Item | Value |
---|---|
geneid | 221393 |
ensemblid | ENSG00000153294.12 |
hgncid | 19011 |
symbol | ADGRF4 |
name | adhesion G protein-coupled receptor F4 |
refseq_nuc | NM_153838.5 |
refseq_prot | NP_722580.3 |
ensembl_nuc | ENST00000283303.3 |
ensembl_prot | ENSP00000283303.2 |
mane_status | MANE Select |
chr | chr6 |
start | 47698580 |
end | 47722014 |
strand | + |
ver | v1.2 |
region | chr6:47698580-47722014 |
region5000 | chr6:47693580-47727014 |
regionname0 | ADGRF4_chr6_47698580_47722014 |
regionname5000 | ADGRF4_chr6_47693580_47727014 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 695 | 307 | 58 | 70 | 143 | 12 | 23 | 111 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | MKMKS others(690): Show |
chr6 | 47693580 | 47727014 |
a0002 | 1/0 | 695 | 69 | 33 | 4 | 20 | 2 | 9 | 17 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | MKMKS others(690): Show |
chr6 | 47693580 | 47727014 |
a0003 | 0/0 | 695 | 6 | 0 | 1 | 5 | 0 | 0 | 4 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | MKMKS others(690): Show |
chr6 | 47693580 | 47727014 |
a0004 | 0/0 | 695 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | MKMKS others(690): Show |
chr6 | 47693580 | 47727014 |
a0005 | 0/0 | 695 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | MKMKS others(690): Show |
chr6 | 47693580 | 47727014 |
a0006 | 0/0 | 695 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | MKMKS others(690): Show |
chr6 | 47693580 | 47727014 |
a0007 | 0/0 | 695 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | MKMKS others(690): Show |
chr6 | 47693580 | 47727014 |
a0008 | 0/0 | 695 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | MKMKS others(690): Show |
chr6 | 47693580 | 47727014 |
a0009 | 0/0 | 695 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | MKMKS others(690): Show |
chr6 | 47693580 | 47727014 |
a0010 | 0/0 | 695 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | MKMKS others(690): Show |
chr6 | 47693580 | 47727014 |
a0011 | 0/0 | 695 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | MKMKS others(690): Show |
chr6 | 47693580 | 47727014 |
a0012 | 0/0 | 695 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | MKMKS others(690): Show |
chr6 | 47693580 | 47727014 |
a0013 | 0/0 | 695 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | MKMKS others(690): Show |
chr6 | 47693580 | 47727014 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2085 | 296 | 52 | 68 | 140 | 12 | 23 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ATGAA others(2080): Show |
chr6 | 47693580 | 47727014 | ||
a0001c0003 | 0/0 | 2085 | 6 | 5 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ATGAA others(2080): Show |
chr6 | 47693580 | 47727014 | ||
a0001c0005 | 0/0 | 2085 | 3 | 0 | 0 | 3 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ATGAA others(2080): Show |
chr6 | 47693580 | 47727014 | ||
a0001c0007 | 0/0 | 2085 | 2 | 1 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ATGAA others(2080): Show |
chr6 | 47693580 | 47727014 | ||
a0002c0002 | 1/0 | 2085 | 69 | 33 | 4 | 20 | 2 | 9 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ATGAA others(2080): Show |
chr6 | 47693580 | 47727014 | ||
a0003c0004 | 0/0 | 2085 | 6 | 0 | 1 | 5 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ATGAA others(2080): Show |
chr6 | 47693580 | 47727014 | ||
a0004c0008 | 0/0 | 2085 | 2 | 1 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ATGAA others(2080): Show |
chr6 | 47693580 | 47727014 | ||
a0005c0006 | 0/0 | 2085 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ATGAA others(2080): Show |
chr6 | 47693580 | 47727014 | ||
a0006c0015 | 0/0 | 2085 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ATGAA others(2080): Show |
chr6 | 47693580 | 47727014 | ||
a0007c0009 | 0/0 | 2085 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ATGAA others(2080): Show |
chr6 | 47693580 | 47727014 | ||
a0008c0014 | 0/0 | 2085 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ATGAA others(2080): Show |
chr6 | 47693580 | 47727014 | ||
a0009c0016 | 0/0 | 2085 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ATGAA others(2080): Show |
chr6 | 47693580 | 47727014 | ||
a0010c0013 | 0/0 | 2085 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ATGAA others(2080): Show |
chr6 | 47693580 | 47727014 | ||
a0011c0011 | 0/0 | 2085 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ATGAA others(2080): Show |
chr6 | 47693580 | 47727014 | ||
a0012c0012 | 0/0 | 2085 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ATGAA others(2080): Show |
chr6 | 47693580 | 47727014 | ||
a0013c0010 | 0/0 | 2085 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ATGAA others(2080): Show |
chr6 | 47693580 | 47727014 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3128 | 264 | 43 | 56 | 137 | 8 | 19 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ACAGT others(3123): Show |
chr6 | 47693580 | 47727014 |
a0001c0001t0002 | 0/0 | 3127 | 17 | 0 | 12 | 0 | 4 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ACAGT others(3122): Show |
chr6 | 47693580 | 47727014 |
a0001c0001t0003 | 0/0 | 3128 | 5 | 5 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ACAGT others(3123): Show |
chr6 | 47693580 | 47727014 |
a0001c0001t0004 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ACAGT others(3123): Show |
chr6 | 47693580 | 47727014 |
a0001c0001t0005 | 0/0 | 3128 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ACAGT others(3123): Show |
chr6 | 47693580 | 47727014 |
a0001c0001t0007 | 0/0 | 3128 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ACAGT others(3123): Show |
chr6 | 47693580 | 47727014 |
a0001c0001t0008 | 0/0 | 3128 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ACAGT others(3123): Show |
chr6 | 47693580 | 47727014 |
a0001c0001t0009 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ACAGT others(3123): Show |
chr6 | 47693580 | 47727014 |
a0001c0001t0010 | 0/0 | 3128 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ACAGT others(3123): Show |
chr6 | 47693580 | 47727014 |
a0001c0001t0011 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ACAGT others(3123): Show |
chr6 | 47693580 | 47727014 |
a0001c0001t0012 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ACAGT others(3123): Show |
chr6 | 47693580 | 47727014 |
a0001c0001t0013 | 0/0 | 3128 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ACAGT others(3123): Show |
chr6 | 47693580 | 47727014 |
a0001c0001t0014 | 0/0 | 3128 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ACAGT others(3123): Show |
chr6 | 47693580 | 47727014 |
a0001c0003t0001 | 0/0 | 3128 | 6 | 5 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ACAGT others(3123): Show |
chr6 | 47693580 | 47727014 |
a0001c0005t0001 | 0/0 | 3128 | 3 | 0 | 0 | 3 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ACAGT others(3123): Show |
chr6 | 47693580 | 47727014 |
a0001c0007t0001 | 0/0 | 3128 | 2 | 1 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ACAGT others(3123): Show |
chr6 | 47693580 | 47727014 |
a0002c0002t0001 | 1/0 | 3128 | 68 | 32 | 4 | 20 | 2 | 9 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ACAGT others(3123): Show |
chr6 | 47693580 | 47727014 |
a0002c0002t0005 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ACAGT others(3123): Show |
chr6 | 47693580 | 47727014 |
a0003c0004t0001 | 0/0 | 3128 | 6 | 0 | 1 | 5 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ACAGT others(3123): Show |
chr6 | 47693580 | 47727014 |
a0004c0008t0006 | 0/0 | 3128 | 2 | 1 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ACAGT others(3123): Show |
chr6 | 47693580 | 47727014 |
a0005c0006t0001 | 0/0 | 3128 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ACAGT others(3123): Show |
chr6 | 47693580 | 47727014 |
a0006c0015t0004 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ACAGT others(3123): Show |
chr6 | 47693580 | 47727014 |
a0007c0009t0001 | 0/0 | 3128 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ACAGT others(3123): Show |
chr6 | 47693580 | 47727014 |
a0008c0014t0001 | 0/0 | 3128 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ACAGT others(3123): Show |
chr6 | 47693580 | 47727014 |
a0009c0016t0001 | 0/0 | 3128 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ACAGT others(3123): Show |
chr6 | 47693580 | 47727014 |
a0010c0013t0001 | 0/0 | 3128 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ACAGT others(3123): Show |
chr6 | 47693580 | 47727014 |
a0011c0011t0001 | 0/0 | 3128 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ACAGT others(3123): Show |
chr6 | 47693580 | 47727014 |
a0012c0012t0001 | 0/0 | 3128 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ACAGT others(3123): Show |
chr6 | 47693580 | 47727014 |
a0013c0010t0001 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | ACAGT others(3123): Show |
chr6 | 47693580 | 47727014 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 43 | 4 | 18 | 9 | 4 | 8 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0002 | 0/0 | 40 | 4 | 6 | 24 | 2 | 4 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0003 | 0/0 | 30 | 0 | 4 | 26 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0004 | 0/0 | 27 | 0 | 7 | 19 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0008 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0009 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0010 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0011 | 0/0 | 6 | 0 | 5 | 0 | 1 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0014 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0021 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0109 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0002g0006 | 0/0 | 14 | 0 | 10 | 0 | 3 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0003g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0005g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0007g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0008g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0009g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0010g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0011g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0012g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0013g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0014g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0003t0001g0018 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0003t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0003t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0005t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0005t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0007t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0007t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0005 | 0/0 | 16 | 0 | 3 | 8 | 1 | 4 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0007 | 0/0 | 11 | 10 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0019 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0003c0004t0001g0005 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0003c0004t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0003c0004t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0004c0008t0006g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0005c0006t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0006c0015t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0007c0009t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0008c0014t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0009c0016t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0010c0013t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0011c0011t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0012c0012t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0013c0010t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | GBR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00140 | hp1 | a0002 | c0002 | t0001 | g0005 | EUR | GBR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0051 | EUR | FIN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0006 | EUR | FIN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | CHS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00609 | hp2 | a0001 | c0001 | t0008 | g0001 | EAS | CHS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00642 | hp2 | a0001 | c0007 | t0001 | g0064 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01243 | hp2 | a0001 | c0003 | t0001 | g0018 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01255 | hp2 | a0004 | c0008 | t0006 | g0027 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01358 | hp2 | a0003 | c0004 | t0001 | g0005 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01891 | hp1 | a0002 | c0002 | t0001 | g0029 | AFR | ACB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01891 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | ACB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | PEL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01943 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02056 | hp2 | a0003 | c0004 | t0001 | g0058 | EAS | KHV | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02071 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | KHV | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02129 | hp1 | a0001 | c0001 | t0013 | g0015 | EAS | KHV | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02148 