Item | Value |
---|---|
geneid | 81786 |
ensemblid | ENSG00000146054.18 |
hgncid | 16278 |
symbol | TRIM7 |
name | tripartite motif containing 7 |
refseq_nuc | NM_203293.3 |
refseq_prot | NP_976038.1 |
ensembl_nuc | ENST00000274773.12 |
ensembl_prot | ENSP00000274773.7 |
mane_status | MANE Select |
chr | chr5 |
start | 181193924 |
end | 181205196 |
strand | - |
ver | v1.2 |
region | chr5:181193924-181205196 |
region5000 | chr5:181188924-181210196 |
regionname0 | TRIM7_chr5_181193924_181205196 |
regionname5000 | TRIM7_chr5_181188924_181210196 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 511 | 162 | 7 | 47 | 77 | 7 | 23 | 51 | TRIM7_chr5_181188924_181210196 | TRIM7 | MAAVG others(506): Show |
chr5 | 181188924 | 181210196 |
a0002 | 0/0 | 511 | 93 | 22 | 10 | 54 | 2 | 5 | 43 | TRIM7_chr5_181188924_181210196 | TRIM7 | MAAVG others(506): Show |
chr5 | 181188924 | 181210196 |
a0003 | 0/0 | 511 | 35 | 32 | 1 | 2 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | MAAVG others(506): Show |
chr5 | 181188924 | 181210196 |
a0004 | 0/1 | 511 | 34 | 2 | 3 | 19 | 1 | 8 | 15 | TRIM7_chr5_181188924_181210196 | TRIM7 | MAAVG others(506): Show |
chr5 | 181188924 | 181210196 |
a0005 | 0/0 | 511 | 31 | 13 | 3 | 10 | 0 | 5 | 6 | TRIM7_chr5_181188924_181210196 | TRIM7 | MAAVG others(506): Show |
chr5 | 181188924 | 181210196 |
a0006 | 0/0 | 511 | 10 | 9 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | MAAVG others(506): Show |
chr5 | 181188924 | 181210196 |
a0007 | 0/0 | 511 | 6 | 0 | 2 | 3 | 0 | 1 | 3 | TRIM7_chr5_181188924_181210196 | TRIM7 | MAAVG others(506): Show |
chr5 | 181188924 | 181210196 |
a0008 | 0/0 | 511 | 4 | 0 | 0 | 4 | 0 | 0 | 2 | TRIM7_chr5_181188924_181210196 | TRIM7 | MAAVG others(506): Show |
chr5 | 181188924 | 181210196 |
a0009 | 0/0 | 511 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | MAAVG others(506): Show |
chr5 | 181188924 | 181210196 |
a0010 | 0/0 | 511 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | TRIM7_chr5_181188924_181210196 | TRIM7 | MAAVG others(506): Show |
chr5 | 181188924 | 181210196 |
a0011 | 0/0 | 511 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | MAAVG others(506): Show |
chr5 | 181188924 | 181210196 |
a0012 | 0/0 | 511 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | MAAVG others(506): Show |
chr5 | 181188924 | 181210196 |
a0013 | 0/0 | 511 | 2 | 0 | 0 | 1 | 0 | 1 | 1 | TRIM7_chr5_181188924_181210196 | TRIM7 | MAAVG others(506): Show |
chr5 | 181188924 | 181210196 |
a0014 | 0/0 | 511 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | MAAVG others(506): Show |
chr5 | 181188924 | 181210196 |
a0015 | 0/0 | 511 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | MAAVG others(506): Show |
chr5 | 181188924 | 181210196 |
a0016 | 0/0 | 511 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | MAAVG others(506): Show |
chr5 | 181188924 | 181210196 |
a0017 | 0/0 | 511 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | MAAVG others(506): Show |
chr5 | 181188924 | 181210196 |
a0018 | 0/0 | 511 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | MAAVG others(506): Show |
chr5 | 181188924 | 181210196 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1533 | 156 | 6 | 47 | 73 | 7 | 22 | TRIM7_chr5_181188924_181210196 | TRIM7 | ATGGC others(1528): Show |
chr5 | 181188924 | 181210196 | ||
a0001c0016 | 0/0 | 1533 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | ATGGC others(1528): Show |
chr5 | 181188924 | 181210196 | ||
a0001c0022 | 0/0 | 1533 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | ATGGC others(1528): Show |
chr5 | 181188924 | 181210196 | ||
a0001c0023 | 0/0 | 1533 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM7_chr5_181188924_181210196 | TRIM7 | ATGGC others(1528): Show |
chr5 | 181188924 | 181210196 | ||
a0002c0002 | 0/0 | 1533 | 69 | 10 | 3 | 53 | 0 | 3 | TRIM7_chr5_181188924_181210196 | TRIM7 | ATGGC others(1528): Show |
chr5 | 181188924 | 181210196 | ||
a0002c0006 | 0/0 | 1533 | 10 | 10 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | ATGGC others(1528): Show |
chr5 | 181188924 | 181210196 | ||
a0002c0008 | 0/0 | 1533 | 8 | 1 | 5 | 0 | 0 | 2 | TRIM7_chr5_181188924_181210196 | TRIM7 | ATGGC others(1528): Show |
chr5 | 181188924 | 181210196 | ||
a0002c0010 | 0/0 | 1533 | 5 | 1 | 2 | 0 | 2 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | ATGGC others(1528): Show |
chr5 | 181188924 | 181210196 | ||
a0002c0031 | 0/0 | 1533 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | ATGGC others(1528): Show |
chr5 | 181188924 | 181210196 | ||
a0003c0005 | 0/0 | 1533 | 21 | 18 | 1 | 2 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | ATGGC others(1528): Show |
chr5 | 181188924 | 181210196 | ||
a0003c0009 | 0/0 | 1533 | 7 | 7 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | ATGGC others(1528): Show |
chr5 | 181188924 | 181210196 | ||
a0003c0011 | 0/0 | 1533 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | ATGGC others(1528): Show |
chr5 | 181188924 | 181210196 | ||
a0003c0020 | 0/0 | 1533 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | ATGGC others(1528): Show |
chr5 | 181188924 | 181210196 | ||
a0004c0003 | 0/1 | 1533 | 33 | 2 | 3 | 18 | 1 | 8 | TRIM7_chr5_181188924_181210196 | TRIM7 | ATGGC others(1528): Show |
chr5 | 181188924 | 181210196 | ||
a0004c0027 | 0/0 | 1533 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | ATGGC others(1528): Show |
chr5 | 181188924 | 181210196 | ||
a0005c0004 | 0/0 | 1533 | 27 | 12 | 3 | 8 | 0 | 4 | TRIM7_chr5_181188924_181210196 | TRIM7 | ATGGC others(1528): Show |
chr5 | 181188924 | 181210196 | ||
a0005c0015 | 0/0 | 1533 | 4 | 1 | 0 | 2 | 0 | 1 | TRIM7_chr5_181188924_181210196 | TRIM7 | ATGGC others(1528): Show |
chr5 | 181188924 | 181210196 | ||
a0006c0007 | 0/0 | 1533 | 9 | 8 | 1 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | ATGGC others(1528): Show |
chr5 | 181188924 | 181210196 | ||
a0006c0025 | 0/0 | 1533 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | ATGGC others(1528): Show |
chr5 | 181188924 | 181210196 | ||
a0007c0012 | 0/0 | 1533 | 5 | 0 | 1 | 3 | 0 | 1 | TRIM7_chr5_181188924_181210196 | TRIM7 | ATGGC others(1528): Show |
chr5 | 181188924 | 181210196 | ||
a0007c0033 | 0/0 | 1533 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | ATGGC others(1528): Show |
chr5 | 181188924 | 181210196 | ||
a0008c0014 | 0/0 | 1533 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | ATGGC others(1528): Show |
chr5 | 181188924 | 181210196 | ||
a0009c0017 | 0/0 | 1533 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | ATGGC others(1528): Show |
chr5 | 181188924 | 181210196 | ||
a0010c0013 | 0/0 | 1533 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | ATGGC others(1528): Show |
chr5 | 181188924 | 181210196 | ||
a0011c0019 | 0/0 | 1533 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | ATGGC others(1528): Show |
chr5 | 181188924 | 181210196 | ||
a0012c0026 | 0/0 | 1533 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM7_chr5_181188924_181210196 | TRIM7 | ATGGC others(1528): Show |
chr5 | 181188924 | 181210196 | ||
a0012c0028 | 0/0 | 1533 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM7_chr5_181188924_181210196 | TRIM7 | ATGGC others(1528): Show |
chr5 | 181188924 | 181210196 | ||
a0013c0018 | 0/0 | 1533 | 2 | 0 | 0 | 1 | 0 | 1 | TRIM7_chr5_181188924_181210196 | TRIM7 | ATGGC others(1528): Show |
chr5 | 181188924 | 181210196 | ||
a0014c0029 | 0/0 | 1533 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | ATGGC others(1528): Show |
chr5 | 181188924 | 181210196 | ||
a0015c0024 | 0/0 | 1533 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | ATGGC others(1528): Show |
chr5 | 181188924 | 181210196 | ||
a0016c0032 | 0/0 | 1533 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | ATGGC others(1528): Show |
chr5 | 181188924 | 181210196 | ||
a0017c0021 | 0/0 | 1533 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | ATGGC others(1528): Show |
chr5 | 181188924 | 181210196 | ||
a0018c0030 | 0/0 | 1533 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM7_chr5_181188924_181210196 | TRIM7 | ATGGC others(1528): Show |
chr5 | 181188924 | 181210196 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2864 | 156 | 6 | 47 | 73 | 7 | 22 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2859): Show |
chr5 | 181188924 | 181210196 |
a0001c0016t0001 | 0/0 | 2864 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2859): Show |
chr5 | 181188924 | 181210196 |
a0001c0022t0002 | 0/0 | 2863 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2858): Show |
chr5 | 181188924 | 181210196 |
a0001c0023t0001 | 0/0 | 2864 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2859): Show |
chr5 | 181188924 | 181210196 |
a0002c0002t0001 | 0/0 | 2864 | 67 | 9 | 3 | 52 | 0 | 3 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2859): Show |
chr5 | 181188924 | 181210196 |
a0002c0002t0002 | 0/0 | 2863 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2858): Show |
chr5 | 181188924 | 181210196 |
a0002c0002t0010 | 0/0 | 2864 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2859): Show |
chr5 | 181188924 | 181210196 |
a0002c0006t0002 | 0/0 | 2863 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2858): Show |
chr5 | 181188924 | 181210196 |
a0002c0006t0003 | 0/0 | 2864 | 9 | 9 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2859): Show |
chr5 | 181188924 | 181210196 |
a0002c0008t0001 | 0/0 | 2864 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2859): Show |
chr5 | 181188924 | 181210196 |
a0002c0008t0002 | 0/0 | 2863 | 7 | 0 | 5 | 0 | 0 | 2 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2858): Show |
chr5 | 181188924 | 181210196 |
a0002c0010t0001 | 0/0 | 2864 | 4 | 0 | 2 | 0 | 2 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2859): Show |
chr5 | 181188924 | 181210196 |
a0002c0010t0002 | 0/0 | 2863 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2858): Show |
chr5 | 181188924 | 181210196 |
a0002c0031t0001 | 0/0 | 2864 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2859): Show |
chr5 | 181188924 | 181210196 |
a0003c0005t0002 | 0/0 | 2863 | 17 | 14 | 1 | 2 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2858): Show |
chr5 | 181188924 | 181210196 |
a0003c0005t0004 | 0/0 | 2864 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2859): Show |
chr5 | 181188924 | 181210196 |
a0003c0005t0006 | 0/0 | 2863 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2858): Show |
chr5 | 181188924 | 181210196 |
a0003c0009t0002 | 0/0 | 2863 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2858): Show |
