Item | Value |
---|---|
geneid | 667 |
ensemblid | ENSG00000151914.22 |
hgncid | 1090 |
symbol | DST |
name | dystonin |
refseq_nuc | NM_001723.7 |
refseq_prot | NP_001714.1 |
ensembl_nuc | ENST00000370765.11 |
ensembl_prot | ENSP00000359801.6 |
mane_status | MANE Plus Clinical |
chr | chr6 |
start | 56614597 |
end | 56642889 |
strand | - |
ver | v1.2 |
region | chr6:56614597-56642889 |
region5000 | chr6:56609597-56647889 |
regionname0 | DST_chr6_56614597_56642889 |
regionname5000 | DST_chr6_56609597_56647889 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 2649 | 166 | 32 | 28 | 79 | 6 | 19 | 59 | DST_chr6_56609597_56647889 | DST | MHSSS others(2644): Show |
chr6 | 56609597 | 56647889 |
a0002 | 0/0 | 2649 | 96 | 12 | 23 | 44 | 4 | 13 | 35 | DST_chr6_56609597_56647889 | DST | MHSSS others(2644): Show |
chr6 | 56609597 | 56647889 |
a0003 | 0/0 | 2649 | 11 | 10 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | MHSSS others(2644): Show |
chr6 | 56609597 | 56647889 |
a0004 | 0/0 | 2649 | 10 | 9 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | MHSSS others(2644): Show |
chr6 | 56609597 | 56647889 |
a0005 | 0/0 | 2649 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | MHSSS others(2644): Show |
chr6 | 56609597 | 56647889 |
a0006 | 0/0 | 2649 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | MHSSS others(2644): Show |
chr6 | 56609597 | 56647889 |
a0007 | 0/0 | 2649 | 4 | 0 | 2 | 0 | 2 | 0 | 0 | DST_chr6_56609597_56647889 | DST | MHSSS others(2644): Show |
chr6 | 56609597 | 56647889 |
a0008 | 0/0 | 2649 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | MHSSS others(2644): Show |
chr6 | 56609597 | 56647889 |
a0009 | 0/0 | 2649 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | MHSSS others(2644): Show |
chr6 | 56609597 | 56647889 |
a0010 | 0/0 | 2649 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | MHSSS others(2644): Show |
chr6 | 56609597 | 56647889 |
a0011 | 0/0 | 2649 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | MHSSS others(2644): Show |
chr6 | 56609597 | 56647889 |
a0012 | 0/0 | 2649 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | MHSSS others(2644): Show |
chr6 | 56609597 | 56647889 |
a0013 | 0/0 | 2649 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | MHSSS others(2644): Show |
chr6 | 56609597 | 56647889 |
a0014 | 0/0 | 2649 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | MHSSS others(2644): Show |
chr6 | 56609597 | 56647889 |
a0015 | 0/0 | 2649 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | MHSSS others(2644): Show |
chr6 | 56609597 | 56647889 |
a0016 | 0/0 | 2649 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | MHSSS others(2644): Show |
chr6 | 56609597 | 56647889 |
a0017 | 0/0 | 2649 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | MHSSS others(2644): Show |
chr6 | 56609597 | 56647889 |
a0018 | 0/0 | 2649 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | MHSSS others(2644): Show |
chr6 | 56609597 | 56647889 |
a0019 | 0/0 | 2649 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | MHSSS others(2644): Show |
chr6 | 56609597 | 56647889 |
a0020 | 0/0 | 2649 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | MHSSS others(2644): Show |
chr6 | 56609597 | 56647889 |
a0021 | 0/0 | 2649 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DST_chr6_56609597_56647889 | DST | MHSSS others(2644): Show |
chr6 | 56609597 | 56647889 |
a0022 | 0/0 | 2649 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DST_chr6_56609597_56647889 | DST | MHSSS others(2644): Show |
chr6 | 56609597 | 56647889 |
a0023 | 0/0 | 2649 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | MHSSS others(2644): Show |
chr6 | 56609597 | 56647889 |
a0024 | 0/0 | 2649 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | MHSSS others(2644): Show |
chr6 | 56609597 | 56647889 |
a0025 | 0/0 | 2649 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DST_chr6_56609597_56647889 | DST | MHSSS others(2644): Show |
chr6 | 56609597 | 56647889 |
a0026 | 0/0 | 2649 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DST_chr6_56609597_56647889 | DST | MHSSS others(2644): Show |
chr6 | 56609597 | 56647889 |
a0027 | 0/0 | 2649 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | MHSSS others(2644): Show |
chr6 | 56609597 | 56647889 |
a0028 | 0/0 | 2649 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | MHSSS others(2644): Show |
chr6 | 56609597 | 56647889 |
a0029 | 0/0 | 2620 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DST_chr6_56609597_56647889 | DST | MHSSS others(2615): Show |
chr6 | 56609597 | 56647889 |
a0030 | 0/0 | 2649 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DST_chr6_56609597_56647889 | DST | MHSSS others(2644): Show |
chr6 | 56609597 | 56647889 |
a0031 | 0/0 | 2649 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | MHSSS others(2644): Show |
chr6 | 56609597 | 56647889 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 7947 | 159 | 32 | 26 | 78 | 6 | 15 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0001c0012 | 0/0 | 7947 | 2 | 0 | 0 | 0 | 0 | 2 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0001c0014 | 0/0 | 7947 | 2 | 0 | 2 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0001c0034 | 0/0 | 7947 | 1 | 0 | 0 | 0 | 0 | 1 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0001c0035 | 0/0 | 7947 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0001c0037 | 0/0 | 7947 | 1 | 0 | 0 | 0 | 0 | 1 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0002c0002 | 0/0 | 7947 | 71 | 4 | 22 | 31 | 4 | 10 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0002c0003 | 0/0 | 7947 | 14 | 0 | 1 | 10 | 0 | 3 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0002c0005 | 0/0 | 7947 | 8 | 8 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0002c0015 | 0/0 | 7947 | 2 | 0 | 0 | 2 | 0 | 0 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0002c0031 | 0/0 | 7947 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0003c0004 | 0/0 | 7947 | 11 | 10 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0004c0006 | 0/0 | 7947 | 7 | 6 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0004c0011 | 0/0 | 7947 | 3 | 3 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0005c0007 | 0/0 | 7947 | 5 | 5 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0005c0020 | 0/0 | 7947 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0006c0010 | 0/0 | 7947 | 3 | 3 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0006c0016 | 0/0 | 7947 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0006c0022 | 0/0 | 7947 | 1 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0007c0009 | 0/0 | 7947 | 4 | 0 | 2 | 0 | 2 | 0 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0008c0008 | 0/0 | 7947 | 4 | 4 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0009c0013 | 0/0 | 7947 | 2 | 0 | 2 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0010c0036 | 0/0 | 7947 | 1 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0011c0025 | 0/0 | 7947 | 1 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0012c0028 | 0/0 | 7947 | 1 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0013c0041 | 0/0 | 7947 | 1 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0014c0038 | 0/0 | 7947 | 1 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0015c0026 | 0/0 | 7947 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0016c0032 | 0/0 | 7947 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0017c0043 | 0/0 | 7947 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0018c0024 | 0/0 | 7947 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0019c0030 | 0/0 | 7947 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0020c0018 | 0/0 | 7947 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0021c0017 | 0/0 | 7947 | 1 | 0 | 0 | 0 | 0 | 1 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0022c0039 | 0/0 | 7947 | 1 | 0 | 0 | 0 | 0 | 1 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0023c0042 | 0/0 | 7947 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0024c0019 | 0/0 | 7947 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0025c0040 | 0/0 | 7947 | 1 | 0 | 0 | 0 | 0 | 1 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0026c0044 | 0/0 | 7947 | 1 | 0 | 0 | 0 | 0 | 1 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0027c0021 | 0/0 | 7947 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0028c0027 | 0/0 | 7947 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0029c0033 | 0/0 | 7966 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | ATGCA others(7961): Show |
chr6 | 56609597 | 56647889 | ||
a0030c0029 | 0/0 | 7947 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 | ||
a0031c0023 | 0/0 | 7947 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | ATGCA others(7942): Show |
chr6 | 56609597 | 56647889 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 8971 | 145 | 31 | 26 | 67 | 6 | 14 | DST_chr6_56609597_56647889 | DST | AGCTG others(8966): Show |
chr6 | 56609597 | 56647889 |
a0001c0001t0002 | 0/0 | 8973 | 2 | 0 | 0 | 2 | 0 | 0 | DST_chr6_56609597_56647889 | DST | AGCTG others(8968): Show |
chr6 | 56609597 | 56647889 |
a0001c0001t0004 | 0/0 | 8971 | 7 | 0 | 0 | 7 | 0 | 0 | DST_chr6_56609597_56647889 | DST | AGCTG others(8966): Show |
chr6 | 56609597 | 56647889 |
a0001c0001t0005 | 0/0 | 8971 | 2 | 0 | 0 | 2 | 0 | 0 | DST_chr6_56609597_56647889 | DST | AGCTG others(8966): Show |
chr6 | 56609597 | 56647889 |
a0001c0001t0007 | 0/1 | 8971 | 2 | 0 | 0 | 0 | 0 | 1 | DST_chr6_56609597_56647889 | DST | AGCTG others(8966): Show |
chr6 | 56609597 | 56647889 |
a0001c0001t0008 | 0/0 | 8971 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | AGCTG others(8966): Show |
chr6 | 56609597 | 56647889 |
a0001c0012t0001 | 0/0 | 8971 | 2 | 0 | 0 | 0 | 0 | 2 | DST_chr6_56609597_56647889 | DST | AGCTG others(8966): Show |
chr6 | 56609597 | 56647889 |
a0001c0014t0001 | 0/0 | 8971 | 2 | 0 | 2 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | AGCTG others(8966): Show |
chr6 | 56609597 | 56647889 |
a0001c0034t0001 | 0/0 | 8971 | 1 | 0 | 0 | 0 | 0 | 1 | DST_chr6_56609597_56647889 | DST | AGCTG others(8966): Show |
chr6 | 56609597 | 56647889 |
a0001c0035t0001 | 0/0 | 8971 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | AGCTG others(8966): Show |
chr6 | 56609597 | 56647889 |
a0001c0037t0001 | 0/0 | 8971 | 1 | 0 | 0 | 0 | 0 | 1 | DST_chr6_56609597_56647889 | DST | AGCTG others(8966): Show |
chr6 | 56609597 | 56647889 |
a0002c0002t0002 | 0/0 | 8973 | 71 | 4 | 22 | 31 | 4 | 10 | DST_chr6_56609597_56647889 | DST | AGCTG others(8968): Show |
chr6 | 56609597 | 56647889 |
a0002c0003t0002 | 0/0 | 8973 | 14 | 0 | 1 | 10 | 0 | 3 | DST_chr6_56609597_56647889 | DST | AGCTG others(8968): Show |
chr6 | 56609597 | 56647889 |
a0002c0005t0001 | 0/0 | 8971 | 3 | 3 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | AGCTG others(8966): Show |
chr6 | 56609597 | 56647889 |
a0002c0005t0003 | 0/0 | 8972 | 5 | 5 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | AGCTG others(8967): Show |
chr6 | 56609597 | 56647889 |
a0002c0015t0002 | 0/0 | 8973 | 2 | 0 | 0 | 2 | 0 | 0 | DST_chr6_56609597_56647889 | DST | AGCTG others(8968): Show |
chr6 | 56609597 | 56647889 |
a0002c0031t0002 | 0/0 | 8973 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | AGCTG others(8968): Show |
chr6 | 56609597 | 56647889 |
a0003c0004t0003 | 0/0 | 8972 | 11 | 10 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | AGCTG others(8967): Show |
chr6 | 56609597 | 56647889 |
a0004c0006t0003 | 0/0 | 8972 | 7 | 6 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | AGCTG others(8967): Show |
chr6 | 56609597 | 56647889 |
a0004c0011t0006 | 0/0 | 8972 | 3 | 3 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | AGCTG others(8967): Show |
chr6 | 56609597 | 56647889 |
a0005c0007t0003 | 0/0 | 8972 | 5 | 5 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | AGCTG others(8967): Show |
chr6 | 56609597 | 56647889 |
a0005c0020t0001 | 0/0 | 8971 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | AGCTG others(8966): Show |
chr6 | 56609597 | 56647889 |
a0006c0010t0001 | 0/0 | 8971 | 3 | 3 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | AGCTG others(8966): Show |
chr6 | 56609597 | 56647889 |
a0006c0016t0001 | 0/0 | 8971 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | AGCTG others(8966): Show |
chr6 | 56609597 | 56647889 |
a0006c0022t0001 | 0/0 | 8971 | 1 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | AGCTG others(8966): Show |
chr6 | 56609597 | 56647889 |
a0007c0009t0001 | 0/0 | 8971 | 4 | 0 | 2 | 0 | 2 | 0 | DST_chr6_56609597_56647889 | DST | AGCTG others(8966): Show |
chr6 | 56609597 | 56647889 |
a0008c0008t0001 | 0/0 | 8971 | 4 | 4 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | AGCTG others(8966): Show |
chr6 | 56609597 | 56647889 |
a0009c0013t0001 | 0/0 | 8971 | 2 | 0 | 2 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | AGCTG others(8966): Show |
chr6 | 56609597 | 56647889 |
a0010c0036t0001 | 0/0 | 8971 | 1 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | AGCTG others(8966): Show |
chr6 | 56609597 | 56647889 |
a0011c0025t0007 | 0/0 | 8971 | 1 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | AGCTG others(8966): Show |
chr6 | 56609597 | 56647889 |
a0012c0028t0002 | 0/0 | 8973 | 1 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | AGCTG others(8968): Show |
chr6 | 56609597 | 56647889 |
a0013c0041t0001 | 0/0 | 8971 | 1 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | AGCTG others(8966): Show |
chr6 | 56609597 | 56647889 |
a0014c0038t0001 | 0/0 | 8971 | 1 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | AGCTG others(8966): Show |
chr6 | 56609597 | 56647889 |
a0015c0026t0005 | 0/0 | 8971 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | AGCTG others(8966): Show |
chr6 | 56609597 | 56647889 |
a0016c0032t0002 | 0/0 | 8973 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | AGCTG others(8968): Show |
chr6 | 56609597 | 56647889 |
a0017c0043t0001 | 0/0 | 8971 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | AGCTG others(8966): Show |
chr6 | 56609597 | 56647889 |
a0018c0024t0003 | 0/0 | 8972 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | AGCTG others(8967): Show |
chr6 | 56609597 | 56647889 |
a0019c0030t0001 | 0/0 | 8971 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | AGCTG others(8966): Show |
chr6 | 56609597 | 56647889 |
a0020c0018t0003 | 0/0 | 8972 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | AGCTG others(8967): Show |
chr6 | 56609597 | 56647889 |
a0021c0017t0009 | 0/0 | 8972 | 1 | 0 | 0 | 0 | 0 | 1 | DST_chr6_56609597_56647889 | DST | AGCTG others(8967): Show |
chr6 | 56609597 | 56647889 |
a0022c0039t0002 | 0/0 | 8973 | 1 | 0 | 0 | 0 | 0 | 1 | DST_chr6_56609597_56647889 | DST | AGCTG others(8968): Show |
chr6 | 56609597 | 56647889 |
a0023c0042t0001 | 0/0 | 8971 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | AGCTG others(8966): Show |
chr6 | 56609597 | 56647889 |
a0024c0019t0003 | 0/0 | 8972 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | AGCTG others(8967): Show |
chr6 | 56609597 | 56647889 |
a0025c0040t0002 | 0/0 | 8973 | 1 | 0 | 0 | 0 | 0 | 1 | DST_chr6_56609597_56647889 | DST | AGCTG others(8968): Show |
chr6 | 56609597 | 56647889 |
a0026c0044t0001 | 0/0 | 8971 | 1 | 0 | 0 | 0 | 0 | 1 | DST_chr6_56609597_56647889 | DST | AGCTG others(8966): Show |