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | CDX | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02257 | hp1 | a0002 | c0002 | t0001 | g0019 | AFR | ACB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02257 | hp2 | a0001 | c0007 | t0001 | g0053 | AFR | ACB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | ACB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | ACB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02280 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | ACB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02451 | hp2 | a0002 | c0002 | t0001 | g0028 | AFR | ACB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02572 | hp2 | a0006 | c0015 | t0004 | g0006 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02602 | hp1 | a0002 | c0002 | t0001 | g0062 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0005 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02615 | hp2 | a0001 | c0003 | t0001 | g0018 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02630 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02735 | hp1 | a0001 | c0001 | t0014 | g0001 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0083 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0048 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02809 | hp2 | a0001 | c0001 | t0011 | g0008 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02818 | hp2 | a0001 | c0003 | t0001 | g0035 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02895 | hp2 | a0002 | c0002 | t0001 | g0026 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02897 | hp2 | a0002 | c0002 | t0001 | g0026 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02922 | hp1 | a0002 | c0002 | t0001 | g0054 | AFR | ESN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02965 | hp1 | a0001 | c0003 | t0001 | g0120 | AFR | ESN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02965 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | ESN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02970 | hp1 | a0002 | c0002 | t0005 | g0028 | AFR | ESN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02970 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | ESN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02976 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | ESN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02976 | hp2 | a0001 | c0001 | t0012 | g0012 | AFR | ESN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03017 | hp1 | a0007 | c0009 | t0001 | g0090 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03017 | hp2 | a0002 | c0002 | t0001 | g0005 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03041 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0063 | AFR | MSL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03098 | hp2 | a0004 | c0008 | t0006 | g0027 | AFR | MSL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03130 | hp1 | a0001 | c0001 | t0009 | g0001 | AFR | ESN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03139 | hp2 | a0001 | c0003 | t0001 | g0018 | AFR | ESN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | ESN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | MSL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03209 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | MSL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0049 | AFR | MSL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03225 | hp2 | a0002 | c0002 | t0001 | g0044 | AFR | MSL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03486 | hp1 | a0002 | c0002 | t0001 | g0127 | AFR | MSL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03486 | hp2 | a0002 | c0002 | t0001 | g0032 | AFR | MSL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03579 | hp1 | a0002 | c0002 | t0001 | g0029 | AFR | MSL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0056 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | STU | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03688 | hp2 | a0001 | c0001 | t0007 | g0089 | SAS | STU | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0005 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03710 | hp2 | a0008 | c0014 | t0001 | g0005 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03831 | hp1 | a0009 | c0016 | t0001 | g0096 | SAS | BEB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03927 | hp2 | a0001 | c0001 | t0005 | g0035 | SAS | BEB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0060 | SAS | BEB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG04115 | hp2 | a0010 | c0013 | t0001 | g0101 | SAS | STU | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG04184 | hp2 | a0002 | c0002 | t0001 | g0005 | SAS | BEB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0055 | SAS | STU | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18522 | hp2 | a0002 | c0002 | t0001 | g0047 | AFR | YRI | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | YRI | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18939 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18940 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18943 | hp2 | a0003 | c0004 | t0001 | g0005 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18946 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18954 | hp1 | a0003 | c0004 | t0001 | g0005 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18954 | hp2 | a0011 | c0011 | t0001 | g0076 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18959 | hp1 | a0003 | c0004 | t0001 | g0005 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18962 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18962 | hp2 | a0001 | c0005 | t0001 | g0124 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18966 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18968 | hp2 | a0005 | c0006 | t0001 | g0004 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18969 | hp1 | a0012 | c0012 | t0001 | g0004 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18972 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18972 | hp2 | a0001 | c0005 | t0001 | g0003 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18977 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18982 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18993 | hp2 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18994 | hp2 | a0005 | c0006 | t0001 | g0004 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19003 | hp2 | a0003 | c0004 | t0001 | g0110 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19005 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | LWK | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19030 | hp2 | a0002 | c0002 | t0001 | g0043 | AFR | LWK | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19043 | hp1 | a0002 | c0002 | t0001 | g0032 | AFR | LWK | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19043 | hp2 | a0013 | c0010 | t0001 | g0086 | AFR | LWK | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19077 | hp1 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19084 | hp1 | a0001 | c0001 | t0010 | g0073 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19086 | hp1 | a0001 | c0005 | t0001 | g0003 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19240 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | YRI | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19240 | hp2 | a0002 | c0002 | t0001 | g0046 | AFR | YRI | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ASW | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ASW | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0006 | EUR | TSI | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0034 | EUR | TSI | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0082 | EUR | TSI | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0006 | EUR | TSI | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02109 | hp1 | a0002 | c0002 | t0001 | g0042 | AFR | ACB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02109 | hp2 | a0002 | c0002 | t0001 | g0065 | AFR | ACB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02486 | hp2 | a0001 | c0003 | t0001 | g0018 | AFR | ACB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | USA | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | USA | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | USA | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | USA | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0061 | AFR | LWK | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA21309 | hp2 | a0002 | c0002 | t0001 | g0045 | AFR | LWK | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0109 | REF | REF | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0019 | REF | REF | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:47707278 | C | G | 1 | a0004 | 2 | HG01255.hp2 HG03098.hp2 |
missense_variant | MODERATE | c.33C>G | p.Cys11Trp | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/10 | 264/3128 | 33/2088 | 11/695 | chr6 | 47707278 | |||
chr6:47712520 | C | T | 1 | a0004 | 2 | HG01255.hp2 HG03098.hp2 |
missense_variant | MODERATE | c.464C>T | p.Thr155Ile | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 5/10 | 695/3128 | 464/2088 | 155/695 | chr6 | 47712520 | |||
chr6:47713828 | G | A | 1 | a0007 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.583G>A | p.Asp195Asn | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 814/3128 | 583/2088 | 195/695 | chr6 | 47713828 | |||
chr6:47713929 | C | G | 1 | a0009 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.684C>G | p.His228Gln | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 915/3128 | 684/2088 | 228/695 | chr6 | 47713929 | |||
chr6:47713975 | G | T | 1 | a0003 | 6 | HG01358.hp2 HG02056.hp2 NA18943.hp2 others(3): Show |
missense_variant | MODERATE | c.730G>T | p.Gly244Trp | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 961/3128 | 730/2088 | 244/695 | chr6 | 47713975 | |||
chr6:47713982 | A | G | 1 | a0006 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.737A>G | p.His246Arg | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 968/3128 | 737/2088 | 246/695 | chr6 | 47713982 | |||
chr6:47714189 | A | G | 1 | a0004 | 2 | HG01255.hp2 HG03098.hp2 |
missense_variant | MODERATE | c.944A>G | p.Gln315Arg | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 1175/3128 | 944/2088 | 315/695 | chr6 | 47714189 | |||
chr6:47714399 | T | C | 1 | a0004 | 2 | HG01255.hp2 HG03098.hp2 |
missense_variant | MODERATE | c.1154T>C | p.Met385Thr | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 1385/3128 | 1154/2088 | 385/695 | chr6 | 47714399 | |||
chr6:47714422 | T | C | 1 | a0004 | 2 | HG01255.hp2 HG03098.hp2 |
missense_variant | MODERATE | c.1177T>C | p.Ser393Pro | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 1408/3128 | 1177/2088 | 393/695 | chr6 | 47714422 | |||
chr6:47714531 | G | A | 1 | a0004 | 2 | HG01255.hp2 HG03098.hp2 |
missense_variant | MODERATE | c.1286G>A | p.Arg429Gln | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 1517/3128 | 1286/2088 | 429/695 | chr6 | 47714531 | |||
chr6:47714533 | G | A | 1 | a0005 | 2 | NA18968.hp2 NA18994.hp2 |
missense_variant | MODERATE | c.1288G>A | p.Val430Met | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 1519/3128 | 1288/2088 | 430/695 | chr6 | 47714533 | |||
chr6:47714560 | C | T | 1 | a0008 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.1315C>T | p.Arg439Cys | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 1546/3128 | 1315/2088 | 439/695 | chr6 | 47714560 | |||
chr6:47714783 | G | A | 1 | a0013 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.1538G>A | p.Arg513Gln | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 1769/3128 | 1538/2088 | 513/695 | chr6 | 47714783 | |||
chr6:47714868 | A | C | 9 | a0001 a0004 a0005 others(6): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(313): Show |
missense_variant | MODERATE | c.1623A>C | p.Lys541Asn | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 1854/3128 | 1623/2088 | 541/695 | chr6 | 47714868 | |||
chr6:47714935 | A | G | 1 | a0004 | 2 | HG01255.hp2 HG03098.hp2 |
missense_variant | MODERATE | c.1690A>G | p.Ile564Val | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 1921/3128 | 1690/2088 | 564/695 | chr6 | 47714935 | |||
chr6:47714946 | C | G | 1 | a0004 | 2 | HG01255.hp2 HG03098.hp2 |
missense_variant | MODERATE | c.1701C>G | p.Phe567Leu | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 1932/3128 | 1701/2088 | 567/695 | chr6 | 47714946 | |||
chr6:47714968 | A | T | 1 | a0010 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.1723A>T | p.Ile575Phe | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 1954/3128 | 1723/2088 | 575/695 | chr6 | 47714968 | |||
chr6:47715107 | G | C | 1 | a0011 | 1 | NA18954.hp2 | missense_variant | MODERATE | c.1862G>C | p.Gly621Ala | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 2093/3128 | 1862/2088 | 621/695 | chr6 | 47715107 | |||
chr6:47716837 | T | C | 1 | a0004 | 2 | HG01255.hp2 HG03098.hp2 |
missense_variant | MODERATE | c.1964T>C | p.Met655Thr | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 7/10 | 2195/3128 | 1964/2088 | 655/695 | chr6 | 47716837 | |||
chr6:47718417 | C | G | 1 | a0004 | 2 | HG01255.hp2 HG03098.hp2 |
