geneid | 4131 |
---|---|
ensemblid | ENSG00000131711.15 |
hgncid | 6836 |
symbol | MAP1B |
name | microtubule associated protein 1B |
refseq_nuc | NM_005909.5 |
refseq_prot | NP_005900.2 |
ensembl_nuc | ENST00000296755.12 |
ensembl_prot | ENSP00000296755.7 |
mane_status | MANE Select |
chr | chr5 |
start | 72107475 |
end | 72209565 |
strand | + |
ver | v1.2 |
region | chr5:72107475-72209565 |
region5000 | chr5:72102475-72214565 |
regionname0 | MAP1B_chr5_72107475_72209565 |
regionname5000 | MAP1B_chr5_72102475_72214565 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 2468 | 289 | 77 | 49 | 119 | 10 | 33 | 88 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0002 | 1/0 | 2468 | 22 | 1 | 16 | 3 | 0 | 1 | 2 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0003 | 0/0 | 2468 | 5 | 0 | 5 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0004 | 0/0 | 2468 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0005 | 0/0 | 2468 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0006 | 0/0 | 2468 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0007 | 0/0 | 2468 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0008 | 0/0 | 2468 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0009 | 0/0 | 2468 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0010 | 0/0 | 2472 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0011 | 0/0 | 2468 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0012 | 0/0 | 2468 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0013 | 0/0 | 2468 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0014 | 0/0 | 2468 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0015 | 0/0 | 2468 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0016 | 0/0 | 2468 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0017 | 0/0 | 2468 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 7407 | 122 | 30 | 22 | 48 | 3 | 18 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
c0002 | 0/0 | 7407 | 100 | 10 | 17 | 58 | 5 | 10 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
c0003 | 1/0 | 7407 | 18 | 1 | 14 | 1 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
c0004 | 0/0 | 7407 | 18 | 6 | 3 | 4 | 2 | 3 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
c0005 | 0/0 | 7407 | 17 | 16 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
c0006 | 0/0 | 7407 | 7 | 6 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
c0007 | 0/0 | 7407 | 5 | 0 | 5 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
c0008 | 0/0 | 7407 | 4 | 0 | 0 | 4 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
c0009 | 0/0 | 7407 | 4 | 1 | 3 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
c0010 | 0/0 | 7407 | 4 | 4 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
c0011 | 0/0 | 7407 | 4 | 3 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
c0012 | 0/0 | 7407 | 3 | 0 | 0 | 3 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
c0013 | 0/0 | 7407 | 3 | 3 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
c0014 | 0/0 | 7407 | 2 | 0 | 2 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
c0015 | 0/0 | 7407 | 2 | 0 | 0 | 2 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
c0016 | 0/0 | 7407 | 2 | 1 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
c0017 | 0/0 | 7407 | 2 | 0 | 0 | 2 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
c0018 | 0/0 | 7407 | 2 | 0 | 0 | 2 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
c0019 | 0/0 | 7407 | 2 | 1 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
c0020 | 0/0 | 7407 | 2 | 1 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
c0021 | 0/0 | 7407 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
c0022 | 0/0 | 7407 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
c0023 | 0/0 | 7419 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
c0024 | 0/0 | 7407 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
c0025 | 0/0 | 7407 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
c0026 | 0/0 | 7407 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
c0027 | 0/0 | 7407 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
c0028 | 0/0 | 7407 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
c0029 | 0/0 | 7407 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
c0030 | 0/0 | 7407 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
c0031 | 0/0 | 7407 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
c0032 | 0/0 | 7407 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
c0033 | 0/0 | 7407 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
c0034 | 0/0 | 7407 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
c0035 | 0/0 | 7407 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
c0036 | 0/0 | 7407 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
c0037 | 0/0 | 7407 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
c0038 | 0/0 | 7407 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
c0039 | 0/0 | 7407 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 4385 | 77 | 23 | 12 | 31 | 2 | 9 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
t0002 | 0/0 | 4385 | 59 | 4 | 8 | 36 | 0 | 11 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
t0003 | 0/1 | 4384 | 40 | 0 | 9 | 25 | 3 | 2 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
t0004 | 0/0 | 4374 | 20 | 2 | 10 | 0 | 3 | 5 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
t0005 | 0/0 | 4384 | 18 | 15 | 2 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
t0006 | 0/0 | 4384 | 17 | 1 | 16 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
t0007 | 0/0 | 4386 | 12 | 7 | 3 | 0 | 1 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
t0008 | 0/0 | 4384 | 9 | 8 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
t0009 | 0/0 | 4385 | 9 | 0 | 0 | 9 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
t0010 | 0/0 | 4385 | 9 | 0 | 3 | 5 | 1 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
t0011 | 0/0 | 4386 | 8 | 4 | 1 | 3 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
t0012 | 0/0 | 4384 | 7 | 7 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
t0013 | 0/0 | 4384 | 7 | 1 | 3 | 3 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
t0014 | 0/0 | 4384 | 5 | 2 | 0 | 3 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
t0015 | 0/0 | 4381 | 5 | 1 | 0 | 3 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
t0016 | 0/0 | 4383 | 4 | 1 | 0 | 3 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
t0017 | 0/0 | 4375 | 4 | 1 | 2 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
t0018 | 0/0 | 4385 | 4 | 4 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
t0019 | 0/0 | 4374 | 3 | 0 | 2 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
t0020 | 0/0 | 4385 | 2 | 2 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
t0021 | 0/0 | 4384 | 2 | 2 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
t0022 | 0/0 | 4386 | 2 | 2 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
t0023 | 0/0 | 4384 | 2 | 0 | 1 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
t0024 | 0/0 | 4383 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
t0025 | 0/0 | 4385 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
t0026 | 0/0 | 4385 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
t0027 | 0/0 | 4383 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
t0028 | 0/0 | 4385 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
t0029 | 0/0 | 4385 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
t0030 | 0/0 | 4385 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
t0031 | 0/0 | 4374 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
t0032 | 0/0 | 4384 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
t0033 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
t0034 | 0/0 | 4386 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
t0035 | 0/0 | 4375 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
t0036 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
t0037 | 0/0 | 4385 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
t0038 | 1/0 | 4384 | 1 | 0 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
t0039 | 0/0 | 4386 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
t0040 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0224 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0325 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 7407 | 122 | 30 | 22 | 48 | 3 | 18 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0002 | 0/0 | 7407 | 100 | 10 | 17 | 58 | 5 | 10 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0004 | 0/0 | 7407 | 18 | 6 | 3 | 4 | 2 | 3 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0005 | 0/0 | 7407 | 17 | 16 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0006 | 0/0 | 7407 | 7 | 6 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0008 | 0/0 | 7407 | 4 | 0 | 0 | 4 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0009 | 0/0 | 7407 | 4 | 1 | 3 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0017 | 0/0 | 7407 | 2 | 0 | 0 | 2 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0018 | 0/0 | 7407 | 2 | 0 | 0 | 2 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0019 | 0/0 | 7407 | 2 | 1 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0020 | 0/0 | 7407 | 2 | 1 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0022 | 0/0 | 7407 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0025 | 0/0 | 7407 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0026 | 0/0 | 7407 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0028 | 0/0 | 7407 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0029 | 0/0 | 7407 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0034 | 0/0 | 7407 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0036 | 0/0 | 7407 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0038 | 0/0 | 7407 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0039 | 0/0 | 7407 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0002c0003 | 1/0 | 7407 | 18 | 1 | 14 | 1 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0002c0014 | 0/0 | 7407 | 2 | 0 | 2 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0002c0015 | 0/0 | 7407 | 2 | 0 | 0 | 2 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0003c0007 | 0/0 | 7407 | 5 | 0 | 5 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0004c0010 | 0/0 | 7407 | 4 | 4 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0005c0012 | 0/0 | 7407 | 3 | 0 | 0 | 3 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0005c0030 | 0/0 | 7407 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0006c0011 | 0/0 | 7407 | 4 | 3 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0007c0013 | 0/0 | 7407 | 3 | 3 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0008c0016 | 0/0 | 7407 | 2 | 1 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0009c0021 | 0/0 | 7407 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0010c0023 | 0/0 | 7419 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0011c0032 | 0/0 | 7407 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0012c0027 | 0/0 | 7407 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0013c0031 | 0/0 | 7407 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0014c0033 | 0/0 | 7407 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0015c0024 | 0/0 | 7407 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0016c0035 | 0/0 | 7407 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0017c0037 | 0/0 | 7407 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 11791 | 53 | 13 | 7 | 23 | 2 | 8 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0001t0002 | 0/0 | 11791 | 12 | 0 | 1 | 9 | 0 | 2 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0001t0003 | 0/1 | 11790 | 1 | 0 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0001t0004 | 0/0 | 11780 | 15 | 2 | 7 | 0 | 1 | 5 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0001t0005 | 0/0 | 11790 | 4 | 2 | 1 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0001t0007 | 0/0 | 11792 | 4 | 3 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0001t0009 | 0/0 | 11791 | 4 | 0 | 0 | 4 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0001t0010 | 0/0 | 11791 | 6 | 0 | 3 | 3 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0001t0011 | 0/0 | 11792 | 2 | 0 | 0 | 2 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0001t0012 | 0/0 | 11790 | 7 | 7 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0001t0014 | 0/0 | 11790 | 2 | 0 | 0 | 2 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0001t0015 | 0/0 | 11787 | 2 | 1 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0001t0019 | 0/0 | 11780 | 3 | 0 | 2 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0001t0020 | 0/0 | 11791 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0001t0021 | 0/0 | 11790 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0001t0024 | 0/0 | 11789 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0001t0026 | 0/0 | 11791 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0001t0028 | 0/0 | 11791 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0001t0035 | 0/0 | 11781 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0001t0039 | 0/0 | 11792 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0002t0001 | 0/0 | 11791 | 7 | 0 | 1 | 6 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0002t0002 | 0/0 | 11791 | 32 | 4 | 2 | 18 | 0 | 8 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0002t0003 | 0/0 | 11790 | 35 | 0 | 8 | 22 | 3 | 2 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0002t0004 | 0/0 | 11780 | 4 | 0 | 2 | 0 | 2 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0002t0009 | 0/0 | 11791 | 4 | 0 | 0 | 4 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0002t0010 | 0/0 | 11791 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0002t0011 | 0/0 | 11792 | 2 | 2 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0002t0013 | 0/0 | 11790 | 6 | 1 | 3 | 2 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0002t0014 | 0/0 | 11790 | 3 | 2 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0002t0016 | 0/0 | 11789 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0002t0023 | 0/0 | 11790 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0002t0027 | 0/0 | 11789 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0002t0030 | 0/0 | 11791 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0002t0031 | 0/0 | 11780 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0002t0032 | 0/0 | 11790 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0004t0001 | 0/0 | 11791 | 3 | 3 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0004t0002 | 0/0 | 11791 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0004t0005 | 0/0 | 11790 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0004t0007 | 0/0 | 11792 | 2 | 1 | 0 | 0 | 1 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0004t0010 | 0/0 | 11791 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0004t0011 | 0/0 | 11792 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0004t0015 | 0/0 | 11787 | 3 | 0 | 0 | 2 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0004t0017 | 0/0 | 11781 | 4 | 1 | 2 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0004t0022 | 0/0 | 11792 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0004t0034 | 0/0 | 11792 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0005t0001 | 0/0 | 11791 | 3 | 3 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0005t0005 | 0/0 | 11790 | 5 | 5 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0005t0008 | 0/0 | 11790 | 7 | 6 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0005t0020 | 0/0 | 11791 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0005t0021 | 0/0 | 11790 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0006t0005 | 0/0 | 11790 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0006t0007 | 0/0 | 11792 | 2 | 1 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0006t0018 | 0/0 | 11791 | 3 | 3 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0006t0022 | 0/0 | 11792 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0008t0002 | 0/0 | 11791 | 2 | 0 | 0 | 2 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0008t0003 | 0/0 | 11790 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0008t0037 | 0/0 | 11791 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0009t0001 | 0/0 | 11791 | 3 | 0 | 3 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0009t0007 | 0/0 | 11792 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0017t0002 | 0/0 | 11791 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0017t0003 | 0/0 | 11790 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0018t0001 | 0/0 | 11791 | 2 | 0 | 0 | 2 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0019t0007 | 0/0 | 11792 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0019t0040 | 0/0 | 11792 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0020t0007 | 0/0 | 11792 | 2 | 1 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0022t0002 | 0/0 | 11791 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0025t0001 | 0/0 | 11791 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0026t0008 | 0/0 | 11790 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0028t0025 | 0/0 | 11791 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0029t0005 | 0/0 | 11790 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0034t0005 | 0/0 | 11790 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0036t0008 | 0/0 | 11790 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0038t0013 | 0/0 | 11790 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0001c0039t0018 | 0/0 | 11791 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0002c0003t0006 | 0/0 | 11790 | 15 | 1 | 14 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0002c0003t0016 | 0/0 | 11789 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0002c0003t0023 | 0/0 | 11790 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0002c0003t0038 | 1/0 | 11790 | 1 | 0 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0002c0014t0004 | 0/0 | 11780 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0002c0014t0006 | 0/0 | 11790 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0002c0015t0016 | 0/0 | 11789 | 2 | 0 | 0 | 2 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0003c0007t0002 | 0/0 | 11791 | 5 | 0 | 5 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0004c0010t0005 | 0/0 | 11790 | 4 | 4 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0005c0012t0002 | 0/0 | 11791 | 3 | 0 | 0 | 3 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0005c0030t0002 | 0/0 | 11791 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0006c0011t0001 | 0/0 | 11791 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0006c0011t0011 | 0/0 | 11792 | 3 | 2 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0007c0013t0001 | 0/0 | 11791 | 2 | 2 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0007c0013t0029 | 0/0 | 11791 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0008c0016t0001 | 0/0 | 11791 | 2 | 1 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0009c0021t0036 | 0/0 | 11792 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0010c0023t0006 | 0/0 | 11802 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0011c0032t0033 | 0/0 | 11792 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0012c0027t0010 | 0/0 | 11791 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0013c0031t0003 | 0/0 | 11790 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0014c0033t0009 | 0/0 | 11791 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0015c0024t0003 | 0/0 | 11790 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0016c0035t0005 | 0/0 | 11790 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
a0017c0037t0002 | 0/0 | 11791 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | copy fasta | chr5 | 72102475 | 72214565 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0003g0325 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0004g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0004g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0004g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0004g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0004g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0004g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0004g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0005g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0005g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0005g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0007g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0007g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0007g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0007g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0009g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0009g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0009g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0009g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0010g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0010g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0010g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0010g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0010g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0010g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0011g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0011g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0012g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0012g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0012g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0012g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0012g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0012g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0012g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0014g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0014g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0015g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0015g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0019g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0019g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0019g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0020g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0021g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0024g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0026g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0028g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0035g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0039g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0004g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0004g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0004g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0009g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0009g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0009g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0009g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0010g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0011g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0011g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0013g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0013g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0013g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0013g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0013g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0013g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0014g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0014g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0016g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0023g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0027g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0030g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0031g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0032g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0004t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0004t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0004t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0004t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0004t0005g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0004t0007g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0004t0007g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0004t0010g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0004t0011g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0004t0015g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0004t0015g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0004t0015g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0004t0017g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0004t0017g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0004t0017g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0004t0017g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0004t0022g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0004t0034g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0005t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0005t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0005t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0005t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0005t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0005t0005g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0005t0005g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0005t0005g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0005t0008g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0005t0008g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0005t0008g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0005t0008g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0005t0008g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0005t0008g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0005t0008g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0005t0020g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0005t0021g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0006t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0006t0007g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0006t0007g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0006t0018g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0006t0018g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0006t0018g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0006t0022g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0008t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0008t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0008t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0008t0037g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0009t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0009t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0009t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0009t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0017t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0017t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0018t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0018t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0019t0007g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0019t0040g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0020t0007g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0020t0007g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0022t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0025t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0026t0008g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0028t0025g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0029t0005g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0034t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0036t0008g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0038t0013g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0039t0018g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0003t0006g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0003t0006g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0003t0006g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0003t0006g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0003t0006g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0003t0006g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0003t0006g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0003t0006g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0003t0006g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0003t0006g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0003t0006g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0003t0006g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0003t0006g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0003t0006g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0003t0006g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0003t0016g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0003t0023g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0003t0038g0224 