chr5 | 181188924 | 181210196 |
a0003c0009t0007 | 0/0 | 2863 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2858): Show |
chr5 | 181188924 | 181210196 |
a0003c0009t0008 | 0/0 | 2863 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2858): Show |
chr5 | 181188924 | 181210196 |
a0003c0011t0002 | 0/0 | 2863 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2858): Show |
chr5 | 181188924 | 181210196 |
a0003c0020t0002 | 0/0 | 2863 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2858): Show |
chr5 | 181188924 | 181210196 |
a0004c0003t0001 | 0/1 | 2864 | 33 | 2 | 3 | 18 | 1 | 8 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2859): Show |
chr5 | 181188924 | 181210196 |
a0004c0027t0001 | 0/0 | 2864 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2859): Show |
chr5 | 181188924 | 181210196 |
a0005c0004t0001 | 0/0 | 2864 | 25 | 11 | 2 | 8 | 0 | 4 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2859): Show |
chr5 | 181188924 | 181210196 |
a0005c0004t0002 | 0/0 | 2863 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2858): Show |
chr5 | 181188924 | 181210196 |
a0005c0015t0001 | 0/0 | 2864 | 4 | 1 | 0 | 2 | 0 | 1 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2859): Show |
chr5 | 181188924 | 181210196 |
a0006c0007t0002 | 0/0 | 2863 | 9 | 8 | 1 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2858): Show |
chr5 | 181188924 | 181210196 |
a0006c0025t0002 | 0/0 | 2863 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2858): Show |
chr5 | 181188924 | 181210196 |
a0007c0012t0001 | 0/0 | 2864 | 5 | 0 | 1 | 3 | 0 | 1 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2859): Show |
chr5 | 181188924 | 181210196 |
a0007c0033t0001 | 0/0 | 2864 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2859): Show |
chr5 | 181188924 | 181210196 |
a0008c0014t0001 | 0/0 | 2864 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2859): Show |
chr5 | 181188924 | 181210196 |
a0009c0017t0002 | 0/0 | 2863 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2858): Show |
chr5 | 181188924 | 181210196 |
a0009c0017t0005 | 0/0 | 2863 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2858): Show |
chr5 | 181188924 | 181210196 |
a0010c0013t0001 | 0/0 | 2864 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2859): Show |
chr5 | 181188924 | 181210196 |
a0011c0019t0001 | 0/0 | 2864 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2859): Show |
chr5 | 181188924 | 181210196 |
a0012c0026t0001 | 0/0 | 2864 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2859): Show |
chr5 | 181188924 | 181210196 |
a0012c0028t0001 | 0/0 | 2864 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2859): Show |
chr5 | 181188924 | 181210196 |
a0013c0018t0001 | 0/0 | 2864 | 2 | 0 | 0 | 1 | 0 | 1 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2859): Show |
chr5 | 181188924 | 181210196 |
a0014c0029t0001 | 0/0 | 2864 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2859): Show |
chr5 | 181188924 | 181210196 |
a0015c0024t0001 | 0/0 | 2864 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2859): Show |
chr5 | 181188924 | 181210196 |
a0016c0032t0009 | 0/0 | 2864 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2859): Show |
chr5 | 181188924 | 181210196 |
a0017c0021t0003 | 0/0 | 2864 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2859): Show |
chr5 | 181188924 | 181210196 |
a0018c0030t0001 | 0/0 | 2864 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM7_chr5_181188924_181210196 | TRIM7 | AGTGG others(2859): Show |
chr5 | 181188924 | 181210196 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 1/0 | 99 | 5 | 24 | 51 | 5 | 13 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0001c0001t0001g0004 | 0/0 | 12 | 0 | 10 | 0 | 0 | 2 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0001c0001t0001g0008 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0001c0001t0001g0009 | 0/0 | 7 | 0 | 1 | 3 | 2 | 1 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0001c0001t0001g0013 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0001c0016t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0001c0016t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0001c0016t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0001c0022t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0001c0023t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0002c0002t0001g0002 | 0/0 | 56 | 6 | 3 | 44 | 0 | 3 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0002c0002t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0002c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0002c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0002c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0002c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0002c0002t0010g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0002c0006t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0002c0006t0003g0006 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0002c0006t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0002c0008t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0002c0008t0002g0015 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0002c0008t0002g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0002c0010t0001g0017 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0002c0010t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0002c0010t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0002c0031t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0003c0005t0002g0007 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0003c0005t0002g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0003c0005t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0003c0005t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0003c0005t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0003c0005t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0003c0005t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0003c0005t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0003c0005t0004g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0003c0005t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0003c0005t0006g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0003c0009t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0003c0009t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0003c0009t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0003c0009t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0003c0009t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0003c0009t0007g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0003c0009t0008g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0003c0011t0002g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0003c0011t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0003c0020t0002g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0004c0003t0001g0003 | 0/1 | 19 | 1 | 1 | 8 | 1 | 7 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0004c0003t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0004c0003t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0004c0003t0001g0037 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0004c0003t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0004c0003t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0004c0003t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0004c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0004c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0004c0027t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0005c0004t0001g0005 | 0/0 | 11 | 0 | 1 | 6 | 0 | 4 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0005c0004t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0005c0004t0001g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0005c0004t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0005c0004t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0005c0004t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0005c0004t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0005c0004t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0005c0004t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0005c0004t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0005c0004t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0005c0004t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0005c0004t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0005c0015t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0005c0015t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0005c0015t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0005c0015t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0006c0007t0002g0014 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0006c0007t0002g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0006c0007t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0006c0007t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0006c0025t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0007c0012t0001g0010 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0007c0033t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0008c0014t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0009c0017t0002g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0009c0017t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0010c0013t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0010c0013t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0010c0013t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0011c0019t0001g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0012c0026t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0012c0028t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0013c0018t0001g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0014c0029t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0015c0024t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0016c0032t0009g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0017c0021t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
