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02683 | hp2 | a0002 | c0001 | t0001 | g0025 | SAS | PJL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02698 | hp1 | a0002 | c0001 | t0001 | g0037 | SAS | PJL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02698 | hp2 | a0003 | c0003 | t0001 | g0133 | SAS | PJL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02717 | hp1 | a0002 | c0006 | t0001 | g0021 | AFR | GWD | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02717 | hp2 | a0002 | c0001 | t0001 | g0099 | AFR | GWD | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02723 | hp1 | a0002 | c0001 | t0001 | g0189 | AFR | GWD | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | GWD | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02738 | hp1 | a0002 | c0001 | t0001 | g0019 | SAS | PJL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02738 | hp2 | a0003 | c0003 | t0001 | g0134 | SAS | PJL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02809 | hp1 | a0001 | c0005 | t0001 | g0027 | AFR | GWD | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02809 | hp2 | a0002 | c0001 | t0001 | g0190 | AFR | GWD | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02818 | hp1 | a0002 | c0014 | t0001 | g0176 | AFR | GWD | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0040 | AFR | GWD | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02886 | hp1 | a0002 | c0001 | t0001 | g0105 | AFR | GWD | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02886 | hp2 | a0001 | c0020 | t0001 | g0026 | AFR | GWD | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02895 | hp1 | a0003 | c0003 | t0001 | g0153 | AFR | GWD | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02895 | hp2 | a0002 | c0001 | t0001 | g0001 | AFR | GWD | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02896 | hp1 | a0002 | c0006 | t0001 | g0048 | AFR | GWD | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02896 | hp2 | a0002 | c0001 | t0001 | g0114 | AFR | GWD | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02897 | hp1 | a0002 | c0006 | t0001 | g0048 | AFR | GWD | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02897 | hp2 | a0003 | c0003 | t0001 | g0158 | AFR | GWD | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02922 | hp1 | a0002 | c0001 | t0001 | g0007 | AFR | ESN | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02922 | hp2 | a0002 | c0006 | t0001 | g0020 | AFR | ESN | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02965 | hp1 | a0008 | c0016 | t0001 | g0031 | AFR | ESN | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | ESN | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | ESN | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0041 | AFR | ESN | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02976 | hp1 | a0002 | c0006 | t0001 | g0062 | AFR | ESN | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02976 | hp2 | a0002 | c0001 | t0001 | g0006 | AFR | ESN | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03017 | hp1 | a0002 | c0001 | t0001 | g0016 | SAS | PJL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03017 | hp2 | a0002 | c0001 | t0001 | g0013 | SAS | PJL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03041 | hp1 | a0001 | c0005 | t0001 | g0027 | AFR | GWD | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0040 | AFR | GWD | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03098 | hp1 | a0002 | c0001 | t0001 | g0053 | AFR | MSL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03098 | hp2 | a0002 | c0006 | t0001 | g0021 | AFR | MSL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03130 | hp1 | a0002 | c0001 | t0001 | g0051 | AFR | ESN | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03130 | hp2 | a0002 | c0001 | t0001 | g0007 | AFR | ESN | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0032 | AFR | ESN | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | ESN | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03195 | hp1 | a0001 | c0005 | t0001 | g0184 | AFR | ESN | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03195 | hp2 | a0004 | c0007 | t0001 | g0058 | AFR | ESN | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03209 | hp1 | a0003 | c0003 | t0001 | g0047 | AFR | MSL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | MSL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0022 | AFR | MSL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03225 | hp2 | a0001 | c0005 | t0001 | g0186 | AFR | MSL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03239 | hp1 | a0002 | c0001 | t0001 | g0001 | SAS | PJL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03239 | hp2 | a0002 | c0001 | t0001 | g0006 | SAS | PJL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03453 | hp1 | a0002 | c0001 | t0001 | g0050 | AFR | MSL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03453 | hp2 | a0002 | c0006 | t0001 | g0020 | AFR | MSL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03486 | hp1 | a0002 | c0006 | t0001 | g0119 | AFR | MSL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0074 | AFR | MSL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03490 | hp1 | a0003 | c0003 | t0001 | g0005 | SAS | PJL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03490 | hp2 | a0002 | c0001 | t0001 | g0039 | SAS | PJL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03491 | hp1 | a0003 | c0003 | t0001 | g0142 | SAS | PJL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03491 | hp2 | a0002 | c0001 | t0001 | g0203 | SAS | PJL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03492 | hp1 | a0002 | c0001 | t0001 | g0200 | SAS | PJL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03492 | hp2 | a0002 | c0001 | t0001 | g0039 | SAS | PJL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03516 | hp1 | a0004 | c0007 | t0001 | g0059 | AFR | ESN | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0015 | AFR | ESN | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03540 | hp1 | a0005 | c0010 | t0001 | g0122 | AFR | GWD | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03540 | hp2 | a0002 | c0001 | t0001 | g0188 | AFR | GWD | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03579 | hp1 | a0002 | c0006 | t0001 | g0120 | AFR | MSL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | MSL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03654 | hp1 | a0002 | c0001 | t0001 | g0025 | SAS | PJL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03654 | hp2 | a0003 | c0003 | t0001 | g0144 | SAS | PJL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0003 | SAS | PJL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03669 | hp2 | a0002 | c0001 | t0001 | g0180 | SAS | PJL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03688 | hp1 | a0002 | c0001 | t0001 | g0006 | SAS | STU | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03688 | hp2 | a0009 | c0011 | t0001 | g0010 | SAS | STU | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03704 | hp1 | a0002 | c0001 | t0001 | g0006 | SAS | PJL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03704 | hp2 | a0003 | c0003 | t0001 | g0138 | SAS | PJL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03710 | hp1 | a0002 | c0001 | t0001 | g0013 | SAS | PJL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03710 | hp2 | a0003 | c0003 | t0001 | g0005 | SAS | PJL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03834 | hp1 | a0003 | c0003 | t0001 | g0159 | SAS | BEB | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03834 | hp2 | a0003 | c0003 | t0001 | g0135 | SAS | BEB | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03927 | hp1 | a0002 | c0001 | t0001 | g0177 | SAS | BEB | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03927 | hp2 | a0002 | c0001 | t0001 | g0101 | SAS | BEB | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0130 | SAS | BEB | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03942 | hp2 | a0001 | c0004 | t0001 | g0172 | SAS | BEB | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG04115 | hp1 | a0001 | c0004 | t0001 | g0002 | SAS | STU | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG04115 | hp2 | a0003 | c0003 | t0001 | g0005 | SAS | STU | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG04184 | hp1 | a0003 | c0003 | t0001 | g0149 | SAS | BEB | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG04184 | hp2 | a0002 | c0001 | t0001 | g0063 | SAS | BEB | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG04199 | hp1 | a0002 | c0001 | t0001 | g0035 | SAS | STU | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG04199 | hp2 | a0003 | c0003 | t0001 | g0143 | SAS | STU | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG04204 | hp1 | a0001 | c0004 | t0001 | g0010 | SAS | STU | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG04204 | hp2 | a0002 | c0001 | t0001 | g0179 | SAS | STU | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG04228 | hp1 | a0001 | c0004 | t0001 | g0002 | SAS | STU | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0015 | SAS | STU | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18522 | hp1 | a0002 | c0001 | t0001 | g0052 | AFR | YRI | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18522 | hp2 | a0002 | c0001 | t0001 | g0050 | AFR | YRI | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | CHB | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18612 | hp2 | a0001 | c0004 | t0001 | g0010 | EAS | CHB | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18747 | hp1 | a0003 | c0003 | t0001 | g0044 | EAS | CHB | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | CHB | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18906 | hp1 | a0002 | c0001 | t0001 | g0001 | AFR | YRI | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18906 | hp2 | a0001 | c0004 | t0001 | g0113 | AFR | YRI | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18939 | hp1 | a0002 | c0001 | t0001 | g0018 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18939 | hp2 | a0003 | c0003 | t0001 | g0044 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18943 | hp1 | a0003 | c0003 | t0001 | g0012 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18946 | hp2 | a0002 | c0001 | t0001 | g0006 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18947 | hp1 | a0001 | c0005 | t0001 | g0008 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18947 | hp2 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18948 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18949 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18949 | hp2 | a0001 | c0004 | t0001 | g0169 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18950 | hp2 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18951 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18952 | hp1 | a0003 | c0003 | t0001 | g0023 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18952 | hp2 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18953 | hp2 | a0001 | c0004 | t0001 | g0010 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18954 | hp2 | a0002 | c0001 | t0001 | g0007 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18956 | hp2 | a0003 | c0003 | t0001 | g0154 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18957 | hp1 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18957 | hp2 | a0001 | c0005 | t0001 | g0183 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18960 | hp2 | a0003 | c0003 | t0001 | g0005 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18961 | hp1 | a0002 | c0001 | t0001 | g0018 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18962 | hp1 | a0001 | c0004 | t0001 | g0010 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18963 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18964 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18966 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18967 | hp1 | a0003 | c0003 | t0001 | g0005 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18967 | hp2 | a0001 | c0004 | t0001 | g0010 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18968 | hp1 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18969 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18970 | hp2 | a0003 | c0003 | t0001 | g0005 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18971 | hp1 | a0001 | c0005 | t0001 | g0008 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18971 | hp2 | a0003 | c0003 | t0001 | g0023 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18972 | hp1 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18974 | hp1 | a0002 | c0001 | t0001 | g0006 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18974 | hp2 | a0002 | c0001 | t0001 | g0116 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18975 | hp2 | a0002 | c0001 | t0001 | g0007 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18977 | hp1 | a0001 | c0005 | t0001 | g0008 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18978 | hp1 | a0002 | c0001 | t0001 | g0199 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18983 | hp1 | a0003 | c0003 | t0001 | g0012 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18983 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18984 | hp2 | a0003 | c0003 | t0001 | g0045 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18985 | hp1 | a0003 | c0003 | t0001 | g0146 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18986 | hp1 | a0002 | c0001 | t0001 | g0198 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18986 | hp2 | a0003 | c0003 | t0001 | g0139 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18987 | hp2 | a0002 | c0001 | t0001 | g0111 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18990 | hp1 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18990 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18991 | hp2 | a0003 | c0003 | t0003 | g0151 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18992 | hp1 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18992 | hp2 | a0002 | c0001 | t0001 | g0204 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18993 | hp1 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18994 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18994 | hp2 | a0001 | c0005 | t0001 | g0195 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18995 | hp1 | a0003 | c0003 | t0001 | g0012 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18997 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18997 | hp2 | a0002 | c0001 | t0001 | g0202 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18998 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18998 | hp2 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18999 | hp1 | a0001 | c0005 | t0001 | g0008 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18999 | hp2 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19000 | hp1 | a0001 | c0005 | t0002 | g0008 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19000 | hp2 | a0003 | c0003 | t0001 | g0046 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19001 | hp1 | a0001 | c0004 | t0001 | g0171 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19001 | hp2 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19003 | hp1 | a0002 | c0001 | t0001 | g0055 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19003 | hp2 | a0003 | c0003 | t0001 | g0005 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19005 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19007 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19009 | hp2 | a0001 | c0004 | t0001 | g0167 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19010 | hp1 | a0003 | c0003 | t0001 | g0012 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19011 | hp1 | a0003 | c0003 | t0001 | g0162 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19011 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0070 | AFR | LWK | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0075 | AFR | LWK | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19043 | hp1 | a0002 | c0006 | t0001 | g0021 | AFR | LWK | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19043 | hp2 | a0002 | c0001 | t0001 | g0007 | AFR | LWK | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19054 | hp1 | a0002 | c0001 | t0001 | g0104 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19054 | hp2 | a0001 | c0004 | t0001 | g0049 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19056 | hp2 | a0002 | c0001 | t0001 | g0006 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19057 | hp1 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19057 | hp2 | a0002 | c0001 | t0001 | g0042 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19058 | hp2 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19059 | hp1 | a0003 | c0003 | t0001 | g0043 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19059 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19060 | hp1 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19060 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19063 | hp1 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19064 | hp2 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19065 | hp1 | a0001 | c0004 | t0001 | g0049 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19065 | hp2 | a0001 | c0005 | t0002 | g0008 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19068 | hp1 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19068 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19070 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19070 | hp2 | a0002 | c0001 | t0001 | g0056 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19074 | hp2 | a0001 | c0005 | t0001 | g0008 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19077 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19077 | hp2 | a0003 | c0003 | t0001 | g0141 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19078 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19078 | hp2 | a0001 | c0004 | t0001 | g0174 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19080 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19081 | hp1 | a0002 | c0001 | t0001 | g0055 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19081 | hp2 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19082 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19085 | hp1 | a0001 | c0004 | t0001 | g0010 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19085 | hp2 | a0001 | c0021 | t0001 | g0008 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19086 | hp1 | a0001 | c0004 | t0001 | g0170 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19086 | hp2 | a0003 | c0003 | t0001 | g0152 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19088 | hp1 | a0001 | c0005 | t0001 | g0008 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19091 | hp1 | a0003 | c0003 | t0001 | g0043 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19091 | hp2 | a0002 | c0001 | t0001 | g0007 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0124 | AFR | YRI | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0076 | AFR | YRI | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA20129 | hp1 | a0002 | c0001 | t0001 | g0016 | AFR | ASW | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA20129 | hp2 | a0003 | c0012 | t0001 | g0197 | AFR | ASW | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA20752 | hp1 | a0002 | c0001 | t0001 | g0194 | EUR | TSI | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA20752 | hp2 | a0002 | c0001 | t0001 | g0117 | EUR | TSI | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA20805 | hp1 | a0003 | c0003 | t0001 | g0014 | EUR | TSI | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA20805 | hp2 | a0002 | c0001 | t0001 | g0013 | EUR | TSI | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA20905 | hp1 | a0002 | c0001 | t0001 | g0006 | SAS | GIH | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA20905 | hp2 | a0003 | c0003 | t0001 | g0132 | SAS | GIH | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01123 | hp1 | a0002 | c0001 | t0001 | g0016 | AMR | CLM | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02109 | hp1 | a0001 | c0005 | t0001 | g0185 | AFR | ACB | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0123 | AFR | ACB | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02486 | hp1 | a0002 | c0001 | t0001 | g0035 | AFR | ACB | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0071 | AFR | ACB | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0128 | AFR | ACB | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG02559 | hp2 | a0002 | c0001 | t0001 | g0019 | AFR | ACB | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03471 | hp1 | a0001 | c0005 | t0001 | g0026 | AFR | MSL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0127 | AFR | MSL | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG06807 | hp1 | a0002 | c0006 | t0001 | g0020 | AFR | USA | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| HG06807 | hp2 | a0002 | c0001 | t0001 | g0001 | AFR | USA | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18955 | hp1 | a0003 | c0003 | t0001 | g0156 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA20300 | hp1 | a0002 | c0001 | t0001 | g0053 | AFR | USA | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA20300 | hp2 | a0001 | c0004 | t0001 | g0191 | AFR | USA | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA21309 | hp1 | a0002 | c0001 | t0001 | g0205 | AFR | LWK | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| NA21309 | hp2 | a0002 | c0001 | t0001 | g0006 | AFR | LWK | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| homoSapiens | chm13v2 | a0002 | c0001 | t0001 | g0196 | REF | REF | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0003 | REF | REF | LSR_chr19_35244002_35272964 | LSR | chr19 | 35244002 | 35272964 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:35250465 | G | C | 1 | a0007 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.260G>C | p.Arg87Pro | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/10 | 281/1932 | 260/1806 | 87/601 | chr19 | 35250465 | |||
| chr19:35250476 | G | A | 1 | a0005 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.271G>A | p.Ala91Thr | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/10 | 292/1932 | 271/1806 | 91/601 | chr19 | 35250476 | |||
