Item | Value |
---|---|
geneid | 51091 |
ensemblid | ENSG00000109618.13 |
hgncid | 30605 |
symbol | SEPSECS |
name | Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase |
refseq_nuc | NM_016955.4 |
refseq_prot | NP_058651.3 |
ensembl_nuc | ENST00000382103.7 |
ensembl_prot | ENSP00000371535.2 |
mane_status | MANE Select |
chr | chr4 |
start | 25120014 |
end | 25160449 |
strand | - |
ver | v1.2 |
region | chr4:25120014-25160449 |
region5000 | chr4:25115014-25165449 |
regionname0 | SEPSECS_chr4_25120014_25160449 |
regionname5000 | SEPSECS_chr4_25115014_25165449 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 501 | 387 | 74 | 71 | 186 | 13 | 41 | 143 | SEPSECS_chr4_25115014_25165449 | SEPSECS | MNRES others(496): Show |
chr4 | 25115014 | 25165449 |
a0002 | 0/0 | 501 | 61 | 16 | 10 | 27 | 1 | 7 | 24 | SEPSECS_chr4_25115014_25165449 | SEPSECS | MNRES others(496): Show |
chr4 | 25115014 | 25165449 |
a0003 | 0/0 | 501 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | MNRES others(496): Show |
chr4 | 25115014 | 25165449 |
a0004 | 0/0 | 501 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | MNRES others(496): Show |
chr4 | 25115014 | 25165449 |
a0005 | 0/0 | 501 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | MNRES others(496): Show |
chr4 | 25115014 | 25165449 |
a0006 | 0/0 | 501 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | MNRES others(496): Show |
chr4 | 25115014 | 25165449 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1503 | 385 | 74 | 71 | 184 | 13 | 41 | SEPSECS_chr4_25115014_25165449 | SEPSECS | ATGAA others(1498): Show |
chr4 | 25115014 | 25165449 | ||
a0001c0004 | 0/0 | 1503 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | ATGAA others(1498): Show |
chr4 | 25115014 | 25165449 | ||
a0001c0006 | 0/0 | 1503 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | ATGAA others(1498): Show |
chr4 | 25115014 | 25165449 | ||
a0002c0002 | 0/0 | 1503 | 61 | 16 | 10 | 27 | 1 | 7 | SEPSECS_chr4_25115014_25165449 | SEPSECS | ATGAA others(1498): Show |
chr4 | 25115014 | 25165449 | ||
a0003c0003 | 0/0 | 1503 | 5 | 4 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | ATGAA others(1498): Show |
chr4 | 25115014 | 25165449 | ||
a0004c0008 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | ATGAA others(1498): Show |
chr4 | 25115014 | 25165449 | ||
a0005c0005 | 0/0 | 1503 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | ATGAA others(1498): Show |
chr4 | 25115014 | 25165449 | ||
a0006c0007 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | ATGAA others(1498): Show |
chr4 | 25115014 | 25165449 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 5503 | 194 | 27 | 34 | 111 | 4 | 17 | SEPSECS_chr4_25115014_25165449 | SEPSECS | GAGTT others(5498): Show |
chr4 | 25115014 | 25165449 |
a0001c0001t0002 | 0/1 | 5503 | 87 | 6 | 19 | 39 | 6 | 16 | SEPSECS_chr4_25115014_25165449 | SEPSECS | GAGTT others(5498): Show |
chr4 | 25115014 | 25165449 |
a0001c0001t0003 | 0/0 | 5503 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | GAGTT others(5498): Show |
chr4 | 25115014 | 25165449 |
a0001c0001t0004 | 0/0 | 5503 | 47 | 1 | 12 | 24 | 3 | 7 | SEPSECS_chr4_25115014_25165449 | SEPSECS | GAGTT others(5498): Show |
chr4 | 25115014 | 25165449 |
a0001c0001t0005 | 0/0 | 5503 | 6 | 6 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | GAGTT others(5498): Show |
chr4 | 25115014 | 25165449 |
a0001c0001t0006 | 0/0 | 5501 | 8 | 8 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | GAGTT others(5496): Show |
chr4 | 25115014 | 25165449 |
a0001c0001t0007 | 0/0 | 5506 | 6 | 6 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | GAGTT others(5501): Show |
chr4 | 25115014 | 25165449 |
a0001c0001t0008 | 0/0 | 5503 | 5 | 4 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | GAGTT others(5498): Show |
chr4 | 25115014 | 25165449 |
a0001c0001t0009 | 0/0 | 5503 | 5 | 4 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | GAGTT others(5498): Show |
chr4 | 25115014 | 25165449 |
a0001c0001t0010 | 0/0 | 5499 | 3 | 2 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | GAGTT others(5494): Show |
chr4 | 25115014 | 25165449 |
a0001c0001t0011 | 0/0 | 5503 | 3 | 0 | 0 | 3 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | GAGTT others(5498): Show |
chr4 | 25115014 | 25165449 |
a0001c0001t0012 | 0/0 | 5503 | 2 | 0 | 0 | 2 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | GAGTT others(5498): Show |
chr4 | 25115014 | 25165449 |
a0001c0001t0013 | 0/0 | 5503 | 2 | 1 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | GAGTT others(5498): Show |
chr4 | 25115014 | 25165449 |
a0001c0001t0014 | 0/0 | 5503 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | GAGTT others(5498): Show |
chr4 | 25115014 | 25165449 |
a0001c0001t0015 | 0/0 | 5503 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | GAGTT others(5498): Show |
chr4 | 25115014 | 25165449 |
a0001c0001t0016 | 0/0 | 5503 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | GAGTT others(5498): Show |
chr4 | 25115014 | 25165449 |
a0001c0001t0017 | 0/0 | 5503 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | GAGTT others(5498): Show |
chr4 | 25115014 | 25165449 |
a0001c0001t0018 | 0/0 | 5499 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | GAGTT others(5494): Show |
chr4 | 25115014 | 25165449 |
a0001c0001t0019 | 0/0 | 5503 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | GAGTT others(5498): Show |
chr4 | 25115014 | 25165449 |
a0001c0001t0020 | 0/0 | 5503 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | GAGTT others(5498): Show |
chr4 | 25115014 | 25165449 |
a0001c0001t0021 | 0/0 | 5503 | 1 | 0 | 0 | 0 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | GAGTT others(5498): Show |
chr4 | 25115014 | 25165449 |
a0001c0001t0022 | 0/0 | 5503 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | GAGTT others(5498): Show |
chr4 | 25115014 | 25165449 |
a0001c0001t0023 | 0/0 | 5503 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | GAGTT others(5498): Show |
chr4 | 25115014 | 25165449 |
a0001c0001t0024 | 0/0 | 5503 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | GAGTT others(5498): Show |
chr4 | 25115014 | 25165449 |
a0001c0001t0025 | 0/0 | 5503 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | GAGTT others(5498): Show |
chr4 | 25115014 | 25165449 |
a0001c0001t0026 | 0/0 | 5503 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | GAGTT others(5498): Show |
chr4 | 25115014 | 25165449 |
a0001c0001t0027 | 0/0 | 5503 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | GAGTT others(5498): Show |
chr4 | 25115014 | 25165449 |
a0001c0001t0028 | 0/0 | 5503 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | GAGTT others(5498): Show |
chr4 | 25115014 | 25165449 |
a0001c0001t0029 | 0/0 | 5503 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | GAGTT others(5498): Show |
chr4 | 25115014 | 25165449 |
a0001c0004t0001 | 0/0 | 5503 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | GAGTT others(5498): Show |
chr4 | 25115014 | 25165449 |
a0001c0006t0001 | 0/0 | 5503 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | GAGTT others(5498): Show |
chr4 | 25115014 | 25165449 |
a0002c0002t0003 | 0/0 | 5503 | 61 | 16 | 10 | 27 | 1 | 7 | SEPSECS_chr4_25115014_25165449 | SEPSECS | GAGTT others(5498): Show |
chr4 | 25115014 | 25165449 |
a0003c0003t0005 | 0/0 | 5503 | 5 | 4 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | GAGTT others(5498): Show |
chr4 | 25115014 | 25165449 |
a0004c0008t0001 | 0/0 | 5503 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | GAGTT others(5498): Show |
chr4 | 25115014 | 25165449 |
a0005c0005t0001 | 0/0 | 5503 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | GAGTT others(5498): Show |
chr4 | 25115014 | 25165449 |
a0006c0007t0001 | 0/0 | 5503 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | GAGTT others(5498): Show |
chr4 | 25115014 | 25165449 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0005 | 0/0 | 7 | 0 | 3 | 3 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0013 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0157 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0001 | 0/0 | 15 | 1 | 2 | 9 | 1 | 2 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0010 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0011 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0023 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0182 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0003g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0004g0002 | 0/0 | 8 | 0 | 6 | 1 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0004g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0004g0009 | 0/0 | 5 | 0 | 0 | 3 | 1 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0004g0036 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0004g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0004g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0004g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0004g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0004g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0004g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0004g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0004g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0005g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0005g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0005g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0005g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0005g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0006g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0006g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0006g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0006g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0006g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0007g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0007g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0007g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0007g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0007g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0008g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0008g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0008g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0008g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0009g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0009g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0009g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0009g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0009g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0010g0043 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0010g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0011g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0011g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0012g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0012g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0013g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0013g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0014g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0015g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0016g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0017g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0018g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0019g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0020g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0021g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0022g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0023g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0024g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0025g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0026g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0027g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0028g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0001t0029g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0004t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0001c0006t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0002c0002t0003g0004 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0002c0002t0003g0007 | 0/0 | 6 | 0 | 2 | 2 | 0 | 2 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0002c0002t0003g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0002c0002t0003g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0002c0002t0003g0016 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0002c0002t0003g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0002c0002t0003g0058 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0002c0002t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0002c0002t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0002c0002t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0002c0002t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0002c0002t0003g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0002c0002t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0002c0002t0003g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0002c0002t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0002c0002t0003g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0002c0002t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0002c0002t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0002c0002t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0002c0002t0003g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0002c0002t0003g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0002c0002t0003g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0002c0002t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0002c0002t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0002c0002t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0002c0002t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0002c0002t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0002c0002t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0002c0002t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0002c0002t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0002c0002t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0002c0002t0003g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0002c0002t0003g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0002c0002t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0002c0002t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0002c0002t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0002c0002t0003g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0003c0003t0005g0017 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0003c0003t0005g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0003c0003t0005g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0004c0008t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0005c0005t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