a0018c0030t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0004 | c0003 | t0001 | g0003 | EUR | GBR | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG00408 | hp1 | a0005 | c0004 | t0001 | g0088 | EAS | CHS | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG00423 | hp2 | a0005 | c0015 | t0001 | g0070 | EAS | CHS | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | CHS | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG00544 | hp1 | a0008 | c0014 | t0001 | g0011 | EAS | CHS | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG00544 | hp2 | a0004 | c0003 | t0001 | g0003 | EAS | CHS | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG00597 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG00621 | hp2 | a0004 | c0003 | t0001 | g0037 | EAS | CHS | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG00735 | hp1 | a0005 | c0004 | t0002 | g0090 | AMR | PUR | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG00735 | hp2 | a0004 | c0003 | t0001 | g0003 | AMR | PUR | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01069 | hp1 | a0002 | c0008 | t0002 | g0020 | AMR | PUR | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01106 | hp2 | a0002 | c0008 | t0002 | g0020 | AMR | PUR | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01167 | hp2 | a0006 | c0007 | t0002 | g0014 | AMR | PUR | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01168 | hp1 | a0002 | c0008 | t0002 | g0015 | AMR | PUR | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01169 | hp2 | a0002 | c0008 | t0002 | g0015 | AMR | PUR | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01175 | hp2 | a0007 | c0033 | t0001 | g0121 | AMR | PUR | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01243 | hp1 | a0003 | c0005 | t0002 | g0007 | AMR | PUR | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01243 | hp2 | a0011 | c0019 | t0001 | g0038 | AMR | PUR | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01255 | hp2 | a0014 | c0029 | t0001 | g0095 | AMR | CLM | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01256 | hp1 | a0007 | c0012 | t0001 | g0010 | AMR | CLM | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01257 | hp2 | a0005 | c0004 | t0001 | g0005 | AMR | CLM | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01261 | hp2 | a0002 | c0010 | t0001 | g0065 | AMR | CLM | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01361 | hp1 | a0004 | c0003 | t0001 | g0036 | AMR | CLM | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01516 | hp2 | a0002 | c0010 | t0001 | g0017 | EUR | IBS | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01517 | hp2 | a0002 | c0010 | t0001 | g0017 | EUR | IBS | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01884 | hp1 | a0003 | c0005 | t0002 | g0118 | AFR | ACB | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01884 | hp2 | a0003 | c0005 | t0002 | g0119 | AFR | ACB | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01891 | hp2 | a0002 | c0006 | t0003 | g0006 | AFR | ACB | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01943 | hp1 | a0002 | c0008 | t0002 | g0020 | AMR | PEL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01943 | hp2 | a0004 | c0003 | t0001 | g0036 | AMR | PEL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01952 | hp1 | a0005 | c0004 | t0001 | g0033 | AMR | PEL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01993 | hp1 | a0015 | c0024 | t0001 | g0053 | AMR | PEL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02015 | hp2 | a0004 | c0003 | t0001 | g0003 | EAS | KHV | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02040 | hp2 | a0005 | c0004 | t0001 | g0087 | EAS | KHV | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02055 | hp1 | a0003 | c0011 | t0002 | g0016 | AFR | ACB | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02055 | hp2 | a0005 | c0004 | t0001 | g0032 | AFR | ACB | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02074 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02083 | hp2 | a0005 | c0004 | t0001 | g0005 | EAS | KHV | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02129 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02132 | hp2 | a0008 | c0014 | t0001 | g0011 | EAS | KHV | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0078 | EAS | KHV | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02145 | hp1 | a0001 | c0022 | t0002 | g0044 | AFR | ACB | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02145 | hp2 | a0003 | c0011 | t0002 | g0016 | AFR | ACB | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CDX | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02155 | hp2 | a0004 | c0003 | t0001 | g0039 | EAS | CDX | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CDX | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02165 | hp2 | a0001 | c0016 | t0001 | g0031 | EAS | CDX | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02257 | hp1 | a0004 | c0003 | t0001 | g0037 | AFR | ACB | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02257 | hp2 | a0006 | c0025 | t0002 | g0066 | AFR | ACB | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02258 | hp1 | a0016 | c0032 | t0009 | g0111 | AFR | ACB | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02258 | hp2 | a0002 | c0006 | t0003 | g0006 | AFR | ACB | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02280 | hp1 | a0003 | c0011 | t0002 | g0016 | AFR | ACB | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02280 | hp2 | a0003 | c0020 | t0002 | g0042 | AFR | ACB | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02451 | hp1 | a0003 | c0009 | t0002 | g0110 | AFR | ACB | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02451 | hp2 | a0005 | c0015 | t0001 | g0074 | AFR | ACB | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02572 | hp1 | a0002 | c0006 | t0003 | g0006 | AFR | GWD | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02572 | hp2 | a0003 | c0005 | t0002 | g0022 | AFR | GWD | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02602 | hp2 | a0005 | c0004 | t0001 | g0005 | SAS | PJL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02615 | hp1 | a0005 | c0004 | t0002 | g0091 | AFR | GWD | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02615 | hp2 | a0005 | c0004 | t0001 | g0085 | AFR | GWD | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | GWD | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0075 | AFR | GWD | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02630 | hp1 | a0011 | c0019 | t0001 | g0038 | AFR | GWD | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02630 | hp2 | a0005 | c0004 | t0001 | g0093 | AFR | GWD | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02647 | hp1 | a0002 | c0002 | t0002 | g0067 | AFR | GWD | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02683 | hp1 | a0005 | c0004 | t0001 | g0005 | SAS | PJL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02683 | hp2 | a0004 | c0003 | t0001 | g0003 | SAS | PJL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02717 | hp1 | a0005 | c0004 | t0001 | g0086 | AFR | GWD | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02717 | hp2 | a0003 | c0011 | t0002 | g0103 | AFR | GWD | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02723 | hp1 | a0003 | c0005 | t0002 | g0007 | AFR | GWD | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02723 | hp2 | a0006 | c0007 | t0002 | g0014 | AFR | GWD | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02735 | hp1 | a0005 | c0004 | t0001 | g0005 | SAS | PJL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02809 | hp1 | a0003 | c0005 | t0004 | g0041 | AFR | GWD | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02809 | hp2 | a0003 | c0005 | t0006 | g0112 | AFR | GWD | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02818 | hp1 | a0003 | c0005 | t0002 | g0007 | AFR | GWD | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02818 | hp2 | a0003 | c0009 | t0002 | g0107 | AFR | GWD | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02886 | hp1 | a0002 | c0010 | t0002 | g0064 | AFR | GWD | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02886 | hp2 | a0017 | c0021 | t0003 | g0043 | AFR | GWD | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02895 | hp1 | a0005 | c0004 | t0001 | g0089 | AFR | GWD | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02895 | hp2 | a0005 | c0004 | t0001 | g0035 | AFR | GWD | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02896 | hp1 | a0003 | c0005 | t0004 | g0041 | AFR | GWD | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02896 | hp2 | a0002 | c0006 | t0003 | g0006 | AFR | GWD | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02897 | hp1 | a0005 | c0004 | t0001 | g0035 | AFR | GWD | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02897 | hp2 | a0003 | c0005 | t0004 | g0117 | AFR | GWD | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02922 | hp1 | a0006 | c0007 | t0002 | g0019 | AFR | ESN | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02922 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | ESN | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02965 | hp1 | a0003 | c0005 | t0002 | g0116 | AFR | ESN | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02965 | hp2 | a0003 | c0020 | t0002 | g0042 | AFR | ESN | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02976 | hp1 | a0009 | c0017 | t0002 | g0023 | AFR | ESN | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02976 | hp2 | a0002 | c0008 | t0001 | g0092 | AFR | ESN | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03017 | hp2 | a0012 | c0026 | t0001 | g0094 | SAS | PJL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03041 | hp1 | a0002 | c0006 | t0003 | g0006 | AFR | GWD | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03041 | hp2 | a0006 | c0007 | t0002 | g0014 | AFR | GWD | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03098 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | MSL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03098 | hp2 | a0005 | c0004 | t0001 | g0034 | AFR | MSL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03130 | hp1 | a0003 | c0009 | t0002 | g0108 | AFR | ESN | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03130 | hp2 | a0002 | c0006 | t0003 | g0006 | AFR | ESN | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03139 | hp1 | a0003 | c0005 | t0002 | g0022 | AFR | ESN | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03139 | hp2 | a0006 | c0007 | t0002 | g0084 | AFR | ESN | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03209 | hp1 | a0002 | c0006 | t0003 | g0046 | AFR | MSL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03209 | hp2 | a0003 | c0005 | t0002 | g0007 | AFR | MSL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03225 | hp1 | a0003 | c0005 | t0002 | g0007 | AFR | MSL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03225 | hp2 | a0003 | c0009 | t0002 | g0109 | AFR | MSL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03239 | hp2 | a0004 | c0003 | t0001 | g0003 | SAS | PJL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03453 