| chr19:35250477 | C | G | 1 | a0005 | 1 | HG02004.hp1 | missense_variant | MODERATE | c.272C>G | p.Ala91Gly | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/10 | 293/1932 | 272/1806 | 91/601 | chr19 | 35250477 | |||
| chr19:35250573 | G | A | 1 | a0009 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.368G>A | p.Arg123His | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/10 | 389/1932 | 368/1806 | 123/601 | chr19 | 35250573 | |||
| chr19:35250639 | G | A | 1 | a0006 | 1 | HG02135.hp1 | missense_variant | MODERATE | c.434G>A | p.Arg145Gln | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/10 | 455/1932 | 434/1806 | 145/601 | chr19 | 35250639 | |||
| chr19:35266524 | G | A | 2 | a0003 a0006 |
84 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(81): Show |
missense_variant | MODERATE | c.944G>A | p.Ser315Asn | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 6/10 | 965/1932 | 944/1806 | 315/601 | chr19 | 35266524 | |||
| chr19:35267372 | G | GGGA | 5 | a0002 a0003 a0005 others(2): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
disruptive_inframe_insertion | MODERATE | c.1410_1412dupGAG | p.Arg471dup | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 9/10 | 1434/1932 | 1413/1806 | 471/601 | INFO_REALIGN_3_PRIME | chr19 | 35267372 | ||
| chr19:35267537 | G | T | 1 | a0004 | 3 | HG02451.hp1 HG03195.hp2 HG03516.hp1 |
missense_variant | MODERATE | c.1573G>T | p.Asp525Tyr | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 9/10 | 1594/1932 | 1573/1806 | 525/601 | chr19 | 35267537 | |||
| chr19:35267610 | A | G | 1 | a0008 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.1646A>G | p.Lys549Arg | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 9/10 | 1667/1932 | 1646/1806 | 549/601 | chr19 | 35267610 | |||
| chr19:35267962 | C | T | 1 | a0003 | 1 | NA18991.hp2 | splice_region_variant | LOW | c.*103C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 10/10 | chr19 | 35267962 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:35250343 | G | A | 1 | a0001c0008 | 1 | HG02056.hp1 | synonymous_variant | LOW | c.138G>A | p.Val46Val | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/10 | 159/1932 | 138/1806 | 46/601 | chr19 | 35250343 | |||
| chr19:35250472 | C | T | 3 | a0001c0005 a0001c0020 a0001c0021 |
24 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(21): Show |
synonymous_variant | LOW | c.267C>T | p.Ala89Ala | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/10 | 288/1932 | 267/1806 | 89/601 | chr19 | 35250472 | |||
| chr19:35250553 | T | C | 10 | a0001c0004 a0001c0005 a0001c0020 others(7): Show |
219 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(216): Show |
synonymous_variant | LOW | c.348T>C | p.Val116Val | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/10 | 369/1932 | 348/1806 | 116/601 | chr19 | 35250553 | |||
| chr19:35259045 | C | T | 1 | a0001c0021 | 1 | NA19085.hp2 | synonymous_variant | LOW | c.555C>T | p.Tyr185Tyr | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 3/10 | 576/1932 | 555/1806 | 185/601 | chr19 | 35259045 | |||
| chr19:35262692 | C | T | 1 | a0003c0018 | 1 | HG01361.hp2 | splice_region_variant&synonymous_variant | LOW | c.778C>T | p.Leu260Leu | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/10 | 799/1932 | 778/1806 | 260/601 | chr19 | 35262692 | |||
| chr19:35266876 | C | T | 1 | a0001c0017 | 1 | HG01175.hp1 | synonymous_variant | LOW | c.1053C>T | p.Asp351Asp | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 8/10 | 1074/1932 | 1053/1806 | 351/601 | chr19 | 35266876 | |||
| chr19:35266888 | G | T | 1 | a0002c0014 | 1 | HG02818.hp1 | synonymous_variant | LOW | c.1065G>T | p.Arg355Arg | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 8/10 | 1086/1932 | 1065/1806 | 355/601 | chr19 | 35266888 | |||
| chr19:35267134 | C | T | 1 | a0002c0013 | 1 | HG00738.hp2 | synonymous_variant | LOW | c.1170C>T | p.His390His | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 9/10 | 1191/1932 | 1170/1806 | 390/601 | chr19 | 35267134 | |||
| chr19:35267527 | C | T | 1 | a0001c0020 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.1563C>T | p.His521His | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 9/10 | 1584/1932 | 1563/1806 | 521/601 | chr19 | 35267527 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:35267931 | C | T | 1 | a0001c0005t0002 | 2 | NA19000.hp1 NA19065.hp2 |
3_prime_UTR_variant | MODIFIER | c.*72C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 10/10 | 72 | chr19 | 35267931 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:35249135 | C | T | 1 | a0003c0003t0001g0206 | 1 | HG00735.hp2 | splice_region_variant&intron_variant | LOW | c.109+4C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 1/9 | chr19 | 35249135 | |||||||
| chr19:35249166 | C | G | 60 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0049 others(57): Show |
116 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.109+35C>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 1/9 | chr19 | 35249166 | |||||||
| chr19:35249170 | A | G | 1 | a0002c0001t0001g0055 | 2 | NA19003.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.109+39A>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 1/9 | chr19 | 35249170 | |||||||
| chr19:35249304 | T | C | 60 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0049 others(57): Show |
116 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.109+173T>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 1/9 | chr19 | 35249304 | |||||||
| chr19:35249429 | C | T | 1 | a0002c0001t0001g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.109+298C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 1/9 | chr19 | 35249429 | |||||||
| chr19:35249499 | G | A | 1 | a0002c0001t0001g0056 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.109+368G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 1/9 | chr19 | 35249499 | |||||||
| chr19:35249859 | A | G | 1 | a0002c0006t0001g0048 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.110-456A>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 1/9 | chr19 | 35249859 | |||||||
| chr19:35249903 | C | A | 17 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0049 others(14): Show |
51 | HG00140.hp1 HG00558.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.110-412C>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 1/9 | chr19 | 35249903 | |||||||
| chr19:35250167 | CACTGGTC others(10): Show |
C | 9 | a0002c0001t0001g0054 a0002c0001t0001g0055 a0002c0001t0001g0198 others(6): Show |
11 | HG00544.hp1 HG02083.hp1 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.110-146_110-130del others(17): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr19 | 35250167 | ||||||
| chr19:35250189 | A | G | 9 | a0002c0001t0001g0054 a0002c0001t0001g0055 a0002c0001t0001g0198 others(6): Show |
11 | HG00544.hp1 HG02083.hp1 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.110-126A>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 1/9 | chr19 | 35250189 | |||||||
| chr19:35250795 | C | CT | 93 | a0001c0002t0001g0130 a0001c0004t0001g0002 a0001c0004t0001g0010 others(90): Show |
186 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.454+153dupT | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35250795 | ||||||
| chr19:35250795 | C | CTT | 15 | a0001c0004t0001g0173 a0001c0004t0001g0174 a0001c0004t0001g0175 others(12): Show |
17 | HG00544.hp1 HG02080.hp2 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.454+152_454+153dup others(2): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35250795 | ||||||
| chr19:35251054 | G | A | 1 | a0001c0002t0001g0028 | 2 | NA18977.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.454+395G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35251054 | |||||||
| chr19:35251072 | C | T | 17 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0049 others(14): Show |
51 | HG00140.hp1 HG00558.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.454+413C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35251072 | |||||||
| chr19:35251094 | G | A | 1 | a0002c0001t0001g0057 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.454+435G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35251094 | |||||||
| chr19:35251116 | T | C | 5 | a0002c0006t0001g0062 a0004c0007t0001g0058 a0004c0007t0001g0059 others(2): Show |
5 | HG02257.hp1 HG02451.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.454+457T>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35251116 | |||||||
| chr19:35251148 | A | T | 1 | a0003c0003t0001g0161 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.454+489A>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35251148 | |||||||
| chr19:35251273 | G | T | 59 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0049 others(56): Show |
115 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.454+614G>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35251273 | |||||||
| chr19:35251397 | A | T | 1 | a0003c0012t0001g0197 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.454+738A>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35251397 | |||||||
| chr19:35251440 | G | A | 1 | a0002c0001t0001g0063 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.454+781G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35251440 | |||||||
| chr19:35251508 | G | C | 1 | a0003c0003t0001g0129 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.454+849G>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35251508 | |||||||
| chr19:35251624 | A | T | 1 | a0002c0014t0001g0176 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.454+965A>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35251624 | |||||||
| chr19:35251819 | C | T | 4 | a0002c0001t0001g0016 a0002c0001t0001g0192 a0002c0001t0001g0193 others(1): Show |
7 | HG01099.hp1 HG01123.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.454+1160C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35251819 | |||||||
| chr19:35251835 | A | AC | 12 | a0002c0001t0001g0016 a0002c0001t0001g0025 a0002c0001t0001g0050 others(9): Show |
18 | HG01099.hp1 HG01123.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.454+1178dupC | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35251835 | ||||||
| chr19:35251843 | C | CTGTTTTT others(5): Show |
1 | a0002c0006t0001g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.454+1185_454+1186i others(14): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35251843 | ||||||
| chr19:35251843 | C | CTTTTTTT others(6): Show |
9 | a0002c0006t0001g0020 a0002c0006t0001g0021 a0002c0006t0001g0048 others(6): Show |
14 | HG02622.hp2 HG02698.hp2 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.454+1193_454+1194i others(15): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35251843 | ||||||
| chr19:35251843 | C | CTTTTTTT others(7): Show |
2 | a0003c0003t0001g0134 a0003c0003t0001g0135 |
2 | HG02738.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.454+1193_454+1194i others(16): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35251843 | ||||||
| chr19:35251843 | C | CTTTTTTT others(9): Show |
1 | a0003c0018t0001g0136 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.454+1193_454+1194i others(18): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35251843 | ||||||