chr6 | 56609597 | 56647889 |
a0027c0021t0001 | 0/0 | 8971 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | AGCTG others(8966): Show |
chr6 | 56609597 | 56647889 |
a0028c0027t0002 | 0/0 | 8973 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | AGCTG others(8968): Show |
chr6 | 56609597 | 56647889 |
a0029c0033t0001 | 0/0 | 8990 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | AGCTG others(8985): Show |
chr6 | 56609597 | 56647889 |
a0030c0029t0001 | 0/0 | 8971 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | AGCTG others(8966): Show |
chr6 | 56609597 | 56647889 |
a0031c0023t0001 | 0/0 | 8971 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | AGCTG others(8966): Show |
chr6 | 56609597 | 56647889 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 30 | 3 | 9 | 12 | 2 | 4 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0003 | 0/0 | 12 | 11 | 0 | 0 | 0 | 1 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0005 | 0/0 | 6 | 0 | 3 | 1 | 0 | 2 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0013 | 1/0 | 3 | 0 | 0 | 2 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0031 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0004g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0005g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0007g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0007g0106 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0001t0008g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0012t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0014t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0034t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0035t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0001c0037t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0002t0002g0002 | 0/0 | 25 | 0 | 8 | 11 | 1 | 5 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0002t0002g0006 | 0/0 | 6 | 1 | 3 | 2 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0002t0002g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0002t0002g0016 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0002t0002g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0002t0002g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0002t0002g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0002t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0002t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0002t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0002t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0002t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0002t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0002t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0002t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0002t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0003t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0003t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0003t0002g0036 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0003t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0003t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0003t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0003t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0003t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0003t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0003t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0003t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0005t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0005t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0005t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0005t0003g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0005t0003g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0015t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0015t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0002c0031t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0003c0004t0003g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0003c0004t0003g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0003c0004t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0003c0004t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0003c0004t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0003c0004t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0003c0004t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0004c0006t0003g0007 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0004c0006t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0004c0006t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0004c0006t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0004c0011t0006g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0004c0011t0006g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0004c0011t0006g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0005c0007t0003g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0005c0007t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0005c0007t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0005c0007t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0005c0020t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0006c0010t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0006c0010t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0006c0010t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0006c0016t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0006c0022t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0007c0009t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0007c0009t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0007c0009t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0008c0008t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0008c0008t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0008c0008t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0009c0013t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0010c0036t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0011c0025t0007g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0012c0028t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0013c0041t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0014c0038t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0015c0026t0005g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0016c0032t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0017c0043t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0018c0024t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0019c0030t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0020c0018t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0021c0017t0009g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0022c0039t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0023c0042t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0024c0019t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0025c0040t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0026c0044t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0027c0021t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0028c0027t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0029c0033t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0030c0029t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
a0031c0023t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG00099 | hp2 | a0002 | c0002 | t0002 | g0033 | EUR | GBR | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0143 | EUR | GBR | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG00323 | hp1 | a0002 | c0002 | t0002 | g0188 | EUR | FIN | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG00323 | hp2 | a0002 | c0002 | t0002 | g0194 | EUR | FIN | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG00408 | hp2 | a0002 | c0003 | t0002 | g0036 | EAS | CHS | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG00423 | hp1 | a0002 | c0002 | t0002 | g0176 | EAS | CHS | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG00438 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG00597 | hp1 | a0002 | c0002 | t0002 | g0131 | EAS | CHS | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG00609 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG00642 | hp2 | a0002 | c0002 | t0002 | g0150 | AMR | PUR | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG00673 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG00733 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | PUR | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG00735 | hp1 | a0010 | c0036 | t0001 | g0104 | AMR | PUR | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG00735 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG00741 | hp1 | a0002 | c0002 | t0002 | g0200 | AMR | PUR | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG00741 | hp2 | a0009 | c0013 | t0001 | g0030 | AMR | PUR | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01069 | hp1 | a0004 | c0006 | t0003 | g0007 | AMR | PUR | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01071 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01074 | hp1 | a0011 | c0025 | t0007 | g0124 | AMR | PUR | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01081 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01106 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01109 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | PUR | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01169 | hp1 | a0009 | c0013 | t0001 | g0030 | AMR | PUR | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01169 | hp2 | a0002 | c0002 | t0002 | g0172 | AMR | PUR | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01175 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | PUR | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01192 | hp1 | a0001 | c0014 | t0001 | g0023 | AMR | PUR | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01192 | hp2 | a0002 | c0002 | t0002 | g0173 | AMR | PUR | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01243 | hp1 | a0002 | c0002 | t0002 | g0120 | AMR | PUR | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01255 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01256 | hp1 | a0002 | c0002 | t0002 | g0021 | AMR | CLM | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01256 | hp2 | a0012 | c0028 | t0002 | g0177 | AMR | CLM | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01257 | hp2 | a0007 | c0009 | t0001 | g0032 | AMR | CLM | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01258 | hp1 | a0002 | c0002 | t0002 | g0021 | AMR | CLM | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01258 | hp2 | a0007 | c0009 | t0001 | g0032 | AMR | CLM | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01261 | hp2 | a0002 | c0002 | t0002 | g0033 | AMR | CLM | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01358 | hp1 | a0006 | c0022 | t0001 | g0058 | AMR | CLM | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01358 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01361 | hp2 | a0002 | c0003 | t0002 | g0076 | AMR | CLM | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01433 | hp1 | a0013 | c0041 | t0001 | g0074 | AMR | CLM | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01496 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01496 | hp2 | a0001 | c0014 | t0001 | g0023 | AMR | CLM | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01515 | hp1 | a0007 | c0009 | t0001 | g0155 | EUR | IBS | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01515 | hp2 | a0002 | c0002 | t0002 | g0002 | EUR | IBS | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0154 | EUR | IBS | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01517 | hp2 | a0007 | c0009 | t0001 | g0092 | EUR | IBS | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01884 | hp2 | a0006 | c0010 | t0001 | g0043 | AFR | ACB | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01891 | hp1 | a0008 | c0008 | t0001 | g0018 | AFR | ACB | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01928 | hp1 | a0014 | c0038 | t0001 | g0148 | AMR | PEL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01952 | hp1 | a0002 | c0002 | t0002 | g0035 | AMR | PEL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01975 | hp1 | a0002 | c0002 | t0002 | g0016 | AMR | PEL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02004 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02015 | hp2 | a0002 | c0002 | t0002 | g0035 | EAS | KHV | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02027 | hp2 | a0015 | c0026 | t0005 | g0125 | EAS | KHV | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02055 | hp1 | a0004 | c0011 | t0006 | g0045 | AFR | ACB | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02071 | hp1 | a0001 | c0001 | t0005 | g0027 | EAS | KHV | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02074 | hp1 | a0016 | c0032 | t0002 | g0179 | EAS | KHV | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02074 | hp2 | a0017 | c0043 | t0001 | g0117 | EAS | KHV | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02080 | hp2 | a0002 | c0003 | t0002 | g0110 | EAS | KHV | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02129 | hp2 | a0002 | c0003 | t0002 | g0174 | EAS | KHV | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02132 | hp1 | a0003 | c0004 | t0003 | g0054 | EAS | KHV | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02145 | hp2 | a0018 | c0024 | t0003 | g0063 | AFR | ACB | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02257 | hp1 | a0002 | c0005 | t0003 | g0026 | AFR | ACB | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02258 | hp1 | a0003 | c0004 | t0003 | g0017 | AFR | ACB | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02280 | hp1 | a0002 | c0005 | t0003 | g0014 | AFR | ACB | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02280 | hp2 | a0002 | c0005 | t0001 | g0067 | AFR | ACB | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02300 | hp2 | a0002 | c0002 | t0002 | g0139 | AMR | PEL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02451 | hp1 | a0004 | c0006 | t0003 | g0047 | AFR | ACB | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02451 | hp2 | a0003 | c0004 | t0003 | g0008 | AFR | ACB | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02523 | hp1 | a0001 | c0001 | t0005 | g0027 | EAS | KHV | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02572 | hp2 | a0004 | c0006 | t0003 | g0046 | AFR | GWD | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02602 | hp1 | a0002 | c0002 | t0002 | g0186 | SAS | PJL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02602 | hp2 | a0021 | c0017 | t0009 | g0039 | SAS | PJL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02615 | hp2 | a0004 | c0011 | t0006 | g0044 | AFR | GWD | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02622 | hp1 | a0004 | c0006 | t0003 | g0048 | AFR | GWD | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02622 | hp2 | a0005 | c0007 | t0003 | g0061 | AFR | GWD | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02647 | hp2 | a0003 | c0004 | t0003 | g0008 | AFR | GWD | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02683 | hp1 | a0001 | c0001 | t0007 | g0099 | SAS | PJL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02683 | hp2 | a0022 | c0039 | t0002 | g0190 | SAS | PJL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02717 | hp1 | a0002 | c0005 | t0003 | g0014 | AFR | GWD | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02723 | hp2 | a0004 | c0006 | t0003 | g0007 | AFR | GWD | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02735 | hp1 | a0002 | c0003 | t0002 | g0169 | SAS | PJL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02738 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02809 | hp2 | a0002 | c0005 | t0003 | g0026 | AFR | GWD | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02818 | hp1 | a0005 | c0020 | t0001 | g0062 | AFR | GWD | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02886 | hp2 | a0003 | c0004 | t0003 | g0008 | AFR | GWD | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02895 | hp1 | a0002 | c0002 | t0002 | g0016 | AFR | GWD | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02895 | hp2 | a0002 | c0005 | t0001 | g0140 | AFR | GWD | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02897 | hp1 | a0023 | c0042 | t0001 | g0198 | AFR | GWD | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02897 | hp2 | a0002 | c0002 | t0002 | g0016 | AFR | GWD | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02922 | hp1 | a0003 | c0004 | t0003 | g0017 | AFR | ESN | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02965 | hp2 | a0003 | c0004 | t0003 | g0051 | AFR | ESN | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02976 | hp2 | a0002 | c0005 | t0003 | g0014 | AFR | ESN | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03017 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03041 | hp2 | a0005 | c0007 | t0003 | g0060 | AFR | GWD | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03098 | hp1 | a0002 | c0002 | t0002 | g0199 | AFR | MSL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03098 | hp2 | a0005 | c0007 | t0003 | g0019 | AFR | MSL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03139 | hp2 | a0024 | c0019 | t0003 | g0065 | AFR | ESN | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03195 | hp1 | a0005 | c0007 | t0003 | g0019 | AFR | ESN | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03195 | hp2 | a0006 | c0010 | t0001 | g0041 | AFR | ESN | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03209 | hp2 | a0006 | c0010 | t0001 | g0042 | AFR | MSL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03225 | hp1 | a0001 | c0001 | t0008 | g0123 | AFR | MSL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03225 | hp2 | a0004 | c0006 | t0003 | g0007 | AFR | MSL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03239 | hp1 | a0001 | c0012 | t0001 | g0022 | SAS | PJL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03239 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03453 | hp2 | a0003 | c0004 | t0003 | g0008 | AFR | MSL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03486 | hp2 | a0004 | c0006 | t0003 | g0007 | AFR | MSL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03490 | hp1 | a0002 | c0002 | t0002 | g0189 | SAS | PJL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03516 | hp1 | a0002 | c0005 | t0001 | g0068 | AFR | ESN | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | MSL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03579 | hp2 | a0008 | c0008 | t0001 | g0052 | AFR | MSL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03654 | hp1 | a0002 | c0003 | t0002 | g0075 | SAS | PJL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03654 | hp2 | a0025 | c0040 | t0002 | g0191 | SAS | PJL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03669 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03688 | hp1 | a0002 | c0002 | t0002 | g0137 | SAS | STU | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03831 | hp2 | a0002 | c0003 | t0002 | g0036 | SAS | BEB | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03834 | hp2 | a0001 | c0034 | t0001 | g0122 | SAS | BEB | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03927 | hp1 | a0002 | c0002 | t0002 | g0138 | SAS | BEB | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03927 | hp2 | a0001 | c0012 | t0001 | g0022 | SAS | BEB | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03942 | hp2 | a0002 | c0002 | t0002 | g0187 | SAS | BEB | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | STU | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | STU | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | STU | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG04199 | hp2 | a0001 | c0037 | t0001 | g0142 | SAS | STU | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG04204 | hp1 | a0026 | c0044 | t0001 | g0197 | SAS | STU | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | STU | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | YRI | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18522 | hp2 | a0005 | c0007 | t0003 | g0059 | AFR | YRI | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHB | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18612 | hp2 | a0028 | c0027 | t0002 | g0171 | EAS | CHB | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18939 | hp1 | a0002 | c0003 | t0002 | g0024 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18940 | hp1 | a0002 | c0015 | t0002 | g0098 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18942 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18946 | hp2 | a0002 | c0003 | t0002 | g0167 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18947 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18949 | hp1 | a0001 | c0035 | t0001 | g0085 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18949 | hp2 | a0002 | c0002 | t0002 | g0184 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18950 | hp1 | a0002 | c0003 | t0002 | g0034 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18952 | hp2 | a0002 | c0015 | t0002 | g0181 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18956 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18957 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18962 | hp1 | a0002 | c0002 | t0002 | g0151 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18963 | hp2 | a0002 | c0002 | t0002 | g0038 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18965 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18965 | hp2 | a0002 | c0002 | t0002 | g0182 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18967 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18970 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18973 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18973 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18977 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18979 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18982 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18994 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18998 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19011 | hp1 | a0002 | c0003 | t0002 | g0107 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19011 | hp2 | a0002 | c0031 | t0002 | g0178 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19030 | hp2 | a0008 | c0008 | t0001 | g0053 | AFR | LWK | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19043 | hp1 | a0003 | c0004 | t0003 | g0050 | AFR | LWK | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19043 | hp2 | a0004 | c0011 | t0006 | g0049 | AFR | LWK | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19054 | hp2 | a0002 | c0002 | t0002 | g0170 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19058 | hp2 | a0002 | c0003 | t0002 | g0034 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19059 | hp2 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19063 | hp2 | a0001 | c0001 | t0004 | g0116 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19064 | hp2 | a0001 | c0001 | t0004 | g0105 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19066 | hp2 | a0002 | c0002 | t0002 | g0118 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19068 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19075 | hp1 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19081 | hp1 | a0002 | c0002 | t0002 | g0109 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19081 | hp2 | a0001 | c0001 | t0004 | g0111 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19084 | hp2 | a0002 | c0003 | t0002 | g0175 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19085 | hp1 | a0029 | c0033 | t0001 | g0103 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19085 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19086 | hp2 | a0030 | c0029 | t0001 | g0081 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19087 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19088 | hp1 | a0002 | c0003 | t0002 | g0024 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19090 | hp1 | a0002 | c0002 | t0002 | g0119 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA19091 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA20129 | hp2 | a0031 | c0023 | t0001 | g0066 | AFR | ASW | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | TSI | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0072 | EUR | TSI | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | GIH | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA20905 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | GIH | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02486 | hp2 | a0003 | c0004 | t0003 | g0056 | AFR | ACB | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02559 | hp1 | a0019 | c0030 | t0001 | g0159 | AFR | ACB | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG02559 | hp2 | a0020 | c0018 | t0003 | g0064 | AFR | ACB | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03471 | hp1 | a0006 | c0016 | t0001 | g0057 | AFR | MSL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG03471 | hp2 | a0008 | c0008 | t0001 | g0018 | AFR | MSL | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG06807 | hp1 | a0003 | c0004 | t0003 | g0040 | AFR | USA | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
HG06807 | hp2 | a0027 | c0021 | t0001 | g0055 | AFR | USA | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA18955 | hp2 | a0002 | c0002 | t0002 | g0038 | EAS | JPT | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
NA20300 | hp2 | a0002 | c0002 | t0002 | g0006 | AFR | USA | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
homoSapiens | chm13v2 | a0001 | c0001 | t0007 | g0106 | REF | REF | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0013 | REF | REF | DST_chr6_56609597_56647889 | DST | chr6 | 56609597 | 56647889 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:56615702 | T | C | 1 | a0021 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.7765A>G | p.Ile2589Val | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 24/24 | 7866/8971 | 7765/7950 | 2589/2649 | chr6 | 56615702 | |||
chr6:56615741 | T | TTGATAAC others(12): Show |
1 | a0029 | 1 | NA19085.hp1 | frameshift_variant | HIGH | c.7707_7725dupGGTTCA others(13): Show |
p.Ile2576fs | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 24/24 | 7826/8971 | 7725/7950 | 2575/2649 | chr6 | 56615741 | |||
chr6:56616608 | T | C | 1 | a0016 | 1 | HG02074.hp1 | missense_variant | MODERATE | c.6859A>G | p.Ser2287Gly | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 24/24 | 6960/8971 | 6859/7950 | 2287/2649 | chr6 | 56616608 | |||
chr6:56617094 | C | T | 1 | a0020 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.6373G>A | p.Val2125Ile | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 24/24 | 6474/8971 | 6373/7950 | 2125/2649 | chr6 | 56617094 | |||
chr6:56617289 | C | T | 1 | a0024 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.6178G>A | p.Asp2060Asn | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 24/24 | 6279/8971 | 6178/7950 | 2060/2649 | chr6 | 56617289 | |||
chr6:56618003 | C | G | 15 | a0002 a0003 a0004 others(12): Show |
141 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(138): Show |
missense_variant | MODERATE | c.6031G>C | p.Val2011Leu | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/24 | 6132/8971 | 6031/7950 | 2011/2649 | chr6 | 56618003 | |||
chr6:56618515 | C | T | 1 | a0019 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.5519G>A | p.Arg1840His | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/24 | 5620/8971 | 5519/7950 | 1840/2649 | chr6 | 56618515 | |||
chr6:56618549 | G | C | 1 | a0008 | 4 | HG01891.hp1 HG03471.hp2 HG03579.hp2 others(1): Show |
missense_variant | MODERATE | c.5485C>G | p.Gln1829Glu | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/24 | 5586/8971 | 5485/7950 | 1829/2649 | chr6 | 56618549 | |||
chr6:56618606 | A | G | 2 | a0018 a0020 |
2 | HG02145.hp2 HG02559.hp2 |
missense_variant | MODERATE | c.5428T>C | p.Tyr1810His | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/24 | 5529/8971 | 5428/7950 | 1810/2649 | chr6 | 56618606 | |||
chr6:56618840 | T | A | 1 | a0029 | 1 | NA19085.hp1 | missense_variant | MODERATE | c.5194A>T | p.Met1732Leu | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/24 | 5295/8971 | 5194/7950 | 1732/2649 | chr6 | 56618840 | |||
chr6:56618889 | C | A | 1 | a0029 | 1 | NA19085.hp1 | missense_variant | MODERATE | c.5145G>T | p.Arg1715Ser | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/24 | 5246/8971 | 5145/7950 | 1715/2649 | chr6 | 56618889 | |||
chr6:56618902 | T | A | 1 | a0029 | 1 | NA19085.hp1 | missense_variant | MODERATE | c.5132A>T | p.Glu1711Val | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/24 | 5233/8971 | 5132/7950 | 1711/2649 | chr6 | 56618902 | |||
chr6:56618915 | C | T | 1 | a0029 | 1 | NA19085.hp1 | missense_variant | MODERATE | c.5119G>A | p.Ala1707Thr | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/24 | 5220/8971 | 5119/7950 | 1707/2649 | chr6 | 56618915 | |||
chr6:56618916 | T | A | 1 | a0029 | 1 | NA19085.hp1 | missense_variant | MODERATE | c.5118A>T | p.Gln1706His | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/24 | 5219/8971 | 5118/7950 | 1706/2649 | chr6 | 56618916 | |||
chr6:56618917 | T | C | 1 | a0029 | 1 | NA19085.hp1 | missense_variant | MODERATE | c.5117A>G | p.Gln1706Arg | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/24 | 5218/8971 | 5117/7950 | 1706/2649 | chr6 | 56618917 | |||
chr6:56618937 | C | A | 1 | a0029 | 1 | NA19085.hp1 | missense_variant | MODERATE | c.5097G>T | p.Glu1699Asp | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/24 | 5198/8971 | 5097/7950 | 1699/2649 | chr6 | 56618937 | |||
chr6:56618938 | T | A | 1 | a0029 | 1 | NA19085.hp1 | missense_variant | MODERATE | c.5096A>T | p.Glu1699Val | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/24 | 5197/8971 | 5096/7950 | 1699/2649 | chr6 | 56618938 | |||
chr6:56618947 | C | T | 1 | a0029 | 1 | NA19085.hp1 | missense_variant | MODERATE | c.5087G>A | p.Arg1696Gln | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/24 | 5188/8971 | 5087/7950 | 1696/2649 | chr6 | 56618947 | |||
chr6:56619073 | G | A | 1 | a0009 | 2 | HG00741.hp2 HG01169.hp1 |
missense_variant | MODERATE | c.4961C>T | p.Ala1654Val | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/24 | 5062/8971 | 4961/7950 | 1654/2649 | chr6 | 56619073 | |||
chr6:56619257 | T | G | 1 | a0010 | 1 | HG00735.hp1 | missense_variant | MODERATE | c.4777A>C | p.Ile1593Leu | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/24 | 4878/8971 | 4777/7950 | 1593/2649 | chr6 | 56619257 | |||