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | MSL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03453 | hp2 | a0005 | c0004 | t0001 | g0034 | AFR | MSL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03486 | hp1 | a0003 | c0005 | t0002 | g0022 | AFR | MSL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03486 | hp2 | a0002 | c0006 | t0003 | g0006 | AFR | MSL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03516 | hp1 | a0006 | c0007 | t0002 | g0019 | AFR | ESN | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03516 | hp2 | a0002 | c0006 | t0003 | g0006 | AFR | ESN | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03540 | hp1 | a0005 | c0004 | t0001 | g0033 | AFR | GWD | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03540 | hp2 | a0006 | c0007 | t0002 | g0014 | AFR | GWD | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03579 | hp1 | a0006 | c0007 | t0002 | g0019 | AFR | MSL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03579 | hp2 | a0003 | c0005 | t0002 | g0007 | AFR | MSL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03654 | hp2 | a0001 | c0023 | t0001 | g0047 | SAS | PJL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03669 | hp1 | a0012 | c0028 | t0001 | g0097 | SAS | PJL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03669 | hp2 | a0004 | c0003 | t0001 | g0003 | SAS | PJL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03688 | hp1 | a0005 | c0015 | t0001 | g0079 | SAS | STU | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03688 | hp2 | a0013 | c0018 | t0001 | g0030 | SAS | STU | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03704 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03704 | hp2 | a0004 | c0003 | t0001 | g0003 | SAS | PJL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03831 | hp2 | a0007 | c0012 | t0001 | g0010 | SAS | BEB | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03834 | hp1 | a0004 | c0003 | t0001 | g0003 | SAS | BEB | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | BEB | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03927 | hp1 | a0004 | c0003 | t0001 | g0099 | SAS | BEB | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03942 | hp1 | a0018 | c0030 | t0001 | g0101 | SAS | BEB | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG04115 | hp2 | a0004 | c0003 | t0001 | g0003 | SAS | STU | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG04199 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | STU | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG04204 | hp1 | a0005 | c0004 | t0001 | g0005 | SAS | STU | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG04204 | hp2 | a0002 | c0008 | t0002 | g0015 | SAS | STU | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG04228 | hp2 | a0004 | c0003 | t0001 | g0003 | SAS | STU | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18522 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | YRI | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18522 | hp2 | a0006 | c0007 | t0002 | g0083 | AFR | YRI | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18612 | hp2 | a0010 | c0013 | t0001 | g0059 | EAS | CHB | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18747 | hp1 | a0003 | c0005 | t0002 | g0114 | EAS | CHB | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18747 | hp2 | a0003 | c0005 | t0002 | g0115 | EAS | CHB | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18906 | hp1 | a0003 | c0009 | t0007 | g0106 | AFR | YRI | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18906 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | YRI | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18940 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18942 | hp1 | a0002 | c0002 | t0010 | g0080 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18942 | hp2 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18943 | hp2 | a0008 | c0014 | t0001 | g0011 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18944 | hp1 | a0004 | c0003 | t0001 | g0003 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18944 | hp2 | a0004 | c0003 | t0001 | g0021 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18945 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18946 | hp1 | a0004 | c0003 | t0001 | g0003 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18946 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18947 | hp1 | a0004 | c0003 | t0001 | g0039 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18949 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18953 | hp1 | a0010 | c0013 | t0001 | g0061 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18953 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18956 | hp2 | a0005 | c0015 | t0001 | g0082 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18959 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18961 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18962 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18963 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18963 | hp2 | a0004 | c0003 | t0001 | g0096 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18966 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18968 | hp1 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18969 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18975 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18977 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18981 | hp1 | a0008 | c0014 | t0001 | g0011 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18981 | hp2 | a0004 | c0003 | t0001 | g0003 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18983 | hp1 | a0001 | c0016 | t0001 | g0071 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18985 | hp2 | a0005 | c0004 | t0001 | g0005 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18986 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18987 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18987 | hp2 | a0005 | c0004 | t0001 | g0005 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18989 | hp1 | a0010 | c0013 | t0001 | g0029 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18989 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18990 | hp1 | a0001 | c0016 | t0001 | g0031 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18992 | hp1 | a0004 | c0003 | t0001 | g0040 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18992 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18993 | hp1 | a0004 | c0003 | t0001 | g0003 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18994 | hp1 | a0004 | c0003 | t0001 | g0098 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18999 | hp1 | a0010 | c0013 | t0001 | g0029 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA18999 | hp2 | a0005 | c0004 | t0001 | g0005 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19000 | hp2 | a0004 | c0003 | t0001 | g0021 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19003 | hp2 | a0004 | c0027 | t0001 | g0100 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19004 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19005 | hp1 | a0005 | c0004 | t0001 | g0005 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19010 | hp2 | a0004 | c0003 | t0001 | g0003 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19011 | hp1 | a0007 | c0012 | t0001 | g0010 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19011 | hp2 | a0005 | c0004 | t0001 | g0005 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19030 | hp1 | a0003 | c0009 | t0008 | g0104 | AFR | LWK | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19030 | hp2 | a0005 | c0004 | t0001 | g0032 | AFR | LWK | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19043 | hp1 | a0003 | c0011 | t0002 | g0016 | AFR | LWK | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19043 | hp2 | a0002 | c0002 | t0001 | g0069 | AFR | LWK | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19056 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19057 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19060 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19062 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19063 | hp1 | a0007 | c0012 | t0001 | g0010 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19063 | hp2 | a0007 | c0012 | t0001 | g0010 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19064 | hp2 | a0004 | c0003 | t0001 | g0021 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19065 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19068 | hp2 | a0013 | c0018 | t0001 | g0030 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19070 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19075 | hp1 | a0004 | c0003 | t0001 | g0040 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19082 | hp1 | a0002 | c0031 | t0001 | g0102 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19087 | hp1 | a0004 | c0003 | t0001 | g0003 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19088 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19089 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19089 | hp2 | a0001 | c0016 | t0001 | g0072 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19240 | hp1 | a0009 | c0017 | t0002 | g0023 | AFR | YRI | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA19240 | hp2 | a0003 | c0005 | t0002 | g0113 | AFR | YRI | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | GIH | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA20905 | hp2 | a0002 | c0008 | t0002 | g0015 | SAS | GIH | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG01123 | hp2 | a0002 | c0010 | t0001 | g0017 | AMR | CLM | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02109 | hp1 | a0009 | c0017 | t0005 | g0120 | AFR | ACB | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02486 | hp1 | a0003 | c0009 | t0002 | g0105 | AFR | ACB | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG02559 | hp2 | a0004 | c0003 | t0001 | g0003 | AFR | ACB | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03471 | hp1 | a0002 | c0006 | t0002 | g0045 | AFR | MSL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG03471 | hp2 | a0003 | c0005 | t0002 | g0007 | AFR | MSL | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG06807 | hp1 | a0009 | c0017 | t0002 | g0023 | AFR | USA | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
HG06807 | hp2 | a0003 | c0005 | t0002 | g0007 | AFR | USA | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