a0006c0007t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0060 | EUR | GBR | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0181 | EUR | GBR | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG00140 | hp1 | a0001 | c0001 | t0004 | g0009 | EUR | GBR | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0122 | EUR | GBR | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | FIN | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG00423 | hp2 | a0001 | c0001 | t0029 | g0323 | EAS | CHS | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG00438 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | CHS | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | CHS | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG00558 | hp1 | a0001 | c0001 | t0004 | g0137 | EAS | CHS | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG00609 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | CHS | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | CHS | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0171 | AMR | PUR | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG00642 | hp2 | a0002 | c0002 | t0003 | g0007 | AMR | PUR | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG00673 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | CHS | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG00733 | hp1 | a0002 | c0002 | t0003 | g0004 | AMR | PUR | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0146 | AMR | PUR | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0161 | AMR | PUR | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG00741 | hp1 | a0001 | c0001 | t0010 | g0043 | AMR | PUR | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01069 | hp1 | a0002 | c0002 | t0003 | g0303 | AMR | PUR | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01069 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01071 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01106 | hp1 | a0001 | c0001 | t0004 | g0126 | AMR | PUR | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01109 | hp2 | a0003 | c0003 | t0005 | g0017 | AMR | PUR | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01167 | hp1 | a0001 | c0001 | t0027 | g0216 | AMR | PUR | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0183 | AMR | PUR | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01169 | hp1 | a0001 | c0001 | t0017 | g0217 | AMR | PUR | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0196 | AMR | PUR | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01243 | hp1 | a0001 | c0001 | t0013 | g0193 | AMR | PUR | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | CLM | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01256 | hp2 | a0002 | c0002 | t0003 | g0314 | AMR | CLM | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0163 | AMR | CLM | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | CLM | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | CLM | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | CLM | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01261 | hp1 | a0001 | c0001 | t0008 | g0264 | AMR | CLM | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01346 | hp1 | a0001 | c0001 | t0009 | g0213 | AMR | CLM | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01358 | hp2 | a0002 | c0002 | t0003 | g0007 | AMR | CLM | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01433 | hp1 | a0001 | c0001 | t0004 | g0072 | AMR | CLM | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0199 | AMR | CLM | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | CLM | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01515 | hp1 | a0001 | c0001 | t0004 | g0036 | EUR | IBS | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0010 | EUR | IBS | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0148 | EUR | IBS | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01517 | hp1 | a0001 | c0001 | t0004 | g0036 | EUR | IBS | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0010 | EUR | IBS | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01884 | hp1 | a0001 | c0001 | t0009 | g0188 | AFR | ACB | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01884 | hp2 | a0001 | c0001 | t0013 | g0194 | AFR | ACB | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01891 | hp1 | a0001 | c0001 | t0009 | g0192 | AFR | ACB | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01928 | hp1 | a0001 | c0001 | t0004 | g0130 | AMR | PEL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0203 | AMR | PEL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PEL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01943 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PEL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01952 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | PEL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01975 | hp2 | a0002 | c0002 | t0003 | g0016 | AMR | PEL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | PEL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01978 | hp2 | a0001 | c0001 | t0004 | g0142 | AMR | PEL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01981 | hp1 | a0002 | c0002 | t0003 | g0313 | AMR | PEL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01981 | hp2 | a0001 | c0001 | t0004 | g0140 | AMR | PEL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01993 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | PEL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | KHV | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | KHV | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02055 | hp1 | a0001 | c0001 | t0004 | g0125 | AFR | ACB | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | KHV | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | KHV | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | KHV | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02083 | hp2 | a0002 | c0002 | t0003 | g0305 | EAS | KHV | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02129 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | KHV | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | KHV | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02145 | hp1 | a0001 | c0001 | t0007 | g0271 | AFR | ACB | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02148 | hp2 | a0002 | c0002 | t0003 | g0016 | AMR | PEL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | CDX | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02155 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | CDX | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | CDX | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | CDX | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02258 | hp1 | a0002 | c0002 | t0003 | g0015 | AFR | ACB | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02258 | hp2 | a0001 | c0001 | t0005 | g0067 | AFR | ACB | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02273 | hp2 | a0002 | c0002 | t0003 | g0016 | AMR | PEL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02293 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | PEL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02300 | hp1 | a0002 | c0002 | t0003 | g0016 | AMR | PEL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | PEL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02451 | hp2 | a0001 | c0001 | t0025 | g0190 | AFR | ACB | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02523 | hp1 | a0001 | c0006 | t0001 | g0092 | EAS | KHV | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02523 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | KHV | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0201 | AFR | GWD | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02572 | hp2 | a0001 | c0001 | t0006 | g0256 | AFR | GWD | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02602 | hp1 | a0001 | c0001 | t0004 | g0009 | SAS | PJL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0204 | SAS | PJL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02615 | hp1 | a0002 | c0002 | t0003 | g0298 | AFR | GWD | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02615 | hp2 | a0001 | c0001 | t0007 | g0054 | AFR | GWD | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02630 | hp1 | a0002 | c0002 | t0003 | g0296 | AFR | GWD | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0173 | AFR | GWD | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02647 | hp2 | a0001 | c0001 | t0006 | g0052 | AFR | GWD | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0167 | SAS | PJL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02683 | hp2 | a0001 | c0001 | t0004 | g0131 | SAS | PJL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02717 | hp1 | a0001 | c0001 | t0005 | g0027 | AFR | GWD | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02717 | hp2 | a0002 | c0002 | t0003 | g0015 | AFR | GWD | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02723 | hp1 | a0001 | c0001 | t0019 | g0116 | AFR | GWD | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02723 | hp2 | a0001 | c0001 | t0010 | g0151 | AFR | GWD | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02735 | hp1 | a0002 | c0002 | t0003 | g0301 | SAS | PJL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0195 | SAS | PJL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0211 | SAS | PJL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02809 | hp1 | a0001 | c0001 | t0007 | g0274 | AFR | GWD | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02818 | hp2 | a0002 | c0002 | t0003 | g0292 | AFR | GWD | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02886 | hp1 | a0003 | c0003 | t0005 | g0017 | AFR | GWD | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02886 | hp2 | a0001 | c0001 | t0010 | g0043 | AFR | GWD | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02895 | hp2 | a0001 | c0001 | t0018 | g0152 | AFR | GWD | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02896 | hp1 | a0001 | c0001 | t0005 | g0069 | AFR | GWD | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02896 | hp2 | a0001 | c0001 | t0028 | g0153 | AFR | GWD | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02897 | hp2 | a0001 | c0001 | t0005 | g0027 | AFR | GWD | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02922 | hp1 | a0001 | c0001 | t0015 | g0191 | AFR | ESN | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02922 | hp2 | a0001 | c0001 | t0005 | g0066 | AFR | ESN | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02965 | hp2 | a0001 | c0001 | t0006 | g0262 | AFR | ESN | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0321 | AFR | ESN | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02970 | hp2 | a0001 | c0001 | t0006 | g0052 | AFR | ESN | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02976 | hp1 | a0001 | c0001 | t0006 | g0024 | AFR | ESN | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02976 | hp2 | a0001 | c0001 | t0009 | g0189 | AFR | ESN | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0174 | SAS | PJL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03041 | hp1 | a0001 | c0001 | t0007 | g0054 | AFR | GWD | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03098 | hp2 | a0002 | c0002 | t0003 | g0014 | AFR | MSL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03130 | hp2 | a0002 | c0002 | t0003 | g0290 | AFR | ESN | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03139 | hp1 | a0002 | c0002 | t0003 | g0014 | AFR | ESN | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03139 | hp2 | a0001 | c0001 | t0006 | g0024 | AFR | ESN | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03195 | hp1 | a0001 | c0001 | t0023 | g0128 | AFR | ESN | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | MSL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03209 | hp2 | a0002 | c0002 | t0003 | g0302 | AFR | MSL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03225 | hp2 | a0002 | c0002 | t0003 | g0014 | AFR | MSL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03453 | hp1 | a0004 | c0008 | t0001 | g0322 | AFR | MSL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03453 | hp2 | a0002 | c0002 | t0003 | g0015 | AFR | MSL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03486 | hp2 | a0001 | c0001 | t0006 | g0255 | AFR | MSL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03490 | hp1 | a0002 | c0002 | t0003 | g0058 | SAS | PJL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0040 | SAS | PJL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03491 | hp1 | a0001 | c0001 | t0004 | g0002 | SAS | PJL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03516 | hp1 | a0001 | c0001 | t0008 | g0266 | AFR | ESN | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03540 | hp1 | a0003 | c0003 | t0005 | g0017 | AFR | GWD | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | GWD | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03579 | hp1 | a0001 | c0001 | t0005 | g0068 | AFR | MSL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | MSL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0198 | SAS | PJL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03688 | hp1 | a0001 | c0001 | t0021 | g0268 | SAS | STU | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03688 | hp2 | a0002 | c0002 | t0003 | g0293 | SAS | STU | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0175 | SAS | PJL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0073 | SAS | BEB | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03834 | hp1 | a0001 | c0001 | t0004 | g0132 | SAS | BEB | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03927 | hp1 | a0002 | c0002 | t0003 | g0295 | SAS | BEB | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | BEB | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03942 | hp1 | a0001 | c0001 | t0004 | g0141 | SAS | BEB | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03942 | hp2 | a0002 | c0002 | t0003 | g0007 | SAS | BEB | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | STU | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0170 | SAS | STU | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0202 | SAS | BEB | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG04184 | hp2 | a0002 | c0002 | t0003 | g0318 | SAS | BEB | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | STU | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0164 | SAS | STU | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | STU | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0243 | SAS | STU | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0210 | SAS | STU | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG04228 | hp2 | a0002 | c0002 | t0003 | g0007 | SAS | STU | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18522 | hp1 | a0001 | c0001 | t0020 | g0280 | AFR | YRI | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18522 | hp2 | a0001 | c0001 | t0008 | g0053 | AFR | YRI | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHB | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | CHB | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | CHB | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | CHB | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | YRI | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18906 | hp2 | a0002 | c0002 | t0003 | g0291 | AFR | YRI | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18939 | hp1 | a0001 | c0001 | t0004 | g0038 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18940 | hp2 | a0001 | c0001 | t0011 | g0138 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18942 | hp1 | a0001 | c0001 | t0011 | g0037 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18944 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18945 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18945 | hp2 | a0002 | c0002 | t0003 | g0026 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18946 | hp2 | a0001 | c0001 | t0004 | g0220 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18948 | hp1 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18949 | hp2 | a0001 | c0001 | t0022 | g0127 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18950 | hp2 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18953 | hp2 | a0002 | c0002 | t0003 | g0306 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18959 | hp1 | a0001 | c0001 | t0004 | g0038 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18959 | hp2 | a0001 | c0001 | t0012 | g0094 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18960 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18963 | hp1 | a0001 | c0001 | t0004 | g0240 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18965 | hp1 | a0002 | c0002 | t0003 | g0304 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18966 | hp1 | a0002 | c0002 | t0003 | g0307 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18967 | hp2 | a0001 | c0001 | t0004 | g0143 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18969 | hp1 | a0002 | c0002 | t0003 | g0294 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18969 | hp2 | a0001 | c0001 | t0016 | g0095 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18971 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18971 | hp2 | a0002 | c0002 | t0003 | g0026 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18973 | hp1 | a0002 | c0002 | t0003 | g0312 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18980 | hp1 | a0002 | c0002 | t0003 | g0317 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18982 | hp1 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18983 | hp1 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18983 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18985 | hp2 | a0002 | c0002 | t0003 | g0316 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18987 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18988 | hp1 | a0001 | c0001 | t0026 | g0133 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18989 | hp1 | a0002 | c0002 | t0003 | g0310 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18989 | hp2 | a0001 | c0001 | t0004 | g0241 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18993 | hp2 | a0002 | c0002 | t0003 | g0308 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18995 | hp2 | a0005 | c0005 | t0001 | g0062 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18999 