Item | Value |
---|---|
geneid | 89866 |
ensemblid | ENSG00000120341.19 |
hgncid | 30301 |
symbol | SEC16B |
name | SEC16 homolog B, endoplasmic reticulum export factor |
refseq_nuc | NM_033127.4 |
refseq_prot | NP_149118.2 |
ensembl_nuc | ENST00000308284.11 |
ensembl_prot | ENSP00000308339.6 |
mane_status | MANE Select |
chr | chr1 |
start | 177928788 |
end | 177970058 |
strand | - |
ver | v1.2 |
region | chr1:177928788-177970058 |
region5000 | chr1:177923788-177975058 |
regionname0 | SEC16B_chr1_177928788_177970058 |
regionname5000 | SEC16B_chr1_177923788_177975058 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1060 | 119 | 25 | 26 | 41 | 7 | 20 | 29 | SEC16B_chr1_177923788_177975058 | SEC16B | MELWA others(1055): Show |
chr1 | 177923788 | 177975058 |
a0002 | 0/0 | 1060 | 68 | 15 | 13 | 27 | 4 | 9 | 22 | SEC16B_chr1_177923788_177975058 | SEC16B | MELWA others(1055): Show |
chr1 | 177923788 | 177975058 |
a0003 | 0/1 | 1060 | 68 | 15 | 13 | 33 | 1 | 5 | 26 | SEC16B_chr1_177923788_177975058 | SEC16B | MELWA others(1055): Show |
chr1 | 177923788 | 177975058 |
a0004 | 0/0 | 1060 | 57 | 3 | 9 | 40 | 0 | 5 | 31 | SEC16B_chr1_177923788_177975058 | SEC16B | MELWA others(1055): Show |
chr1 | 177923788 | 177975058 |
a0005 | 0/0 | 1060 | 13 | 10 | 3 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | MELWA others(1055): Show |
chr1 | 177923788 | 177975058 |
a0006 | 0/0 | 1060 | 11 | 0 | 0 | 10 | 1 | 0 | 9 | SEC16B_chr1_177923788_177975058 | SEC16B | MELWA others(1055): Show |
chr1 | 177923788 | 177975058 |
a0007 | 0/0 | 1060 | 10 | 1 | 5 | 3 | 0 | 1 | 3 | SEC16B_chr1_177923788_177975058 | SEC16B | MELWA others(1055): Show |
chr1 | 177923788 | 177975058 |
a0008 | 1/0 | 1060 | 9 | 2 | 1 | 5 | 0 | 0 | 4 | SEC16B_chr1_177923788_177975058 | SEC16B | MELWA others(1055): Show |
chr1 | 177923788 | 177975058 |
a0009 | 0/0 | 1071 | 8 | 0 | 1 | 7 | 0 | 0 | 6 | SEC16B_chr1_177923788_177975058 | SEC16B | MELWA others(1066): Show |
chr1 | 177923788 | 177975058 |
a0010 | 0/0 | 1071 | 3 | 0 | 1 | 2 | 0 | 0 | 2 | SEC16B_chr1_177923788_177975058 | SEC16B | MELWA others(1066): Show |
chr1 | 177923788 | 177975058 |
a0011 | 0/0 | 1060 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | MELWA others(1055): Show |
chr1 | 177923788 | 177975058 |
a0012 | 0/0 | 1060 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | MELWA others(1055): Show |
chr1 | 177923788 | 177975058 |
a0013 | 0/0 | 1060 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | MELWA others(1055): Show |
chr1 | 177923788 | 177975058 |
a0014 | 0/0 | 1060 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | MELWA others(1055): Show |
chr1 | 177923788 | 177975058 |
a0015 | 0/0 | 1060 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | MELWA others(1055): Show |
chr1 | 177923788 | 177975058 |
a0016 | 0/0 | 1060 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | MELWA others(1055): Show |
chr1 | 177923788 | 177975058 |
a0017 | 0/0 | 1060 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | MELWA others(1055): Show |
chr1 | 177923788 | 177975058 |
a0018 | 0/0 | 1060 | 2 | 1 | 0 | 1 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | MELWA others(1055): Show |
chr1 | 177923788 | 177975058 |
a0019 | 0/0 | 1060 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | MELWA others(1055): Show |
chr1 | 177923788 | 177975058 |
a0020 | 0/0 | 1060 | 2 | 0 | 0 | 1 | 0 | 1 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | MELWA others(1055): Show |
chr1 | 177923788 | 177975058 |
a0021 | 0/0 | 1060 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SEC16B_chr1_177923788_177975058 | SEC16B | MELWA others(1055): Show |
chr1 | 177923788 | 177975058 |
a0022 | 0/0 | 1060 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SEC16B_chr1_177923788_177975058 | SEC16B | MELWA others(1055): Show |
chr1 | 177923788 | 177975058 |
a0023 | 0/0 | 1071 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | MELWA others(1066): Show |
chr1 | 177923788 | 177975058 |
a0024 | 0/0 | 1060 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | MELWA others(1055): Show |
chr1 | 177923788 | 177975058 |
a0025 | 0/0 | 1060 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | MELWA others(1055): Show |
chr1 | 177923788 | 177975058 |
a0026 | 0/0 | 1060 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | MELWA others(1055): Show |
chr1 | 177923788 | 177975058 |
a0027 | 0/0 | 1060 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | MELWA others(1055): Show |
chr1 | 177923788 | 177975058 |
a0028 | 0/0 | 1060 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | MELWA others(1055): Show |
chr1 | 177923788 | 177975058 |
a0029 | 0/0 | 1060 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | MELWA others(1055): Show |
chr1 | 177923788 | 177975058 |
a0030 | 0/0 | 1060 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | MELWA others(1055): Show |
chr1 | 177923788 | 177975058 |
a0031 | 0/0 | 1060 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | MELWA others(1055): Show |
chr1 | 177923788 | 177975058 |
a0032 | 0/0 | 1060 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | MELWA others(1055): Show |
chr1 | 177923788 | 177975058 |
a0033 | 0/0 | 1060 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | MELWA others(1055): Show |
chr1 | 177923788 | 177975058 |
a0034 | 0/0 | 1060 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | MELWA others(1055): Show |
chr1 | 177923788 | 177975058 |
a0035 | 0/0 | 1060 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | MELWA others(1055): Show |
chr1 | 177923788 | 177975058 |
a0036 | 0/0 | 1060 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | MELWA others(1055): Show |
chr1 | 177923788 | 177975058 |
a0037 | 0/0 | 1060 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | MELWA others(1055): Show |
chr1 | 177923788 | 177975058 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0004 | 0/0 | 3180 | 28 | 1 | 4 | 20 | 0 | 3 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0001c0005 | 0/0 | 3180 | 28 | 3 | 2 | 17 | 0 | 6 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0001c0006 | 0/0 | 3180 | 26 | 4 | 12 | 1 | 3 | 6 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0001c0007 | 0/0 | 3180 | 17 | 9 | 6 | 1 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0001c0013 | 0/0 | 3180 | 6 | 0 | 2 | 0 | 2 | 2 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0001c0017 | 0/0 | 3180 | 3 | 1 | 0 | 0 | 0 | 2 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0001c0021 | 0/0 | 3180 | 3 | 3 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0001c0036 | 0/0 | 3180 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0001c0048 | 0/0 | 3180 | 1 | 0 | 0 | 0 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0001c0052 | 0/0 | 3180 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0001c0053 | 0/0 | 3180 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0001c0061 | 0/0 | 3180 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0001c0063 | 0/0 | 3180 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0001c0065 | 0/0 | 3180 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0002c0001 | 0/0 | 3180 | 68 | 15 | 13 | 27 | 4 | 9 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0003c0003 | 0/0 | 3180 | 44 | 1 | 11 | 27 | 0 | 5 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0003c0008 | 0/0 | 3180 | 17 | 14 | 1 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0003c0018 | 0/0 | 3180 | 3 | 0 | 0 | 3 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0003c0026 | 0/1 | 3180 | 2 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0003c0055 | 0/0 | 3180 | 1 | 0 | 0 | 0 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0003c0057 | 0/0 | 3180 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0004c0002 | 0/0 | 3180 | 44 | 1 | 9 | 29 | 0 | 5 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0004c0010 | 0/0 | 3180 | 10 | 0 | 0 | 10 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0004c0027 | 0/0 | 3180 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0004c0067 | 0/0 | 3180 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0005c0011 | 0/0 | 3180 | 8 | 6 | 2 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0005c0016 | 0/0 | 3180 | 4 | 3 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0005c0054 | 0/0 | 3180 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0006c0009 | 0/0 | 3180 | 11 | 0 | 0 | 10 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0007c0014 | 0/0 | 3180 | 5 | 1 | 3 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0007c0029 | 0/0 | 3180 | 2 | 0 | 2 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0007c0034 | 0/0 | 3180 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0007c0049 | 0/0 | 3180 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0008c0012 | 1/0 | 3180 | 7 | 1 | 0 | 5 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0008c0041 | 0/0 | 3180 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0008c0044 | 0/0 | 3180 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0009c0015 | 0/0 | 3213 | 5 | 0 | 1 | 4 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3208): Show |
chr1 | 177923788 | 177975058 | ||
a0009c0030 | 0/0 | 3213 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3208): Show |
chr1 | 177923788 | 177975058 | ||
a0009c0069 | 0/0 | 3213 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3208): Show |
chr1 | 177923788 | 177975058 | ||
a0010c0035 | 0/0 | 3213 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3208): Show |
chr1 | 177923788 | 177975058 | ||
a0010c0070 | 0/0 | 3213 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3208): Show |
chr1 | 177923788 | 177975058 | ||
a0011c0025 | 0/0 | 3180 | 2 | 1 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0011c0050 | 0/0 | 3180 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0012c0019 | 0/0 | 3180 | 3 | 2 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0013c0020 | 0/0 | 3180 | 3 | 3 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0014c0032 | 0/0 | 3180 | 2 | 0 | 1 | 0 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0015c0047 | 0/0 | 3180 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0015c0062 | 0/0 | 3180 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0016c0024 | 0/0 | 3180 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0017c0031 | 0/0 | 3180 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0018c0045 | 0/0 | 3180 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0018c0068 | 0/0 | 3180 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0019c0028 | 0/0 | 3180 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0020c0022 | 0/0 | 3180 | 2 | 0 | 0 | 1 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0021c0033 | 0/0 | 3180 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0022c0023 | 0/0 | 3180 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0023c0071 | 0/0 | 3213 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3208): Show |
chr1 | 177923788 | 177975058 | ||
a0024c0043 | 0/0 | 3180 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0025c0051 | 0/0 | 3180 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0026c0038 | 0/0 | 3180 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0027c0039 | 0/0 | 3180 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0028c0037 | 0/0 | 3180 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0029c0064 | 0/0 | 3180 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0030c0040 | 0/0 | 3180 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0031c0042 | 0/0 | 3180 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0032c0046 | 0/0 | 3180 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0033c0059 | 0/0 | 3180 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0034c0058 | 0/0 | 3180 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0035c0060 | 0/0 | 3180 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0036c0066 | 0/0 | 3180 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 | ||
a0037c0056 | 0/0 | 3180 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | ATGGA others(3175): Show |
chr1 | 177923788 | 177975058 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0004t0001 | 0/0 | 4486 | 19 | 1 | 3 | 12 | 0 | 3 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0001c0004t0004 | 0/0 | 4486 | 9 | 0 | 1 | 8 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0001c0005t0001 | 0/0 | 4486 | 20 | 3 | 1 | 10 | 0 | 6 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0001c0005t0002 | 0/0 | 4486 | 3 | 0 | 0 | 3 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0001c0005t0004 | 0/0 | 4486 | 4 | 0 | 0 | 4 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0001c0005t0017 | 0/0 | 4486 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0001c0006t0001 | 0/0 | 4486 | 24 | 3 | 11 | 1 | 3 | 6 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0001c0006t0007 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0001c0006t0018 | 0/0 | 4486 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0001c0007t0001 | 0/0 | 4486 | 11 | 5 | 4 | 1 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0001c0007t0006 | 0/0 | 4486 | 5 | 4 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0001c0007t0007 | 0/0 | 4486 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0001c0013t0001 | 0/0 | 4486 | 6 | 0 | 2 | 0 | 2 | 2 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0001c0017t0001 | 0/0 | 4486 | 3 | 1 | 0 | 0 | 0 | 2 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0001c0021t0001 | 0/0 | 4486 | 3 | 3 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0001c0036t0001 | 0/0 | 4486 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0001c0048t0001 | 0/0 | 4486 | 1 | 0 | 0 | 0 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0001c0052t0012 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0001c0053t0001 | 0/0 | 4486 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0001c0061t0001 | 0/0 | 4486 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0001c0063t0001 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0001c0065t0001 | 0/0 | 4486 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0002c0001t0002 | 0/0 | 4486 | 66 | 15 | 11 | 27 | 4 | 9 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0002c0001t0014 | 0/0 | 4486 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0002c0001t0020 | 0/0 | 4486 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0003c0003t0003 | 0/0 | 4486 | 42 | 1 | 11 | 26 | 0 | 4 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0003c0003t0013 | 0/0 | 4486 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0003c0003t0015 | 0/0 | 4486 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0003c0008t0003 | 0/0 | 4486 | 17 | 14 | 1 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0003c0018t0003 | 0/0 | 4486 | 3 | 0 | 0 | 3 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0003c0026t0003 | 0/1 | 4486 | 2 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0003c0055t0003 | 0/0 | 4486 | 1 | 0 | 0 | 0 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0003c0057t0003 | 0/0 | 4486 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0004c0002t0001 | 0/0 | 4486 | 2 | 0 | 0 | 1 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0004c0002t0004 | 0/0 | 4486 | 39 | 1 | 9 | 25 | 0 | 4 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0004c0002t0008 | 0/0 | 4486 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0004c0002t0009 | 0/0 | 4486 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0004c0010t0002 | 0/0 | 4486 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0004c0010t0004 | 0/0 | 4486 | 7 | 0 | 0 | 7 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0004c0010t0008 | 0/0 | 4486 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0004c0010t0009 | 0/0 | 4486 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0004c0027t0006 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0004c0027t0019 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0004c0067t0008 | 0/0 | 4486 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0005c0011t0002 | 0/0 | 4486 | 8 | 6 | 2 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0005c0016t0002 | 0/0 | 4486 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0005c0016t0003 | 0/0 | 4486 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0005c0016t0005 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0005c0054t0005 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0006c0009t0004 | 0/0 | 4486 | 11 | 0 | 0 | 10 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0007c0014t0002 | 0/0 | 4486 | 5 | 1 | 3 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0007c0029t0002 | 0/0 | 4486 | 2 | 0 | 2 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0007c0034t0002 | 0/0 | 4486 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0007c0049t0002 | 0/0 | 4486 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0008c0012t0001 | 1/0 | 4486 | 6 | 0 | 0 | 5 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0008c0012t0011 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0008c0041t0007 | 0/0 | 4486 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0008c0044t0001 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0009c0015t0002 | 0/0 | 4519 | 5 | 0 | 1 | 4 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4514): Show |
chr1 | 177923788 | 177975058 |
a0009c0030t0002 | 0/0 | 4519 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4514): Show |
chr1 | 177923788 | 177975058 |
a0009c0069t0001 | 0/0 | 4519 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4514): Show |
chr1 | 177923788 | 177975058 |
a0010c0035t0002 | 0/0 | 4519 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4514): Show |
chr1 | 177923788 | 177975058 |
a0010c0070t0002 | 0/0 | 4519 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4514): Show |
chr1 | 177923788 | 177975058 |
a0011c0025t0005 | 0/0 | 4486 | 2 | 1 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0011c0050t0005 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0012c0019t0001 | 0/0 | 4486 | 2 | 1 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0012c0019t0006 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0013c0020t0001 | 0/0 | 4486 | 3 | 3 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0014c0032t0003 | 0/0 | 4486 | 2 | 0 | 1 | 0 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0015c0047t0004 | 0/0 | 4486 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0015c0062t0004 | 0/0 | 4486 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0016c0024t0010 | 0/0 | 4486 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0017c0031t0001 | 0/0 | 4486 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0018c0045t0002 | 0/0 | 4486 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0018c0068t0002 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0019c0028t0005 | 0/0 | 4486 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0020c0022t0003 | 0/0 | 4486 | 2 | 0 | 0 | 1 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0021c0033t0003 | 0/0 | 4486 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0022c0023t0001 | 0/0 | 4486 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0023c0071t0002 | 0/0 | 4519 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4514): Show |
chr1 | 177923788 | 177975058 |
a0024c0043t0003 | 0/0 | 4486 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0025c0051t0007 | 0/0 | 4486 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0026c0038t0001 | 0/0 | 4486 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0027c0039t0004 | 0/0 | 4486 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0028c0037t0003 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0029c0064t0003 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0030c0040t0001 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0031c0042t0005 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0032c0046t0001 | 0/0 | 4486 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0033c0059t0003 | 0/0 | 4486 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0034c0058t0004 | 0/0 | 4486 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0035c0060t0001 | 0/0 | 4486 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0036c0066t0003 | 0/0 | 4486 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
a0037c0056t0016 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | AGCTC others(4481): Show |
chr1 | 177923788 | 177975058 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0004t0001g0012 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0004g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0004g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0004g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0004g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0001g0024 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0004g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0017g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0001g0010 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0001g0011 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0007g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0018g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0007t0001g0020 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0007t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0007t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0007t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0007t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0007t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0007t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0007t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0007t0006g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0007t0006g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0007t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0007t0007g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0013t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0013t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0013t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0013t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0017t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0017t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0017t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0021t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0021t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0021t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0036t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0036t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0048t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0052t0012g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0053t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0061t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0063t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0065t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0002 | 0/0 | 7 | 0 | 0 | 3 | 2 | 2 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0005 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0018 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0014g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0020g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0003 | 0/0 | 7 | 0 | 4 | 2 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0016 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0021 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0013g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0015g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0008t0003g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0008t0003g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0008t0003g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0008t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0008t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0008t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0008t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0008t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0008t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0008t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0008t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0008t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0008t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0008t0003g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0018t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0018t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0018t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0026t0003g0182 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0026t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0055t0003g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0057t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0001 | 0/0 | 8 | 0 | 0 | 6 | 0 | 2 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0019 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0008g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0009g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0010t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0010t0004g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0010t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0010t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0010t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0010t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0010t0008g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0010t0009g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0027t0006g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0027t0019g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0067t0008g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0005c0011t0002g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0005c0011t0002g0014 