| chr19:35251843 | C | CTTTTTTT others(11): Show |
2 | a0001c0004t0001g0163 a0001c0004t0001g0173 |
2 | HG01070.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.454+1193_454+1194i others(20): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35251843 | ||||||
| chr19:35251843 | C | CTTTTTTT others(12): Show |
8 | a0001c0004t0001g0002 a0001c0004t0001g0049 a0001c0004t0001g0164 others(5): Show |
34 | HG00140.hp1 HG00558.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.454+1193_454+1194i others(21): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35251843 | ||||||
| chr19:35251843 | C | CTTTTTTT others(13): Show |
8 | a0001c0004t0001g0010 a0001c0004t0001g0169 a0001c0004t0001g0170 others(5): Show |
16 | HG01257.hp2 HG01258.hp2 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.454+1193_454+1194i others(22): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35251843 | ||||||
| chr19:35251843 | C | CTTTTTTT others(14): Show |
10 | a0002c0001t0001g0016 a0002c0001t0001g0025 a0002c0001t0001g0050 others(7): Show |
16 | HG01099.hp1 HG01123.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.454+1193_454+1194i others(23): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35251843 | ||||||
| chr19:35251843 | C | CTTTTTTT others(15): Show |
13 | a0002c0001t0001g0051 a0002c0001t0001g0054 a0002c0001t0001g0055 others(10): Show |
16 | HG00544.hp1 HG02083.hp1 HG02129.hp2 others(13): Show |
intron_variant | MODIFIER | c.454+1193_454+1194i others(24): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35251843 | ||||||
| chr19:35251843 | C | CTTTTTTT others(17): Show |
1 | a0002c0001t0001g0190 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.454+1193_454+1194i others(26): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35251843 | ||||||
| chr19:35251843 | C | CTTTTTTT others(18): Show |
1 | a0002c0001t0001g0052 | 2 | HG01884.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.454+1193_454+1194i others(27): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35251843 | ||||||
| chr19:35251843 | C | CTTTTTTT others(19): Show |
1 | a0002c0001t0001g0053 | 2 | HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.454+1193_454+1194i others(28): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35251843 | ||||||
| chr19:35251843 | C | CTTTTTTT others(20): Show |
1 | a0001c0002t0001g0123 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.454+1193_454+1194i others(29): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35251843 | ||||||
| chr19:35251843 | C | CTTTTTTT others(21): Show |
9 | a0001c0002t0001g0124 a0003c0003t0001g0009 a0003c0003t0001g0043 others(6): Show |
20 | HG01256.hp2 HG01358.hp1 HG01934.hp1 others(17): Show |
intron_variant | MODIFIER | c.454+1193_454+1194i others(30): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35251843 | ||||||
| chr19:35251843 | C | CTTTTTTT others(22): Show |
16 | a0001c0002t0001g0040 a0001c0002t0001g0125 a0001c0002t0001g0126 others(13): Show |
32 | HG00544.hp2 HG00621.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.454+1193_454+1194i others(31): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35251843 | ||||||
| chr19:35251843 | C | CTTTTTTT others(23): Show |
13 | a0001c0002t0001g0022 a0001c0002t0001g0127 a0001c0002t0001g0128 others(10): Show |
26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.454+1193_454+1194i others(32): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35251843 | ||||||
| chr19:35251843 | C | CTTTTTTT others(24): Show |
8 | a0001c0002t0001g0041 a0003c0003t0001g0047 a0003c0003t0001g0129 others(5): Show |
10 | HG01516.hp1 HG01981.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.454+1193_454+1194i others(33): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35251843 | ||||||
| chr19:35251843 | C | CTTTTTTT others(25): Show |
1 | a0001c0004t0001g0191 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.454+1193_454+1194i others(34): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35251843 | ||||||
| chr19:35251843 | C | CTTTTTTT others(27): Show |
1 | a0003c0003t0001g0159 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.454+1193_454+1194i others(36): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35251843 | ||||||
| chr19:35251843 | C | CTTTTTTT others(35): Show |
1 | a0003c0003t0001g0160 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.454+1193_454+1194i others(44): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35251843 | ||||||
| chr19:35251857 | C | T | 45 | a0003c0003t0001g0005 a0003c0003t0001g0009 a0003c0003t0001g0012 others(42): Show |
83 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.454+1198C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35251857 | |||||||
| chr19:35251981 | C | T | 1 | a0002c0001t0001g0179 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.454+1322C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35251981 | |||||||
| chr19:35251983 | C | T | 62 | a0001c0002t0001g0022 a0001c0002t0001g0040 a0001c0002t0001g0041 others(59): Show |
109 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.454+1324C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35251983 | |||||||
| chr19:35251995 | C | T | 39 | a0001c0004t0001g0113 a0002c0001t0001g0001 a0002c0001t0001g0006 others(36): Show |
103 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.454+1336C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35251995 | |||||||
| chr19:35252025 | G | A | 10 | a0002c0001t0001g0016 a0002c0001t0001g0025 a0002c0001t0001g0050 others(7): Show |
16 | HG01099.hp1 HG01123.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.454+1366G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35252025 | |||||||
| chr19:35252086 | G | A | 1 | a0002c0001t0001g0179 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.454+1427G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35252086 | |||||||
| chr19:35252108 | A | G | 16 | a0001c0002t0001g0022 a0001c0002t0001g0040 a0001c0002t0001g0041 others(13): Show |
25 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.454+1449A>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35252108 | |||||||
| chr19:35252118 | G | A | 37 | a0003c0003t0001g0005 a0003c0003t0001g0009 a0003c0003t0001g0012 others(34): Show |
72 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.454+1459G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35252118 | |||||||
| chr19:35252231 | ATCGACTA others(4): Show |
A | 1 | a0002c0001t0001g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.454+1576_454+1586d others(13): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35252231 | ||||||
| chr19:35252266 | G | A | 10 | a0002c0001t0001g0016 a0002c0001t0001g0025 a0002c0001t0001g0050 others(7): Show |
16 | HG01099.hp1 HG01123.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.454+1607G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35252266 | |||||||
| chr19:35252291 | G | A | 46 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0049 others(43): Show |
99 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.454+1632G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35252291 | |||||||
| chr19:35252301 | T | C | 1 | a0002c0001t0001g0098 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.454+1642T>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35252301 | |||||||
| chr19:35252360 | T | C | 62 | a0001c0002t0001g0022 a0001c0002t0001g0040 a0001c0002t0001g0041 others(59): Show |
109 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.454+1701T>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35252360 | |||||||
| chr19:35252576 | G | A | 1 | a0002c0001t0001g0057 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.454+1917G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35252576 | |||||||
| chr19:35252608 | C | T | 1 | a0001c0002t0001g0097 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.454+1949C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35252608 | |||||||
| chr19:35252648 | C | CA | 58 | a0001c0002t0001g0015 a0001c0002t0001g0029 a0001c0002t0001g0065 others(55): Show |
103 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.454+2010dupA | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35252648 | ||||||
| chr19:35252648 | CA | C | 35 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0001c0002t0001g0094 others(32): Show |
74 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.454+2010delA | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35252648 | ||||||
| chr19:35252648 | CAA | C | 27 | a0001c0004t0001g0174 a0001c0005t0001g0008 a0001c0005t0001g0026 others(24): Show |
44 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.454+2009_454+2010d others(4): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35252648 | ||||||
| chr19:35252656 | A | G | 1 | a0001c0004t0001g0191 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.454+1997A>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35252656 | |||||||
| chr19:35252677 | T | C | 1 | a0002c0001t0001g0104 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.454+2018T>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35252677 | |||||||
| chr19:35252773 | G | A | 12 | a0002c0001t0001g0016 a0002c0001t0001g0025 a0002c0001t0001g0050 others(9): Show |
18 | HG01099.hp1 HG01123.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.454+2114G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35252773 | |||||||
| chr19:35252940 | G | T | 1 | a0002c0006t0001g0096 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.454+2281G>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35252940 | |||||||
| chr19:35252948 | G | A | 1 | a0001c0004t0001g0191 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.454+2289G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35252948 | |||||||
| chr19:35253019 | TTGAAA | T | 45 | a0003c0003t0001g0005 a0003c0003t0001g0009 a0003c0003t0001g0012 others(42): Show |
83 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.454+2366_454+2370d others(7): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35253019 | ||||||
| chr19:35253036 | T | C | 1 | a0002c0001t0001g0105 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.454+2377T>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35253036 | |||||||
| chr19:35253176 | C | T | 1 | a0001c0004t0001g0168 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.454+2517C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35253176 | |||||||
| chr19:35253180 | C | T | 45 | a0003c0003t0001g0005 a0003c0003t0001g0009 a0003c0003t0001g0012 others(42): Show |
83 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.454+2521C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35253180 | |||||||
| chr19:35253181 | G | A | 3 | a0001c0004t0001g0049 a0001c0004t0001g0171 a0001c0004t0001g0175 |
4 | HG02080.hp2 NA19001.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.454+2522G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35253181 | |||||||
| chr19:35253200 | A | G | 3 | a0002c0001t0001g0052 a0002c0001t0001g0053 a0002c0001t0001g0190 |
5 | HG01884.hp1 HG02809.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.454+2541A>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35253200 | |||||||