chr6:56619634 | C | T | 1 | a0031 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.4400G>A | p.Arg1467His | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/24 | 4501/8971 | 4400/7950 | 1467/2649 | chr6 | 56619634 | |||
chr6:56619745 | G | A | 1 | a0008 | 4 | HG01891.hp1 HG03471.hp2 HG03579.hp2 others(1): Show |
missense_variant | MODERATE | c.4289C>T | p.Ala1430Val | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/24 | 4390/8971 | 4289/7950 | 1430/2649 | chr6 | 56619745 | |||
chr6:56619974 | G | T | 1 | a0019 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.4060C>A | p.Gln1354Lys | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/24 | 4161/8971 | 4060/7950 | 1354/2649 | chr6 | 56619974 | |||
chr6:56620225 | T | C | 1 | a0007 | 4 | HG01257.hp2 HG01258.hp2 HG01515.hp1 others(1): Show |
missense_variant | MODERATE | c.3809A>G | p.Lys1270Arg | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/24 | 3910/8971 | 3809/7950 | 1270/2649 | chr6 | 56620225 | |||
chr6:56620246 | A | G | 1 | a0030 | 1 | NA19086.hp2 | missense_variant | MODERATE | c.3788T>C | p.Leu1263Pro | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/24 | 3889/8971 | 3788/7950 | 1263/2649 | chr6 | 56620246 | |||
chr6:56620598 | T | C | 1 | a0014 | 1 | HG01928.hp1 | missense_variant | MODERATE | c.3436A>G | p.Met1146Val | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/24 | 3537/8971 | 3436/7950 | 1146/2649 | chr6 | 56620598 | |||
chr6:56620688 | G | A | 1 | a0005 | 6 | HG02622.hp2 HG02818.hp1 HG03041.hp2 others(3): Show |
missense_variant | MODERATE | c.3346C>T | p.His1116Tyr | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/24 | 3447/8971 | 3346/7950 | 1116/2649 | chr6 | 56620688 | |||
chr6:56620698 | C | G | 1 | a0012 | 1 | HG01256.hp2 | missense_variant | MODERATE | c.3336G>C | p.Glu1112Asp | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/24 | 3437/8971 | 3336/7950 | 1112/2649 | chr6 | 56620698 | |||
chr6:56628047 | A | C | 2 | a0004 a0031 |
11 | HG01069.hp1 HG02055.hp1 HG02451.hp1 others(8): Show |
missense_variant | MODERATE | c.2979T>G | p.Asn993Lys | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 19/24 | 3080/8971 | 2979/7950 | 993/2649 | chr6 | 56628047 | |||
chr6:56629261 | C | A | 1 | a0022 | 1 | HG02683.hp2 | missense_variant | MODERATE | c.2853G>T | p.Gln951His | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 18/24 | 2954/8971 | 2853/7950 | 951/2649 | chr6 | 56629261 | |||
chr6:56629356 | T | G | 1 | a0025 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.2758A>C | p.Met920Leu | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 18/24 | 2859/8971 | 2758/7950 | 920/2649 | chr6 | 56629356 | |||
chr6:56629395 | C | T | 1 | a0028 | 1 | NA18612.hp2 | missense_variant | MODERATE | c.2719G>A | p.Glu907Lys | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 18/24 | 2820/8971 | 2719/7950 | 907/2649 | chr6 | 56629395 | |||
chr6:56632934 | C | A | 1 | a0013 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.2114G>T | p.Gly705Val | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 14/24 | 2215/8971 | 2114/7950 | 705/2649 | chr6 | 56632934 | |||
chr6:56634196 | C | T | 1 | a0006 | 5 | HG01358.hp1 HG01884.hp2 HG03195.hp2 others(2): Show |
missense_variant | MODERATE | c.1946G>A | p.Ser649Asn | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 13/24 | 2047/8971 | 1946/7950 | 649/2649 | chr6 | 56634196 | |||
chr6:56634474 | T | A | 1 | a0023 | 1 | HG02897.hp1 | missense_variant | MODERATE | c.1871A>T | p.Asp624Val | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 12/24 | 1972/8971 | 1871/7950 | 624/2649 | chr6 | 56634474 | |||
chr6:56634502 | C | A | 1 | a0027 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.1843G>T | p.Val615Phe | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 12/24 | 1944/8971 | 1843/7950 | 615/2649 | chr6 | 56634502 | |||
chr6:56639763 | G | A | 1 | a0017 | 1 | HG02074.hp2 | missense_variant | MODERATE | c.1019C>T | p.Thr340Ile | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 6/24 | 1120/8971 | 1019/7950 | 340/2649 | chr6 | 56639763 | |||
chr6:56640032 | C | T | 1 | a0015 | 1 | HG02027.hp2 | missense_variant | MODERATE | c.905G>A | p.Gly302Asp | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 5/24 | 1006/8971 | 905/7950 | 302/2649 | chr6 | 56640032 | |||
chr6:56640283 | G | C | 1 | a0026 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.739C>G | p.Pro247Ala | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 4/24 | 840/8971 | 739/7950 | 247/2649 | chr6 | 56640283 | |||
chr6:56640591 | C | T | 1 | a0011 | 1 | HG01074.hp1 | missense_variant | MODERATE | c.431G>A | p.Arg144His | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 4/24 | 532/8971 | 431/7950 | 144/2649 | chr6 | 56640591 | |||
chr6:56642691 | A | G | 11 | a0003 a0004 a0005 others(8): Show |
42 | HG01069.hp1 HG01358.hp1 HG01884.hp2 others(39): Show |
missense_variant | MODERATE | c.98T>C | p.Leu33Ser | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 1/24 | 199/8971 | 98/7950 | 33/2649 | chr6 | 56642691 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:56615976 | C | T | 2 | a0005c0020 a0031c0023 |
2 | HG02818.hp1 NA20129.hp2 |
synonymous_variant | LOW | c.7491G>A | p.Lys2497Lys | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 24/24 | 7592/8971 | 7491/7950 | 2497/2649 | chr6 | 56615976 | |||
chr6:56616108 | C | T | 1 | a0002c0031 | 1 | NA19011.hp2 | synonymous_variant | LOW | c.7359G>A | p.Leu2453Leu | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 24/24 | 7460/8971 | 7359/7950 | 2453/2649 | chr6 | 56616108 | |||
chr6:56616834 | T | C | 1 | a0021c0017 | 1 | HG02602.hp2 | synonymous_variant | LOW | c.6633A>G | p.Ala2211Ala | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 24/24 | 6734/8971 | 6633/7950 | 2211/2649 | chr6 | 56616834 | |||
chr6:56616969 | C | T | 1 | a0001c0012 | 2 | HG03239.hp1 HG03927.hp2 |
synonymous_variant | LOW | c.6498G>A | p.Val2166Val | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 24/24 | 6599/8971 | 6498/7950 | 2166/2649 | chr6 | 56616969 | |||
chr6:56618028 | G | A | 1 | a0006c0010 | 3 | HG01884.hp2 HG03195.hp2 HG03209.hp2 |
synonymous_variant | LOW | c.6006C>T | p.Asn2002Asn | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/24 | 6107/8971 | 6006/7950 | 2002/2649 | chr6 | 56618028 | |||
chr6:56618268 | T | C | 1 | a0001c0034 | 1 | HG03834.hp2 | synonymous_variant | LOW | c.5766A>G | p.Glu1922Glu | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/24 | 5867/8971 | 5766/7950 | 1922/2649 | chr6 | 56618268 | |||
chr6:56618676 | G | A | 1 | a0001c0035 | 1 | NA18949.hp1 | synonymous_variant | LOW | c.5358C>T | p.Asn1786Asn | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/24 | 5459/8971 | 5358/7950 | 1786/2649 | chr6 | 56618676 | |||
chr6:56618940 | C | T | 1 | a0029c0033 | 1 | NA19085.hp1 | synonymous_variant | LOW | c.5094G>A | p.Gly1698Gly | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/24 | 5195/8971 | 5094/7950 | 1698/2649 | chr6 | 56618940 | |||
chr6:56618964 | A | G | 1 | a0029c0033 | 1 | NA19085.hp1 | synonymous_variant | LOW | c.5070T>C | p.Ala1690Ala | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/24 | 5171/8971 | 5070/7950 | 1690/2649 | chr6 | 56618964 | |||
chr6:56618979 | A | G | 4 | a0002c0005 a0006c0010 a0006c0016 others(1): Show |
13 | HG01358.hp1 HG01884.hp2 HG02257.hp1 others(10): Show |
synonymous_variant | LOW | c.5055T>C | p.Asn1685Asn | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/24 | 5156/8971 | 5055/7950 | 1685/2649 | chr6 | 56618979 | |||
chr6:56619054 | T | G | 2 | a0003c0004 a0024c0019 |
12 | HG02132.hp1 HG02258.hp1 HG02451.hp2 others(9): Show |
synonymous_variant | LOW | c.4980A>C | p.Val1660Val | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/24 | 5081/8971 | 4980/7950 | 1660/2649 | chr6 | 56619054 | |||
chr6:56619300 | C | T | 1 | a0001c0037 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.4734G>A | p.Glu1578Glu | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/24 | 4835/8971 | 4734/7950 | 1578/2649 | chr6 | 56619300 | |||
chr6:56619360 | G | A | 1 | a0001c0014 | 2 | HG01192.hp1 HG01496.hp2 |
synonymous_variant | LOW | c.4674C>T | p.Leu1558Leu | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/24 | 4775/8971 | 4674/7950 | 1558/2649 | chr6 | 56619360 | |||
chr6:56619570 | G | A | 1 | a0002c0015 | 2 | NA18940.hp1 NA18952.hp2 |
synonymous_variant | LOW | c.4464C>T | p.Asp1488Asp | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/24 | 4565/8971 | 4464/7950 | 1488/2649 | chr6 | 56619570 | |||
chr6:56619924 | T | C | 1 | a0001c0037 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.4110A>G | p.Glu1370Glu | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/24 | 4211/8971 | 4110/7950 | 1370/2649 | chr6 | 56619924 | |||
chr6:56619960 | C | T | 19 | a0002c0002 a0002c0005 a0002c0031 others(16): Show |
118 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(115): Show |
synonymous_variant | LOW | c.4074G>A | p.Lys1358Lys | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/24 | 4175/8971 | 4074/7950 | 1358/2649 | chr6 | 56619960 | |||
chr6:56629273 | A | G | 1 | a0021c0017 | 1 | HG02602.hp2 | synonymous_variant | LOW | c.2841T>C | p.Asn947Asn | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 18/24 | 2942/8971 | 2841/7950 | 947/2649 | chr6 | 56629273 | |||
chr6:56631291 | G | A | 2 | a0005c0007 a0005c0020 |
6 | HG02622.hp2 HG02818.hp1 HG03041.hp2 others(3): Show |
synonymous_variant | LOW | c.2451C>T | p.Val817Val | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 16/24 | 2552/8971 | 2451/7950 | 817/2649 | chr6 | 56631291 | |||
chr6:56634464 | G | A | 1 | a0005c0007 | 5 | HG02622.hp2 HG03041.hp2 HG03098.hp2 others(2): Show |
splice_region_variant&synonymous_variant | LOW | c.1881C>T | p.Asn627Asn | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 12/24 | 1982/8971 | 1881/7950 | 627/2649 | chr6 | 56634464 | |||
chr6:56639705 | T | C | 1 | a0006c0022 | 1 | HG01358.hp1 | synonymous_variant | LOW | c.1077A>G | p.Ala359Ala | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 6/24 | 1178/8971 | 1077/7950 | 359/2649 | chr6 | 56639705 | |||
chr6:56640028 | T | G | 1 | a0031c0023 | 1 | NA20129.hp2 | synonymous_variant | LOW | c.909A>C | p.Ser303Ser | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 5/24 | 1010/8971 | 909/7950 | 303/2649 | chr6 | 56640028 | |||
chr6:56640265 | A | G | 15 | a0003c0004 a0004c0006 a0004c0011 others(12): Show |
42 | HG01069.hp1 HG01358.hp1 HG01884.hp2 others(39): Show |
synonymous_variant | LOW | c.757T>C | p.Leu253Leu | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 4/24 | 858/8971 | 757/7950 | 253/2649 | chr6 | 56640265 | |||
chr6:56640476 | T | C | 1 | a0018c0024 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.546A>G | p.Ser182Ser | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 4/24 | 647/8971 | 546/7950 | 182/2649 | chr6 | 56640476 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:56614784 | T | A | 1 | a0004c0011t0006 | 3 | HG02055.hp1 HG02615.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*733A>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 24/24 | 733 | chr6 | 56614784 | ||||||
chr6:56614851 | G | A | 1 | a0021c0017t0009 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*666C>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 24/24 | 666 | chr6 | 56614851 | ||||||
chr6:56614914 | T | C | 2 | a0001c0001t0005 a0015c0026t0005 |
3 | HG02027.hp2 HG02071.hp1 HG02523.hp1 |
3_prime_UTR_variant | MODIFIER | c.*603A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 24/24 | 603 | chr6 | 56614914 | ||||||
chr6:56614922 | C | G | 2 | a0001c0001t0005 a0015c0026t0005 |
3 | HG02027.hp2 HG02071.hp1 HG02523.hp1 |
3_prime_UTR_variant | MODIFIER | c.*595G>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 24/24 | 595 | chr6 | 56614922 | ||||||
chr6:56615253 | G | A | 1 | a0001c0001t0008 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*264C>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 24/24 | 264 | chr6 | 56615253 | ||||||
chr6:56615254 | T | TA | 9 | a0002c0005t0003 a0003c0004t0003 a0004c0006t0003 others(6): Show |
35 | HG01069.hp1 HG02055.hp1 HG02132.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*262dupT | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 24/24 | 262 | chr6 | 56615254 | ||||||
chr6:56615254 | T | TAA | 10 | a0001c0001t0002 a0002c0002t0002 a0002c0003t0002 others(7): Show |
95 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*261_*262dupTT | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 24/24 | 262 | chr6 | 56615254 | ||||||
chr6:56615348 | T | G | 2 | a0001c0001t0007 a0011c0025t0007 |
2 | HG01074.hp1 HG02683.hp1 |
3_prime_UTR_variant | MODIFIER | c.*169A>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 24/24 | 169 | chr6 | 56615348 | ||||||
chr6:56615468 | C | T | 1 | a0001c0001t0004 | 7 | NA18956.hp1 NA18957.hp2 NA18970.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*49G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 24/24 | 49 | chr6 | 56615468 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:56617493 | C | A | 1 | a0001c0001t0001g0160 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.6049-75G>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/23 | chr6 | 56617493 | |||||||
chr6:56617581 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.6049-163A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/23 | chr6 | 56617581 | |||||||
chr6:56617655 | G | A | 63 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0009 others(60): Show |
110 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.6049-237C>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/23 | chr6 | 56617655 | |||||||
chr6:56617707 | C | T | 3 | a0008c0008t0001g0018 a0008c0008t0001g0052 a0008c0008t0001g0053 |
4 | HG01891.hp1 HG03471.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.6048+279G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/23 | chr6 | 56617707 | |||||||
chr6:56617753 | C | T | 1 | a0002c0002t0002g0137 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.6048+233G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/23 | chr6 | 56617753 | |||||||
chr6:56617838 | G | C | 8 | a0003c0004t0003g0008 a0003c0004t0003g0017 a0003c0004t0003g0040 others(5): Show |
12 | HG02132.hp1 HG02258.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.6048+148C>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/23 | chr6 | 56617838 | |||||||
chr6:56617906 | A | C | 57 | a0001c0001t0002g0132 a0002c0002t0002g0002 a0002c0002t0002g0006 others(54): Show |
100 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.6048+80T>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 23/23 | chr6 | 56617906 | |||||||
chr6:56620838 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3319-123T>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56620838 | |||||||
chr6:56621035 | G | A | 1 | a0001c0001t0004g0111 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.3319-320C>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56621035 | |||||||
chr6:56621191 | T | C | 5 | a0001c0001t0001g0088 a0002c0002t0002g0009 a0002c0002t0002g0109 others(2): Show |