missense_variant | MODERATE | c.2063C>G | p.Ser688Cys | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/10 | 2294/3128 | 2063/2088 | 688/695 | chr6 | 47718417 | |||
chr6:47718431 | C | T | 1 | a0012 | 1 | NA18969.hp1 | missense_variant | MODERATE | c.2077C>T | p.Arg693Cys | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/10 | 2308/3128 | 2077/2088 | 693/695 | chr6 | 47718431 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:47712410 | T | C | 1 | a0004c0008 | 2 | HG01255.hp2 HG03098.hp2 |
synonymous_variant | LOW | c.354T>C | p.His118His | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 5/10 | 585/3128 | 354/2088 | 118/695 | chr6 | 47712410 | |||
chr6:47712521 | A | G | 1 | a0004c0008 | 2 | HG01255.hp2 HG03098.hp2 |
synonymous_variant | LOW | c.465A>G | p.Thr155Thr | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 5/10 | 696/3128 | 465/2088 | 155/695 | chr6 | 47712521 | |||
chr6:47712572 | A | T | 1 | a0001c0007 | 2 | HG00642.hp2 HG02257.hp2 |
synonymous_variant | LOW | c.516A>T | p.Thr172Thr | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 5/10 | 747/3128 | 516/2088 | 172/695 | chr6 | 47712572 | |||
chr6:47714319 | A | G | 1 | a0001c0005 | 3 | NA18962.hp2 NA18972.hp2 NA19086.hp1 |
synonymous_variant | LOW | c.1074A>G | p.Arg358Arg | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 1305/3128 | 1074/2088 | 358/695 | chr6 | 47714319 | |||
chr6:47714523 | G | A | 1 | a0004c0008 | 2 | HG01255.hp2 HG03098.hp2 |
synonymous_variant | LOW | c.1278G>A | p.Val426Val | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 1509/3128 | 1278/2088 | 426/695 | chr6 | 47714523 | |||
chr6:47714574 | C | T | 1 | a0001c0003 | 6 | HG01243.hp2 HG02486.hp2 HG02615.hp2 others(3): Show |
synonymous_variant | LOW | c.1329C>T | p.Ile443Ile | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 1560/3128 | 1329/2088 | 443/695 | chr6 | 47714574 | |||
chr6:47714937 | C | T | 1 | a0004c0008 | 2 | HG01255.hp2 HG03098.hp2 |
synonymous_variant | LOW | c.1692C>T | p.Ile564Ile | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 1923/3128 | 1692/2088 | 564/695 | chr6 | 47714937 | |||
chr6:47714943 | G | A | 1 | a0004c0008 | 2 | HG01255.hp2 HG03098.hp2 |
synonymous_variant | LOW | c.1698G>A | p.Ala566Ala | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 1929/3128 | 1698/2088 | 566/695 | chr6 | 47714943 | |||
chr6:47717339 | G | C | 1 | a0004c0008 | 2 | HG01255.hp2 HG03098.hp2 |
synonymous_variant | LOW | c.2022G>C | p.Ser674Ser | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 8/10 | 2253/3128 | 2022/2088 | 674/695 | chr6 | 47717339 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:47698637 | C | T | 1 | a0001c0001t0014 | 1 | HG02735.hp1 | 5_prime_UTR_variant | MODIFIER | c.-174C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/10 | 8609 | chr6 | 47698637 | ||||||
chr6:47698661 | C | T | 1 | a0004c0008t0006 | 2 | HG01255.hp2 HG03098.hp2 |
5_prime_UTR_variant | MODIFIER | c.-150C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/10 | 8585 | chr6 | 47698661 | ||||||
chr6:47698734 | T | G | 1 | a0004c0008t0006 | 2 | HG01255.hp2 HG03098.hp2 |
5_prime_UTR_variant | MODIFIER | c.-77T>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/10 | 8512 | chr6 | 47698734 | ||||||
chr6:47721265 | G | T | 1 | a0001c0001t0013 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*60G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 10/10 | 2823 | chr6 | 47721265 | ||||||
chr6:47721328 | T | C | 1 | a0004c0008t0006 | 2 | HG01255.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*123T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 10/10 | 2886 | chr6 | 47721328 | ||||||
chr6:47721345 | C | T | 1 | a0001c0001t0012 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*140C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 10/10 | 2903 | chr6 | 47721345 | ||||||
chr6:47721349 | C | T | 1 | a0004c0008t0006 | 2 | HG01255.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*144C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 10/10 | 2907 | chr6 | 47721349 | ||||||
chr6:47721358 | G | A | 1 | a0001c0001t0007 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*153G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 10/10 | 2916 | chr6 | 47721358 | ||||||
chr6:47721541 | G | C | 1 | a0001c0001t0008 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*336G>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 10/10 | 3099 | chr6 | 47721541 | ||||||
chr6:47721640 | T | C | 1 | a0001c0001t0009 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*435T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 10/10 | 3198 | chr6 | 47721640 | ||||||
chr6:47721641 | C | T | 1 | a0004c0008t0006 | 2 | HG01255.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*436C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 10/10 | 3199 | chr6 | 47721641 | ||||||
chr6:47721670 | T | A | 1 | a0001c0001t0010 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*465T>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 10/10 | 3228 | chr6 | 47721670 | ||||||
chr6:47721692 | C | T | 2 | a0001c0001t0003 a0001c0001t0012 |
6 | HG02258.hp1 HG02717.hp2 HG02976.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*487C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 10/10 | 3250 | chr6 | 47721692 | ||||||
chr6:47721757 | C | T | 1 | a0001c0001t0011 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*552C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 10/10 | 3315 | chr6 | 47721757 | ||||||
chr6:47721867 | GA | G | 1 | a0001c0001t0002 | 17 | HG00323.hp2 HG00733.hp1 HG00738.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*671delA | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 10/10 | 3434 | INFO_REALIGN_3_PRIME | chr6 | 47721867 | |||||
chr6:47721996 | C | T | 2 | a0001c0001t0005 a0002c0002t0005 |
2 | HG02970.hp1 HG03927.hp2 |
3_prime_UTR_variant | MODIFIER | c.*791C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 10/10 | 3554 | chr6 | 47721996 | ||||||
chr6:47721997 | G | T | 2 | a0001c0001t0004 a0006c0015t0004 |
2 | HG02572.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*792G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 10/10 | 3555 | chr6 | 47721997 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:47698859 | C | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.-17+65C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47698859 | |||||||
chr6:47698930 | C | T | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+136C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47698930 | |||||||
chr6:47699005 | T | C | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+211T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699005 | |||||||
chr6:47699042 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-17+248A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699042 | |||||||
chr6:47699124 | T | C | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+330T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699124 | |||||||
chr6:47699126 | G | T | 3 | a0001c0001t0001g0041 a0001c0001t0003g0012 a0001c0001t0012g0012 |
7 | HG02258.hp1 HG02717.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17+332G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699126 | |||||||
chr6:47699166 | G | T | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(128): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.-17+372G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699166 | |||||||
chr6:47699185 | T | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.-17+391T>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699185 | |||||||
chr6:47699342 | G | A | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+548G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699342 | |||||||
chr6:47699342 | G | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.-17+548G>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699342 | |||||||
chr6:47699368 | T | A | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+574T>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699368 | |||||||
chr6:47699427 | A | G | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+633A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699427 | |||||||
chr6:47699428 | C | G | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+634C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699428 | |||||||
chr6:47699433 | G | A | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+639G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699433 | |||||||
chr6:47699447 | G | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(128): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.-17+653G>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699447 | |||||||
chr6:47699450 | T | C | 1 | a0002c0002t0001g0042 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-17+656T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699450 | |||||||
chr6:47699499 | A | G | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+705A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699499 | |||||||
chr6:47699509 | T | C | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+715T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699509 | |||||||
chr6:47699559 | A | G | 1 | a0002c0002t0001g0127 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-17+765A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699559 | |||||||
chr6:47699575 | A | T | 11 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0039 others(8): Show |
45 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.-17+781A>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699575 | |||||||
chr6:47699590 | G | A | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+796G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699590 | |||||||
chr6:47699640 | T | C | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+846T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699640 | |||||||
chr6:47699715 | T | A | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+921T>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699715 | |||||||
chr6:47699768 | C | A | 1 | a0001c0001t0004g0049 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-17+974C>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699768 | |||||||
chr6:47699774 | A | T | 1 | a0002c0002t0001g0038 | 2 | NA18977.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.-17+980A>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699774 | |||||||
chr6:47699853 | G | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0050 |
9 | NA18945.hp1 NA18955.hp1 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.-17+1059G>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699853 | |||||||
chr6:47699903 | T | C | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+1109T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699903 | |||||||
chr6:47699903 | T | TAC | 67 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(64): Show |
182 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.-17+1129_-17+1130d others(4): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 47699903 | ||||||
chr6:47699903 | T | TACAC | 5 | a0001c0007t0001g0053 a0002c0002t0001g0028 a0002c0002t0001g0051 others(2): Show |
5 | HG00280.hp1 HG02257.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17+1127_-17+1130d others(6): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 47699903 | ||||||
chr6:47699903 | TACAC | T | 28 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0023 others(25): Show |
80 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.-17+1127_-17+1130d others(6): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 47699903 | ||||||
chr6:47699903 | TACACAC | T | 2 | a0001c0003t0001g0018 a0001c0003t0001g0120 |
5 | HG01243.hp2 HG02486.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17+1125_-17+1130d others(8): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 47699903 | ||||||
chr6:47699921 | C | G | 1 | a0001c0001t0001g0099 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-17+1127C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699921 | |||||||
chr6:47699925 | G | C | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+1131G>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699925 | |||||||
chr6:47699927 | C | G | 1 | a0001c0001t0001g0099 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-17+1133C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699927 | |||||||
chr6:47699927 | C | T | 1 | a0002c0002t0001g0038 | 2 | NA18977.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.-17+1133C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699927 | |||||||
chr6:47699928 | G | A | 2 | a0002c0002t0001g0028 a0002c0002t0005g0028 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-17+1134G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699928 | |||||||
chr6:47699933 | A | AC | 10 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0097 others(7): Show |
16 | HG00099.hp2 HG01069.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.-17+1150dupC | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 47699933 | ||||||
chr6:47699933 | A | C | 1 | a0001c0001t0001g0119 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-17+1139A>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699933 | |||||||