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0014t0004g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0014t0006g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0015t0016g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0015t0016g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0003c0007t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0003c0007t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0003c0007t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0003c0007t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0003c0007t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0004c0010t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0004c0010t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0004c0010t0005g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0004c0010t0005g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0005c0012t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0005c0012t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0005c0012t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0005c0030t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0006c0011t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0006c0011t0011g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0006c0011t0011g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0006c0011t0011g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0007c0013t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0007c0013t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0007c0013t0029g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0008c0016t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0008c0016t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0009c0021t0036g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0010c0023t0006g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0011c0032t0033g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0012c0027t0010g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0013c0031t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0014c0033t0009g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0015c0024t0003g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0016c0035t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0017c0037t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0004 | g0194 | EUR | GBR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00099 | hp2 | a0001 | c0002 | t0003 | g0177 | EUR | GBR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0312 | EUR | GBR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00140 | hp2 | a0001 | c0002 | t0003 | g0087 | EUR | GBR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | CHS | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0074 | EAS | CHS | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00558 | hp1 | a0001 | c0004 | t0015 | g0304 | EAS | CHS | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00558 | hp2 | a0001 | c0002 | t0009 | g0231 | EAS | CHS | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00609 | hp1 | a0002 | c0015 | t0016 | g0206 | EAS | CHS | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0305 | EAS | CHS | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00621 | hp1 | a0001 | c0008 | t0002 | g0110 | EAS | CHS | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00621 | hp2 | a0001 | c0002 | t0013 | g0020 | EAS | CHS | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0149 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00639 | hp2 | a0001 | c0001 | t0010 | g0230 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00642 | hp2 | a0001 | c0001 | t0004 | g0299 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00673 | hp1 | a0001 | c0001 | t0026 | g0202 | EAS | CHS | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00673 | hp2 | a0001 | c0002 | t0003 | g0109 | EAS | CHS | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00733 | hp1 | a0002 | c0003 | t0006 | g0195 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00733 | hp2 | a0001 | c0004 | t0005 | g0104 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00735 | hp1 | a0002 | c0003 | t0006 | g0168 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0081 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00738 | hp1 | a0002 | c0003 | t0006 | g0143 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00738 | hp2 | a0001 | c0004 | t0017 | g0165 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00741 | hp1 | a0008 | c0016 | t0001 | g0333 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00741 | hp2 | a0001 | c0005 | t0008 | g0038 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01069 | hp1 | a0001 | c0002 | t0004 | g0003 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01069 | hp2 | a0001 | c0001 | t0028 | g0176 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01070 | hp1 | a0001 | c0002 | t0023 | g0141 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01070 | hp2 | a0001 | c0001 | t0005 | g0156 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01071 | hp1 | a0001 | c0002 | t0004 | g0003 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01074 | hp1 | a0001 | c0002 | t0003 | g0174 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01074 | hp2 | a0006 | c0011 | t0011 | g0137 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01081 | hp1 | a0002 | c0003 | t0006 | g0142 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01081 | hp2 | a0001 | c0001 | t0019 | g0238 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01099 | hp2 | a0001 | c0002 | t0003 | g0309 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01106 | hp1 | a0002 | c0014 | t0006 | g0088 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01106 | hp2 | a0001 | c0001 | t0004 | g0310 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01109 | hp1 | a0002 | c0014 | t0004 | g0082 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01109 | hp2 | a0001 | c0002 | t0002 | g0161 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01167 | hp1 | a0003 | c0007 | t0002 | g0095 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01167 | hp2 | a0001 | c0006 | t0007 | g0260 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01168 | hp1 | a0001 | c0002 | t0003 | g0148 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01168 | hp2 | a0001 | c0009 | t0001 | g0060 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01169 | hp1 | a0001 | c0009 | t0001 | g0059 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01169 | hp2 | a0003 | c0007 | t0002 | g0096 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01192 | hp2 | a0001 | c0001 | t0004 | g0022 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01243 | hp2 | a0001 | c0020 | t0007 | g0261 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01255 | hp1 | a0001 | c0001 | t0004 | g0196 | AMR | CLM | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01255 | hp2 | a0001 | c0002 | t0013 | g0226 | AMR | CLM | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01257 | hp1 | a0002 | c0003 | t0006 | g0170 | AMR | CLM | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01257 | hp2 | a0001 | c0002 | t0002 | g0072 | AMR | CLM | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01261 | hp1 | a0002 | c0003 | t0006 | g0011 | AMR | CLM | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01261 | hp2 | a0001 | c0001 | t0010 | g0007 | AMR | CLM | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01346 | hp1 | a0001 | c0002 | t0013 | g0227 | AMR | CLM | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01346 | hp2 | a0001 | c0001 | t0004 | g0192 | AMR | CLM | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01358 | hp1 | a0001 | c0002 | t0013 | g0018 | AMR | CLM | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01358 | hp2 | a0001 | c0009 | t0001 | g0331 | AMR | CLM | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01361 | hp1 | a0001 | c0001 | t0019 | g0242 | AMR | CLM | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01361 | hp2 | a0015 | c0024 | t0003 | g0329 | AMR | CLM | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01433 | hp1 | a0001 | c0019 | t0007 | g0026 | AMR | CLM | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01433 | hp2 | a0003 | c0007 | t0002 | g0119 | AMR | CLM | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0052 | EUR | IBS | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01515 | hp2 | a0001 | c0004 | t0010 | g0237 | EUR | IBS | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01884 | hp1 | a0001 | c0002 | t0014 | g0001 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01884 | hp2 | a0001 | c0005 | t0001 | g0005 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01891 | hp1 | a0001 | c0001 | t0007 | g0255 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01891 | hp2 | a0001 | c0002 | t0011 | g0266 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01928 | hp1 | a0001 | c0002 | t0003 | g0296 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01934 | hp1 | a0002 | c0003 | t0006 | g0294 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01934 | hp2 | a0001 | c0001 | t0004 | g0025 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01943 | hp1 | a0002 | c0003 | t0006 | g0167 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01943 | hp2 | a0001 | c0002 | t0003 | g0290 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01975 | hp1 | a0003 | c0007 | t0002 | g0080 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01975 | hp2 | a0002 | c0003 | t0006 | g0218 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01978 | hp1 | a0001 | c0002 | t0003 | g0012 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01978 | hp2 | a0001 | c0001 | t0010 | g0229 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01981 | hp1 | a0001 | c0002 | t0003 | g0085 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01981 | hp2 | a0002 | c0003 | t0006 | g0151 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01993 | hp1 | a0010 | c0023 | t0006 | g0166 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01993 | hp2 | a0002 | c0003 | t0006 | g0197 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02004 | hp1 | a0002 | c0003 | t0006 | g0171 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02004 | hp2 | a0003 | c0007 | t0002 | g0094 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02015 | hp1 | a0001 | c0002 | t0003 | g0204 | EAS | KHV | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02055 | hp1 | a0001 | c0029 | t0005 | g0073 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | KHV | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02071 | hp1 | a0001 | c0001 | t0039 | g0019 | EAS | KHV | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02071 | hp2 | a0001 | c0002 | t0002 | g0187 | EAS | KHV | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02074 | hp1 | a0001 | c0002 | t0002 | g0017 | EAS | KHV | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02074 | hp2 | a0001 | c0002 | t0010 | g0225 | EAS | KHV | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | KHV | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02080 | hp2 | a0001 | c0001 | t0015 | g0113 | EAS | KHV | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | KHV | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02132 | hp2 | a0001 | c0002 | t0002 | g0205 | EAS | KHV | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02135 | hp1 | a0001 | c0001 | t0011 | g0105 | EAS | KHV | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02135 | hp2 | a0001 | c0004 | t0011 | g0326 | EAS | KHV | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02145 | hp1 | a0001 | c0005 | t0021 | g0135 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02145 | hp2 | a0001 | c0001 | t0015 | g0121 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02148 | hp1 | a0001 | c0002 | t0003 | g0219 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02148 | hp2 | a0001 | c0004 | t0017 | g0057 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02155 | hp1 | a0001 | c0038 | t0013 | g0021 | EAS | CDX | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02257 | hp1 | a0001 | c0005 | t0005 | g0125 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02257 | hp2 | a0001 | c0019 | t0040 | g0245 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02258 | hp1 | a0001 | c0001 | t0005 | g0139 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02258 | hp2 | a0001 | c0001 | t0021 | g0269 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02280 | hp1 | a0001 | c0004 | t0017 | g0191 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02280 | hp2 | a0001 | c0005 | t0020 | g0259 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0292 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02300 | hp2 | a0002 | c0003 | t0006 | g0162 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02451 | hp1 | a0001 | c0006 | t0018 | g0068 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02451 | hp2 | a0001 | c0005 | t0005 | g0258 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | KHV | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | KHV | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02572 | hp1 | a0001 | c0001 | t0012 | g0314 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02572 | hp2 | a0001 | c0001 | t0007 | g0116 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02602 | hp1 | a0001 | c0001 | t0004 | g0102 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02602 | hp2 | a0001 | c0001 | t0004 | g0065 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02622 | hp1 | a0001 | c0002 | t0002 | g0217 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02630 | hp1 | a0001 | c0005 | t0001 | g0271 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02630 | hp2 | a0001 | c0005 | t0008 | g0335 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02647 | hp1 | a0004 | c0010 | t0005 | g0332 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02647 | hp2 | a0001 | c0005 | t0008 | g0134 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02683 | hp1 | a0001 | c0001 | t0019 | g0247 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02683 | hp2 | a0001 | c0025 | t0001 | g0086 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02717 | hp2 | a0001 | c0004 | t0001 | g0190 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02723 | hp1 | a0001 | c0002 | t0002 | g0037 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02723 | hp2 | a0009 | c0021 | t0036 | g0042 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02738 | hp1 | a0001 | c0004 | t0034 | g0216 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02738 | hp2 | a0001 | c0002 | t0002 | g0010 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02818 | hp1 | a0001 | c0034 | t0005 | g0033 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02886 | hp1 | a0001 | c0026 | t0008 | g0027 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02886 | hp2 | a0001 | c0009 | t0007 | g0040 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02895 | hp1 | a0001 | c0001 | t0012 | g0053 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02895 | hp2 | a0001 | c0004 | t0007 | g0140 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02897 | hp1 | a0011 | c0032 | t0033 | g0222 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02897 | hp2 | a0001 | c0001 | t0012 | g0054 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02922 | hp1 | a0004 | c0010 | t0005 | g0256 | AFR | ESN | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02922 | hp2 | a0001 | c0002 | t0016 | g0153 | AFR | ESN | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02965 | hp1 | a0006 | c0011 | t0011 | g0136 | AFR | ESN | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02965 | hp2 | a0001 | c0005 | t0001 | g0307 | AFR | ESN | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02976 | hp1 | a0001 | c0005 | t0005 | g0155 | AFR | ESN | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0147 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03017 | hp2 | a0001 | c0002 | t0003 | g0118 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03041 | hp2 | a0001 | c0004 | t0001 | g0337 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03098 | hp1 | a0001 | c0005 | t0008 | g0030 | AFR | MSL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03098 | hp2 | a0001 | c0006 | t0022 | g0036 | AFR | MSL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03130 | hp1 | a0007 | c0013 | t0001 | g0123 | AFR | ESN | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03130 | hp2 | a0001 | c0005 | t0005 | g0043 | AFR | ESN | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03139 | hp1 | a0001 | c0005 | t0008 | g0107 | AFR | ESN | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03139 | hp2 | a0007 | c0013 | t0029 | g0124 | AFR | ESN | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03195 | hp1 | a0001 | c0005 | t0005 | g0221 | AFR | ESN | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03195 | hp2 | a0007 | c0013 | t0001 | g0265 | AFR | ESN | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03209 | hp1 | a0001 | c0005 | t0008 | g0253 | AFR | MSL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | MSL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03225 | hp1 | a0006 | c0011 | t0001 | g0254 | AFR | MSL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03225 | hp2 | a0001 | c0001 | t0012 | g0009 | AFR | MSL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03239 | hp2 | a0001 | c0001 | t0007 | g0049 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03453 | hp1 | a0001 | c0002 | t0002 | g0268 | AFR | MSL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03453 | hp2 | a0008 | c0016 | t0001 | g0262 | AFR | MSL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03486 | hp1 | a0016 | c0035 | t0005 | g0044 | AFR | MSL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0336 | AFR | MSL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03491 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03492 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03492 | hp2 | a0001 | c0002 | t0002 | g0092 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03516 | hp1 | a0001 | c0001 | t0007 | g0270 | AFR | ESN | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03540 | hp1 | a0001 | c0002 | t0002 | g0108 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03540 | hp2 | a0001 | c0036 | t0008 | g0122 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03579 | hp1 | a0001 | c0005 | t0008 | g0032 | AFR | MSL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03579 | hp2 | a0001 | c0001 | t0004 | g0324 | AFR | MSL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03654 | hp2 | a0001 | c0001 | t0035 | g0303 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03669 | hp1 | a0002 | c0003 | t0023 | g0243 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0159 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03688 | hp1 | a0001 | c0002 | t0002 | g0152 | SAS | STU | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03688 | hp2 | a0001 | c0004 | t0017 | g0061 | SAS | STU | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03710 | hp1 | a0001 | c0001 | t0004 | g0097 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03831 | hp2 | a0001 | c0002 | t0002 | g0008 | SAS | BEB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03927 | hp2 | a0001 | c0002 | t0002 | g0169 | SAS | BEB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | BEB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG04115 | hp1 | a0001 | c0001 | t0004 | g0048 | SAS | STU | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG04115 | hp2 | a0001 | c0002 | t0003 | g0175 | SAS | STU | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG04199 | hp1 | a0001 | c0022 | t0002 | g0150 | SAS | STU | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG04199 | hp2 | a0001 | c0001 | t0004 | g0252 | SAS | STU | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG04204 | hp1 | a0001 | c0002 | t0002 | g0051 | SAS | STU | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG04204 | hp2 | a0001 | c0004 | t0015 | g0186 | SAS | STU | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18522 | hp1 | a0001 | c0002 | t0011 | g0154 | AFR | YRI | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18522 | hp2 | a0001 | c0001 | t0005 | g0157 | AFR | YRI | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | CHB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18612 | hp2 | a0001 | c0002 | t0002 | g0201 | EAS | CHB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18747 | hp1 | a0001 | c0002 | t0002 | g0276 | EAS | CHB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | CHB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18906 | hp1 | a0006 | c0011 | t0011 | g0138 | AFR | YRI | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18906 | hp2 | a0001 | c0002 | t0014 | g0001 | AFR | YRI | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18941 | hp2 | a0001 | c0001 | t0010 | g0232 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18942 | hp2 | a0001 | c0002 | t0002 | g0098 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18943 | hp1 | a0001 | c0008 | t0003 | g0184 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18944 | hp1 | a0001 | c0002 | t0002 | g0181 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18944 | hp2 | a0001 | c0002 | t0002 | g0079 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18945 | hp2 | a0001 | c0002 | t0003 | g0066 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18946 | hp2 | a0001 | c0002 | t0003 | g0172 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18947 | hp1 | a0001 | c0004 | t0002 | g0180 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18947 | hp2 | a0001 | c0002 | t0003 | g0295 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18953 | hp1 | a0001 | c0002 | t0003 | g0126 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18953 | hp2 | a0001 | c0001 | t0005 | g0286 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18957 | hp2 | a0001 | c0001 | t0014 | g0091 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18959 | hp1 | a0001 | c0002 | t0027 | g0100 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18959 | hp2 | a0001 | c0017 | t0002 | g0055 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18960 | hp1 | a0012 | c0027 | t0010 | g0235 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18960 | hp2 | a0001 | c0002 | t0003 | g0321 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18963 | hp1 | a0005 | c0012 | t0002 | g0322 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18963 | hp2 | a0001 | c0002 | t0003 | g0306 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18966 | hp1 | a0001 | c0018 | t0001 | g0077 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18966 | hp2 | a0002 | c0015 | t0016 | g0016 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18967 | hp2 | a0017 | c0037 | t0002 | g0318 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18968 | hp1 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18970 | hp1 | a0001 | c0002 | t0003 | g0099 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18970 | hp2 | a0001 | c0018 | t0001 | g0289 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18971 | hp1 | a0005 | c0030 | t0002 | g0297 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18971 | hp2 | a0001 | c0002 | t0013 | g0248 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18973 | hp1 | a0001 | c0001 | t0009 | g0241 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18973 | hp2 | a0005 | c0012 | t0002 | g0317 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18974 | hp1 | a0001 | c0002 | t0002 | g0283 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18974 | hp2 | a0001 | c0002 | t0003 | g0173 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18977 | hp1 | a0001 | c0002 | t0003 | g0288 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18978 | hp1 | a0001 | c0002 | t0003 | g0300 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18978 | hp2 | a0001 | c0002 | t0030 | g0067 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18979 | hp1 | a0001 | c0001 | t0009 | g0239 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18979 | hp2 | a0001 | c0002 | t0003 | g0212 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18982 | hp1 | a0001 | c0001 | t0024 | g0208 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18982 | hp2 | a0001 | c0004 | t0015 | g0272 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18983 | hp1 | a0001 | c0002 | t0002 | g0214 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18983 | hp2 | a0001 | c0017 | t0003 | g0070 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18984 | hp2 | a0001 | c0002 | t0009 | g0249 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18985 | hp2 | a0013 | c0031 | t0003 | g0046 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18986 | hp1 | a0001 | c0002 | t0003 | g0279 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18986 | hp2 | a0001 | c0001 | t0010 | g0244 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18991 | hp2 | a0001 | c0002 | t0003 | g0103 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18995 | hp2 | a0001 | c0002 | t0003 | g0323 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18998 | hp2 | a0001 | c0001 | t0010 | g0246 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19002 | hp1 | a0001 | c0002 | t0009 | g0228 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19002 | hp2 | a0001 | c0002 | t0002 | g0056 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19003 | hp1 | a0001 | c0002 | t0032 | g0274 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19007 | hp1 | a0001 | c0002 | t0014 | g0179 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19007 | hp2 | a0001 | c0001 | t0014 | g0090 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19009 | hp2 | a0001 | c0001 | t0009 | g0240 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19011 | hp1 | a0001 | c0008 | t0037 | g0075 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19011 | hp2 | a0001 | c0002 | t0003 | g0058 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | LWK | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19030 | hp2 | a0001 | c0006 | t0018 | g0035 | AFR | LWK | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19043 | hp1 | a0001 | c0028 | t0025 | g0039 | AFR | LWK | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19043 | hp2 | a0004 | c0010 | t0005 | g0133 | AFR | LWK | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19057 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19060 | hp2 | a0001 | c0002 | t0009 | g0236 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19062 | hp1 | a0002 | c0003 | t0016 | g0302 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19062 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19063 | hp2 | a0001 | c0002 | t0002 | g0203 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19066 | hp1 | a0001 | c0002 | t0003 | g0308 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19066 | hp2 | a0001 | c0002 | t0002 | g0298 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19068 | hp2 | a0001 | c0008 | t0002 | g0281 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19077 | hp1 | a0001 | c0002 | t0002 | g0315 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19077 | hp2 | a0014 | c0033 | t0009 | g0234 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19081 | hp1 | a0005 | c0012 | t0002 | g0316 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19082 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19082 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19085 | hp2 | a0001 | c0001 | t0009 | g0233 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19086 | hp1 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19086 | hp2 | a0001 | c0002 | t0003 | g0084 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19087 | hp1 | a0001 | c0002 | t0003 | g0301 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19087 | hp2 | a0001 | c0002 | t0031 | g0207 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19088 | hp1 | a0001 | c0001 | t0011 | g0280 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19088 | hp2 | a0001 | c0002 | t0002 | g0106 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19240 | hp1 | a0001 | c0004 | t0022 | g0034 | AFR | YRI | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19240 | hp2 | a0004 | c0010 | t0005 | g0334 | AFR | YRI | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA20129 | hp1 | a0001 | c0002 | t0013 | g0223 | AFR | ASW | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA20129 | hp2 | a0001 | c0006 | t0018 | g0215 | AFR | ASW | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA20752 | hp1 | a0001 | c0002 | t0003 | g0158 | EUR | TSI | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA20752 | hp2 | a0001 | c0002 | t0004 | g0193 | EUR | TSI | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA20805 | hp1 | a0001 | c0004 | t0007 | g0327 | EUR | TSI | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA20805 | hp2 | a0001 | c0001 | t0004 | g0213 | EUR | TSI | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01123 | hp2 | a0002 | c0003 | t0006 | g0047 | AMR | CLM | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02109 | hp2 | a0001 | c0006 | t0005 | g0064 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02486 | hp1 | a0001 | c0001 | t0012 | g0045 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02486 | hp2 | a0001 | c0039 | t0018 | g0013 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02559 | hp1 | a0001 | c0001 | t0012 | g0145 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02559 | hp2 | a0001 | c0001 | t0020 | g0128 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03471 | hp1 | a0001 | c0006 | t0007 | g0263 | AFR | MSL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03471 | hp2 | a0001 | c0001 | t0012 | g0031 | AFR | MSL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG06807 | hp1 | a0001 | c0001 | t0004 | g0251 | AFR | USA | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | USA | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18955 | hp1 | a0001 | c0002 | t0002 | g0029 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | USA | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA20300 | hp2 | a0002 | c0003 | t0006 | g0293 | AFR | USA | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA21309 | hp1 | a0001 | c0020 | t0007 | g0130 | AFR | LWK | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA21309 | hp2 | a0001 | c0004 | t0001 | g0330 | AFR | LWK | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0325 | REF | REF | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