9 | NA18939.hp1 NA18963.hp1 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.3319-476A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56621191 | |||||||
chr6:56621202 | A | G | 8 | a0004c0006t0003g0007 a0004c0006t0003g0046 a0004c0006t0003g0047 others(5): Show |
11 | HG01069.hp1 HG02055.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.3319-487T>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56621202 | |||||||
chr6:56621317 | T | C | 7 | a0001c0001t0001g0015 a0001c0001t0001g0100 a0001c0001t0001g0128 others(4): Show |
10 | HG00438.hp1 HG00621.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.3319-602A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56621317 | |||||||
chr6:56621520 | A | G | 3 | a0001c0001t0001g0158 a0001c0001t0001g0161 a0001c0001t0001g0192 |
3 | HG00408.hp1 HG02523.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.3319-805T>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56621520 | |||||||
chr6:56621638 | G | C | 2 | a0002c0002t0002g0176 a0002c0002t0002g0182 |
2 | HG00423.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.3319-923C>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56621638 | |||||||
chr6:56621676 | T | C | 5 | a0005c0007t0003g0019 a0005c0007t0003g0059 a0005c0007t0003g0060 others(2): Show |
6 | HG02622.hp2 HG02818.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.3319-961A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56621676 | |||||||
chr6:56621679 | T | C | 3 | a0018c0024t0003g0063 a0020c0018t0003g0064 a0024c0019t0003g0065 |
3 | HG02145.hp2 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3319-964A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56621679 | |||||||
chr6:56621741 | G | A | 7 | a0004c0006t0003g0007 a0004c0006t0003g0046 a0004c0006t0003g0047 others(4): Show |
10 | HG01069.hp1 HG02055.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.3319-1026C>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56621741 | |||||||
chr6:56621795 | A | T | 11 | a0003c0004t0003g0008 a0003c0004t0003g0017 a0003c0004t0003g0040 others(8): Show |
16 | HG01891.hp1 HG02132.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3319-1080T>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56621795 | |||||||
chr6:56621915 | A | G | 3 | a0002c0005t0001g0140 a0002c0005t0003g0014 a0002c0005t0003g0026 |
6 | HG02257.hp1 HG02280.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.3319-1200T>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56621915 | |||||||
chr6:56621921 | T | C | 2 | a0002c0005t0003g0014 a0002c0005t0003g0026 |
5 | HG02257.hp1 HG02280.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.3319-1206A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56621921 | |||||||
chr6:56622028 | T | G | 4 | a0018c0024t0003g0063 a0020c0018t0003g0064 a0021c0017t0009g0039 others(1): Show |
4 | HG02145.hp2 HG02559.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.3319-1313A>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56622028 | |||||||
chr6:56622044 | G | T | 1 | a0001c0001t0001g0102 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3319-1329C>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56622044 | |||||||
chr6:56622072 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3319-1357A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56622072 | |||||||
chr6:56622097 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3319-1382T>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56622097 | |||||||
chr6:56622324 | A | G | 2 | a0002c0005t0001g0067 a0002c0005t0001g0068 |
2 | HG02280.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3319-1609T>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56622324 | |||||||
chr6:56622337 | A | C | 1 | a0002c0002t0002g0176 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3319-1622T>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56622337 | |||||||
chr6:56622448 | C | T | 8 | a0004c0006t0003g0007 a0004c0006t0003g0046 a0004c0006t0003g0047 others(5): Show |
11 | HG01069.hp1 HG02055.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.3319-1733G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56622448 | |||||||
chr6:56622450 | C | T | 1 | a0001c0001t0002g0132 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.3319-1735G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56622450 | |||||||
chr6:56622523 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3319-1808G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56622523 | |||||||
chr6:56622569 | C | CA | 13 | a0001c0001t0001g0012 a0001c0001t0001g0086 a0001c0001t0001g0087 others(10): Show |
15 | HG00621.hp2 HG00733.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.3319-1855dupT | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56622569 | |||||||
chr6:56622569 | CA | C | 28 | a0001c0001t0001g0031 a0001c0001t0001g0078 a0001c0001t0001g0096 others(25): Show |
35 | HG00408.hp1 HG00733.hp1 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.3319-1855delT | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56622569 | |||||||
chr6:56622569 | CAA | C | 76 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0028 others(73): Show |
138 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.3319-1856_3319-185 others(6): Show |
DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56622569 | |||||||
chr6:56622569 | CAAA | C | 6 | a0001c0001t0001g0165 a0002c0015t0002g0098 a0004c0006t0003g0047 others(3): Show |
6 | HG02055.hp1 HG02451.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.3319-1857_3319-185 others(7): Show |
DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56622569 | |||||||
chr6:56622569 | CAAAA | C | 5 | a0005c0007t0003g0019 a0005c0007t0003g0059 a0005c0007t0003g0060 others(2): Show |
6 | HG02622.hp2 HG03041.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.3319-1858_3319-185 others(8): Show |
DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56622569 | |||||||
chr6:56622793 | G | C | 3 | a0018c0024t0003g0063 a0020c0018t0003g0064 a0024c0019t0003g0065 |
3 | HG02145.hp2 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3318+1737C>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56622793 | |||||||
chr6:56622815 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3318+1715T>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56622815 | |||||||
chr6:56622993 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3318+1537A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56622993 | |||||||
chr6:56623021 | G | A | 7 | a0003c0004t0003g0008 a0003c0004t0003g0017 a0003c0004t0003g0040 others(4): Show |
12 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.3318+1509C>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56623021 | |||||||
chr6:56623259 | T | A | 1 | a0024c0019t0003g0065 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3318+1271A>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56623259 | |||||||
chr6:56623423 | G | C | 1 | a0026c0044t0001g0197 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3318+1107C>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56623423 | |||||||
chr6:56623453 | C | T | 1 | a0021c0017t0009g0039 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3318+1077G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56623453 | |||||||
chr6:56623455 | C | CCTT | 8 | a0004c0006t0003g0007 a0004c0006t0003g0046 a0004c0006t0003g0047 others(5): Show |
11 | HG01069.hp1 HG02055.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.3318+1074_3318+107 others(7): Show |
DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56623455 | |||||||
chr6:56623475 | G | A | 3 | a0018c0024t0003g0063 a0020c0018t0003g0064 a0024c0019t0003g0065 |
3 | HG02145.hp2 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3318+1055C>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56623475 | |||||||
chr6:56623673 | C | T | 17 | a0003c0004t0003g0008 a0003c0004t0003g0017 a0003c0004t0003g0040 others(14): Show |
22 | HG01358.hp1 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.3318+857G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56623673 | |||||||
chr6:56623878 | T | C | 7 | a0004c0006t0003g0007 a0004c0006t0003g0046 a0004c0006t0003g0047 others(4): Show |
10 | HG01069.hp1 HG02055.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.3318+652A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56623878 | |||||||
chr6:56623934 | T | C | 2 | a0005c0007t0003g0060 a0005c0007t0003g0061 |
2 | HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3318+596A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56623934 | |||||||
chr6:56624000 | C | A | 1 | a0024c0019t0003g0065 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3318+530G>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56624000 | |||||||
chr6:56624138 | C | T | 17 | a0003c0004t0003g0008 a0003c0004t0003g0017 a0003c0004t0003g0040 others(14): Show |
22 | HG01358.hp1 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.3318+392G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56624138 | |||||||
chr6:56624215 | G | A | 7 | a0004c0006t0003g0007 a0004c0006t0003g0046 a0004c0006t0003g0047 others(4): Show |
10 | HG01069.hp1 HG02055.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.3318+315C>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56624215 | |||||||
chr6:56624246 | G | A | 9 | a0004c0006t0003g0007 a0004c0006t0003g0046 a0004c0006t0003g0047 others(6): Show |
12 | HG01069.hp1 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.3318+284C>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56624246 | |||||||
chr6:56624339 | T | A | 1 | a0031c0023t0001g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3318+191A>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56624339 | |||||||
chr6:56624420 | C | T | 3 | a0008c0008t0001g0018 a0008c0008t0001g0052 a0008c0008t0001g0053 |
4 | HG01891.hp1 HG03471.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.3318+110G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56624420 | |||||||
chr6:56624428 | T | C | 1 | a0001c0001t0001g0108 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.3318+102A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 22/23 | chr6 | 56624428 | |||||||
chr6:56624631 | G | T | 2 | a0002c0005t0001g0067 a0002c0005t0001g0068 |
2 | HG02280.hp2 HG03516.hp1 |
splice_region_variant&intron_variant | LOW | c.3220-3C>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 21/23 | chr6 | 56624631 | |||||||
chr6:56624678 | C | G | 1 | a0021c0017t0009g0039 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3220-50G>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 21/23 | chr6 | 56624678 | |||||||
chr6:56624692 | T | C | 1 | a0027c0021t0001g0055 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3220-64A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 21/23 | chr6 | 56624692 | |||||||
chr6:56624739 | C | T | 1 | a0018c0024t0003g0063 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3220-111G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 21/23 | chr6 | 56624739 | |||||||
chr6:56624749 | C | A | 1 | a0001c0001t0001g0164 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3220-121G>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 21/23 | chr6 | 56624749 | |||||||
chr6:56624836 | C | T | 8 | a0004c0006t0003g0007 a0004c0006t0003g0046 a0004c0006t0003g0047 others(5): Show |
11 | HG01069.hp1 HG02055.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.3220-208G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 21/23 | chr6 | 56624836 | |||||||
chr6:56624903 | A | C | 1 | a0001c0001t0001g0088 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3219+254T>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 21/23 | chr6 | 56624903 | |||||||
chr6:56624948 | T | C | 1 | a0024c0019t0003g0065 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3219+209A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 21/23 | chr6 | 56624948 | |||||||
chr6:56625296 | T | C | 1 | a0002c0002t0002g0186 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3112-32A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 20/23 | chr6 | 56625296 | |||||||
chr6:56625313 | A | G | 8 | a0004c0006t0003g0007 a0004c0006t0003g0046 a0004c0006t0003g0047 others(5): Show |
11 | HG01069.hp1 HG02055.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.3112-49T>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 20/23 | chr6 | 56625313 | |||||||
chr6:56625542 | C | T | 1 | a0002c0005t0001g0067 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3112-278G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 20/23 | chr6 | 56625542 | |||||||
chr6:56625676 | G | A | 2 | a0002c0002t0002g0009 a0002c0002t0002g0109 |
5 | NA18965.hp1 NA18967.hp2 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.3112-412C>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 20/23 | chr6 | 56625676 | |||||||
chr6:56625677 | G | A | 5 | a0005c0007t0003g0019 a0005c0007t0003g0059 a0005c0007t0003g0060 others(2): Show |
6 | HG02622.hp2 HG02818.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.3112-413C>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 20/23 | chr6 | 56625677 | |||||||
chr6:56625721 | T | C | 35 | a0002c0005t0001g0067 a0002c0005t0001g0068 a0003c0004t0003g0008 others(32): Show |
44 | HG01069.hp1 HG01358.hp1 HG01884.hp2 others(41): Show |
intron_variant | MODIFIER | c.3112-457A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 20/23 | chr6 | 56625721 | |||||||
chr6:56625737 | T | TAA | 12 | a0003c0004t0003g0008 a0003c0004t0003g0017 a0003c0004t0003g0040 others(9): Show |
17 | HG01891.hp1 HG02132.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.3112-475_3112-474d others(4): Show |
DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 20/23 | chr6 | 56625737 | |||||||
chr6:56625737 | TA | T | 22 | a0001c0001t0001g0029 a0001c0001t0001g0093 a0001c0001t0001g0096 others(19): Show |
28 | HG00323.hp1 HG01069.hp1 HG01346.hp1 others(25): Show |
intron_variant | MODIFIER | c.3112-474delT | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 20/23 | chr6 | 56625737 | |||||||
chr6:56625955 | C | T | 8 | a0004c0006t0003g0007 a0004c0006t0003g0046 a0004c0006t0003g0047 others(5): Show |
11 | HG01069.hp1 HG02055.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.3112-691G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 20/23 | chr6 | 56625955 | |||||||
chr6:56625972 | T | TA | 7 | a0001c0001t0001g0071 a0001c0001t0001g0083 a0001c0001t0001g0136 others(4): Show |
7 | HG01361.hp1 HG01361.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.3112-709dupT | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 20/23 | chr6 | 56625972 | |||||||
chr6:56625972 | T | TAA | 7 | a0004c0006t0003g0007 a0004c0006t0003g0046 a0004c0006t0003g0048 others(4): Show |
10 | HG01069.hp1 HG02055.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.3112-710_3112-709d others(4): Show |
DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 20/23 | chr6 | 56625972 | |||||||
chr6:56625972 | TA | T | 27 | a0001c0001t0001g0095 a0002c0003t0002g0034 a0002c0003t0002g0174 others(24): Show |
34 | HG01358.hp1 HG01884.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.3112-709delT | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 20/23 | chr6 | 56625972 | |||||||
chr6:56625991 | C | A | 4 | a0002c0002t0002g0009 a0002c0002t0002g0109 a0002c0003t0002g0024 others(1): Show |