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0005c0011t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0005c0011t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0005c0016t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0005c0016t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0005c0016t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0005c0016t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0005c0054t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0006c0009t0004g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0006c0009t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0006c0009t0004g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0006c0009t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0006c0009t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0006c0009t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0006c0009t0004g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0007c0014t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0007c0014t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0007c0014t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0007c0014t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0007c0014t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0007c0029t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0007c0029t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0007c0034t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0007c0034t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0007c0049t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0008c0012t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0008c0012t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0008c0012t0001g0146 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0008c0012t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0008c0012t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0008c0012t0011g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0008c0041t0007g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0008c0044t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0009c0015t0002g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0009c0015t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0009c0015t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0009c0030t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0009c0030t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0009c0069t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0010c0035t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0010c0035t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0010c0070t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0011c0025t0005g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0011c0025t0005g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0011c0050t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0012c0019t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0012c0019t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0012c0019t0006g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0013c0020t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0013c0020t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0014c0032t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0014c0032t0003g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0015c0047t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0015c0062t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0016c0024t0010g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0016c0024t0010g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0017c0031t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0017c0031t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0018c0045t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0018c0068t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0019c0028t0005g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0020c0022t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0020c0022t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0021c0033t0003g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0022c0023t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0022c0023t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0023c0071t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0024c0043t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0025c0051t0007g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0026c0038t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0027c0039t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0028c0037t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0029c0064t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0030c0040t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0031c0042t0005g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0032c0046t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0033c0059t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0034c0058t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0035c0060t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0036c0066t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0037c0056t0016g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0014 | c0032 | t0003 | g0129 | EUR | GBR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00099 | hp2 | a0001 | c0006 | t0001 | g0011 | EUR | GBR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00140 | hp1 | a0001 | c0048 | t0001 | g0124 | EUR | GBR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00140 | hp2 | a0002 | c0001 | t0002 | g0036 | EUR | GBR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00280 | hp1 | a0001 | c0006 | t0001 | g0170 | EUR | FIN | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00280 | hp2 | a0006 | c0009 | t0004 | g0135 | EUR | FIN | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00323 | hp1 | a0002 | c0001 | t0002 | g0002 | EUR | FIN | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00323 | hp2 | a0001 | c0006 | t0001 | g0011 | EUR | FIN | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00408 | hp1 | a0003 | c0003 | t0003 | g0079 | EAS | CHS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00408 | hp2 | a0004 | c0002 | t0004 | g0040 | EAS | CHS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00423 | hp1 | a0006 | c0009 | t0004 | g0294 | EAS | CHS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00423 | hp2 | a0023 | c0071 | t0002 | g0205 | EAS | CHS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00438 | hp1 | a0002 | c0001 | t0002 | g0305 | EAS | CHS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00438 | hp2 | a0001 | c0065 | t0001 | g0279 | EAS | CHS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00544 | hp1 | a0003 | c0003 | t0003 | g0080 | EAS | CHS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00544 | hp2 | a0015 | c0047 | t0004 | g0122 | EAS | CHS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00558 | hp1 | a0003 | c0003 | t0003 | g0274 | EAS | CHS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00558 | hp2 | a0004 | c0067 | t0008 | g0200 | EAS | CHS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00597 | hp1 | a0001 | c0005 | t0002 | g0272 | EAS | CHS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00597 | hp2 | a0002 | c0001 | t0002 | g0295 | EAS | CHS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00609 | hp1 | a0009 | c0069 | t0001 | g0201 | EAS | CHS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00609 | hp2 | a0004 | c0010 | t0002 | g0278 | EAS | CHS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00621 | hp1 | a0004 | c0002 | t0004 | g0001 | EAS | CHS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00621 | hp2 | a0001 | c0004 | t0001 | g0243 | EAS | CHS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00639 | hp1 | a0001 | c0004 | t0001 | g0260 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00639 | hp2 | a0001 | c0007 | t0001 | g0020 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00642 | hp1 | a0001 | c0007 | t0001 | g0020 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00642 | hp2 | a0007 | c0029 | t0002 | g0209 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00733 | hp1 | a0001 | c0007 | t0007 | g0287 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00733 | hp2 | a0007 | c0014 | t0002 | g0164 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00735 | hp1 | a0024 | c0043 | t0003 | g0145 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00735 | hp2 | a0002 | c0001 | t0002 | g0120 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00738 | hp1 | a0001 | c0005 | t0001 | g0084 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00738 | hp2 | a0010 | c0070 | t0002 | g0203 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00741 | hp1 | a0003 | c0026 | t0003 | g0220 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00741 | hp2 | a0001 | c0006 | t0001 | g0011 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01069 | hp1 | a0001 | c0007 | t0006 | g0027 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01069 | hp2 | a0003 | c0003 | t0003 | g0003 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01070 | hp1 | a0005 | c0011 | t0002 | g0014 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01070 | hp2 | a0001 | c0006 | t0001 | g0181 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01071 | hp1 | a0005 | c0011 | t0002 | g0014 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01071 | hp2 | a0003 | c0003 | t0003 | g0003 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01074 | hp1 | a0025 | c0051 | t0007 | g0059 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01074 | hp2 | a0002 | c0001 | t0002 | g0018 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01081 | hp1 | a0001 | c0007 | t0001 | g0185 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01081 | hp2 | a0001 | c0006 | t0001 | g0010 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01099 | hp1 | a0011 | c0025 | t0005 | g0177 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01099 | hp2 | a0007 | c0029 | t0002 | g0186 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01106 | hp1 | a0003 | c0003 | t0003 | g0105 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01106 | hp2 | a0001 | c0006 | t0001 | g0208 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01109 | hp1 | a0005 | c0016 | t0002 | g0229 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01109 | hp2 | a0001 | c0004 | t0001 | g0134 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01168 | hp1 | a0001 | c0013 | t0001 | g0035 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01168 | hp2 | a0007 | c0014 | t0002 | g0087 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01169 | hp1 | a0001 | c0013 | t0001 | g0035 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01169 | hp2 | a0001 | c0004 | t0001 | g0072 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01175 | hp1 | a0008 | c0041 | t0007 | g0151 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01175 | hp2 | a0001 | c0007 | t0001 | g0112 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01192 | hp1 | a0001 | c0006 | t0001 | g0056 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01192 | hp2 | a0002 | c0001 | t0002 | g0005 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01243 | hp1 | a0003 | c0003 | t0003 | g0288 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01243 | hp2 | a0012 | c0019 | t0001 | g0073 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01255 | hp1 | a0003 | c0003 | t0003 | g0021 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01255 | hp2 | a0002 | c0001 | t0014 | g0304 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01257 | hp1 | a0002 | c0001 | t0002 | g0216 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01257 | hp2 | a0003 | c0003 | t0003 | g0050 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01258 | hp1 | a0003 | c0003 | t0003 | g0109 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01258 | hp2 | a0002 | c0001 | t0002 | g0044 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01261 | hp1 | a0009 | c0015 | t0002 | g0204 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01261 | hp2 | a0007 | c0014 | t0002 | g0178 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01346 | hp1 | a0026 | c0038 | t0001 | g0237 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01346 | hp2 | a0001 | c0004 | t0004 | g0261 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01358 | hp1 | a0003 | c0003 | t0003 | g0003 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01358 | hp2 | a0002 | c0001 | t0002 | g0044 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01361 | hp1 | a0004 | c0002 | t0004 | g0171 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01361 | hp2 | a0004 | c0002 | t0004 | g0019 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01433 | hp1 | a0001 | c0006 | t0018 | g0180 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01433 | hp2 | a0004 | c0002 | t0004 | g0160 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01496 | hp1 | a0001 | c0006 | t0001 | g0011 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01496 | hp2 | a0004 | c0002 | t0004 | g0019 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01515 | hp1 | a0001 | c0013 | t0001 | g0032 | EUR | IBS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01515 | hp2 | a0001 | c0007 | t0001 | g0113 | EUR | IBS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01517 | hp1 | a0002 | c0001 | t0002 | g0036 | EUR | IBS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01517 | hp2 | a0001 | c0013 | t0001 | g0032 | EUR | IBS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01884 | hp1 | a0016 | c0024 | t0010 | g0057 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01884 | hp2 | a0001 | c0004 | t0001 | g0060 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01891 | hp1 | a0001 | c0005 | t0001 | g0110 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01891 | hp2 | a0003 | c0008 | t0003 | g0033 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01928 | hp1 | a0001 | c0006 | t0001 | g0115 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01928 | hp2 | a0004 | c0002 | t0004 | g0257 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01943 | hp1 | a0001 | c0006 | t0001 | g0010 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01943 | hp2 | a0002 | c0001 | t0002 | g0005 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01952 | hp1 | a0003 | c0003 | t0003 | g0050 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01952 | hp2 | a0004 | c0002 | t0004 | g0017 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01978 | hp1 | a0002 | c0001 | t0002 | g0142 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01978 | hp2 | a0002 | c0001 | t0002 | g0005 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01981 | hp1 | a0002 | c0001 | t0020 | g0308 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01981 | hp2 | a0004 | c0002 | t0004 | g0017 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01993 | hp1 | a0002 | c0001 | t0002 | g0005 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01993 | hp2 | a0003 | c0003 | t0003 | g0016 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02004 | hp1 | a0002 | c0001 | t0002 | g0121 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02004 | hp2 | a0003 | c0003 | t0003 | g0003 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02027 | hp1 | a0027 | c0039 | t0004 | g0251 | EAS | KHV | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02027 | hp2 | a0002 | c0001 | t0002 | g0152 | EAS | KHV | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02040 | hp1 | a0003 | c0003 | t0015 | g0107 | EAS | KHV | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02040 | hp2 | a0004 | c0002 | t0004 | g0255 | EAS | KHV | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02055 | hp1 | a0003 | c0008 | t0003 | g0061 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02055 | hp2 | a0001 | c0063 | t0001 | g0127 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02071 | hp1 | a0004 | c0002 | t0004 | g0001 | EAS | KHV | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02071 | hp2 | a0002 | c0001 | t0002 | g0212 | EAS | KHV | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02074 | hp1 | a0008 | c0012 | t0001 | g0249 | EAS | KHV | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02074 | hp2 | a0001 | c0004 | t0001 | g0244 | EAS | KHV | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02080 | hp1 | a0015 | c0062 | t0004 | g0265 | EAS | KHV | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02080 | hp2 | a0001 | c0005 | t0001 | g0024 | EAS | KHV | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02083 | hp1 | a0001 | c0004 | t0001 | g0153 | EAS | KHV | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02083 | hp2 | a0004 | c0010 | t0004 | g0192 | EAS | KHV | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02129 | hp1 | a0003 | c0003 | t0003 | g0191 | EAS | KHV | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02129 | hp2 | a0001 | c0053 | t0001 | g0252 | EAS | KHV | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02132 | hp1 | a0001 | c0005 | t0002 | g0108 | EAS | KHV | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02132 | hp2 | a0001 | c0004 | t0001 | g0012 | EAS | KHV | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02135 | hp1 | a0001 | c0005 | t0001 | g0042 | EAS | KHV | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02135 | hp2 | a0004 | c0002 | t0004 | g0174 | EAS | KHV | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02145 | hp1 | a0028 | c0037 | t0003 | g0224 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02145 | hp2 | a0004 | c0027 | t0019 | g0307 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02148 | hp1 | a0004 | c0002 | t0004 | g0219 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02148 | hp2 | a0001 | c0006 | t0001 | g0010 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02155 | hp1 | a0001 | c0004 | t0001 | g0238 | EAS | CDX | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02155 | hp2 | a0002 | c0001 | t0002 | g0214 | EAS | CDX | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02165 | hp1 | a0003 | c0003 | t0003 | g0114 | EAS | CDX | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02165 | hp2 | a0001 | c0004 | t0001 | g0012 | EAS | CDX | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02257 | hp1 | a0005 | c0011 | t0002 | g0013 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02257 | hp2 | a0001 | c0007 | t0001 | g0020 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02258 | hp1 | a0002 | c0001 | t0002 | g0008 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02258 | hp2 | a0001 | c0017 | t0001 | g0064 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02280 | hp1 | a0003 | c0008 | t0003 | g0300 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02280 | hp2 | a0001 | c0007 | t0006 | g0027 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02293 | hp1 | a0001 | c0006 | t0001 | g0165 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02293 | hp2 | a0001 | c0005 | t0017 | g0130 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02300 | hp1 | a0004 | c0002 | t0004 | g0017 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02300 | hp2 | a0014 | c0032 | t0003 | g0266 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02451 | hp1 | a0029 | c0064 | t0003 | g0132 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02451 | hp2 | a0005 | c0011 | t0002 | g0013 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02572 | hp1 | a0012 | c0019 | t0006 | g0051 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02572 | hp2 | a0001 | c0005 | t0001 | g0047 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02602 | hp1 | a0003 | c0003 | t0013 | g0198 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02602 | hp2 | a0004 | c0002 | t0001 | g0123 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02615 | hp1 | a0002 | c0001 | t0002 | g0007 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02615 | hp2 | a0001 | c0005 | t0001 | g0047 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02622 | hp1 | a0003 | c0008 | t0003 | g0230 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02622 | hp2 | a0018 | c0068 | t0002 | g0089 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02630 | hp1 | a0030 | c0040 | t0001 | g0096 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02630 | hp2 | a0003 | c0008 | t0003 | g0081 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02698 | hp1 | a0001 | c0006 | t0001 | g0166 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02698 | hp2 | a0001 | c0004 | t0001 | g0092 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02717 | hp1 | a0004 | c0027 | t0006 | g0053 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02717 | hp2 | a0001 | c0007 | t0001 | g0099 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02723 | hp1 | a0005 | c0011 | t0002 | g0014 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02723 | hp2 | a0005 | c0054 | t0005 | g0119 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02735 | hp1 | a0002 | c0001 | t0002 | g0018 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02735 | hp2 | a0007 | c0049 | t0002 | g0179 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02738 | hp1 | a0004 | c0002 | t0004 | g0001 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02738 | hp2 | a0003 | c0003 | t0003 | g0003 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02809 | hp1 | a0007 | c0014 | t0002 | g0176 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02809 | hp2 | a0001 | c0006 | t0007 | g0236 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02818 | hp1 | a0031 | c0042 | t0005 | g0093 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02818 | hp2 | a0001 | c0021 | t0001 | g0258 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02886 | hp1 | a0002 | c0001 | t0002 | g0007 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02886 | hp2 | a0003 | c0008 | t0003 | g0088 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02895 | hp1 | a0003 | c0008 | t0003 | g0045 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02895 | hp2 | a0001 | c0007 | t0001 | g0048 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02896 | hp1 | a0003 | c0008 | t0003 | g0030 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02896 | hp2 | a0001 | c0007 | t0006 | g0026 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02897 | hp1 | a0001 | c0007 | t0006 | g0026 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02897 | hp2 | a0001 | c0007 | t0001 | g0048 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02922 | hp1 | a0005 | c0011 | t0002 | g0013 | AFR | ESN | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02922 | hp2 | a0002 | c0001 | t0002 | g0007 | AFR | ESN | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02965 | hp1 | a0019 | c0028 | t0005 | g0029 | AFR | ESN | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02965 | hp2 | a0001 | c0007 | t0001 | g0225 | AFR | ESN | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02970 | hp1 | a0001 | c0006 | t0001 | g0227 | AFR | ESN | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02970 | hp2 | a0005 | c0016 | t0005 | g0133 | AFR | ESN | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02976 | hp1 | a0002 | c0001 | t0002 | g0008 | AFR | ESN | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02976 | hp2 | a0001 | c0036 | t0001 | g0116 | AFR | ESN | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03041 | hp1 | a0002 | c0001 | t0002 | g0231 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03041 | hp2 | a0003 | c0008 | t0003 | g0030 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03098 | hp1 | a0001 | c0006 | t0001 | g0090 | AFR | MSL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03098 | hp2 | a0003 | c0008 | t0003 | g0033 | AFR | MSL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03130 | hp1 | a0013 | c0020 | t0001 | g0028 | AFR | ESN | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03130 | hp2 | a0002 | c0001 | t0002 | g0008 | AFR | ESN | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03139 | hp1 | a0019 | c0028 | t0005 | g0029 | AFR | ESN | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03139 | hp2 | a0003 | c0008 | t0003 | g0226 | AFR | ESN | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03209 | hp1 | a0013 | c0020 | t0001 | g0066 | AFR | MSL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03209 | hp2 | a0001 | c0021 | t0001 | g0259 | AFR | MSL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03225 | hp1 | a0013 | c0020 | t0001 | g0028 | AFR | MSL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03225 | hp2 | a0002 | c0001 | t0002 | g0046 | AFR | MSL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03239 | hp1 | a0002 | c0001 | t0002 | g0172 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03239 | hp2 | a0002 | c0001 | t0002 | g0246 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03453 | hp1 | a0001 | c0007 | t0006 | g0052 | AFR | MSL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03453 | hp2 | a0005 | c0016 | t0003 | g0058 | AFR | MSL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03490 | hp1 | a0001 | c0005 | t0001 | g0293 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03490 | hp2 | a0002 | c0001 | t0002 | g0018 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03491 | hp1 | a0003 | c0003 | t0003 | g0268 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03491 | hp2 | a0002 | c0001 | t0002 | g0002 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03492 | hp1 | a0001 | c0005 | t0001 | g0292 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03492 | hp2 | a0002 | c0001 | t0002 | g0002 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03516 | hp1 | a0005 | c0016 | t0003 | g0235 | AFR | ESN | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03516 | hp2 | a0003 | c0008 | t0003 | g0082 | AFR | ESN | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03579 | hp1 | a0008 | c0044 | t0001 | g0233 | AFR | MSL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03579 | hp2 | a0005 | c0011 | t0002 | g0063 | AFR | MSL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03654 | hp1 | a0001 | c0005 | t0001 | g0277 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03654 | hp2 | a0001 | c0013 | t0001 | g0197 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03669 | hp1 | a0004 | c0002 | t0004 | g0019 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03669 | hp2 | a0001 | c0005 | t0001 | g0193 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03688 | hp1 | a0003 | c0003 | t0003 | g0280 | SAS | STU | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03688 | hp2 | a0001 | c0061 | t0001 | g0269 | SAS | STU | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03704 | hp1 | a0001 | c0006 | t0001 | g0167 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03704 | hp2 | a0001 | c0006 | t0001 | g0175 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03710 | hp1 | a0004 | c0002 | t0004 | g0157 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03710 | hp2 | a0003 | c0003 | t0003 | g0276 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03831 | hp1 | a0001 | c0004 | t0001 | g0012 | SAS | BEB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03831 | hp2 | a0001 | c0006 | t0001 | g0169 | SAS | BEB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03834 | hp1 | a0001 | c0004 | t0001 | g0240 | SAS | BEB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03834 | hp2 | a0002 | c0001 | t0002 | g0148 | SAS | BEB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03927 | hp1 | a0001 | c0017 | t0001 | g0097 | SAS | BEB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03927 | hp2 | a0001 | c0006 | t0001 | g0168 | SAS | BEB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03942 | hp1 | a0001 | c0005 | t0001 | g0273 | SAS | BEB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03942 | hp2 | a0001 | c0017 | t0001 | g0299 | SAS | BEB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG04115 | hp1 | a0001 | c0006 | t0001 | g0010 | SAS | STU | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG04115 | hp2 | a0002 | c0001 | t0002 | g0143 | SAS | STU | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG04184 | hp1 | a0020 | c0022 | t0003 | g0144 | SAS | BEB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG04184 | hp2 | a0001 | c0013 | t0001 | g0131 | SAS | BEB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG04204 | hp1 | a0004 | c0002 | t0004 | g0001 | SAS | STU | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG04204 | hp2 | a0002 | c0001 | t0002 | g0140 | SAS | STU | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG04228 | hp1 | a0001 | c0005 | t0001 | g0024 | SAS | STU | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG04228 | hp2 | a0032 | c0046 | t0001 | g0162 | SAS | STU | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18522 | hp1 | a0003 | c0008 | t0003 | g0045 | AFR | YRI | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18522 | hp2 | a0005 | c0011 | t0002 | g0118 | AFR | YRI | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18612 | hp1 | a0004 | c0002 | t0004 | g0282 | EAS | CHB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18612 | hp2 | a0003 | c0008 | t0003 | g0101 | EAS | CHB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18906 | hp1 | a0016 | c0024 | t0010 | g0065 | AFR | YRI | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18906 | hp2 | a0002 | c0001 | t0002 | g0007 | AFR | YRI | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18939 | hp1 | a0004 | c0002 | t0004 | g0161 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18939 | hp2 | a0002 | c0001 | t0002 | g0043 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18942 | hp1 | a0004 | c0002 | t0004 | g0004 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18942 | hp2 | a0008 | c0012 | t0001 | g0141 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18943 | hp1 | a0006 | c0009 | t0004 | g0095 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18943 | hp2 | a0002 | c0001 | t0002 | g0210 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18944 | hp1 | a0001 | c0004 | t0004 | g0009 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18944 | hp2 | a0002 | c0001 | t0002 | g0083 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18945 | hp1 | a0002 | c0001 | t0002 | g0138 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18945 | hp2 | a0001 | c0005 | t0001 | g0190 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18946 | hp1 | a0001 | c0004 | t0004 | g0103 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18946 | hp2 | a0001 | c0006 | t0001 | g0098 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18947 | hp1 | a0004 | c0002 | t0004 | g0149 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18947 | hp2 | a0001 | c0005 | t0001 | g0290 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18948 | hp1 | a0003 | c0018 | t0003 | g0286 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18948 | hp2 | a0001 | c0004 | t0001 | g0241 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18949 | hp1 | a0003 | c0008 | t0003 | g0100 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18949 | hp2 | a0001 | c0004 | t0004 | g0301 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18950 | hp1 | a0004 | c0002 | t0004 | g0158 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18950 | hp2 | a0002 | c0001 | t0002 | g0023 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18951 | hp1 | a0004 | c0002 | t0004 | g0004 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18951 | hp2 | a0008 | c0012 | t0001 | g0147 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18952 | hp1 | a0001 | c0004 | t0004 | g0009 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18952 | hp2 | a0001 | c0005 | t0001 | g0031 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18953 | hp1 | a0004 | c0002 | t0004 | g0154 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18953 | hp2 | a0004 | c0010 | t0004 | g0077 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18954 | hp1 | a0002 | c0001 | t0002 | g0002 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18954 | hp2 | a0003 | c0003 | t0003 | g0270 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18959 | hp1 | a0004 | c0002 | t0001 | g0207 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18959 | hp2 | a0003 | c0003 | t0003 | g0086 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18960 | hp1 | a0001 | c0004 | t0001 | g0239 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18960 | hp2 | a0002 | c0001 | t0002 | g0002 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18961 | hp1 | a0009 | c0030 | t0002 | g0183 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18961 | hp2 | a0004 | c0002 | t0004 | g0004 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18962 | hp1 | a0006 | c0009 | t0004 | g0250 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18962 | hp2 | a0001 | c0005 | t0001 | g0024 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18963 | hp1 | a0002 | c0001 | t0002 | g0247 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18963 | hp2 | a0001 | c0007 | t0001 | g0302 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18964 | hp1 | a0033 | c0059 | t0003 | g0078 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18964 | hp2 | a0009 | c0015 | t0002 | g0022 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18965 | hp1 | a0006 | c0009 | t0004 | g0211 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18965 | hp2 | a0003 | c0003 | t0003 | g0195 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18966 | hp1 | a0010 | c0035 | t0002 | g0298 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18966 | hp2 | a0001 | c0004 | t0001 | g0012 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18969 | hp1 | a0004 | c0010 | t0009 | g0188 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18969 | hp2 | a0006 | c0009 | t0004 | g0139 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18970 | hp1 | a0003 | c0003 | t0003 | g0296 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18970 | hp2 | a0002 | c0001 | t0002 | g0136 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18971 | hp1 | a0004 | c0002 | t0004 | g0156 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18971 | hp2 | a0004 | c0010 | t0008 | g0264 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18974 | hp1 | a0002 | c0001 | t0002 | g0281 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18974 | hp2 | a0003 | c0003 | t0003 | g0267 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18975 | hp1 | a0009 | c0030 | t0002 | g0184 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18975 | hp2 | a0002 | c0001 | t0002 | g0002 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18977 | hp1 | a0002 | c0001 | t0002 | g0291 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18977 | hp2 | a0008 | c0012 | t0001 | g0037 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18979 | hp1 | a0003 | c0003 | t0003 | g0271 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18979 | hp2 | a0001 | c0004 | t0001 | g0245 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18981 | hp1 | a0004 | c0002 | t0004 | g0039 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18981 | hp2 | a0001 | c0005 | t0004 | g0025 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18982 | hp1 | a0004 | c0010 | t0004 | g0075 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18982 | hp2 | a0003 | c0003 | t0003 | g0041 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18983 | hp1 | a0007 | c0034 | t0002 | g0128 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18983 | hp2 | a0004 | c0002 | t0004 | g0001 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18986 | hp1 | a0001 | c0005 | t0002 | g0221 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18986 | hp2 | a0004 | c0002 | t0008 | g0038 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18987 | hp1 | a0021 | c0033 | t0003 | g0049 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18987 | hp2 | a0006 | c0009 | t0004 | g0006 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18988 | hp1 | a0010 | c0035 | t0002 | g0297 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18988 | hp2 | a0003 | c0018 | t0003 | g0217 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18989 | hp1 | a0006 | c0009 | t0004 | g0006 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18989 | hp2 | a0001 | c0005 | t0001 | g0104 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18990 | hp1 | a0003 | c0003 | t0003 | g0016 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18990 | hp2 | a0004 | c0002 | t0004 | g0040 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18993 | hp1 | a0002 | c0001 | t0002 | g0137 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18993 | hp2 | a0001 | c0004 | t0004 | g0009 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18995 | hp1 | a0003 | c0003 | t0003 | g0275 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18995 | hp2 | a0004 | c0010 | t0004 | g0015 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19000 | hp1 | a0003 | c0003 | t0003 | g0041 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19000 | hp2 | a0002 | c0001 | t0002 | g0248 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19002 | hp1 | a0004 | c0010 | t0004 | g0015 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19002 | hp2 | a0020 | c0022 | t0003 | g0213 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19005 | hp1 | a0003 | c0003 | t0003 | g0016 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19005 | hp2 | a0034 | c0058 | t0004 | g0076 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19009 | hp1 | a0006 | c0009 | t0004 | g0006 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19009 | hp2 | a0004 | c0002 | t0008 | g0038 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19010 | hp1 | a0006 | c0009 | t0004 | g0006 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19010 | hp2 | a0002 | c0001 | t0002 | g0254 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19011 | hp1 | a0001 | c0004 | t0004 | g0034 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19011 | hp2 | a0001 | c0005 | t0001 | g0031 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19012 | hp1 | a0009 | c0015 | t0002 | g0022 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19012 | hp2 | a0007 | c0034 | t0002 | g0289 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19043 | hp1 | a0001 | c0021 | t0001 | g0306 | AFR | LWK | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19043 | hp2 | a0008 | c0012 | t0011 | g0069 | AFR | LWK | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19054 | hp1 | a0004 | c0002 | t0004 | g0001 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19054 | hp2 | a0006 | c0009 | t0004 | g0006 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19057 | hp1 | a0003 | c0003 | t0003 | g0106 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19057 | hp2 | a0004 | c0002 | t0004 | g0004 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19058 | hp1 | a0003 | c0057 | t0003 | g0194 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19058 | hp2 | a0001 | c0004 | t0001 | g0242 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19060 | hp1 | a0001 | c0005 | t0004 | g0025 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19060 | hp2 | a0004 | c0010 | t0004 | g0015 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19062 | hp1 | a0021 | c0033 | t0003 | g0049 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19062 | hp2 | a0004 | c0002 | t0004 | g0039 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19063 | hp1 | a0001 | c0005 | t0001 | g0042 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19063 | hp2 | a0004 | c0002 | t0004 | g0126 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19064 | hp1 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19064 | hp2 | a0002 | c0001 | t0002 | g0206 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19065 | hp1 | a0003 | c0018 | t0003 | g0173 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19065 | hp2 | a0003 | c0003 | t0003 | g0263 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19067 | hp1 | a0001 | c0004 | t0004 | g0034 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19067 | hp2 | a0022 | c0023 | t0001 | g0283 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19068 | hp1 | a0001 | c0005 | t0004 | g0196 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19068 | hp2 | a0004 | c0002 | t0004 | g0155 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19070 | hp1 | a0004 | c0002 | t0004 | g0001 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19070 | hp2 | a0009 | c0015 | t0002 | g0202 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19072 | hp1 | a0004 | c0002 | t0004 | g0001 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19072 | hp2 | a0018 | c0045 | t0002 | g0218 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19074 | hp1 | a0002 | c0001 | t0002 | g0005 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19074 | hp2 | a0004 | c0010 | t0004 | g0074 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19077 | hp1 | a0001 | c0004 | t0004 | g0009 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19077 | hp2 | a0004 | c0002 | t0009 | g0159 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19079 | hp1 | a0003 | c0003 | t0003 | g0222 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19079 | hp2 | a0003 | c0003 | t0003 | g0262 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19080 | hp1 | a0003 | c0003 | t0003 | g0085 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19080 | hp2 | a0002 | c0001 | t0002 | g0023 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19081 | hp1 | a0001 | c0005 | t0001 | g0187 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19081 | hp2 | a0004 | c0002 | t0004 | g0004 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19082 | hp1 | a0003 | c0003 | t0003 | g0021 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19082 | hp2 | a0002 | c0001 | t0002 | g0253 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19083 | hp1 | a0008 | c0012 | t0001 | g0037 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19083 | hp2 | a0002 | c0001 | t0002 | g0023 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19084 | hp1 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19084 | hp2 | a0001 | c0004 | t0001 | g0102 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19085 | hp1 | a0003 | c0003 | t0003 | g0021 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19085 | hp2 | a0022 | c0023 | t0001 | g0284 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19088 | hp1 | a0035 | c0060 | t0001 | g0189 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19088 | hp2 | a0007 | c0014 | t0002 | g0163 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19089 | hp1 | a0002 | c0001 | t0002 | g0094 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19089 | hp2 | a0036 | c0066 | t0003 | g0199 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19090 | hp1 | a0009 | c0015 | t0002 | g0022 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19090 | hp2 | a0003 | c0003 | t0003 | g0223 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19091 | hp1 | a0002 | c0001 | t0002 | g0043 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19091 | hp2 | a0001 | c0005 | t0004 | g0025 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19240 | hp1 | a0001 | c0052 | t0012 | g0055 | AFR | YRI | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19240 | hp2 | a0017 | c0031 | t0001 | g0067 | AFR | YRI | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA20129 | hp1 | a0002 | c0001 | t0002 | g0046 | AFR | ASW | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA20129 | hp2 | a0004 | c0002 | t0004 | g0256 | AFR | ASW | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA20805 | hp1 | a0002 | c0001 | t0002 | g0002 | EUR | TSI | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA20805 | hp2 | a0003 | c0055 | t0003 | g0303 | EUR | TSI | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01123 | hp1 | a0003 | c0008 | t0003 | g0125 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01123 | hp2 | a0001 | c0006 | t0001 | g0285 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02109 | hp1 | a0011 | c0025 | t0005 | g0234 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02109 | hp2 | a0002 | c0001 | t0002 | g0232 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02486 | hp1 | a0011 | c0050 | t0005 | g0062 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02486 | hp2 | a0017 | c0031 | t0001 | g0054 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02559 | hp1 | a0012 | c0019 | t0001 | g0228 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02559 | hp2 | a0003 | c0008 | t0003 | g0068 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03471 | hp1 | a0001 | c0036 | t0001 | g0117 | AFR | MSL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03471 | hp2 | a0002 | c0001 | t0002 | g0008 | AFR | MSL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG06807 | hp1 | a0002 | c0001 | t0002 | g0150 | AFR | USA | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG06807 | hp2 | a0001 | c0006 | t0001 | g0071 | AFR | USA | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA20300 | hp1 | a0003 | c0003 | t0003 | g0091 | AFR | USA | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA20300 | hp2 | a0002 | c0001 | t0002 | g0215 | AFR | USA | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA21309 | hp1 | a0002 | c0001 | t0002 | g0070 | AFR | LWK | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA21309 | hp2 | a0037 | c0056 | t0016 | g0111 | AFR | LWK | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
homoSapiens | chm13v2 | a0003 | c0026 | t0003 | g0182 | REF | REF | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
homoSapiens | grch38p0 | a0008 | c0012 | t0001 | g0146 | REF | REF | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:177930564 | T | C | 3 | a0012 a0013 a0030 |
7 | HG01243.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
missense_variant | MODERATE | c.3092A>G | p.Asn1031Ser | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 25/26 | 3325/4486 | 3092/3183 | 1031/1060 | chr1 | 177930564 | |||
chr1:177932503 | A | G | 1 | a0016 | 2 | HG01884.hp1 NA18906.hp1 |
missense_variant | MODERATE | c.2999T>C | p.Leu1000Ser | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/26 | 3232/4486 | 2999/3183 | 1000/1060 | chr1 | 177932503 | |||
chr1:177933233 | G | A | 2 | a0019 a0031 |
3 | HG02818.hp1 HG02965.hp1 HG03139.hp1 |
missense_variant | MODERATE | c.2804C>T | p.Ser935Leu | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 22/26 | 3037/4486 | 2804/3183 | 935/1060 | chr1 | 177933233 | |||
chr1:177933252 | C | A | 9 | a0002 a0005 a0007 others(6): Show |
104 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(101): Show |
missense_variant | MODERATE | c.2785G>T | p.Ala929Ser | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 22/26 | 3018/4486 | 2785/3183 | 929/1060 | chr1 | 177933252 | |||
chr1:177933278 | G | A | 1 | a0034 | 1 | NA19005.hp2 | missense_variant | MODERATE | c.2759C>T | p.Ser920Leu | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 22/26 | 2992/4486 | 2759/3183 | 920/1060 | chr1 | 177933278 | |||
chr1:177933590 | C | T | 8 | a0002 a0005 a0007 others(5): Show |
101 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(98): Show |
missense_variant | MODERATE | c.2618G>A | p.Ser873Asn | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 21/26 | 2851/4486 | 2618/3183 | 873/1060 | chr1 | 177933590 | |||
chr1:177933618 | G | C | 17 | a0002 a0003 a0005 others(14): Show |
179 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(176): Show |
missense_variant | MODERATE | c.2590C>G | p.Pro864Ala | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 21/26 | 2823/4486 | 2590/3183 | 864/1060 | chr1 | 177933618 | |||
chr1:177936334 | C | A | 6 | a0002 a0006 a0007 others(3): Show |
94 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
missense_variant | MODERATE | c.2535G>T | p.Gln845His | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/26 | 2768/4486 | 2535/3183 | 845/1060 | chr1 | 177936334 | |||
chr1:177936351 | A | T | 1 | a0035 | 1 | NA19088.hp1 | missense_variant | MODERATE | c.2518T>A | p.Ser840Thr | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/26 | 2751/4486 | 2518/3183 | 840/1060 | chr1 | 177936351 | |||
chr1:177937372 | G | A | 1 | a0011 | 3 | HG01099.hp1 HG02109.hp1 HG02486.hp1 |
missense_variant | MODERATE | c.2345C>T | p.Ser782Phe | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 19/26 | 2578/4486 | 2345/3183 | 782/1060 | chr1 | 177937372 | |||
chr1:177939710 | G | T | 1 | a0032 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.2195C>A | p.Thr732Lys | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/26 | 2428/4486 | 2195/3183 | 732/1060 | chr1 | 177939710 | |||
chr1:177939717 | C | T | 8 | a0004 a0009 a0010 others(5): Show |
72 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(69): Show |
missense_variant | MODERATE | c.2188G>A | p.Gly730Arg | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/26 | 2421/4486 | 2188/3183 | 730/1060 | chr1 | 177939717 | |||
chr1:177939725 | G | A | 1 | a0025 | 1 | HG01074.hp1 | missense_variant | MODERATE | c.2180C>T | p.Ser727Leu | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/26 | 2413/4486 | 2180/3183 | 727/1060 | chr1 | 177939725 | |||
chr1:177939758 | A | G | 1 | a0022 | 2 | NA19067.hp2 NA19085.hp2 |
missense_variant | MODERATE | c.2147T>C | p.Ile716Thr | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/26 | 2380/4486 | 2147/3183 | 716/1060 | chr1 | 177939758 | |||
chr1:177941995 | C | T | 1 | a0021 | 2 | NA18987.hp1 NA19062.hp1 |
missense_variant | MODERATE | c.1927G>A | p.Val643Met | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 16/26 | 2160/4486 | 1927/3183 | 643/1060 | chr1 | 177941995 | |||
chr1:177951984 | G | A | 1 | a0017 | 2 | HG02486.hp2 NA19240.hp2 |
missense_variant | MODERATE | c.1475C>T | p.Thr492Met | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/26 | 1708/4486 | 1475/3183 | 492/1060 | chr1 | 177951984 | |||
chr1:177958344 | T | C | 1 | a0029 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.1153A>G | p.Ile385Val | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/26 | 1386/4486 | 1153/3183 | 385/1060 | chr1 | 177958344 | |||
chr1:177960366 | C | G | 1 | a0014 | 2 | HG00099.hp1 HG02300.hp2 |
missense_variant | MODERATE | c.974G>C | p.Arg325Thr | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 8/26 | 1207/4486 | 974/3183 | 325/1060 | chr1 | 177960366 | |||
chr1:177960813 | A | G | 1 | a0037 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.914T>C | p.Leu305Pro | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 7/26 | 1147/4486 | 914/3183 | 305/1060 | chr1 | 177960813 | |||
chr1:177960852 | T | C | 29 | a0001 a0003 a0004 others(26): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
missense_variant | MODERATE | c.875A>G | p.His292Arg | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 7/26 | 1108/4486 | 875/3183 | 292/1060 | chr1 | 177960852 | |||
chr1:177960892 | G | GAGGGATG others(26): Show |
3 | a0009 a0010 a0023 |
12 | HG00423.hp2 HG00609.hp1 HG00738.hp2 others(9): Show |
conservative_inframe_insertion | MODERATE | c.802_834dupGGTCCCAA others(25): Show |
p.Pro278_His279insGl others(31): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 7/26 | 1067/4486 | 834/3183 | 278/1060 | chr1 | 177960892 | |||
chr1:177961698 | G | A | 2 | a0013 a0017 |
5 | HG02486.hp2 HG03130.hp1 HG03209.hp1 others(2): Show |
missense_variant | MODERATE | c.679C>T | p.Arg227Cys | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 6/26 | 912/4486 | 679/3183 | 227/1060 | chr1 | 177961698 | |||