homoSapiens_grch38 | hp1 | a0002 | c0003 | t0038 | g0224 | REF | REF | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:72183772
|
G | A | 1 | a0009 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.316G>A | p.Val106Ile | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/7 | 373/11790 | 316/7407 | 106/2468 | chr5 | 72183772 | ||
chr5:72194797
|
C | T | 1 | a0017 | 1 | NA18967.hp2 | missense_variant | MODERATE | c.1442C>T | p.Ala481Val | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 1499/11790 | 1442/7407 | 481/2468 | chr5 | 72194797 | ||
chr5:72195135
|
A | G | 15 | a0001a0003a0004others(12): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
missense_variant | MODERATE | c.1780A>G | p.Ile594Val | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 1837/11790 | 1780/7407 | 594/2468 | chr5 | 72195135 | ||
chr5:72195415
|
A | C | 1 | a0010 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.2060A>C | p.Glu687Ala | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 2117/11790 | 2060/7407 | 687/2468 | chr5 | 72195415 | ||
chr5:72195484
|
A | G | 1 | a0006 | 4 | HG01074.hp2 HG02965.hp1 HG03225.hp1 others(1): Show |
missense_variant | MODERATE | c.2129A>G | p.Lys710Arg | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 2186/11790 | 2129/7407 | 710/2468 | chr5 | 72195484 | ||
chr5:72195741
|
G | A | 1 | a0015 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.2386G>A | p.Ala796Thr | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 2443/11790 | 2386/7407 | 796/2468 | chr5 | 72195741 | ||
chr5:72195742
|
C | T | 1 | a0016 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.2387C>T | p.Ala796Val | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 2444/11790 | 2387/7407 | 796/2468 | chr5 | 72195742 | ||
chr5:72195961
|
A | G | 1 | a0007 | 3 | HG03130.hp1 HG03139.hp2 HG03195.hp2 |
missense_variant | MODERATE | c.2606A>G | p.Glu869Gly | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 2663/11790 | 2606/7407 | 869/2468 | chr5 | 72195961 | ||
chr5:72196294
|
C | T | 1 | a0014 | 1 | NA19077.hp2 | missense_variant | MODERATE | c.2939C>T | p.Ala980Val | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 2996/11790 | 2939/7407 | 980/2468 | chr5 | 72196294 | ||
chr5:72196591
|
G | A | 1 | a0008 | 2 | HG00741.hp1 HG03453.hp2 |
missense_variant | MODERATE | c.3236G>A | p.Arg1079Gln | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 3293/11790 | 3236/7407 | 1079/2468 | chr5 | 72196591 | ||
chr5:72197242
|
C | T | 1 | a0004 | 4 | HG02647.hp1 HG02922.hp1 NA19043.hp2 others(1): Show |
missense_variant | MODERATE | c.3887C>T | p.Pro1296Leu | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 3944/11790 | 3887/7407 | 1296/2468 | chr5 | 72197242 | ||
chr5:72197388
|
T | G | 1 | a0011 | 1 | HG02897.hp1 | missense_variant | MODERATE | c.4033T>G | p.Ser1345Ala | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 4090/11790 | 4033/7407 | 1345/2468 | chr5 | 72197388 | ||
chr5:72197424
|
C | T | 1 | a0013 | 1 | NA18985.hp2 | missense_variant | MODERATE | c.4069C>T | p.Pro1357Ser | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 4126/11790 | 4069/7407 | 1357/2468 | chr5 | 72197424 | ||
chr5:72197866
|
A | C | 1 | a0010 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.4511A>C | p.Gln1504Pro | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 4568/11790 | 4511/7407 | 1504/2468 | chr5 | 72197866 | ||
chr5:72197867
|
A | C | 1 | a0010 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.4512A>C | p.Gln1504His | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 4569/11790 | 4512/7407 | 1504/2468 | chr5 | 72197867 | ||
chr5:72197869
|
T | C | 1 | a0010 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.4514T>C | p.Ile1505Thr | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 4571/11790 | 4514/7407 | 1505/2468 | chr5 | 72197869 | ||
chr5:72197871
|
G | C | 1 | a0010 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.4516G>C | p.Asp1506His | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 4573/11790 | 4516/7407 | 1506/2468 | chr5 | 72197871 | ||
chr5:72197877
|
A | G | 1 | a0010 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.4522A>G | p.Ser1508Gly | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 4579/11790 | 4522/7407 | 1508/2468 | chr5 | 72197877 | ||
chr5:72197878
|
G | A | 1 | a0010 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.4523G>A | p.Ser1508Asn | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 4580/11790 | 4523/7407 | 1508/2468 | chr5 | 72197878 | ||
chr5:72197879
|
T | G | 1 | a0010 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.4524T>G | p.Ser1508Arg | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 4581/11790 | 4524/7407 | 1508/2468 | chr5 | 72197879 | ||
chr5:72197881
|
A | T | 1 | a0010 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.4526A>T | p.Gln1509Leu | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 4583/11790 | 4526/7407 | 1509/2468 | chr5 | 72197881 | ||
chr5:72197917
|
T | G | 1 | a0010 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.4562T>G | p.Ile1521Ser | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 4619/11790 | 4562/7407 | 1521/2468 | chr5 | 72197917 | ||
chr5:72197982
|
T | G | 1 | a0010 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.4627T>G | p.Tyr1543Asp | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 4684/11790 | 4627/7407 | 1543/2468 | chr5 | 72197982 | ||
chr5:72197990
|
T | G | 1 | a0010 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.4635T>G | p.His1545Gln | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 4692/11790 | 4635/7407 | 1545/2468 | chr5 | 72197990 | ||
chr5:72197991
|
A | T | 1 | a0010 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.4636A>T | p.Met1546Leu | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 4693/11790 | 4636/7407 | 1546/2468 | chr5 | 72197991 | ||
chr5:72197998
|
G | GGTGCAGC others(5): Show |
1 | a0010 | 1 | HG01993.hp1 | disruptive_inframe_insertion | MODERATE | c.4643_4644insGTGCAG others(6): Show |
p.Gly1548_Val1549ins others(12): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 4701/11790 | 4644/7407 | 1548/2468 | chr5 | 72197998 | ||
chr5:72198853
|
G | A | 1 | a0012 | 1 | NA18960.hp1 | missense_variant | MODERATE | c.5498G>A | p.Arg1833His | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 5555/11790 | 5498/7407 | 1833/2468 | chr5 | 72198853 | ||
chr5:72198867
|
T | C | 1 | a0003 | 5 | HG01167.hp1 HG01169.hp2 HG01433.hp2 others(2): Show |
missense_variant | MODERATE | c.5512T>C | p.Phe1838Leu | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 5569/11790 | 5512/7407 | 1838/2468 | chr5 | 72198867 | ||
chr5:72199104
|
A | C | 1 | a0015 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.5749A>C | p.Ser1917Arg | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 5806/11790 | 5749/7407 | 1917/2468 | chr5 | 72199104 | ||
chr5:72199362
|
G | C | 1 | a0005 | 4 | NA18963.hp1 NA18971.hp1 NA18973.hp2 others(1): Show |
missense_variant | MODERATE | c.6007G>C | p.Asp2003His | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 6064/11790 | 6007/7407 | 2003/2468 | chr5 | 72199362 | ||
chr5:72199978
|
G | A | 1 | a0005 | 4 | NA18963.hp1 NA18971.hp1 NA18973.hp2 others(1): Show |
missense_variant | MODERATE | c.6623G>A | p.Arg2208His | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 6680/11790 | 6623/7407 | 2208/2468 | chr5 | 72199978 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:72107627
|
C | T | 1 | a0001c0039 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.96C>T | p.Phe32Phe | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/7 | 153/11790 | 96/7407 | 32/2468 | chr5 | 72107627 | ||
chr5:72115762
|
A | G | 1 | a0001c0038 | 1 | HG02155.hp1 | synonymous_variant | LOW | c.249A>G | p.Val83Val | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/7 | 306/11790 | 249/7407 | 83/2468 | chr5 | 72115762 | ||
chr5:72193868
|
C | T | 4 | a0001c0006a0001c0020a0001c0039others(1): Show | 11 | HG01167.hp2 HG01243.hp2 HG02109.hp2 others(8): Show |
splice_region_variant&synonymous_variant | LOW | c.513C>T | p.Ile171Ile | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 570/11790 | 513/7407 | 171/2468 | chr5 | 72193868 | ||
chr5:72194798
|
G | A | 1 | a0001c0022 | 1 | HG04199.hp1 | synonymous_variant | LOW | c.1443G>A | p.Ala481Ala | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 1500/11790 | 1443/7407 | 481/2468 | chr5 | 72194798 | ||
chr5:72194850
|
C | T | 1 | a0001c0036 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.1495C>T | p.Leu499Leu | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 1552/11790 | 1495/7407 | 499/2468 | chr5 | 72194850 | ||
chr5:72195134
|
A | G | 1 | a0007c0013 | 3 | HG03130.hp1 HG03139.hp2 HG03195.hp2 |
synonymous_variant | LOW | c.1779A>G | p.Pro593Pro | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 1836/11790 | 1779/7407 | 593/2468 | chr5 | 72195134 | ||
chr5:72195674
|
C | T | 1 | a0002c0015 | 2 | HG00609.hp1 NA18966.hp2 |
synonymous_variant | LOW | c.2319C>T | p.Ala773Ala | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 2376/11790 | 2319/7407 | 773/2468 | chr5 | 72195674 | ||
chr5:72196037
|
G | A | 3 | a0001c0006a0001c0020a0001c0039 | 10 | HG01167.hp2 HG01243.hp2 HG02109.hp2 others(7): Show |
synonymous_variant | LOW | c.2682G>A | p.Glu894Glu | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 2739/11790 | 2682/7407 | 894/2468 | chr5 | 72196037 | ||
chr5:72196082
|
T | C | 1 | a0007c0013 | 3 | HG03130.hp1 HG03139.hp2 HG03195.hp2 |
synonymous_variant | LOW | c.2727T>C | p.Pro909Pro | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 2784/11790 | 2727/7407 | 909/2468 | chr5 | 72196082 | ||
chr5:72196238
|
C | T | 1 | a0001c0034 | 1 | HG02818.hp1 | synonymous_variant | LOW | c.2883C>T | p.His961His | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 2940/11790 | 2883/7407 | 961/2468 | chr5 | 72196238 | ||
chr5:72196259
|
G | A | 1 | a0001c0025 | 1 | HG02683.hp2 | synonymous_variant | LOW | c.2904G>A | p.Lys968Lys | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 2961/11790 | 2904/7407 | 968/2468 | chr5 | 72196259 | ||
chr5:72196613
|
T | C | 1 | a0001c0026 | 1 | HG02886.hp1 | synonymous_variant | LOW | c.3258T>C | p.His1086His | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 3315/11790 | 3258/7407 | 1086/2468 | chr5 | 72196613 | ||
chr5:72196907
|
C | T | 4 | a0001c0004a0001c0019a0001c0034others(1): Show | 22 | HG00558.hp1 HG00733.hp2 HG00738.hp2 others(19): Show |
synonymous_variant | LOW | c.3552C>T | p.Asn1184Asn | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 3609/11790 | 3552/7407 | 1184/2468 | chr5 | 72196907 | ||
chr5:72197324
|
A | G | 1 | a0001c0018 | 2 | NA18966.hp1 NA18970.hp2 |
synonymous_variant | LOW | c.3969A>G | p.Pro1323Pro | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 4026/11790 | 3969/7407 | 1323/2468 | chr5 | 72197324 | ||
chr5:72197381
|
C | T | 1 | a0001c0017 | 2 | NA18959.hp2 NA18983.hp2 |
synonymous_variant | LOW | c.4026C>T | p.Asp1342Asp | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 4083/11790 | 4026/7407 | 1342/2468 | chr5 | 72197381 | ||
chr5:72197981
|
G | T | 1 | a0010c0023 | 1 | HG01993.hp1 | synonymous_variant | LOW | c.4626G>T | p.Thr1542Thr | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 4683/11790 | 4626/7407 | 1542/2468 | chr5 | 72197981 | ||
chr5:72198050
|
A | T | 3 | a0001c0005a0001c0026a0001c0036 | 19 | HG00741.hp2 HG01884.hp2 HG02145.hp1 others(16): Show |
synonymous_variant | LOW | c.4695A>T | p.Pro1565Pro | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 4752/11790 | 4695/7407 | 1565/2468 | chr5 | 72198050 | ||
chr5:72198548
|
C | A | 1 | a0001c0008 | 4 | HG00621.hp1 NA18943.hp1 NA19011.hp1 others(1): Show |
synonymous_variant | LOW | c.5193C>A | p.Ser1731Ser | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 5250/11790 | 5193/7407 | 1731/2468 | chr5 | 72198548 | ||
chr5:72199079
|
G | A | 2 | a0001c0004a0001c0009 | 22 | HG00558.hp1 HG00733.hp2 HG00738.hp2 others(19): Show |
synonymous_variant | LOW | c.5724G>A | p.Lys1908Lys | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 5781/11790 | 5724/7407 | 1908/2468 | chr5 | 72199079 | ||
chr5:72199145
|
C | T | 1 | a0005c0030 | 1 | NA18971.hp1 | synonymous_variant | LOW | c.5790C>T | p.Thr1930Thr | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 5847/11790 | 5790/7407 | 1930/2468 | chr5 | 72199145 | ||
chr5:72199214
|
T | C | 13 | a0001c0002a0001c0008a0001c0017others(10): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(121): Show |
synonymous_variant | LOW | c.5859T>C | p.Gly1953Gly | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 5916/11790 | 5859/7407 | 1953/2468 | chr5 | 72199214 | ||
chr5:72199493
|
G | A | 1 | a0001c0029 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.6138G>A | p.Glu2046Glu | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 6195/11790 | 6138/7407 | 2046/2468 | chr5 | 72199493 | ||
chr5:72199517
|
A | C | 1 | a0001c0028 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.6162A>C | p.Ala2054Ala | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 6219/11790 | 6162/7407 | 2054/2468 | chr5 | 72199517 | ||
chr5:72199901
|
C | T | 1 | a0006c0011 | 4 | HG01074.hp2 HG02965.hp1 HG03225.hp1 others(1): Show |
synonymous_variant | LOW | c.6546C>T | p.Asp2182Asp | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 6603/11790 | 6546/7407 | 2182/2468 | chr5 | 72199901 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:72107479
|
T | A | 84 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(81): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
5_prime_UTR_variant | MODIFIER | c.-53T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/7 | 53 | chr5 | 72107479 | |||||
chr5:72205473
|
C | A | 1 | a0001c0001t0024 | 1 | NA18982.hp1 | 3_prime_UTR_variant | MODIFIER | c.*234C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 234 | chr5 | 72205473 | |||||
chr5:72205571
|
G | A | 4 | a0001c0005t0008a0001c0026t0008a0001c0028t0025others(1): Show | 10 | HG00741.hp2 HG02630.hp2 HG02647.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*332G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 332 | chr5 | 72205571 | |||||
chr5:72205795
|
A | G | 1 | a0001c0008t0037 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*556A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 556 | chr5 | 72205795 | |||||
chr5:72206699
|
C | CT | 11 | a0001c0001t0007a0001c0001t0035a0001c0004t0007others(8): Show | 17 | HG01167.hp2 HG01243.hp2 HG01433.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1469dupT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 1470 | INFO_REALIGN_3_PRIME | chr5 | 72206699 | ||||
chr5:72206717
|
C | T | 10 | a0001c0001t0007a0001c0001t0035a0001c0004t0007others(7): Show | 16 | HG01167.hp2 HG01243.hp2 HG01433.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1478C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 1478 | chr5 | 72206717 | |||||
chr5:72206723
|
A | G | 4 | a0001c0004t0022a0001c0006t0018a0001c0006t0022others(1): Show | 6 | HG02451.hp1 HG02486.hp2 HG03098.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1484A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 1484 | chr5 | 72206723 | |||||
chr5:72207295
|
A | G | 1 | a0001c0002t0032 | 1 | NA19003.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2056A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 2056 | chr5 | 72207295 | |||||
chr5:72207378
|
C | G | 1 | a0001c0002t0031 | 1 | NA19087.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2139C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 2139 | chr5 | 72207378 | |||||
chr5:72207588
|
G | A | 2 | a0001c0001t0020a0001c0005t0020 | 2 | HG02280.hp2 HG02559.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2349G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 2349 | chr5 | 72207588 | |||||
chr5:72207680
|
C | G | 73 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(70): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
3_prime_UTR_variant | MODIFIER | c.*2441C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 2441 | chr5 | 72207680 | |||||
chr5:72207860
|
C | A | 95 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(92): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
3_prime_UTR_variant | MODIFIER | c.*2621C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 2621 | chr5 | 72207860 | |||||
chr5:72207946
|
TTCTC | T | 3 | a0001c0001t0015a0001c0004t0015a0001c0004t0017 | 9 | HG00558.hp1 HG00738.hp2 HG02080.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2721_*2724delCTCT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 2721 | INFO_REALIGN_3_PRIME | chr5 | 72207946 | ||||
chr5:72207962
|
C | CT | 22 | a0001c0001t0002a0001c0001t0009a0001c0001t0011others(19): Show | 81 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*2744dupT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 2745 | INFO_REALIGN_3_PRIME | chr5 | 72207962 | ||||
chr5:72207962
|
CT | C | 16 | a0001c0001t0005a0001c0001t0024a0001c0002t0016others(13): Show | 33 | HG00609.hp1 HG00733.hp2 HG00741.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2744delT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 2744 | INFO_REALIGN_3_PRIME | chr5 | 72207962 | ||||
chr5:72207962
|
CTTTTTTT others(4): Show |
C | 6 | a0001c0001t0004a0001c0001t0019a0001c0001t0035others(3): Show | 25 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2734_*2744delTTTT others(7): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 2734 | INFO_REALIGN_3_PRIME | chr5 | 72207962 | ||||
chr5:72207964
|
T | C | 11 | a0001c0001t0007a0001c0001t0020a0001c0001t0026others(8): Show | 17 | HG00673.hp1 HG01167.hp2 HG01243.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2725T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 2725 | chr5 | 72207964 | |||||
chr5:72207965
|
T | C | 1 | a0001c0004t0034 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2726T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 2726 | chr5 | 72207965 | |||||
chr5:72208086
|
T | TA | 62 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(59): Show | 193 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*2848dupA | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 2849 | INFO_REALIGN_3_PRIME | chr5 | 72208086 | ||||
chr5:72208450
|
G | A | 1 | a0001c0001t0028 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3211G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3211 | chr5 | 72208450 | |||||
chr5:72208466
|
C | A | 2 | a0001c0001t0021a0001c0005t0021 | 2 | HG02145.hp1 HG02258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3227C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3227 | chr5 | 72208466 | |||||
chr5:72208794
|
G | A | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3555G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3555 | chr5 | 72208794 | |||||
chr5:72208795
|
C | A | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3556C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3556 | chr5 | 72208795 | |||||
chr5:72208797
|
G | T | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3558G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3558 | chr5 | 72208797 | |||||
chr5:72208798
|
C | T | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3559C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3559 | chr5 | 72208798 | |||||
chr5:72208799
|
T | G | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3560T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3560 | chr5 | 72208799 | |||||
chr5:72208800
|
C | G | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3561C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3561 | chr5 | 72208800 | |||||
chr5:72208806
|
T | A | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3567T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3567 | chr5 | 72208806 | |||||
chr5:72208807
|
T | A | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3568T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3568 | chr5 | 72208807 | |||||
chr5:72208808
|
C | A | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3569C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3569 | chr5 | 72208808 | |||||
chr5:72208813
|
T | G | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3574T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3574 | chr5 | 72208813 | |||||
chr5:72208814
|
T | G | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3575T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3575 | chr5 | 72208814 | |||||
chr5:72208817
|
C | G | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3578C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3578 | chr5 | 72208817 | |||||
chr5:72208819
|
T | A | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3580T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3580 | chr5 | 72208819 | |||||
chr5:72208820
|
T | A | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3581T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3581 | chr5 | 72208820 | |||||
chr5:72208821
|
T | G | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3582T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3582 | chr5 | 72208821 | |||||
chr5:72208822
|
C | A | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3583C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3583 | chr5 | 72208822 | |||||
chr5:72208825
|
G | T | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3586G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3586 | chr5 | 72208825 | |||||
chr5:72208832
|
T | A | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3593T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3593 | chr5 | 72208832 | |||||
chr5:72208840
|
C | A | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3601C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3601 | chr5 | 72208840 | |||||
chr5:72208841
|
C | A | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3602C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3602 | chr5 | 72208841 | |||||
chr5:72208852
|
G | T | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3613G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3613 | chr5 | 72208852 | |||||
chr5:72208853
|
G | T | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3614G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3614 | chr5 | 72208853 | |||||
chr5:72208855
|
T | C | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3616T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3616 | chr5 | 72208855 | |||||
chr5:72208856
|
C | A | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3617C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3617 | chr5 | 72208856 | |||||
chr5:72208859
|
G | C | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3620G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3620 | chr5 | 72208859 | |||||
chr5:72208860
|
C | T | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3621C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3621 | chr5 | 72208860 | |||||
chr5:72208864
|
G | C | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3625G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3625 | chr5 | 72208864 | |||||
chr5:72208892
|
CT | C | 3 | a0001c0001t0012a0001c0001t0021a0001c0005t0021 | 9 | HG02145.hp1 HG02258.hp2 HG02486.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3664delT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3664 | INFO_REALIGN_3_PRIME | chr5 | 72208892 | ||||
chr5:72209045
|
TTAAAAC | T | 1 | a0001c0004t0017 | 4 | HG00738.hp2 HG02148.hp2 HG02280.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3809_*3814delAAAC others(2): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3809 | INFO_REALIGN_3_PRIME | chr5 | 72209045 | ||||
chr5:72209135
|
G | T | 1 | a0001c0002t0031 | 1 | NA19087.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3896G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3896 | chr5 | 72209135 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:72107730
|
G | GC | 6 | a0001c0001t0001g0336a0001c0001t0001g0338a0001c0004t0001g0337others(3): Show | 6 | HG00741.hp1 HG02055.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.184+20dupC | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 72107730 | |||||
chr5:72107892
|
G | C | 1 | a0001c0005t0001g0005 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.184+177G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72107892 | ||||||
chr5:72108044
|
G | T | 1 | a0004c0010t0005g0332 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.184+329G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72108044 | ||||||
chr5:72108290
|
G | GC | 23 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0024others(20): Show | 23 | HG00621.hp2 HG00642.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.184+583dupC | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 72108290 | |||||
chr5:72108349
|
A | G | 1 | a0001c0009t0001g0331 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.184+634A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72108349 | ||||||