chr6:47699933 | AC | A | 44 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(41): Show |
139 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.-17+1150delC | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 47699933 | ||||||
chr6:47699933 | ACC | A | 30 | a0001c0001t0001g0041 a0001c0001t0001g0085 a0001c0001t0003g0012 others(27): Show |
60 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.-17+1149_-17+1150d others(4): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 47699933 | ||||||
chr6:47699936 | C | A | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+1142C>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699936 | |||||||
chr6:47699939 | C | T | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+1145C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699939 | |||||||
chr6:47699986 | T | G | 2 | a0002c0002t0001g0028 a0002c0002t0005g0028 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-17+1192T>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699986 | |||||||
chr6:47700045 | G | A | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+1251G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700045 | |||||||
chr6:47700047 | A | G | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+1253A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700047 | |||||||
chr6:47700057 | T | C | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+1263T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700057 | |||||||
chr6:47700071 | A | C | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+1277A>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700071 | |||||||
chr6:47700106 | A | G | 2 | a0002c0002t0001g0028 a0002c0002t0005g0028 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-17+1312A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700106 | |||||||
chr6:47700113 | C | T | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+1319C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700113 | |||||||
chr6:47700204 | AG | A | 1 | a0002c0002t0001g0020 | 3 | NA18962.hp1 NA18977.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-17+1411delG | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700204 | |||||||
chr6:47700206 | A | T | 1 | a0002c0002t0001g0020 | 3 | NA18962.hp1 NA18977.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-17+1412A>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700206 | |||||||
chr6:47700207 | T | G | 1 | a0002c0002t0001g0020 | 3 | NA18962.hp1 NA18977.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-17+1413T>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700207 | |||||||
chr6:47700210 | C | T | 1 | a0002c0002t0001g0020 | 3 | NA18962.hp1 NA18977.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-17+1416C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700210 | |||||||
chr6:47700211 | A | T | 1 | a0002c0002t0001g0020 | 3 | NA18962.hp1 NA18977.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-17+1417A>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700211 | |||||||
chr6:47700277 | T | C | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+1483T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700277 | |||||||
chr6:47700300 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-17+1506G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700300 | |||||||
chr6:47700357 | A | G | 2 | a0001c0001t0002g0031 a0001c0001t0002g0082 |
3 | HG01081.hp1 HG01934.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-17+1563A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700357 | |||||||
chr6:47700523 | T | C | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+1729T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700523 | |||||||
chr6:47700636 | C | T | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+1842C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700636 | |||||||
chr6:47700761 | A | C | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+1967A>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700761 | |||||||
chr6:47700935 | T | C | 71 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(68): Show |
186 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.-17+2141T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700935 | |||||||
chr6:47700938 | A | ATTCTGAC others(20): Show |
1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+2146_-17+2147i others(29): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 47700938 | ||||||
chr6:47700944 | T | G | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+2150T>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700944 | |||||||
chr6:47700968 | T | A | 1 | a0001c0001t0001g0099 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-17+2174T>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700968 | |||||||
chr6:47700987 | G | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(52): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-17+2193G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700987 | |||||||
chr6:47700988 | G | T | 1 | a0002c0002t0001g0065 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-17+2194G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700988 | |||||||
chr6:47700989 | G | T | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+2195G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700989 | |||||||
chr6:47701021 | C | T | 3 | a0001c0001t0001g0085 a0002c0002t0001g0032 a0013c0010t0001g0086 |
4 | HG03453.hp1 HG03486.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17+2227C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47701021 | |||||||
chr6:47701044 | A | C | 18 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(15): Show |
77 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.-17+2250A>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47701044 | |||||||
chr6:47701144 | C | G | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+2350C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47701144 | |||||||
chr6:47701185 | G | A | 31 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0023 others(28): Show |
86 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.-17+2391G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47701185 | |||||||
chr6:47701315 | T | C | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+2521T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47701315 | |||||||
chr6:47701364 | C | A | 1 | a0001c0001t0001g0100 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-17+2570C>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47701364 | |||||||
chr6:47701372 | G | A | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+2578G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47701372 | |||||||
chr6:47701400 | G | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(137): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.-17+2606G>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47701400 | |||||||
chr6:47701401 | T | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(137): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.-17+2607T>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47701401 | |||||||
chr6:47701466 | A | C | 56 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(53): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.-17+2672A>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47701466 | |||||||
chr6:47701476 | G | A | 1 | a0010c0013t0001g0101 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-17+2682G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47701476 | |||||||
chr6:47701494 | G | A | 2 | a0001c0001t0001g0036 a0001c0001t0001g0102 |
3 | HG02896.hp2 HG02897.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-17+2700G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47701494 | |||||||
chr6:47701693 | A | C | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+2899A>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47701693 | |||||||
chr6:47701708 | G | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(53): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.-17+2914G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47701708 | |||||||
chr6:47701750 | A | T | 51 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(48): Show |
141 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.-17+2956A>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47701750 | |||||||
chr6:47701920 | G | T | 31 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0023 others(28): Show |
86 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.-17+3126G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47701920 | |||||||
chr6:47701937 | G | A | 2 | a0002c0002t0001g0029 a0002c0002t0001g0054 |
3 | HG01891.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-17+3143G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47701937 | |||||||
chr6:47701956 | C | A | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+3162C>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47701956 | |||||||
chr6:47701957 | G | A | 1 | a0002c0002t0001g0025 | 2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-17+3163G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47701957 | |||||||
chr6:47702015 | A | G | 1 | a0001c0007t0001g0053 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-17+3221A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702015 | |||||||
chr6:47702026 | A | G | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+3232A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702026 | |||||||
chr6:47702058 | C | G | 1 | a0001c0001t0001g0017 | 4 | HG02451.hp1 HG02615.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17+3264C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702058 | |||||||
chr6:47702100 | A | G | 1 | a0001c0001t0004g0049 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-17+3306A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702100 | |||||||
chr6:47702201 | A | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(51): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.-17+3407A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702201 | |||||||
chr6:47702254 | GTGTGT | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0097 |
7 | HG00099.hp2 HG01069.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17+3463_-17+3467d others(7): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 47702254 | ||||||
chr6:47702261 | G | A | 1 | a0007c0009t0001g0090 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-17+3467G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702261 | |||||||
chr6:47702302 | T | C | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+3508T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702302 | |||||||
chr6:47702407 | G | A | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+3613G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702407 | |||||||
chr6:47702434 | T | G | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+3640T>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702434 | |||||||
chr6:47702443 | C | T | 51 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(48): Show |
141 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.-17+3649C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702443 | |||||||
chr6:47702474 | T | C | 57 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(54): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.-17+3680T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702474 | |||||||
chr6:47702533 | G | A | 43 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(40): Show |
129 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.-17+3739G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702533 | |||||||
chr6:47702645 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-17+3851C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702645 | |||||||
chr6:47702662 | T | G | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+3868T>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702662 | |||||||
chr6:47702879 | G | A | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+4085G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702879 | |||||||
chr6:47702887 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-17+4093C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702887 | |||||||
chr6:47702900 | A | G | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+4106A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702900 | |||||||
chr6:47702939 | G | A | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+4145G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702939 | |||||||
chr6:47702954 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-17+4160G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702954 | |||||||
chr6:47702990 | T | C | 2 | a0002c0002t0001g0051 a0002c0002t0001g0055 |
2 | HG00280.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-17+4196T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702990 | |||||||
chr6:47703069 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-16-4161C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47703069 | |||||||
chr6:47703288 | C | T | 50 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(47): Show |
140 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.-16-3942C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47703288 | |||||||