| chr19:35253281 | C | T | 1 | a0001c0005t0001g0187 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.454+2622C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35253281 | |||||||
| chr19:35253285 | A | G | 6 | a0001c0005t0001g0026 a0001c0005t0001g0027 a0001c0005t0001g0184 others(3): Show |
9 | HG00642.hp2 HG00735.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.454+2626A>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35253285 | |||||||
| chr19:35253526 | G | T | 11 | a0002c0001t0001g0016 a0002c0001t0001g0025 a0002c0001t0001g0050 others(8): Show |
17 | HG01099.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.454+2867G>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35253526 | |||||||
| chr19:35253615 | A | G | 1 | a0002c0006t0001g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.454+2956A>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35253615 | |||||||
| chr19:35253789 | C | T | 1 | a0001c0002t0001g0091 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.454+3130C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35253789 | |||||||
| chr19:35253983 | TC | T | 49 | a0002c0001t0001g0051 a0002c0001t0001g0188 a0002c0001t0001g0189 others(46): Show |
88 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.454+3326delC | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35253983 | ||||||
| chr19:35254013 | A | G | 16 | a0002c0001t0001g0016 a0002c0001t0001g0025 a0002c0001t0001g0050 others(13): Show |
26 | HG01099.hp1 HG01123.hp1 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.454+3354A>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35254013 | |||||||
| chr19:35254093 | T | G | 1 | a0002c0001t0001g0106 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.454+3434T>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35254093 | |||||||
| chr19:35254135 | C | G | 1 | a0002c0001t0001g0039 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.454+3476C>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35254135 | |||||||
| chr19:35254169 | C | T | 1 | a0003c0012t0001g0197 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.454+3510C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35254169 | |||||||
| chr19:35254185 | G | A | 11 | a0002c0001t0001g0006 a0002c0001t0001g0013 a0002c0001t0001g0035 others(8): Show |
28 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.454+3526G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35254185 | |||||||
| chr19:35254196 | T | C | 4 | a0002c0001t0001g0165 a0002c0001t0001g0181 a0002c0006t0001g0021 others(1): Show |
6 | HG02615.hp1 HG02622.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.454+3537T>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35254196 | |||||||
| chr19:35254282 | G | A | 13 | a0001c0005t0001g0008 a0001c0005t0001g0026 a0001c0005t0001g0027 others(10): Show |
24 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.454+3623G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35254282 | |||||||
| chr19:35254456 | A | G | 2 | a0002c0001t0001g0165 a0002c0001t0001g0181 |
2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.454+3797A>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35254456 | |||||||
| chr19:35254468 | C | T | 1 | a0001c0002t0001g0128 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.454+3809C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35254468 | |||||||
| chr19:35254484 | G | T | 2 | a0002c0001t0001g0165 a0002c0001t0001g0181 |
2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.454+3825G>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35254484 | |||||||
| chr19:35254549 | C | T | 2 | a0002c0001t0001g0165 a0002c0001t0001g0181 |
2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.454+3890C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35254549 | |||||||
| chr19:35254638 | C | T | 2 | a0002c0001t0001g0165 a0002c0001t0001g0181 |
2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.454+3979C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35254638 | |||||||
| chr19:35254683 | T | A | 3 | a0002c0001t0001g0052 a0002c0001t0001g0053 a0002c0001t0001g0190 |
5 | HG01884.hp1 HG02809.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.454+4024T>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35254683 | |||||||
| chr19:35254722 | G | C | 2 | a0002c0001t0001g0165 a0002c0001t0001g0181 |
2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.454+4063G>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35254722 | |||||||
| chr19:35254882 | C | T | 1 | a0001c0004t0001g0167 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.455-4063C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35254882 | |||||||
| chr19:35255013 | T | C | 1 | a0002c0001t0001g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.455-3932T>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35255013 | |||||||
| chr19:35255103 | G | A | 1 | a0002c0006t0001g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.455-3842G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35255103 | |||||||
| chr19:35255165 | C | T | 2 | a0002c0001t0001g0165 a0002c0001t0001g0181 |
2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.455-3780C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35255165 | |||||||
| chr19:35255169 | G | C | 185 | a0001c0002t0001g0004 a0001c0002t0001g0015 a0001c0002t0001g0017 others(182): Show |
380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.455-3776G>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35255169 | |||||||
| chr19:35255206 | C | T | 3 | a0002c0001t0001g0052 a0002c0001t0001g0053 a0002c0001t0001g0190 |
5 | HG01884.hp1 HG02809.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.455-3739C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35255206 | |||||||
| chr19:35255311 | C | T | 1 | a0002c0001t0001g0181 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.455-3634C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35255311 | |||||||
| chr19:35255479 | C | T | 9 | a0002c0001t0001g0019 a0002c0001t0001g0038 a0002c0001t0001g0057 others(6): Show |
11 | HG00738.hp2 HG01109.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.455-3466C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35255479 | |||||||
| chr19:35255518 | G | A | 1 | a0002c0001t0001g0118 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.455-3427G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35255518 | |||||||
| chr19:35255606 | A | C | 1 | a0002c0014t0001g0176 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.455-3339A>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35255606 | |||||||
| chr19:35255639 | A | G | 1 | a0002c0006t0001g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.455-3306A>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35255639 | |||||||
| chr19:35255703 | T | C | 1 | a0003c0003t0001g0149 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.455-3242T>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35255703 | |||||||
| chr19:35255803 | A | G | 40 | a0001c0004t0001g0113 a0002c0001t0001g0001 a0002c0001t0001g0007 others(37): Show |
93 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.455-3142A>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35255803 | |||||||
| chr19:35255865 | A | G | 3 | a0002c0001t0001g0051 a0002c0001t0001g0188 a0002c0001t0001g0189 |
4 | HG02258.hp2 HG02723.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.455-3080A>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35255865 | |||||||
| chr19:35255896 | G | A | 93 | a0001c0004t0001g0113 a0002c0001t0001g0001 a0002c0001t0001g0007 others(90): Show |
189 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.455-3049G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35255896 | |||||||
| chr19:35255915 | T | C | 2 | a0002c0001t0001g0165 a0002c0001t0001g0181 |
2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.455-3030T>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35255915 | |||||||
| chr19:35256106 | C | T | 5 | a0001c0002t0001g0017 a0001c0002t0001g0031 a0001c0002t0001g0032 others(2): Show |
8 | HG01257.hp1 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.455-2839C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35256106 | |||||||
| chr19:35256183 | A | G | 2 | a0002c0001t0001g0165 a0002c0001t0001g0181 |
2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.455-2762A>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35256183 | |||||||
| chr19:35256220 | C | T | 1 | a0002c0014t0001g0176 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.455-2725C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35256220 | |||||||
| chr19:35256221 | G | A | 1 | a0002c0001t0001g0165 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.455-2724G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35256221 | |||||||
| chr19:35256233 | CA | C | 49 | a0001c0002t0001g0090 a0001c0005t0001g0183 a0002c0001t0001g0109 others(46): Show |
87 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.455-2696delA | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35256233 | ||||||
| chr19:35256275 | A | T | 1 | a0002c0001t0001g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.455-2670A>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35256275 | |||||||
| chr19:35256276 | T | C | 1 | a0002c0001t0001g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.455-2669T>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35256276 | |||||||
| chr19:35256278 | G | T | 1 | a0002c0001t0001g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.455-2667G>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35256278 | |||||||
| chr19:35256279 | G | T | 1 | a0002c0001t0001g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.455-2666G>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35256279 | |||||||
| chr19:35256281 | A | T | 1 | a0002c0001t0001g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.455-2664A>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35256281 | |||||||
| chr19:35256284 | A | T | 1 | a0002c0001t0001g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.455-2661A>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35256284 | |||||||
| chr19:35256286 | A | C | 1 | a0002c0001t0001g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.455-2659A>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35256286 | |||||||
| chr19:35256287 | A | C | 1 | a0002c0001t0001g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.455-2658A>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35256287 | |||||||
| chr19:35256289 | G | A | 1 | a0002c0001t0001g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.455-2656G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35256289 | |||||||
| chr19:35256290 | A | T | 1 | a0002c0001t0001g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.455-2655A>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35256290 | |||||||
| chr19:35256680 | T | A | 1 | a0002c0014t0001g0176 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.455-2265T>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35256680 | |||||||
| chr19:35256699 | G | GATGA | 15 | a0001c0002t0001g0086 a0001c0002t0001g0087 a0001c0002t0001g0088 others(12): Show |