chr5:72108384
|
T | C | 1 | a0001c0026t0008g0027 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.184+669T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72108384 | ||||||
chr5:72108487
|
G | C | 1 | a0001c0001t0001g0006 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.184+772G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72108487 | ||||||
chr5:72108557
|
T | C | 2 | a0001c0001t0002g0028a0001c0002t0002g0029 | 2 | HG02523.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.184+842T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72108557 | ||||||
chr5:72108567
|
C | G | 31 | a0001c0001t0001g0311a0001c0001t0001g0312a0001c0001t0001g0313others(28): Show | 31 | HG00140.hp1 HG00741.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.184+852C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72108567 | ||||||
chr5:72108571
|
G | A | 2 | a0001c0005t0008g0030a0004c0010t0005g0332 | 2 | HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.184+856G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72108571 | ||||||
chr5:72108571
|
G | C | 1 | a0001c0001t0012g0031 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.184+856G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72108571 | ||||||
chr5:72108572
|
G | A | 2 | a0001c0005t0008g0032a0001c0034t0005g0033 | 2 | HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.184+857G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72108572 | ||||||
chr5:72108580
|
G | A | 1 | a0001c0001t0010g0007 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.184+865G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72108580 | ||||||
chr5:72108601
|
G | A | 12 | a0001c0001t0001g0041a0001c0001t0012g0045a0001c0002t0002g0037others(9): Show | 12 | HG00741.hp2 HG02486.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.184+886G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72108601 | ||||||
chr5:72108703
|
C | A | 1 | a0001c0026t0008g0027 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.184+988C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72108703 | ||||||
chr5:72108750
|
G | T | 2 | a0001c0001t0001g0338a0008c0016t0001g0333 | 2 | HG00741.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.184+1035G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72108750 | ||||||
chr5:72108764
|
C | T | 1 | a0001c0005t0001g0307 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.184+1049C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72108764 | ||||||
chr5:72109053
|
C | A | 1 | a0013c0031t0003g0046 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.184+1338C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72109053 | ||||||
chr5:72109205
|
C | T | 37 | a0001c0001t0001g0024a0001c0001t0001g0273a0001c0001t0001g0275others(34): Show | 38 | HG00558.hp1 HG00609.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.184+1490C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72109205 | ||||||
chr5:72109235
|
T | TA | 83 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0063others(80): Show | 83 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.184+1532dupA | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 72109235 | |||||
chr5:72109248
|
G | A | 1 | a0001c0001t0001g0338 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.184+1533G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72109248 | ||||||
chr5:72109248
|
G | GA | 59 | a0001c0001t0001g0041a0001c0001t0001g0127a0001c0001t0001g0129others(56): Show | 59 | HG00140.hp1 HG00741.hp1 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.184+1541dupA | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 72109248 | |||||
chr5:72109496
|
A | G | 1 | a0001c0004t0015g0272 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.184+1781A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72109496 | ||||||
chr5:72109582
|
G | T | 1 | a0001c0001t0001g0120 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.184+1867G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72109582 | ||||||
chr5:72109685
|
C | T | 36 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(33): Show | 36 | HG00140.hp1 HG00741.hp1 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.184+1970C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72109685 | ||||||
chr5:72109759
|
T | C | 1 | a0001c0005t0008g0030 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.184+2044T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72109759 | ||||||
chr5:72109902
|
G | C | 1 | a0004c0010t0005g0133 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.184+2187G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72109902 | ||||||
chr5:72109909
|
C | T | 24 | a0001c0001t0001g0311a0001c0001t0001g0312a0001c0001t0001g0313others(21): Show | 24 | HG00140.hp1 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.184+2194C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72109909 | ||||||
chr5:72109912
|
T | C | 1 | a0001c0005t0008g0134 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.184+2197T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72109912 | ||||||
chr5:72110077
|
A | T | 55 | a0001c0001t0001g0024a0001c0001t0001g0257a0001c0001t0001g0264others(52): Show | 56 | HG00558.hp1 HG00609.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.184+2362A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72110077 | ||||||
chr5:72110234
|
G | C | 6 | a0001c0001t0005g0139a0001c0004t0007g0140a0001c0005t0021g0135others(3): Show | 6 | HG01074.hp2 HG02145.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.184+2519G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72110234 | ||||||
chr5:72110549
|
A | G | 1 | a0003c0007t0002g0119 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.184+2834A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72110549 | ||||||
chr5:72110661
|
A | G | 1 | a0001c0002t0003g0118 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.184+2946A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72110661 | ||||||
chr5:72110730
|
C | T | 2 | a0001c0001t0002g0028a0001c0002t0002g0029 | 2 | HG02523.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.184+3015C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72110730 | ||||||
chr5:72110843
|
T | C | 32 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0120others(29): Show | 32 | HG00140.hp1 HG01070.hp1 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.184+3128T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72110843 | ||||||
chr5:72110866
|
C | T | 1 | a0001c0001t0020g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.184+3151C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72110866 | ||||||
chr5:72110950
|
T | A | 4 | a0001c0002t0002g0037a0001c0004t0022g0034a0001c0006t0018g0035others(1): Show | 4 | HG02723.hp1 HG03098.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.184+3235T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72110950 | ||||||
chr5:72111028
|
T | A | 4 | a0001c0001t0001g0311a0001c0001t0001g0312a0001c0001t0004g0310others(1): Show | 4 | HG00140.hp1 HG01099.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.184+3313T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72111028 | ||||||
chr5:72111053
|
T | G | 1 | a0001c0001t0001g0313 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.184+3338T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72111053 | ||||||
chr5:72111102
|
C | CT | 17 | a0001c0001t0001g0041a0001c0001t0001g0127a0001c0001t0012g0045others(14): Show | 17 | HG00741.hp2 HG02257.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.184+3392dupT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 72111102 | |||||
chr5:72111250
|
C | T | 1 | a0001c0039t0018g0013 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.184+3535C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72111250 | ||||||
chr5:72111283
|
A | T | 3 | a0001c0005t0008g0134a0001c0005t0008g0253a0006c0011t0001g0254 | 3 | HG02647.hp2 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.184+3568A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72111283 | ||||||
chr5:72111296
|
T | A | 5 | a0001c0001t0012g0053a0001c0001t0012g0054a0001c0001t0015g0121others(2): Show | 5 | HG02145.hp2 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.184+3581T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72111296 | ||||||
chr5:72111423
|
A | T | 3 | a0001c0001t0004g0022a0001c0001t0004g0251a0001c0001t0004g0252 | 3 | HG01192.hp2 HG04199.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.184+3708A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72111423 | ||||||
chr5:72111604
|
T | A | 2 | a0007c0013t0001g0123a0007c0013t0029g0124 | 2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.184+3889T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72111604 | ||||||
chr5:72111647
|
A | T | 2 | a0001c0001t0001g0127a0001c0002t0003g0126 | 2 | NA18945.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.184+3932A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72111647 | ||||||
chr5:72111717
|
G | C | 234 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0024others(231): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.185-3981G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72111717 | ||||||
chr5:72111738
|
A | G | 1 | a0001c0002t0004g0003 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.185-3960A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72111738 | ||||||
chr5:72111768
|
C | T | 31 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0120others(28): Show | 31 | HG00140.hp1 HG01070.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.185-3930C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72111768 | ||||||
chr5:72111831
|
G | C | 236 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0024others(233): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.185-3867G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72111831 | ||||||
chr5:72111877
|
T | G | 1 | a0001c0004t0017g0057 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.185-3821T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72111877 | ||||||
chr5:72112063
|
T | G | 234 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0024others(231): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.185-3635T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72112063 | ||||||
chr5:72112173
|
C | G | 1 | a0001c0005t0001g0271 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.185-3525C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72112173 | ||||||
chr5:72112426
|
C | T | 7 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(4): Show | 7 | HG02622.hp2 HG02886.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.185-3272C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72112426 | ||||||
chr5:72112488
|
C | T | 1 | a0001c0038t0013g0021 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.185-3210C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72112488 | ||||||
chr5:72112641
|
A | G | 1 | a0001c0001t0007g0270 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.185-3057A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72112641 | ||||||
chr5:72112923
|
G | A | 1 | a0001c0001t0020g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.185-2775G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72112923 | ||||||
chr5:72112984
|
A | C | 19 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(16): Show | 19 | HG00741.hp1 HG02055.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.185-2714A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72112984 | ||||||
chr5:72113040
|
A | G | 234 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0024others(231): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.185-2658A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72113040 | ||||||
chr5:72113092
|
C | A | 55 | a0001c0001t0001g0024a0001c0001t0001g0257a0001c0001t0001g0264others(52): Show | 56 | HG00558.hp1 HG00609.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.185-2606C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72113092 | ||||||
chr5:72113116
|
A | G | 1 | a0001c0005t0005g0221 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.185-2582A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72113116 | ||||||
chr5:72113144
|
C | A | 1 | a0001c0005t0008g0038 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.185-2554C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72113144 | ||||||
chr5:72113168
|
T | G | 1 | a0001c0002t0003g0058 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.185-2530T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72113168 | ||||||
chr5:72113184
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.185-2514A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72113184 | ||||||
chr5:72113297
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.185-2401A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72113297 | ||||||
chr5:72113388
|
C | T | 1 | a0001c0001t0001g0220 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.185-2310C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72113388 | ||||||
chr5:72113482
|
A | C | 31 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0120others(28): Show | 31 | HG00140.hp1 HG01070.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.185-2216A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72113482 | ||||||
chr5:72113493
|
A | C | 2 | a0001c0002t0003g0219a0002c0003t0006g0218 | 2 | HG01975.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.185-2205A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72113493 | ||||||
chr5:72113556
|
A | G | 50 | a0001c0001t0001g0041a0001c0001t0001g0050a0001c0001t0001g0052others(47): Show | 50 | HG00140.hp1 HG00741.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.185-2142A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72113556 | ||||||
chr5:72113742
|
A | C | 302 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0024others(299): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.185-1956A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72113742 | ||||||
chr5:72113767
|
T | C | 2 | a0002c0003t0006g0142a0002c0003t0006g0143 | 2 | HG00738.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.185-1931T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72113767 | ||||||
chr5:72113866
|
G | C | 2 | a0001c0001t0001g0144a0004c0010t0005g0133 | 2 | HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.185-1832G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72113866 | ||||||
chr5:72114028
|
T | C | 1 | a0001c0039t0018g0013 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.185-1670T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72114028 | ||||||
chr5:72114090
|
T | C | 1 | a0001c0002t0002g0062 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.185-1608T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72114090 | ||||||
chr5:72114190
|
T | C | 1 | a0001c0001t0001g0063 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.185-1508T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72114190 | ||||||
chr5:72114192
|
T | C | 1 | a0001c0006t0005g0064 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.185-1506T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72114192 | ||||||
chr5:72114220
|
T | C | 1 | a0001c0001t0012g0145 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.185-1478T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72114220 | ||||||
chr5:72114227
|
G | A | 108 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0144others(105): Show | 111 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.185-1471G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72114227 | ||||||
chr5:72114243
|
A | G | 108 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0144others(105): Show | 111 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.185-1455A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72114243 | ||||||
chr5:72114285
|
A | T | 31 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0120others(28): Show | 31 | HG00140.hp1 HG01070.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.185-1413A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72114285 | ||||||
chr5:72114372
|
A | G | 4 | a0001c0001t0012g0053a0001c0001t0012g0054a0001c0001t0015g0121others(1): Show | 4 | HG02145.hp2 HG02818.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.185-1326A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72114372 | ||||||
chr5:72114498
|
T | G | 2 | a0001c0001t0002g0028a0001c0002t0002g0029 | 2 | HG02523.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.185-1200T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72114498 | ||||||
chr5:72114507
|
G | T | 1 | a0001c0039t0018g0013 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.185-1191G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72114507 | ||||||
chr5:72114518
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.185-1180T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72114518 | ||||||
chr5:72114529
|
G | C | 234 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0024others(231): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.185-1169G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72114529 | ||||||
chr5:72115095
|
G | A | 2 | a0001c0001t0002g0028a0001c0002t0002g0029 | 2 | HG02523.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.185-603G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72115095 | ||||||
chr5:72115172
|
G | A | 7 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(4): Show | 7 | HG02622.hp2 HG02886.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.185-526G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72115172 | ||||||
chr5:72115177
|
T | G | 234 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0024others(231): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.185-521T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72115177 | ||||||
chr5:72115369
|
C | T | 1 | a0004c0010t0005g0332 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.185-329C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72115369 | ||||||
chr5:72115465
|
A | G | 4 | a0001c0001t0001g0267a0001c0002t0002g0268a0001c0002t0011g0266others(1): Show | 4 | HG01891.hp2 HG02109.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.185-233A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72115465 | ||||||
chr5:72115479
|
C | T | 62 | a0001c0001t0001g0063a0001c0001t0001g0071a0001c0001t0001g0083others(59): Show | 62 | HG00140.hp2 HG00408.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.185-219C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72115479 | ||||||
chr5:72115593
|
C | G | 2 | a0001c0001t0002g0028a0001c0002t0002g0029 | 2 | HG02523.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.185-105C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72115593 | ||||||
chr5:72115845
|
A | G | 1 | a0001c0001t0007g0116 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.286+46A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72115845 | ||||||
chr5:72115891
|
T | C | 160 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0050others(157): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.286+92T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72115891 | ||||||
chr5:72116040
|
A | T | 53 | a0001c0001t0001g0024a0001c0001t0001g0264a0001c0001t0001g0267others(50): Show | 54 | HG00558.hp1 HG00609.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.286+241A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72116040 | ||||||
chr5:72116049
|
C | T | 159 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0050others(156): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.286+250C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72116049 | ||||||
chr5:72116118
|
A | G | 8 | a0001c0001t0001g0336a0001c0001t0001g0338a0001c0001t0012g0314others(5): Show | 8 | HG00741.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.286+319A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72116118 | ||||||
chr5:72116150
|
T | C | 1 | a0001c0001t0012g0009 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.286+351T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72116150 | ||||||
chr5:72116309
|
A | G | 7 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(4): Show | 7 | HG02622.hp2 HG02886.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.286+510A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72116309 | ||||||
chr5:72116386
|
T | C | 13 | a0001c0001t0001g0336a0001c0001t0001g0338a0001c0001t0012g0053others(10): Show | 13 | HG00741.hp1 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.286+587T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72116386 | ||||||
chr5:72116417
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.286+618T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72116417 | ||||||
chr5:72116465
|
A | G | 52 | a0001c0001t0001g0024a0001c0001t0001g0264a0001c0001t0001g0267others(49): Show | 53 | HG00558.hp1 HG00609.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.286+666A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72116465 | ||||||
chr5:72116544
|
G | A | 7 | a0001c0001t0001g0336a0001c0001t0001g0338a0001c0004t0001g0337others(4): Show | 7 | HG00741.hp1 HG02055.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.286+745G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72116544 | ||||||
chr5:72116546
|
A | G | 160 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0050others(157): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.286+747A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72116546 | ||||||
chr5:72116627
|
T | G | 1 | a0013c0031t0003g0046 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.286+828T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72116627 | ||||||
chr5:72117121
|
T | TGAAAAAT others(322): Show |
1 | a0001c0002t0032g0274 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.286+1337_286+1338i others(331): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72117121 | |||||
chr5:72117121
|
T | TGAAAAAT others(325): Show |
1 | a0001c0005t0001g0271 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.286+1337_286+1338i others(334): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72117121 | |||||
chr5:72117121
|
T | TGAAAAAT others(330): Show |
1 | a0001c0001t0001g0275 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.286+1337_286+1338i others(339): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72117121 | |||||
chr5:72117121
|
T | TGAAAAAT others(331): Show |
8 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0002t0002g0217others(5): Show | 8 | HG01167.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.286+1337_286+1338i others(340): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72117121 | |||||
chr5:72117121
|
T | TGAAAAAT others(332): Show |
12 | a0001c0001t0001g0264a0001c0001t0001g0282a0001c0001t0001g0284others(9): Show | 12 | HG01099.hp1 HG01243.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.286+1337_286+1338i others(341): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72117121 | |||||
chr5:72117121
|
T | TGAAAAAT others(333): Show |
5 | a0001c0001t0001g0267a0001c0001t0001g0287a0001c0001t0005g0286others(2): Show | 5 | HG02109.hp1 HG02258.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.286+1337_286+1338i others(342): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72117121 | |||||
chr5:72117121
|
T | TGAAAAAT others(337): Show |
1 | a0001c0002t0002g0268 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.286+1337_286+1338i others(346): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72117121 | |||||
chr5:72117121
|
T | TGAAAAAT others(338): Show |
4 | a0001c0002t0003g0288a0001c0002t0003g0290a0001c0017t0002g0055others(1): Show | 4 | HG01943.hp2 NA18959.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.286+1337_286+1338i others(347): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72117121 | |||||
chr5:72117121
|
T | TGAAAAAT others(339): Show |
7 | a0001c0001t0001g0024a0001c0001t0001g0291a0001c0001t0002g0292others(4): Show | 7 | HG01928.hp1 HG01934.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.286+1337_286+1338i others(348): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72117121 | |||||
chr5:72117121
|
T | TGAAAAAT others(340): Show |
2 | a0001c0002t0002g0298a0005c0030t0002g0297 | 2 | NA18971.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.286+1337_286+1338i others(349): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72117121 | |||||
chr5:72117121
|
T | TGAAAAAT others(341): Show |
3 | a0001c0001t0004g0299a0001c0002t0003g0004a0001c0002t0003g0300 | 4 | HG00642.hp2 NA18978.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+1337_286+1338i others(350): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72117121 | |||||
chr5:72117121
|
T | TGAAAAAT others(342): Show |
3 | a0001c0002t0003g0301a0001c0005t0001g0005a0002c0003t0016g0302 | 3 | HG01884.hp2 NA19062.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.286+1337_286+1338i others(351): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72117121 | |||||
chr5:72117121
|
T | TGAAAAAT others(343): Show |
1 | a0001c0001t0035g0303 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.286+1337_286+1338i others(352): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72117121 | |||||
chr5:72117121
|
T | TGAAAAAT others(346): Show |
2 | a0001c0002t0001g0305a0001c0004t0015g0304 | 2 | HG00558.hp1 HG00609.hp2 |
intron_variant | MODIFIER | c.286+1337_286+1338i others(355): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72117121 | |||||
chr5:72117121
|
T | TGAAAAAT others(348): Show |
1 | a0001c0002t0003g0306 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.286+1337_286+1338i others(357): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72117121 | |||||
chr5:72117267
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.286+1468C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72117267 | ||||||
chr5:72117268
|
G | A | 213 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0024others(210): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.286+1469G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72117268 | ||||||
chr5:72117327
|
G | A | 160 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0050others(157): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.286+1528G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72117327 | ||||||
chr5:72117376
|
T | A | 1 | a0001c0001t0002g0147 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.286+1577T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72117376 | ||||||
chr5:72117447
|
T | C | 1 | a0001c0002t0003g0148 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.286+1648T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72117447 | ||||||
chr5:72117492
|
A | G | 213 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0024others(210): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.286+1693A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72117492 | ||||||
chr5:72117516
|
G | A | 4 | a0001c0005t0021g0135a0006c0011t0011g0136a0006c0011t0011g0137others(1): Show | 4 | HG01074.hp2 HG02145.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+1717G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72117516 | ||||||
chr5:72117530
|
T | C | 1 | a0001c0002t0001g0149 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.286+1731T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72117530 | ||||||
chr5:72117541
|
T | C | 1 | a0001c0002t0001g0149 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.286+1742T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72117541 | ||||||
chr5:72117624
|
C | G | 1 | a0001c0001t0001g0328 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.286+1825C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72117624 | ||||||
chr5:72117791
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.286+1992C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72117791 | ||||||
chr5:72117801
|
G | A | 70 | a0001c0001t0001g0063a0001c0001t0001g0071a0001c0001t0001g0083others(67): Show | 70 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.286+2002G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72117801 | ||||||
chr5:72117801
|
G | T | 1 | a0001c0001t0012g0314 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.286+2002G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72117801 | ||||||