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19001 | hp2 | a0002 | c0002 | t0003 | g0299 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19002 | hp1 | a0002 | c0002 | t0003 | g0311 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19003 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19004 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19011 | hp2 | a0001 | c0001 | t0004 | g0270 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0209 | AFR | LWK | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19030 | hp2 | a0002 | c0002 | t0003 | g0014 | AFR | LWK | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19043 | hp1 | a0002 | c0002 | t0003 | g0297 | AFR | LWK | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19043 | hp2 | a0001 | c0001 | t0024 | g0169 | AFR | LWK | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19054 | hp1 | a0002 | c0002 | t0003 | g0309 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19057 | hp1 | a0002 | c0002 | t0003 | g0026 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19057 | hp2 | a0001 | c0001 | t0011 | g0037 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19062 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19066 | hp2 | a0001 | c0001 | t0012 | g0103 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19072 | hp1 | a0002 | c0002 | t0003 | g0300 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19077 | hp2 | a0001 | c0001 | t0004 | g0139 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19078 | hp1 | a0002 | c0002 | t0003 | g0315 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19080 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19081 | hp1 | a0001 | c0004 | t0001 | g0059 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19081 | hp2 | a0001 | c0001 | t0014 | g0166 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19083 | hp2 | a0001 | c0001 | t0004 | g0135 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19088 | hp1 | a0001 | c0001 | t0004 | g0136 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19090 | hp2 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19240 | hp1 | a0001 | c0001 | t0007 | g0273 | AFR | YRI | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | YRI | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA20129 | hp1 | a0006 | c0007 | t0001 | g0089 | AFR | ASW | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ASW | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0180 | EUR | TSI | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA20805 | hp2 | a0002 | c0002 | t0003 | g0058 | EUR | TSI | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA20905 | hp1 | a0001 | c0001 | t0004 | g0134 | SAS | GIH | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | GIH | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG01123 | hp2 | a0001 | c0001 | t0004 | g0129 | AMR | CLM | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | ACB | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02109 | hp2 | a0002 | c0002 | t0003 | g0015 | AFR | ACB | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02486 | hp1 | a0001 | c0001 | t0009 | g0187 | AFR | ACB | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02486 | hp2 | a0003 | c0003 | t0005 | g0071 | AFR | ACB | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02559 | hp1 | a0003 | c0003 | t0005 | g0070 | AFR | ACB | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG02559 | hp2 | a0001 | c0001 | t0007 | g0272 | AFR | ACB | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03471 | hp1 | a0001 | c0001 | t0006 | g0024 | AFR | MSL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG03471 | hp2 | a0001 | c0001 | t0008 | g0265 | AFR | MSL | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | USA | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | USA | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA20300 | hp1 | a0002 | c0002 | t0003 | g0289 | AFR | USA | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA20300 | hp2 | a0001 | c0001 | t0008 | g0053 | AFR | USA | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | LWK | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0172 | AFR | LWK | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0182 | REF | REF | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0157 | REF | REF | SEPSECS_chr4_25115014_25165449 | SEPSECS | chr4 | 25115014 | 25165449 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:25124043 | C | T | 1 | a0003 | 5 | HG01109.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
missense_variant | MODERATE | c.1394G>A | p.Arg465Gln | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 11/11 | 1474/5503 | 1394/1506 | 465/501 | chr4 | 25124043 | |||
chr4:25124081 | C | G | 1 | a0002 | 61 | HG00438.hp2 HG00642.hp2 HG00733.hp1 others(58): Show |
missense_variant | MODERATE | c.1356G>C | p.Lys452Asn | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 11/11 | 1436/5503 | 1356/1506 | 452/501 | chr4 | 25124081 | |||
chr4:25125761 | C | T | 1 | a0005 | 1 | NA18995.hp2 | missense_variant | MODERATE | c.1144G>A | p.Glu382Lys | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 10/11 | 1224/5503 | 1144/1506 | 382/501 | chr4 | 25125761 | |||
chr4:25144853 | G | A | 1 | a0006 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.947C>T | p.Ala316Val | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/11 | 1027/5503 | 947/1506 | 316/501 | chr4 | 25144853 | |||
chr4:25160296 | C | A | 1 | a0004 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.74G>T | p.Arg25Leu | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 1/11 | 154/5503 | 74/1506 | 25/501 | chr4 | 25160296 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:25125777 | T | C | 1 | a0001c0006 | 1 | HG02523.hp1 | synonymous_variant | LOW | c.1128A>G | p.Thr376Thr | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 10/11 | 1208/5503 | 1128/1506 | 376/501 | chr4 | 25125777 | |||
chr4:25160325 | C | T | 1 | a0001c0004 | 1 | NA19081.hp1 | synonymous_variant | LOW | c.45G>A | p.Pro15Pro | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 1/11 | 125/5503 | 45/1506 | 15/501 | chr4 | 25160325 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:25120061 | T | A | 1 | a0001c0001t0013 | 2 | HG01243.hp1 HG01884.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3870A>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 11/11 | 3870 | chr4 | 25120061 | ||||||
chr4:25120083 | G | A | 3 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0018 |
9 | HG00741.hp1 HG01261.hp1 HG02723.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3848C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 11/11 | 3848 | chr4 | 25120083 | ||||||
chr4:25120156 | T | C | 1 | a0001c0001t0023 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3775A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 11/11 | 3775 | chr4 | 25120156 | ||||||
chr4:25120529 | T | C | 1 | a0001c0001t0024 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3402A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 11/11 | 3402 | chr4 | 25120529 | ||||||
chr4:25120592 | C | T | 1 | a0001c0001t0021 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3339G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 11/11 | 3339 | chr4 | 25120592 | ||||||
chr4:25120680 | G | A | 1 | a0001c0001t0026 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3251C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 11/11 | 3251 | chr4 | 25120680 | ||||||
chr4:25120965 | T | C | 2 | a0001c0001t0017 a0001c0001t0027 |
2 | HG01167.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2966A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 11/11 | 2966 | chr4 | 25120965 | ||||||
chr4:25121091 | A | G | 2 | a0001c0001t0010 a0001c0001t0018 |
4 | HG00741.hp1 HG02723.hp2 HG02886.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2840T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 11/11 | 2840 | chr4 | 25121091 | ||||||
chr4:25121237 | T | C | 2 | a0001c0001t0003 a0002c0002t0003 |
62 | HG00438.hp2 HG00642.hp2 HG00733.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*2694A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 11/11 | 2694 | chr4 | 25121237 | ||||||
chr4:25121268 | C | G | 1 | a0001c0001t0020 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2663G>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 11/11 | 2663 | chr4 | 25121268 | ||||||
chr4:25121722 | T | C | 2 | a0001c0001t0005 a0003c0003t0005 |
11 | HG01109.hp2 HG02258.hp2 HG02486.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2209A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 11/11 | 2209 | chr4 | 25121722 | ||||||
chr4:25121773 | A | G | 1 | a0001c0001t0019 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2158T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 11/11 | 2158 | chr4 | 25121773 | ||||||
chr4:25121808 | T | C | 2 | a0001c0001t0010 a0001c0001t0018 |
4 | HG00741.hp1 HG02723.hp2 HG02886.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2123A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 11/11 | 2123 | chr4 | 25121808 | ||||||
chr4:25121839 | G | A | 1 | a0001c0001t0025 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2092C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 11/11 | 2092 | chr4 | 25121839 | ||||||
chr4:25121890 | C | G | 1 | a0001c0001t0018 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2041G>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 11/11 | 2041 | chr4 | 25121890 | ||||||
chr4:25122283 | C | T | 1 | a0001c0001t0022 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1648G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 11/11 | 1648 | chr4 | 25122283 | ||||||
chr4:25122317 | A | G | 1 | a0001c0001t0012 | 2 | NA18959.hp2 NA19066.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1614T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 11/11 | 1614 | chr4 | 25122317 | ||||||
chr4:25122890 | A | G | 1 | a0001c0001t0006 | 8 | HG02572.hp2 HG02647.hp2 HG02965.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1041T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 11/11 | 1041 | chr4 | 25122890 | ||||||
chr4:25123124 | T | C | 5 | a0001c0001t0002 a0001c0001t0014 a0001c0001t0022 others(2): Show |
90 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*807A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 11/11 | 807 | chr4 | 25123124 | ||||||
chr4:25123250 | T | G | 2 | a0001c0001t0009 a0001c0001t0025 |
6 | HG01346.hp1 HG01884.hp1 HG01891.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*681A>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 11/11 | 681 | chr4 | 25123250 | ||||||
chr4:25123293 | C | G | 2 | a0001c0001t0005 a0003c0003t0005 |
11 | HG01109.hp2 HG02258.hp2 HG02486.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*638G>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 11/11 | 638 | chr4 | 25123293 | ||||||
chr4:25123476 | G | A | 5 | a0001c0001t0004 a0001c0001t0011 a0001c0001t0017 others(2): Show |
53 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*455C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 11/11 | 455 | chr4 | 25123476 | ||||||
chr4:25123477 | G | A | 1 | a0001c0001t0028 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*454C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 11/11 | 454 | chr4 | 25123477 | ||||||
chr4:25123558 | ATT | A | 1 | a0001c0001t0006 | 8 | HG02572.hp2 HG02647.hp2 HG02965.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*371_*372delAA | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 11/11 | 371 | chr4 | 25123558 | ||||||
chr4:25123673 | CTTAA | C | 2 | a0001c0001t0010 a0001c0001t0018 |
4 | HG00741.hp1 HG02723.hp2 HG02886.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*254_*257delTTAA | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 11/11 | 254 | chr4 | 25123673 | ||||||
chr4:25123678 | T | C | 1 | a0001c0001t0011 | 3 | NA18940.hp2 NA18942.hp1 NA19057.hp2 |
3_prime_UTR_variant | MODIFIER | c.*253A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 11/11 | 253 | chr4 | 25123678 | ||||||
chr4:25123690 | C | T | 1 | a0001c0001t0017 | 1 | HG01169.hp1 | 3_prime_UTR_variant | MODIFIER | c.*241G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 11/11 | 241 | chr4 | 25123690 | ||||||
chr4:25123694 | C | CAAA | 1 | a0001c0001t0007 | 6 | HG02145.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*236_*237insTTT | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 11/11 | 236 | chr4 | 25123694 | ||||||
chr4:25123708 | C | T | 2 | a0001c0001t0012 a0001c0001t0016 |
3 | NA18959.hp2 NA18969.hp2 NA19066.hp2 |
3_prime_UTR_variant | MODIFIER | c.*223G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 11/11 | 223 | chr4 | 25123708 | ||||||
chr4:25123883 | A | G | 1 | a0001c0001t0015 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*48T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 11/11 | 48 | chr4 | 25123883 | ||||||
chr4:25123894 | A | C | 1 | a0001c0001t0014 | 1 | NA19081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*37T>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 11/11 | 37 | chr4 | 25123894 | ||||||
chr4:25160426 | C | A | 1 | a0001c0001t0029 | 1 | HG00423.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-57G>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 1/11 | chr4 | 25160426 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:25124306 | C | G | 1 | a0001c0001t0002g0170 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1212-81G>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 10/10 | chr4 | 25124306 | |||||||
chr4:25124789 | G | T | 4 | a0001c0001t0002g0047 a0001c0001t0002g0165 a0001c0001t0002g0178 others(1): Show |
5 | NA18955.hp1 NA18956.hp2 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1212-564C>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 10/10 | chr4 | 25124789 | |||||||
chr4:25124956 | G | A | 2 | a0001c0001t0004g0136 a0001c0001t0004g0139 |
2 | NA19077.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1212-731C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 10/10 | chr4 | 25124956 | |||||||
chr4:25125009 | T | C | 1 | a0001c0001t0001g0249 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1211+685A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 10/10 | chr4 | 25125009 | |||||||
chr4:25125038 | A | T | 2 | a0001c0001t0004g0136 a0001c0001t0004g0139 |
2 | NA19077.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1211+656T>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 10/10 | chr4 | 25125038 | |||||||
chr4:25125119 | T | C | 3 | a0001c0001t0010g0043 a0001c0001t0010g0151 a0001c0001t0018g0152 |
4 | HG00741.hp1 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1211+575A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 10/10 | chr4 | 25125119 | |||||||
chr4:25125145 | T | C | 20 | a0001c0001t0001g0003 a0001c0001t0001g0049 a0001c0001t0001g0221 others(17): Show |
28 | HG00423.hp2 HG00597.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.1211+549A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 10/10 | chr4 | 25125145 | |||||||
chr4:25125356 | G | A | 32 | a0001c0001t0004g0002 a0001c0001t0004g0006 a0001c0001t0004g0009 others(29): Show |
53 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.1211+338C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 10/10 | chr4 | 25125356 | |||||||
chr4:25125366 | C | T | 318 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(315): Show |
451 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(448): Show |
intron_variant | MODIFIER | c.1211+328G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 10/10 | chr4 | 25125366 | |||||||
chr4:25125539 | C | A | 5 | a0001c0001t0006g0024 a0001c0001t0006g0052 a0001c0001t0006g0255 others(2): Show |
8 | HG02572.hp2 HG02647.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1211+155G>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 10/10 | chr4 | 25125539 | |||||||
chr4:25125687 | T | C | 26 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0050 others(23): Show |
33 | HG00544.hp2 HG00621.hp1 HG01255.hp2 others(30): Show |
splice_region_variant&intron_variant | LOW | c.1211+7A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 10/10 | chr4 | 25125687 | |||||||
chr4:25125818 | G | T | 1 | a0001c0001t0001g0288 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1121-34C>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 9/10 | chr4 | 25125818 | |||||||
chr4:25126233 | G | A | 8 | a0001c0001t0001g0030 a0001c0001t0001g0078 a0001c0001t0001g0104 others(5): Show |