24 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.455-2216_455-2213d others(6): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35256699 | ||||||
| chr19:35256699 | G | GATGAATG others(1): Show |
7 | a0001c0005t0001g0027 a0001c0005t0001g0182 a0001c0005t0001g0184 others(4): Show |
9 | HG00735.hp1 HG02109.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.455-2220_455-2213d others(10): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35256699 | ||||||
| chr19:35256699 | G | GATGAATG others(5): Show |
2 | a0001c0005t0001g0186 a0004c0007t0001g0061 |
2 | HG02451.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.455-2224_455-2213d others(14): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35256699 | ||||||
| chr19:35256699 | GATGA | G | 27 | a0001c0002t0001g0004 a0001c0002t0001g0015 a0001c0002t0001g0028 others(24): Show |
70 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.455-2216_455-2213d others(6): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35256699 | ||||||
| chr19:35256707 | A | G | 1 | a0001c0002t0001g0034 | 2 | HG00140.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.455-2238A>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35256707 | |||||||
| chr19:35256717 | TGAATGAA others(9): Show |
T | 2 | a0002c0001t0001g0165 a0002c0001t0001g0181 |
2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.455-2224_455-2209d others(18): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35256717 | ||||||
| chr19:35256725 | TGAATGAA others(1): Show |
T | 44 | a0001c0004t0001g0113 a0002c0001t0001g0001 a0002c0001t0001g0007 others(41): Show |
93 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.455-2216_455-2209d others(10): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35256725 | ||||||
| chr19:35256725 | TGAATGAA others(5): Show |
T | 44 | a0003c0003t0001g0005 a0003c0003t0001g0009 a0003c0003t0001g0012 others(41): Show |
81 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.455-2216_455-2205d others(14): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35256725 | ||||||
| chr19:35256729 | TGAAA | T | 12 | a0002c0001t0001g0001 a0002c0001t0001g0007 a0002c0001t0001g0018 others(9): Show |
20 | HG00621.hp2 HG01192.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.455-2203_455-2200d others(6): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35256729 | ||||||
| chr19:35256729 | TGAAAGAA others(5): Show |
T | 1 | a0003c0003t0001g0009 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.455-2211_455-2200d others(14): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35256729 | ||||||
| chr19:35256733 | A | T | 8 | a0002c0001t0001g0054 a0002c0001t0001g0055 a0002c0001t0001g0198 others(5): Show |
10 | HG00544.hp1 HG02129.hp2 HG03491.hp2 others(7): Show |
intron_variant | MODIFIER | c.455-2212A>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35256733 | |||||||
| chr19:35256737 | A | T | 1 | a0003c0012t0001g0197 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.455-2208A>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35256737 | |||||||
| chr19:35256760 | C | T | 93 | a0001c0004t0001g0113 a0002c0001t0001g0001 a0002c0001t0001g0007 others(90): Show |
189 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.455-2185C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35256760 | |||||||
| chr19:35256892 | A | C | 1 | a0002c0006t0001g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.455-2053A>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35256892 | |||||||
| chr19:35256895 | G | A | 1 | a0002c0006t0001g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.455-2050G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35256895 | |||||||
| chr19:35257217 | T | G | 1 | a0002c0006t0001g0119 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.455-1728T>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35257217 | |||||||
| chr19:35257307 | G | A | 3 | a0002c0001t0001g0052 a0002c0001t0001g0053 a0002c0001t0001g0190 |
5 | HG01884.hp1 HG02809.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.455-1638G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35257307 | |||||||
| chr19:35257339 | C | T | 3 | a0002c0001t0001g0052 a0002c0001t0001g0053 a0002c0001t0001g0190 |
5 | HG01884.hp1 HG02809.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.455-1606C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35257339 | |||||||
| chr19:35257351 | C | T | 1 | a0002c0001t0001g0117 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.455-1594C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35257351 | |||||||
| chr19:35257379 | C | T | 2 | a0002c0001t0001g0165 a0002c0001t0001g0181 |
2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.455-1566C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35257379 | |||||||
| chr19:35257550 | A | G | 1 | a0001c0002t0001g0085 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.455-1395A>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35257550 | |||||||
| chr19:35257644 | G | C | 1 | a0002c0014t0001g0176 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.455-1301G>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35257644 | |||||||
| chr19:35257687 | G | A | 2 | a0002c0001t0001g0013 a0002c0001t0001g0106 |
6 | HG00741.hp1 HG01167.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.455-1258G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35257687 | |||||||
| chr19:35257726 | A | G | 9 | a0002c0001t0001g0054 a0002c0001t0001g0055 a0002c0001t0001g0198 others(6): Show |
11 | HG00544.hp1 HG02083.hp1 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.455-1219A>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35257726 | |||||||
| chr19:35257803 | A | G | 12 | a0002c0001t0001g0006 a0002c0001t0001g0013 a0002c0001t0001g0035 others(9): Show |
29 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.455-1142A>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35257803 | |||||||
| chr19:35257879 | A | G | 12 | a0002c0001t0001g0006 a0002c0001t0001g0013 a0002c0001t0001g0035 others(9): Show |
29 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.455-1066A>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35257879 | |||||||
| chr19:35257881 | A | G | 1 | a0002c0001t0001g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.455-1064A>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35257881 | |||||||
| chr19:35257957 | G | A | 3 | a0002c0001t0001g0052 a0002c0001t0001g0053 a0002c0001t0001g0190 |
5 | HG01884.hp1 HG02809.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.455-988G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35257957 | |||||||
| chr19:35258142 | G | C | 1 | a0002c0006t0001g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.455-803G>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35258142 | |||||||
| chr19:35258256 | G | A | 1 | a0001c0002t0001g0078 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.455-689G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35258256 | |||||||
| chr19:35258266 | C | A | 1 | a0003c0003t0001g0150 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.455-679C>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35258266 | |||||||
| chr19:35258360 | T | C | 121 | a0001c0004t0001g0113 a0002c0001t0001g0001 a0002c0001t0001g0006 others(118): Show |
238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.455-585T>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35258360 | |||||||
| chr19:35258377 | C | T | 1 | a0001c0002t0001g0084 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.455-568C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35258377 | |||||||
| chr19:35258439 | G | A | 1 | a0002c0001t0001g0179 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.455-506G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35258439 | |||||||
| chr19:35258455 | C | CA | 47 | a0001c0002t0001g0065 a0001c0002t0001g0070 a0001c0002t0001g0086 others(44): Show |
85 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.455-476dupA | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr19 | 35258455 | ||||||
| chr19:35258458 | A | AC | 40 | a0001c0004t0001g0113 a0002c0001t0001g0001 a0002c0001t0001g0007 others(37): Show |
93 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.455-487_455-486ins others(1): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35258458 | |||||||
| chr19:35258458 | A | C | 4 | a0002c0001t0001g0054 a0002c0001t0001g0055 a0002c0001t0001g0202 others(1): Show |
6 | HG00544.hp1 HG02129.hp2 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.455-487A>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35258458 | |||||||
| chr19:35258459 | A | C | 23 | a0001c0002t0001g0029 a0001c0002t0001g0083 a0001c0002t0001g0085 others(20): Show |
43 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.455-486A>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35258459 | |||||||
| chr19:35258462 | A | C | 1 | a0002c0001t0001g0116 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.455-483A>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35258462 | |||||||
| chr19:35258570 | A | G | 1 | a0002c0006t0001g0119 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.455-375A>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35258570 | |||||||
| chr19:35258660 | T | C | 166 | a0001c0002t0001g0022 a0001c0002t0001g0040 a0001c0002t0001g0041 others(163): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.455-285T>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 2/9 | chr19 | 35258660 | |||||||
| chr19:35259104 | T | C | 1 | a0002c0001t0001g0111 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.574+40T>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 3/9 | chr19 | 35259104 | |||||||
| chr19:35259165 | C | G | 1 | a0002c0001t0001g0105 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.574+101C>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 3/9 | chr19 | 35259165 | |||||||
| chr19:35259329 | C | T | 3 | a0002c0001t0001g0052 a0002c0001t0001g0053 a0002c0001t0001g0190 |
5 | HG01884.hp1 HG02809.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.574+265C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 3/9 | chr19 | 35259329 | |||||||
| chr19:35259331 | C | A | 1 | a0001c0002t0001g0075 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.574+267C>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 3/9 | chr19 | 35259331 | |||||||
| chr19:35259337 | T | A | 1 | a0001c0002t0001g0075 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.574+273T>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 3/9 | chr19 | 35259337 | |||||||
| chr19:35259361 | C | T | 11 | a0001c0002t0001g0022 a0001c0002t0001g0040 a0001c0002t0001g0041 others(8): Show |
15 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.574+297C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 3/9 | chr19 | 35259361 | |||||||
| chr19:35259632 | T | C | 2 | a0002c0001t0001g0165 a0002c0001t0001g0181 |
2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.574+568T>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 3/9 | chr19 | 35259632 | |||||||
| chr19:35259636 | C | CA | 30 | a0001c0002t0001g0066 a0001c0002t0001g0071 a0001c0002t0001g0072 others(27): Show |