chr5:72117818
|
T | G | 7 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(4): Show | 7 | HG02622.hp2 HG02886.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.286+2019T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72117818 | ||||||
chr5:72117831
|
T | A | 1 | a0001c0022t0002g0150 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.286+2032T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72117831 | ||||||
chr5:72118145
|
A | G | 1 | a0001c0001t0020g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.286+2346A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72118145 | ||||||
chr5:72118339
|
A | G | 160 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0050others(157): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.286+2540A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72118339 | ||||||
chr5:72118369
|
T | C | 1 | a0001c0001t0020g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.286+2570T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72118369 | ||||||
chr5:72118369
|
TA | T | 52 | a0001c0001t0001g0024a0001c0001t0001g0264a0001c0001t0001g0267others(49): Show | 53 | HG00558.hp1 HG00609.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.286+2579delA | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72118369 | |||||
chr5:72118380
|
A | G | 7 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(4): Show | 7 | HG02622.hp2 HG02886.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.286+2581A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72118380 | ||||||
chr5:72118455
|
T | C | 2 | a0001c0001t0012g0053a0001c0001t0012g0054 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+2656T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72118455 | ||||||
chr5:72118637
|
G | A | 1 | a0001c0039t0018g0013 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.286+2838G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72118637 | ||||||
chr5:72118773
|
G | A | 114 | a0001c0001t0001g0014a0001c0001t0001g0129a0001c0001t0001g0131others(111): Show | 117 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.286+2974G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72118773 | ||||||
chr5:72118805
|
A | G | 53 | a0001c0001t0001g0024a0001c0001t0001g0264a0001c0001t0001g0267others(50): Show | 54 | HG00558.hp1 HG00609.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.286+3006A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72118805 | ||||||
chr5:72118832
|
C | T | 146 | a0001c0001t0001g0014a0001c0001t0001g0050a0001c0001t0001g0052others(143): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.286+3033C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72118832 | ||||||
chr5:72118852
|
G | A | 10 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0002t0002g0056others(7): Show | 10 | NA18946.hp1 NA18960.hp2 NA18963.hp1 others(7): Show |
intron_variant | MODIFIER | c.286+3053G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72118852 | ||||||
chr5:72118876
|
T | G | 1 | a0001c0006t0005g0064 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.286+3077T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72118876 | ||||||
chr5:72118973
|
A | G | 159 | a0001c0001t0001g0014a0001c0001t0001g0050a0001c0001t0001g0052others(156): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.286+3174A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72118973 | ||||||
chr5:72118985
|
C | A | 146 | a0001c0001t0001g0014a0001c0001t0001g0050a0001c0001t0001g0052others(143): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.286+3186C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72118985 | ||||||
chr5:72119306
|
C | G | 159 | a0001c0001t0001g0014a0001c0001t0001g0050a0001c0001t0001g0052others(156): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.286+3507C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72119306 | ||||||
chr5:72119329
|
G | A | 1 | a0002c0003t0006g0151 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.286+3530G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72119329 | ||||||
chr5:72119569
|
G | A | 2 | a0001c0009t0007g0040a0001c0028t0025g0039 | 2 | HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.286+3770G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72119569 | ||||||
chr5:72119595
|
C | A | 116 | a0001c0001t0001g0014a0001c0001t0001g0129a0001c0001t0001g0131others(113): Show | 119 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.286+3796C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72119595 | ||||||
chr5:72119755
|
T | C | 1 | a0001c0001t0020g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.286+3956T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72119755 | ||||||
chr5:72119802
|
C | T | 30 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0120others(27): Show | 30 | HG00140.hp1 HG01070.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.286+4003C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72119802 | ||||||
chr5:72119803
|
G | A | 1 | a0001c0002t0002g0072 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.286+4004G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72119803 | ||||||
chr5:72119859
|
A | C | 2 | a0001c0001t0002g0069a0001c0001t0015g0113 | 2 | HG00408.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.286+4060A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72119859 | ||||||
chr5:72119990
|
G | A | 1 | a0001c0020t0007g0261 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.286+4191G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72119990 | ||||||
chr5:72120095
|
C | G | 53 | a0001c0001t0001g0024a0001c0001t0001g0264a0001c0001t0001g0267others(50): Show | 54 | HG00558.hp1 HG00609.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.286+4296C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72120095 | ||||||
chr5:72120425
|
CT | C | 54 | a0001c0001t0001g0024a0001c0001t0001g0144a0001c0001t0001g0264others(51): Show | 55 | HG00558.hp1 HG00609.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.286+4643delT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72120425 | |||||
chr5:72120465
|
C | G | 1 | a0001c0001t0001g0114 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.286+4666C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72120465 | ||||||
chr5:72120494
|
G | T | 5 | a0001c0001t0001g0144a0001c0005t0008g0134a0001c0005t0008g0253others(2): Show | 5 | HG02647.hp2 HG03041.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+4695G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72120494 | ||||||
chr5:72120518
|
G | A | 1 | a0001c0001t0012g0314 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.286+4719G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72120518 | ||||||
chr5:72120549
|
C | T | 1 | a0001c0004t0034g0216 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.286+4750C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72120549 | ||||||
chr5:72120574
|
A | G | 2 | a0001c0001t0002g0028a0001c0002t0002g0029 | 2 | HG02523.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.286+4775A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72120574 | ||||||
chr5:72120590
|
A | AT | 6 | a0001c0001t0012g0053a0001c0001t0012g0054a0001c0001t0015g0121others(3): Show | 6 | HG02145.hp2 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.286+4800dupT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72120590 | |||||
chr5:72120590
|
AT | A | 5 | a0001c0001t0001g0014a0001c0001t0012g0314a0001c0005t0001g0005others(2): Show | 5 | HG00642.hp1 HG01884.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.286+4800delT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72120590 | |||||
chr5:72120640
|
A | C | 1 | a0001c0004t0001g0337 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.286+4841A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72120640 | ||||||
chr5:72120665
|
A | C | 1 | a0001c0002t0002g0214 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.286+4866A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72120665 | ||||||
chr5:72120800
|
A | G | 65 | a0001c0001t0001g0006a0001c0001t0001g0063a0001c0001t0001g0071others(62): Show | 65 | HG00140.hp2 HG00408.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.286+5001A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72120800 | ||||||
chr5:72120857
|
G | A | 2 | a0001c0001t0002g0028a0001c0002t0002g0029 | 2 | HG02523.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.286+5058G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72120857 | ||||||
chr5:72121067
|
C | T | 2 | a0001c0001t0002g0028a0001c0002t0002g0029 | 2 | HG02523.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.286+5268C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72121067 | ||||||
chr5:72121111
|
G | C | 1 | a0001c0002t0002g0079 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.286+5312G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72121111 | ||||||
chr5:72121213
|
A | G | 2 | a0001c0005t0008g0134a0006c0011t0001g0254 | 2 | HG02647.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.286+5414A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72121213 | ||||||
chr5:72121291
|
T | C | 1 | a0001c0001t0020g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.286+5492T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72121291 | ||||||
chr5:72121295
|
C | T | 4 | a0001c0001t0004g0022a0001c0001t0004g0213a0001c0001t0004g0251others(1): Show | 4 | HG01192.hp2 HG04199.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+5496C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72121295 | ||||||
chr5:72121337
|
T | G | 7 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(4): Show | 7 | HG02622.hp2 HG02886.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.286+5538T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72121337 | ||||||
chr5:72121844
|
A | G | 19 | a0001c0001t0001g0111a0001c0001t0001g0211a0001c0001t0001g0313others(16): Show | 19 | HG00609.hp1 HG00621.hp1 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.286+6045A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72121844 | ||||||
chr5:72121938
|
G | A | 11 | a0001c0001t0007g0270a0001c0001t0012g0053a0001c0001t0012g0054others(8): Show | 11 | HG01167.hp2 HG01243.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.286+6139G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72121938 | ||||||
chr5:72121960
|
T | C | 1 | a0001c0002t0002g0203 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.286+6161T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72121960 | ||||||
chr5:72121983
|
G | T | 1 | a0001c0001t0026g0202 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.286+6184G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72121983 | ||||||
chr5:72122065
|
G | A | 3 | a0001c0001t0001g0220a0001c0004t0001g0330a0001c0005t0008g0030 | 3 | HG03098.hp1 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.286+6266G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72122065 | ||||||
chr5:72122238
|
G | A | 3 | a0001c0002t0011g0154a0001c0002t0014g0001a0001c0002t0016g0153 | 4 | HG01884.hp1 HG02922.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+6439G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72122238 | ||||||
chr5:72122281
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.286+6482C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72122281 | ||||||
chr5:72122301
|
T | C | 1 | a0001c0001t0002g0028 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.286+6502T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72122301 | ||||||
chr5:72122376
|
G | A | 1 | a0001c0005t0008g0030 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.286+6577G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72122376 | ||||||
chr5:72122556
|
C | T | 2 | a0001c0017t0003g0070a0002c0003t0016g0302 | 2 | NA18983.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.286+6757C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72122556 | ||||||
chr5:72122641
|
C | CTTT | 7 | a0001c0001t0012g0031a0001c0001t0012g0145a0001c0001t0020g0128others(4): Show | 7 | HG02559.hp1 HG02559.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.286+6857_286+6859d others(5): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72122641 | |||||
chr5:72122641
|
CT | C | 10 | a0001c0001t0001g0052a0001c0001t0005g0156a0001c0001t0005g0157others(7): Show | 10 | HG01070.hp1 HG01070.hp2 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.286+6859delT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72122641 | |||||
chr5:72122737
|
G | T | 3 | a0001c0001t0002g0069a0001c0001t0015g0113a0003c0007t0002g0080 | 3 | HG00408.hp1 HG01975.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.286+6938G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72122737 | ||||||
chr5:72122750
|
T | C | 1 | a0001c0002t0002g0315 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.286+6951T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72122750 | ||||||
chr5:72122785
|
C | CCCAGGAG | 7 | a0001c0001t0012g0031a0001c0001t0012g0145a0001c0001t0020g0128others(4): Show | 7 | HG02559.hp1 HG02559.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.286+6990_286+6996d others(9): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72122785 | |||||
chr5:72122811
|
A | G | 3 | a0001c0001t0001g0006a0001c0002t0001g0200a0001c0002t0002g0201 | 3 | HG02155.hp2 NA18612.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.286+7012A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72122811 | ||||||
chr5:72122881
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.286+7082G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72122881 | ||||||
chr5:72123062
|
C | G | 1 | a0008c0016t0001g0333 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.286+7263C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72123062 | ||||||
chr5:72123183
|
A | G | 10 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(7): Show | 10 | HG02622.hp2 HG02818.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.286+7384A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72123183 | ||||||
chr5:72123325
|
C | T | 1 | a0001c0001t0002g0147 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.286+7526C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72123325 | ||||||
chr5:72123472
|
G | GT | 168 | a0001c0001t0001g0024a0001c0001t0001g0041a0001c0001t0001g0063others(165): Show | 171 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(168): Show |
intron_variant | MODIFIER | c.286+7681dupT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72123472 | |||||
chr5:72123481
|
G | T | 1 | a0001c0002t0003g0212 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.286+7682G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72123481 | ||||||
chr5:72123505
|
GA | G | 10 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(7): Show | 10 | HG02622.hp2 HG02818.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.286+7707delA | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72123505 | ||||||
chr5:72123523
|
C | T | 10 | a0001c0001t0001g0071a0001c0001t0007g0116a0001c0002t0002g0108others(7): Show | 10 | HG01074.hp2 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.286+7724C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72123523 | ||||||
chr5:72123585
|
C | T | 2 | a0001c0001t0012g0314a0001c0005t0001g0005 | 2 | HG01884.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.286+7786C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72123585 | ||||||
chr5:72123586
|
G | A | 2 | a0001c0001t0002g0028a0001c0039t0018g0013 | 2 | HG02486.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.286+7787G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72123586 | ||||||
chr5:72123607
|
C | T | 1 | a0001c0005t0008g0335 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.286+7808C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72123607 | ||||||
chr5:72123728
|
C | A | 10 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(7): Show | 10 | HG02622.hp2 HG02818.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.286+7929C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72123728 | ||||||
chr5:72123884
|
A | G | 336 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0024others(333): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.286+8085A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72123884 | ||||||
chr5:72123929
|
C | T | 4 | a0001c0001t0012g0031a0001c0001t0012g0145a0001c0005t0005g0221others(1): Show | 4 | HG02559.hp1 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.286+8130C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72123929 | ||||||
chr5:72124358
|
T | G | 3 | a0001c0002t0011g0154a0001c0002t0014g0001a0001c0002t0016g0153 | 4 | HG01884.hp1 HG02922.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+8559T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72124358 | ||||||
chr5:72124385
|
A | G | 1 | a0001c0001t0004g0097 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.286+8586A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72124385 | ||||||
chr5:72124450
|
C | T | 8 | a0001c0001t0001g0287a0001c0002t0001g0305a0001c0002t0003g0279others(5): Show | 8 | HG00609.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.286+8651C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72124450 | ||||||
chr5:72124460
|
A | C | 1 | a0001c0005t0005g0125 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.286+8661A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72124460 | ||||||
chr5:72124466
|
A | T | 1 | a0001c0005t0005g0125 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.286+8667A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72124466 | ||||||
chr5:72124534
|
G | T | 1 | a0001c0039t0018g0013 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.286+8735G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72124534 | ||||||
chr5:72124545
|
G | A | 1 | a0001c0001t0007g0116 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.286+8746G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72124545 | ||||||
chr5:72124617
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.286+8818C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72124617 | ||||||
chr5:72124624
|
T | C | 5 | a0001c0001t0004g0081a0001c0002t0003g0158a0002c0003t0006g0011others(2): Show | 5 | HG00735.hp2 HG01109.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+8825T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72124624 | ||||||
chr5:72124862
|
C | A | 3 | a0001c0002t0011g0154a0001c0002t0014g0001a0001c0002t0016g0153 | 4 | HG01884.hp1 HG02922.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+9063C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72124862 | ||||||
chr5:72124924
|
G | T | 10 | a0001c0002t0002g0106a0001c0002t0003g0004a0001c0002t0003g0219others(7): Show | 11 | HG01928.hp1 HG01943.hp2 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.286+9125G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72124924 | ||||||
chr5:72124956
|
C | T | 1 | a0001c0001t0007g0116 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.286+9157C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72124956 | ||||||
chr5:72125160
|
C | T | 1 | a0001c0001t0001g0182 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.286+9361C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72125160 | ||||||
chr5:72125204
|
TAGG | T | 34 | a0001c0001t0001g0093a0001c0001t0001g0120a0001c0001t0001g0250others(31): Show | 35 | HG00099.hp2 HG00408.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.286+9408_286+9410d others(5): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72125204 | |||||
chr5:72125285
|
T | C | 3 | a0001c0002t0002g0203a0001c0002t0002g0205a0001c0008t0002g0110 | 3 | HG00621.hp1 HG02132.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.286+9486T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72125285 | ||||||
chr5:72125658
|
A | G | 2 | a0001c0001t0012g0314a0001c0005t0001g0005 | 2 | HG01884.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.286+9859A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72125658 | ||||||
chr5:72125721
|
A | AT | 135 | a0001c0001t0001g0024a0001c0001t0001g0041a0001c0001t0001g0063others(132): Show | 138 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.286+9923dupT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72125721 | |||||
chr5:72125841
|
G | A | 1 | a0001c0039t0018g0013 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.286+10042G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72125841 | ||||||
chr5:72125880
|
T | TAAGAATT others(308): Show |
1 | a0001c0001t0001g0199 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.286+10098_286+1009 others(319): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72125880 | |||||
chr5:72125880
|
T | TAAGAATT others(309): Show |
9 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(6): Show | 9 | HG02622.hp2 HG02897.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.286+10098_286+1009 others(320): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72125880 | |||||
chr5:72125903
|
A | G | 10 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(7): Show | 10 | HG02622.hp2 HG02818.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.286+10104A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72125903 | ||||||
chr5:72126076
|
C | G | 7 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(4): Show | 7 | HG02622.hp2 HG02818.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.286+10277C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72126076 | ||||||
chr5:72126133
|
G | A | 10 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(7): Show | 10 | HG02622.hp2 HG02818.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.286+10334G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72126133 | ||||||
chr5:72126181
|
G | A | 174 | a0001c0001t0001g0024a0001c0001t0001g0041a0001c0001t0001g0063others(171): Show | 177 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(174): Show |
intron_variant | MODIFIER | c.286+10382G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72126181 | ||||||
chr5:72126275
|
C | G | 10 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(7): Show | 10 | HG02622.hp2 HG02818.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.286+10476C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72126275 | ||||||
chr5:72126338
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.286+10539G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72126338 | ||||||
chr5:72126359
|
T | C | 154 | a0001c0001t0001g0024a0001c0001t0001g0041a0001c0001t0001g0063others(151): Show | 157 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(154): Show |
intron_variant | MODIFIER | c.286+10560T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72126359 | ||||||
chr5:72126361
|
A | G | 1 | a0001c0001t0001g0336 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.286+10562A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72126361 | ||||||
chr5:72126525
|
C | G | 2 | a0001c0001t0001g0144a0004c0010t0005g0133 | 2 | HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.286+10726C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72126525 | ||||||
chr5:72126549
|
A | G | 12 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(9): Show | 12 | HG02486.hp2 HG02523.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.286+10750A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72126549 | ||||||
chr5:72126816
|
C | A | 1 | a0001c0002t0003g0126 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.286+11017C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72126816 | ||||||
chr5:72126922
|
T | C | 1 | a0003c0007t0002g0080 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.286+11123T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72126922 | ||||||
chr5:72127160
|
T | C | 1 | a0001c0001t0002g0028 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.286+11361T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72127160 | ||||||
chr5:72127164
|
G | A | 2 | a0001c0001t0002g0028a0001c0005t0008g0030 | 2 | HG02523.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.286+11365G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72127164 | ||||||
chr5:72127172
|
C | T | 4 | a0001c0001t0001g0093a0001c0001t0001g0120a0001c0001t0002g0147others(1): Show | 4 | HG02738.hp2 HG03017.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.286+11373C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72127172 | ||||||
chr5:72127336
|
T | C | 1 | a0001c0001t0020g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.286+11537T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72127336 | ||||||
chr5:72127342
|
T | G | 1 | a0001c0001t0001g0127 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.286+11543T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72127342 | ||||||
chr5:72127398
|
A | G | 135 | a0001c0001t0001g0024a0001c0001t0001g0041a0001c0001t0001g0063others(132): Show | 138 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.286+11599A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72127398 | ||||||
chr5:72127414
|
G | T | 9 | a0001c0001t0001g0336a0001c0001t0001g0338a0001c0004t0001g0337others(6): Show | 9 | HG00741.hp1 HG00741.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.286+11615G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72127414 | ||||||
chr5:72127525
|
A | G | 5 | a0001c0001t0004g0081a0001c0002t0003g0158a0002c0003t0006g0011others(2): Show | 5 | HG00735.hp2 HG01109.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+11726A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72127525 | ||||||
chr5:72127599
|
A | C | 9 | a0001c0001t0001g0071a0001c0002t0002g0108a0001c0005t0005g0043others(6): Show | 9 | HG01074.hp2 HG02109.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.286+11800A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72127599 | ||||||
chr5:72127741
|
C | T | 2 | a0003c0007t0002g0095a0003c0007t0002g0096 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.286+11942C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72127741 | ||||||
chr5:72127983
|
G | A | 1 | a0001c0001t0002g0028 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.286+12184G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72127983 | ||||||
chr5:72128061
|
A | C | 10 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(7): Show | 10 | HG02622.hp2 HG02818.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.286+12262A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72128061 | ||||||
chr5:72128105
|
C | T | 9 | a0001c0001t0001g0336a0001c0001t0001g0338a0001c0004t0001g0337others(6): Show | 9 | HG00741.hp1 HG00741.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.286+12306C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72128105 | ||||||
chr5:72128178
|
A | G | 1 | a0004c0010t0005g0332 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.286+12379A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72128178 | ||||||
chr5:72128257
|
G | A | 1 | a0001c0001t0003g0325 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.286+12458G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72128257 | ||||||
chr5:72128408
|
T | A | 10 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(7): Show | 10 | HG02622.hp2 HG02818.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.286+12609T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72128408 | ||||||
chr5:72128408
|
TA | T | 155 | a0001c0001t0001g0024a0001c0001t0001g0041a0001c0001t0001g0063others(152): Show | 158 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(155): Show |
intron_variant | MODIFIER | c.286+12624delA | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72128408 | |||||
chr5:72128410
|
A | T | 4 | a0001c0001t0001g0071a0001c0001t0001g0220a0001c0004t0001g0330others(1): Show | 4 | HG03098.hp1 HG03209.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+12611A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72128410 | ||||||
chr5:72128420
|
A | C | 1 | a0001c0001t0011g0105 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.286+12621A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72128420 | ||||||
chr5:72128664
|
A | C | 10 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(7): Show | 10 | HG02622.hp2 HG02818.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.286+12865A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72128664 | ||||||