NA21309 | hp2 | a0002 | c0002 | t0001 | g0068 | AFR | LWK | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
homoSapiens | chm13v2 | a0004 | c0003 | t0001 | g0003 | REF | REF | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | TRIM7_chr5_181188924_181210196 | TRIM7 | chr5 | 181188924 | 181210196 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:181195167 | C | G | 1 | a0009 | 1 | HG02109.hp1 | stop_lost | HIGH | c.1535G>C | p.Ter512Serext*? | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 7/7 | 1621/2864 | 1535/1536 | 512/511 | chr5 | 181195167 | |||
chr5:181195194 | G | A | 1 | a0011 | 2 | HG01243.hp2 HG02630.hp1 |
missense_variant | MODERATE | c.1508C>T | p.Thr503Met | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 7/7 | 1594/2864 | 1508/1536 | 503/511 | chr5 | 181195194 | |||
chr5:181195354 | G | A | 1 | a0013 | 2 | HG03688.hp2 NA19068.hp2 |
missense_variant | MODERATE | c.1348C>T | p.Arg450Trp | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 7/7 | 1434/2864 | 1348/1536 | 450/511 | chr5 | 181195354 | |||
chr5:181195609 | G | T | 1 | a0015 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.1093C>A | p.Arg365Ser | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 7/7 | 1179/2864 | 1093/1536 | 365/511 | chr5 | 181195609 | |||
chr5:181195615 | C | T | 8 | a0004 a0005 a0010 others(5): Show |
75 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(72): Show |
missense_variant | MODERATE | c.1087G>A | p.Gly363Ser | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 7/7 | 1173/2864 | 1087/1536 | 363/511 | chr5 | 181195615 | |||
chr5:181199104 | G | A | 1 | a0008 | 4 | HG00544.hp1 HG02132.hp2 NA18943.hp2 others(1): Show |
missense_variant | MODERATE | c.863C>T | p.Thr288Met | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 4/7 | 949/2864 | 863/1536 | 288/511 | chr5 | 181199104 | |||
chr5:181199899 | G | C | 1 | a0009 | 4 | HG02109.hp1 HG02976.hp1 HG06807.hp1 others(1): Show |
missense_variant | MODERATE | c.801C>G | p.Ser267Arg | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 3/7 | 887/2864 | 801/1536 | 267/511 | chr5 | 181199899 | |||
chr5:181199927 | A | G | 11 | a0002 a0003 a0004 others(8): Show |
214 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(211): Show |
missense_variant | MODERATE | c.773T>C | p.Val258Ala | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 3/7 | 859/2864 | 773/1536 | 258/511 | chr5 | 181199927 | |||
chr5:181200027 | C | T | 1 | a0009 | 4 | HG02109.hp1 HG02976.hp1 HG06807.hp1 others(1): Show |
missense_variant | MODERATE | c.673G>A | p.Ala225Thr | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 3/7 | 759/2864 | 673/1536 | 225/511 | chr5 | 181200027 | |||
chr5:181200048 | C | T | 1 | a0006 | 10 | HG01167.hp2 HG02257.hp2 HG02723.hp2 others(7): Show |
missense_variant | MODERATE | c.652G>A | p.Ala218Thr | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 3/7 | 738/2864 | 652/1536 | 218/511 | chr5 | 181200048 | |||
chr5:181204762 | C | G | 1 | a0017 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.349G>C | p.Gly117Arg | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 1/7 | 435/2864 | 349/1536 | 117/511 | chr5 | 181204762 | |||
chr5:181204828 | G | C | 5 | a0004 a0011 a0012 others(2): Show |
39 | HG00099.hp1 HG00544.hp2 HG00621.hp2 others(36): Show |
missense_variant | MODERATE | c.283C>G | p.Gln95Glu | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 1/7 | 369/2864 | 283/1536 | 95/511 | chr5 | 181204828 | |||
chr5:181204894 | G | A | 3 | a0003 a0009 a0016 |
40 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(37): Show |
missense_variant | MODERATE | c.217C>T | p.Pro73Ser | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 1/7 | 303/2864 | 217/1536 | 73/511 | chr5 | 181204894 | |||
chr5:181205058 | G | A | 1 | a0007 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.53C>T | p.Ala18Val | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 1/7 | 139/2864 | 53/1536 | 18/511 | chr5 | 181205058 | |||
chr5:181205059 | C | A | 1 | a0007 | 5 | HG01256.hp1 HG03831.hp2 NA19011.hp1 others(2): Show |
missense_variant | MODERATE | c.52G>T | p.Ala18Ser | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 1/7 | 138/2864 | 52/1536 | 18/511 | chr5 | 181205059 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:181195223 | G | A | 1 | a0003c0011 | 5 | HG02055.hp1 HG02145.hp2 HG02280.hp1 others(2): Show |
synonymous_variant | LOW | c.1479C>T | p.Arg493Arg | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 7/7 | 1565/2864 | 1479/1536 | 493/511 | chr5 | 181195223 | |||
chr5:181195454 | C | T | 1 | a0004c0027 | 1 | NA19003.hp2 | synonymous_variant | LOW | c.1248G>A | p.Glu416Glu | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 7/7 | 1334/2864 | 1248/1536 | 416/511 | chr5 | 181195454 | |||
chr5:181198210 | G | T | 1 | a0011c0019 | 2 | HG01243.hp2 HG02630.hp1 |
synonymous_variant | LOW | c.997C>A | p.Arg333Arg | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/7 | 1083/2864 | 997/1536 | 333/511 | chr5 | 181198210 | |||
chr5:181204760 | C | T | 1 | a0001c0023 | 1 | HG03654.hp2 | synonymous_variant | LOW | c.351G>A | p.Gly117Gly | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 1/7 | 437/2864 | 351/1536 | 117/511 | chr5 | 181204760 | |||
chr5:181204778 | A | G | 11 | a0001c0016 a0001c0022 a0002c0002 others(8): Show |
115 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
synonymous_variant | LOW | c.333T>C | p.Ala111Ala | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 1/7 | 419/2864 | 333/1536 | 111/511 | chr5 | 181204778 | |||
chr5:181204778 | A | T | 4 | a0002c0010 a0003c0009 a0003c0011 others(1): Show |
18 | HG01123.hp2 HG01261.hp2 HG01516.hp2 others(15): Show |
synonymous_variant | LOW | c.333T>A | p.Ala111Ala | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 1/7 | 419/2864 | 333/1536 | 111/511 | chr5 | 181204778 | |||
chr5:181204817 | T | C | 23 | a0001c0016 a0002c0002 a0002c0008 others(20): Show |
209 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(206): Show |
synonymous_variant | LOW | c.294A>G | p.Ala98Ala | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 1/7 | 380/2864 | 294/1536 | 98/511 | chr5 | 181204817 | |||
chr5:181204850 | G | C | 1 | a0002c0031 | 1 | NA19082.hp1 | synonymous_variant | LOW | c.261C>G | p.Pro87Pro | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 1/7 | 347/2864 | 261/1536 | 87/511 | chr5 | 181204850 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:181193942 | T | TC | 17 | a0001c0022t0002 a0002c0002t0002 a0002c0006t0002 others(14): Show |
59 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1223_*1224insG | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 7/7 | 1223 | chr5 | 181193942 | ||||||
chr5:181193978 | C | T | 17 | a0001c0022t0002 a0002c0002t0002 a0002c0006t0002 others(14): Show |
59 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1188G>A | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 7/7 | 1188 | chr5 | 181193978 | ||||||
chr5:181194088 | A | G | 1 | a0016c0032t0009 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1078T>C | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 7/7 | 1078 | chr5 | 181194088 | ||||||
chr5:181194118 | C | G | 17 | a0001c0022t0002 a0002c0002t0002 a0002c0006t0002 others(14): Show |
59 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1048G>C | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 7/7 | 1048 | chr5 | 181194118 | ||||||
chr5:181194410 | C | T | 17 | a0001c0022t0002 a0002c0002t0002 a0002c0006t0002 others(14): Show |
59 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*756G>A | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 7/7 | 756 | chr5 | 181194410 | ||||||
chr5:181194472 | CAG | C | 17 | a0001c0022t0002 a0002c0002t0002 a0002c0006t0002 others(14): Show |
59 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*692_*693delCT | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 7/7 | 692 | chr5 | 181194472 | ||||||
chr5:181194561 | C | T | 2 | a0003c0005t0004 a0003c0009t0008 |
4 | HG02809.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*605G>A | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 7/7 | 605 | chr5 | 181194561 | ||||||
chr5:181194585 | C | T | 1 | a0003c0009t0007 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*581G>A | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 7/7 | 581 | chr5 | 181194585 | ||||||
chr5:181194595 | A | C | 17 | a0001c0022t0002 a0002c0002t0002 a0002c0006t0002 others(14): Show |
59 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*571T>G | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 7/7 | 571 | chr5 | 181194595 | ||||||
chr5:181194636 | G | T | 17 | a0001c0022t0002 a0002c0002t0002 a0002c0006t0002 others(14): Show |
59 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*530C>A | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 7/7 | 530 | chr5 | 181194636 | ||||||
chr5:181194771 | G | A | 1 | a0002c0002t0010 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*395C>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 7/7 | 395 | chr5 | 181194771 | ||||||
chr5:181194982 | C | G | 3 | a0002c0006t0003 a0003c0005t0006 a0017c0021t0003 |
11 | HG01891.hp2 HG02258.hp2 HG02572.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*184G>C | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 7/7 | 184 | chr5 | 181194982 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:181195758 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1025-81A>G | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181195758 | |||||||
chr5:181195810 | G | C | 2 | a0006c0007t0002g0019 a0006c0007t0002g0083 |
4 | HG02922.hp1 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1025-133C>G | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181195810 | |||||||
chr5:181195841 | G | A | 1 | a0003c0005t0006g0112 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1025-164C>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181195841 | |||||||
chr5:181195913 | C | A | 15 | a0001c0001t0001g0009 a0003c0005t0002g0114 a0004c0003t0001g0003 others(12): Show |
45 | HG00099.hp1 HG00544.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.1025-236G>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181195913 | |||||||
chr5:181196021 | G | A | 28 | a0002c0002t0002g0067 a0002c0006t0002g0045 a0002c0010t0002g0064 others(25): Show |
49 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.1025-344C>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181196021 | |||||||
chr5:181196040 | A | G | 2 | a0002c0006t0003g0006 a0002c0006t0003g0046 |