9 | HG00423.hp1 HG00609.hp1 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.1121-449C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 9/10 | chr4 | 25126233 | |||||||
chr4:25126348 | G | A | 2 | a0001c0001t0001g0269 a0001c0001t0021g0268 |
2 | HG02165.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1121-564C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 9/10 | chr4 | 25126348 | |||||||
chr4:25126719 | G | A | 2 | a0001c0001t0013g0193 a0001c0001t0013g0194 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1120+545C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 9/10 | chr4 | 25126719 | |||||||
chr4:25126782 | A | G | 2 | a0001c0001t0001g0269 a0001c0001t0021g0268 |
2 | HG02165.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1120+482T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 9/10 | chr4 | 25126782 | |||||||
chr4:25126938 | G | A | 122 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0002g0001 others(119): Show |
180 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.1120+326C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 9/10 | chr4 | 25126938 | |||||||
chr4:25126952 | G | C | 49 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0025 others(46): Show |
63 | HG00544.hp2 HG00621.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.1120+312C>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 9/10 | chr4 | 25126952 | |||||||
chr4:25127031 | G | A | 1 | a0001c0001t0002g0170 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1120+233C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 9/10 | chr4 | 25127031 | |||||||
chr4:25127051 | T | G | 1 | a0001c0001t0002g0211 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1120+213A>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 9/10 | chr4 | 25127051 | |||||||
chr4:25127114 | C | T | 1 | a0001c0001t0006g0024 | 3 | HG02976.hp1 HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1120+150G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 9/10 | chr4 | 25127114 | |||||||
chr4:25127160 | A | G | 4 | a0001c0001t0008g0053 a0001c0001t0008g0264 a0001c0001t0008g0265 others(1): Show |
5 | HG01261.hp1 HG03471.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1120+104T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 9/10 | chr4 | 25127160 | |||||||
chr4:25127252 | A | G | 10 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0035 others(7): Show |
19 | HG00738.hp2 HG01358.hp1 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.1120+12T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 9/10 | chr4 | 25127252 | |||||||
chr4:25127374 | T | C | 1 | a0001c0001t0001g0269 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1027-17A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25127374 | |||||||
chr4:25127929 | A | G | 1 | a0001c0001t0001g0258 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1027-572T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25127929 | |||||||
chr4:25127947 | C | T | 1 | a0001c0001t0015g0191 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1027-590G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25127947 | |||||||
chr4:25127969 | A | T | 2 | a0001c0001t0001g0049 a0001c0001t0001g0230 |
3 | NA18984.hp2 NA18998.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.1027-612T>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25127969 | |||||||
chr4:25128084 | G | A | 2 | a0001c0001t0001g0269 a0001c0001t0021g0268 |
2 | HG02165.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1027-727C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25128084 | |||||||
chr4:25128108 | T | G | 20 | a0001c0001t0001g0003 a0001c0001t0001g0049 a0001c0001t0001g0221 others(17): Show |
28 | HG00423.hp2 HG00597.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.1027-751A>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25128108 | |||||||
chr4:25128429 | T | TAACAAA | 5 | a0001c0001t0007g0054 a0001c0001t0007g0271 a0001c0001t0007g0272 others(2): Show |
6 | HG02145.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1027-1078_1027-107 others(10): Show |
SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25128429 | |||||||
chr4:25128429 | TAACAAA | T | 31 | a0001c0001t0001g0003 a0001c0001t0001g0049 a0001c0001t0001g0221 others(28): Show |
40 | HG00423.hp2 HG00597.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.1027-1078_1027-107 others(10): Show |
SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25128429 | |||||||
chr4:25128429 | TAACAAAA others(5): Show |
T | 12 | a0001c0001t0005g0027 a0001c0001t0005g0066 a0001c0001t0005g0067 others(9): Show |
16 | HG01109.hp2 HG01261.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1027-1084_1027-107 others(16): Show |
SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25128429 | |||||||
chr4:25128443 | A | C | 61 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0011 others(58): Show |
90 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.1027-1086T>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25128443 | |||||||
chr4:25128493 | T | C | 3 | a0001c0001t0010g0043 a0001c0001t0010g0151 a0001c0001t0018g0152 |
4 | HG00741.hp1 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1027-1136A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25128493 | |||||||
chr4:25128558 | G | T | 2 | a0001c0001t0001g0049 a0001c0001t0001g0230 |
3 | NA18984.hp2 NA18998.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.1027-1201C>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25128558 | |||||||
chr4:25128661 | C | T | 13 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0057 others(10): Show |
18 | HG00639.hp1 HG01192.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1027-1304G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25128661 | |||||||
chr4:25129189 | A | C | 3 | a0001c0001t0001g0269 a0001c0001t0001g0288 a0001c0001t0021g0268 |
3 | HG02165.hp1 HG03579.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1027-1832T>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25129189 | |||||||
chr4:25129379 | T | G | 61 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0011 others(58): Show |
90 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.1027-2022A>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25129379 | |||||||
chr4:25129421 | C | T | 3 | a0001c0001t0001g0269 a0001c0001t0001g0288 a0001c0001t0021g0268 |
3 | HG02165.hp1 HG03579.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1027-2064G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25129421 | |||||||
chr4:25129454 | T | C | 32 | a0001c0001t0004g0002 a0001c0001t0004g0006 a0001c0001t0004g0009 others(29): Show |
53 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.1027-2097A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25129454 | |||||||
chr4:25129600 | A | T | 61 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0011 others(58): Show |
90 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.1027-2243T>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25129600 | |||||||
chr4:25129644 | G | A | 1 | a0001c0001t0002g0171 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1027-2287C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25129644 | |||||||
chr4:25129685 | T | C | 3 | a0001c0001t0001g0269 a0001c0001t0001g0288 a0001c0001t0021g0268 |
3 | HG02165.hp1 HG03579.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1027-2328A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25129685 | |||||||
chr4:25129837 | T | C | 2 | a0001c0001t0001g0269 a0001c0001t0021g0268 |
2 | HG02165.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1027-2480A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25129837 | |||||||
chr4:25129939 | T | A | 3 | a0001c0001t0001g0269 a0001c0001t0001g0288 a0001c0001t0021g0268 |
3 | HG02165.hp1 HG03579.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1027-2582A>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25129939 | |||||||
chr4:25130182 | T | A | 1 | a0001c0001t0028g0153 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1027-2825A>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25130182 | |||||||
chr4:25130195 | T | C | 64 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0002g0001 others(61): Show |
93 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.1027-2838A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25130195 | |||||||
chr4:25130503 | C | T | 1 | a0001c0001t0004g0038 | 2 | NA18939.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.1027-3146G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25130503 | |||||||
chr4:25130633 | A | G | 32 | a0001c0001t0004g0002 a0001c0001t0004g0006 a0001c0001t0004g0009 others(29): Show |
53 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.1027-3276T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25130633 | |||||||
chr4:25130809 | C | T | 71 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0018 others(68): Show |
95 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.1027-3452G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25130809 | |||||||
chr4:25130872 | G | A | 176 | a0001c0001t0001g0003 a0001c0001t0001g0049 a0001c0001t0001g0221 others(173): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1027-3515C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25130872 | |||||||
chr4:25130878 | A | G | 2 | a0002c0002t0003g0306 a0002c0002t0003g0310 |
2 | NA18953.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.1027-3521T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25130878 | |||||||
chr4:25130971 | A | C | 3 | a0001c0001t0001g0223 a0001c0001t0001g0225 a0001c0001t0001g0231 |
3 | HG02071.hp2 HG02135.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.1027-3614T>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25130971 | |||||||
chr4:25131203 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1027-3846G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25131203 | |||||||
chr4:25131204 | G | A | 1 | a0001c0001t0002g0181 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1027-3847C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25131204 | |||||||
chr4:25131223 | G | A | 3 | a0001c0001t0001g0269 a0001c0001t0001g0288 a0001c0001t0021g0268 |
3 | HG02165.hp1 HG03579.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1027-3866C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25131223 | |||||||
chr4:25131287 | C | T | 2 | a0001c0001t0013g0193 a0001c0001t0013g0194 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1027-3930G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25131287 | |||||||
chr4:25131348 | G | C | 3 | a0001c0001t0001g0269 a0001c0001t0001g0288 a0001c0001t0021g0268 |
3 | HG02165.hp1 HG03579.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1027-3991C>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25131348 | |||||||
chr4:25131413 | G | C | 1 | a0001c0001t0002g0200 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1027-4056C>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25131413 | |||||||
chr4:25131443 | T | C | 311 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(308): Show |
441 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(438): Show |
intron_variant | MODIFIER | c.1027-4086A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25131443 | |||||||
chr4:25131482 | T | C | 1 | a0001c0001t0001g0320 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1027-4125A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25131482 | |||||||
chr4:25131534 | G | A | 5 | a0001c0001t0009g0187 a0001c0001t0009g0188 a0001c0001t0009g0189 others(2): Show |
5 | HG01346.hp1 HG01884.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1027-4177C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25131534 | |||||||
chr4:25131543 | G | A | 5 | a0001c0001t0006g0024 a0001c0001t0006g0052 a0001c0001t0006g0255 others(2): Show |
8 | HG02572.hp2 HG02647.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1027-4186C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25131543 | |||||||
chr4:25131625 | G | C | 1 | a0001c0001t0001g0251 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1027-4268C>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25131625 | |||||||
chr4:25131742 | C | T | 240 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(237): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.1027-4385G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25131742 | |||||||
chr4:25131893 | C | T | 1 | a0001c0001t0001g0041 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1027-4536G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25131893 | |||||||
chr4:25131940 | T | G | 1 | a0001c0001t0001g0226 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1027-4583A>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25131940 | |||||||
chr4:25131980 | T | C | 3 | a0001c0001t0001g0020 a0001c0001t0001g0109 a0001c0001t0001g0218 |
5 | HG00438.hp1 HG00544.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.1027-4623A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25131980 | |||||||
chr4:25131984 | C | T | 1 | a0001c0001t0002g0172 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1027-4627G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25131984 | |||||||
chr4:25132019 | T | C | 8 | a0001c0001t0005g0027 a0001c0001t0005g0066 a0001c0001t0005g0067 others(5): Show |
11 | HG01109.hp2 HG02258.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1027-4662A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25132019 | |||||||
chr4:25132047 | G | A | 153 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0002g0001 others(150): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1027-4690C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25132047 | |||||||
chr4:25132211 | A | G | 2 | a0001c0001t0001g0225 a0001c0001t0001g0231 |
2 | HG02071.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.1027-4854T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25132211 | |||||||
chr4:25132376 | A | G | 1 | a0001c0001t0004g0130 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1027-5019T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25132376 | |||||||
chr4:25132423 | A | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0049 a0001c0001t0001g0221 others(136): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.1027-5066T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25132423 | |||||||
chr4:25132872 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1027-5515G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25132872 | |||||||
chr4:25133182 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1027-5825G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25133182 | |||||||
chr4:25133287 | A | C | 10 | a0001c0001t0003g0321 a0002c0002t0003g0014 a0002c0002t0003g0015 others(7): Show |
16 | HG02109.hp2 HG02258.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.1027-5930T>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25133287 | |||||||
chr4:25133423 | G | A | 6 | a0001c0001t0005g0066 a0001c0001t0005g0067 a0001c0001t0005g0068 others(3): Show |
8 | HG01109.hp2 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1027-6066C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25133423 | |||||||
chr4:25133473 | C | T | 240 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(237): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.1027-6116G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25133473 | |||||||
chr4:25133822 | T | A | 1 | a0001c0001t0001g0236 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1027-6465A>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25133822 | |||||||
chr4:25133948 | T | C | 4 | a0001c0001t0001g0057 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
5 | HG01257.hp2 HG01258.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.1027-6591A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25133948 | |||||||
chr4:25133957 | T | C | 2 | a0001c0001t0013g0193 a0001c0001t0013g0194 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1027-6600A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25133957 | |||||||
chr4:25134028 | G | A | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG03669.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1027-6671C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25134028 | |||||||
chr4:25134077 | A | T | 8 | a0001c0001t0005g0027 a0001c0001t0005g0066 a0001c0001t0005g0067 others(5): Show |
11 | HG01109.hp2 HG02258.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1027-6720T>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25134077 | |||||||
chr4:25134083 | A | G | 1 | a0001c0001t0021g0268 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1027-6726T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25134083 | |||||||