chr5:72128834
|
G | A | 15 | a0001c0001t0001g0063a0001c0001t0001g0101a0001c0001t0009g0239others(12): Show | 15 | HG02135.hp1 NA18942.hp2 NA18943.hp1 others(12): Show |
intron_variant | MODIFIER | c.286+13035G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72128834 | ||||||
chr5:72128971
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.286+13172T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72128971 | ||||||
chr5:72129120
|
TC | T | 3 | a0001c0002t0011g0154a0001c0002t0014g0001a0001c0002t0016g0153 | 4 | HG01884.hp1 HG02922.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+13323delC | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72129120 | |||||
chr5:72129326
|
T | C | 1 | a0001c0001t0012g0314 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.286+13527T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72129326 | ||||||
chr5:72129384
|
T | C | 3 | a0001c0001t0001g0183a0001c0001t0004g0102a0001c0022t0002g0150 | 3 | HG02602.hp1 HG03942.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.286+13585T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72129384 | ||||||
chr5:72129505
|
C | T | 4 | a0001c0002t0003g0109a0001c0002t0003g0204a0001c0002t0013g0020others(1): Show | 4 | HG00621.hp2 HG00673.hp2 HG02015.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+13706C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72129505 | ||||||
chr5:72129515
|
C | T | 10 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(7): Show | 10 | HG02622.hp2 HG02818.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.286+13716C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72129515 | ||||||
chr5:72129530
|
C | G | 2 | a0001c0001t0012g0314a0001c0005t0001g0005 | 2 | HG01884.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.286+13731C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72129530 | ||||||
chr5:72129532
|
A | G | 16 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(13): Show | 16 | HG02559.hp1 HG02559.hp2 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.286+13733A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72129532 | ||||||
chr5:72129547
|
A | G | 41 | a0001c0001t0001g0114a0001c0001t0001g0164a0001c0001t0001g0275others(38): Show | 41 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.286+13748A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72129547 | ||||||
chr5:72129555
|
C | T | 11 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(8): Show | 11 | HG02622.hp2 HG02818.hp2 HG02897.hp1 others(8): Show |
intron_variant | MODIFIER | c.286+13756C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72129555 | ||||||
chr5:72129556
|
T | C | 11 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(8): Show | 11 | HG02622.hp2 HG02818.hp2 HG02897.hp1 others(8): Show |
intron_variant | MODIFIER | c.286+13757T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72129556 | ||||||
chr5:72129657
|
G | A | 1 | a0001c0001t0014g0091 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.286+13858G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72129657 | ||||||
chr5:72130098
|
C | T | 9 | a0001c0001t0001g0336a0001c0001t0001g0338a0001c0004t0001g0337others(6): Show | 9 | HG00741.hp1 HG00741.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.286+14299C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72130098 | ||||||
chr5:72130125
|
A | T | 5 | a0001c0001t0012g0031a0001c0001t0012g0145a0001c0005t0005g0221others(2): Show | 5 | HG02559.hp1 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+14326A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72130125 | ||||||
chr5:72130146
|
T | A | 2 | a0001c0001t0001g0250a0001c0002t0003g0172 | 2 | NA18946.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.286+14347T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72130146 | ||||||
chr5:72130194
|
A | AAC | 8 | a0001c0001t0001g0287a0001c0002t0001g0305a0001c0002t0003g0279others(5): Show | 8 | HG00609.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.286+14396_286+1439 others(6): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72130194 | |||||
chr5:72130194
|
A | AC | 281 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0041others(278): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.286+14395_286+1439 others(5): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72130194 | ||||||
chr5:72130213
|
C | T | 9 | a0001c0001t0001g0336a0001c0001t0001g0338a0001c0004t0001g0337others(6): Show | 9 | HG00741.hp1 HG00741.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.286+14414C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72130213 | ||||||
chr5:72130219
|
G | A | 1 | a0001c0004t0011g0326 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.286+14420G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72130219 | ||||||
chr5:72130268
|
C | T | 3 | a0001c0002t0011g0154a0001c0002t0014g0001a0001c0002t0016g0153 | 4 | HG01884.hp1 HG02922.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+14469C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72130268 | ||||||
chr5:72130302
|
A | G | 1 | a0001c0001t0001g0014 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.286+14503A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72130302 | ||||||
chr5:72130392
|
T | A | 2 | a0001c0001t0012g0314a0001c0005t0001g0005 | 2 | HG01884.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.286+14593T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72130392 | ||||||
chr5:72130507
|
A | G | 1 | a0001c0001t0004g0252 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.286+14708A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72130507 | ||||||
chr5:72130637
|
A | G | 150 | a0001c0001t0001g0024a0001c0001t0001g0041a0001c0001t0001g0071others(147): Show | 153 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.286+14838A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72130637 | ||||||
chr5:72130704
|
G | A | 11 | a0001c0001t0001g0071a0001c0001t0007g0116a0001c0002t0002g0037others(8): Show | 11 | HG01074.hp2 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.286+14905G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72130704 | ||||||
chr5:72130818
|
G | A | 336 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0024others(333): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.286+15019G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72130818 | ||||||
chr5:72131042
|
A | G | 3 | a0001c0001t0001g0127a0001c0002t0003g0126a0001c0004t0005g0104 | 3 | HG00733.hp2 NA18945.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.286+15243A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72131042 | ||||||
chr5:72131083
|
G | T | 10 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(7): Show | 10 | HG02622.hp2 HG02818.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.286+15284G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72131083 | ||||||
chr5:72131125
|
T | C | 1 | a0001c0001t0026g0202 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.286+15326T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72131125 | ||||||
chr5:72131187
|
G | A | 10 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(7): Show | 10 | HG02622.hp2 HG02818.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.286+15388G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72131187 | ||||||
chr5:72131309
|
T | G | 3 | a0001c0001t0012g0053a0001c0001t0012g0054a0001c0039t0018g0013 | 3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+15510T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72131309 | ||||||
chr5:72131674
|
G | A | 3 | a0001c0001t0012g0053a0001c0001t0012g0054a0001c0039t0018g0013 | 3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+15875G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72131674 | ||||||
chr5:72131818
|
C | T | 11 | a0001c0001t0001g0071a0001c0001t0007g0116a0001c0002t0002g0037others(8): Show | 11 | HG01074.hp2 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.286+16019C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72131818 | ||||||
chr5:72131896
|
G | A | 1 | a0001c0005t0021g0135 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.286+16097G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72131896 | ||||||
chr5:72131957
|
T | C | 9 | a0001c0001t0001g0336a0001c0001t0001g0338a0001c0004t0001g0337others(6): Show | 9 | HG00741.hp1 HG00741.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.286+16158T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72131957 | ||||||
chr5:72132082
|
A | G | 133 | a0001c0001t0001g0024a0001c0001t0001g0041a0001c0001t0001g0071others(130): Show | 135 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.286+16283A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72132082 | ||||||
chr5:72132345
|
C | T | 3 | a0001c0001t0012g0053a0001c0001t0012g0054a0001c0039t0018g0013 | 3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+16546C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72132345 | ||||||
chr5:72132467
|
T | C | 2 | a0001c0006t0018g0068a0009c0021t0036g0042 | 2 | HG02451.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.286+16668T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72132467 | ||||||
chr5:72132498
|
G | A | 2 | a0001c0005t0005g0155a0001c0005t0005g0258 | 2 | HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.286+16699G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72132498 | ||||||
chr5:72132537
|
A | G | 2 | a0001c0001t0012g0314a0001c0005t0001g0005 | 2 | HG01884.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.286+16738A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72132537 | ||||||
chr5:72132699
|
G | A | 8 | a0001c0001t0001g0146a0001c0001t0005g0139a0001c0001t0012g0045others(5): Show | 8 | HG01243.hp1 HG02145.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.286+16900G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72132699 | ||||||
chr5:72132858
|
T | C | 1 | a0001c0005t0020g0259 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.286+17059T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72132858 | ||||||
chr5:72132873
|
T | C | 2 | a0001c0034t0005g0033a0016c0035t0005g0044 | 2 | HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.286+17074T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72132873 | ||||||
chr5:72132964
|
G | T | 7 | a0001c0001t0005g0139a0001c0001t0012g0045a0001c0001t0021g0269others(4): Show | 7 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.286+17165G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72132964 | ||||||
chr5:72133319
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.286+17520C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72133319 | ||||||
chr5:72133358
|
C | T | 3 | a0001c0001t0012g0314a0001c0005t0001g0005a0002c0003t0006g0171 | 3 | HG01884.hp2 HG02004.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.286+17559C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72133358 | ||||||
chr5:72133396
|
C | A | 1 | a0001c0001t0005g0139 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.286+17597C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72133396 | ||||||
chr5:72133696
|
T | A | 3 | a0001c0001t0012g0053a0001c0001t0012g0054a0001c0039t0018g0013 | 3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+17897T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72133696 | ||||||
chr5:72133733
|
T | C | 1 | a0001c0004t0007g0140 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.286+17934T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72133733 | ||||||
chr5:72133764
|
G | A | 10 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(7): Show | 10 | HG02622.hp2 HG02818.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.286+17965G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72133764 | ||||||
chr5:72133874
|
G | A | 3 | a0001c0001t0012g0053a0001c0001t0012g0054a0001c0039t0018g0013 | 3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+18075G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72133874 | ||||||
chr5:72133935
|
A | C | 3 | a0001c0001t0012g0053a0001c0001t0012g0054a0001c0039t0018g0013 | 3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+18136A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72133935 | ||||||
chr5:72134016
|
C | T | 3 | a0001c0001t0012g0053a0001c0001t0012g0054a0001c0039t0018g0013 | 3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+18217C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72134016 | ||||||
chr5:72134102
|
G | A | 3 | a0001c0001t0012g0053a0001c0001t0012g0054a0001c0039t0018g0013 | 3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+18303G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72134102 | ||||||
chr5:72134330
|
T | C | 3 | a0001c0001t0012g0053a0001c0001t0012g0054a0001c0039t0018g0013 | 3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+18531T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72134330 | ||||||
chr5:72134345
|
G | T | 1 | a0001c0001t0012g0045 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.286+18546G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72134345 | ||||||
chr5:72134410
|
T | C | 333 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0024others(330): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.286+18611T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72134410 | ||||||
chr5:72134410
|
T | G | 2 | a0001c0001t0001g0220a0001c0004t0001g0330 | 2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.286+18611T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72134410 | ||||||
chr5:72134515
|
TAAG | T | 119 | a0001c0001t0001g0024a0001c0001t0001g0041a0001c0001t0001g0071others(116): Show | 121 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.286+18722_286+1872 others(7): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72134515 | |||||
chr5:72134548
|
C | T | 3 | a0001c0001t0012g0053a0001c0001t0012g0054a0001c0039t0018g0013 | 3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+18749C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72134548 | ||||||
chr5:72134590
|
A | T | 1 | a0001c0006t0007g0263 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.286+18791A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72134590 | ||||||
chr5:72134795
|
A | G | 3 | a0001c0001t0012g0053a0001c0001t0012g0054a0001c0039t0018g0013 | 3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+18996A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72134795 | ||||||
chr5:72134806
|
G | T | 3 | a0001c0001t0012g0053a0001c0001t0012g0054a0001c0039t0018g0013 | 3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+19007G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72134806 | ||||||
chr5:72135068
|
G | A | 168 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0041others(165): Show | 171 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(168): Show |
intron_variant | MODIFIER | c.286+19269G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72135068 | ||||||
chr5:72135106
|
A | G | 38 | a0001c0001t0001g0093a0001c0001t0001g0120a0001c0001t0001g0250others(35): Show | 39 | HG00099.hp2 HG00408.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.286+19307A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72135106 | ||||||
chr5:72135140
|
C | A | 3 | a0001c0001t0012g0053a0001c0001t0012g0054a0001c0039t0018g0013 | 3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+19341C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72135140 | ||||||
chr5:72135397
|
G | C | 3 | a0001c0001t0012g0053a0001c0001t0012g0054a0001c0039t0018g0013 | 3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+19598G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72135397 | ||||||
chr5:72135401
|
T | G | 1 | a0001c0001t0001g0185 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.286+19602T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72135401 | ||||||
chr5:72135614
|
A | T | 3 | a0001c0001t0012g0053a0001c0001t0012g0054a0001c0039t0018g0013 | 3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+19815A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72135614 | ||||||
chr5:72135708
|
T | TGAAAAAG others(312): Show |
1 | a0001c0001t0012g0054 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.286+19921_286+1992 others(323): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72135708 | |||||
chr5:72135708
|
T | TGAAAAAG others(313): Show |
2 | a0001c0001t0012g0053a0001c0039t0018g0013 | 2 | HG02486.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.286+19921_286+1992 others(324): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72135708 | |||||
chr5:72135844
|
T | C | 1 | a0001c0002t0002g0056 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.286+20045T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72135844 | ||||||
chr5:72135889
|
G | A | 161 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0041others(158): Show | 164 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(161): Show |
intron_variant | MODIFIER | c.286+20090G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72135889 | ||||||
chr5:72135952
|
T | A | 1 | a0001c0002t0003g0309 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.286+20153T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72135952 | ||||||
chr5:72136069
|
C | T | 1 | a0001c0001t0004g0251 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.286+20270C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72136069 | ||||||
chr5:72136106
|
T | C | 1 | a0001c0004t0015g0186 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.286+20307T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72136106 | ||||||
chr5:72136344
|
T | C | 3 | a0001c0001t0012g0053a0001c0001t0012g0054a0001c0039t0018g0013 | 3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+20545T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72136344 | ||||||
chr5:72136393
|
A | G | 16 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(13): Show | 16 | HG01884.hp2 HG02486.hp2 HG02523.hp2 others(13): Show |
intron_variant | MODIFIER | c.286+20594A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72136393 | ||||||
chr5:72136396
|
C | G | 12 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(9): Show | 12 | HG01884.hp2 HG02572.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.286+20597C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72136396 | ||||||
chr5:72136870
|
C | T | 2 | a0001c0001t0001g0220a0001c0004t0001g0330 | 2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.286+21071C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72136870 | ||||||
chr5:72137163
|
A | G | 3 | a0001c0002t0011g0154a0001c0002t0014g0001a0001c0002t0016g0153 | 4 | HG01884.hp1 HG02922.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+21364A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72137163 | ||||||
chr5:72137456
|
G | C | 1 | a0001c0002t0032g0274 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.286+21657G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72137456 | ||||||
chr5:72137511
|
A | G | 2 | a0001c0001t0001g0220a0001c0004t0001g0330 | 2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.286+21712A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72137511 | ||||||
chr5:72137615
|
C | T | 3 | a0001c0001t0012g0053a0001c0001t0012g0054a0001c0039t0018g0013 | 3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+21816C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72137615 | ||||||
chr5:72137777
|
C | T | 10 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(7): Show | 10 | HG02622.hp2 HG02818.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.286+21978C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72137777 | ||||||
chr5:72138483
|
C | A | 2 | a0001c0034t0005g0033a0016c0035t0005g0044 | 2 | HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.286+22684C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72138483 | ||||||
chr5:72138487
|
C | T | 2 | a0001c0001t0012g0314a0001c0005t0001g0005 | 2 | HG01884.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.286+22688C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72138487 | ||||||
chr5:72138674
|
G | A | 3 | a0001c0001t0012g0053a0001c0001t0012g0054a0001c0039t0018g0013 | 3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+22875G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72138674 | ||||||
chr5:72138724
|
T | C | 1 | a0001c0001t0002g0028 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.286+22925T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72138724 | ||||||
chr5:72139494
|
A | G | 2 | a0001c0034t0005g0033a0016c0035t0005g0044 | 2 | HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.286+23695A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72139494 | ||||||
chr5:72139508
|
C | T | 1 | a0001c0002t0003g0118 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.286+23709C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72139508 | ||||||
chr5:72139509
|
G | A | 1 | a0004c0010t0005g0332 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.286+23710G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72139509 | ||||||
chr5:72139526
|
C | T | 2 | a0001c0001t0004g0025a0001c0001t0004g0324 | 2 | HG01934.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.286+23727C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72139526 | ||||||
chr5:72139678
|
G | T | 3 | a0001c0001t0012g0053a0001c0001t0012g0054a0001c0039t0018g0013 | 3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+23879G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72139678 | ||||||
chr5:72139747
|
T | C | 132 | a0001c0001t0001g0024a0001c0001t0001g0041a0001c0001t0001g0071others(129): Show | 134 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.286+23948T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72139747 | ||||||
chr5:72139868
|
C | T | 3 | a0001c0001t0001g0284a0001c0002t0002g0023a0012c0027t0010g0235 | 3 | NA18960.hp1 NA19060.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.286+24069C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72139868 | ||||||
chr5:72139966
|
C | CT | 9 | a0001c0001t0001g0014a0001c0001t0001g0250a0001c0001t0007g0270others(6): Show | 9 | HG00642.hp1 HG01167.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.286+24180dupT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72139966 | |||||
chr5:72139988
|
G | T | 3 | a0001c0001t0004g0022a0001c0001t0004g0251a0001c0001t0004g0252 | 3 | HG01192.hp2 HG04199.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.286+24189G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72139988 | ||||||
chr5:72140024
|
C | A | 1 | a0001c0001t0001g0014 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.286+24225C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72140024 | ||||||
chr5:72140024
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.286+24225C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72140024 | ||||||
chr5:72140333
|
A | G | 1 | a0001c0001t0001g0336 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.286+24534A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72140333 | ||||||
chr5:72140432
|
G | C | 1 | a0001c0002t0002g0187 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.286+24633G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72140432 | ||||||
chr5:72140527
|
G | A | 161 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0041others(158): Show | 164 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(161): Show |
intron_variant | MODIFIER | c.286+24728G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72140527 | ||||||
chr5:72140564
|
A | G | 1 | a0004c0010t0005g0332 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.286+24765A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72140564 | ||||||
chr5:72140897
|
G | A | 7 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(4): Show | 7 | HG02622.hp2 HG02818.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.286+25098G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72140897 | ||||||
chr5:72140923
|
A | T | 1 | a0001c0001t0001g0285 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.286+25124A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72140923 | ||||||
chr5:72141028
|
C | G | 1 | a0004c0010t0005g0332 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.286+25229C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72141028 | ||||||
chr5:72141035
|
A | G | 9 | a0001c0001t0001g0336a0001c0001t0001g0338a0001c0004t0001g0337others(6): Show | 9 | HG00741.hp1 HG00741.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.286+25236A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72141035 | ||||||
chr5:72141231
|
C | G | 6 | a0001c0001t0001g0063a0001c0001t0001g0101a0001c0002t0002g0062others(3): Show | 6 | NA18942.hp2 NA18943.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.286+25432C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72141231 | ||||||
chr5:72141266
|
G | C | 1 | a0002c0003t0006g0162 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.286+25467G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72141266 | ||||||
chr5:72141435
|
A | G | 195 | a0001c0001t0001g0024a0001c0001t0001g0041a0001c0001t0001g0071others(192): Show | 198 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(195): Show |
intron_variant | MODIFIER | c.286+25636A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72141435 | ||||||
chr5:72141641
|
C | G | 8 | a0001c0001t0001g0287a0001c0002t0001g0305a0001c0002t0003g0279others(5): Show | 8 | HG00609.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.286+25842C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72141641 | ||||||
chr5:72142054
|
C | T | 1 | a0014c0033t0009g0234 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.286+26255C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72142054 | ||||||
chr5:72142222
|
A | T | 108 | a0001c0001t0001g0014a0001c0001t0001g0111a0001c0001t0001g0117others(105): Show | 109 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.286+26423A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72142222 | ||||||
chr5:72142409
|
C | T | 21 | a0001c0001t0001g0041a0001c0001t0002g0189a0001c0001t0003g0325others(18): Show | 22 | HG00558.hp1 HG01928.hp1 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.286+26610C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72142409 | ||||||
chr5:72142610
|
G | A | 1 | a0001c0022t0002g0150 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.286+26811G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72142610 | ||||||
chr5:72142641
|
A | G | 2 | a0001c0001t0002g0069a0001c0001t0015g0113 | 2 | HG00408.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.286+26842A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72142641 | ||||||
chr5:72142651
|
A | G | 1 | a0001c0001t0002g0028 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.286+26852A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72142651 | ||||||
chr5:72142678
|
A | T | 4 | a0001c0005t0008g0134a0001c0005t0008g0253a0004c0010t0005g0332others(1): Show | 4 | HG02647.hp1 HG02647.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+26879A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72142678 | ||||||
chr5:72142731
|
T | TA | 11 | a0001c0001t0002g0069a0001c0001t0004g0213a0001c0001t0015g0113others(8): Show | 11 | HG00408.hp1 HG00733.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.286+26945dupA | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72142731 | |||||
chr5:72142829
|
G | C | 5 | a0001c0001t0012g0314a0001c0005t0008g0134a0001c0005t0008g0253others(2): Show | 5 | HG02572.hp1 HG02647.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.286+27030G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72142829 | ||||||
chr5:72142985
|
T | C | 2 | a0001c0034t0005g0033a0016c0035t0005g0044 | 2 | HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.286+27186T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72142985 | ||||||
chr5:72143109
|
T | C | 4 | a0001c0005t0008g0134a0001c0005t0008g0253a0004c0010t0005g0332others(1): Show | 4 | HG02647.hp1 HG02647.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+27310T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72143109 | ||||||
chr5:72143141
|
A | G | 2 | a0001c0001t0004g0097a0001c0001t0004g0251 | 2 | HG03710.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.286+27342A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72143141 | ||||||
chr5:72143349
|