chr6:47703329 | T | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.-16-3901T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47703329 | |||||||
chr6:47703407 | G | A | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-3823G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47703407 | |||||||
chr6:47703695 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-16-3535C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47703695 | |||||||
chr6:47703696 | A | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.-16-3534A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47703696 | |||||||
chr6:47703787 | A | G | 1 | a0002c0002t0001g0025 | 2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-16-3443A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47703787 | |||||||
chr6:47703974 | C | T | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-3256C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47703974 | |||||||
chr6:47704012 | A | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(53): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.-16-3218A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47704012 | |||||||
chr6:47704053 | C | CT | 7 | a0001c0001t0001g0010 a0001c0001t0001g0080 a0001c0001t0001g0085 others(4): Show |
14 | HG01255.hp2 HG03098.hp2 HG03453.hp1 others(11): Show |
intron_variant | MODIFIER | c.-16-3164dupT | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 47704053 | ||||||
chr6:47704089 | A | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.-16-3141A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47704089 | |||||||
chr6:47704187 | A | G | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-3043A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47704187 | |||||||
chr6:47704246 | G | A | 50 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(47): Show |
140 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.-16-2984G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47704246 | |||||||
chr6:47704280 | G | A | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-2950G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47704280 | |||||||
chr6:47704327 | G | A | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-2903G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47704327 | |||||||
chr6:47704333 | A | C | 1 | a0001c0001t0001g0126 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-16-2897A>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47704333 | |||||||
chr6:47704367 | C | G | 50 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(47): Show |
140 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.-16-2863C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47704367 | |||||||
chr6:47704453 | T | C | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-2777T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47704453 | |||||||
chr6:47704505 | A | G | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-2725A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47704505 | |||||||
chr6:47704519 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-16-2711A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47704519 | |||||||
chr6:47704543 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-2687G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47704543 | |||||||
chr6:47704595 | T | TCAAAATG others(317): Show |
1 | a0001c0001t0004g0049 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-16-2622_-16-2621i others(326): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 47704595 | ||||||
chr6:47704638 | G | C | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-2592G>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47704638 | |||||||
chr6:47704742 | T | C | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-2488T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47704742 | |||||||
chr6:47704778 | G | A | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-2452G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47704778 | |||||||
chr6:47704797 | G | A | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-2433G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47704797 | |||||||
chr6:47705072 | A | G | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(128): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.-16-2158A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47705072 | |||||||
chr6:47705079 | C | T | 1 | a0001c0001t0001g0011 | 6 | HG00099.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16-2151C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47705079 | |||||||
chr6:47705126 | C | T | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-2104C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47705126 | |||||||
chr6:47705139 | G | T | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | NA18985.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-16-2091G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47705139 | |||||||
chr6:47705178 | C | T | 2 | a0002c0002t0001g0032 a0013c0010t0001g0086 |
3 | HG03486.hp2 NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-16-2052C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47705178 | |||||||
chr6:47705181 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-16-2049C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47705181 | |||||||
chr6:47705223 | G | A | 1 | a0001c0001t0004g0049 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-16-2007G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47705223 | |||||||
chr6:47705254 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-16-1976G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47705254 | |||||||
chr6:47705308 | A | C | 1 | a0002c0002t0001g0065 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-16-1922A>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47705308 | |||||||
chr6:47705323 | G | T | 5 | a0002c0002t0001g0026 a0002c0002t0001g0042 a0002c0002t0001g0045 others(2): Show |
6 | HG02109.hp1 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16-1907G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47705323 | |||||||
chr6:47705342 | T | C | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-1888T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47705342 | |||||||
chr6:47705344 | G | A | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-1886G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47705344 | |||||||
chr6:47705457 | T | C | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-1773T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47705457 | |||||||
chr6:47705469 | T | C | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-1761T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47705469 | |||||||
chr6:47705567 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-16-1663T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47705567 | |||||||
chr6:47705578 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-16-1652G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47705578 | |||||||
chr6:47705664 | A | T | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-1566A>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47705664 | |||||||
chr6:47706030 | T | C | 1 | a0001c0001t0001g0041 | 2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-16-1200T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47706030 | |||||||
chr6:47706110 | A | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(104): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.-16-1120A>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47706110 | |||||||
chr6:47706288 | A | T | 2 | a0001c0001t0001g0066 a0001c0001t0001g0079 |
2 | NA18961.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.-16-942A>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47706288 | |||||||
chr6:47706351 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-16-879C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47706351 | |||||||
chr6:47706414 | G | A | 1 | a0001c0001t0001g0041 | 2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-16-816G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47706414 | |||||||
chr6:47706517 | C | T | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-713C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47706517 | |||||||
chr6:47706585 | T | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(51): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.-16-645T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47706585 | |||||||
chr6:47706623 | A | G | 52 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(49): Show |
142 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.-16-607A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47706623 | |||||||
chr6:47706686 | A | T | 1 | a0001c0007t0001g0064 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-16-544A>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47706686 | |||||||
chr6:47706741 | G | A | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-489G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47706741 | |||||||
chr6:47706811 | C | G | 1 | a0001c0001t0001g0125 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-16-419C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47706811 | |||||||
chr6:47706854 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-16-376A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47706854 | |||||||
chr6:47706863 | A | G | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-367A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47706863 | |||||||
chr6:47706871 | G | A | 1 | a0002c0002t0001g0065 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-16-359G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47706871 | |||||||
chr6:47706947 | A | G | 1 | a0013c0010t0001g0086 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-16-283A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47706947 | |||||||
chr6:47706983 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(52): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-16-247G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47706983 | |||||||
chr6:47707161 | C | G | 2 | a0001c0001t0001g0100 a0001c0001t0001g0128 |
2 | HG02486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-16-69C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47707161 | |||||||
chr6:47707183 | G | A | 1 | a0002c0002t0001g0056 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-16-47G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47707183 | |||||||
chr6:47707356 | C | T | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.93+18C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47707356 | |||||||
chr6:47707366 | C | T | 1 | a0001c0003t0001g0120 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.93+28C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47707366 | |||||||
chr6:47707375 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.93+37A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47707375 | |||||||
chr6:47707377 | C | G | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.93+39C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47707377 | |||||||
chr6:47707553 | C | T | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.93+215C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47707553 | |||||||
chr6:47707561 | G | C | 31 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0023 others(28): Show |
86 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.93+223G>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47707561 | |||||||
chr6:47707614 | C | T | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.93+276C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47707614 | |||||||
chr6:47707619 | A | G | 1 | a0002c0002t0001g0020 | 3 | NA18962.hp1 NA18977.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.93+281A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47707619 | |||||||
chr6:47707738 | A | G | 23 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(20): Show |
88 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.93+400A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47707738 | |||||||
chr6:47707770 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.93+432T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47707770 | |||||||
chr6:47707814 | T | A | 1 | a0013c0010t0001g0086 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.94-410T>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47707814 | |||||||
chr6:47707850 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.94-374G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47707850 | |||||||
chr6:47708034 | G | A | 2 | a0002c0002t0001g0032 a0002c0002t0001g0045 |
3 | HG03486.hp2 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.94-190G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47708034 | |||||||
chr6:47708043 | C | T | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.94-181C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47708043 | |||||||
chr6:47708061 | A | G | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.94-163A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47708061 | |||||||