chr4:25134124 | C | CA | 61 | a0001c0001t0001g0075 a0001c0001t0001g0088 a0001c0001t0001g0093 others(58): Show |
91 | HG00423.hp1 HG00438.hp2 HG00642.hp2 others(88): Show |
intron_variant | MODIFIER | c.1027-6768dupT | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25134124 | |||||||
chr4:25134124 | C | CAA | 32 | a0001c0001t0004g0002 a0001c0001t0004g0006 a0001c0001t0004g0009 others(29): Show |
55 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1027-6769_1027-676 others(6): Show |
SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25134124 | |||||||
chr4:25134124 | C | CAAA | 9 | a0001c0001t0004g0073 a0001c0001t0004g0131 a0001c0001t0004g0140 others(6): Show |
10 | HG00741.hp1 HG01978.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.1027-6770_1027-676 others(7): Show |
SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25134124 | |||||||
chr4:25134124 | CA | C | 49 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0025 others(46): Show |
64 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.1027-6768delT | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25134124 | |||||||
chr4:25134320 | A | ATG | 19 | a0001c0001t0001g0022 a0001c0001t0001g0045 a0001c0001t0001g0077 others(16): Show |
23 | HG01346.hp1 HG01884.hp1 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.1027-6965_1027-696 others(6): Show |
SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25134320 | |||||||
chr4:25134320 | A | ATGTG | 61 | a0001c0001t0001g0155 a0001c0001t0001g0185 a0001c0001t0002g0001 others(58): Show |
95 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.1027-6967_1027-696 others(8): Show |
SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25134320 | |||||||
chr4:25134320 | A | ATGTGTG | 30 | a0001c0001t0001g0237 a0001c0001t0002g0167 a0001c0001t0002g0168 others(27): Show |
48 | HG00438.hp2 HG00642.hp2 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.1027-6969_1027-696 others(10): Show |
SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25134320 | |||||||
chr4:25134320 | A | ATGTGTGT others(1): Show |
7 | a0001c0001t0002g0209 a0001c0001t0002g0243 a0002c0002t0003g0302 others(4): Show |
7 | HG03209.hp2 HG04184.hp2 HG04204.hp2 others(4): Show |
intron_variant | MODIFIER | c.1027-6971_1027-696 others(12): Show |
SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25134320 | |||||||
chr4:25134320 | A | ATGTGTGT others(3): Show |
18 | a0001c0001t0001g0003 a0001c0001t0001g0049 a0001c0001t0001g0221 others(15): Show |
26 | HG00423.hp2 HG00597.hp2 HG01943.hp1 others(23): Show |
intron_variant | MODIFIER | c.1027-6973_1027-696 others(14): Show |
SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25134320 | |||||||
chr4:25134320 | A | ATGTGTGT others(9): Show |
1 | a0001c0001t0001g0228 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1027-6979_1027-696 others(20): Show |
SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25134320 | |||||||
chr4:25134320 | ATG | A | 33 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(30): Show |
40 | HG00140.hp2 HG00741.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.1027-6965_1027-696 others(6): Show |
SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25134320 | |||||||
chr4:25134320 | ATGTG | A | 35 | a0001c0001t0001g0082 a0001c0001t0001g0097 a0001c0001t0001g0114 others(32): Show |
55 | HG00140.hp1 HG00609.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1027-6967_1027-696 others(8): Show |
SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25134320 | |||||||
chr4:25134320 | ATGTGTG | A | 33 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0050 others(30): Show |
42 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.1027-6969_1027-696 others(10): Show |
SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25134320 | |||||||
chr4:25134364 | C | T | 4 | a0001c0001t0001g0025 a0001c0001t0001g0253 a0001c0001t0001g0261 others(1): Show |
6 | NA18948.hp2 NA18956.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.1027-7007G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25134364 | |||||||
chr4:25134581 | C | T | 1 | a0001c0001t0028g0153 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1027-7224G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25134581 | |||||||
chr4:25134717 | T | C | 2 | a0001c0001t0001g0269 a0001c0001t0021g0268 |
2 | HG02165.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1027-7360A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25134717 | |||||||
chr4:25135046 | G | C | 3 | a0001c0001t0002g0173 a0001c0001t0002g0201 a0001c0001t0002g0209 |
3 | HG02572.hp1 HG02647.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1027-7689C>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25135046 | |||||||
chr4:25135122 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1027-7765A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25135122 | |||||||
chr4:25135148 | A | C | 1 | a0001c0001t0015g0191 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1027-7791T>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25135148 | |||||||
chr4:25135290 | A | T | 2 | a0001c0001t0001g0288 a0001c0001t0004g0129 |
2 | HG01123.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1027-7933T>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25135290 | |||||||
chr4:25135325 | GACT | G | 32 | a0001c0001t0004g0002 a0001c0001t0004g0006 a0001c0001t0004g0009 others(29): Show |
53 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.1027-7971_1027-796 others(7): Show |
SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25135325 | |||||||
chr4:25135483 | C | T | 5 | a0001c0001t0007g0054 a0001c0001t0007g0271 a0001c0001t0007g0272 others(2): Show |
6 | HG02145.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1027-8126G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25135483 | |||||||
chr4:25135743 | T | A | 2 | a0001c0001t0001g0288 a0001c0001t0001g0320 |
2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1027-8386A>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25135743 | |||||||
chr4:25135754 | C | T | 1 | a0001c0001t0005g0067 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1027-8397G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25135754 | |||||||
chr4:25135784 | C | T | 176 | a0001c0001t0001g0003 a0001c0001t0001g0049 a0001c0001t0001g0221 others(173): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1027-8427G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25135784 | |||||||
chr4:25136155 | G | A | 1 | a0001c0001t0002g0202 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1026+8619C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25136155 | |||||||
chr4:25136227 | T | G | 3 | a0001c0001t0010g0043 a0001c0001t0010g0151 a0001c0001t0018g0152 |
4 | HG00741.hp1 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026+8547A>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25136227 | |||||||
chr4:25136264 | G | A | 1 | a0001c0001t0002g0174 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1026+8510C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25136264 | |||||||
chr4:25136308 | T | C | 2 | a0001c0001t0001g0107 a0001c0001t0012g0103 |
2 | NA19066.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1026+8466A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25136308 | |||||||
chr4:25136432 | T | G | 70 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0018 others(67): Show |
94 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.1026+8342A>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25136432 | |||||||
chr4:25136433 | C | A | 70 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0018 others(67): Show |
94 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.1026+8341G>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25136433 | |||||||
chr4:25136589 | T | C | 1 | a0002c0002t0003g0310 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1026+8185A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25136589 | |||||||
chr4:25136616 | A | G | 1 | a0002c0002t0003g0295 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1026+8158T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25136616 | |||||||
chr4:25136734 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1026+8040G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25136734 | |||||||
chr4:25136815 | T | C | 13 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0057 others(10): Show |
18 | HG00639.hp1 HG01192.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1026+7959A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25136815 | |||||||
chr4:25136853 | G | T | 1 | a0001c0001t0005g0066 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1026+7921C>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25136853 | |||||||
chr4:25136891 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1026+7883T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25136891 | |||||||
chr4:25136943 | T | C | 1 | a0001c0001t0002g0165 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1026+7831A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25136943 | |||||||
chr4:25137137 | T | C | 32 | a0001c0001t0004g0002 a0001c0001t0004g0006 a0001c0001t0004g0009 others(29): Show |
53 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.1026+7637A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25137137 | |||||||
chr4:25137308 | C | T | 3 | a0001c0001t0010g0043 a0001c0001t0010g0151 a0001c0001t0018g0152 |
4 | HG00741.hp1 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026+7466G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25137308 | |||||||
chr4:25137350 | C | T | 2 | a0001c0001t0001g0269 a0001c0001t0021g0268 |
2 | HG02165.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1026+7424G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25137350 | |||||||
chr4:25137364 | C | T | 27 | a0002c0002t0003g0004 a0002c0002t0003g0007 a0002c0002t0003g0016 others(24): Show |
45 | HG00438.hp2 HG00642.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.1026+7410G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25137364 | |||||||
chr4:25137390 | A | T | 311 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(308): Show |
441 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(438): Show |
intron_variant | MODIFIER | c.1026+7384T>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25137390 | |||||||
chr4:25137505 | A | G | 5 | a0001c0001t0006g0024 a0001c0001t0006g0052 a0001c0001t0006g0255 others(2): Show |
8 | HG02572.hp2 HG02647.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1026+7269T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25137505 | |||||||
chr4:25137576 | G | C | 3 | a0001c0001t0001g0107 a0001c0001t0012g0103 a0001c0004t0001g0059 |
3 | NA19066.hp2 NA19078.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1026+7198C>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25137576 | |||||||
chr4:25137611 | G | A | 1 | a0001c0001t0004g0241 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1026+7163C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25137611 | |||||||
chr4:25137692 | C | T | 2 | a0001c0001t0005g0027 a0001c0001t0005g0069 |
3 | HG02717.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1026+7082G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25137692 | |||||||
chr4:25137820 | A | G | 3 | a0001c0001t0001g0269 a0001c0001t0001g0288 a0001c0001t0021g0268 |
3 | HG02165.hp1 HG03579.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1026+6954T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25137820 | |||||||
chr4:25137916 | G | A | 37 | a0002c0002t0003g0004 a0002c0002t0003g0007 a0002c0002t0003g0014 others(34): Show |
61 | HG00438.hp2 HG00642.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.1026+6858C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25137916 | |||||||
chr4:25138337 | T | C | 1 | a0001c0001t0001g0288 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1026+6437A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25138337 | |||||||
chr4:25138422 | C | T | 1 | a0001c0001t0002g0048 | 2 | HG01978.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1026+6352G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25138422 | |||||||
chr4:25138621 | C | T | 1 | a0002c0002t0003g0305 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1026+6153G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25138621 | |||||||
chr4:25138807 | CA | C | 3 | a0001c0001t0001g0269 a0001c0001t0001g0288 a0001c0001t0021g0268 |
3 | HG02165.hp1 HG03579.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1026+5966delT | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25138807 | |||||||
chr4:25138828 | G | A | 1 | a0001c0001t0002g0196 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1026+5946C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25138828 | |||||||
chr4:25138870 | T | G | 2 | a0001c0001t0002g0175 a0001c0001t0002g0203 |
2 | HG01928.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1026+5904A>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25138870 | |||||||
chr4:25139144 | T | A | 1 | a0001c0001t0003g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1026+5630A>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25139144 | |||||||
chr4:25139145 | C | A | 1 | a0001c0001t0003g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1026+5629G>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25139145 | |||||||
chr4:25139268 | T | C | 1 | a0001c0001t0028g0153 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1026+5506A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25139268 | |||||||
chr4:25139384 | C | CT | 265 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0012 others(262): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.1026+5389dupA | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25139384 | |||||||
chr4:25139384 | C | CTT | 25 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0061 others(22): Show |
27 | HG00733.hp2 HG01106.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.1026+5388_1026+538 others(6): Show |
SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25139384 | |||||||
chr4:25139578 | G | T | 2 | a0001c0001t0013g0193 a0001c0001t0013g0194 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1026+5196C>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25139578 | |||||||
chr4:25139626 | T | C | 3 | a0001c0001t0010g0043 a0001c0001t0010g0151 a0001c0001t0018g0152 |
4 | HG00741.hp1 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026+5148A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25139626 | |||||||
chr4:25139724 | G | T | 32 | a0001c0001t0004g0002 a0001c0001t0004g0006 a0001c0001t0004g0009 others(29): Show |
53 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.1026+5050C>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25139724 | |||||||
chr4:25139919 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1026+4855G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25139919 | |||||||
chr4:25139959 | T | C | 1 | a0001c0001t0001g0258 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1026+4815A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25139959 | |||||||
chr4:25139996 | T | C | 1 | a0001c0001t0001g0278 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1026+4778A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25139996 | |||||||
chr4:25140015 | G | C | 1 | a0001c0001t0002g0176 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1026+4759C>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25140015 | |||||||
chr4:25140078 | A | G | 64 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0002g0001 others(61): Show |
93 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.1026+4696T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25140078 | |||||||
chr4:25140104 | C | T | 1 | a0001c0001t0001g0090 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1026+4670G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25140104 | |||||||
chr4:25140182 | C | T | 2 | a0001c0001t0006g0255 a0001c0001t0006g0256 |
2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1026+4592G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25140182 | |||||||
chr4:25140420 | G | A | 318 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(315): Show |
451 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(448): Show |
intron_variant | MODIFIER | c.1026+4354C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25140420 | |||||||
chr4:25140431 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1026+4343A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25140431 | |||||||