35 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.574+586dupA | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 35259636 | ||||||
| chr19:35259781 | G | A | 12 | a0002c0001t0001g0006 a0002c0001t0001g0013 a0002c0001t0001g0035 others(9): Show |
29 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.574+717G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 3/9 | chr19 | 35259781 | |||||||
| chr19:35259806 | A | G | 3 | a0001c0002t0001g0126 a0001c0002t0001g0127 a0001c0002t0001g0128 |
3 | HG02280.hp2 HG02559.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.574+742A>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 3/9 | chr19 | 35259806 | |||||||
| chr19:35259884 | C | T | 1 | a0001c0002t0001g0089 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.574+820C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 3/9 | chr19 | 35259884 | |||||||
| chr19:35259984 | A | G | 1 | a0003c0003t0001g0145 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.574+920A>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 3/9 | chr19 | 35259984 | |||||||
| chr19:35260012 | C | T | 1 | a0002c0001t0001g0194 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.574+948C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 3/9 | chr19 | 35260012 | |||||||
| chr19:35260291 | C | CT | 82 | a0001c0002t0001g0033 a0001c0002t0001g0086 a0002c0001t0001g0001 others(79): Show |
169 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.574+1245dupT | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 35260291 | ||||||
| chr19:35260291 | C | CTT | 26 | a0002c0001t0001g0007 a0002c0001t0001g0052 a0002c0001t0001g0053 others(23): Show |
39 | HG00544.hp1 HG00738.hp1 HG01175.hp2 others(36): Show |
intron_variant | MODIFIER | c.574+1244_574+1245d others(4): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 35260291 | ||||||
| chr19:35260291 | C | CTTT | 13 | a0002c0001t0001g0006 a0002c0001t0001g0013 a0002c0001t0001g0035 others(10): Show |
31 | HG00099.hp2 HG00621.hp2 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.574+1243_574+1245d others(5): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 35260291 | ||||||
| chr19:35260291 | CT | C | 7 | a0001c0005t0001g0008 a0001c0005t0001g0182 a0001c0005t0001g0183 others(4): Show |
15 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.574+1245delT | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 35260291 | ||||||
| chr19:35260405 | C | T | 45 | a0003c0003t0001g0005 a0003c0003t0001g0009 a0003c0003t0001g0012 others(42): Show |
83 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.574+1341C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 3/9 | chr19 | 35260405 | |||||||
| chr19:35260418 | G | A | 123 | a0002c0001t0001g0001 a0002c0001t0001g0006 a0002c0001t0001g0007 others(120): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.574+1354G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 3/9 | chr19 | 35260418 | |||||||
| chr19:35260457 | A | G | 9 | a0002c0001t0001g0054 a0002c0001t0001g0055 a0002c0001t0001g0198 others(6): Show |
11 | HG00544.hp1 HG02083.hp1 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.574+1393A>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 3/9 | chr19 | 35260457 | |||||||
| chr19:35260501 | G | A | 7 | a0001c0002t0001g0011 a0001c0002t0001g0067 a0001c0002t0001g0078 others(4): Show |
11 | HG02056.hp1 HG02165.hp2 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.575-1424G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 3/9 | chr19 | 35260501 | |||||||
| chr19:35260526 | C | A | 2 | a0002c0001t0001g0165 a0002c0001t0001g0181 |
2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.575-1399C>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 3/9 | chr19 | 35260526 | |||||||
| chr19:35260529 | G | A | 1 | a0003c0003t0001g0137 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.575-1396G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 3/9 | chr19 | 35260529 | |||||||
| chr19:35260600 | G | C | 1 | a0002c0001t0001g0165 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.575-1325G>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 3/9 | chr19 | 35260600 | |||||||
| chr19:35260776 | G | A | 93 | a0002c0001t0001g0001 a0002c0001t0001g0007 a0002c0001t0001g0016 others(90): Show |
188 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.575-1149G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 3/9 | chr19 | 35260776 | |||||||
| chr19:35260833 | A | AAC | 8 | a0001c0002t0001g0031 a0001c0002t0001g0080 a0001c0002t0001g0097 others(5): Show |
8 | HG01257.hp1 HG02055.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.575-1071_575-1070d others(4): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 35260833 | ||||||
| chr19:35260856 | G | A | 32 | a0001c0002t0001g0022 a0001c0002t0001g0040 a0001c0002t0001g0041 others(29): Show |
71 | HG00140.hp1 HG00558.hp2 HG00673.hp2 others(68): Show |
intron_variant | MODIFIER | c.575-1069G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 3/9 | chr19 | 35260856 | |||||||
| chr19:35260870 | A | G | 3 | a0001c0002t0001g0031 a0001c0002t0001g0097 a0008c0016t0001g0031 |
3 | HG01257.hp1 HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.575-1055A>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 3/9 | chr19 | 35260870 | |||||||
| chr19:35261053 | T | C | 1 | a0001c0005t0001g0184 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.575-872T>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 3/9 | chr19 | 35261053 | |||||||
| chr19:35261160 | G | A | 1 | a0001c0004t0001g0166 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.575-765G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 3/9 | chr19 | 35261160 | |||||||
| chr19:35261269 | G | A | 4 | a0003c0003t0001g0132 a0003c0003t0001g0133 a0003c0003t0001g0134 others(1): Show |
4 | HG02698.hp2 HG02738.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.575-656G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 3/9 | chr19 | 35261269 | |||||||
| chr19:35261284 | T | C | 1 | a0001c0017t0001g0073 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.575-641T>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 3/9 | chr19 | 35261284 | |||||||
| chr19:35261372 | T | C | 3 | a0002c0001t0001g0052 a0002c0001t0001g0053 a0002c0001t0001g0190 |
5 | HG01884.hp1 HG02809.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.575-553T>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 3/9 | chr19 | 35261372 | |||||||
| chr19:35261482 | A | C | 3 | a0002c0001t0001g0052 a0002c0001t0001g0053 a0002c0001t0001g0190 |
5 | HG01884.hp1 HG02809.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.575-443A>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 3/9 | chr19 | 35261482 | |||||||
| chr19:35261525 | C | T | 47 | a0001c0002t0001g0072 a0003c0003t0001g0005 a0003c0003t0001g0009 others(44): Show |
85 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.575-400C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 3/9 | chr19 | 35261525 | |||||||
| chr19:35261585 | T | C | 7 | a0002c0006t0001g0020 a0002c0006t0001g0021 a0002c0006t0001g0048 others(4): Show |
12 | HG02622.hp2 HG02717.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.575-340T>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 3/9 | chr19 | 35261585 | |||||||
| chr19:35261766 | G | A | 1 | a0002c0001t0001g0105 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.575-159G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 3/9 | chr19 | 35261766 | |||||||
| chr19:35261788 | A | G | 38 | a0002c0001t0001g0001 a0002c0001t0001g0007 a0002c0001t0001g0016 others(35): Show |
90 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.575-137A>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 3/9 | chr19 | 35261788 | |||||||
| chr19:35262014 | G | A | 13 | a0002c0001t0001g0006 a0002c0001t0001g0013 a0002c0001t0001g0035 others(10): Show |
31 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.631+33G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 4/9 | chr19 | 35262014 | |||||||
| chr19:35262032 | C | T | 1 | a0001c0004t0001g0164 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.631+51C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 4/9 | chr19 | 35262032 | |||||||
| chr19:35262142 | G | A | 2 | a0001c0002t0001g0074 a0003c0003t0001g0138 |
2 | HG03486.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.631+161G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 4/9 | chr19 | 35262142 | |||||||
| chr19:35262208 | C | T | 1 | a0003c0012t0001g0197 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.631+227C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 4/9 | chr19 | 35262208 | |||||||
| chr19:35262212 | G | A | 1 | a0002c0001t0001g0112 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.631+231G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 4/9 | chr19 | 35262212 | |||||||
| chr19:35262353 | C | T | 3 | a0001c0002t0001g0069 a0001c0002t0001g0079 a0001c0002t0001g0082 |
3 | NA18966.hp2 NA18975.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.632-193C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 4/9 | chr19 | 35262353 | |||||||
| chr19:35262474 | T | C | 1 | a0002c0006t0001g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.632-72T>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 4/9 | chr19 | 35262474 | |||||||
| chr19:35262703 | C | T | 1 | a0003c0003t0001g0162 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.778+11C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35262703 | |||||||
| chr19:35262847 | T | G | 1 | a0002c0001t0001g0114 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.778+155T>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35262847 | |||||||
| chr19:35262904 | C | T | 1 | a0003c0003t0001g0044 | 2 | NA18747.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.778+212C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35262904 | |||||||
| chr19:35263096 | A | G | 46 | a0001c0002t0001g0072 a0003c0003t0001g0005 a0003c0003t0001g0009 others(43): Show |
84 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.778+404A>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35263096 | |||||||
| chr19:35263098 | G | A | 3 | a0002c0001t0001g0051 a0002c0001t0001g0188 a0002c0001t0001g0189 |
4 | HG02258.hp2 HG02723.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.778+406G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35263098 | |||||||
| chr19:35263100 | T | C | 4 | a0002c0001t0001g0052 a0002c0001t0001g0053 a0002c0001t0001g0190 others(1): Show |
6 | HG01884.hp1 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.778+408T>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35263100 | |||||||
| chr19:35263108 | A | C | 13 | a0002c0001t0001g0006 a0002c0001t0001g0013 a0002c0001t0001g0035 others(10): Show |
31 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.778+416A>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35263108 | |||||||
| chr19:35263196 | G | A | 1 | a0001c0002t0001g0123 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.778+504G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35263196 | |||||||