chr1:177965898 | T | A | 1 | a0036 | 1 | NA19089.hp2 | missense_variant | MODERATE | c.407A>T | p.Glu136Val | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/26 | 640/4486 | 407/3183 | 136/1060 | chr1 | 177965898 | |||
chr1:177967735 | C | G | 1 | a0026 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.247G>C | p.Val83Leu | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/26 | 480/4486 | 247/3183 | 83/1060 | chr1 | 177967735 | |||
chr1:177967761 | G | A | 1 | a0023 | 1 | HG00423.hp2 | missense_variant | MODERATE | c.221C>T | p.Ser74Phe | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/26 | 454/4486 | 221/3183 | 74/1060 | chr1 | 177967761 | |||
chr1:177967930 | C | T | 1 | a0028 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.52G>A | p.Ala18Thr | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/26 | 285/4486 | 52/3183 | 18/1060 | chr1 | 177967930 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:177932520 | G | A | 17 | a0002c0001 a0005c0011 a0005c0016 others(14): Show |
104 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(101): Show |
synonymous_variant | LOW | c.2982C>T | p.Gly994Gly | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/26 | 3215/4486 | 2982/3183 | 994/1060 | chr1 | 177932520 | |||
chr1:177932523 | C | T | 17 | a0002c0001 a0005c0011 a0005c0016 others(14): Show |
104 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(101): Show |
synonymous_variant | LOW | c.2979G>A | p.Ala993Ala | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/26 | 3212/4486 | 2979/3183 | 993/1060 | chr1 | 177932523 | |||
chr1:177933244 | G | A | 1 | a0016c0024 | 2 | HG01884.hp1 NA18906.hp1 |
synonymous_variant | LOW | c.2793C>T | p.Asp931Asp | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 22/26 | 3026/4486 | 2793/3183 | 931/1060 | chr1 | 177933244 | |||
chr1:177933253 | G | A | 7 | a0001c0007 a0001c0048 a0001c0061 others(4): Show |
23 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(20): Show |
synonymous_variant | LOW | c.2784C>T | p.Pro928Pro | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 22/26 | 3017/4486 | 2784/3183 | 928/1060 | chr1 | 177933253 | |||
chr1:177933271 | G | A | 2 | a0001c0052 a0037c0056 |
2 | NA19240.hp1 NA21309.hp2 |
synonymous_variant | LOW | c.2766C>T | p.Pro922Pro | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 22/26 | 2999/4486 | 2766/3183 | 922/1060 | chr1 | 177933271 | |||
chr1:177937218 | G | A | 1 | a0001c0036 | 2 | HG02976.hp2 HG03471.hp1 |
synonymous_variant | LOW | c.2499C>T | p.Gly833Gly | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 19/26 | 2732/4486 | 2499/3183 | 833/1060 | chr1 | 177937218 | |||
chr1:177940655 | C | T | 1 | a0003c0057 | 1 | NA19058.hp1 | synonymous_variant | LOW | c.2082G>A | p.Arg694Arg | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 17/26 | 2315/4486 | 2082/3183 | 694/1060 | chr1 | 177940655 | |||
chr1:177954305 | T | G | 12 | a0001c0006 a0001c0013 a0001c0048 others(9): Show |
45 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(42): Show |
synonymous_variant | LOW | c.1437A>C | p.Pro479Pro | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/26 | 1670/4486 | 1437/3183 | 479/1060 | chr1 | 177954305 | |||
chr1:177960386 | G | A | 6 | a0009c0015 a0009c0030 a0009c0069 others(3): Show |
12 | HG00423.hp2 HG00609.hp1 HG00738.hp2 others(9): Show |
synonymous_variant | LOW | c.954C>T | p.Ser318Ser | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 8/26 | 1187/4486 | 954/3183 | 318/1060 | chr1 | 177960386 | |||
chr1:177960805 | G | A | 21 | a0001c0004 a0001c0007 a0001c0021 others(18): Show |
98 | HG00438.hp2 HG00621.hp2 HG00639.hp1 others(95): Show |
synonymous_variant | LOW | c.922C>T | p.Leu308Leu | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 7/26 | 1155/4486 | 922/3183 | 308/1060 | chr1 | 177960805 | |||
chr1:177961729 | T | A | 2 | a0001c0021 a0001c0036 |
5 | HG02818.hp2 HG02976.hp2 HG03209.hp2 others(2): Show |
synonymous_variant | LOW | c.648A>T | p.Ser216Ser | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 6/26 | 881/4486 | 648/3183 | 216/1060 | chr1 | 177961729 | |||
chr1:177961732 | T | C | 1 | a0003c0055 | 1 | NA20805.hp2 | splice_region_variant&synonymous_variant | LOW | c.645A>G | p.Pro215Pro | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 6/26 | 878/4486 | 645/3183 | 215/1060 | chr1 | 177961732 | |||
chr1:177965915 | T | A | 18 | a0001c0005 a0001c0013 a0001c0061 others(15): Show |
105 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(102): Show |
synonymous_variant | LOW | c.390A>T | p.Pro130Pro | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/26 | 623/4486 | 390/3183 | 130/1060 | chr1 | 177965915 | |||
chr1:177967874 | G | A | 8 | a0001c0036 a0004c0067 a0009c0015 others(5): Show |
14 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(11): Show |
synonymous_variant | LOW | c.108C>T | p.Val36Val | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/26 | 341/4486 | 108/3183 | 36/1060 | chr1 | 177967874 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:177928824 | T | C | 63 | a0001c0004t0004 a0001c0005t0002 a0001c0005t0004 others(60): Show |
281 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(278): Show |
3_prime_UTR_variant | MODIFIER | c.*1034A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 26/26 | 1034 | chr1 | 177928824 | ||||||
chr1:177928840 | C | T | 34 | a0001c0004t0004 a0001c0005t0004 a0001c0005t0017 others(31): Show |
163 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*1018G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 26/26 | 1018 | chr1 | 177928840 | ||||||
chr1:177928847 | G | A | 2 | a0001c0006t0018 a0002c0001t0014 |
2 | HG01255.hp2 HG01433.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1011C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 26/26 | 1011 | chr1 | 177928847 | ||||||
chr1:177928980 | C | T | 1 | a0037c0056t0016 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*878G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 26/26 | 878 | chr1 | 177928980 | ||||||
chr1:177928981 | G | A | 1 | a0003c0003t0015 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*877C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 26/26 | 877 | chr1 | 177928981 | ||||||
chr1:177929217 | A | G | 2 | a0004c0002t0009 a0004c0010t0009 |
2 | NA18969.hp1 NA19077.hp2 |
3_prime_UTR_variant | MODIFIER | c.*641T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 26/26 | 641 | chr1 | 177929217 | ||||||
chr1:177929409 | T | C | 1 | a0016c0024t0010 | 2 | HG01884.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*449A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 26/26 | 449 | chr1 | 177929409 | ||||||
chr1:177929421 | A | T | 1 | a0016c0024t0010 | 2 | HG01884.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*437T>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 26/26 | 437 | chr1 | 177929421 | ||||||
chr1:177929444 | G | C | 12 | a0001c0004t0004 a0001c0005t0004 a0004c0002t0004 others(9): Show |
78 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*414C>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 26/26 | 414 | chr1 | 177929444 | ||||||
chr1:177929526 | C | T | 6 | a0005c0016t0005 a0005c0054t0005 a0011c0025t0005 others(3): Show |
8 | HG01099.hp1 HG02109.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*332G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 26/26 | 332 | chr1 | 177929526 | ||||||
chr1:177929556 | C | T | 1 | a0003c0003t0013 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*302G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 26/26 | 302 | chr1 | 177929556 | ||||||
chr1:177929579 | C | T | 1 | a0001c0052t0012 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*279G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 26/26 | 279 | chr1 | 177929579 | ||||||
chr1:177929664 | C | T | 51 | a0001c0004t0004 a0001c0005t0002 a0001c0005t0004 others(48): Show |
266 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(263): Show |
3_prime_UTR_variant | MODIFIER | c.*194G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 26/26 | 194 | chr1 | 177929664 | ||||||
chr1:177929710 | C | A | 3 | a0004c0002t0008 a0004c0010t0008 a0004c0067t0008 |
4 | HG00558.hp2 NA18971.hp2 NA18986.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*148G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 26/26 | 148 | chr1 | 177929710 | ||||||
chr1:177929741 | C | T | 1 | a0008c0012t0011 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*117G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 26/26 | 117 | chr1 | 177929741 | ||||||
chr1:177969922 | C | T | 3 | a0001c0007t0006 a0004c0027t0006 a0012c0019t0006 |
7 | HG01069.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-97G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/26 | 1941 | chr1 | 177969922 | ||||||
chr1:177969926 | G | A | 1 | a0004c0027t0019 | 1 | HG02145.hp2 | 5_prime_UTR_variant | MODIFIER | c.-101C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/26 | 1945 | chr1 | 177969926 | ||||||
chr1:177970032 | T | A | 1 | a0002c0001t0020 | 1 | HG01981.hp1 | 5_prime_UTR_variant | MODIFIER | c.-207A>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/26 | 2051 | chr1 | 177970032 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:177929970 | A | G | 1 | a0006c0009t0004g0139 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.3112-41T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 25/25 | chr1 | 177929970 | |||||||
chr1:177929986 | G | C | 65 | a0003c0003t0003g0003 a0003c0003t0003g0016 a0003c0003t0003g0021 others(62): Show |
81 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.3112-57C>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 25/25 | chr1 | 177929986 | |||||||
chr1:177930147 | G | T | 2 | a0002c0001t0002g0044 a0002c0001t0002g0216 |
3 | HG01257.hp1 HG01258.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.3112-218C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 25/25 | chr1 | 177930147 | |||||||
chr1:177930180 | A | G | 1 | a0003c0003t0003g0222 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.3112-251T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 25/25 | chr1 | 177930180 | |||||||
chr1:177930328 | A | G | 1 | a0003c0003t0003g0091 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3111+217T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 25/25 | chr1 | 177930328 | |||||||
chr1:177930427 | C | T | 199 | a0001c0004t0004g0009 a0001c0004t0004g0034 a0001c0004t0004g0103 others(196): Show |
276 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.3111+118G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 25/25 | chr1 | 177930427 | |||||||
chr1:177930703 | G | A | 1 | a0024c0043t0003g0145 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3013-60C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177930703 | |||||||
chr1:177930712 | A | G | 1 | a0001c0004t0001g0092 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3013-69T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177930712 | |||||||
chr1:177930722 | T | C | 1 | a0004c0002t0004g0161 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.3013-79A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177930722 | |||||||
chr1:177930963 | T | C | 116 | a0001c0004t0004g0009 a0001c0004t0004g0034 a0001c0004t0004g0103 others(113): Show |
162 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.3013-320A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177930963 | |||||||
chr1:177931006 | A | G | 1 | a0001c0006t0001g0169 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3013-363T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177931006 | |||||||
chr1:177931160 | C | T | 7 | a0005c0016t0005g0133 a0005c0054t0005g0119 a0011c0025t0005g0177 others(4): Show |
7 | HG01099.hp1 HG01884.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.3013-517G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177931160 | |||||||
chr1:177931211 | G | A | 6 | a0001c0017t0001g0064 a0001c0021t0001g0258 a0001c0021t0001g0259 others(3): Show |
6 | HG02258.hp2 HG02486.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.3013-568C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177931211 | |||||||
chr1:177931255 | A | G | 1 | a0002c0001t0002g0070 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3013-612T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177931255 | |||||||
chr1:177931396 | A | G | 7 | a0005c0016t0005g0133 a0005c0054t0005g0119 a0011c0025t0005g0177 others(4): Show |
8 | HG01099.hp1 HG02109.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.3013-753T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177931396 | |||||||
chr1:177931405 | T | TAG | 5 | a0002c0001t0002g0083 a0002c0001t0002g0136 a0002c0001t0002g0247 others(2): Show |
5 | NA18944.hp2 NA18963.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.3013-764_3013-763d others(4): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177931405 | |||||||
chr1:177931445 | T | TA | 3 | a0001c0005t0004g0196 a0004c0010t0004g0015 a0004c0010t0004g0074 |
5 | NA18995.hp2 NA19002.hp1 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.3013-803dupT | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177931445 | |||||||
chr1:177931481 | C | T | 199 | a0001c0004t0004g0009 a0001c0004t0004g0034 a0001c0004t0004g0103 others(196): Show |
276 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.3013-838G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177931481 | |||||||
chr1:177931525 | C | T | 7 | a0005c0016t0005g0133 a0005c0054t0005g0119 a0011c0025t0005g0177 others(4): Show |
8 | HG01099.hp1 HG02109.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.3013-882G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177931525 | |||||||
chr1:177931532 | A | G | 1 | a0001c0021t0001g0306 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3013-889T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177931532 | |||||||
chr1:177931858 | C | T | 1 | a0001c0004t0001g0239 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.3012+632G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177931858 | |||||||
chr1:177931885 | C | T | 2 | a0003c0008t0003g0088 a0028c0037t0003g0224 |
2 | HG02145.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3012+605G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177931885 | |||||||
chr1:177931964 | A | G | 1 | a0018c0068t0002g0089 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3012+526T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177931964 | |||||||
chr1:177931985 | G | GA | 9 | a0001c0006t0007g0236 a0005c0016t0005g0133 a0005c0054t0005g0119 others(6): Show |
10 | HG01074.hp1 HG01099.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.3012+504dupT | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177931985 | |||||||
chr1:177932161 | A | G | 4 | a0001c0005t0001g0190 a0001c0005t0001g0273 a0001c0006t0001g0056 others(1): Show |
4 | HG01192.hp1 HG03942.hp1 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.3012+329T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177932161 | |||||||
chr1:177932179 | C | T | 1 | a0004c0002t0004g0158 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.3012+311G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177932179 | |||||||
chr1:177932343 | CT | C | 2 | a0019c0028t0005g0029 a0031c0042t0005g0093 |
3 | HG02818.hp1 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3012+146delA | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177932343 | |||||||
chr1:177932428 | T | A | 5 | a0005c0016t0005g0133 a0005c0054t0005g0119 a0011c0025t0005g0177 others(2): Show |
5 | HG01099.hp1 HG02109.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.3012+62A>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177932428 | |||||||
chr1:177932438 | A | G | 1 | a0001c0013t0001g0131 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3012+52T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177932438 | |||||||
chr1:177932484 | G | A | 64 | a0002c0001t0002g0002 a0002c0001t0002g0005 a0002c0001t0002g0007 others(61): Show |
92 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(89): Show |
splice_region_variant&intron_variant | LOW | c.3012+6C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177932484 | |||||||
chr1:177932578 | T | C | 137 | a0002c0001t0002g0002 a0002c0001t0002g0005 a0002c0001t0002g0007 others(134): Show |
182 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.2933-9A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 23/25 | chr1 | 177932578 | |||||||
chr1:177932606 | A | G | 177 | a0001c0004t0004g0009 a0001c0004t0004g0034 a0001c0004t0004g0103 others(174): Show |
251 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.2933-37T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 23/25 | chr1 | 177932606 | |||||||
chr1:177932642 | C | T | 3 | a0001c0005t0004g0196 a0004c0010t0004g0015 a0004c0010t0004g0074 |
5 | NA18995.hp2 NA19002.hp1 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.2932+56G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 23/25 | chr1 | 177932642 | |||||||
chr1:177932692 | C | T | 1 | a0001c0063t0001g0127 | 1 | HG02055.hp2 | splice_region_variant&intron_variant | LOW | c.2932+6G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 23/25 | chr1 | 177932692 | |||||||
chr1:177933003 | A | G | 3 | a0001c0021t0001g0306 a0001c0036t0001g0116 a0001c0036t0001g0117 |
3 | HG02976.hp2 HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2824-197T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 22/25 | chr1 | 177933003 | |||||||
chr1:177933114 | G | A | 1 | a0026c0038t0001g0237 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2823+100C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 22/25 | chr1 | 177933114 | |||||||
chr1:177933347 | G | A | 75 | a0002c0001t0002g0002 a0002c0001t0002g0005 a0002c0001t0002g0007 others(72): Show |
104 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.2725-35C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 21/25 | chr1 | 177933347 | |||||||
chr1:177933875 | C | T | 1 | a0003c0008t0003g0230 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2572-239G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177933875 | |||||||
chr1:177933969 | A | C | 69 | a0001c0017t0001g0064 a0002c0001t0002g0002 a0002c0001t0002g0005 others(66): Show |
98 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.2572-333T>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177933969 | |||||||
chr1:177933987 | G | GC | 5 | a0002c0001t0002g0212 a0002c0001t0002g0248 a0002c0001t0002g0254 others(2): Show |
6 | HG02071.hp2 HG02818.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2572-352dupG | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177933987 | |||||||
chr1:177933989 | T | C | 69 | a0001c0017t0001g0064 a0002c0001t0002g0002 a0002c0001t0002g0005 others(66): Show |
98 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.2572-353A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177933989 | |||||||
chr1:177933995 | C | CA | 9 | a0001c0005t0002g0108 a0001c0005t0002g0272 a0001c0021t0001g0306 others(6): Show |
9 | HG00597.hp1 HG02055.hp2 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2572-360dupT | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177933995 | |||||||
chr1:177933996 | A | C | 206 | a0001c0004t0001g0012 a0001c0004t0001g0072 a0001c0004t0001g0092 others(203): Show |
268 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.2572-360T>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177933996 | |||||||
chr1:177933997 | A | C | 3 | a0001c0006t0001g0071 a0001c0007t0001g0112 a0005c0011t0002g0063 |
3 | HG01175.hp2 HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2572-361T>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177933997 | |||||||
chr1:177934135 | CT | C | 64 | a0001c0006t0001g0285 a0001c0017t0001g0064 a0002c0001t0002g0002 others(61): Show |
89 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.2572-500delA | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177934135 | |||||||
chr1:177934146 | T | A | 219 | a0001c0004t0001g0012 a0001c0004t0001g0072 a0001c0004t0001g0092 others(216): Show |
289 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.2572-510A>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177934146 | |||||||
chr1:177934147 | T | C | 1 | a0001c0006t0001g0167 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2572-511A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177934147 | |||||||
chr1:177934234 | C | T | 1 | a0004c0027t0019g0307 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2572-598G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177934234 | |||||||
chr1:177934239 | A | T | 2 | a0001c0036t0001g0116 a0001c0036t0001g0117 |
2 | HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2572-603T>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177934239 | |||||||
chr1:177934443 | T | C | 28 | a0001c0004t0004g0009 a0001c0004t0004g0034 a0001c0004t0004g0103 others(25): Show |
37 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.2572-807A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177934443 | |||||||
chr1:177934624 | A | G | 3 | a0001c0005t0001g0042 a0001c0005t0001g0187 a0009c0069t0001g0201 |
4 | HG00609.hp1 HG02135.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.2572-988T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177934624 | |||||||
chr1:177934661 | C | T | 32 | a0001c0004t0001g0012 a0001c0004t0001g0072 a0001c0004t0001g0092 others(29): Show |
40 | HG00609.hp1 HG00621.hp2 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.2572-1025G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177934661 | |||||||
chr1:177934707 | T | G | 1 | a0001c0006t0001g0115 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2572-1071A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177934707 | |||||||
chr1:177934708 | G | C | 1 | a0001c0052t0012g0055 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2572-1072C>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177934708 | |||||||
chr1:177934976 | C | T | 3 | a0011c0025t0005g0177 a0011c0025t0005g0234 a0011c0050t0005g0062 |
3 | HG01099.hp1 HG02109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.2571+1322G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177934976 | |||||||
chr1:177935105 | G | T | 34 | a0001c0004t0001g0260 a0001c0005t0001g0031 a0001c0005t0001g0104 others(31): Show |
40 | HG00280.hp1 HG00639.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.2571+1193C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177935105 | |||||||
chr1:177935194 | G | A | 3 | a0001c0063t0001g0127 a0005c0016t0005g0133 a0005c0054t0005g0119 |
3 | HG02055.hp2 HG02723.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2571+1104C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177935194 | |||||||
chr1:177935267 | ATGCCTCC others(8): Show |
A | 6 | a0012c0019t0001g0073 a0012c0019t0001g0228 a0012c0019t0006g0051 others(3): Show |
7 | HG01243.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2571+1016_2571+103 others(19): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177935267 | |||||||
chr1:177935293 | T | C | 166 | a0001c0004t0001g0012 a0001c0004t0001g0072 a0001c0004t0001g0092 others(163): Show |
220 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.2571+1005A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177935293 | |||||||
chr1:177935326 | A | G | 285 | a0001c0004t0001g0012 a0001c0004t0001g0072 a0001c0004t0001g0092 others(282): Show |
380 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(377): Show |
intron_variant | MODIFIER | c.2571+972T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177935326 | |||||||
chr1:177935360 | T | C | 88 | a0001c0004t0004g0009 a0001c0004t0004g0034 a0001c0004t0004g0103 others(85): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.2571+938A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177935360 | |||||||
chr1:177935545 | G | T | 34 | a0004c0002t0001g0207 a0004c0002t0004g0001 a0004c0002t0004g0004 others(31): Show |
53 | HG00408.hp2 HG00621.hp1 HG01361.hp1 others(50): Show |
intron_variant | MODIFIER | c.2571+753C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177935545 | |||||||
chr1:177935560 | A | G | 1 | a0001c0006t0018g0180 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2571+738T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177935560 | |||||||
chr1:177935616 | T | C | 133 | a0001c0004t0001g0260 a0001c0004t0004g0009 a0001c0004t0004g0034 others(130): Show |
176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.2571+682A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177935616 | |||||||
chr1:177935662 | GA | G | 90 | a0001c0004t0001g0012 a0001c0004t0001g0072 a0001c0004t0001g0092 others(87): Show |
109 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.2571+635delT | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177935662 | |||||||
chr1:177935781 | T | C | 25 | a0001c0004t0001g0260 a0001c0005t0001g0031 a0001c0005t0001g0104 others(22): Show |
31 | HG00280.hp1 HG00639.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.2571+517A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177935781 | |||||||
chr1:177935794 | T | G | 9 | a0003c0008t0003g0033 a0003c0008t0003g0045 a0003c0008t0003g0061 others(6): Show |
15 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.2571+504A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177935794 | |||||||
chr1:177935817 | G | A | 39 | a0004c0002t0001g0123 a0004c0002t0001g0207 a0004c0002t0004g0001 others(36): Show |
60 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.2571+481C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177935817 | |||||||
chr1:177935836 | T | C | 38 | a0004c0002t0001g0123 a0004c0002t0001g0207 a0004c0002t0004g0001 others(35): Show |
58 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.2571+462A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177935836 | |||||||
chr1:177935998 | C | T | 1 | a0037c0056t0016g0111 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2571+300G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177935998 | |||||||