chr6:47708130 | C | T | 1 | a0002c0002t0001g0044 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.94-94C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47708130 | |||||||
chr6:47708150 | A | C | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.94-74A>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47708150 | |||||||
chr6:47708152 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.94-72G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47708152 | |||||||
chr6:47708153 | G | T | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.94-71G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47708153 | |||||||
chr6:47708155 | G | C | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.94-69G>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47708155 | |||||||
chr6:47708156 | C | A | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.94-68C>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47708156 | |||||||
chr6:47708157 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.94-67C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47708157 | |||||||
chr6:47708158 | T | A | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.94-66T>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47708158 | |||||||
chr6:47708159 | C | G | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.94-65C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47708159 | |||||||
chr6:47708161 | A | G | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.94-63A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47708161 | |||||||
chr6:47708163 | G | T | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.94-61G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47708163 | |||||||
chr6:47708164 | C | G | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.94-60C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47708164 | |||||||
chr6:47708166 | G | T | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.94-58G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47708166 | |||||||
chr6:47708186 | C | T | 36 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0015 others(33): Show |
104 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.94-38C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47708186 | |||||||
chr6:47708298 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.148+20T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47708298 | |||||||
chr6:47708375 | C | T | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.148+97C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47708375 | |||||||
chr6:47708402 | C | T | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.148+124C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47708402 | |||||||
chr6:47708414 | C | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(51): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.148+136C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47708414 | |||||||
chr6:47708448 | T | C | 1 | a0001c0001t0001g0034 | 2 | HG01346.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.148+170T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47708448 | |||||||
chr6:47708450 | C | T | 1 | a0001c0001t0007g0089 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.148+172C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47708450 | |||||||
chr6:47708513 | A | G | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.148+235A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47708513 | |||||||
chr6:47708624 | G | A | 1 | a0001c0001t0002g0082 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.148+346G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47708624 | |||||||
chr6:47708660 | C | G | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.148+382C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47708660 | |||||||
chr6:47708707 | A | T | 52 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(49): Show |
142 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.148+429A>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47708707 | |||||||
chr6:47708759 | G | A | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.148+481G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47708759 | |||||||
chr6:47708783 | T | C | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.148+505T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47708783 | |||||||
chr6:47708889 | T | C | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.148+611T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47708889 | |||||||
chr6:47708890 | T | C | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.148+612T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47708890 | |||||||
chr6:47708955 | T | C | 1 | a0001c0001t0001g0107 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.148+677T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47708955 | |||||||
chr6:47709006 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.148+728C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47709006 | |||||||
chr6:47709077 | C | CAAGGTTT others(93): Show |
1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.148+807_148+808ins others(100): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 47709077 | ||||||
chr6:47709096 | G | A | 2 | a0001c0001t0002g0031 a0001c0001t0002g0082 |
3 | HG01081.hp1 HG01934.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.148+818G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47709096 | |||||||
chr6:47709104 | T | G | 3 | a0001c0001t0004g0049 a0001c0007t0001g0053 a0001c0007t0001g0064 |
3 | HG00642.hp2 HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.148+826T>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47709104 | |||||||
chr6:47709223 | T | A | 5 | a0001c0001t0001g0041 a0001c0001t0001g0085 a0001c0001t0003g0012 others(2): Show |
9 | HG02258.hp1 HG02717.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.148+945T>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47709223 | |||||||
chr6:47709238 | A | G | 1 | a0001c0001t0001g0113 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.148+960A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47709238 | |||||||
chr6:47709254 | A | G | 1 | a0009c0016t0001g0096 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.148+976A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47709254 | |||||||
chr6:47709291 | C | T | 2 | a0001c0007t0001g0053 a0001c0007t0001g0064 |
2 | HG00642.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.148+1013C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47709291 | |||||||
chr6:47709362 | T | C | 23 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(20): Show |
88 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.148+1084T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47709362 | |||||||
chr6:47709451 | A | T | 1 | a0002c0002t0001g0025 | 2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.148+1173A>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47709451 | |||||||
chr6:47709479 | A | G | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(129): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.148+1201A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47709479 | |||||||
chr6:47709502 | A | G | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.148+1224A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47709502 | |||||||
chr6:47709582 | T | C | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.149-1153T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47709582 | |||||||
chr6:47709639 | T | A | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.149-1096T>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47709639 | |||||||
chr6:47709710 | G | A | 2 | a0002c0002t0001g0029 a0002c0002t0001g0054 |
3 | HG01891.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.149-1025G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47709710 | |||||||
chr6:47709849 | G | GTTTT | 23 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(20): Show |
91 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.149-879_149-876dup others(4): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 47709849 | ||||||
chr6:47709849 | G | GTTTTT | 29 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0023 others(26): Show |
81 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.149-880_149-876dup others(5): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 47709849 | ||||||
chr6:47709860 | G | T | 4 | a0001c0001t0001g0041 a0001c0001t0003g0012 a0001c0001t0003g0063 others(1): Show |
8 | HG02258.hp1 HG02717.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-875G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47709860 | |||||||
chr6:47709925 | C | T | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.149-810C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47709925 | |||||||
chr6:47709958 | AATGTGTC others(2): Show |
A | 2 | a0002c0002t0001g0013 a0002c0002t0001g0057 |
5 | NA18939.hp2 NA18940.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.149-773_149-765del others(9): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 47709958 | ||||||
chr6:47709969 | T | C | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.149-766T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47709969 | |||||||
chr6:47709980 | C | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(51): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.149-755C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47709980 | |||||||
chr6:47710051 | G | A | 2 | a0002c0002t0001g0028 a0002c0002t0005g0028 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.149-684G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47710051 | |||||||
chr6:47710095 | C | A | 1 | a0003c0004t0001g0058 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.149-640C>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47710095 | |||||||
chr6:47710150 | G | A | 52 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(49): Show |
142 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.149-585G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47710150 | |||||||
chr6:47710199 | A | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(52): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.149-536A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47710199 | |||||||
chr6:47710393 | C | T | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.149-342C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47710393 | |||||||
chr6:47710446 | C | T | 25 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(22): Show |
93 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.149-289C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47710446 | |||||||
chr6:47710475 | C | A | 1 | a0002c0002t0001g0059 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.149-260C>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47710475 | |||||||
chr6:47710543 | T | C | 1 | a0001c0001t0001g0069 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.149-192T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47710543 | |||||||
chr6:47710551 | G | A | 1 | a0002c0002t0001g0060 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.149-184G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47710551 | |||||||
chr6:47710577 | C | G | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.149-158C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47710577 | |||||||
chr6:47710653 | G | A | 1 | a0002c0002t0001g0060 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.149-82G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47710653 | |||||||
chr6:47710676 | A | G | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.149-59A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47710676 | |||||||
chr6:47710719 | CT | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(51): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.149-9delT | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 47710719 | ||||||
chr6:47710722 | T | C | 1 | a0002c0002t0001g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.149-13T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47710722 | |||||||
chr6:47710922 | A | G | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.300+36A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47710922 | |||||||
chr6:47710942 | C | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(104): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.300+56C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47710942 | |||||||
chr6:47710982 | C | G | 51 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(48): Show |
141 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.300+96C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47710982 | |||||||
chr6:47710983 | A | G | 1 | a0002c0002t0001g0062 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.300+97A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47710983 | |||||||
chr6:47711077 | T | C | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.300+191T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47711077 | |||||||
chr6:47711093 | C | G | 1 | a0002c0002t0001g0061 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.300+207C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47711093 | |||||||
chr6:47711112 | CA | C | 47 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(44): Show |