8 | NA18939.hp1 NA18965.hp1 NA18967.hp2 others(5): Show |
intron_variant | MODIFIER | c.3112-727G>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 20/23 | chr6 | 56625991 | |||||||
chr6:56625992 | C | A | 10 | a0002c0002t0002g0009 a0002c0002t0002g0109 a0004c0006t0003g0007 others(7): Show |
16 | HG01069.hp1 HG02055.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.3112-728G>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 20/23 | chr6 | 56625992 | |||||||
chr6:56626042 | G | A | 33 | a0003c0004t0003g0008 a0003c0004t0003g0017 a0003c0004t0003g0040 others(30): Show |
42 | HG01069.hp1 HG01358.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.3112-778C>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 20/23 | chr6 | 56626042 | |||||||
chr6:56626045 | G | A | 8 | a0004c0006t0003g0007 a0004c0006t0003g0046 a0004c0006t0003g0047 others(5): Show |
11 | HG01069.hp1 HG02055.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.3112-781C>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 20/23 | chr6 | 56626045 | |||||||
chr6:56626200 | A | T | 1 | a0001c0001t0001g0144 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3112-936T>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 20/23 | chr6 | 56626200 | |||||||
chr6:56626220 | A | G | 1 | a0001c0001t0001g0144 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3112-956T>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 20/23 | chr6 | 56626220 | |||||||
chr6:56626409 | A | G | 1 | a0005c0020t0001g0062 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3111+795T>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 20/23 | chr6 | 56626409 | |||||||
chr6:56626498 | T | TA | 8 | a0004c0006t0003g0007 a0004c0006t0003g0046 a0004c0006t0003g0047 others(5): Show |
11 | HG01069.hp1 HG02055.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.3111+705_3111+706i others(3): Show |
DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 20/23 | chr6 | 56626498 | |||||||
chr6:56626546 | T | C | 1 | a0001c0001t0001g0166 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3111+658A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 20/23 | chr6 | 56626546 | |||||||
chr6:56626593 | G | A | 1 | a0003c0004t0003g0017 | 2 | HG02258.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.3111+611C>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 20/23 | chr6 | 56626593 | |||||||
chr6:56626731 | G | C | 1 | a0031c0023t0001g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3111+473C>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 20/23 | chr6 | 56626731 | |||||||
chr6:56626733 | T | C | 1 | a0003c0004t0003g0054 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3111+471A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 20/23 | chr6 | 56626733 | |||||||
chr6:56626767 | T | C | 4 | a0005c0007t0003g0019 a0005c0007t0003g0059 a0005c0007t0003g0060 others(1): Show |
5 | HG02622.hp2 HG03041.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.3111+437A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 20/23 | chr6 | 56626767 | |||||||
chr6:56626829 | A | G | 1 | a0002c0003t0002g0034 | 2 | NA18950.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.3111+375T>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 20/23 | chr6 | 56626829 | |||||||
chr6:56626877 | C | G | 1 | a0002c0003t0002g0169 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3111+327G>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 20/23 | chr6 | 56626877 | |||||||
chr6:56626918 | C | A | 5 | a0005c0007t0003g0019 a0005c0007t0003g0059 a0005c0007t0003g0060 others(2): Show |
6 | HG02622.hp2 HG02818.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.3111+286G>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 20/23 | chr6 | 56626918 | |||||||
chr6:56626989 | G | A | 1 | a0011c0025t0007g0124 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.3111+215C>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 20/23 | chr6 | 56626989 | |||||||
chr6:56626993 | C | T | 1 | a0002c0002t0002g0120 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3111+211G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 20/23 | chr6 | 56626993 | |||||||
chr6:56627025 | G | A | 3 | a0002c0005t0001g0140 a0002c0005t0003g0014 a0002c0005t0003g0026 |
6 | HG02257.hp1 HG02280.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.3111+179C>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 20/23 | chr6 | 56627025 | |||||||
chr6:56627042 | G | A | 8 | a0004c0006t0003g0007 a0004c0006t0003g0046 a0004c0006t0003g0047 others(5): Show |
11 | HG01069.hp1 HG02055.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.3111+162C>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 20/23 | chr6 | 56627042 | |||||||
chr6:56627049 | G | A | 3 | a0002c0002t0002g0172 a0002c0002t0002g0188 a0002c0002t0002g0189 |
3 | HG00323.hp1 HG01169.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.3111+155C>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 20/23 | chr6 | 56627049 | |||||||
chr6:56627051 | C | T | 1 | a0031c0023t0001g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3111+153G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 20/23 | chr6 | 56627051 | |||||||
chr6:56627094 | A | T | 17 | a0003c0004t0003g0008 a0003c0004t0003g0017 a0003c0004t0003g0040 others(14): Show |
22 | HG01358.hp1 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.3111+110T>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 20/23 | chr6 | 56627094 | |||||||
chr6:56627153 | G | C | 10 | a0005c0007t0003g0019 a0005c0007t0003g0059 a0005c0007t0003g0060 others(7): Show |
11 | HG01358.hp1 HG01884.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.3111+51C>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 20/23 | chr6 | 56627153 | |||||||
chr6:56627180 | A | C | 2 | a0001c0001t0001g0094 a0001c0001t0001g0156 |
2 | HG02293.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.3111+24T>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 20/23 | chr6 | 56627180 | |||||||
chr6:56627389 | C | T | 3 | a0001c0001t0001g0069 a0002c0005t0001g0067 a0002c0005t0001g0068 |
3 | HG02280.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3028-102G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 19/23 | chr6 | 56627389 | |||||||
chr6:56627471 | C | G | 1 | a0002c0002t0002g0173 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3028-184G>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 19/23 | chr6 | 56627471 | |||||||
chr6:56627533 | C | G | 3 | a0008c0008t0001g0018 a0008c0008t0001g0052 a0008c0008t0001g0053 |
4 | HG01891.hp1 HG03471.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.3028-246G>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 19/23 | chr6 | 56627533 | |||||||
chr6:56627568 | A | T | 5 | a0005c0007t0003g0019 a0005c0007t0003g0059 a0005c0007t0003g0060 others(2): Show |
6 | HG02622.hp2 HG02818.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.3028-281T>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 19/23 | chr6 | 56627568 | |||||||
chr6:56627867 | A | G | 1 | a0008c0008t0001g0052 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3027+132T>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 19/23 | chr6 | 56627867 | |||||||
chr6:56627983 | A | T | 1 | a0001c0001t0001g0121 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3027+16T>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 19/23 | chr6 | 56627983 | |||||||
chr6:56628233 | G | T | 1 | a0001c0037t0001g0142 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2865-72C>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 18/23 | chr6 | 56628233 | |||||||
chr6:56628275 | C | G | 33 | a0003c0004t0003g0008 a0003c0004t0003g0017 a0003c0004t0003g0040 others(30): Show |
42 | HG01069.hp1 HG01358.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.2865-114G>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 18/23 | chr6 | 56628275 | |||||||
chr6:56628307 | C | T | 1 | a0031c0023t0001g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2865-146G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 18/23 | chr6 | 56628307 | |||||||
chr6:56628603 | G | C | 1 | a0024c0019t0003g0065 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2865-442C>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 18/23 | chr6 | 56628603 | |||||||
chr6:56628734 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2864+516C>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 18/23 | chr6 | 56628734 | |||||||
chr6:56628756 | G | A | 2 | a0001c0001t0001g0072 a0013c0041t0001g0074 |
2 | HG01433.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2864+494C>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 18/23 | chr6 | 56628756 | |||||||
chr6:56628898 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0093 |
3 | NA18971.hp2 NA18981.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.2864+352G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 18/23 | chr6 | 56628898 | |||||||
chr6:56629173 | C | T | 1 | a0006c0016t0001g0057 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2864+77G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 18/23 | chr6 | 56629173 | |||||||
chr6:56629199 | C | T | 2 | a0018c0024t0003g0063 a0020c0018t0003g0064 |
2 | HG02145.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2864+51G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 18/23 | chr6 | 56629199 | |||||||
chr6:56629235 | A | T | 2 | a0018c0024t0003g0063 a0020c0018t0003g0064 |
2 | HG02145.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2864+15T>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 18/23 | chr6 | 56629235 | |||||||
chr6:56629683 | CA | C | 3 | a0001c0001t0001g0154 a0007c0009t0001g0092 a0007c0009t0001g0155 |
3 | HG01515.hp1 HG01517.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2671-241delT | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 17/23 | chr6 | 56629683 | |||||||
chr6:56629752 | C | T | 1 | a0005c0020t0001g0062 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2671-309G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 17/23 | chr6 | 56629752 | |||||||
chr6:56629919 | T | C | 1 | a0006c0022t0001g0058 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2670+326A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 17/23 | chr6 | 56629919 | |||||||
chr6:56629957 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2670+288T>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 17/23 | chr6 | 56629957 | |||||||
chr6:56630044 | G | C | 1 | a0004c0011t0006g0049 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2670+201C>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 17/23 | chr6 | 56630044 | |||||||
chr6:56630072 | C | G | 7 | a0003c0004t0003g0008 a0003c0004t0003g0017 a0003c0004t0003g0040 others(4): Show |
12 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.2670+173G>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 17/23 | chr6 | 56630072 | |||||||
chr6:56630130 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2670+115C>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 17/23 | chr6 | 56630130 | |||||||
chr6:56630511 | A | G | 1 | a0004c0006t0003g0046 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2532-128T>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 16/23 | chr6 | 56630511 | |||||||
chr6:56630785 | C | CT | 9 | a0001c0001t0001g0091 a0005c0007t0003g0019 a0005c0007t0003g0059 others(6): Show |
10 | HG02145.hp2 HG02559.hp2 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.2532-403dupA | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 16/23 | chr6 | 56630785 | |||||||
chr6:56630785 | CTTTTTTT others(1): Show |
C | 23 | a0003c0004t0003g0008 a0003c0004t0003g0017 a0003c0004t0003g0040 others(20): Show |
31 | HG01069.hp1 HG01358.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.2532-410_2532-403d others(10): Show |
DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 16/23 | chr6 | 56630785 | |||||||
chr6:56630846 | G | A | 1 | a0004c0011t0006g0049 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2531+365C>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 16/23 | chr6 | 56630846 | |||||||
chr6:56631002 | C | T | 1 | a0002c0002t0002g0172 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2531+209G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 16/23 | chr6 | 56631002 | |||||||
chr6:56631060 | G | A | 1 | a0002c0003t0002g0167 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2531+151C>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 16/23 | chr6 | 56631060 | |||||||
chr6:56631439 | G | A | 2 | a0018c0024t0003g0063 a0020c0018t0003g0064 |
2 | HG02145.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2353-50C>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 15/23 | chr6 | 56631439 | |||||||
chr6:56631459 | G | T | 33 | a0003c0004t0003g0008 a0003c0004t0003g0017 a0003c0004t0003g0040 others(30): Show |
42 | HG01069.hp1 HG01358.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.2353-70C>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 15/23 | chr6 | 56631459 | |||||||
chr6:56631536 | T | C | 33 | a0003c0004t0003g0008 a0003c0004t0003g0017 a0003c0004t0003g0040 others(30): Show |
42 | HG01069.hp1 HG01358.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.2353-147A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 15/23 | chr6 | 56631536 | |||||||
chr6:56631796 | A | G | 3 | a0003c0004t0003g0050 a0003c0004t0003g0054 a0003c0004t0003g0056 |
3 | HG02132.hp1 HG02486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2352+87T>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 15/23 | chr6 | 56631796 | |||||||
chr6:56631803 | A | G | 1 | a0031c0023t0001g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2352+80T>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 15/23 | chr6 | 56631803 | |||||||
chr6:56631851 | A | C | 2 | a0002c0002t0002g0033 a0028c0027t0002g0171 |
3 | HG00099.hp2 HG01261.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.2352+32T>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 15/23 | chr6 | 56631851 | |||||||
chr6:56632170 | C | A | 1 | a0027c0021t0001g0055 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2195-130G>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 14/23 | chr6 | 56632170 | |||||||
chr6:56632291 | C | T | 27 | a0003c0004t0003g0008 a0003c0004t0003g0017 a0003c0004t0003g0040 others(24): Show |
35 | HG01069.hp1 HG01358.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.2195-251G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 14/23 | chr6 | 56632291 | |||||||
chr6:56632367 | T | C | 5 | a0006c0010t0001g0041 a0006c0010t0001g0042 a0006c0010t0001g0043 others(2): Show |
5 | HG01358.hp1 HG01884.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2195-327A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 14/23 | chr6 | 56632367 | |||||||
chr6:56632607 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2194+247T>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 14/23 | chr6 | 56632607 | |||||||
chr6:56633135 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2011-98C>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 13/23 | chr6 | 56633135 | |||||||
chr6:56633194 | G | GT | 21 | a0003c0004t0003g0008 a0003c0004t0003g0017 a0003c0004t0003g0040 others(18): Show |
29 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.2011-158_2011-157i others(3): Show |
DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 13/23 | chr6 | 56633194 | |||||||
chr6:56633194 | G | GTT | 5 | a0004c0011t0006g0044 a0006c0010t0001g0041 a0006c0010t0001g0042 others(2): Show |
5 | HG01884.hp2 HG02615.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2011-158_2011-157i others(4): Show |
DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 13/23 | chr6 | 56633194 | |||||||
chr6:56633194 | G | GTTT | 3 | a0005c0020t0001g0062 a0006c0022t0001g0058 a0031c0023t0001g0066 |
3 | HG01358.hp1 HG02818.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2011-158_2011-157i others(5): Show |
DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 13/23 | chr6 | 56633194 | |||||||
chr6:56633194 | G | GTTTT | 4 | a0005c0007t0003g0019 a0005c0007t0003g0059 a0005c0007t0003g0060 others(1): Show |
5 | HG02622.hp2 HG03041.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2011-158_2011-157i others(6): Show |
DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 13/23 | chr6 | 56633194 | |||||||
chr6:56633195 | G | T | 39 | a0001c0001t0001g0069 a0002c0005t0001g0067 a0002c0005t0001g0068 others(36): Show |
51 | HG01069.hp1 HG01358.hp1 HG01884.hp2 others(48): Show |
intron_variant | MODIFIER | c.2011-158C>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 13/23 | chr6 | 56633195 | |||||||
chr6:56633211 | T | C | 2 | a0018c0024t0003g0063 a0020c0018t0003g0064 |
2 | HG02145.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2011-174A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 13/23 | chr6 | 56633211 | |||||||
chr6:56633233 | C | CT | 6 | a0001c0001t0001g0089 a0001c0001t0001g0127 a0001c0001t0001g0128 others(3): Show |
6 | HG00621.hp1 HG02027.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.2011-197dupA | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 13/23 | chr6 | 56633233 | |||||||
chr6:56633233 | C | CTTTTTTT others(1): Show |
18 | a0001c0001t0001g0069 a0002c0005t0001g0067 a0002c0005t0001g0068 others(15): Show |
21 | HG01069.hp1 HG01358.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.2011-204_2011-197d others(10): Show |
DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 13/23 | chr6 | 56633233 | |||||||
chr6:56633233 | C | CTTTTTTT others(2): Show |
10 | a0003c0004t0003g0050 a0003c0004t0003g0054 a0005c0007t0003g0019 others(7): Show |
12 | HG01891.hp1 HG02132.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.2011-205_2011-197d others(11): Show |
DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 13/23 | chr6 | 56633233 | |||||||
chr6:56633233 | C | CTTTTTTT others(3): Show |
5 | a0003c0004t0003g0008 a0003c0004t0003g0017 a0003c0004t0003g0040 others(2): Show |
9 | HG02258.hp1 HG02451.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.2011-206_2011-197d others(12): Show |
DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 13/23 | chr6 | 56633233 | |||||||
chr6:56633233 | C | CTTTTTTT others(4): Show |
2 | a0003c0004t0003g0056 a0005c0020t0001g0062 |
2 | HG02486.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2011-207_2011-197d others(13): Show |
DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 13/23 | chr6 | 56633233 | |||||||
chr6:56633233 | C | CTTTTTTT others(7): Show |
1 | a0031c0023t0001g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2011-197_2011-196i others(16): Show |
DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 13/23 | chr6 | 56633233 | |||||||
chr6:56633250 | G | A | 24 | a0003c0004t0003g0008 a0003c0004t0003g0017 a0003c0004t0003g0040 others(21): Show |
32 | HG01069.hp1 HG01358.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.2011-213C>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 13/23 | chr6 | 56633250 | |||||||
chr6:56633267 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2011-230G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 13/23 | chr6 | 56633267 | |||||||
chr6:56633296 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2011-259C>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 13/23 | chr6 | 56633296 | |||||||
chr6:56633375 | T | C | 80 | a0001c0001t0001g0180 a0001c0001t0001g0183 a0001c0001t0001g0185 others(77): Show |
126 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.2011-338A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 13/23 | chr6 | 56633375 | |||||||
chr6:56633381 | T | C | 2 | a0002c0002t0002g0037 a0002c0002t0002g0151 |
3 | NA18962.hp1 NA19059.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.2011-344A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 13/23 | chr6 | 56633381 | |||||||
chr6:56633462 | G | A | 28 | a0003c0004t0003g0008 a0003c0004t0003g0017 a0003c0004t0003g0040 others(25): Show |
36 | HG01069.hp1 HG01358.hp1 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.2011-425C>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 13/23 | chr6 | 56633462 | |||||||
chr6:56633516 | G | A | 1 | a0027c0021t0001g0055 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2011-479C>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 13/23 | chr6 | 56633516 | |||||||
chr6:56633591 | C | G | 1 | a0001c0001t0001g0152 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2010+541G>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 13/23 | chr6 | 56633591 | |||||||
chr6:56633594 | A | G | 1 | a0001c0001t0001g0087 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2010+538T>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 13/23 | chr6 | 56633594 | |||||||
chr6:56633608 | C | G | 2 | a0001c0001t0001g0080 a0001c0001t0001g0086 |
2 | HG00733.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.2010+524G>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 13/23 | chr6 | 56633608 | |||||||
chr6:56633652 | C | A | 4 | a0001c0001t0001g0112 a0001c0001t0004g0010 a0001c0001t0004g0111 others(1): Show |
7 | NA18956.hp1 NA18957.hp2 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.2010+480G>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 13/23 | chr6 | 56633652 | |||||||
chr6:56633663 | G | T | 1 | a0001c0034t0001g0122 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2010+469C>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 13/23 | chr6 | 56633663 | |||||||
chr6:56633701 | C | T | 2 | a0001c0001t0001g0143 a0001c0037t0001g0142 |
2 | HG00140.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2010+431G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 13/23 | chr6 | 56633701 | |||||||
chr6:56633902 | C | T | 2 | a0001c0001t0001g0084 a0001c0035t0001g0085 |
2 | NA18949.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.2010+230G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 13/23 | chr6 | 56633902 | |||||||
chr6:56634275 | A | G | 4 | a0005c0007t0003g0019 a0005c0007t0003g0059 a0005c0007t0003g0060 others(1): Show |
5 | HG02622.hp2 HG03041.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1884-17T>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 12/23 | chr6 | 56634275 | |||||||
chr6:56634346 | C | T | 1 | a0005c0007t0003g0059 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1884-88G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 12/23 | chr6 | 56634346 | |||||||
chr6:56634378 | G | C | 1 | a0002c0002t0002g0150 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1883+84C>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 12/23 | chr6 | 56634378 | |||||||
chr6:56634391 | T | C | 27 | a0003c0004t0003g0008 a0003c0004t0003g0017 a0003c0004t0003g0040 others(24): Show |
35 | HG01069.hp1 HG01358.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.1883+71A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 12/23 | chr6 | 56634391 | |||||||
chr6:56634402 | C | T | 1 | a0031c0023t0001g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1883+60G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 12/23 | chr6 | 56634402 | |||||||
chr6:56634429 | C | T | 1 | a0002c0002t0002g0151 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1883+33G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 12/23 | chr6 | 56634429 | |||||||
chr6:56634707 | C | G | 7 | a0005c0007t0003g0019 a0005c0007t0003g0059 a0005c0007t0003g0060 others(4): Show |
8 | HG02145.hp2 HG02559.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1729-91G>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 11/23 | chr6 | 56634707 | |||||||
chr6:56634981 | G | C | 1 | a0021c0017t0009g0039 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1576-28C>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 10/23 | chr6 | 56634981 | |||||||
chr6:56635144 | C | T | 1 | a0031c0023t0001g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1576-191G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 10/23 | chr6 | 56635144 | |||||||
chr6:56635152 | C | A | 5 | a0006c0010t0001g0041 a0006c0010t0001g0042 a0006c0010t0001g0043 others(2): Show |
5 | HG01358.hp1 HG01884.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1576-199G>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 10/23 | chr6 | 56635152 | |||||||
chr6:56635208 | T | G | 1 | a0001c0001t0001g0113 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1576-255A>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 10/23 | chr6 | 56635208 | |||||||
chr6:56635346 | C | T | 11 | a0003c0004t0003g0008 a0003c0004t0003g0017 a0003c0004t0003g0040 others(8): Show |
16 | HG01891.hp1 HG02132.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1575+243G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 10/23 | chr6 | 56635346 | |||||||
chr6:56635353 | G | A | 3 | a0002c0005t0001g0140 a0002c0005t0003g0014 a0002c0005t0003g0026 |
6 | HG02257.hp1 HG02280.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1575+236C>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 10/23 | chr6 | 56635353 | |||||||
chr6:56635502 | C | T | 1 | a0002c0002t0002g0150 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1575+87G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 10/23 | chr6 | 56635502 | |||||||
chr6:56635770 | A | C | 2 | a0001c0001t0001g0070 a0001c0001t0001g0083 |
2 | NA19068.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1450-56T>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 9/23 | chr6 | 56635770 | |||||||
chr6:56636029 | C | A | 1 | a0021c0017t0009g0039 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1450-315G>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 9/23 | chr6 | 56636029 | |||||||
chr6:56636236 | A | ATT | 12 | a0001c0001t0001g0013 a0001c0001t0001g0114 a0001c0001t0001g0192 others(9): Show |
15 | HG01891.hp1 HG02258.hp1 HG02818.hp2 others(12): Show |
intron_variant | MODIFIER | c.1449+320_1449+321i others(4): Show |
DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 9/23 | chr6 | 56636236 | |||||||
chr6:56636238 | A | T | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.1449+319T>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 9/23 | chr6 | 56636238 | |||||||
chr6:56636240 | A | T | 4 | a0001c0001t0001g0069 a0002c0005t0001g0067 a0002c0005t0001g0068 others(1): Show |
4 | HG02280.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1449+317T>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 9/23 | chr6 | 56636240 | |||||||
chr6:56636254 | A | T | 1 | a0002c0002t0002g0200 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1449+303T>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 9/23 | chr6 | 56636254 | |||||||
chr6:56636255 | T | C | 3 | a0018c0024t0003g0063 a0020c0018t0003g0064 a0021c0017t0009g0039 |
3 | HG02145.hp2 HG02559.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.1449+302A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 9/23 | chr6 | 56636255 | |||||||
chr6:56636257 | C | T | 2 | a0002c0005t0001g0140 a0003c0004t0003g0008 |
5 | HG02451.hp2 HG02647.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1449+300G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 9/23 | chr6 | 56636257 | |||||||
chr6:56636267 | CAA | C | 1 | a0003c0004t0003g0008 | 4 | HG02451.hp2 HG02647.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1449+288_1449+289d others(4): Show |
DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 9/23 | chr6 | 56636267 | |||||||
chr6:56636269 | A | C | 2 | a0002c0005t0001g0140 a0024c0019t0003g0065 |
2 | HG02895.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1449+288T>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 9/23 | chr6 | 56636269 | |||||||
chr6:56636269 | AAC | A | 9 | a0001c0001t0001g0088 a0002c0005t0003g0014 a0002c0005t0003g0026 others(6): Show |
13 | HG02257.hp1 HG02280.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.1449+286_1449+287d others(4): Show |
DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 9/23 | chr6 | 56636269 | |||||||
chr6:56636269 | AACACAC | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0165 |
5 | HG02965.hp1 HG03041.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1449+282_1449+287d others(8): Show |
DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 9/23 | chr6 | 56636269 | |||||||
chr6:56636271 | C | A | 2 | a0002c0005t0001g0140 a0024c0019t0003g0065 |
2 | HG02895.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1449+286G>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 9/23 | chr6 | 56636271 | |||||||
chr6:56636273 | C | A | 1 | a0003c0004t0003g0008 | 4 | HG02451.hp2 HG02647.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1449+284G>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 9/23 | chr6 | 56636273 | |||||||
chr6:56636289 | T | C | 1 | a0031c0023t0001g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1449+268A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 9/23 | chr6 | 56636289 | |||||||
chr6:56636348 | GTA | G | 2 | a0001c0001t0001g0028 a0031c0023t0001g0066 |
3 | HG00639.hp1 HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1449+207_1449+208d others(4): Show |
DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 9/23 | chr6 | 56636348 | |||||||
chr6:56636358 | GTGTGTGT others(71): Show |
G | 2 | a0001c0001t0001g0082 a0030c0029t0001g0081 |
2 | NA19058.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1449+121_1449+198d others(80): Show |
DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 9/23 | chr6 | 56636358 | |||||||
chr6:56636364 | G | GTA | 3 | a0001c0001t0001g0069 a0002c0005t0001g0067 a0002c0005t0001g0068 |
3 | HG02280.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1449+191_1449+192d others(4): Show |
DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 9/23 | chr6 | 56636364 | |||||||
chr6:56636373 | T | C | 8 | a0005c0007t0003g0019 a0005c0007t0003g0059 a0005c0007t0003g0060 others(5): Show |
9 | HG02145.hp2 HG02559.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1449+184A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 9/23 | chr6 | 56636373 | |||||||
chr6:56636386 | G | A | 1 | a0002c0002t0002g0184 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1449+171C>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 9/23 | chr6 | 56636386 | |||||||
chr6:56636394 | G | A | 1 | a0031c0023t0001g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1449+163C>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 9/23 | chr6 | 56636394 | |||||||
chr6:56636394 | G | GTATGTGT others(33): Show |
1 | a0002c0002t0002g0187 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1449+123_1449+162d others(42): Show |
DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 9/23 | chr6 | 56636394 | |||||||