9 | HG01891.hp2 HG02258.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1025-363T>C | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181196040 | |||||||
chr5:181196051 | T | C | 1 | a0002c0002t0001g0069 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1025-374A>G | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181196051 | |||||||
chr5:181196104 | A | G | 12 | a0002c0008t0001g0092 a0003c0009t0002g0105 a0003c0009t0008g0104 others(9): Show |
16 | HG00735.hp1 HG01952.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1025-427T>C | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181196104 | |||||||
chr5:181196120 | G | A | 1 | a0001c0001t0001g0025 | 2 | NA18959.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.1025-443C>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181196120 | |||||||
chr5:181196195 | C | T | 1 | a0002c0002t0001g0068 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1025-518G>A | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181196195 | |||||||
chr5:181196245 | C | T | 1 | a0010c0013t0001g0059 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1025-568G>A | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181196245 | |||||||
chr5:181196320 | T | C | 10 | a0003c0005t0002g0007 a0003c0005t0002g0022 a0003c0005t0002g0113 others(7): Show |
20 | HG01243.hp1 HG01884.hp2 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.1025-643A>G | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181196320 | |||||||
chr5:181196367 | C | T | 2 | a0002c0010t0002g0064 a0003c0009t0002g0107 |
2 | HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1025-690G>A | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181196367 | |||||||
chr5:181196409 | C | G | 5 | a0006c0007t0002g0014 a0006c0007t0002g0019 a0006c0007t0002g0083 others(2): Show |
10 | HG01167.hp2 HG02257.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1025-732G>C | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181196409 | |||||||
chr5:181196489 | T | C | 1 | a0003c0005t0002g0113 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1025-812A>G | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181196489 | |||||||
chr5:181196680 | G | C | 1 | a0003c0005t0002g0115 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1025-1003C>G | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181196680 | |||||||
chr5:181196939 | G | C | 1 | a0003c0009t0002g0110 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1024+1244C>G | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181196939 | |||||||
chr5:181196989 | G | A | 1 | a0001c0001t0001g0026 | 2 | HG01109.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1024+1194C>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181196989 | |||||||
chr5:181197069 | G | A | 9 | a0002c0008t0001g0092 a0005c0004t0001g0032 a0005c0004t0001g0033 others(6): Show |
13 | HG00735.hp1 HG01952.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1024+1114C>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181197069 | |||||||
chr5:181197087 | C | A | 1 | a0005c0004t0001g0088 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1024+1096G>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181197087 | |||||||
chr5:181197135 | G | A | 4 | a0002c0008t0002g0015 a0002c0008t0002g0020 a0005c0015t0001g0070 others(1): Show |
10 | HG00423.hp2 HG01069.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.1024+1048C>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181197135 | |||||||
chr5:181197148 | C | CA | 17 | a0001c0016t0001g0072 a0002c0002t0001g0068 a0002c0008t0001g0092 others(14): Show |
31 | HG00408.hp1 HG01257.hp2 HG01952.hp1 others(28): Show |
intron_variant | MODIFIER | c.1024+1034dupT | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181197148 | |||||||
chr5:181197148 | CA | C | 30 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0002c0002t0002g0067 others(27): Show |
44 | HG01167.hp2 HG01884.hp1 HG02055.hp1 others(41): Show |
intron_variant | MODIFIER | c.1024+1034delT | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181197148 | |||||||
chr5:181197213 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1024+970C>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181197213 | |||||||
chr5:181197374 | C | T | 1 | a0003c0005t0002g0113 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1024+809G>A | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181197374 | |||||||
chr5:181197414 | G | C | 31 | a0002c0002t0002g0067 a0002c0006t0002g0045 a0002c0008t0002g0015 others(28): Show |
56 | HG00423.hp2 HG01069.hp1 HG01106.hp2 others(53): Show |
intron_variant | MODIFIER | c.1024+769C>G | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181197414 | |||||||
chr5:181197483 | G | A | 1 | a0005c0004t0001g0086 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1024+700C>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181197483 | |||||||
chr5:181197486 | A | G | 2 | a0005c0015t0001g0070 a0013c0018t0001g0030 |
3 | HG00423.hp2 HG03688.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1024+697T>C | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181197486 | |||||||
chr5:181197516 | A | C | 31 | a0002c0002t0002g0067 a0002c0006t0002g0045 a0002c0010t0002g0064 others(28): Show |
52 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(49): Show |
intron_variant | MODIFIER | c.1024+667T>G | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181197516 | |||||||
chr5:181197518 | C | T | 2 | a0002c0002t0002g0067 a0003c0020t0002g0042 |
3 | HG02280.hp2 HG02647.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1024+665G>A | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181197518 | |||||||
chr5:181197520 | G | A | 31 | a0002c0002t0002g0067 a0002c0006t0002g0045 a0002c0010t0002g0064 others(28): Show |
52 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(49): Show |
intron_variant | MODIFIER | c.1024+663C>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181197520 | |||||||
chr5:181197569 | A | G | 31 | a0002c0002t0002g0067 a0002c0006t0002g0045 a0002c0010t0002g0064 others(28): Show |
52 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(49): Show |
intron_variant | MODIFIER | c.1024+614T>C | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181197569 | |||||||
chr5:181197570 | G | T | 31 | a0002c0002t0002g0067 a0002c0006t0002g0045 a0002c0010t0002g0064 others(28): Show |
52 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(49): Show |
intron_variant | MODIFIER | c.1024+613C>A | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181197570 | |||||||
chr5:181197590 | T | A | 31 | a0002c0002t0002g0067 a0002c0006t0002g0045 a0002c0010t0002g0064 others(28): Show |
52 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(49): Show |
intron_variant | MODIFIER | c.1024+593A>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181197590 | |||||||
chr5:181197592 | C | G | 31 | a0002c0002t0002g0067 a0002c0006t0002g0045 a0002c0010t0002g0064 others(28): Show |
52 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(49): Show |
intron_variant | MODIFIER | c.1024+591G>C | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181197592 | |||||||
chr5:181197631 | G | A | 2 | a0002c0006t0003g0006 a0002c0006t0003g0046 |
9 | HG01891.hp2 HG02258.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1024+552C>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181197631 | |||||||
chr5:181197722 | G | A | 15 | a0002c0008t0001g0092 a0005c0004t0001g0005 a0005c0004t0001g0032 others(12): Show |
29 | HG00408.hp1 HG00735.hp1 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.1024+461C>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181197722 | |||||||
chr5:181197917 | G | A | 2 | a0002c0008t0002g0015 a0002c0008t0002g0020 |
7 | HG01069.hp1 HG01106.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1024+266C>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181197917 | |||||||
chr5:181198046 | G | A | 1 | a0016c0032t0009g0111 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1024+137C>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181198046 | |||||||
chr5:181198068 | A | C | 9 | a0002c0008t0001g0092 a0005c0004t0001g0032 a0005c0004t0001g0033 others(6): Show |
13 | HG00735.hp1 HG01952.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1024+115T>G | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 6/6 | chr5 | 181198068 | |||||||
chr5:181198254 | G | A | 14 | a0004c0003t0001g0003 a0004c0003t0001g0021 a0004c0003t0001g0036 others(11): Show |
38 | HG00099.hp1 HG00544.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.989-36C>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 5/6 | chr5 | 181198254 | |||||||
chr5:181198373 | G | A | 4 | a0006c0007t0002g0019 a0006c0007t0002g0083 a0006c0007t0002g0084 others(1): Show |
6 | HG02257.hp2 HG02922.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.989-155C>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 5/6 | chr5 | 181198373 | |||||||
chr5:181198487 | C | A | 14 | a0002c0002t0001g0002 a0002c0002t0001g0018 a0002c0002t0001g0073 others(11): Show |
73 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.988+203G>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 5/6 | chr5 | 181198487 | |||||||
chr5:181198494 | G | C | 55 | a0002c0002t0001g0068 a0002c0002t0001g0069 a0002c0002t0002g0067 others(52): Show |
103 | HG00408.hp1 HG00423.hp2 HG00735.hp1 others(100): Show |
intron_variant | MODIFIER | c.988+196C>G | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 5/6 | chr5 | 181198494 | |||||||
chr5:181198672 | T | C | 52 | a0002c0002t0001g0068 a0002c0002t0002g0067 a0002c0006t0002g0045 others(49): Show |
93 | HG00408.hp1 HG00423.hp2 HG00735.hp1 others(90): Show |
intron_variant | MODIFIER | c.988+18A>G | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 5/6 | chr5 | 181198672 | |||||||
chr5:181199030 | G | A | 13 | a0002c0002t0001g0002 a0002c0002t0001g0018 a0002c0002t0001g0073 others(10): Show |
72 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.872+65C>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 4/6 | chr5 | 181199030 | |||||||
chr5:181199036 | G | C | 36 | a0001c0001t0001g0056 a0002c0002t0002g0067 a0002c0006t0002g0045 others(33): Show |
61 | HG00423.hp2 HG01069.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.872+59C>G | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 4/6 | chr5 | 181199036 | |||||||
chr5:181199224 | A | G | 49 | a0002c0002t0002g0067 a0002c0006t0002g0045 a0002c0008t0001g0092 others(46): Show |