133 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.300+243delA | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 47711112 | ||||||
chr6:47711112 | CAA | C | 57 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(54): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.300+242_300+243del others(2): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 47711112 | ||||||
chr6:47711125 | A | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(52): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.300+239A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47711125 | |||||||
chr6:47711240 | A | G | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.300+354A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47711240 | |||||||
chr6:47711280 | T | C | 1 | a0002c0002t0001g0007 | 11 | HG01069.hp2 HG01891.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.300+394T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47711280 | |||||||
chr6:47711366 | A | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(104): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.300+480A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47711366 | |||||||
chr6:47711477 | G | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0030 |
6 | HG01175.hp2 HG02572.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.300+591G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47711477 | |||||||
chr6:47711540 | C | T | 1 | a0001c0001t0001g0041 | 2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.300+654C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47711540 | |||||||
chr6:47711550 | C | A | 1 | a0009c0016t0001g0096 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.300+664C>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47711550 | |||||||
chr6:47711550 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.300+664C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47711550 | |||||||
chr6:47711555 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.300+669C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47711555 | |||||||
chr6:47711621 | A | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(137): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.300+735A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47711621 | |||||||
chr6:47711796 | G | C | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.301-561G>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47711796 | |||||||
chr6:47711850 | A | G | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.301-507A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47711850 | |||||||
chr6:47711889 | G | A | 35 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0015 others(32): Show |
103 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.301-468G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47711889 | |||||||
chr6:47711900 | AG | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(51): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.301-456delG | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47711900 | |||||||
chr6:47712053 | G | A | 1 | a0001c0007t0001g0064 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.301-304G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47712053 | |||||||
chr6:47712055 | T | C | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.301-302T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47712055 | |||||||
chr6:47712096 | A | G | 1 | a0001c0001t0004g0049 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.301-261A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47712096 | |||||||
chr6:47712100 | G | A | 5 | a0001c0001t0001g0041 a0001c0001t0001g0085 a0001c0001t0003g0012 others(2): Show |
9 | HG02258.hp1 HG02717.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.301-257G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47712100 | |||||||
chr6:47712180 | T | C | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.301-177T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47712180 | |||||||
chr6:47712184 | C | A | 1 | a0001c0001t0001g0121 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.301-173C>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47712184 | |||||||
chr6:47712625 | A | G | 1 | a0002c0002t0001g0065 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.552+17A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 5/9 | chr6 | 47712625 | |||||||
chr6:47712714 | A | C | 50 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(47): Show |
140 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.552+106A>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 5/9 | chr6 | 47712714 | |||||||
chr6:47712847 | G | A | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.552+239G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 5/9 | chr6 | 47712847 | |||||||
chr6:47712870 | G | A | 1 | a0001c0001t0001g0091 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.552+262G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 5/9 | chr6 | 47712870 | |||||||
chr6:47712882 | A | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0095 |
4 | HG01099.hp2 HG01123.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.552+274A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 5/9 | chr6 | 47712882 | |||||||
chr6:47712936 | G | T | 50 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(47): Show |
140 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.552+328G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 5/9 | chr6 | 47712936 | |||||||
chr6:47712979 | G | A | 1 | a0002c0002t0001g0127 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.552+371G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 5/9 | chr6 | 47712979 | |||||||
chr6:47713025 | G | C | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.552+417G>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 5/9 | chr6 | 47713025 | |||||||
chr6:47713260 | T | A | 1 | a0001c0001t0001g0092 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.553-538T>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 5/9 | chr6 | 47713260 | |||||||
chr6:47713275 | A | AT | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(128): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.553-523_553-522ins others(1): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 5/9 | chr6 | 47713275 | |||||||
chr6:47713297 | A | T | 1 | a0001c0001t0004g0049 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.553-501A>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 5/9 | chr6 | 47713297 | |||||||
chr6:47713451 | T | G | 1 | a0002c0002t0001g0127 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.553-347T>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 5/9 | chr6 | 47713451 | |||||||
chr6:47713505 | A | G | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.553-293A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 5/9 | chr6 | 47713505 | |||||||
chr6:47713758 | T | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(102): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.553-40T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 5/9 | chr6 | 47713758 | |||||||
chr6:47715213 | C | T | 36 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0015 others(33): Show |
105 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.1932+36C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47715213 | |||||||
chr6:47715255 | A | C | 1 | a0001c0001t0001g0016 | 4 | HG00544.hp2 NA18942.hp2 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.1932+78A>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47715255 | |||||||
chr6:47715321 | A | G | 45 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(42): Show |
131 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.1932+144A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47715321 | |||||||
chr6:47715428 | G | A | 2 | a0001c0007t0001g0053 a0001c0007t0001g0064 |
2 | HG00642.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1932+251G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47715428 | |||||||
chr6:47715615 | A | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0092 others(1): Show |
14 | HG00741.hp1 HG02451.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1932+438A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47715615 | |||||||
chr6:47715682 | C | T | 5 | a0001c0001t0001g0041 a0001c0001t0001g0085 a0001c0001t0003g0012 others(2): Show |
9 | HG02258.hp1 HG02717.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1932+505C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47715682 | |||||||
chr6:47715696 | G | C | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1932+519G>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47715696 | |||||||
chr6:47715757 | G | T | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1932+580G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47715757 | |||||||
chr6:47715776 | A | G | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1932+599A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47715776 | |||||||
chr6:47715827 | T | C | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1932+650T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47715827 | |||||||
chr6:47715864 | A | G | 1 | a0002c0002t0001g0054 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1932+687A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47715864 | |||||||
chr6:47715900 | C | G | 26 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
94 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.1932+723C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47715900 | |||||||
chr6:47715900 | C | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(76): Show |
222 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.1932+723C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47715900 | |||||||
chr6:47715935 | A | C | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1932+758A>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47715935 | |||||||
chr6:47715983 | A | ATT | 5 | a0002c0002t0001g0028 a0002c0002t0001g0032 a0002c0002t0001g0045 others(2): Show |
6 | HG02451.hp2 HG02970.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1933-808_1933-807d others(4): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 47715983 | ||||||
chr6:47715983 | AT | A | 32 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(29): Show |
95 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.1933-807delT | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 47715983 | ||||||
chr6:47715983 | ATT | A | 25 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(22): Show |
90 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.1933-808_1933-807d others(4): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 47715983 | ||||||
chr6:47715998 | T | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(88): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.1933-808T>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47715998 | |||||||
chr6:47715998 | T | TA | 13 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0021 others(10): Show |
34 | HG00323.hp2 HG00642.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.1933-808_1933-807i others(3): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47715998 | |||||||
chr6:47715999 | T | A | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(101): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.1933-807T>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47715999 | |||||||
chr6:47716033 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1933-773C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47716033 | |||||||
chr6:47716099 | T | C | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1933-707T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47716099 | |||||||
chr6:47716217 | C | CCTGTGAC others(7): Show |
1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1933-587_1933-586i others(16): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 47716217 | ||||||
chr6:47716417 | C | T | 1 | a0002c0002t0001g0025 | 2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1933-389C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47716417 | |||||||
chr6:47716473 | T | A | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1933-333T>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47716473 | |||||||
chr6:47716487 | C | T | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1933-319C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47716487 | |||||||
chr6:47716653 | C | T | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1933-153C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47716653 | |||||||
chr6:47716659 | A | G | 1 | a0002c0002t0001g0061 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1933-147A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47716659 | |||||||
chr6:47716670 | A | G | 1 | a0002c0002t0001g0026 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1933-136A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47716670 | |||||||
chr6:47716727 | T | C | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1933-79T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47716727 | |||||||