chr1:177936039 | T | C | 134 | a0001c0004t0001g0260 a0001c0004t0004g0009 a0001c0004t0004g0034 others(131): Show |
177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.2571+259A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177936039 | |||||||
chr1:177936055 | G | A | 3 | a0001c0006t0007g0236 a0005c0016t0002g0229 a0025c0051t0007g0059 |
3 | HG01074.hp1 HG01109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2571+243C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177936055 | |||||||
chr1:177936131 | C | T | 3 | a0001c0006t0001g0098 a0022c0023t0001g0283 a0022c0023t0001g0284 |
3 | NA18946.hp2 NA19067.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.2571+167G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177936131 | |||||||
chr1:177936135 | C | T | 9 | a0004c0010t0002g0278 a0009c0015t0002g0022 a0009c0015t0002g0202 others(6): Show |
11 | HG00423.hp2 HG00609.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.2571+163G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177936135 | |||||||
chr1:177936588 | C | T | 1 | a0002c0001t0002g0143 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2504-223G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 19/25 | chr1 | 177936588 | |||||||
chr1:177936752 | C | T | 2 | a0019c0028t0005g0029 a0031c0042t0005g0093 |
3 | HG02818.hp1 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2504-387G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 19/25 | chr1 | 177936752 | |||||||
chr1:177936867 | G | A | 1 | a0014c0032t0003g0266 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2503+347C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 19/25 | chr1 | 177936867 | |||||||
chr1:177936919 | T | G | 207 | a0001c0004t0001g0260 a0001c0004t0004g0009 a0001c0004t0004g0034 others(204): Show |
272 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.2503+295A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 19/25 | chr1 | 177936919 | |||||||
chr1:177936930 | A | C | 2 | a0012c0019t0001g0073 a0030c0040t0001g0096 |
2 | HG01243.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2503+284T>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 19/25 | chr1 | 177936930 | |||||||
chr1:177937157 | C | T | 66 | a0002c0001t0002g0002 a0002c0001t0002g0005 a0002c0001t0002g0007 others(63): Show |
94 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.2503+57G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 19/25 | chr1 | 177937157 | |||||||
chr1:177937201 | G | A | 1 | a0001c0052t0012g0055 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2503+13C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 19/25 | chr1 | 177937201 | |||||||
chr1:177937522 | G | A | 72 | a0001c0004t0001g0012 a0001c0004t0001g0072 a0001c0004t0001g0092 others(69): Show |
86 | HG00280.hp1 HG00609.hp1 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.2204-9C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177937522 | |||||||
chr1:177937624 | A | G | 1 | a0001c0006t0001g0227 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2204-111T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177937624 | |||||||
chr1:177937654 | T | C | 1 | a0003c0003t0003g0080 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2204-141A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177937654 | |||||||
chr1:177937706 | T | G | 12 | a0004c0002t0008g0038 a0004c0010t0002g0278 a0004c0067t0008g0200 others(9): Show |
15 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.2204-193A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177937706 | |||||||
chr1:177937998 | A | T | 1 | a0002c0001t0002g0137 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2204-485T>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177937998 | |||||||
chr1:177938118 | A | G | 3 | a0001c0017t0001g0064 a0016c0024t0010g0057 a0016c0024t0010g0065 |
3 | HG01884.hp1 HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2204-605T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177938118 | |||||||
chr1:177938298 | G | A | 6 | a0001c0006t0007g0236 a0004c0027t0006g0053 a0005c0016t0002g0229 others(3): Show |
7 | HG01074.hp1 HG01109.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2204-785C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177938298 | |||||||
chr1:177938301 | AAGATCTT others(9): Show |
A | 92 | a0001c0004t0001g0012 a0001c0004t0001g0072 a0001c0004t0001g0092 others(89): Show |
123 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.2204-804_2204-789d others(18): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177938301 | |||||||
chr1:177938328 | T | C | 3 | a0001c0006t0007g0236 a0005c0016t0002g0229 a0025c0051t0007g0059 |
3 | HG01074.hp1 HG01109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2204-815A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177938328 | |||||||
chr1:177938328 | T | G | 1 | a0001c0006t0001g0181 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2204-815A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177938328 | |||||||
chr1:177938376 | A | G | 92 | a0001c0004t0001g0012 a0001c0004t0001g0072 a0001c0004t0001g0092 others(89): Show |
123 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.2204-863T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177938376 | |||||||
chr1:177938769 | A | G | 1 | a0003c0003t0003g0191 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2203+933T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177938769 | |||||||
chr1:177938838 | G | A | 55 | a0001c0006t0007g0236 a0004c0002t0001g0123 a0004c0002t0001g0207 others(52): Show |
78 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.2203+864C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177938838 | |||||||
chr1:177938893 | G | A | 1 | a0004c0002t0004g0155 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2203+809C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177938893 | |||||||
chr1:177938963 | G | A | 1 | a0001c0007t0001g0048 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2203+739C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177938963 | |||||||
chr1:177938966 | A | T | 1 | a0002c0001t0002g0143 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2203+736T>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177938966 | |||||||
chr1:177939012 | C | T | 9 | a0004c0010t0002g0278 a0009c0015t0002g0022 a0009c0015t0002g0202 others(6): Show |
11 | HG00423.hp2 HG00609.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.2203+690G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177939012 | |||||||
chr1:177939186 | A | G | 55 | a0001c0006t0007g0236 a0004c0002t0001g0123 a0004c0002t0001g0207 others(52): Show |
78 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.2203+516T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177939186 | |||||||
chr1:177939187 | C | G | 295 | a0001c0004t0001g0012 a0001c0004t0001g0072 a0001c0004t0001g0092 others(292): Show |
391 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(388): Show |
intron_variant | MODIFIER | c.2203+515G>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177939187 | |||||||
chr1:177939234 | C | T | 5 | a0001c0006t0007g0236 a0005c0016t0002g0229 a0019c0028t0005g0029 others(2): Show |
6 | HG01074.hp1 HG01109.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2203+468G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177939234 | |||||||
chr1:177939347 | T | C | 38 | a0004c0002t0001g0123 a0004c0002t0001g0207 a0004c0002t0004g0001 others(35): Show |
58 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.2203+355A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177939347 | |||||||
chr1:177939426 | T | C | 1 | a0001c0006t0001g0170 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2203+276A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177939426 | |||||||
chr1:177939619 | A | G | 1 | a0001c0007t0006g0052 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2203+83T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177939619 | |||||||
chr1:177939645 | G | A | 2 | a0004c0027t0019g0307 a0018c0068t0002g0089 |
2 | HG02145.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2203+57C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177939645 | |||||||
chr1:177939672 | T | C | 6 | a0001c0006t0007g0236 a0004c0027t0006g0053 a0005c0016t0002g0229 others(3): Show |
7 | HG01074.hp1 HG01109.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2203+30A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177939672 | |||||||
chr1:177939835 | G | A | 1 | a0003c0003t0003g0271 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2128-58C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 17/25 | chr1 | 177939835 | |||||||
chr1:177939914 | A | G | 2 | a0001c0036t0001g0116 a0001c0036t0001g0117 |
2 | HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2128-137T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 17/25 | chr1 | 177939914 | |||||||
chr1:177939931 | C | T | 3 | a0001c0017t0001g0064 a0016c0024t0010g0057 a0016c0024t0010g0065 |
3 | HG01884.hp1 HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2128-154G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 17/25 | chr1 | 177939931 | |||||||
chr1:177939991 | C | T | 9 | a0004c0010t0002g0278 a0009c0015t0002g0022 a0009c0015t0002g0202 others(6): Show |
11 | HG00423.hp2 HG00609.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.2128-214G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 17/25 | chr1 | 177939991 | |||||||
chr1:177940059 | A | G | 3 | a0001c0021t0001g0306 a0001c0036t0001g0116 a0001c0036t0001g0117 |
3 | HG02976.hp2 HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2128-282T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 17/25 | chr1 | 177940059 | |||||||
chr1:177940214 | G | A | 4 | a0001c0063t0001g0127 a0005c0016t0005g0133 a0005c0054t0005g0119 others(1): Show |
4 | HG02055.hp2 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2127+396C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 17/25 | chr1 | 177940214 | |||||||
chr1:177940400 | C | T | 1 | a0001c0007t0001g0185 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2127+210G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 17/25 | chr1 | 177940400 | |||||||
chr1:177940451 | G | A | 1 | a0005c0011t0002g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2127+159C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 17/25 | chr1 | 177940451 | |||||||
chr1:177940504 | G | A | 1 | a0002c0001t0002g0295 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2127+106C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 17/25 | chr1 | 177940504 | |||||||
chr1:177940512 | G | T | 1 | a0024c0043t0003g0145 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2127+98C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 17/25 | chr1 | 177940512 | |||||||
chr1:177940524 | T | G | 9 | a0004c0010t0002g0278 a0009c0015t0002g0022 a0009c0015t0002g0202 others(6): Show |
11 | HG00423.hp2 HG00609.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.2127+86A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 17/25 | chr1 | 177940524 | |||||||
chr1:177940543 | T | C | 9 | a0004c0010t0002g0278 a0009c0015t0002g0022 a0009c0015t0002g0202 others(6): Show |
11 | HG00423.hp2 HG00609.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.2127+67A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 17/25 | chr1 | 177940543 | |||||||
chr1:177940585 | A | G | 1 | a0026c0038t0001g0237 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2127+25T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 17/25 | chr1 | 177940585 | |||||||
chr1:177940586 | C | T | 1 | a0001c0006t0007g0236 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2127+24G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 17/25 | chr1 | 177940586 | |||||||
chr1:177940772 | G | C | 1 | a0007c0014t0002g0164 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2023-58C>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 16/25 | chr1 | 177940772 | |||||||
chr1:177941101 | G | A | 38 | a0001c0004t0001g0012 a0001c0004t0001g0072 a0001c0004t0001g0092 others(35): Show |
46 | HG00609.hp1 HG00621.hp2 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.2023-387C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 16/25 | chr1 | 177941101 | |||||||
chr1:177941601 | C | T | 1 | a0002c0001t0002g0008 | 4 | HG02258.hp1 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2022+299G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 16/25 | chr1 | 177941601 | |||||||
chr1:177941667 | A | G | 12 | a0004c0002t0008g0038 a0004c0010t0002g0278 a0004c0067t0008g0200 others(9): Show |
15 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.2022+233T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 16/25 | chr1 | 177941667 | |||||||
chr1:177941748 | T | C | 1 | a0001c0004t0001g0242 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2022+152A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 16/25 | chr1 | 177941748 | |||||||
chr1:177941761 | A | G | 47 | a0001c0004t0001g0012 a0001c0004t0001g0072 a0001c0004t0001g0092 others(44): Show |
56 | HG00609.hp1 HG00621.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.2022+139T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 16/25 | chr1 | 177941761 | |||||||
chr1:177941857 | A | T | 1 | a0001c0052t0012g0055 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2022+43T>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 16/25 | chr1 | 177941857 | |||||||
chr1:177942378 | G | A | 1 | a0002c0001t0002g0036 | 2 | HG00140.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1882-338C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177942378 | |||||||
chr1:177942604 | G | A | 1 | a0014c0032t0003g0129 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1882-564C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177942604 | |||||||
chr1:177942653 | G | A | 1 | a0002c0001t0002g0140 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1882-613C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177942653 | |||||||
chr1:177942787 | G | A | 4 | a0004c0002t0004g0019 a0004c0002t0004g0219 a0004c0002t0004g0256 others(1): Show |
6 | HG01361.hp2 HG01496.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.1882-747C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177942787 | |||||||
chr1:177942836 | G | A | 1 | a0004c0027t0006g0053 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1882-796C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177942836 | |||||||
chr1:177942846 | T | A | 1 | a0001c0021t0001g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1882-806A>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177942846 | |||||||
chr1:177943071 | C | T | 1 | a0004c0027t0006g0053 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1882-1031G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177943071 | |||||||
chr1:177943072 | G | A | 47 | a0004c0002t0001g0123 a0004c0002t0001g0207 a0004c0002t0004g0001 others(44): Show |
69 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.1882-1032C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177943072 | |||||||
chr1:177943112 | C | T | 1 | a0003c0003t0013g0198 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1882-1072G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177943112 | |||||||
chr1:177943113 | G | A | 9 | a0004c0010t0002g0278 a0009c0015t0002g0022 a0009c0015t0002g0202 others(6): Show |
11 | HG00423.hp2 HG00609.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.1882-1073C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177943113 | |||||||
chr1:177943129 | T | C | 3 | a0001c0021t0001g0306 a0001c0036t0001g0116 a0001c0036t0001g0117 |
3 | HG02976.hp2 HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1882-1089A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177943129 | |||||||
chr1:177943194 | A | G | 38 | a0004c0002t0001g0123 a0004c0002t0001g0207 a0004c0002t0004g0001 others(35): Show |
58 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1882-1154T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177943194 | |||||||
chr1:177943283 | A | T | 66 | a0001c0007t0007g0287 a0002c0001t0002g0002 a0002c0001t0002g0005 others(63): Show |
94 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.1882-1243T>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177943283 | |||||||
chr1:177943525 | G | A | 1 | a0002c0001t0002g0142 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1881+1036C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177943525 | |||||||
chr1:177943650 | T | G | 16 | a0001c0006t0007g0236 a0001c0063t0001g0127 a0004c0027t0006g0053 others(13): Show |
17 | HG01074.hp1 HG01099.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1881+911A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177943650 | |||||||
chr1:177943660 | A | G | 1 | a0003c0003t0003g0268 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1881+901T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177943660 | |||||||
chr1:177943680 | T | C | 3 | a0001c0021t0001g0306 a0001c0036t0001g0116 a0001c0036t0001g0117 |
3 | HG02976.hp2 HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1881+881A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177943680 | |||||||
chr1:177943687 | G | A | 35 | a0004c0002t0001g0123 a0004c0002t0001g0207 a0004c0002t0004g0001 others(32): Show |
54 | HG00408.hp2 HG00621.hp1 HG01361.hp1 others(51): Show |
intron_variant | MODIFIER | c.1881+874C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177943687 | |||||||
chr1:177943743 | C | T | 1 | a0004c0027t0006g0053 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1881+818G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177943743 | |||||||
chr1:177943797 | C | T | 41 | a0001c0004t0001g0260 a0001c0005t0001g0031 a0001c0005t0001g0104 others(38): Show |
50 | HG00280.hp1 HG00639.hp1 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.1881+764G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177943797 | |||||||
chr1:177944013 | A | G | 4 | a0003c0003t0003g0106 a0003c0003t0003g0114 a0003c0003t0003g0296 others(1): Show |
4 | HG02165.hp1 NA18970.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.1881+548T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177944013 | |||||||
chr1:177944055 | A | G | 40 | a0003c0018t0003g0217 a0004c0002t0001g0123 a0004c0002t0001g0207 others(37): Show |
60 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.1881+506T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177944055 | |||||||
chr1:177944218 | G | A | 1 | a0004c0002t0004g0160 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1881+343C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177944218 | |||||||
chr1:177944225 | C | G | 1 | a0003c0003t0003g0271 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1881+336G>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177944225 | |||||||
chr1:177944267 | C | G | 96 | a0001c0004t0001g0260 a0001c0005t0001g0031 a0001c0005t0001g0104 others(93): Show |
120 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1881+294G>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177944267 | |||||||
chr1:177944310 | G | A | 1 | a0003c0003t0003g0274 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1881+251C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177944310 | |||||||
chr1:177944384 | T | C | 71 | a0001c0005t0001g0273 a0001c0005t0002g0108 a0001c0005t0002g0272 others(68): Show |
90 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.1881+177A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177944384 | |||||||
chr1:177944440 | T | C | 4 | a0001c0006t0001g0168 a0001c0006t0001g0169 a0001c0006t0001g0175 others(1): Show |
4 | HG01123.hp2 HG03704.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.1881+121A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177944440 | |||||||
chr1:177944533 | G | A | 4 | a0003c0003t0003g0267 a0003c0003t0003g0275 a0003c0008t0003g0100 others(1): Show |
4 | NA18949.hp1 NA18971.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.1881+28C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177944533 | |||||||
chr1:177944726 | C | T | 1 | a0003c0008t0003g0300 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1776-60G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177944726 | |||||||
chr1:177944760 | A | G | 1 | a0003c0003t0003g0105 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1776-94T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177944760 | |||||||
chr1:177944797 | G | A | 1 | a0004c0002t0004g0171 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1776-131C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177944797 | |||||||
chr1:177944845 | T | C | 298 | a0001c0004t0001g0012 a0001c0004t0001g0060 a0001c0004t0001g0072 others(295): Show |
394 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(391): Show |
intron_variant | MODIFIER | c.1776-179A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177944845 | |||||||
chr1:177944917 | G | A | 2 | a0005c0016t0003g0058 a0005c0016t0003g0235 |
2 | HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1776-251C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177944917 | |||||||
chr1:177945051 | C | A | 1 | a0004c0002t0004g0282 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1776-385G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177945051 | |||||||
chr1:177945163 | C | G | 3 | a0002c0001t0002g0018 a0002c0001t0002g0120 a0002c0001t0002g0121 |
5 | HG00735.hp2 HG01074.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1776-497G>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177945163 | |||||||
chr1:177945219 | G | A | 1 | a0002c0001t0002g0206 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1776-553C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177945219 | |||||||
chr1:177945246 | C | G | 6 | a0012c0019t0001g0073 a0012c0019t0001g0228 a0012c0019t0006g0051 others(3): Show |
7 | HG01243.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1776-580G>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177945246 | |||||||
chr1:177945312 | T | G | 2 | a0005c0016t0003g0058 a0005c0016t0003g0235 |
2 | HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1776-646A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177945312 | |||||||
chr1:177945506 | G | T | 1 | a0020c0022t0003g0144 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1776-840C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177945506 | |||||||
chr1:177945590 | C | T | 21 | a0001c0004t0004g0009 a0001c0004t0004g0034 a0001c0004t0004g0103 others(18): Show |
30 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.1775+830G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177945590 | |||||||
chr1:177945593 | A | G | 197 | a0001c0004t0001g0060 a0001c0004t0001g0260 a0001c0004t0004g0009 others(194): Show |
254 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.1775+827T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177945593 | |||||||
chr1:177945598 | A | T | 2 | a0019c0028t0005g0029 a0031c0042t0005g0093 |
3 | HG02818.hp1 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1775+822T>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177945598 | |||||||
chr1:177945611 | C | T | 2 | a0019c0028t0005g0029 a0031c0042t0005g0093 |
3 | HG02818.hp1 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1775+809G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177945611 | |||||||
chr1:177945630 | C | T | 1 | a0001c0052t0012g0055 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1775+790G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177945630 | |||||||
chr1:177945636 | A | G | 1 | a0001c0013t0001g0197 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1775+784T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177945636 | |||||||
chr1:177945755 | G | A | 2 | a0012c0019t0001g0073 a0030c0040t0001g0096 |
2 | HG01243.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1775+665C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177945755 | |||||||
chr1:177945792 | G | A | 2 | a0001c0005t0001g0031 a0001c0005t0001g0104 |
3 | NA18952.hp2 NA18989.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1775+628C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177945792 | |||||||
chr1:177945868 | C | T | 4 | a0003c0008t0003g0033 a0003c0008t0003g0061 a0003c0008t0003g0230 others(1): Show |
5 | HG01891.hp2 HG02055.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1775+552G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177945868 | |||||||
chr1:177945885 | G | A | 62 | a0001c0004t0001g0102 a0001c0005t0001g0024 a0001c0007t0007g0287 others(59): Show |
89 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.1775+535C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177945885 | |||||||
chr1:177946017 | A | G | 2 | a0001c0036t0001g0116 a0001c0036t0001g0117 |
2 | HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1775+403T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177946017 | |||||||
chr1:177946038 | A | G | 6 | a0001c0063t0001g0127 a0005c0054t0005g0119 a0007c0014t0002g0176 others(3): Show |
6 | HG01099.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1775+382T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177946038 | |||||||
chr1:177946339 | A | C | 242 | a0001c0004t0001g0060 a0001c0004t0001g0102 a0001c0004t0001g0260 others(239): Show |
331 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.1775+81T>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177946339 | |||||||
chr1:177946363 | G | A | 17 | a0001c0004t0001g0012 a0001c0004t0001g0072 a0001c0004t0001g0092 others(14): Show |
20 | HG00621.hp2 HG01109.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.1775+57C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177946363 | |||||||
chr1:177946562 | C | T | 4 | a0007c0014t0002g0176 a0011c0025t0005g0177 a0011c0025t0005g0234 others(1): Show |
4 | HG01099.hp1 HG02109.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1664-31G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177946562 | |||||||