C | A | 7 | a0001c0001t0005g0139a0001c0001t0007g0270a0001c0001t0015g0121others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.286+27550C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72143349 | ||||||
chr5:72143436
|
C | G | 3 | a0001c0005t0008g0038a0007c0013t0001g0123a0007c0013t0029g0124 | 3 | HG00741.hp2 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.286+27637C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72143436 | ||||||
chr5:72143447
|
C | T | 1 | a0001c0001t0002g0147 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.286+27648C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72143447 | ||||||
chr5:72143560
|
G | A | 4 | a0001c0005t0008g0134a0001c0005t0008g0253a0004c0010t0005g0332others(1): Show | 4 | HG02647.hp1 HG02647.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+27761G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72143560 | ||||||
chr5:72143658
|
A | G | 2 | a0001c0034t0005g0033a0016c0035t0005g0044 | 2 | HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.286+27859A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72143658 | ||||||
chr5:72143673
|
G | T | 1 | a0001c0001t0012g0314 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.286+27874G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72143673 | ||||||
chr5:72143860
|
TA | T | 10 | a0001c0001t0001g0220a0001c0001t0001g0338a0001c0004t0001g0330others(7): Show | 10 | HG00741.hp1 HG00741.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.286+28062delA | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72143860 | ||||||
chr5:72143933
|
G | A | 1 | a0001c0002t0003g0103 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.286+28134G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72143933 | ||||||
chr5:72144067
|
A | G | 12 | a0001c0001t0001g0146a0001c0001t0001g0267a0001c0001t0012g0045others(9): Show | 12 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.286+28268A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72144067 | ||||||
chr5:72144103
|
A | C | 71 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0111others(68): Show | 71 | HG00099.hp1 HG00621.hp1 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.286+28304A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72144103 | ||||||
chr5:72144304
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.286+28505G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72144304 | ||||||
chr5:72144328
|
G | A | 14 | a0001c0001t0001g0083a0001c0001t0001g0182a0001c0001t0010g0007others(11): Show | 14 | HG00558.hp2 HG00639.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.286+28529G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72144328 | ||||||
chr5:72144329
|
C | T | 4 | a0001c0005t0008g0134a0001c0005t0008g0253a0004c0010t0005g0332others(1): Show | 4 | HG02647.hp1 HG02647.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+28530C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72144329 | ||||||
chr5:72144374
|
C | T | 4 | a0001c0001t0004g0213a0001c0002t0002g0315a0001c0009t0001g0331others(1): Show | 4 | HG01358.hp2 HG01433.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+28575C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72144374 | ||||||
chr5:72144429
|
T | G | 1 | a0001c0002t0003g0174 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.286+28630T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72144429 | ||||||
chr5:72144480
|
A | C | 1 | a0001c0001t0020g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.286+28681A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72144480 | ||||||
chr5:72144550
|
C | T | 2 | a0001c0002t0002g0037a0001c0002t0002g0161 | 2 | HG01109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.286+28751C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72144550 | ||||||
chr5:72144607
|
C | A | 1 | a0001c0002t0002g0092 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.286+28808C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72144607 | ||||||
chr5:72144699
|
G | A | 4 | a0001c0001t0012g0031a0001c0001t0012g0145a0001c0005t0005g0221others(1): Show | 4 | HG02559.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+28900G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72144699 | ||||||
chr5:72144758
|
G | A | 3 | a0001c0002t0011g0154a0001c0002t0014g0001a0001c0002t0016g0153 | 4 | HG01884.hp1 HG02922.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+28959G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72144758 | ||||||
chr5:72144789
|
T | C | 12 | a0001c0001t0005g0139a0001c0001t0007g0270a0001c0001t0012g0314others(9): Show | 12 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.286+28990T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72144789 | ||||||
chr5:72144848
|
G | T | 12 | a0001c0001t0005g0139a0001c0001t0007g0270a0001c0001t0012g0314others(9): Show | 12 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.286+29049G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72144848 | ||||||
chr5:72144887
|
A | G | 2 | a0001c0034t0005g0033a0016c0035t0005g0044 | 2 | HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.286+29088A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72144887 | ||||||
chr5:72145307
|
G | A | 1 | a0001c0002t0031g0207 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.286+29508G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72145307 | ||||||
chr5:72145374
|
TA | T | 15 | a0001c0001t0004g0213a0001c0001t0005g0139a0001c0001t0007g0270others(12): Show | 15 | HG01358.hp2 HG01433.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.286+29587delA | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72145374 | |||||
chr5:72145411
|
T | C | 1 | a0001c0001t0012g0009 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.286+29612T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72145411 | ||||||
chr5:72145641
|
A | T | 14 | a0001c0001t0001g0083a0001c0001t0001g0182a0001c0001t0010g0007others(11): Show | 14 | HG00558.hp2 HG00639.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.286+29842A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72145641 | ||||||
chr5:72145736
|
T | C | 1 | a0001c0002t0023g0141 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.286+29937T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72145736 | ||||||
chr5:72145762
|
T | C | 139 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0111others(136): Show | 140 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(137): Show |
intron_variant | MODIFIER | c.286+29963T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72145762 | ||||||
chr5:72145847
|
G | T | 14 | a0001c0001t0001g0083a0001c0001t0001g0182a0001c0001t0010g0007others(11): Show | 14 | HG00558.hp2 HG00639.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.286+30048G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72145847 | ||||||
chr5:72145873
|
G | A | 16 | a0001c0001t0004g0213a0001c0001t0005g0139a0001c0001t0007g0270others(13): Show | 16 | HG01358.hp2 HG01433.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.286+30074G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72145873 | ||||||
chr5:72145886
|
C | T | 15 | a0001c0001t0004g0213a0001c0001t0005g0139a0001c0001t0007g0270others(12): Show | 15 | HG01358.hp2 HG01433.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.286+30087C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72145886 | ||||||
chr5:72146418
|
T | C | 12 | a0001c0001t0001g0273a0001c0002t0003g0012a0001c0002t0003g0058others(9): Show | 12 | HG00621.hp2 HG00673.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.286+30619T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72146418 | ||||||
chr5:72146680
|
A | G | 1 | a0001c0001t0039g0019 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.286+30881A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72146680 | ||||||
chr5:72146861
|
G | C | 1 | a0001c0001t0002g0028 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.286+31062G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72146861 | ||||||
chr5:72146961
|
C | CT | 15 | a0001c0001t0001g0083a0001c0001t0001g0182a0001c0001t0010g0007others(12): Show | 15 | HG00558.hp2 HG00639.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.286+31180dupT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72146961 | |||||
chr5:72146961
|
CT | C | 7 | a0001c0001t0001g0014a0001c0001t0002g0028a0001c0001t0005g0156others(4): Show | 7 | HG00642.hp1 HG01070.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.286+31180delT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72146961 | |||||
chr5:72147182
|
T | C | 3 | a0001c0001t0001g0006a0001c0002t0001g0200a0001c0002t0002g0201 | 3 | HG02155.hp2 NA18612.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.286+31383T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72147182 | ||||||
chr5:72147248
|
C | T | 2 | a0001c0001t0001g0312a0001c0002t0003g0173 | 2 | HG00140.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.286+31449C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72147248 | ||||||
chr5:72147389
|
C | T | 4 | a0001c0001t0001g0144a0001c0009t0007g0040a0001c0028t0025g0039others(1): Show | 4 | HG02886.hp2 HG03041.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+31590C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72147389 | ||||||
chr5:72147446
|
A | G | 5 | a0001c0001t0001g0273a0001c0002t0003g0012a0001c0002t0003g0084others(2): Show | 5 | HG01978.hp1 HG01981.hp1 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+31647A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72147446 | ||||||
chr5:72147484
|
G | T | 1 | a0001c0005t0008g0030 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.286+31685G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72147484 | ||||||
chr5:72147501
|
G | A | 1 | a0003c0007t0002g0080 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.286+31702G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72147501 | ||||||
chr5:72147588
|
G | A | 1 | a0001c0001t0012g0314 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.286+31789G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72147588 | ||||||
chr5:72147606
|
C | T | 1 | a0001c0002t0002g0217 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.286+31807C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72147606 | ||||||
chr5:72147783
|
G | A | 1 | a0001c0038t0013g0021 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.286+31984G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72147783 | ||||||
chr5:72147795
|
T | C | 2 | a0001c0034t0005g0033a0016c0035t0005g0044 | 2 | HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.286+31996T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72147795 | ||||||
chr5:72148064
|
A | G | 2 | a0001c0006t0007g0260a0001c0020t0007g0261 | 2 | HG01167.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.286+32265A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72148064 | ||||||
chr5:72148447
|
CT | C | 3 | a0001c0001t0011g0280a0001c0002t0002g0276a0001c0008t0002g0281 | 3 | NA18747.hp1 NA19068.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.286+32652delT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72148447 | |||||
chr5:72148517
|
T | G | 15 | a0001c0001t0004g0213a0001c0001t0005g0139a0001c0001t0007g0270others(12): Show | 15 | HG01358.hp2 HG01433.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.286+32718T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72148517 | ||||||
chr5:72148559
|
AG | A | 15 | a0001c0001t0004g0213a0001c0001t0005g0139a0001c0001t0007g0270others(12): Show | 15 | HG01358.hp2 HG01433.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.286+32762delG | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72148559 | |||||
chr5:72148698
|
G | A | 1 | a0001c0005t0005g0125 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.286+32899G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72148698 | ||||||
chr5:72148722
|
T | C | 2 | a0001c0006t0007g0260a0001c0020t0007g0261 | 2 | HG01167.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.286+32923T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72148722 | ||||||
chr5:72148769
|
A | G | 15 | a0001c0001t0004g0213a0001c0001t0005g0139a0001c0001t0007g0270others(12): Show | 15 | HG01358.hp2 HG01433.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.286+32970A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72148769 | ||||||
chr5:72148805
|
C | T | 2 | a0001c0006t0007g0260a0001c0020t0007g0261 | 2 | HG01167.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.286+33006C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72148805 | ||||||
chr5:72148871
|
C | T | 7 | a0001c0001t0005g0139a0001c0001t0007g0270a0001c0001t0015g0121others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.286+33072C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72148871 | ||||||
chr5:72149209
|
A | G | 1 | a0001c0001t0005g0286 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.286+33410A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72149209 | ||||||
chr5:72149238
|
G | A | 1 | a0001c0001t0012g0314 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.286+33439G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72149238 | ||||||
chr5:72149419
|
C | T | 16 | a0001c0001t0004g0213a0001c0001t0005g0139a0001c0001t0007g0270others(13): Show | 16 | HG01358.hp2 HG01433.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.286+33620C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72149419 | ||||||
chr5:72149522
|
A | G | 15 | a0001c0001t0004g0213a0001c0001t0005g0139a0001c0001t0007g0270others(12): Show | 15 | HG01358.hp2 HG01433.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.286+33723A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72149522 | ||||||
chr5:72149538
|
G | T | 1 | a0001c0001t0003g0325 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.286+33739G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72149538 | ||||||
chr5:72149633
|
T | C | 1 | a0001c0002t0002g0205 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.286+33834T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72149633 | ||||||
chr5:72149874
|
C | T | 7 | a0001c0001t0005g0139a0001c0001t0007g0270a0001c0001t0015g0121others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.287-33869C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72149874 | ||||||
chr5:72150112
|
A | G | 1 | a0001c0001t0002g0028 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.287-33631A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72150112 | ||||||
chr5:72150164
|
A | T | 154 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0083others(151): Show | 155 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(152): Show |
intron_variant | MODIFIER | c.287-33579A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72150164 | ||||||
chr5:72150254
|
T | C | 15 | a0001c0001t0004g0213a0001c0001t0005g0139a0001c0001t0007g0270others(12): Show | 15 | HG01358.hp2 HG01433.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.287-33489T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72150254 | ||||||
chr5:72150380
|
C | T | 69 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0111others(66): Show | 69 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.287-33363C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72150380 | ||||||
chr5:72150596
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.287-33147C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72150596 | ||||||
chr5:72150701
|
G | A | 1 | a0001c0005t0008g0335 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.287-33042G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72150701 | ||||||
chr5:72150935
|
G | A | 2 | a0001c0001t0007g0116a0001c0005t0008g0107 | 2 | HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.287-32808G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72150935 | ||||||
chr5:72150979
|
G | A | 7 | a0001c0001t0005g0139a0001c0001t0007g0270a0001c0001t0015g0121others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.287-32764G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72150979 | ||||||
chr5:72151049
|
G | GT | 138 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0083others(135): Show | 139 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(136): Show |
intron_variant | MODIFIER | c.287-32694_287-3269 others(5): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72151049 | ||||||
chr5:72151080
|
A | G | 2 | a0001c0002t0002g0072a0001c0004t0007g0327 | 2 | HG01257.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.287-32663A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72151080 | ||||||
chr5:72151092
|
G | A | 1 | a0001c0026t0008g0027 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.287-32651G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72151092 | ||||||
chr5:72151190
|
A | G | 1 | a0001c0001t0002g0028 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.287-32553A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72151190 | ||||||
chr5:72151316
|
A | G | 12 | a0001c0001t0005g0139a0001c0001t0007g0270a0001c0001t0012g0053others(9): Show | 12 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.287-32427A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72151316 | ||||||
chr5:72151380
|
G | A | 70 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0111others(67): Show | 70 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.287-32363G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72151380 | ||||||
chr5:72151406
|
T | G | 2 | a0001c0001t0002g0069a0001c0001t0015g0113 | 2 | HG00408.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.287-32337T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72151406 | ||||||
chr5:72151441
|
T | C | 1 | a0001c0002t0016g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.287-32302T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72151441 | ||||||
chr5:72151584
|
A | G | 3 | a0001c0002t0011g0154a0001c0002t0014g0001a0001c0002t0016g0153 | 4 | HG01884.hp1 HG02922.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-32159A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72151584 | ||||||
chr5:72151737
|
T | A | 14 | a0001c0001t0001g0083a0001c0001t0001g0182a0001c0001t0010g0007others(11): Show | 14 | HG00558.hp2 HG00639.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.287-32006T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72151737 | ||||||
chr5:72151798
|
A | G | 11 | a0001c0001t0009g0239a0001c0001t0009g0240a0001c0001t0009g0241others(8): Show | 11 | HG02486.hp2 HG02895.hp1 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.287-31945A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72151798 | ||||||
chr5:72151862
|
T | A | 1 | a0001c0001t0002g0209 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.287-31881T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72151862 | ||||||
chr5:72151906
|
A | G | 1 | a0001c0001t0012g0314 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.287-31837A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72151906 | ||||||
chr5:72151973
|
G | A | 1 | a0001c0019t0040g0245 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.287-31770G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72151973 | ||||||
chr5:72152113
|
G | C | 1 | a0001c0004t0010g0237 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.287-31630G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72152113 | ||||||
chr5:72152136
|
T | G | 154 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0083others(151): Show | 155 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(152): Show |
intron_variant | MODIFIER | c.287-31607T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72152136 | ||||||
chr5:72152176
|
G | C | 11 | a0001c0001t0009g0239a0001c0001t0009g0240a0001c0001t0009g0241others(8): Show | 11 | HG02486.hp2 HG02895.hp1 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.287-31567G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72152176 | ||||||
chr5:72152178
|
A | G | 1 | a0001c0001t0002g0147 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.287-31565A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72152178 | ||||||
chr5:72152225
|
G | A | 52 | a0001c0001t0001g0014a0001c0001t0001g0111a0001c0001t0001g0117others(49): Show | 52 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.287-31518G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72152225 | ||||||
chr5:72152237
|
T | C | 1 | a0001c0005t0008g0030 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.287-31506T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72152237 | ||||||
chr5:72152343
|
C | T | 1 | a0001c0002t0002g0051 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.287-31400C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72152343 | ||||||
chr5:72152485
|
C | T | 1 | a0001c0001t0001g0257 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.287-31258C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72152485 | ||||||
chr5:72152508
|
G | T | 2 | a0001c0001t0001g0144a0004c0010t0005g0133 | 2 | HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.287-31235G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72152508 | ||||||
chr5:72152539
|
T | C | 2 | a0001c0001t0001g0287a0001c0002t0003g0279 | 2 | NA18984.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.287-31204T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72152539 | ||||||
chr5:72152541
|
G | A | 1 | a0001c0005t0008g0032 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.287-31202G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72152541 | ||||||
chr5:72152617
|
C | A | 1 | a0001c0001t0001g0336 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.287-31126C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72152617 | ||||||
chr5:72152760
|
T | C | 24 | a0001c0001t0001g0083a0001c0001t0001g0182a0001c0001t0003g0325others(21): Show | 24 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.287-30983T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72152760 | ||||||
chr5:72152810
|
T | A | 2 | a0001c0009t0001g0059a0001c0009t0001g0060 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.287-30933T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72152810 | ||||||
chr5:72152890
|
C | T | 11 | a0001c0001t0009g0239a0001c0001t0009g0240a0001c0001t0009g0241others(8): Show | 11 | HG02486.hp2 HG02895.hp1 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.287-30853C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72152890 | ||||||
chr5:72152921
|
G | A | 4 | a0001c0001t0004g0022a0001c0001t0004g0097a0001c0001t0004g0251others(1): Show | 4 | HG01192.hp2 HG03710.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-30822G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72152921 | ||||||
chr5:72153255
|
A | G | 3 | a0001c0001t0001g0336a0001c0034t0005g0033a0016c0035t0005g0044 | 3 | HG02818.hp1 HG03486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.287-30488A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72153255 | ||||||
chr5:72153278
|
G | C | 23 | a0001c0001t0001g0083a0001c0001t0001g0182a0001c0001t0003g0325others(20): Show | 23 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.287-30465G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72153278 | ||||||
chr5:72153431
|
G | T | 4 | a0001c0002t0002g0056a0001c0018t0001g0077a0005c0012t0002g0316others(1): Show | 4 | NA18966.hp1 NA18971.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-30312G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72153431 | ||||||
chr5:72153520
|
G | T | 4 | a0003c0007t0002g0094a0003c0007t0002g0095a0003c0007t0002g0096others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-30223G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72153520 | ||||||
chr5:72153537
|
G | A | 1 | a0001c0002t0002g0315 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.287-30206G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72153537 | ||||||
chr5:72153903
|
TAA | T | 8 | a0001c0001t0009g0239a0001c0001t0009g0240a0001c0001t0009g0241others(5): Show | 8 | NA18943.hp1 NA18955.hp1 NA18973.hp1 others(5): Show |
intron_variant | MODIFIER | c.287-29831_287-2983 others(6): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72153903 | |||||
chr5:72154097
|
A | G | 8 | a0001c0001t0009g0239a0001c0001t0009g0240a0001c0001t0009g0241others(5): Show | 8 | NA18943.hp1 NA18955.hp1 NA18973.hp1 others(5): Show |
intron_variant | MODIFIER | c.287-29646A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72154097 | ||||||
chr5:72154118
|
G | T | 134 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0083others(131): Show | 135 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.287-29625G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72154118 | ||||||
chr5:72154163
|
C | T | 2 | a0001c0001t0012g0053a0001c0001t0012g0054 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.287-29580C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72154163 | ||||||
chr5:72154188
|
T | C | 22 | a0001c0001t0001g0071a0001c0001t0001g0144a0001c0001t0004g0213others(19): Show | 22 | HG01074.hp2 HG01358.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.287-29555T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72154188 | ||||||
chr5:72154331
|
C | T | 1 | a0001c0001t0002g0028 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.287-29412C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72154331 | ||||||
chr5:72154352
|
C | A | 23 | a0001c0001t0001g0083a0001c0001t0001g0182a0001c0001t0003g0325others(20): Show | 23 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.287-29391C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72154352 | ||||||
chr5:72154605
|
AC | A | 3 | a0001c0005t0008g0134a0001c0005t0008g0253a0006c0011t0001g0254 | 3 | HG02647.hp2 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.287-29137delC | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72154605 | ||||||
chr5:72154766
|
T | C | 4 | a0001c0001t0012g0314a0001c0001t0015g0121a0001c0001t0020g0128others(1): Show | 4 | HG02145.hp2 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-28977T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72154766 | ||||||
chr5:72154931
|
A | G | 1 | a0001c0001t0001g0101 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.287-28812A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72154931 | ||||||
chr5:72154948
|
G | A | 29 | a0001c0001t0001g0083a0001c0001t0001g0182a0001c0001t0003g0325others(26): Show | 29 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.287-28795G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72154948 | ||||||
chr5:72155085
|
C | T | 36 | a0001c0001t0001g0083a0001c0001t0001g0182a0001c0001t0001g0220others(33): Show | 36 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.287-28658C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72155085 | ||||||
chr5:72155128
|
A | G | 28 | a0001c0001t0001g0083a0001c0001t0001g0182a0001c0001t0003g0325others(25): Show | 28 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.287-28615A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72155128 | ||||||
chr5:72155333
|
C | T | 212 | a0001c0001t0001g0014a0001c0001t0001g0050a0001c0001t0001g0052others(209): Show | 213 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.287-28410C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72155333 | ||||||
chr5:72155348
|
A | G | 47 | a0001c0001t0001g0083a0001c0001t0001g0144a0001c0001t0001g0182others(44): Show | 47 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.287-28395A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72155348 | ||||||
chr5:72155383
|
C | T | 34 | a0001c0001t0001g0083a0001c0001t0001g0182a0001c0001t0001g0220others(31): Show | 34 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.287-28360C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72155383 | ||||||
chr5:72155599
|
C | T | 2 | a0001c0006t0007g0260a0001c0020t0007g0261 | 2 | HG01167.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.287-28144C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72155599 | ||||||
chr5:72155654
|
A | G | 1 | a0001c0004t0015g0272 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.287-28089A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72155654 | ||||||
chr5:72155693
|
T | C | 290 | a0001c0001t0001g0014a0001c0001t0001g0050a0001c0001t0001g0052others(287): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.287-28050T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72155693 | ||||||