89 | HG00408.hp1 HG00423.hp2 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.850-107T>C | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 3/6 | chr5 | 181199224 | |||||||
chr5:181199242 | G | A | 1 | a0001c0001t0001g0013 | 4 | HG01070.hp1 HG01071.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.850-125C>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 3/6 | chr5 | 181199242 | |||||||
chr5:181199254 | C | T | 35 | a0002c0002t0002g0067 a0002c0006t0002g0045 a0002c0008t0002g0015 others(32): Show |
62 | HG00423.hp2 HG01069.hp1 HG01106.hp2 others(59): Show |
intron_variant | MODIFIER | c.850-137G>A | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 3/6 | chr5 | 181199254 | |||||||
chr5:181199305 | G | A | 31 | a0002c0002t0002g0067 a0002c0006t0002g0045 a0002c0010t0002g0064 others(28): Show |
52 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(49): Show |
intron_variant | MODIFIER | c.850-188C>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 3/6 | chr5 | 181199305 | |||||||
chr5:181199313 | C | T | 31 | a0002c0002t0002g0067 a0002c0006t0002g0045 a0002c0010t0002g0064 others(28): Show |
52 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(49): Show |
intron_variant | MODIFIER | c.850-196G>A | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 3/6 | chr5 | 181199313 | |||||||
chr5:181199341 | G | A | 35 | a0002c0002t0002g0067 a0002c0006t0002g0045 a0002c0008t0002g0015 others(32): Show |
62 | HG00423.hp2 HG01069.hp1 HG01106.hp2 others(59): Show |
intron_variant | MODIFIER | c.850-224C>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 3/6 | chr5 | 181199341 | |||||||
chr5:181199505 | A | G | 84 | a0002c0002t0001g0002 a0002c0002t0001g0018 a0002c0002t0001g0068 others(81): Show |
215 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(212): Show |
intron_variant | MODIFIER | c.849+346T>C | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 3/6 | chr5 | 181199505 | |||||||
chr5:181199550 | G | T | 14 | a0004c0003t0001g0003 a0004c0003t0001g0021 a0004c0003t0001g0036 others(11): Show |
38 | HG00099.hp1 HG00544.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.849+301C>A | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 3/6 | chr5 | 181199550 | |||||||
chr5:181199596 | G | A | 1 | a0002c0002t0001g0068 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.849+255C>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 3/6 | chr5 | 181199596 | |||||||
chr5:181199643 | G | A | 4 | a0002c0008t0002g0015 a0002c0008t0002g0020 a0005c0015t0001g0070 others(1): Show |
10 | HG00423.hp2 HG01069.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.849+208C>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 3/6 | chr5 | 181199643 | |||||||
chr5:181199654 | T | C | 4 | a0002c0008t0002g0015 a0002c0008t0002g0020 a0005c0015t0001g0070 others(1): Show |
10 | HG00423.hp2 HG01069.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.849+197A>G | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 3/6 | chr5 | 181199654 | |||||||
chr5:181199686 | T | C | 70 | a0002c0002t0001g0068 a0002c0002t0001g0069 a0002c0002t0002g0067 others(67): Show |
142 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.849+165A>G | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 3/6 | chr5 | 181199686 | |||||||
chr5:181200110 | A | T | 1 | a0002c0002t0001g0081 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.619-29T>A | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181200110 | |||||||
chr5:181200111 | C | T | 1 | a0002c0002t0001g0081 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.619-30G>A | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181200111 | |||||||
chr5:181200112 | T | A | 1 | a0002c0002t0001g0081 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.619-31A>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181200112 | |||||||
chr5:181200174 | C | A | 1 | a0001c0001t0001g0026 | 2 | HG01109.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.619-93G>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181200174 | |||||||
chr5:181200223 | C | T | 2 | a0002c0002t0002g0067 a0003c0020t0002g0042 |
3 | HG02280.hp2 HG02647.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.619-142G>A | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181200223 | |||||||
chr5:181200224 | G | A | 34 | a0002c0002t0002g0067 a0002c0006t0002g0045 a0002c0008t0002g0015 others(31): Show |
61 | HG00423.hp2 HG01069.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.619-143C>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181200224 | |||||||
chr5:181200250 | T | C | 35 | a0002c0002t0001g0068 a0002c0002t0001g0069 a0002c0006t0003g0006 others(32): Show |
80 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.619-169A>G | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181200250 | |||||||
chr5:181200273 | A | C | 1 | a0011c0019t0001g0038 | 2 | HG01243.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.619-192T>G | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181200273 | |||||||
chr5:181200615 | C | T | 2 | a0009c0017t0002g0023 a0009c0017t0005g0120 |
4 | HG02109.hp1 HG02976.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.619-534G>A | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181200615 | |||||||
chr5:181200670 | C | T | 1 | a0003c0009t0007g0106 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.619-589G>A | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181200670 | |||||||
chr5:181200814 | G | T | 2 | a0005c0015t0001g0070 a0013c0018t0001g0030 |
3 | HG00423.hp2 HG03688.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.619-733C>A | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181200814 | |||||||
chr5:181200917 | C | T | 19 | a0003c0005t0002g0007 a0003c0005t0002g0022 a0003c0005t0002g0113 others(16): Show |
37 | HG01167.hp2 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.619-836G>A | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181200917 | |||||||
chr5:181200931 | T | C | 1 | a0003c0005t0006g0112 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.619-850A>G | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181200931 | |||||||
chr5:181200936 | T | C | 55 | a0002c0002t0001g0068 a0002c0002t0001g0069 a0002c0002t0002g0067 others(52): Show |
103 | HG00408.hp1 HG00423.hp2 HG00735.hp1 others(100): Show |
intron_variant | MODIFIER | c.619-855A>G | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181200936 | |||||||
chr5:181201064 | C | T | 9 | a0002c0008t0001g0092 a0005c0004t0001g0032 a0005c0004t0001g0033 others(6): Show |
13 | HG00735.hp1 HG01952.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.619-983G>A | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181201064 | |||||||
chr5:181201155 | T | C | 2 | a0009c0017t0002g0023 a0009c0017t0005g0120 |
4 | HG02109.hp1 HG02976.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.619-1074A>G | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181201155 | |||||||
chr5:181201173 | T | C | 4 | a0002c0008t0002g0015 a0002c0008t0002g0020 a0005c0015t0001g0070 others(1): Show |
10 | HG00423.hp2 HG01069.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.619-1092A>G | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181201173 | |||||||
chr5:181201385 | A | T | 1 | a0002c0002t0001g0073 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.619-1304T>A | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181201385 | |||||||
chr5:181201386 | C | A | 1 | a0002c0002t0001g0073 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.619-1305G>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181201386 | |||||||
chr5:181201432 | A | G | 81 | a0002c0002t0001g0002 a0002c0002t0001g0018 a0002c0002t0001g0068 others(78): Show |
205 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.619-1351T>C | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181201432 | |||||||
chr5:181201623 | C | G | 1 | a0002c0002t0001g0018 | 3 | HG00438.hp1 NA18940.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.619-1542G>C | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181201623 | |||||||
chr5:181201687 | A | C | 1 | a0004c0003t0001g0096 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.619-1606T>G | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181201687 | |||||||
chr5:181201731 | A | C | 1 | a0003c0005t0006g0112 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.619-1650T>G | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181201731 | |||||||
chr5:181201779 | G | A | 1 | a0005c0015t0001g0070 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.619-1698C>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181201779 | |||||||
chr5:181201826 | A | G | 29 | a0002c0002t0001g0002 a0002c0002t0001g0018 a0002c0002t0001g0073 others(26): Show |
112 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.618+1719T>C | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181201826 | |||||||
chr5:181201850 | G | C | 2 | a0002c0006t0003g0006 a0002c0006t0003g0046 |
9 | HG01891.hp2 HG02258.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.618+1695C>G | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181201850 | |||||||
chr5:181201946 | G | A | 2 | a0002c0002t0002g0067 a0003c0020t0002g0042 |
3 | HG02280.hp2 HG02647.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.618+1599C>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181201946 | |||||||
chr5:181201989 | G | A | 2 | a0004c0003t0001g0039 a0004c0003t0001g0098 |
3 | HG02155.hp2 NA18947.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.618+1556C>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181201989 | |||||||
chr5:181202178 | C | CT | 6 | a0001c0001t0001g0008 a0005c0004t0001g0005 a0005c0004t0001g0032 others(3): Show |
23 | HG00408.hp1 HG01257.hp2 HG02015.hp1 others(20): Show |
intron_variant | MODIFIER | c.618+1366dupA | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181202178 | |||||||
chr5:181202178 | CT | C | 38 | a0001c0001t0001g0012 a0001c0001t0001g0056 a0001c0016t0001g0072 others(35): Show |
74 | HG00099.hp1 HG00544.hp2 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.618+1366delA | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181202178 | |||||||
chr5:181202178 | CTT | C | 30 | a0002c0002t0001g0002 a0002c0002t0001g0018 a0002c0002t0001g0073 others(27): Show |
103 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.618+1365_618+1366d others(4): Show |
TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181202178 | |||||||
chr5:181202222 | C | A | 1 | a0002c0002t0001g0068 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.618+1323G>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181202222 | |||||||