chr4:25140699 | T | C | 1 | a0001c0001t0001g0281 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1026+4075A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25140699 | |||||||
chr4:25140719 | T | C | 2 | a0001c0001t0001g0049 a0001c0001t0001g0230 |
3 | NA18984.hp2 NA18998.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.1026+4055A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25140719 | |||||||
chr4:25140856 | G | A | 9 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0035 others(6): Show |
18 | HG00738.hp2 HG01358.hp1 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.1026+3918C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25140856 | |||||||
chr4:25140918 | G | GA | 220 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(217): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.1026+3855dupT | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25140918 | |||||||
chr4:25140971 | A | G | 1 | a0001c0001t0006g0024 | 3 | HG02976.hp1 HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1026+3803T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25140971 | |||||||
chr4:25141404 | T | C | 1 | a0001c0001t0023g0128 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1026+3370A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25141404 | |||||||
chr4:25141518 | A | G | 7 | a0001c0001t0008g0053 a0001c0001t0008g0264 a0001c0001t0008g0265 others(4): Show |
9 | HG00741.hp1 HG01261.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1026+3256T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25141518 | |||||||
chr4:25141609 | G | A | 239 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(236): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1026+3165C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25141609 | |||||||
chr4:25141643 | C | T | 1 | a0001c0001t0005g0068 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1026+3131G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25141643 | |||||||
chr4:25141752 | C | A | 1 | a0002c0002t0003g0297 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1026+3022G>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25141752 | |||||||
chr4:25141825 | T | TCTC | 4 | a0001c0001t0001g0269 a0001c0001t0013g0193 a0001c0001t0013g0194 others(1): Show |
4 | HG01243.hp1 HG01884.hp2 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026+2946_1026+294 others(7): Show |
SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25141825 | |||||||
chr4:25141842 | C | T | 1 | a0001c0001t0002g0206 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1026+2932G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25141842 | |||||||
chr4:25141905 | C | G | 1 | a0003c0003t0005g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1026+2869G>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25141905 | |||||||
chr4:25141907 | T | C | 1 | a0001c0001t0002g0178 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1026+2867A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25141907 | |||||||
chr4:25141911 | A | G | 1 | a0001c0001t0001g0288 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1026+2863T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25141911 | |||||||
chr4:25141932 | C | T | 32 | a0001c0001t0004g0002 a0001c0001t0004g0006 a0001c0001t0004g0009 others(29): Show |
53 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.1026+2842G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25141932 | |||||||
chr4:25142105 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1026+2669G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25142105 | |||||||
chr4:25142443 | A | C | 2 | a0001c0001t0009g0187 a0001c0001t0025g0190 |
2 | HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1026+2331T>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25142443 | |||||||
chr4:25142497 | C | A | 2 | a0001c0001t0001g0320 a0001c0001t0003g0321 |
2 | HG02970.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1026+2277G>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25142497 | |||||||
chr4:25142568 | G | GTAAGT | 3 | a0001c0001t0001g0269 a0001c0001t0001g0288 a0001c0001t0021g0268 |
3 | HG02165.hp1 HG03579.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1026+2205_1026+220 others(9): Show |
SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25142568 | |||||||
chr4:25142633 | C | G | 2 | a0001c0001t0001g0085 a0001c0001t0001g0110 |
2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1026+2141G>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25142633 | |||||||
chr4:25142637 | A | G | 1 | a0001c0001t0001g0288 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1026+2137T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25142637 | |||||||
chr4:25142684 | T | C | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | NA18962.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1026+2090A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25142684 | |||||||
chr4:25142697 | A | G | 61 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0011 others(58): Show |
90 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.1026+2077T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25142697 | |||||||
chr4:25142744 | G | A | 5 | a0001c0001t0006g0024 a0001c0001t0006g0052 a0001c0001t0006g0255 others(2): Show |
8 | HG02572.hp2 HG02647.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1026+2030C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25142744 | |||||||
chr4:25142771 | A | G | 1 | a0001c0001t0013g0193 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1026+2003T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25142771 | |||||||
chr4:25142859 | T | A | 5 | a0001c0001t0005g0066 a0001c0001t0005g0067 a0003c0003t0005g0017 others(2): Show |
7 | HG01109.hp2 HG02258.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1026+1915A>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25142859 | |||||||
chr4:25142945 | T | C | 179 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0050 others(176): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1026+1829A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25142945 | |||||||
chr4:25143014 | T | C | 20 | a0001c0001t0001g0003 a0001c0001t0001g0049 a0001c0001t0001g0221 others(17): Show |
28 | HG00423.hp2 HG00597.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.1026+1760A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25143014 | |||||||
chr4:25143121 | C | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0219 |
2 | NA18970.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.1026+1653G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25143121 | |||||||
chr4:25143127 | T | A | 5 | a0001c0001t0005g0066 a0001c0001t0005g0067 a0003c0003t0005g0017 others(2): Show |
7 | HG01109.hp2 HG02258.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1026+1647A>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25143127 | |||||||
chr4:25143147 | T | C | 1 | a0001c0001t0001g0041 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1026+1627A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25143147 | |||||||
chr4:25143151 | T | C | 2 | a0001c0001t0001g0269 a0001c0001t0021g0268 |
2 | HG02165.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1026+1623A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25143151 | |||||||
chr4:25143161 | G | A | 2 | a0001c0001t0001g0225 a0001c0001t0001g0231 |
2 | HG02071.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.1026+1613C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25143161 | |||||||
chr4:25143232 | G | A | 1 | a0001c0001t0023g0128 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1026+1542C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25143232 | |||||||
chr4:25143266 | A | G | 1 | a0003c0003t0005g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1026+1508T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25143266 | |||||||
chr4:25143315 | G | A | 240 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(237): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.1026+1459C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25143315 | |||||||
chr4:25143348 | C | T | 121 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0002g0001 others(118): Show |
179 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.1026+1426G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25143348 | |||||||
chr4:25143391 | A | G | 2 | a0001c0001t0002g0163 a0001c0001t0002g0206 |
2 | HG01257.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.1026+1383T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25143391 | |||||||
chr4:25143434 | C | T | 1 | a0001c0001t0003g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1026+1340G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25143434 | |||||||
chr4:25143508 | T | A | 26 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0050 others(23): Show |
33 | HG00544.hp2 HG00621.hp1 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.1026+1266A>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25143508 | |||||||
chr4:25143649 | T | TA | 3 | a0001c0001t0001g0031 a0001c0001t0001g0084 a0001c0001t0001g0115 |
4 | HG01081.hp2 HG01099.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026+1124dupT | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25143649 | |||||||
chr4:25143887 | T | C | 1 | a0001c0001t0003g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1026+887A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25143887 | |||||||
chr4:25144029 | G | A | 4 | a0001c0001t0001g0279 a0001c0001t0001g0281 a0001c0001t0001g0282 others(1): Show |
4 | HG01243.hp2 HG03209.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026+745C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25144029 | |||||||
chr4:25144079 | G | A | 2 | a0001c0001t0004g0134 a0001c0001t0004g0141 |
2 | HG03942.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1026+695C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25144079 | |||||||
chr4:25144150 | C | A | 3 | a0001c0001t0001g0269 a0001c0001t0001g0288 a0001c0001t0021g0268 |
3 | HG02165.hp1 HG03579.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1026+624G>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25144150 | |||||||
chr4:25144322 | C | T | 2 | a0001c0001t0001g0101 a0001c0001t0001g0249 |
2 | HG03669.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.1026+452G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25144322 | |||||||
chr4:25144326 | C | CA | 107 | a0001c0001t0001g0003 a0001c0001t0001g0049 a0001c0001t0001g0077 others(104): Show |
162 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.1026+447dupT | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25144326 | |||||||
chr4:25144326 | CA | C | 7 | a0001c0001t0001g0018 a0001c0001t0001g0063 a0001c0001t0001g0083 others(4): Show |
10 | HG00558.hp2 HG01167.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.1026+447delT | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25144326 | |||||||
chr4:25144528 | G | C | 1 | a0001c0001t0001g0269 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1026+246C>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25144528 | |||||||
chr4:25144550 | T | C | 32 | a0001c0001t0004g0002 a0001c0001t0004g0006 a0001c0001t0004g0009 others(29): Show |
53 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.1026+224A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25144550 | |||||||
chr4:25144580 | C | G | 1 | a0001c0001t0001g0118 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1026+194G>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25144580 | |||||||
chr4:25144626 | C | G | 1 | a0002c0002t0003g0292 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1026+148G>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25144626 | |||||||
chr4:25144629 | T | C | 9 | a0001c0001t0004g0006 a0001c0001t0004g0039 a0001c0001t0004g0135 others(6): Show |
16 | HG00673.hp1 HG02155.hp2 NA18945.hp1 others(13): Show |
intron_variant | MODIFIER | c.1026+145A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25144629 | |||||||
chr4:25144685 | G | A | 175 | a0001c0001t0001g0003 a0001c0001t0001g0049 a0001c0001t0001g0221 others(172): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1026+89C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 8/10 | chr4 | 25144685 | |||||||
chr4:25144870 | A | C | 21 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0029 others(18): Show |
25 | HG00438.hp1 HG00544.hp1 HG01167.hp2 others(22): Show |
splice_region_variant&intron_variant | LOW | c.935-5T>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 7/10 | chr4 | 25144870 | |||||||
chr4:25144911 | A | G | 1 | a0001c0001t0002g0215 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.935-46T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 7/10 | chr4 | 25144911 | |||||||
chr4:25145217 | T | C | 1 | a0001c0001t0002g0205 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.805-84A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25145217 | |||||||
chr4:25145365 | T | A | 1 | a0001c0001t0002g0048 | 2 | HG01978.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.805-232A>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25145365 | |||||||
chr4:25145445 | T | A | 8 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0147 others(5): Show |
10 | HG01106.hp2 HG01109.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.805-312A>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25145445 | |||||||
chr4:25145479 | G | GTTTACAA others(23): Show |
1 | a0002c0002t0003g0300 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.805-376_805-347dup others(30): Show |
SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25145479 | |||||||
chr4:25145604 | T | C | 37 | a0002c0002t0003g0004 a0002c0002t0003g0007 a0002c0002t0003g0014 others(34): Show |
61 | HG00438.hp2 HG00642.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.805-471A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25145604 | |||||||
chr4:25145652 | T | A | 1 | a0001c0001t0001g0099 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.805-519A>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25145652 | |||||||
chr4:25145677 | C | T | 1 | a0002c0002t0003g0290 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.805-544G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25145677 | |||||||
chr4:25145727 | A | C | 3 | a0001c0001t0010g0043 a0001c0001t0010g0151 a0001c0001t0018g0152 |
4 | HG00741.hp1 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.805-594T>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25145727 | |||||||
chr4:25145746 | T | C | 6 | a0001c0001t0001g0258 a0001c0001t0007g0054 a0001c0001t0007g0271 others(3): Show |
7 | HG02145.hp1 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.805-613A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25145746 | |||||||
chr4:25145878 | A | G | 2 | a0001c0001t0001g0320 a0001c0001t0003g0321 |
2 | HG02970.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.805-745T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25145878 | |||||||
chr4:25145961 | G | C | 1 | a0001c0001t0001g0319 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.805-828C>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25145961 | |||||||
chr4:25146032 | C | T | 1 | a0002c0002t0003g0314 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.805-899G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25146032 | |||||||
chr4:25146108 | G | C | 2 | a0001c0001t0001g0284 a0001c0001t0001g0285 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.805-975C>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25146108 | |||||||
chr4:25146254 | G | A | 3 | a0001c0001t0004g0038 a0001c0001t0004g0137 a0001c0001t0004g0143 |
4 | HG00558.hp1 NA18939.hp1 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.805-1121C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25146254 | |||||||
chr4:25146259 | A | G | 3 | a0001c0001t0010g0043 a0001c0001t0010g0151 a0001c0001t0018g0152 |
4 | HG00741.hp1 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.805-1126T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25146259 | |||||||
chr4:25146284 | G | A | 3 | a0001c0001t0001g0107 a0001c0001t0012g0103 a0001c0004t0001g0059 |
3 | NA19066.hp2 NA19078.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.805-1151C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25146284 | |||||||
chr4:25146339 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.805-1206A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25146339 | |||||||