chr1:177946563 | G | A | 3 | a0002c0001t0002g0018 a0002c0001t0002g0120 a0002c0001t0002g0121 |
5 | HG00735.hp2 HG01074.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1664-32C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177946563 | |||||||
chr1:177946643 | A | G | 33 | a0001c0004t0001g0260 a0001c0005t0001g0031 a0001c0005t0001g0104 others(30): Show |
39 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1664-112T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177946643 | |||||||
chr1:177946648 | A | T | 4 | a0001c0006t0007g0236 a0005c0016t0002g0229 a0005c0016t0003g0058 others(1): Show |
4 | HG01074.hp1 HG01109.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1664-117T>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177946648 | |||||||
chr1:177946679 | C | T | 6 | a0003c0008t0003g0033 a0003c0008t0003g0045 a0003c0008t0003g0061 others(3): Show |
8 | HG01891.hp2 HG02055.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1664-148G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177946679 | |||||||
chr1:177946828 | C | T | 1 | a0001c0052t0012g0055 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1664-297G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177946828 | |||||||
chr1:177946842 | T | C | 1 | a0037c0056t0016g0111 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1664-311A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177946842 | |||||||
chr1:177946889 | T | G | 6 | a0001c0005t0001g0084 a0001c0005t0001g0193 a0001c0005t0001g0277 others(3): Show |
9 | HG00099.hp2 HG00323.hp2 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1664-358A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177946889 | |||||||
chr1:177947046 | A | G | 13 | a0001c0004t0001g0012 a0001c0004t0001g0072 a0001c0004t0001g0092 others(10): Show |
16 | HG00621.hp2 HG01109.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.1664-515T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177947046 | |||||||
chr1:177947248 | C | T | 6 | a0003c0008t0003g0030 a0003c0008t0003g0068 a0003c0008t0003g0081 others(3): Show |
7 | HG02145.hp1 HG02559.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1663+577G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177947248 | |||||||
chr1:177947388 | G | T | 2 | a0019c0028t0005g0029 a0031c0042t0005g0093 |
3 | HG02818.hp1 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1663+437C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177947388 | |||||||
chr1:177947389 | C | T | 2 | a0019c0028t0005g0029 a0031c0042t0005g0093 |
3 | HG02818.hp1 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1663+436G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177947389 | |||||||
chr1:177947692 | C | T | 27 | a0001c0004t0001g0260 a0001c0004t0004g0009 a0001c0004t0004g0034 others(24): Show |
40 | HG00438.hp2 HG00639.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.1663+133G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177947692 | |||||||
chr1:177947693 | G | C | 2 | a0004c0010t0004g0077 a0033c0059t0003g0078 |
2 | NA18953.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.1663+132C>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177947693 | |||||||
chr1:177947730 | G | A | 14 | a0001c0004t0004g0009 a0001c0004t0004g0034 a0001c0004t0004g0103 others(11): Show |
20 | HG00438.hp2 HG00639.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.1663+95C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177947730 | |||||||
chr1:177947736 | C | T | 90 | a0001c0004t0001g0012 a0001c0004t0001g0072 a0001c0004t0001g0092 others(87): Show |
125 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.1663+89G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177947736 | |||||||
chr1:177947737 | G | A | 15 | a0001c0004t0004g0009 a0001c0004t0004g0034 a0001c0004t0004g0103 others(12): Show |
21 | HG00438.hp2 HG00639.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.1663+88C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177947737 | |||||||
chr1:177947754 | A | G | 14 | a0001c0004t0004g0009 a0001c0004t0004g0034 a0001c0004t0004g0103 others(11): Show |
20 | HG00438.hp2 HG00639.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.1663+71T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177947754 | |||||||
chr1:177947755 | A | AAGGGACA others(18): Show |
228 | a0001c0004t0001g0012 a0001c0004t0001g0060 a0001c0004t0001g0072 others(225): Show |
297 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.1663+69_1663+70ins others(25): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177947755 | |||||||
chr1:177947755 | A | G | 14 | a0001c0004t0004g0009 a0001c0004t0004g0034 a0001c0004t0004g0103 others(11): Show |
20 | HG00438.hp2 HG00639.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.1663+70T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177947755 | |||||||
chr1:177947771 | A | AGGTGAGG others(19): Show |
1 | a0001c0006t0001g0168 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1663+53_1663+54ins others(26): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177947771 | |||||||
chr1:177948140 | C | T | 2 | a0004c0027t0019g0307 a0018c0068t0002g0089 |
2 | HG02145.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1546-198G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177948140 | |||||||
chr1:177948281 | C | T | 1 | a0001c0052t0012g0055 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1546-339G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177948281 | |||||||
chr1:177948321 | G | A | 6 | a0001c0006t0007g0236 a0005c0016t0002g0229 a0005c0016t0003g0058 others(3): Show |
7 | HG01074.hp1 HG01109.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1546-379C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177948321 | |||||||
chr1:177948344 | G | A | 72 | a0001c0004t0001g0102 a0001c0005t0001g0024 a0001c0007t0007g0287 others(69): Show |
104 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.1546-402C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177948344 | |||||||
chr1:177948364 | G | A | 11 | a0004c0010t0002g0278 a0007c0014t0002g0178 a0009c0015t0002g0022 others(8): Show |
13 | HG00423.hp2 HG00609.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.1546-422C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177948364 | |||||||
chr1:177948505 | C | G | 1 | a0001c0004t0001g0260 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1546-563G>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177948505 | |||||||
chr1:177948709 | C | T | 3 | a0001c0017t0001g0064 a0016c0024t0010g0057 a0016c0024t0010g0065 |
3 | HG01884.hp1 HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1546-767G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177948709 | |||||||
chr1:177948922 | T | TAC | 51 | a0001c0004t0001g0012 a0001c0004t0001g0072 a0001c0004t0001g0092 others(48): Show |
60 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.1546-982_1546-981d others(4): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177948922 | |||||||
chr1:177948922 | T | TACAC | 74 | a0001c0004t0001g0102 a0001c0004t0001g0243 a0001c0005t0001g0024 others(71): Show |
109 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.1546-984_1546-981d others(6): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177948922 | |||||||
chr1:177948922 | T | TACACAC | 7 | a0002c0001t0002g0005 a0002c0001t0002g0044 a0002c0001t0002g0143 others(4): Show |
12 | HG00544.hp2 HG01192.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1546-986_1546-981d others(8): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177948922 | |||||||
chr1:177948922 | TAC | T | 12 | a0001c0052t0012g0055 a0001c0063t0001g0127 a0003c0008t0003g0033 others(9): Show |
14 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1546-982_1546-981d others(4): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177948922 | |||||||
chr1:177948922 | TACACACA others(1): Show |
T | 28 | a0001c0005t0001g0031 a0001c0005t0001g0104 a0001c0005t0001g0190 others(25): Show |
34 | HG00140.hp1 HG00280.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.1546-988_1546-981d others(10): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177948922 | |||||||
chr1:177948922 | TACACACA others(3): Show |
T | 2 | a0001c0006t0001g0090 a0001c0006t0001g0227 |
2 | HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1546-990_1546-981d others(12): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177948922 | |||||||
chr1:177948992 | G | A | 1 | a0002c0001t0002g0070 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1546-1050C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177948992 | |||||||
chr1:177949030 | A | G | 249 | a0001c0004t0001g0012 a0001c0004t0001g0060 a0001c0004t0001g0072 others(246): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.1546-1088T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949030 | |||||||
chr1:177949233 | C | T | 1 | a0001c0007t0006g0026 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1546-1291G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949233 | |||||||
chr1:177949268 | C | A | 1 | a0020c0022t0003g0144 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1546-1326G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949268 | |||||||
chr1:177949291 | A | G | 1 | a0018c0045t0002g0218 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1546-1349T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949291 | |||||||
chr1:177949364 | G | A | 196 | a0001c0004t0001g0012 a0001c0004t0001g0060 a0001c0004t0001g0072 others(193): Show |
257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.1546-1422C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949364 | |||||||
chr1:177949383 | A | AAC | 35 | a0001c0004t0004g0009 a0001c0005t0001g0042 a0001c0005t0001g0277 others(32): Show |
40 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.1546-1443_1546-144 others(6): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949383 | |||||||
chr1:177949383 | A | AACAC | 19 | a0001c0006t0001g0227 a0003c0003t0003g0050 a0003c0003t0003g0109 others(16): Show |
23 | HG00558.hp2 HG01243.hp1 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.1546-1445_1546-144 others(8): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949383 | |||||||
chr1:177949383 | A | AACACAC | 5 | a0003c0008t0003g0226 a0005c0016t0005g0133 a0009c0015t0002g0022 others(2): Show |
5 | HG01346.hp1 HG02145.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1546-1447_1546-144 others(10): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949383 | |||||||
chr1:177949383 | A | AACACACA others(1): Show |
3 | a0003c0008t0003g0030 a0003c0008t0003g0033 a0003c0008t0003g0081 |
3 | HG01891.hp2 HG02630.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1546-1449_1546-144 others(12): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949383 | |||||||
chr1:177949383 | A | AACACACA others(7): Show |
1 | a0001c0052t0012g0055 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1546-1455_1546-144 others(18): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949383 | |||||||
chr1:177949383 | AAC | A | 23 | a0001c0004t0001g0060 a0001c0004t0001g0260 a0001c0005t0004g0196 others(20): Show |
26 | HG00639.hp1 HG01069.hp1 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.1546-1443_1546-144 others(6): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949383 | |||||||
chr1:177949383 | AACAC | A | 12 | a0001c0005t0001g0290 a0001c0005t0001g0292 a0001c0005t0001g0293 others(9): Show |
12 | HG00558.hp1 HG00733.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.1546-1445_1546-144 others(8): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949383 | |||||||
chr1:177949383 | AACACAC | A | 30 | a0001c0004t0001g0012 a0001c0004t0001g0242 a0001c0005t0001g0031 others(27): Show |
38 | HG00140.hp1 HG00280.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.1546-1447_1546-144 others(10): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949383 | |||||||
chr1:177949383 | AACACACA others(1): Show |
A | 7 | a0001c0004t0001g0134 a0001c0004t0004g0009 a0001c0006t0001g0166 others(4): Show |
7 | HG01109.hp2 HG02486.hp2 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.1546-1449_1546-144 others(12): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949383 | |||||||
chr1:177949383 | AACACACA others(3): Show |
A | 16 | a0001c0004t0001g0012 a0001c0004t0001g0072 a0001c0004t0001g0092 others(13): Show |
16 | HG00621.hp2 HG01123.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.1546-1451_1546-144 others(14): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949383 | |||||||
chr1:177949383 | AACACACA others(5): Show |
A | 3 | a0005c0016t0002g0229 a0025c0051t0007g0059 a0037c0056t0016g0111 |
3 | HG01074.hp1 HG01109.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1546-1453_1546-144 others(16): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949383 | |||||||
chr1:177949383 | AACACACA others(7): Show |
A | 14 | a0001c0004t0001g0012 a0001c0004t0001g0239 a0001c0004t0001g0241 others(11): Show |
16 | HG02129.hp1 HG02165.hp1 NA18948.hp2 others(13): Show |
intron_variant | MODIFIER | c.1546-1455_1546-144 others(18): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949383 | |||||||
chr1:177949383 | AACACACA others(9): Show |
A | 7 | a0002c0001t0002g0005 a0002c0001t0002g0120 a0002c0001t0002g0138 others(4): Show |
8 | HG00735.hp2 HG01993.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1546-1457_1546-144 others(20): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949383 | |||||||
chr1:177949383 | AACACACA others(11): Show |
A | 67 | a0001c0004t0001g0102 a0001c0005t0001g0024 a0001c0061t0001g0269 others(64): Show |
97 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.1546-1459_1546-144 others(22): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949383 | |||||||
chr1:177949383 | AACACACA others(13): Show |
A | 3 | a0001c0017t0001g0064 a0016c0024t0010g0057 a0016c0024t0010g0065 |
3 | HG01884.hp1 HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1546-1461_1546-144 others(24): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949383 | |||||||
chr1:177949417 | CACACACA others(6): Show |
C | 1 | a0003c0003t0003g0223 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1546-1488_1546-147 others(17): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949417 | |||||||
chr1:177949429 | C | A | 2 | a0003c0008t0003g0045 a0003c0008t0003g0300 |
3 | HG02280.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1546-1487G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949429 | |||||||
chr1:177949429 | C | CACACACA others(3): Show |
2 | a0003c0008t0003g0033 a0003c0008t0003g0061 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1546-1488_1546-148 others(14): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949429 | |||||||
chr1:177949431 | A | C | 2 | a0003c0003t0003g0222 a0003c0003t0003g0262 |
2 | NA19079.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1546-1489T>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949431 | |||||||
chr1:177949520 | A | G | 9 | a0001c0007t0001g0048 a0005c0011t0002g0013 a0005c0011t0002g0014 others(6): Show |
14 | HG01070.hp1 HG01071.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.1546-1578T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949520 | |||||||
chr1:177949524 | T | TAGAG | 32 | a0001c0005t0001g0031 a0001c0005t0001g0104 a0001c0005t0001g0190 others(29): Show |
38 | HG00140.hp1 HG00280.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.1546-1586_1546-158 others(8): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949524 | |||||||
chr1:177949554 | A | G | 3 | a0002c0001t0002g0148 a0002c0001t0002g0246 a0007c0014t0002g0087 |
3 | HG01168.hp2 HG03239.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1546-1612T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949554 | |||||||
chr1:177949632 | T | C | 1 | a0001c0004t0001g0244 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1546-1690A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949632 | |||||||
chr1:177949686 | A | G | 197 | a0001c0004t0001g0012 a0001c0004t0001g0060 a0001c0004t0001g0072 others(194): Show |
258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.1546-1744T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949686 | |||||||
chr1:177949709 | C | T | 1 | a0001c0006t0001g0167 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1546-1767G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949709 | |||||||
chr1:177949948 | C | CA | 51 | a0001c0004t0001g0012 a0001c0004t0001g0060 a0001c0004t0001g0072 others(48): Show |
63 | HG00621.hp2 HG01070.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1545+1965dupT | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949948 | |||||||
chr1:177949948 | C | CAA | 117 | a0001c0004t0001g0102 a0001c0004t0001g0260 a0001c0004t0004g0009 others(114): Show |
160 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.1545+1964_1545+196 others(6): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949948 | |||||||
chr1:177949948 | C | CAAA | 32 | a0001c0005t0001g0031 a0001c0005t0001g0104 a0001c0006t0001g0010 others(29): Show |
38 | HG00140.hp1 HG00280.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.1545+1963_1545+196 others(7): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949948 | |||||||
chr1:177949977 | G | A | 1 | a0001c0004t0001g0245 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1545+1937C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949977 | |||||||
chr1:177949978 | T | C | 1 | a0001c0004t0001g0060 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1545+1936A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949978 | |||||||
chr1:177950128 | T | C | 1 | a0004c0002t0004g0156 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1545+1786A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177950128 | |||||||
chr1:177950151 | T | TA | 4 | a0001c0005t0001g0187 a0004c0002t0001g0207 a0004c0002t0004g0004 others(1): Show |
8 | NA18942.hp1 NA18951.hp1 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.1545+1762dupT | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177950151 | |||||||
chr1:177950151 | TA | T | 181 | a0001c0004t0001g0060 a0001c0004t0001g0102 a0001c0004t0001g0260 others(178): Show |
238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.1545+1762delT | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177950151 | |||||||
chr1:177950151 | TAA | T | 25 | a0001c0004t0001g0012 a0001c0004t0001g0072 a0001c0004t0001g0092 others(22): Show |
29 | HG00609.hp2 HG00621.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1545+1761_1545+176 others(6): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177950151 | |||||||
chr1:177950163 | A | T | 1 | a0003c0003t0003g0080 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1545+1751T>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177950163 | |||||||
chr1:177950166 | A | G | 5 | a0001c0021t0001g0258 a0001c0021t0001g0259 a0001c0021t0001g0306 others(2): Show |
5 | HG02818.hp2 HG02976.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1545+1748T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177950166 | |||||||
chr1:177950271 | G | T | 2 | a0005c0016t0005g0133 a0026c0038t0001g0237 |
2 | HG01346.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1545+1643C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177950271 | |||||||
chr1:177950463 | T | C | 15 | a0001c0004t0001g0012 a0001c0004t0001g0072 a0001c0004t0001g0092 others(12): Show |
19 | HG00621.hp2 HG01109.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.1545+1451A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177950463 | |||||||
chr1:177950566 | A | G | 1 | a0005c0016t0003g0235 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1545+1348T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177950566 | |||||||
chr1:177950604 | C | T | 1 | a0004c0002t0004g0040 | 2 | HG00408.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1545+1310G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177950604 | |||||||
chr1:177950951 | G | GGGAAGGA others(81): Show |
1 | a0001c0004t0001g0060 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1545+962_1545+963i others(90): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177950951 | |||||||
chr1:177951131 | G | A | 2 | a0019c0028t0005g0029 a0031c0042t0005g0093 |
3 | HG02818.hp1 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1545+783C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177951131 | |||||||
chr1:177951155 | G | T | 2 | a0001c0063t0001g0127 a0005c0054t0005g0119 |
2 | HG02055.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1545+759C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177951155 | |||||||
chr1:177951256 | A | C | 13 | a0001c0004t0001g0239 a0004c0002t0004g0156 a0004c0010t0002g0278 others(10): Show |
15 | HG00423.hp2 HG00609.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.1545+658T>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177951256 | |||||||
chr1:177951351 | T | C | 3 | a0001c0017t0001g0064 a0016c0024t0010g0057 a0016c0024t0010g0065 |
3 | HG01884.hp1 HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1545+563A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177951351 | |||||||
chr1:177951570 | G | A | 1 | a0026c0038t0001g0237 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1545+344C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177951570 | |||||||
chr1:177951619 | G | A | 108 | a0001c0004t0001g0060 a0001c0004t0001g0102 a0001c0004t0001g0260 others(105): Show |
132 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.1545+295C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177951619 | |||||||
chr1:177951759 | G | A | 1 | a0001c0052t0012g0055 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1545+155C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177951759 | |||||||
chr1:177952018 | C | T | 1 | a0002c0001t0002g0210 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1464-23G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177952018 | |||||||
chr1:177952057 | C | T | 1 | a0003c0003t0003g0085 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1464-62G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177952057 | |||||||
chr1:177952187 | C | T | 1 | a0004c0002t0001g0123 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1464-192G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177952187 | |||||||
chr1:177952299 | T | A | 247 | a0001c0004t0001g0012 a0001c0004t0001g0060 a0001c0004t0001g0072 others(244): Show |
322 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.1464-304A>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177952299 | |||||||
chr1:177952400 | C | A | 2 | a0002c0001t0002g0008 a0030c0040t0001g0096 |
5 | HG02258.hp1 HG02630.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1464-405G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177952400 | |||||||
chr1:177952413 | C | T | 1 | a0005c0011t0002g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1464-418G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177952413 | |||||||
chr1:177952453 | C | A | 1 | a0005c0011t0002g0013 | 3 | HG02257.hp1 HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1464-458G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177952453 | |||||||
chr1:177952490 | C | T | 3 | a0005c0016t0002g0229 a0005c0016t0003g0058 a0025c0051t0007g0059 |
3 | HG01074.hp1 HG01109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1464-495G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177952490 | |||||||
chr1:177952624 | G | A | 1 | a0002c0001t0002g0150 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1464-629C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177952624 | |||||||
chr1:177952911 | T | A | 1 | a0026c0038t0001g0237 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1464-916A>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177952911 | |||||||
chr1:177952912 | C | T | 4 | a0001c0017t0001g0064 a0016c0024t0010g0057 a0016c0024t0010g0065 others(1): Show |
4 | HG01346.hp1 HG01884.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1464-917G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177952912 | |||||||
chr1:177953003 | A | AT | 32 | a0001c0004t0001g0102 a0001c0004t0001g0260 a0001c0004t0004g0009 others(29): Show |
41 | HG00408.hp1 HG00438.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.1464-1009dupA | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177953003 | |||||||
chr1:177953003 | A | ATT | 112 | a0001c0004t0001g0012 a0001c0004t0001g0072 a0001c0004t0001g0092 others(109): Show |
154 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.1464-1010_1464-100 others(6): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177953003 | |||||||
chr1:177953003 | A | ATTT | 7 | a0001c0052t0012g0055 a0003c0003t0003g0222 a0003c0003t0003g0223 others(4): Show |
8 | HG02717.hp1 HG02818.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1464-1011_1464-100 others(7): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177953003 | |||||||
chr1:177953003 | AT | A | 63 | a0001c0006t0001g0010 a0001c0006t0001g0011 a0001c0006t0001g0056 others(60): Show |
79 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.1464-1009delA | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177953003 | |||||||
chr1:177953108 | C | T | 2 | a0001c0006t0007g0236 a0005c0016t0003g0235 |
2 | HG02809.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1464-1113G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177953108 | |||||||
chr1:177953163 | A | G | 216 | a0001c0004t0001g0012 a0001c0004t0001g0072 a0001c0004t0001g0092 others(213): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.1463+1116T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177953163 | |||||||
chr1:177953220 | G | C | 1 | a0037c0056t0016g0111 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1463+1059C>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177953220 | |||||||
chr1:177953336 | C | A | 115 | a0001c0005t0001g0024 a0001c0005t0001g0031 a0001c0005t0001g0042 others(112): Show |
155 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.1463+943G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177953336 | |||||||