chr5:181202342 | G | T | 1 | a0005c0004t0001g0086 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.618+1203C>A | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181202342 | |||||||
chr5:181202421 | C | T | 2 | a0004c0003t0001g0036 a0014c0029t0001g0095 |
3 | HG01255.hp2 HG01361.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.618+1124G>A | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181202421 | |||||||
chr5:181202433 | C | T | 12 | a0002c0006t0002g0045 a0002c0010t0002g0064 a0003c0005t0002g0118 others(9): Show |
15 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.618+1112G>A | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181202433 | |||||||
chr5:181202569 | CT | C | 67 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0002c0002t0001g0002 others(64): Show |
184 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.618+975delA | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181202569 | |||||||
chr5:181202598 | G | A | 2 | a0002c0002t0002g0067 a0003c0020t0002g0042 |
3 | HG02280.hp2 HG02647.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.618+947C>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181202598 | |||||||
chr5:181202606 | T | G | 66 | a0001c0001t0001g0058 a0001c0016t0001g0071 a0002c0002t0001g0002 others(63): Show |
176 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.618+939A>C | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181202606 | |||||||
chr5:181202627 | C | T | 1 | a0017c0021t0003g0043 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.618+918G>A | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181202627 | |||||||
chr5:181202629 | C | T | 1 | a0017c0021t0003g0043 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.618+916G>A | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181202629 | |||||||
chr5:181202636 | G | A | 1 | a0004c0003t0001g0099 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.618+909C>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181202636 | |||||||
chr5:181202649 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0051 |
3 | HG01109.hp1 HG01496.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.618+896G>A | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181202649 | |||||||
chr5:181202668 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.618+877T>C | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181202668 | |||||||
chr5:181202669 | C | T | 1 | a0001c0001t0001g0004 | 12 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.618+876G>A | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181202669 | |||||||
chr5:181202691 | G | C | 1 | a0001c0001t0001g0050 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.618+854C>G | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181202691 | |||||||
chr5:181202711 | C | T | 2 | a0001c0001t0001g0050 a0001c0016t0001g0071 |
2 | HG01106.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.618+834G>A | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181202711 | |||||||
chr5:181202715 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.618+830G>A | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181202715 | |||||||
chr5:181202753 | CA | C | 12 | a0002c0002t0001g0068 a0002c0006t0003g0006 a0003c0005t0002g0007 others(9): Show |
29 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.618+791delT | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181202753 | |||||||
chr5:181202766 | G | A | 1 | a0001c0001t0001g0027 | 2 | HG00673.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.618+779C>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181202766 | |||||||
chr5:181202779 | C | T | 5 | a0001c0001t0001g0028 a0001c0001t0001g0060 a0010c0013t0001g0029 others(2): Show |
7 | NA18612.hp2 NA18953.hp1 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.618+766G>A | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181202779 | |||||||
chr5:181202785 | T | C | 5 | a0001c0001t0001g0028 a0001c0001t0001g0060 a0010c0013t0001g0029 others(2): Show |
7 | NA18612.hp2 NA18953.hp1 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.618+760A>G | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181202785 | |||||||
chr5:181202806 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.618+739G>A | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181202806 | |||||||
chr5:181202812 | C | A | 68 | a0001c0001t0001g0060 a0002c0002t0001g0002 a0002c0002t0001g0018 others(65): Show |
179 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.618+733G>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181202812 | |||||||
chr5:181202813 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.618+732G>A | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181202813 | |||||||
chr5:181202843 | C | T | 4 | a0002c0008t0002g0015 a0002c0008t0002g0020 a0005c0015t0001g0070 others(1): Show |
10 | HG00423.hp2 HG01069.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.618+702G>A | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181202843 | |||||||
chr5:181202897 | C | T | 6 | a0005c0004t0001g0005 a0005c0004t0001g0085 a0005c0004t0001g0086 others(3): Show |
16 | HG00408.hp1 HG01257.hp2 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.618+648G>A | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181202897 | |||||||
chr5:181202999 | T | C | 1 | a0005c0004t0001g0085 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.618+546A>G | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181202999 | |||||||
chr5:181203076 | C | T | 1 | a0002c0002t0001g0076 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.618+469G>A | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181203076 | |||||||
chr5:181203315 | T | TTAA | 2 | a0005c0004t0001g0034 a0005c0004t0001g0093 |
3 | HG02630.hp2 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.618+227_618+229dup others(3): Show |
TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181203315 | |||||||
chr5:181203342 | T | A | 1 | a0003c0005t0002g0119 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.618+203A>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181203342 | |||||||
chr5:181203510 | A | G | 1 | a0002c0002t0001g0075 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.618+35T>C | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181203510 | |||||||
chr5:181203512 | G | C | 19 | a0002c0002t0001g0068 a0002c0002t0001g0069 a0002c0006t0003g0006 others(16): Show |
40 | HG00408.hp1 HG00735.hp1 HG01257.hp2 others(37): Show |
intron_variant | MODIFIER | c.618+33C>G | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 2/6 | chr5 | 181203512 | |||||||
chr5:181203667 | G | A | 4 | a0002c0008t0002g0015 a0002c0008t0002g0020 a0005c0015t0001g0070 others(1): Show |
10 | HG00423.hp2 HG01069.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.523-27C>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 1/6 | chr5 | 181203667 | |||||||
chr5:181203889 | G | C | 1 | a0001c0001t0001g0062 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.523-249C>G | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 1/6 | chr5 | 181203889 | |||||||
chr5:181203908 | GC | G | 10 | a0002c0002t0001g0073 a0002c0008t0001g0092 a0005c0004t0001g0032 others(7): Show |
14 | HG00735.hp1 HG01952.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.523-269delG | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 1/6 | chr5 | 181203908 | |||||||
chr5:181204121 | G | C | 29 | a0002c0002t0001g0002 a0002c0002t0001g0018 a0002c0002t0001g0073 others(26): Show |
112 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.522+468C>G | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 1/6 | chr5 | 181204121 | |||||||
chr5:181204224 | G | A | 1 | a0005c0015t0001g0082 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.522+365C>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 1/6 | chr5 | 181204224 | |||||||
chr5:181204270 | A | T | 7 | a0002c0008t0001g0092 a0005c0004t0001g0032 a0005c0004t0001g0033 others(4): Show |
10 | HG00735.hp1 HG01952.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.522+319T>A | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 1/6 | chr5 | 181204270 | |||||||
chr5:181204342 | G | A | 1 | a0001c0001t0001g0013 | 4 | HG01070.hp1 HG01071.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.522+247C>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 1/6 | chr5 | 181204342 | |||||||
chr5:181204387 | G | A | 33 | a0001c0016t0001g0031 a0001c0016t0001g0071 a0001c0016t0001g0072 others(30): Show |
117 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.522+202C>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 1/6 | chr5 | 181204387 | |||||||
chr5:181204406 | G | C | 2 | a0004c0003t0001g0021 a0004c0027t0001g0100 |
4 | NA18944.hp2 NA19000.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.522+183C>G | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 1/6 | chr5 | 181204406 | |||||||
chr5:181204433 | G | A | 17 | a0002c0002t0001g0002 a0002c0002t0001g0018 a0002c0002t0001g0073 others(14): Show |
77 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.522+156C>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 1/6 | chr5 | 181204433 | |||||||
chr5:181204481 | A | G | 5 | a0006c0007t0002g0014 a0006c0007t0002g0019 a0006c0007t0002g0083 others(2): Show |
10 | HG01167.hp2 HG02257.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.522+108T>C | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 1/6 | chr5 | 181204481 | |||||||
chr5:181204497 | C | G | 14 | a0002c0008t0002g0020 a0004c0003t0001g0003 a0004c0003t0001g0021 others(11): Show |
39 | HG00099.hp1 HG00544.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.522+92G>C | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 1/6 | chr5 | 181204497 | |||||||
chr5:181204498 | G | C | 1 | a0001c0001t0001g0063 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.522+91C>G | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 1/6 | chr5 | 181204498 | |||||||
chr5:181204534 | G | A | 2 | a0009c0017t0002g0023 a0009c0017t0005g0120 |
4 | HG02109.hp1 HG02976.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.522+55C>T | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 1/6 | chr5 | 181204534 | |||||||
chr5:181204544 | CA | C | 36 | a0002c0010t0002g0064 a0003c0005t0002g0007 a0003c0005t0002g0022 others(33): Show |
67 | HG00408.hp1 HG01167.hp2 HG01243.hp1 others(64): Show |
intron_variant | MODIFIER | c.522+44delT | TRIM7 | ENSG00000146054.18 | transcript | ENST00000274773.12 | protein_coding | 1/6 | chr5 | 181204544 |