chr4:25146474 | T | TA | 240 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(237): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.805-1342dupT | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25146474 | |||||||
chr4:25146514 | G | T | 54 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0025 others(51): Show |
71 | HG00544.hp2 HG00621.hp1 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.805-1381C>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25146514 | |||||||
chr4:25146534 | T | C | 1 | a0001c0001t0001g0100 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.805-1401A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25146534 | |||||||
chr4:25146840 | C | T | 5 | a0002c0002t0003g0015 a0002c0002t0003g0289 a0002c0002t0003g0296 others(2): Show |
8 | HG02109.hp2 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.805-1707G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25146840 | |||||||
chr4:25146938 | T | G | 8 | a0001c0001t0005g0027 a0001c0001t0005g0066 a0001c0001t0005g0067 others(5): Show |
11 | HG01109.hp2 HG02258.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.805-1805A>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25146938 | |||||||
chr4:25147124 | A | T | 3 | a0001c0001t0001g0269 a0001c0001t0001g0288 a0001c0001t0021g0268 |
3 | HG02165.hp1 HG03579.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.805-1991T>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25147124 | |||||||
chr4:25147302 | G | C | 3 | a0001c0001t0001g0269 a0001c0001t0001g0288 a0001c0001t0021g0268 |
3 | HG02165.hp1 HG03579.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.805-2169C>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25147302 | |||||||
chr4:25147343 | T | C | 240 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(237): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.805-2210A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25147343 | |||||||
chr4:25147448 | A | G | 5 | a0001c0001t0006g0024 a0001c0001t0006g0052 a0001c0001t0006g0255 others(2): Show |
8 | HG02572.hp2 HG02647.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.805-2315T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25147448 | |||||||
chr4:25147597 | C | A | 1 | a0001c0001t0001g0105 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.805-2464G>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25147597 | |||||||
chr4:25147603 | T | A | 1 | a0001c0001t0001g0258 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.805-2470A>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25147603 | |||||||
chr4:25147921 | G | A | 20 | a0001c0001t0001g0003 a0001c0001t0001g0049 a0001c0001t0001g0221 others(17): Show |
28 | HG00423.hp2 HG00597.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.805-2788C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25147921 | |||||||
chr4:25147926 | G | T | 1 | a0001c0001t0006g0024 | 3 | HG02976.hp1 HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.805-2793C>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25147926 | |||||||
chr4:25148025 | C | G | 2 | a0001c0001t0013g0193 a0001c0001t0013g0194 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.805-2892G>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25148025 | |||||||
chr4:25148092 | T | C | 176 | a0001c0001t0001g0003 a0001c0001t0001g0049 a0001c0001t0001g0221 others(173): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.805-2959A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25148092 | |||||||
chr4:25148123 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.805-2990G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25148123 | |||||||
chr4:25148127 | T | C | 1 | a0001c0001t0001g0252 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.805-2994A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25148127 | |||||||
chr4:25148158 | C | G | 1 | a0001c0001t0002g0238 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.805-3025G>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25148158 | |||||||
chr4:25148269 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.805-3136G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25148269 | |||||||
chr4:25148302 | A | G | 4 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
4 | NA18950.hp1 NA18962.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.805-3169T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25148302 | |||||||
chr4:25148340 | G | A | 8 | a0001c0001t0005g0027 a0001c0001t0005g0066 a0001c0001t0005g0067 others(5): Show |
11 | HG01109.hp2 HG02258.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.805-3207C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25148340 | |||||||
chr4:25148351 | T | A | 1 | a0001c0001t0013g0194 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.805-3218A>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25148351 | |||||||
chr4:25148352 | C | CA | 9 | a0001c0001t0001g0107 a0001c0001t0001g0224 a0001c0001t0001g0225 others(6): Show |
9 | HG00423.hp2 HG00597.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.805-3220dupT | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25148352 | |||||||
chr4:25148352 | CA | C | 226 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0012 others(223): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.805-3220delT | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25148352 | |||||||
chr4:25148352 | CAA | C | 6 | a0001c0001t0001g0084 a0001c0001t0002g0160 a0001c0001t0002g0195 others(3): Show |
6 | HG01081.hp2 HG01192.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.805-3221_805-3220d others(4): Show |
SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25148352 | |||||||
chr4:25148352 | CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0007g0271 a0001c0001t0007g0272 |
2 | HG02145.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.805-3230_805-3220d others(13): Show |
SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25148352 | |||||||
chr4:25148437 | G | A | 1 | a0001c0001t0002g0180 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.805-3304C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25148437 | |||||||
chr4:25148437 | G | T | 1 | a0001c0001t0001g0041 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.805-3304C>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25148437 | |||||||
chr4:25148443 | T | C | 1 | a0001c0001t0008g0266 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.805-3310A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25148443 | |||||||
chr4:25148466 | A | C | 2 | a0002c0002t0003g0016 a0002c0002t0003g0313 |
5 | HG01975.hp2 HG01981.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.805-3333T>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25148466 | |||||||
chr4:25149143 | C | T | 1 | a0001c0001t0013g0193 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.804+2817G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25149143 | |||||||
chr4:25149144 | G | A | 20 | a0001c0001t0001g0003 a0001c0001t0001g0049 a0001c0001t0001g0221 others(17): Show |
28 | HG00423.hp2 HG00597.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.804+2816C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25149144 | |||||||
chr4:25149233 | T | A | 61 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0011 others(58): Show |
90 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.804+2727A>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25149233 | |||||||
chr4:25149263 | G | T | 20 | a0001c0001t0001g0003 a0001c0001t0001g0049 a0001c0001t0001g0221 others(17): Show |
28 | HG00423.hp2 HG00597.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.804+2697C>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25149263 | |||||||
chr4:25149268 | G | C | 7 | a0001c0001t0002g0010 a0001c0001t0002g0060 a0001c0001t0002g0146 others(4): Show |
10 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.804+2692C>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25149268 | |||||||
chr4:25149307 | C | T | 2 | a0001c0001t0004g0125 a0001c0001t0004g0126 |
2 | HG01106.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.804+2653G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25149307 | |||||||
chr4:25149675 | AG | A | 37 | a0002c0002t0003g0004 a0002c0002t0003g0007 a0002c0002t0003g0014 others(34): Show |
61 | HG00438.hp2 HG00642.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.804+2284delC | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25149675 | |||||||
chr4:25149877 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.804+2083A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25149877 | |||||||
chr4:25149912 | T | A | 32 | a0001c0001t0004g0002 a0001c0001t0004g0006 a0001c0001t0004g0009 others(29): Show |
53 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.804+2048A>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25149912 | |||||||
chr4:25150052 | C | T | 4 | a0001c0001t0001g0057 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
5 | HG01257.hp2 HG01258.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.804+1908G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25150052 | |||||||
chr4:25150252 | A | T | 153 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0002g0001 others(150): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.804+1708T>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25150252 | |||||||
chr4:25150391 | C | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0034 a0001c0001t0001g0083 others(1): Show |
9 | HG00558.hp2 HG02135.hp1 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.804+1569G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25150391 | |||||||
chr4:25150392 | G | A | 32 | a0001c0001t0004g0002 a0001c0001t0004g0006 a0001c0001t0004g0009 others(29): Show |
53 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.804+1568C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25150392 | |||||||
chr4:25150577 | T | TA | 11 | a0001c0001t0001g0078 a0001c0001t0001g0105 a0001c0001t0001g0106 others(8): Show |
13 | HG00423.hp1 HG01109.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.804+1382dupT | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25150577 | |||||||
chr4:25150724 | G | A | 22 | a0001c0001t0001g0013 a0001c0001t0001g0055 a0001c0001t0001g0056 others(19): Show |
29 | HG00639.hp1 HG01192.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.804+1236C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25150724 | |||||||
chr4:25150824 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.804+1136C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25150824 | |||||||
chr4:25151069 | T | C | 20 | a0001c0001t0001g0003 a0001c0001t0001g0049 a0001c0001t0001g0221 others(17): Show |
28 | HG00423.hp2 HG00597.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.804+891A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25151069 | |||||||
chr4:25151414 | C | G | 1 | a0001c0001t0028g0153 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.804+546G>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25151414 | |||||||
chr4:25151483 | G | C | 20 | a0001c0001t0001g0003 a0001c0001t0001g0049 a0001c0001t0001g0221 others(17): Show |
28 | HG00423.hp2 HG00597.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.804+477C>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25151483 | |||||||
chr4:25151517 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.804+443G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25151517 | |||||||
chr4:25151561 | T | C | 1 | a0001c0001t0002g0212 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.804+399A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25151561 | |||||||
chr4:25151832 | AAC | A | 20 | a0001c0001t0001g0003 a0001c0001t0001g0049 a0001c0001t0001g0221 others(17): Show |
28 | HG00423.hp2 HG00597.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.804+126_804+127del others(2): Show |
SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 6/10 | chr4 | 25151832 | |||||||
chr4:25152304 | A | C | 1 | a0001c0001t0001g0082 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.702-242T>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 5/10 | chr4 | 25152304 | |||||||
chr4:25152354 | TA | T | 3 | a0001c0001t0010g0043 a0001c0001t0010g0151 a0001c0001t0018g0152 |
4 | HG00741.hp1 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.702-293delT | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 5/10 | chr4 | 25152354 | |||||||
chr4:25153066 | T | C | 8 | a0001c0001t0005g0027 a0001c0001t0005g0066 a0001c0001t0005g0067 others(5): Show |
11 | HG01109.hp2 HG02258.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.702-1004A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 5/10 | chr4 | 25153066 | |||||||
chr4:25153100 | A | G | 1 | a0001c0001t0023g0128 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.702-1038T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 5/10 | chr4 | 25153100 | |||||||
chr4:25153249 | A | G | 1 | a0005c0005t0001g0062 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.702-1187T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 5/10 | chr4 | 25153249 | |||||||
chr4:25153400 | T | G | 20 | a0001c0001t0001g0003 a0001c0001t0001g0049 a0001c0001t0001g0221 others(17): Show |
28 | HG00423.hp2 HG00597.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.702-1338A>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 5/10 | chr4 | 25153400 | |||||||
chr4:25153490 | G | A | 1 | a0001c0001t0001g0254 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.702-1428C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 5/10 | chr4 | 25153490 | |||||||
chr4:25153642 | T | G | 7 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0063 others(4): Show |
9 | HG00140.hp2 HG01168.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.701+1356A>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 5/10 | chr4 | 25153642 | |||||||
chr4:25153685 | C | A | 3 | a0001c0001t0001g0269 a0001c0001t0001g0288 a0001c0001t0021g0268 |
3 | HG02165.hp1 HG03579.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.701+1313G>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 5/10 | chr4 | 25153685 | |||||||
chr4:25154003 | T | G | 4 | a0001c0001t0001g0233 a0001c0001t0001g0235 a0001c0001t0001g0236 others(1): Show |
4 | HG02040.hp2 NA18990.hp2 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.701+995A>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 5/10 | chr4 | 25154003 | |||||||
chr4:25154057 | T | A | 1 | a0001c0001t0001g0254 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.701+941A>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 5/10 | chr4 | 25154057 | |||||||
chr4:25154228 | C | T | 1 | a0001c0001t0002g0060 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.701+770G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 5/10 | chr4 | 25154228 | |||||||
chr4:25154293 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.701+705C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 5/10 | chr4 | 25154293 | |||||||
chr4:25154404 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.701+594G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 5/10 | chr4 | 25154404 | |||||||
chr4:25154609 | C | T | 1 | a0002c0002t0003g0293 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.701+389G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 5/10 | chr4 | 25154609 | |||||||
chr4:25154619 | T | C | 20 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0050 others(17): Show |
26 | HG00544.hp2 HG00621.hp1 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.701+379A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 5/10 | chr4 | 25154619 | |||||||
chr4:25154686 | C | A | 4 | a0001c0001t0001g0025 a0001c0001t0001g0253 a0001c0001t0001g0261 others(1): Show |
6 | NA18948.hp2 NA18956.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.701+312G>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 5/10 | chr4 | 25154686 | |||||||
chr4:25154752 | C | T | 5 | a0001c0001t0006g0024 a0001c0001t0006g0052 a0001c0001t0006g0255 others(2): Show |
8 | HG02572.hp2 HG02647.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.701+246G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 5/10 | chr4 | 25154752 | |||||||
chr4:25154861 | A | G | 64 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0002g0001 others(61): Show |
93 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.701+137T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 5/10 | chr4 | 25154861 | |||||||
chr4:25155173 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.548-22G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 4/10 | chr4 | 25155173 | |||||||