chr1:177953482 | A | G | 115 | a0001c0005t0001g0024 a0001c0005t0001g0031 a0001c0005t0001g0042 others(112): Show |
155 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.1463+797T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177953482 | |||||||
chr1:177953562 | A | C | 13 | a0004c0010t0002g0278 a0007c0014t0002g0178 a0007c0034t0002g0128 others(10): Show |
15 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.1463+717T>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177953562 | |||||||
chr1:177953669 | AT | A | 7 | a0001c0007t0001g0048 a0005c0011t0002g0013 a0005c0011t0002g0014 others(4): Show |
12 | HG01070.hp1 HG01071.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.1463+609delA | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177953669 | |||||||
chr1:177953718 | T | G | 3 | a0001c0006t0001g0170 a0001c0013t0001g0032 a0001c0013t0001g0035 |
5 | HG00280.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1463+561A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177953718 | |||||||
chr1:177953838 | G | A | 3 | a0005c0016t0002g0229 a0005c0016t0003g0058 a0025c0051t0007g0059 |
3 | HG01074.hp1 HG01109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1463+441C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177953838 | |||||||
chr1:177953985 | A | G | 1 | a0003c0018t0003g0217 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1463+294T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177953985 | |||||||
chr1:177954110 | G | A | 1 | a0004c0027t0006g0053 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1463+169C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177954110 | |||||||
chr1:177954189 | G | A | 13 | a0004c0010t0002g0278 a0007c0014t0002g0178 a0007c0034t0002g0128 others(10): Show |
15 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.1463+90C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177954189 | |||||||
chr1:177954396 | A | G | 1 | a0001c0007t0001g0099 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1366-20T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177954396 | |||||||
chr1:177954522 | G | A | 2 | a0001c0006t0001g0090 a0001c0006t0001g0227 |
2 | HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1366-146C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177954522 | |||||||
chr1:177954934 | A | G | 1 | a0026c0038t0001g0237 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1366-558T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177954934 | |||||||
chr1:177955011 | C | A | 35 | a0001c0006t0001g0010 a0001c0006t0001g0011 a0001c0006t0001g0056 others(32): Show |
43 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(40): Show |
intron_variant | MODIFIER | c.1366-635G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955011 | |||||||
chr1:177955137 | T | TAAAAAAT others(273): Show |
1 | a0026c0038t0001g0237 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1366-762_1366-761i others(282): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955137 | |||||||
chr1:177955137 | T | TAAAAAAT others(293): Show |
2 | a0001c0017t0001g0064 a0016c0024t0010g0065 |
2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1366-762_1366-761i others(302): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955137 | |||||||
chr1:177955137 | T | TAAAAAAT others(294): Show |
1 | a0016c0024t0010g0057 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1366-762_1366-761i others(303): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955137 | |||||||
chr1:177955146 | T | C | 1 | a0001c0005t0001g0290 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1366-770A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955146 | |||||||
chr1:177955219 | G | A | 51 | a0001c0006t0001g0010 a0001c0006t0001g0056 a0001c0006t0001g0071 others(48): Show |
58 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.1366-843C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955219 | |||||||
chr1:177955223 | C | A | 7 | a0001c0063t0001g0127 a0005c0016t0002g0229 a0005c0016t0003g0058 others(4): Show |
7 | HG01074.hp1 HG01109.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1366-847G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955223 | |||||||
chr1:177955223 | C | T | 1 | a0001c0006t0001g0165 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1366-847G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955223 | |||||||
chr1:177955339 | A | T | 1 | a0004c0027t0006g0053 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1366-963T>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955339 | |||||||
chr1:177955394 | T | C | 108 | a0001c0005t0001g0024 a0001c0005t0001g0031 a0001c0005t0001g0042 others(105): Show |
148 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.1366-1018A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955394 | |||||||
chr1:177955424 | TGCAACCT others(11): Show |
T | 1 | a0001c0004t0001g0072 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1066_1366-104 others(22): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955424 | |||||||
chr1:177955443 | G | A | 51 | a0001c0006t0001g0010 a0001c0006t0001g0056 a0001c0006t0001g0071 others(48): Show |
58 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.1366-1067C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955443 | |||||||
chr1:177955444 | T | G | 1 | a0001c0004t0001g0072 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1068A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955444 | |||||||
chr1:177955446 | T | G | 1 | a0001c0004t0001g0072 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1070A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955446 | |||||||
chr1:177955448 | A | G | 1 | a0001c0004t0001g0072 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1072T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955448 | |||||||
chr1:177955449 | G | C | 1 | a0001c0004t0001g0072 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1073C>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955449 | |||||||
chr1:177955454 | T | G | 1 | a0001c0004t0001g0072 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1078A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955454 | |||||||
chr1:177955455 | C | A | 1 | a0001c0004t0001g0072 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1079G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955455 | |||||||
chr1:177955463 | T | A | 1 | a0001c0004t0001g0072 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1087A>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955463 | |||||||
chr1:177955465 | A | T | 1 | a0001c0004t0001g0072 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1089T>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955465 | |||||||
chr1:177955468 | C | A | 1 | a0001c0004t0001g0072 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1092G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955468 | |||||||
chr1:177955469 | T | C | 1 | a0001c0004t0001g0072 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1093A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955469 | |||||||
chr1:177955470 | C | T | 1 | a0001c0004t0001g0072 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1094G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955470 | |||||||
chr1:177955478 | G | A | 3 | a0001c0017t0001g0064 a0016c0024t0010g0057 a0016c0024t0010g0065 |
3 | HG01884.hp1 HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1366-1102C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955478 | |||||||
chr1:177955478 | G | C | 1 | a0001c0004t0001g0072 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1102C>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955478 | |||||||
chr1:177955486 | T | A | 1 | a0001c0004t0001g0072 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1110A>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955486 | |||||||
chr1:177955492 | C | A | 1 | a0001c0004t0001g0072 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1116G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955492 | |||||||
chr1:177955497 | C | CTCTCCAA others(8): Show |
1 | a0001c0004t0001g0072 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1122_1366-112 others(19): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955497 | |||||||
chr1:177955500 | T | C | 1 | a0001c0004t0001g0072 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1124A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955500 | |||||||
chr1:177955504 | G | T | 1 | a0001c0004t0001g0072 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1128C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955504 | |||||||
chr1:177955506 | C | A | 1 | a0001c0004t0001g0072 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1130G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955506 | |||||||
chr1:177955508 | G | A | 1 | a0001c0004t0001g0072 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1132C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955508 | |||||||
chr1:177955517 | T | A | 1 | a0001c0004t0001g0072 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1141A>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955517 | |||||||
chr1:177955518 | T | A | 1 | a0001c0004t0001g0072 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1142A>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955518 | |||||||
chr1:177955519 | G | A | 1 | a0001c0004t0001g0072 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1143C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955519 | |||||||
chr1:177955521 | A | T | 1 | a0001c0004t0001g0072 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1145T>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955521 | |||||||
chr1:177955533 | G | T | 1 | a0001c0004t0001g0072 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1157C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955533 | |||||||
chr1:177955536 | G | T | 1 | a0001c0004t0001g0072 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1160C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955536 | |||||||
chr1:177955542 | T | G | 1 | a0001c0004t0001g0072 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1166A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955542 | |||||||
chr1:177955798 | C | A | 1 | a0037c0056t0016g0111 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1366-1422G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955798 | |||||||
chr1:177956033 | A | C | 1 | a0002c0001t0002g0046 | 2 | HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1366-1657T>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177956033 | |||||||
chr1:177956128 | T | A | 43 | a0001c0004t0001g0012 a0001c0004t0001g0072 a0001c0004t0001g0092 others(40): Show |
52 | HG00140.hp1 HG00280.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.1366-1752A>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177956128 | |||||||
chr1:177956166 | A | C | 3 | a0001c0017t0001g0064 a0016c0024t0010g0057 a0016c0024t0010g0065 |
3 | HG01884.hp1 HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1366-1790T>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177956166 | |||||||
chr1:177956225 | A | C | 1 | a0026c0038t0001g0237 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1366-1849T>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177956225 | |||||||
chr1:177956260 | C | A | 35 | a0001c0006t0001g0010 a0001c0006t0001g0056 a0001c0006t0001g0071 others(32): Show |
40 | HG00140.hp1 HG00280.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.1365+1872G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177956260 | |||||||
chr1:177956389 | T | A | 25 | a0001c0006t0001g0010 a0001c0006t0001g0056 a0001c0006t0001g0071 others(22): Show |
30 | HG00140.hp1 HG00280.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.1365+1743A>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177956389 | |||||||
chr1:177956542 | A | G | 16 | a0001c0004t0001g0012 a0001c0004t0001g0072 a0001c0004t0001g0092 others(13): Show |
20 | HG00621.hp2 HG01109.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.1365+1590T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177956542 | |||||||
chr1:177956593 | TTATC | T | 26 | a0001c0004t0001g0102 a0001c0004t0001g0260 a0001c0004t0004g0009 others(23): Show |
34 | HG00438.hp2 HG00639.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1365+1535_1365+153 others(8): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177956593 | |||||||
chr1:177956596 | T | C | 1 | a0026c0038t0001g0237 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1365+1536A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177956596 | |||||||
chr1:177957080 | A | G | 3 | a0001c0017t0001g0064 a0016c0024t0010g0057 a0016c0024t0010g0065 |
3 | HG01884.hp1 HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1365+1052T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177957080 | |||||||
chr1:177957117 | C | G | 1 | a0001c0004t0001g0241 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1365+1015G>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177957117 | |||||||
chr1:177957123 | A | G | 1 | a0006c0009t0004g0135 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1365+1009T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177957123 | |||||||
chr1:177957231 | T | A | 1 | a0005c0016t0005g0133 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1365+901A>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177957231 | |||||||
chr1:177957234 | A | G | 1 | a0037c0056t0016g0111 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1365+898T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177957234 | |||||||
chr1:177957322 | T | TTGTATAA others(328): Show |
1 | a0001c0036t0001g0116 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1365+809_1365+810i others(337): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177957322 | |||||||
chr1:177957376 | T | C | 1 | a0003c0003t0013g0198 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1365+756A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177957376 | |||||||
chr1:177957440 | C | G | 2 | a0004c0002t0004g0149 a0004c0002t0004g0282 |
2 | NA18612.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.1365+692G>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177957440 | |||||||
chr1:177957614 | T | C | 25 | a0001c0004t0001g0060 a0003c0008t0003g0030 a0003c0008t0003g0033 others(22): Show |
29 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.1365+518A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177957614 | |||||||
chr1:177957854 | T | C | 1 | a0002c0001t0002g0148 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1365+278A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177957854 | |||||||
chr1:177957934 | G | A | 1 | a0011c0025t0005g0234 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1365+198C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177957934 | |||||||
chr1:177958053 | A | G | 23 | a0001c0004t0001g0012 a0001c0004t0001g0072 a0001c0004t0001g0092 others(20): Show |
27 | HG00621.hp2 HG01109.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.1365+79T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177958053 | |||||||
chr1:177958519 | C | A | 68 | a0001c0004t0001g0060 a0001c0004t0001g0102 a0001c0004t0001g0260 others(65): Show |
87 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.1135-157G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 9/25 | chr1 | 177958519 | |||||||
chr1:177958593 | C | A | 2 | a0002c0001t0002g0281 a0002c0001t0002g0291 |
2 | NA18974.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.1135-231G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 9/25 | chr1 | 177958593 | |||||||
chr1:177958661 | C | G | 3 | a0001c0017t0001g0064 a0016c0024t0010g0057 a0016c0024t0010g0065 |
3 | HG01884.hp1 HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1134+179G>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 9/25 | chr1 | 177958661 | |||||||
chr1:177958723 | C | T | 2 | a0003c0003t0003g0262 a0003c0003t0003g0263 |
2 | NA19065.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1134+117G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 9/25 | chr1 | 177958723 | |||||||
chr1:177958778 | A | G | 1 | a0001c0005t0017g0130 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1134+62T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 9/25 | chr1 | 177958778 | |||||||
chr1:177959001 | A | T | 1 | a0012c0019t0001g0073 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.999-26T>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 8/25 | chr1 | 177959001 | |||||||
chr1:177959032 | G | A | 1 | a0006c0009t0004g0294 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.999-57C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 8/25 | chr1 | 177959032 | |||||||
chr1:177959088 | A | C | 4 | a0005c0016t0002g0229 a0005c0016t0003g0058 a0025c0051t0007g0059 others(1): Show |
4 | HG01074.hp1 HG01109.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.999-113T>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 8/25 | chr1 | 177959088 | |||||||
chr1:177959130 | G | A | 2 | a0001c0006t0001g0056 a0032c0046t0001g0162 |
2 | HG01192.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.999-155C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 8/25 | chr1 | 177959130 | |||||||
chr1:177959435 | G | T | 1 | a0001c0004t0001g0134 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.999-460C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 8/25 | chr1 | 177959435 | |||||||
chr1:177959478 | G | T | 22 | a0001c0004t0001g0012 a0001c0004t0001g0072 a0001c0004t0001g0092 others(19): Show |
26 | HG00621.hp2 HG01109.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.999-503C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 8/25 | chr1 | 177959478 | |||||||
chr1:177959826 | C | A | 25 | a0001c0006t0001g0010 a0001c0006t0001g0071 a0001c0006t0001g0090 others(22): Show |
28 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.998+516G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 8/25 | chr1 | 177959826 | |||||||
chr1:177959904 | T | A | 1 | a0004c0002t0004g0171 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.998+438A>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 8/25 | chr1 | 177959904 | |||||||
chr1:177959939 | G | T | 1 | a0001c0004t0001g0260 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.998+403C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 8/25 | chr1 | 177959939 | |||||||
chr1:177959953 | C | T | 1 | a0026c0038t0001g0237 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.998+389G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 8/25 | chr1 | 177959953 | |||||||
chr1:177960102 | T | C | 1 | a0001c0052t0012g0055 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.998+240A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 8/25 | chr1 | 177960102 | |||||||
chr1:177960128 | C | T | 1 | a0003c0003t0003g0105 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.998+214G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 8/25 | chr1 | 177960128 | |||||||
chr1:177960160 | TG | T | 15 | a0001c0004t0001g0012 a0001c0004t0001g0072 a0001c0004t0001g0092 others(12): Show |
19 | HG00621.hp2 HG01109.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.998+181delC | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 8/25 | chr1 | 177960160 | |||||||
chr1:177960244 | C | T | 54 | a0001c0004t0001g0060 a0001c0004t0001g0102 a0001c0004t0001g0260 others(51): Show |
70 | HG00438.hp2 HG00639.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.998+98G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 8/25 | chr1 | 177960244 | |||||||
chr1:177960333 | G | A | 1 | a0004c0002t0004g0040 | 2 | HG00408.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.998+9C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 8/25 | chr1 | 177960333 | |||||||
chr1:177960419 | C | T | 148 | a0001c0005t0001g0024 a0001c0005t0001g0031 a0001c0005t0001g0042 others(145): Show |
193 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.937-16G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 7/25 | chr1 | 177960419 | |||||||
chr1:177960471 | A | G | 2 | a0003c0008t0003g0030 a0003c0008t0003g0068 |
3 | HG02559.hp2 HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.937-68T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 7/25 | chr1 | 177960471 | |||||||
chr1:177960493 | G | A | 22 | a0001c0004t0001g0012 a0001c0004t0001g0072 a0001c0004t0001g0092 others(19): Show |
26 | HG00621.hp2 HG01109.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.937-90C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 7/25 | chr1 | 177960493 | |||||||
chr1:177960632 | T | C | 10 | a0009c0015t0002g0022 a0009c0015t0002g0202 a0009c0015t0002g0204 others(7): Show |
12 | HG00423.hp2 HG00609.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.936+159A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 7/25 | chr1 | 177960632 | |||||||
chr1:177960701 | C | T | 22 | a0001c0004t0001g0012 a0001c0004t0001g0072 a0001c0004t0001g0092 others(19): Show |
26 | HG00621.hp2 HG01109.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.936+90G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 7/25 | chr1 | 177960701 | |||||||
chr1:177960780 | G | C | 6 | a0001c0021t0001g0258 a0001c0021t0001g0259 a0001c0021t0001g0306 others(3): Show |
6 | HG02717.hp1 HG02818.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.936+11C>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 7/25 | chr1 | 177960780 | |||||||
chr1:177960961 | T | C | 73 | a0001c0005t0001g0031 a0001c0005t0001g0104 a0001c0005t0001g0292 others(70): Show |
100 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.788-22A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 6/25 | chr1 | 177960961 | |||||||
chr1:177961100 | C | T | 1 | a0004c0010t0008g0264 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.788-161G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 6/25 | chr1 | 177961100 | |||||||
chr1:177961143 | G | A | 14 | a0001c0004t0001g0012 a0001c0004t0001g0072 a0001c0004t0001g0092 others(11): Show |
17 | HG00621.hp2 HG01109.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.788-204C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 6/25 | chr1 | 177961143 | |||||||
chr1:177961143 | G | T | 1 | a0004c0027t0019g0307 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.788-204C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 6/25 | chr1 | 177961143 | |||||||
chr1:177961182 | C | T | 4 | a0004c0002t0001g0207 a0004c0002t0004g0004 a0004c0002t0004g0154 others(1): Show |
8 | NA18942.hp1 NA18951.hp1 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.788-243G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 6/25 | chr1 | 177961182 | |||||||
chr1:177961184 | C | T | 71 | a0001c0005t0001g0031 a0001c0005t0001g0104 a0001c0005t0001g0292 others(68): Show |
98 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.788-245G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 6/25 | chr1 | 177961184 | |||||||
chr1:177961373 | AG | A | 13 | a0004c0002t0004g0017 a0004c0002t0004g0174 a0004c0067t0008g0200 others(10): Show |
17 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(14): Show |
intron_variant | MODIFIER | c.787+216delC | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 6/25 | chr1 | 177961373 | |||||||
chr1:177961507 | G | A | 134 | a0001c0004t0001g0102 a0001c0004t0001g0260 a0001c0004t0004g0009 others(131): Show |
174 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.787+83C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 6/25 | chr1 | 177961507 | |||||||
chr1:177961759 | C | T | 239 | a0001c0004t0001g0012 a0001c0004t0001g0060 a0001c0004t0001g0072 others(236): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.643-25G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177961759 | |||||||
chr1:177961794 | G | A | 1 | a0005c0016t0005g0133 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.643-60C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177961794 | |||||||
chr1:177961820 | C | T | 3 | a0005c0016t0002g0229 a0005c0016t0003g0058 a0025c0051t0007g0059 |
3 | HG01074.hp1 HG01109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.643-86G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177961820 | |||||||
chr1:177961951 | C | T | 139 | a0001c0004t0001g0102 a0001c0004t0001g0260 a0001c0004t0004g0009 others(136): Show |
180 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.643-217G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177961951 | |||||||
chr1:177961987 | G | A | 85 | a0001c0005t0001g0024 a0001c0005t0001g0031 a0001c0005t0001g0042 others(82): Show |
109 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.643-253C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177961987 | |||||||
chr1:177962176 | C | T | 1 | a0004c0010t0009g0188 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.643-442G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177962176 | |||||||
chr1:177962177 | G | T | 1 | a0003c0008t0003g0081 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.643-443C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177962177 | |||||||
chr1:177962221 | G | A | 3 | a0001c0017t0001g0064 a0016c0024t0010g0057 a0016c0024t0010g0065 |
3 | HG01884.hp1 HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.643-487C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177962221 | |||||||
chr1:177962352 | G | C | 5 | a0001c0021t0001g0258 a0001c0021t0001g0259 a0001c0021t0001g0306 others(2): Show |
5 | HG02818.hp2 HG02976.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.643-618C>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177962352 | |||||||
chr1:177962373 | C | A | 142 | a0001c0004t0001g0060 a0001c0004t0001g0102 a0001c0004t0001g0260 others(139): Show |
183 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.643-639G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177962373 | |||||||
chr1:177962397 | C | A | 63 | a0001c0006t0001g0010 a0001c0006t0001g0011 a0001c0006t0001g0056 others(60): Show |