chr6:47716741 | G | A | 1 | a0002c0002t0001g0032 | 2 | HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1933-65G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47716741 | |||||||
chr6:47716748 | A | G | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1933-58A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47716748 | |||||||
chr6:47716755 | G | A | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1933-51G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47716755 | |||||||
chr6:47716771 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1933-35A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47716771 | |||||||
chr6:47716775 | T | C | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1933-31T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47716775 | |||||||
chr6:47716799 | G | T | 5 | a0002c0002t0001g0028 a0002c0002t0001g0032 a0002c0002t0001g0045 others(2): Show |
6 | HG02451.hp2 HG02970.hp1 HG03486.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1933-7G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47716799 | |||||||
chr6:47716855 | G | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(51): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
splice_region_variant&intron_variant | LOW | c.1974+8G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 7/9 | chr6 | 47716855 | |||||||
chr6:47716886 | T | C | 5 | a0002c0002t0001g0028 a0002c0002t0001g0032 a0002c0002t0001g0045 others(2): Show |
6 | HG02451.hp2 HG02970.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1974+39T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 7/9 | chr6 | 47716886 | |||||||
chr6:47716969 | G | T | 1 | a0001c0001t0001g0041 | 2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1974+122G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 7/9 | chr6 | 47716969 | |||||||
chr6:47717191 | T | C | 3 | a0001c0001t0003g0012 a0001c0001t0003g0063 a0001c0001t0012g0012 |
6 | HG02258.hp1 HG02717.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1975-101T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 7/9 | chr6 | 47717191 | |||||||
chr6:47717384 | G | A | 1 | a0001c0001t0004g0049 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2034+33G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 8/9 | chr6 | 47717384 | |||||||
chr6:47717421 | C | T | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2034+70C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 8/9 | chr6 | 47717421 | |||||||
chr6:47717549 | G | A | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2034+198G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 8/9 | chr6 | 47717549 | |||||||
chr6:47717586 | T | C | 1 | a0001c0001t0001g0071 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2034+235T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 8/9 | chr6 | 47717586 | |||||||
chr6:47717740 | C | G | 1 | a0002c0002t0001g0060 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2034+389C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 8/9 | chr6 | 47717740 | |||||||
chr6:47717919 | C | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0023 others(21): Show |
76 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.2035-470C>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 8/9 | chr6 | 47717919 | |||||||
chr6:47718098 | C | A | 4 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0075 others(1): Show |
6 | HG02015.hp1 HG02129.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.2035-291C>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 8/9 | chr6 | 47718098 | |||||||
chr6:47718103 | T | C | 1 | a0001c0001t0001g0079 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2035-286T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 8/9 | chr6 | 47718103 | |||||||
chr6:47718107 | C | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0098 |
2 | NA18978.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.2035-282C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 8/9 | chr6 | 47718107 | |||||||
chr6:47718129 | T | A | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2035-260T>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 8/9 | chr6 | 47718129 | |||||||
chr6:47718167 | G | A | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2035-222G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 8/9 | chr6 | 47718167 | |||||||
chr6:47718215 | C | T | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2035-174C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 8/9 | chr6 | 47718215 | |||||||
chr6:47718228 | A | G | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2035-161A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 8/9 | chr6 | 47718228 | |||||||
chr6:47718342 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2035-47T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 8/9 | chr6 | 47718342 | |||||||
chr6:47718365 | T | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(137): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.2035-24T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 8/9 | chr6 | 47718365 | |||||||
chr6:47718498 | C | G | 2 | a0001c0007t0001g0053 a0001c0007t0001g0064 |
2 | HG00642.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.*3+53C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47718498 | |||||||
chr6:47718499 | C | A | 50 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(47): Show |
140 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.*3+54C>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47718499 | |||||||
chr6:47718635 | G | T | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.*3+190G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47718635 | |||||||
chr6:47718661 | AT | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(51): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.*3+217delT | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47718661 | |||||||
chr6:47718674 | T | A | 1 | a0002c0002t0001g0047 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.*3+229T>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47718674 | |||||||
chr6:47718729 | A | G | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.*3+284A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47718729 | |||||||
chr6:47718856 | C | T | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(128): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.*3+411C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47718856 | |||||||
chr6:47718884 | A | G | 1 | a0013c0010t0001g0086 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.*3+439A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47718884 | |||||||
chr6:47719051 | G | A | 1 | a0001c0007t0001g0053 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.*3+606G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47719051 | |||||||
chr6:47719063 | C | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(51): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.*3+618C>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47719063 | |||||||
chr6:47719163 | T | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(51): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.*3+718T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47719163 | |||||||
chr6:47719271 | T | C | 42 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(39): Show |
128 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.*3+826T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47719271 | |||||||
chr6:47719424 | G | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(51): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.*3+979G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47719424 | |||||||
chr6:47719497 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.*3+1052G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47719497 | |||||||
chr6:47719518 | C | T | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.*3+1073C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47719518 | |||||||
chr6:47719648 | G | C | 1 | a0001c0001t0001g0095 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.*3+1203G>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47719648 | |||||||
chr6:47719657 | C | A | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.*3+1212C>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47719657 | |||||||
chr6:47719666 | G | T | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.*3+1221G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47719666 | |||||||
chr6:47719794 | C | G | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.*3+1349C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47719794 | |||||||
chr6:47719881 | T | C | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.*4-1328T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47719881 | |||||||
chr6:47719922 | G | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0116 |
4 | HG00558.hp1 NA18945.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.*4-1287G>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47719922 | |||||||
chr6:47719949 | G | A | 1 | a0002c0002t0001g0060 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.*4-1260G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47719949 | |||||||
chr6:47719987 | C | G | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.*4-1222C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47719987 | |||||||
chr6:47720082 | C | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0122 |
4 | NA18978.hp2 NA19011.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.*4-1127C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47720082 | |||||||
chr6:47720119 | GATTACAG others(3): Show |
G | 1 | a0001c0005t0001g0124 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.*4-1088_*4-1079del others(10): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 47720119 | ||||||
chr6:47720188 | C | T | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.*4-1021C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47720188 | |||||||
chr6:47720205 | G | A | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.*4-1004G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47720205 | |||||||
chr6:47720279 | G | T | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.*4-930G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47720279 | |||||||
chr6:47720366 | G | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(51): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.*4-843G>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47720366 | |||||||
chr6:47720380 | G | A | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.*4-829G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47720380 | |||||||
chr6:47720392 | G | C | 22 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(19): Show |
85 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.*4-817G>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47720392 | |||||||
chr6:47720456 | A | T | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.*4-753A>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47720456 | |||||||
chr6:47720476 | C | T | 21 | a0002c0002t0001g0005 a0002c0002t0001g0013 a0002c0002t0001g0020 others(18): Show |
46 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.*4-733C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47720476 | |||||||
chr6:47720598 | T | C | 5 | a0002c0002t0001g0028 a0002c0002t0001g0032 a0002c0002t0001g0045 others(2): Show |
6 | HG02451.hp2 HG02970.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.*4-611T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47720598 | |||||||
chr6:47720600 | G | A | 1 | a0001c0007t0001g0053 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.*4-609G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47720600 | |||||||
chr6:47720772 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.*4-437G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47720772 | |||||||
chr6:47720856 | G | T | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.*4-353G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47720856 | |||||||
chr6:47720870 | C | T | 42 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(39): Show |
128 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.*4-339C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47720870 | |||||||
chr6:47720880 | T | C | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.*4-329T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47720880 | |||||||
chr6:47720932 | C | G | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.*4-277C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47720932 | |||||||
chr6:47720933 | G | A | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.*4-276G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47720933 | |||||||
chr6:47721021 | GCCTTTTT others(12): Show |
G | 1 | a0001c0001t0010g0073 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.*4-187_*4-169delCC others(17): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47721021 | |||||||
chr6:47721117 | G | A | 1 | a0004c0008t0006g0027 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.*4-92G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47721117 | |||||||
chr6:47721186 | T | A | 1 | a0001c0001t0002g0082 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.*4-23T>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47721186 |