| chr19:35263237 | C | T | 1 | a0001c0002t0001g0081 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.778+545C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35263237 | |||||||
| chr19:35263238 | G | A | 13 | a0002c0001t0001g0006 a0002c0001t0001g0013 a0002c0001t0001g0035 others(10): Show |
31 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.778+546G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35263238 | |||||||
| chr19:35263365 | A | C | 13 | a0002c0001t0001g0006 a0002c0001t0001g0013 a0002c0001t0001g0035 others(10): Show |
31 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.778+673A>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35263365 | |||||||
| chr19:35263366 | T | A | 1 | a0001c0004t0001g0191 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.778+674T>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35263366 | |||||||
| chr19:35263467 | C | T | 1 | a0002c0001t0001g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.778+775C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35263467 | |||||||
| chr19:35263475 | C | T | 2 | a0002c0001t0001g0200 a0002c0001t0001g0203 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.778+783C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35263475 | |||||||
| chr19:35263494 | T | C | 1 | a0001c0002t0001g0032 | 2 | HG01891.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.778+802T>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35263494 | |||||||
| chr19:35263608 | C | G | 93 | a0002c0001t0001g0001 a0002c0001t0001g0007 a0002c0001t0001g0016 others(90): Show |
188 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.778+916C>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35263608 | |||||||
| chr19:35263699 | A | G | 16 | a0002c0001t0001g0006 a0002c0001t0001g0013 a0002c0001t0001g0035 others(13): Show |
35 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.778+1007A>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35263699 | |||||||
| chr19:35263810 | AT | A | 12 | a0001c0002t0001g0071 a0002c0001t0001g0108 a0003c0003t0001g0012 others(9): Show |
19 | HG00408.hp1 HG00544.hp2 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.778+1133delT | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr19 | 35263810 | ||||||
| chr19:35263811 | T | A | 35 | a0003c0003t0001g0005 a0003c0003t0001g0009 a0003c0003t0001g0014 others(32): Show |
64 | HG00099.hp1 HG00621.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.778+1119T>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35263811 | |||||||
| chr19:35263812 | T | A | 10 | a0003c0003t0001g0012 a0003c0003t0001g0023 a0003c0003t0001g0043 others(7): Show |
17 | HG00408.hp1 HG00544.hp2 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.778+1120T>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35263812 | |||||||
| chr19:35263826 | G | C | 2 | a0002c0001t0001g0037 a0002c0001t0001g0115 |
3 | HG00733.hp1 HG01433.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.778+1134G>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35263826 | |||||||
| chr19:35263862 | A | C | 1 | a0001c0002t0001g0091 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.778+1170A>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35263862 | |||||||
| chr19:35263925 | G | T | 12 | a0002c0001t0001g0006 a0002c0001t0001g0013 a0002c0001t0001g0035 others(9): Show |
30 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.778+1233G>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35263925 | |||||||
| chr19:35263994 | C | T | 1 | a0002c0001t0001g0050 | 2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.778+1302C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35263994 | |||||||
| chr19:35264048 | C | T | 18 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0049 others(15): Show |
52 | HG00140.hp1 HG00558.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.778+1356C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35264048 | |||||||
| chr19:35264073 | C | A | 7 | a0002c0006t0001g0020 a0002c0006t0001g0021 a0002c0006t0001g0048 others(4): Show |
12 | HG02622.hp2 HG02717.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.778+1381C>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35264073 | |||||||
| chr19:35264283 | AG | A | 3 | a0002c0001t0001g0051 a0002c0001t0001g0188 a0002c0001t0001g0189 |
4 | HG02258.hp2 HG02723.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.778+1593delG | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr19 | 35264283 | ||||||
| chr19:35264310 | A | G | 1 | a0003c0003t0001g0132 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.778+1618A>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35264310 | |||||||
| chr19:35264355 | A | G | 4 | a0001c0002t0001g0031 a0001c0002t0001g0032 a0001c0002t0001g0097 others(1): Show |
5 | HG01257.hp1 HG01891.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.778+1663A>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35264355 | |||||||
| chr19:35264434 | T | G | 1 | a0001c0002t0001g0034 | 2 | HG00140.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.778+1742T>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35264434 | |||||||
| chr19:35264440 | C | T | 3 | a0003c0003t0001g0045 a0003c0003t0001g0139 a0003c0003t0001g0141 |
4 | HG02056.hp2 NA18984.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.778+1748C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35264440 | |||||||
| chr19:35264460 | C | G | 3 | a0002c0001t0001g0050 a0002c0006t0001g0062 a0007c0009t0001g0060 |
4 | HG02257.hp1 HG02976.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.778+1768C>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35264460 | |||||||
| chr19:35264483 | G | A | 16 | a0002c0001t0001g0006 a0002c0001t0001g0013 a0002c0001t0001g0035 others(13): Show |
35 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.778+1791G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35264483 | |||||||
| chr19:35264509 | C | T | 3 | a0002c0001t0001g0051 a0002c0001t0001g0188 a0002c0001t0001g0189 |
4 | HG02258.hp2 HG02723.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.778+1817C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35264509 | |||||||
| chr19:35264624 | T | C | 1 | a0003c0003t0001g0156 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.779-1735T>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35264624 | |||||||
| chr19:35264803 | C | T | 3 | a0002c0001t0001g0051 a0002c0001t0001g0188 a0002c0001t0001g0189 |
4 | HG02258.hp2 HG02723.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.779-1556C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35264803 | |||||||
| chr19:35264939 | CAG | C | 45 | a0003c0003t0001g0005 a0003c0003t0001g0009 a0003c0003t0001g0012 others(42): Show |
83 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.779-1417_779-1416d others(4): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr19 | 35264939 | ||||||
| chr19:35264971 | C | T | 1 | a0005c0010t0001g0122 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.779-1388C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35264971 | |||||||
| chr19:35264973 | G | C | 1 | a0001c0002t0001g0097 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.779-1386G>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35264973 | |||||||
| chr19:35265119 | C | T | 1 | a0002c0006t0001g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.779-1240C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35265119 | |||||||
| chr19:35265252 | C | A | 16 | a0002c0001t0001g0006 a0002c0001t0001g0013 a0002c0001t0001g0035 others(13): Show |
35 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.779-1107C>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35265252 | |||||||
| chr19:35265275 | T | C | 13 | a0002c0001t0001g0006 a0002c0001t0001g0013 a0002c0001t0001g0035 others(10): Show |
31 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.779-1084T>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35265275 | |||||||
| chr19:35265633 | T | TAGGAAGG others(5): Show |
6 | a0003c0003t0001g0024 a0003c0003t0001g0129 a0003c0003t0001g0153 others(3): Show |
8 | HG00735.hp2 HG01081.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.779-723_779-722ins others(12): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr19 | 35265633 | ||||||
| chr19:35265633 | T | TAGGGAGG others(5): Show |
48 | a0002c0001t0001g0165 a0002c0001t0001g0181 a0002c0006t0001g0020 others(45): Show |
89 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.779-717_779-706dup others(12): Show |
LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr19 | 35265633 | ||||||
| chr19:35265784 | C | T | 1 | a0001c0002t0001g0030 | 2 | NA18980.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.779-575C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35265784 | |||||||
| chr19:35265819 | T | TG | 106 | a0001c0002t0001g0086 a0002c0001t0001g0001 a0002c0001t0001g0007 others(103): Show |
203 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.779-537dupG | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr19 | 35265819 | ||||||
| chr19:35265832 | C | T | 55 | a0002c0001t0001g0165 a0002c0001t0001g0181 a0002c0006t0001g0020 others(52): Show |
98 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.779-527C>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35265832 | |||||||
| chr19:35266013 | T | C | 1 | a0002c0001t0001g0202 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.779-346T>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35266013 | |||||||
| chr19:35266306 | G | T | 7 | a0002c0006t0001g0020 a0002c0006t0001g0021 a0002c0006t0001g0048 others(4): Show |
12 | HG02622.hp2 HG02717.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.779-53G>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35266306 | |||||||
| chr19:35266344 | A | G | 1 | a0003c0003t0001g0142 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.779-15A>G | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35266344 | |||||||
| chr19:35266347 | G | A | 39 | a0002c0001t0001g0001 a0002c0001t0001g0007 a0002c0001t0001g0016 others(36): Show |
91 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.779-12G>A | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 5/9 | chr19 | 35266347 | |||||||
| chr19:35266566 | A | C | 29 | a0001c0002t0001g0022 a0001c0002t0001g0040 a0001c0002t0001g0041 others(26): Show |
67 | HG00140.hp1 HG00558.hp2 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.952+34A>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 6/9 | chr19 | 35266566 | |||||||
| chr19:35266983 | G | C | 1 | a0002c0001t0001g0198 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1144+16G>C | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 8/9 | chr19 | 35266983 | |||||||
| chr19:35267010 | G | T | 9 | a0001c0002t0001g0022 a0001c0002t0001g0040 a0001c0002t0001g0041 others(6): Show |
13 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1144+43G>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 8/9 | chr19 | 35267010 | |||||||
| chr19:35267051 | G | T | 1 | a0001c0005t0001g0185 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1145-58G>T | LSR | ENSG00000105699.17 | transcript | ENST00000605618.6 | protein_coding | 8/9 | chr19 | 35267051 |