88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.643-663G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177962397 | |||||||
chr1:177962546 | T | C | 3 | a0005c0016t0002g0229 a0005c0016t0003g0058 a0025c0051t0007g0059 |
3 | HG01074.hp1 HG01109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.643-812A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177962546 | |||||||
chr1:177962758 | T | G | 1 | a0002c0001t0002g0150 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.643-1024A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177962758 | |||||||
chr1:177962789 | G | T | 4 | a0001c0004t0001g0060 a0001c0017t0001g0064 a0016c0024t0010g0057 others(1): Show |
4 | HG01884.hp1 HG01884.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.643-1055C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177962789 | |||||||
chr1:177962861 | C | T | 14 | a0001c0004t0001g0012 a0001c0004t0001g0072 a0001c0004t0001g0092 others(11): Show |
18 | HG00621.hp2 HG01109.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.643-1127G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177962861 | |||||||
chr1:177962864 | T | G | 4 | a0001c0004t0001g0060 a0001c0017t0001g0064 a0016c0024t0010g0057 others(1): Show |
4 | HG01884.hp1 HG01884.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.643-1130A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177962864 | |||||||
chr1:177962876 | G | A | 4 | a0001c0017t0001g0064 a0016c0024t0010g0057 a0016c0024t0010g0065 others(1): Show |
4 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.643-1142C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177962876 | |||||||
chr1:177962907 | GACCAGCC others(489): Show |
G | 11 | a0001c0004t0001g0153 a0002c0001t0002g0005 a0002c0001t0002g0044 others(8): Show |
16 | HG00597.hp2 HG01192.hp2 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.642+768_643-1174de others(1): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177962907 | |||||||
chr1:177962965 | G | A | 1 | a0001c0004t0001g0060 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.642+1206C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177962965 | |||||||
chr1:177962969 | A | G | 242 | a0001c0004t0001g0012 a0001c0004t0001g0060 a0001c0004t0001g0072 others(239): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.642+1202T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177962969 | |||||||
chr1:177963167 | T | C | 11 | a0004c0067t0008g0200 a0009c0015t0002g0022 a0009c0015t0002g0202 others(8): Show |
13 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(10): Show |
intron_variant | MODIFIER | c.642+1004A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177963167 | |||||||
chr1:177963228 | T | C | 138 | a0001c0004t0001g0102 a0001c0004t0001g0260 a0001c0004t0004g0009 others(135): Show |
179 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.642+943A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177963228 | |||||||
chr1:177963249 | G | T | 3 | a0001c0017t0001g0064 a0016c0024t0010g0057 a0016c0024t0010g0065 |
3 | HG01884.hp1 HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.642+922C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177963249 | |||||||
chr1:177963276 | G | A | 3 | a0001c0021t0001g0306 a0001c0036t0001g0116 a0001c0036t0001g0117 |
3 | HG02976.hp2 HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.642+895C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177963276 | |||||||
chr1:177963318 | T | G | 3 | a0005c0016t0002g0229 a0005c0016t0003g0058 a0025c0051t0007g0059 |
3 | HG01074.hp1 HG01109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.642+853A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177963318 | |||||||
chr1:177963327 | G | A | 1 | a0001c0063t0001g0127 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.642+844C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177963327 | |||||||
chr1:177963343 | G | C | 43 | a0001c0004t0001g0102 a0001c0004t0001g0260 a0001c0004t0004g0009 others(40): Show |
58 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.642+828C>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177963343 | |||||||
chr1:177963464 | A | G | 249 | a0001c0004t0001g0012 a0001c0004t0001g0060 a0001c0004t0001g0072 others(246): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.642+707T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177963464 | |||||||
chr1:177963683 | TA | T | 4 | a0001c0004t0001g0060 a0001c0017t0001g0064 a0016c0024t0010g0057 others(1): Show |
4 | HG01884.hp1 HG01884.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.642+487delT | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177963683 | |||||||
chr1:177963764 | A | G | 3 | a0005c0016t0002g0229 a0005c0016t0003g0058 a0025c0051t0007g0059 |
3 | HG01074.hp1 HG01109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.642+407T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177963764 | |||||||
chr1:177963791 | G | A | 3 | a0005c0016t0002g0229 a0005c0016t0003g0058 a0025c0051t0007g0059 |
3 | HG01074.hp1 HG01109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.642+380C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177963791 | |||||||
chr1:177963925 | C | T | 1 | a0004c0027t0006g0053 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.642+246G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177963925 | |||||||
chr1:177964007 | A | G | 3 | a0001c0017t0001g0064 a0016c0024t0010g0057 a0016c0024t0010g0065 |
3 | HG01884.hp1 HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.642+164T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177964007 | |||||||
chr1:177964145 | C | T | 1 | a0003c0003t0003g0280 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.642+26G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177964145 | |||||||
chr1:177964155 | C | A | 1 | a0001c0006t0001g0175 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.642+16G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177964155 | |||||||
chr1:177964155 | C | T | 1 | a0004c0010t0008g0264 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.642+16G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177964155 | |||||||
chr1:177964308 | G | A | 135 | a0001c0004t0001g0102 a0001c0004t0001g0260 a0001c0004t0004g0009 others(132): Show |
176 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.534-29C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 4/25 | chr1 | 177964308 | |||||||
chr1:177964348 | C | T | 1 | a0037c0056t0016g0111 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.534-69G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 4/25 | chr1 | 177964348 | |||||||
chr1:177964370 | C | T | 81 | a0001c0005t0001g0024 a0001c0005t0001g0031 a0001c0005t0001g0042 others(78): Show |
105 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.534-91G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 4/25 | chr1 | 177964370 | |||||||
chr1:177964402 | T | C | 4 | a0001c0004t0001g0060 a0001c0017t0001g0064 a0016c0024t0010g0057 others(1): Show |
4 | HG01884.hp1 HG01884.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.534-123A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 4/25 | chr1 | 177964402 | |||||||
chr1:177964538 | A | G | 2 | a0003c0003t0003g0262 a0003c0003t0003g0263 |
2 | NA19065.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.534-259T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 4/25 | chr1 | 177964538 | |||||||
chr1:177964548 | G | A | 4 | a0007c0014t0002g0176 a0011c0025t0005g0177 a0011c0025t0005g0234 others(1): Show |
4 | HG01099.hp1 HG02109.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.534-269C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 4/25 | chr1 | 177964548 | |||||||
chr1:177964670 | A | T | 4 | a0001c0004t0001g0060 a0001c0017t0001g0064 a0016c0024t0010g0057 others(1): Show |
4 | HG01884.hp1 HG01884.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.533+377T>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 4/25 | chr1 | 177964670 | |||||||
chr1:177964686 | A | G | 1 | a0001c0004t0001g0060 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.533+361T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 4/25 | chr1 | 177964686 | |||||||
chr1:177964694 | A | C | 169 | a0001c0004t0001g0012 a0001c0004t0001g0060 a0001c0004t0001g0072 others(166): Show |
215 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(212): Show |
intron_variant | MODIFIER | c.533+353T>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 4/25 | chr1 | 177964694 | |||||||
chr1:177964697 | G | A | 1 | a0008c0041t0007g0151 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.533+350C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 4/25 | chr1 | 177964697 | |||||||
chr1:177964779 | C | T | 1 | a0001c0005t0001g0031 | 2 | NA18952.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.533+268G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 4/25 | chr1 | 177964779 | |||||||
chr1:177964809 | C | T | 1 | a0037c0056t0016g0111 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.533+238G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 4/25 | chr1 | 177964809 | |||||||
chr1:177964892 | A | C | 2 | a0001c0052t0012g0055 a0028c0037t0003g0224 |
2 | HG02145.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.533+155T>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 4/25 | chr1 | 177964892 | |||||||
chr1:177964909 | T | C | 141 | a0001c0004t0001g0102 a0001c0004t0001g0260 a0001c0004t0004g0009 others(138): Show |
182 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.533+138A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 4/25 | chr1 | 177964909 | |||||||
chr1:177964987 | G | T | 14 | a0001c0004t0001g0012 a0001c0004t0001g0072 a0001c0004t0001g0092 others(11): Show |
18 | HG00621.hp2 HG01109.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.533+60C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 4/25 | chr1 | 177964987 | |||||||
chr1:177965216 | G | T | 79 | a0001c0005t0001g0024 a0001c0005t0001g0031 a0001c0005t0001g0042 others(76): Show |
103 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.413-49C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/25 | chr1 | 177965216 | |||||||
chr1:177965324 | A | G | 2 | a0001c0007t0001g0048 a0005c0011t0002g0013 |
5 | HG02257.hp1 HG02451.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.413-157T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/25 | chr1 | 177965324 | |||||||
chr1:177965332 | T | C | 138 | a0001c0004t0001g0102 a0001c0004t0001g0260 a0001c0004t0004g0009 others(135): Show |
179 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.413-165A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/25 | chr1 | 177965332 | |||||||
chr1:177965400 | G | GGTGTGTG others(1): Show |
13 | a0001c0063t0001g0127 a0004c0067t0008g0200 a0009c0015t0002g0022 others(10): Show |
15 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(12): Show |
intron_variant | MODIFIER | c.413-241_413-234dup others(8): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/25 | chr1 | 177965400 | |||||||
chr1:177965400 | G | GGTGTGTG others(3): Show |
78 | a0001c0005t0001g0024 a0001c0005t0001g0031 a0001c0005t0001g0042 others(75): Show |
102 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.413-243_413-234dup others(10): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/25 | chr1 | 177965400 | |||||||
chr1:177965400 | G | GGTGTGTG others(5): Show |
36 | a0001c0004t0001g0102 a0001c0004t0001g0260 a0001c0004t0004g0009 others(33): Show |
45 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.413-245_413-234dup others(12): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/25 | chr1 | 177965400 | |||||||
chr1:177965400 | G | GGTGTGTG others(7): Show |
12 | a0001c0007t0001g0048 a0003c0008t0003g0030 a0003c0008t0003g0068 others(9): Show |
18 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.413-247_413-234dup others(14): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/25 | chr1 | 177965400 | |||||||
chr1:177965400 | G | GGTGTGTG others(9): Show |
1 | a0012c0019t0006g0051 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.413-249_413-234dup others(16): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/25 | chr1 | 177965400 | |||||||
chr1:177965400 | G | GGTGTGTG others(13): Show |
5 | a0001c0052t0012g0055 a0003c0008t0003g0045 a0005c0011t0002g0063 others(2): Show |
6 | HG01243.hp2 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.413-234_413-233ins others(20): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/25 | chr1 | 177965400 | |||||||
chr1:177965400 | G | GGTGTGTG others(15): Show |
14 | a0001c0004t0001g0012 a0001c0004t0001g0072 a0001c0004t0001g0092 others(11): Show |
17 | HG00621.hp2 HG01109.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.413-234_413-233ins others(22): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/25 | chr1 | 177965400 | |||||||
chr1:177965400 | G | GGTGTGTG others(17): Show |
7 | a0001c0004t0001g0239 a0001c0004t0001g0240 a0001c0017t0001g0064 others(4): Show |
8 | HG01884.hp1 HG02258.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.413-234_413-233ins others(24): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/25 | chr1 | 177965400 | |||||||
chr1:177965400 | G | GGTGTGTG others(19): Show |
1 | a0001c0004t0001g0238 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.413-234_413-233ins others(26): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/25 | chr1 | 177965400 | |||||||
chr1:177965400 | G | GGTGTGTG others(21): Show |
1 | a0001c0004t0001g0060 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.413-234_413-233ins others(28): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/25 | chr1 | 177965400 | |||||||
chr1:177965456 | T | C | 141 | a0001c0004t0001g0102 a0001c0004t0001g0260 a0001c0004t0004g0009 others(138): Show |
182 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.413-289A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/25 | chr1 | 177965456 | |||||||
chr1:177965472 | C | T | 3 | a0005c0016t0002g0229 a0005c0016t0003g0058 a0025c0051t0007g0059 |
3 | HG01074.hp1 HG01109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.413-305G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/25 | chr1 | 177965472 | |||||||
chr1:177965477 | T | C | 5 | a0007c0014t0002g0176 a0011c0025t0005g0177 a0011c0025t0005g0234 others(2): Show |
5 | HG01099.hp1 HG02109.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.413-310A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/25 | chr1 | 177965477 | |||||||
chr1:177965491 | T | C | 1 | a0025c0051t0007g0059 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.413-324A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/25 | chr1 | 177965491 | |||||||
chr1:177965611 | A | G | 13 | a0001c0021t0001g0258 a0001c0021t0001g0259 a0001c0021t0001g0306 others(10): Show |
14 | HG01243.hp2 HG02145.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.412+282T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/25 | chr1 | 177965611 | |||||||
chr1:177965832 | G | C | 4 | a0007c0014t0002g0176 a0011c0025t0005g0177 a0011c0025t0005g0234 others(1): Show |
4 | HG01099.hp1 HG02109.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.412+61C>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/25 | chr1 | 177965832 | |||||||
chr1:177966017 | C | A | 4 | a0007c0014t0002g0176 a0011c0025t0005g0177 a0011c0025t0005g0234 others(1): Show |
4 | HG01099.hp1 HG02109.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.300-12G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177966017 | |||||||
chr1:177966027 | T | A | 1 | a0003c0026t0003g0220 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.300-22A>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177966027 | |||||||
chr1:177966031 | C | T | 1 | a0001c0063t0001g0127 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.300-26G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177966031 | |||||||
chr1:177966068 | A | G | 138 | a0001c0004t0001g0060 a0001c0004t0001g0102 a0001c0004t0001g0260 others(135): Show |
179 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.300-63T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177966068 | |||||||
chr1:177966140 | A | G | 248 | a0001c0004t0001g0012 a0001c0004t0001g0060 a0001c0004t0001g0072 others(245): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.300-135T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177966140 | |||||||
chr1:177966209 | T | C | 5 | a0001c0006t0001g0181 a0001c0006t0018g0180 a0001c0048t0001g0124 others(2): Show |
5 | HG00140.hp1 HG01070.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.300-204A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177966209 | |||||||
chr1:177966295 | C | A | 2 | a0003c0003t0003g0085 a0003c0003t0003g0086 |
2 | NA18959.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.300-290G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177966295 | |||||||
chr1:177966308 | C | T | 134 | a0001c0004t0001g0102 a0001c0004t0001g0260 a0001c0004t0004g0009 others(131): Show |
175 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.300-303G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177966308 | |||||||
chr1:177966392 | C | A | 1 | a0005c0016t0002g0229 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.300-387G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177966392 | |||||||
chr1:177966530 | G | A | 42 | a0001c0004t0001g0102 a0001c0004t0001g0260 a0001c0004t0004g0009 others(39): Show |
57 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.300-525C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177966530 | |||||||
chr1:177966572 | ATT | A | 133 | a0001c0004t0001g0102 a0001c0004t0001g0260 a0001c0004t0004g0009 others(130): Show |
174 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.300-569_300-568del others(2): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177966572 | |||||||
chr1:177966678 | G | A | 1 | a0001c0004t0001g0060 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.300-673C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177966678 | |||||||
chr1:177966795 | G | A | 134 | a0001c0004t0001g0102 a0001c0004t0001g0260 a0001c0004t0004g0009 others(131): Show |
175 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.300-790C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177966795 | |||||||
chr1:177966836 | A | T | 1 | a0002c0001t0020g0308 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.300-831T>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177966836 | |||||||
chr1:177966892 | T | C | 137 | a0001c0004t0001g0102 a0001c0004t0001g0260 a0001c0004t0004g0009 others(134): Show |
178 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.299+791A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177966892 | |||||||
chr1:177967109 | G | A | 2 | a0001c0021t0001g0258 a0001c0021t0001g0259 |
2 | HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.299+574C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177967109 | |||||||
chr1:177967268 | G | A | 5 | a0003c0008t0003g0045 a0005c0011t0002g0063 a0012c0019t0001g0073 others(2): Show |
6 | HG01243.hp2 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.299+415C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177967268 | |||||||
chr1:177967346 | A | C | 248 | a0001c0004t0001g0012 a0001c0004t0001g0060 a0001c0004t0001g0072 others(245): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.299+337T>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177967346 | |||||||
chr1:177967390 | A | G | 28 | a0001c0004t0001g0102 a0001c0004t0001g0260 a0001c0004t0004g0009 others(25): Show |
36 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.299+293T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177967390 | |||||||
chr1:177967401 | T | G | 105 | a0001c0004t0001g0153 a0001c0006t0001g0010 a0001c0006t0001g0011 others(102): Show |
139 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.299+282A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177967401 | |||||||
chr1:177967464 | T | G | 126 | a0001c0004t0001g0102 a0001c0004t0001g0260 a0001c0004t0004g0009 others(123): Show |
161 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.299+219A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177967464 | |||||||
chr1:177967556 | C | T | 3 | a0005c0016t0002g0229 a0005c0016t0003g0058 a0025c0051t0007g0059 |
3 | HG01074.hp1 HG01109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.299+127G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177967556 | |||||||
chr1:177967671 | C | T | 1 | a0005c0016t0005g0133 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.299+12G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177967671 | |||||||
chr1:177968143 | A | C | 3 | a0001c0006t0001g0071 a0004c0027t0019g0307 a0018c0068t0002g0089 |
3 | HG02145.hp2 HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-58-104T>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177968143 | |||||||
chr1:177968163 | T | C | 1 | a0003c0003t0003g0280 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-58-124A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177968163 | |||||||
chr1:177968241 | C | T | 2 | a0001c0036t0001g0116 a0001c0036t0001g0117 |
2 | HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-58-202G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177968241 | |||||||
chr1:177968306 | A | G | 159 | a0001c0004t0001g0012 a0001c0004t0001g0060 a0001c0004t0001g0072 others(156): Show |
215 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.-58-267T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177968306 | |||||||
chr1:177968396 | C | T | 1 | a0001c0006t0001g0115 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-58-357G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177968396 | |||||||
chr1:177968419 | C | T | 1 | a0003c0003t0003g0114 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-58-380G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177968419 | |||||||
chr1:177968430 | T | C | 2 | a0001c0005t0001g0292 a0001c0005t0001g0293 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-58-391A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177968430 | |||||||
chr1:177968577 | C | T | 1 | a0011c0025t0005g0234 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-58-538G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177968577 | |||||||
chr1:177968585 | G | A | 1 | a0002c0001t0002g0206 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-58-546C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177968585 | |||||||
chr1:177968603 | T | C | 161 | a0001c0004t0001g0012 a0001c0004t0001g0060 a0001c0004t0001g0072 others(158): Show |
212 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(209): Show |
intron_variant | MODIFIER | c.-58-564A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177968603 | |||||||
chr1:177968620 | A | G | 166 | a0001c0004t0001g0012 a0001c0004t0001g0060 a0001c0004t0001g0072 others(163): Show |
219 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(216): Show |
intron_variant | MODIFIER | c.-58-581T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177968620 | |||||||
chr1:177968829 | A | G | 31 | a0001c0004t0001g0060 a0001c0006t0001g0090 a0001c0006t0001g0227 others(28): Show |
39 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.-58-790T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177968829 | |||||||
chr1:177968922 | G | A | 18 | a0001c0005t0002g0221 a0002c0001t0002g0005 a0002c0001t0002g0043 others(15): Show |
24 | HG00741.hp1 HG01192.hp2 HG01257.hp1 others(21): Show |
intron_variant | MODIFIER | c.-58-883C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177968922 | |||||||
chr1:177968995 | C | T | 28 | a0001c0004t0001g0060 a0001c0005t0001g0047 a0001c0006t0001g0227 others(25): Show |
37 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.-59+889G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177968995 | |||||||
chr1:177969099 | T | G | 3 | a0001c0006t0001g0056 a0001c0052t0012g0055 a0016c0024t0010g0057 |
3 | HG01192.hp1 HG01884.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-59+785A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177969099 | |||||||
chr1:177969108 | T | C | 6 | a0001c0004t0004g0301 a0001c0007t0001g0302 a0001c0017t0001g0299 others(3): Show |
6 | HG01255.hp2 HG02280.hp1 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.-59+776A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177969108 | |||||||
chr1:177969302 | G | A | 98 | a0001c0004t0001g0012 a0001c0004t0001g0238 a0001c0004t0001g0239 others(95): Show |
123 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.-59+582C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177969302 | |||||||
chr1:177969463 | G | A | 1 | a0001c0021t0001g0306 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-59+421C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177969463 | |||||||
chr1:177969577 | A | G | 40 | a0001c0004t0001g0060 a0001c0004t0001g0072 a0001c0005t0001g0031 others(37): Show |
54 | HG00408.hp1 HG00544.hp1 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.-59+307T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177969577 | |||||||
chr1:177969611 | G | A | 1 | a0002c0001t0002g0305 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-59+273C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177969611 | |||||||
chr1:177969837 | C | T | 39 | a0001c0004t0001g0060 a0001c0004t0001g0072 a0001c0005t0001g0031 others(36): Show |
53 | HG00408.hp1 HG00544.hp1 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.-59+47G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177969837 | |||||||
chr1:177969838 | G | T | 4 | a0001c0006t0001g0056 a0001c0052t0012g0055 a0016c0024t0010g0057 others(1): Show |
4 | HG01192.hp1 HG01884.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-59+46C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177969838 | |||||||
chr1:177969854 | G | C | 1 | a0001c0021t0001g0306 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-59+30C>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177969854 |