chr4:25155174 | A | C | 1 | a0001c0001t0002g0046 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.548-23T>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 4/10 | chr4 | 25155174 | |||||||
chr4:25155364 | T | G | 5 | a0001c0001t0009g0187 a0001c0001t0009g0188 a0001c0001t0009g0189 others(2): Show |
5 | HG01346.hp1 HG01884.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.548-213A>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 4/10 | chr4 | 25155364 | |||||||
chr4:25155810 | C | G | 1 | a0001c0001t0001g0233 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.547+227G>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 4/10 | chr4 | 25155810 | |||||||
chr4:25155934 | T | C | 1 | a0001c0001t0002g0183 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.547+103A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 4/10 | chr4 | 25155934 | |||||||
chr4:25155937 | G | A | 1 | a0001c0001t0001g0254 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.547+100C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 4/10 | chr4 | 25155937 | |||||||
chr4:25156239 | AC | A | 3 | a0001c0001t0001g0020 a0001c0001t0001g0109 a0001c0001t0001g0218 |
5 | HG00438.hp1 HG00544.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.389-45delG | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 3/10 | chr4 | 25156239 | |||||||
chr4:25156333 | A | C | 17 | a0001c0001t0001g0013 a0001c0001t0001g0055 a0001c0001t0001g0056 others(14): Show |
23 | HG00639.hp1 HG01192.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.389-138T>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 3/10 | chr4 | 25156333 | |||||||
chr4:25156403 | TA | T | 317 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(314): Show |
450 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(447): Show |
intron_variant | MODIFIER | c.389-209delT | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 3/10 | chr4 | 25156403 | |||||||
chr4:25156405 | A | T | 1 | a0001c0001t0001g0288 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.389-210T>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 3/10 | chr4 | 25156405 | |||||||
chr4:25156470 | C | T | 1 | a0001c0001t0008g0264 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.389-275G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 3/10 | chr4 | 25156470 | |||||||
chr4:25156471 | A | G | 1 | a0001c0001t0008g0264 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.389-276T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 3/10 | chr4 | 25156471 | |||||||
chr4:25156475 | C | G | 1 | a0001c0001t0008g0264 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.389-280G>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 3/10 | chr4 | 25156475 | |||||||
chr4:25156518 | C | G | 1 | a0001c0001t0001g0226 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.389-323G>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 3/10 | chr4 | 25156518 | |||||||
chr4:25156528 | C | A | 2 | a0001c0001t0013g0193 a0001c0001t0013g0194 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.388+328G>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 3/10 | chr4 | 25156528 | |||||||
chr4:25156600 | C | T | 61 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0011 others(58): Show |
90 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.388+256G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 3/10 | chr4 | 25156600 | |||||||
chr4:25156640 | G | A | 8 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0147 others(5): Show |
10 | HG01106.hp2 HG01109.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.388+216C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 3/10 | chr4 | 25156640 | |||||||
chr4:25156665 | G | A | 1 | a0001c0001t0002g0146 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.388+191C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 3/10 | chr4 | 25156665 | |||||||
chr4:25156707 | C | CA | 89 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0028 others(86): Show |
119 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.388+148dupT | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 3/10 | chr4 | 25156707 | |||||||
chr4:25156707 | C | CAA | 57 | a0001c0001t0001g0285 a0001c0001t0001g0319 a0001c0001t0001g0320 others(54): Show |
81 | HG00438.hp2 HG00621.hp2 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.388+147_388+148dup others(2): Show |
SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 3/10 | chr4 | 25156707 | |||||||
chr4:25156707 | C | CAAA | 11 | a0001c0001t0002g0214 a0002c0002t0003g0007 a0002c0002t0003g0295 others(8): Show |
18 | HG00642.hp2 HG01109.hp2 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.388+146_388+148dup others(3): Show |
SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 3/10 | chr4 | 25156707 | |||||||
chr4:25156707 | C | CAAAAAAA others(6): Show |
4 | a0001c0001t0008g0053 a0001c0001t0008g0264 a0001c0001t0008g0265 others(1): Show |
5 | HG01261.hp1 HG03471.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.388+136_388+148dup others(13): Show |
SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 3/10 | chr4 | 25156707 | |||||||
chr4:25156707 | CA | C | 10 | a0001c0001t0001g0003 a0001c0001t0001g0049 a0001c0001t0001g0221 others(7): Show |
18 | HG00423.hp2 HG01943.hp1 HG02135.hp2 others(15): Show |
intron_variant | MODIFIER | c.388+148delT | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 3/10 | chr4 | 25156707 | |||||||
chr4:25156707 | CAA | C | 6 | a0001c0001t0004g0009 a0001c0001t0004g0073 a0001c0001t0004g0140 others(3): Show |
10 | HG00140.hp1 HG00609.hp2 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.388+147_388+148del others(2): Show |
SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 3/10 | chr4 | 25156707 | |||||||
chr4:25156707 | CAAA | C | 28 | a0001c0001t0001g0269 a0001c0001t0004g0002 a0001c0001t0004g0006 others(25): Show |
45 | HG00558.hp1 HG00673.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.388+146_388+148del others(3): Show |
SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 3/10 | chr4 | 25156707 | |||||||
chr4:25156707 | CAAAAAAA others(1): Show |
C | 6 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0147 others(3): Show |
8 | HG01106.hp2 HG01109.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.388+141_388+148del others(8): Show |
SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 3/10 | chr4 | 25156707 | |||||||
chr4:25156707 | CAAAAAAA others(3): Show |
C | 8 | a0002c0002t0003g0014 a0002c0002t0003g0015 a0002c0002t0003g0289 others(5): Show |
14 | HG02109.hp2 HG02258.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.388+139_388+148del others(10): Show |
SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 3/10 | chr4 | 25156707 | |||||||
chr4:25156707 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0002g0146 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.388+136_388+148del others(13): Show |
SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 3/10 | chr4 | 25156707 | |||||||
chr4:25157050 | G | A | 3 | a0001c0001t0001g0269 a0001c0001t0001g0288 a0001c0001t0021g0268 |
3 | HG02165.hp1 HG03579.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.270-76C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 2/10 | chr4 | 25157050 | |||||||
chr4:25157128 | T | C | 32 | a0001c0001t0004g0002 a0001c0001t0004g0006 a0001c0001t0004g0009 others(29): Show |
53 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.270-154A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 2/10 | chr4 | 25157128 | |||||||
chr4:25157168 | T | C | 3 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0285 |
3 | HG01257.hp2 HG01258.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.270-194A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 2/10 | chr4 | 25157168 | |||||||
chr4:25157274 | C | A | 5 | a0001c0001t0007g0054 a0001c0001t0007g0271 a0001c0001t0007g0272 others(2): Show |
6 | HG02145.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.270-300G>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 2/10 | chr4 | 25157274 | |||||||
chr4:25157372 | A | T | 1 | a0002c0002t0003g0318 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.270-398T>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 2/10 | chr4 | 25157372 | |||||||
chr4:25157539 | C | CT | 13 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(10): Show |
16 | HG01255.hp1 HG02027.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.270-566dupA | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 2/10 | chr4 | 25157539 | |||||||
chr4:25157539 | CT | C | 50 | a0001c0001t0001g0063 a0001c0001t0001g0123 a0001c0001t0001g0234 others(47): Show |
76 | HG00438.hp2 HG00642.hp2 HG00733.hp1 others(73): Show |
intron_variant | MODIFIER | c.270-566delA | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 2/10 | chr4 | 25157539 | |||||||
chr4:25157558 | G | T | 32 | a0001c0001t0004g0002 a0001c0001t0004g0006 a0001c0001t0004g0009 others(29): Show |
53 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.270-584C>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 2/10 | chr4 | 25157558 | |||||||
chr4:25157638 | A | G | 1 | a0002c0002t0003g0293 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.270-664T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 2/10 | chr4 | 25157638 | |||||||
chr4:25157747 | A | G | 1 | a0001c0001t0001g0275 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.270-773T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 2/10 | chr4 | 25157747 | |||||||
chr4:25157768 | A | T | 20 | a0001c0001t0001g0013 a0001c0001t0001g0055 a0001c0001t0001g0056 others(17): Show |
27 | HG00639.hp1 HG01243.hp2 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.270-794T>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 2/10 | chr4 | 25157768 | |||||||
chr4:25157814 | A | G | 1 | a0001c0001t0023g0128 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.270-840T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 2/10 | chr4 | 25157814 | |||||||
chr4:25157840 | C | T | 6 | a0001c0001t0001g0028 a0001c0001t0001g0061 a0001c0001t0001g0074 others(3): Show |
7 | NA18953.hp1 NA18964.hp2 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.270-866G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 2/10 | chr4 | 25157840 | |||||||
chr4:25157841 | G | A | 1 | a0001c0001t0002g0215 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.270-867C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 2/10 | chr4 | 25157841 | |||||||
chr4:25157854 | T | G | 2 | a0001c0001t0017g0217 a0001c0001t0027g0216 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.270-880A>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 2/10 | chr4 | 25157854 | |||||||
chr4:25158012 | A | G | 1 | a0001c0001t0022g0127 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.269+941T>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 2/10 | chr4 | 25158012 | |||||||
chr4:25158034 | C | T | 2 | a0001c0001t0004g0125 a0001c0001t0004g0126 |
2 | HG01106.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.269+919G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 2/10 | chr4 | 25158034 | |||||||
chr4:25158130 | C | A | 1 | a0001c0001t0001g0124 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.269+823G>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 2/10 | chr4 | 25158130 | |||||||
chr4:25158271 | G | C | 4 | a0001c0001t0008g0053 a0001c0001t0008g0264 a0001c0001t0008g0265 others(1): Show |
5 | HG01261.hp1 HG03471.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.269+682C>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 2/10 | chr4 | 25158271 | |||||||
chr4:25158379 | TATTAACT others(4): Show |
T | 71 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0018 others(68): Show |
95 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.269+563_269+573del others(11): Show |
SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 2/10 | chr4 | 25158379 | |||||||
chr4:25158414 | T | C | 1 | a0001c0001t0001g0267 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.269+539A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 2/10 | chr4 | 25158414 | |||||||
chr4:25158444 | T | C | 1 | a0001c0001t0001g0218 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.269+509A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 2/10 | chr4 | 25158444 | |||||||
chr4:25158577 | C | CA | 22 | a0001c0001t0001g0003 a0001c0001t0001g0049 a0001c0001t0001g0219 others(19): Show |
30 | HG00423.hp2 HG00597.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.269+375dupT | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 2/10 | chr4 | 25158577 | |||||||
chr4:25158805 | T | C | 2 | a0001c0001t0001g0269 a0001c0001t0021g0268 |
2 | HG02165.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.269+148A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 2/10 | chr4 | 25158805 | |||||||
chr4:25158868 | A | C | 2 | a0001c0001t0004g0072 a0001c0001t0004g0073 |
2 | HG01433.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.269+85T>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 2/10 | chr4 | 25158868 | |||||||
chr4:25158888 | C | A | 1 | a0001c0001t0002g0238 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.269+65G>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 2/10 | chr4 | 25158888 | |||||||
chr4:25159110 | T | TA | 58 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0025 others(55): Show |
76 | HG00544.hp2 HG00621.hp1 HG00639.hp1 others(73): Show |
splice_region_variant&intron_variant | LOW | c.115-4dupT | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 1/10 | chr4 | 25159110 | |||||||
chr4:25159110 | TA | T | 18 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0064 others(15): Show |
24 | HG01109.hp2 HG01168.hp2 HG01192.hp1 others(21): Show |
splice_region_variant&intron_variant | LOW | c.115-4delT | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 1/10 | chr4 | 25159110 | |||||||
chr4:25159470 | A | T | 1 | a0001c0001t0001g0319 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.115-363T>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 1/10 | chr4 | 25159470 | |||||||
chr4:25159486 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.115-379C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 1/10 | chr4 | 25159486 | |||||||
chr4:25159550 | T | C | 1 | a0002c0002t0003g0318 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.115-443A>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 1/10 | chr4 | 25159550 | |||||||
chr4:25159635 | G | T | 5 | a0001c0001t0007g0054 a0001c0001t0007g0271 a0001c0001t0007g0272 others(2): Show |
6 | HG02145.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-528C>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 1/10 | chr4 | 25159635 | |||||||
chr4:25159658 | G | A | 3 | a0001c0001t0001g0269 a0001c0001t0001g0288 a0001c0001t0021g0268 |
3 | HG02165.hp1 HG03579.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.115-551C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 1/10 | chr4 | 25159658 | |||||||
chr4:25159665 | G | C | 1 | a0001c0001t0004g0270 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.115-558C>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 1/10 | chr4 | 25159665 | |||||||
chr4:25159917 | G | A | 20 | a0001c0001t0001g0013 a0001c0001t0001g0055 a0001c0001t0001g0056 others(17): Show |
27 | HG00639.hp1 HG01243.hp2 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.114+339C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 1/10 | chr4 | 25159917 | |||||||
chr4:25160020 | T | G | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | NA19012.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.114+236A>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 1/10 | chr4 | 25160020 | |||||||
chr4:25160045 | T | G | 1 | a0001c0001t0001g0288 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.114+211A>C | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 1/10 | chr4 | 25160045 | |||||||
chr4:25160093 | G | C | 37 | a0002c0002t0003g0004 a0002c0002t0003g0007 a0002c0002t0003g0014 others(34): Show |
61 | HG00438.hp2 HG00642.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.114+163C>G | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 1/10 | chr4 | 25160093 | |||||||
chr4:25160172 | G | A | 3 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0003g0321 |
3 | HG02970.hp1 HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.114+84C>T | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 1/10 | chr4 | 25160172 | |||||||
chr4:25160242 | C | T | 1 | a0001c0001t0002g0060 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.114+14G>A | SEPSECS | ENSG00000109618.13 | transcript | ENST00000382103.7 | protein_coding | 1/10 | chr4 | 25160242 |