chr6:56636402 | G | GTA | 4 | a0005c0007t0003g0019 a0005c0007t0003g0059 a0005c0007t0003g0060 others(1): Show |
5 | HG02622.hp2 HG03041.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1449+153_1449+154d others(4): Show |
DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 9/23 | chr6 | 56636402 | |||||||
chr6:56636411 | T | C | 3 | a0018c0024t0003g0063 a0020c0018t0003g0064 a0024c0019t0003g0065 |
3 | HG02145.hp2 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1449+146A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 9/23 | chr6 | 56636411 | |||||||
chr6:56636428 | A | G | 3 | a0018c0024t0003g0063 a0020c0018t0003g0064 a0024c0019t0003g0065 |
3 | HG02145.hp2 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1449+129T>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 9/23 | chr6 | 56636428 | |||||||
chr6:56636438 | G | A | 1 | a0017c0043t0001g0117 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1449+119C>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 9/23 | chr6 | 56636438 | |||||||
chr6:56636531 | T | C | 3 | a0018c0024t0003g0063 a0020c0018t0003g0064 a0024c0019t0003g0065 |
3 | HG02145.hp2 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1449+26A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 9/23 | chr6 | 56636531 | |||||||
chr6:56636718 | T | G | 1 | a0003c0004t0003g0056 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1354-66A>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 8/23 | chr6 | 56636718 | |||||||
chr6:56636724 | C | T | 17 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0121 others(14): Show |
25 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.1354-72G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 8/23 | chr6 | 56636724 | |||||||
chr6:56636791 | T | C | 1 | a0001c0001t0001g0141 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1354-139A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 8/23 | chr6 | 56636791 | |||||||
chr6:56636953 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1354-301G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 8/23 | chr6 | 56636953 | |||||||
chr6:56637104 | C | CA | 3 | a0004c0011t0006g0044 a0004c0011t0006g0045 a0004c0011t0006g0049 |
3 | HG02055.hp1 HG02615.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1354-453dupT | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 8/23 | chr6 | 56637104 | |||||||
chr6:56637108 | C | A | 3 | a0004c0011t0006g0044 a0004c0011t0006g0045 a0004c0011t0006g0049 |
3 | HG02055.hp1 HG02615.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1354-456G>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 8/23 | chr6 | 56637108 | |||||||
chr6:56637108 | C | CA | 24 | a0001c0001t0001g0025 a0001c0001t0002g0115 a0001c0001t0004g0116 others(21): Show |
33 | HG01069.hp1 HG01358.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.1354-457dupT | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 8/23 | chr6 | 56637108 | |||||||
chr6:56637108 | CA | C | 9 | a0001c0001t0001g0005 a0001c0001t0001g0126 a0001c0001t0001g0143 others(6): Show |
14 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.1354-457delT | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 8/23 | chr6 | 56637108 | |||||||
chr6:56637112 | A | C | 2 | a0026c0044t0001g0197 a0031c0023t0001g0066 |
2 | HG04204.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1354-460T>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 8/23 | chr6 | 56637112 | |||||||
chr6:56637119 | C | A | 4 | a0005c0007t0003g0019 a0005c0007t0003g0059 a0005c0007t0003g0060 others(1): Show |
5 | HG02622.hp2 HG03041.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1354-467G>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 8/23 | chr6 | 56637119 | |||||||
chr6:56637141 | T | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0078 |
4 | NA18957.hp1 NA18967.hp1 NA19075.hp2 others(1): Show |
intron_variant | MODIFIER | c.1354-489A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 8/23 | chr6 | 56637141 | |||||||
chr6:56637289 | C | T | 1 | a0005c0020t0001g0062 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1354-637G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 8/23 | chr6 | 56637289 | |||||||
chr6:56637298 | A | G | 1 | a0031c0023t0001g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1354-646T>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 8/23 | chr6 | 56637298 | |||||||
chr6:56637479 | A | C | 5 | a0005c0007t0003g0019 a0005c0007t0003g0059 a0005c0007t0003g0060 others(2): Show |
6 | HG02622.hp2 HG02818.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1354-827T>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 8/23 | chr6 | 56637479 | |||||||
chr6:56637724 | A | T | 1 | a0031c0023t0001g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1354-1072T>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 8/23 | chr6 | 56637724 | |||||||
chr6:56637866 | C | T | 2 | a0002c0005t0003g0014 a0002c0005t0003g0026 |
5 | HG02257.hp1 HG02280.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1354-1214G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 8/23 | chr6 | 56637866 | |||||||
chr6:56637872 | G | A | 4 | a0005c0007t0003g0019 a0005c0007t0003g0059 a0005c0007t0003g0060 others(1): Show |
5 | HG02622.hp2 HG03041.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1354-1220C>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 8/23 | chr6 | 56637872 | |||||||
chr6:56638070 | T | G | 1 | a0031c0023t0001g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1353+1189A>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 8/23 | chr6 | 56638070 | |||||||
chr6:56638084 | T | C | 7 | a0004c0006t0003g0007 a0004c0006t0003g0046 a0004c0006t0003g0047 others(4): Show |
10 | HG01069.hp1 HG02055.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1353+1175A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 8/23 | chr6 | 56638084 | |||||||
chr6:56638106 | TATTA | T | 24 | a0003c0004t0003g0008 a0003c0004t0003g0017 a0003c0004t0003g0040 others(21): Show |
32 | HG01069.hp1 HG01358.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1353+1149_1353+115 others(8): Show |
DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 8/23 | chr6 | 56638106 | |||||||
chr6:56638129 | C | G | 3 | a0018c0024t0003g0063 a0020c0018t0003g0064 a0024c0019t0003g0065 |
3 | HG02145.hp2 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1353+1130G>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 8/23 | chr6 | 56638129 | |||||||
chr6:56638416 | T | C | 5 | a0003c0004t0003g0050 a0003c0004t0003g0054 a0003c0004t0003g0056 others(2): Show |
5 | HG02132.hp1 HG02486.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1353+843A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 8/23 | chr6 | 56638416 | |||||||
chr6:56638618 | T | C | 1 | a0005c0007t0003g0061 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1353+641A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 8/23 | chr6 | 56638618 | |||||||
chr6:56638639 | T | C | 5 | a0006c0010t0001g0041 a0006c0010t0001g0042 a0006c0010t0001g0043 others(2): Show |
5 | HG01358.hp1 HG01884.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1353+620A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 8/23 | chr6 | 56638639 | |||||||
chr6:56638656 | G | A | 1 | a0002c0002t0002g0038 | 2 | NA18955.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1353+603C>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 8/23 | chr6 | 56638656 | |||||||
chr6:56638688 | T | G | 1 | a0002c0002t0002g0194 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1353+571A>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 8/23 | chr6 | 56638688 | |||||||
chr6:56638714 | A | G | 5 | a0005c0007t0003g0019 a0005c0007t0003g0059 a0005c0007t0003g0060 others(2): Show |
6 | HG02622.hp2 HG02818.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1353+545T>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 8/23 | chr6 | 56638714 | |||||||
chr6:56639056 | G | T | 1 | a0001c0001t0001g0080 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1353+203C>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 8/23 | chr6 | 56639056 | |||||||
chr6:56639057 | G | T | 1 | a0001c0001t0001g0080 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1353+202C>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 8/23 | chr6 | 56639057 | |||||||
chr6:56639101 | A | G | 2 | a0006c0016t0001g0057 a0006c0022t0001g0058 |
2 | HG01358.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1353+158T>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 8/23 | chr6 | 56639101 | |||||||
chr6:56639122 | T | C | 3 | a0018c0024t0003g0063 a0020c0018t0003g0064 a0024c0019t0003g0065 |
3 | HG02145.hp2 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1353+137A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 8/23 | chr6 | 56639122 | |||||||
chr6:56639413 | T | C | 2 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
2 | NA18997.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1248+37A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 7/23 | chr6 | 56639413 | |||||||
chr6:56640063 | G | A | 1 | a0031c0023t0001g0066 | 1 | NA20129.hp2 | splice_region_variant&intron_variant | LOW | c.880-6C>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 4/23 | chr6 | 56640063 | |||||||
chr6:56640084 | A | T | 1 | a0024c0019t0003g0065 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.880-27T>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 4/23 | chr6 | 56640084 | |||||||
chr6:56640829 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.417-224G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 3/23 | chr6 | 56640829 | |||||||
chr6:56640932 | G | C | 1 | a0018c0024t0003g0063 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.417-327C>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 3/23 | chr6 | 56640932 | |||||||
chr6:56641115 | C | CAG | 36 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0015 others(33): Show |
50 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.417-512_417-511dup others(2): Show |
DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 3/23 | chr6 | 56641115 | |||||||
chr6:56641115 | C | CAGAG | 9 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(6): Show |
9 | HG00741.hp1 HG01361.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.417-514_417-511dup others(4): Show |
DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 3/23 | chr6 | 56641115 | |||||||
chr6:56641115 | C | CAGAGAG | 7 | a0001c0001t0008g0123 a0001c0034t0001g0122 a0002c0005t0003g0014 others(4): Show |
10 | HG02280.hp1 HG02622.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.417-516_417-511dup others(6): Show |
DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 3/23 | chr6 | 56641115 | |||||||
chr6:56641115 | C | CAGAGAGA others(3): Show |
1 | a0001c0001t0001g0121 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.417-520_417-511dup others(10): Show |
DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 3/23 | chr6 | 56641115 | |||||||
chr6:56641115 | C | CAGAGAGA others(7): Show |
2 | a0006c0010t0001g0043 a0024c0019t0003g0065 |
2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.417-524_417-511dup others(14): Show |
DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 3/23 | chr6 | 56641115 | |||||||
chr6:56641115 | C | CAGAGAGA others(9): Show |
1 | a0006c0010t0001g0042 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.417-526_417-511dup others(16): Show |
DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 3/23 | chr6 | 56641115 | |||||||
chr6:56641115 | C | CAGAGAGA others(13): Show |
1 | a0006c0010t0001g0041 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.417-530_417-511dup others(20): Show |
DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 3/23 | chr6 | 56641115 | |||||||
chr6:56641115 | CAGAG | C | 4 | a0002c0002t0002g0016 a0006c0016t0001g0057 a0006c0022t0001g0058 others(1): Show |
6 | HG01358.hp1 HG01975.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.417-514_417-511del others(4): Show |
DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 3/23 | chr6 | 56641115 | |||||||
chr6:56641438 | A | C | 4 | a0005c0007t0003g0019 a0005c0007t0003g0059 a0005c0007t0003g0060 others(1): Show |
5 | HG02622.hp2 HG03041.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.416+509T>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 3/23 | chr6 | 56641438 | |||||||
chr6:56641456 | C | T | 1 | a0003c0004t0003g0040 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.416+491G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 3/23 | chr6 | 56641456 | |||||||
chr6:56641591 | G | A | 2 | a0020c0018t0003g0064 a0031c0023t0001g0066 |
2 | HG02559.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.416+356C>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 3/23 | chr6 | 56641591 | |||||||
chr6:56641596 | A | G | 1 | a0002c0002t0002g0120 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.416+351T>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 3/23 | chr6 | 56641596 | |||||||
chr6:56641600 | A | C | 1 | a0001c0001t0001g0070 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.416+347T>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 3/23 | chr6 | 56641600 | |||||||
chr6:56641659 | T | C | 1 | a0002c0002t0002g0199 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.416+288A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 3/23 | chr6 | 56641659 | |||||||
chr6:56641678 | C | G | 1 | a0021c0017t0009g0039 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.416+269G>C | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 3/23 | chr6 | 56641678 | |||||||
chr6:56641687 | A | C | 2 | a0002c0002t0002g0118 a0002c0002t0002g0119 |
2 | NA19066.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.416+260T>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 3/23 | chr6 | 56641687 | |||||||
chr6:56641710 | G | A | 2 | a0001c0001t0001g0201 a0002c0002t0002g0200 |
2 | HG00741.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.416+237C>T | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 3/23 | chr6 | 56641710 | |||||||
chr6:56641736 | C | T | 24 | a0003c0004t0003g0008 a0003c0004t0003g0017 a0003c0004t0003g0040 others(21): Show |
32 | HG01069.hp1 HG01358.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.416+211G>A | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 3/23 | chr6 | 56641736 | |||||||
chr6:56642232 | T | C | 1 | a0024c0019t0003g0065 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.262-131A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 2/23 | chr6 | 56642232 | |||||||
chr6:56642315 | G | C | 1 | a0031c0023t0001g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.261+95C>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 2/23 | chr6 | 56642315 | |||||||
chr6:56642337 | T | C | 141 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(138): Show |
219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.261+73A>G | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 2/23 | chr6 | 56642337 | |||||||
chr6:56642373 | TC | T | 3 | a0001c0001t0001g0069 a0002c0005t0001g0067 a0002c0005t0001g0068 |
3 | HG02280.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.261+36delG | DST | ENSG00000151914.22 | transcript | ENST00000370765.11 | protein_coding | 2/23 | chr6 | 56642373 |