chr5:72155766
|
C | CT | 24 | a0001c0001t0001g0014a0001c0001t0001g0319a0001c0001t0001g0320others(21): Show | 25 | HG00642.hp1 HG01099.hp2 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.287-27959dupT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72155766 | |||||
chr5:72155766
|
C | CTT | 40 | a0001c0001t0001g0111a0001c0001t0001g0117a0001c0001t0001g0160others(37): Show | 40 | HG00099.hp1 HG00621.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.287-27960_287-2795 others(6): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72155766 | |||||
chr5:72155766
|
C | CTTT | 7 | a0001c0001t0001g0198a0001c0002t0001g0078a0001c0004t0034g0216others(4): Show | 7 | HG01928.hp2 HG01934.hp1 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.287-27961_287-2795 others(7): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72155766 | |||||
chr5:72155766
|
CT | C | 37 | a0001c0001t0001g0083a0001c0001t0001g0144a0001c0001t0001g0182others(34): Show | 37 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.287-27959delT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72155766 | |||||
chr5:72155770
|
T | TC | 13 | a0001c0001t0001g0071a0001c0001t0007g0116a0001c0002t0002g0108others(10): Show | 13 | HG01074.hp2 HG02109.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.287-27973_287-2797 others(5): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72155770 | ||||||
chr5:72155799
|
C | T | 89 | a0001c0001t0001g0014a0001c0001t0001g0111a0001c0001t0001g0117others(86): Show | 90 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.287-27944C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72155799 | ||||||
chr5:72155881
|
C | T | 7 | a0001c0001t0012g0053a0001c0001t0012g0054a0001c0001t0012g0314others(4): Show | 7 | HG02486.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.287-27862C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72155881 | ||||||
chr5:72155995
|
G | T | 3 | a0001c0001t0011g0280a0001c0002t0002g0276a0001c0008t0002g0281 | 3 | NA18747.hp1 NA19068.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.287-27748G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72155995 | ||||||
chr5:72156052
|
C | G | 1 | a0001c0002t0002g0002 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.287-27691C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72156052 | ||||||
chr5:72156267
|
G | A | 234 | a0001c0001t0001g0014a0001c0001t0001g0050a0001c0001t0001g0052others(231): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.287-27476G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72156267 | ||||||
chr5:72156275
|
A | G | 8 | a0001c0001t0009g0239a0001c0001t0009g0240a0001c0001t0009g0241others(5): Show | 8 | NA18943.hp1 NA18955.hp1 NA18973.hp1 others(5): Show |
intron_variant | MODIFIER | c.287-27468A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72156275 | ||||||
chr5:72156318
|
G | A | 2 | a0001c0001t0012g0314a0001c0001t0020g0128 | 2 | HG02559.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.287-27425G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72156318 | ||||||
chr5:72156423
|
G | A | 288 | a0001c0001t0001g0014a0001c0001t0001g0050a0001c0001t0001g0052others(285): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.287-27320G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72156423 | ||||||
chr5:72156735
|
G | T | 8 | a0001c0001t0009g0239a0001c0001t0009g0240a0001c0001t0009g0241others(5): Show | 8 | NA18943.hp1 NA18955.hp1 NA18973.hp1 others(5): Show |
intron_variant | MODIFIER | c.287-27008G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72156735 | ||||||
chr5:72156753
|
C | T | 1 | a0001c0001t0002g0147 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.287-26990C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72156753 | ||||||
chr5:72156998
|
C | G | 1 | a0001c0001t0001g0336 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.287-26745C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72156998 | ||||||
chr5:72157021
|
T | A | 3 | a0001c0001t0003g0325a0001c0001t0004g0025a0001c0001t0004g0324 | 3 | HG01934.hp2 HG03579.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.287-26722T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72157021 | ||||||
chr5:72157519
|
C | G | 1 | a0001c0002t0003g0321 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.287-26224C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72157519 | ||||||
chr5:72157520
|
G | A | 4 | a0001c0001t0001g0006a0001c0002t0001g0200a0001c0002t0002g0201others(1): Show | 4 | HG02155.hp2 NA18612.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-26223G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72157520 | ||||||
chr5:72157574
|
C | G | 2 | a0001c0006t0018g0035a0001c0006t0022g0036 | 2 | HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.287-26169C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72157574 | ||||||
chr5:72157959
|
C | T | 1 | a0001c0002t0002g0203 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.287-25784C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72157959 | ||||||
chr5:72157987
|
C | T | 1 | a0001c0001t0019g0247 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.287-25756C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72157987 | ||||||
chr5:72158006
|
A | AT | 12 | a0001c0001t0001g0014a0001c0001t0001g0041a0001c0001t0001g0188others(9): Show | 13 | HG00642.hp1 HG01109.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.287-25716dupT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72158006 | |||||
chr5:72158006
|
A | ATTT | 7 | a0001c0001t0009g0240a0001c0001t0009g0241a0001c0001t0014g0090others(4): Show | 7 | NA18943.hp1 NA18955.hp1 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.287-25718_287-2571 others(7): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72158006 | |||||
chr5:72158006
|
AT | A | 51 | a0001c0001t0001g0083a0001c0001t0001g0111a0001c0001t0001g0182others(48): Show | 51 | HG00558.hp2 HG00639.hp2 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.287-25716delT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72158006 | |||||
chr5:72158006
|
ATT | A | 200 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0063others(197): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.287-25717_287-2571 others(6): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72158006 | |||||
chr5:72158122
|
C | T | 10 | a0001c0001t0001g0144a0001c0001t0012g0053a0001c0001t0012g0054others(7): Show | 10 | HG02145.hp2 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.287-25621C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72158122 | ||||||
chr5:72158233
|
A | G | 2 | a0001c0006t0007g0260a0001c0020t0007g0261 | 2 | HG01167.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.287-25510A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72158233 | ||||||
chr5:72158324
|
T | C | 2 | a0001c0001t0001g0220a0001c0004t0001g0330 | 2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.287-25419T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72158324 | ||||||
chr5:72158348
|
T | C | 246 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0063others(243): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.287-25395T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72158348 | ||||||
chr5:72158360
|
A | T | 1 | a0001c0001t0001g0014 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.287-25383A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72158360 | ||||||
chr5:72158373
|
A | G | 19 | a0001c0001t0001g0071a0001c0001t0007g0116a0001c0001t0009g0239others(16): Show | 19 | HG01074.hp2 HG02109.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.287-25370A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72158373 | ||||||
chr5:72158442
|
G | A | 246 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0063others(243): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.287-25301G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72158442 | ||||||
chr5:72158445
|
G | A | 1 | a0001c0002t0001g0149 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.287-25298G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72158445 | ||||||
chr5:72158456
|
A | G | 8 | a0001c0001t0009g0239a0001c0001t0009g0240a0001c0001t0009g0241others(5): Show | 8 | NA18943.hp1 NA18955.hp1 NA18973.hp1 others(5): Show |
intron_variant | MODIFIER | c.287-25287A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72158456 | ||||||
chr5:72158476
|
A | G | 10 | a0001c0001t0001g0220a0001c0001t0002g0028a0001c0004t0001g0330others(7): Show | 10 | HG00741.hp2 HG02523.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.287-25267A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72158476 | ||||||
chr5:72158484
|
T | C | 1 | a0001c0001t0015g0121 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.287-25259T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72158484 | ||||||
chr5:72158510
|
G | T | 1 | a0001c0001t0026g0202 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.287-25233G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72158510 | ||||||
chr5:72158684
|
T | C | 2 | a0001c0001t0012g0053a0001c0001t0012g0054 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.287-25059T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72158684 | ||||||
chr5:72158719
|
C | T | 14 | a0001c0001t0001g0083a0001c0001t0001g0182a0001c0001t0010g0007others(11): Show | 14 | HG00558.hp2 HG00639.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.287-25024C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72158719 | ||||||
chr5:72158881
|
T | C | 1 | a0001c0002t0002g0203 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.287-24862T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72158881 | ||||||
chr5:72158955
|
A | G | 2 | a0001c0001t0001g0144a0004c0010t0005g0133 | 2 | HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.287-24788A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72158955 | ||||||
chr5:72158956
|
C | T | 233 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0063others(230): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.287-24787C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72158956 | ||||||
chr5:72159087
|
T | C | 5 | a0001c0001t0012g0053a0001c0001t0012g0054a0001c0034t0005g0033others(2): Show | 5 | HG02486.hp2 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.287-24656T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72159087 | ||||||
chr5:72159433
|
CAGAT | C | 243 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0063others(240): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.287-24303_287-2430 others(8): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72159433 | |||||
chr5:72159447
|
A | G | 194 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0063others(191): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.287-24296A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72159447 | ||||||
chr5:72159706
|
A | G | 2 | a0001c0001t0001g0115a0001c0001t0001g0120 | 2 | HG03491.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.287-24037A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72159706 | ||||||
chr5:72159761
|
C | T | 8 | a0001c0001t0012g0053a0001c0001t0012g0054a0001c0001t0012g0314others(5): Show | 8 | HG02145.hp2 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.287-23982C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72159761 | ||||||
chr5:72159781
|
C | A | 1 | a0001c0004t0034g0216 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.287-23962C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72159781 | ||||||
chr5:72159791
|
A | G | 210 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0063others(207): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.287-23952A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72159791 | ||||||
chr5:72159927
|
G | A | 236 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0063others(233): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.287-23816G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72159927 | ||||||
chr5:72159927
|
G | T | 7 | a0001c0001t0001g0220a0001c0001t0002g0028a0001c0004t0001g0330others(4): Show | 7 | HG00741.hp2 HG02523.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.287-23816G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72159927 | ||||||
chr5:72159985
|
G | A | 2 | a0001c0001t0001g0144a0004c0010t0005g0133 | 2 | HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.287-23758G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72159985 | ||||||
chr5:72160120
|
C | T | 2 | a0001c0006t0005g0064a0009c0021t0036g0042 | 2 | HG02109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.287-23623C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72160120 | ||||||
chr5:72160218
|
T | TA | 62 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0129others(59): Show | 63 | HG00140.hp1 HG00642.hp1 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.287-23510dupA | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72160218 | |||||
chr5:72160218
|
T | TAA | 218 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0063others(215): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.287-23511_287-2351 others(6): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72160218 | |||||
chr5:72160266
|
G | A | 4 | a0001c0001t0004g0213a0001c0002t0002g0315a0001c0009t0001g0331others(1): Show | 4 | HG01358.hp2 HG01433.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-23477G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72160266 | ||||||
chr5:72160382
|
A | G | 8 | a0001c0001t0009g0239a0001c0001t0009g0240a0001c0001t0009g0241others(5): Show | 8 | NA18943.hp1 NA18955.hp1 NA18973.hp1 others(5): Show |
intron_variant | MODIFIER | c.287-23361A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72160382 | ||||||
chr5:72160660
|
ATAGGCAA others(13): Show |
A | 1 | a0001c0002t0002g0214 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.287-23080_287-2306 others(24): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72160660 | |||||
chr5:72160795
|
A | G | 210 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0063others(207): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.287-22948A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72160795 | ||||||
chr5:72161004
|
C | T | 1 | a0002c0003t0006g0294 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.287-22739C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72161004 | ||||||
chr5:72161181
|
C | T | 262 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0063others(259): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.287-22562C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72161181 | ||||||
chr5:72161201
|
G | A | 42 | a0001c0001t0001g0063a0001c0001t0001g0101a0001c0001t0001g0127others(39): Show | 42 | HG00140.hp2 HG00621.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.287-22542G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72161201 | ||||||
chr5:72161358
|
A | G | 19 | a0001c0001t0001g0071a0001c0001t0007g0116a0001c0001t0009g0239others(16): Show | 19 | HG01074.hp2 HG02109.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.287-22385A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72161358 | ||||||
chr5:72161441
|
T | C | 1 | a0001c0004t0017g0061 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.287-22302T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72161441 | ||||||
chr5:72161567
|
C | T | 6 | a0001c0001t0001g0220a0001c0004t0001g0330a0001c0005t0008g0030others(3): Show | 6 | HG00741.hp2 HG03098.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-22176C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72161567 | ||||||
chr5:72161618
|
C | T | 1 | a0001c0001t0001g0336 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.287-22125C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72161618 | ||||||
chr5:72161685
|
A | C | 5 | a0001c0001t0001g0144a0001c0004t0001g0337a0001c0005t0008g0335others(2): Show | 5 | HG02630.hp2 HG03041.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.287-22058A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72161685 | ||||||
chr5:72161771
|
A | G | 2 | a0001c0034t0005g0033a0016c0035t0005g0044 | 2 | HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.287-21972A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72161771 | ||||||
chr5:72161906
|
G | A | 2 | a0001c0001t0001g0111a0001c0001t0010g0246 | 2 | NA18941.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.287-21837G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72161906 | ||||||
chr5:72161926
|
C | G | 1 | a0001c0005t0008g0038 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.287-21817C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72161926 | ||||||
chr5:72161943
|
C | T | 1 | a0001c0005t0008g0030 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.287-21800C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72161943 | ||||||
chr5:72161956
|
C | CA | 30 | a0001c0001t0001g0083a0001c0001t0001g0182a0001c0001t0002g0210others(27): Show | 30 | HG00558.hp2 HG00642.hp2 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.287-21767dupA | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72161956 | |||||
chr5:72161956
|
CA | C | 181 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0063others(178): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.287-21767delA | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72161956 | |||||
chr5:72161956
|
CAA | C | 29 | a0001c0001t0001g0071a0001c0001t0001g0146a0001c0001t0001g0257others(26): Show | 29 | HG01074.hp2 HG01168.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.287-21768_287-2176 others(6): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72161956 | |||||
chr5:72161973
|
A | AAAG | 6 | a0001c0001t0001g0220a0001c0004t0001g0330a0001c0005t0008g0030others(3): Show | 6 | HG00741.hp2 HG03098.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-21768_287-2176 others(7): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72161973 | |||||
chr5:72161974
|
AAAG | A | 23 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(20): Show | 24 | HG00140.hp1 HG00741.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.287-21766_287-2176 others(7): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72161974 | |||||
chr5:72161974
|
AAAGAAAG | A | 6 | a0001c0001t0010g0007a0001c0001t0010g0229a0001c0001t0010g0230others(3): Show | 6 | HG00639.hp2 HG01106.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.287-21766_287-2176 others(11): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72161974 | |||||
chr5:72161986
|
A | G | 193 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0063others(190): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.287-21757A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72161986 | ||||||
chr5:72162014
|
ACAGC | A | 7 | a0001c0001t0001g0220a0001c0001t0002g0028a0001c0004t0001g0330others(4): Show | 7 | HG00741.hp2 HG02523.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.287-21725_287-2172 others(8): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72162014 | |||||
chr5:72162251
|
A | G | 1 | a0004c0010t0005g0332 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.287-21492A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72162251 | ||||||
chr5:72162295
|
C | T | 142 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0063others(139): Show | 144 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.287-21448C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72162295 | ||||||
chr5:72162393
|
G | A | 30 | a0001c0001t0001g0083a0001c0001t0001g0182a0001c0001t0002g0210others(27): Show | 30 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.287-21350G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72162393 | ||||||
chr5:72162394
|
G | A | 8 | a0001c0001t0009g0239a0001c0001t0009g0240a0001c0001t0009g0241others(5): Show | 8 | NA18943.hp1 NA18955.hp1 NA18973.hp1 others(5): Show |
intron_variant | MODIFIER | c.287-21349G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72162394 | ||||||
chr5:72162403
|
CT | C | 6 | a0001c0001t0001g0220a0001c0004t0001g0330a0001c0005t0008g0030others(3): Show | 6 | HG00741.hp2 HG03098.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-21330delT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72162403 | |||||
chr5:72162602
|
A | C | 1 | a0001c0004t0010g0237 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.287-21141A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72162602 | ||||||
chr5:72162644
|
G | A | 243 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0063others(240): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.287-21099G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72162644 | ||||||
chr5:72162691
|
G | A | 2 | a0001c0006t0007g0260a0001c0020t0007g0261 | 2 | HG01167.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.287-21052G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72162691 | ||||||
chr5:72162704
|
G | C | 1 | a0001c0001t0002g0028 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.287-21039G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72162704 | ||||||
chr5:72162784
|
T | A | 1 | a0001c0004t0015g0304 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.287-20959T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72162784 | ||||||
chr5:72162992
|
G | A | 1 | a0001c0005t0008g0030 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.287-20751G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72162992 | ||||||
chr5:72163012
|
G | A | 1 | a0001c0001t0020g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.287-20731G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163012 | ||||||
chr5:72163172
|
G | A | 6 | a0001c0001t0001g0052a0001c0001t0004g0048a0001c0001t0007g0049others(3): Show | 6 | HG01070.hp1 HG01515.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-20571G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163172 | ||||||
chr5:72163185
|
G | A | 1 | a0001c0002t0002g0017 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.287-20558G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163185 | ||||||
chr5:72163227
|
C | CA | 14 | a0001c0001t0001g0071a0001c0001t0001g0336a0001c0001t0001g0338others(11): Show | 14 | HG01074.hp2 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.287-20495dupA | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72163227 | |||||
chr5:72163227
|
CA | C | 196 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0093others(193): Show | 198 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.287-20495delA | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72163227 | |||||
chr5:72163227
|
CAA | C | 35 | a0001c0001t0001g0083a0001c0001t0001g0182a0001c0001t0002g0210others(32): Show | 35 | HG00099.hp1 HG00558.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.287-20496_287-2049 others(6): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72163227 | |||||
chr5:72163245
|
A | G | 2 | a0001c0004t0015g0272a0001c0022t0002g0150 | 2 | HG04199.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.287-20498A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163245 | ||||||
chr5:72163307
|
A | G | 1 | a0001c0008t0002g0110 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.287-20436A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163307 | ||||||
chr5:72163322
|
G | A | 262 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0063others(259): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.287-20421G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163322 | ||||||
chr5:72163448
|
A | G | 1 | a0001c0001t0002g0028 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.287-20295A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163448 | ||||||
chr5:72163461
|
G | A | 11 | a0001c0001t0001g0071a0001c0001t0007g0116a0001c0002t0002g0108others(8): Show | 11 | HG01074.hp2 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.287-20282G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163461 | ||||||
chr5:72163497
|
C | G | 1 | a0001c0005t0020g0259 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.287-20246C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163497 | ||||||
chr5:72163639
|
C | T | 20 | a0001c0001t0001g0111a0001c0001t0001g0183a0001c0001t0001g0211others(17): Show | 20 | HG00621.hp1 HG00673.hp1 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.287-20104C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163639 | ||||||
chr5:72163643
|
A | C | 28 | a0001c0001t0001g0083a0001c0001t0001g0182a0001c0001t0002g0210others(25): Show | 28 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.287-20100A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163643 | ||||||
chr5:72163706
|
G | T | 8 | a0001c0001t0012g0053a0001c0001t0012g0054a0001c0001t0012g0314others(5): Show | 8 | HG02145.hp2 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.287-20037G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163706 | ||||||
chr5:72163904
|
T | C | 6 | a0001c0002t0003g0109a0001c0002t0003g0204a0001c0002t0013g0020others(3): Show | 6 | HG00621.hp2 HG00673.hp2 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-19839T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163904 | ||||||
chr5:72163916
|
CT | C | 7 | a0001c0001t0001g0264a0001c0001t0001g0267a0001c0002t0002g0217others(4): Show | 7 | HG01099.hp1 HG01884.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.287-19814delT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72163916 | |||||
chr5:72163917
|
TTTTTTTT others(6): Show |
T | 1 | a0001c0002t0003g0126 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.287-19813_287-1980 others(17): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72163917 | |||||
chr5:72163925
|
T | C | 1 | a0001c0004t0011g0326 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.287-19818T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163925 | ||||||
chr5:72163925
|
T | TC | 34 | a0001c0001t0001g0014a0001c0001t0001g0129a0001c0001t0001g0131others(31): Show | 35 | HG00140.hp1 HG00642.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.287-19818_287-1981 others(5): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163925 | ||||||
chr5:72163926
|
T | C | 248 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0063others(245): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.287-19817T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163926 | ||||||
chr5:72163927
|
T | C | 1 | a0001c0002t0003g0085 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.287-19816T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163927 | ||||||
chr5:72163928
|
TTC | T | 31 | a0001c0001t0001g0083a0001c0001t0001g0182a0001c0001t0002g0112others(28): Show | 31 | HG00558.hp2 HG00639.hp2 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.287-19813_287-1981 others(6): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72163928 | |||||
chr5:72163929
|
T | C | 1 | a0001c0002t0009g0236 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.287-19814T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163929 | ||||||
chr5:72163929
|
TC | T | 178 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0063others(175): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.287-19813delC | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163929 | ||||||
chr5:72163930
|
C | CT | 21 | a0001c0001t0001g0014a0001c0001t0001g0131a0001c0001t0001g0188others(18): Show | 21 | HG00140.hp1 HG00642.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.287-19792dupT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72163930 | |||||
chr5:72163930
|
C | CTT | 6 | a0001c0001t0001g0129a0001c0001t0001g0132a0001c0001t0001g0338others(3): Show | 7 | HG01884.hp1 HG02055.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.287-19793_287-1979 others(6): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72163930 | |||||
chr5:72163930
|
C | T | 48 | a0001c0001t0001g0101a0001c0001t0001g0183a0001c0001t0002g0292others(45): Show | 48 | HG00609.hp2 HG00621.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.287-19813C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163930 | ||||||
chr5:72163931
|
T | C | 11 | a0001c0001t0009g0239a0001c0001t0009g0240a0001c0001t0009g0241others(8): Show | 11 | HG02630.hp2 HG03041.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.287-19812T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163931 | ||||||
chr5:72163932
|
T | C | 17 | a0001c0001t0001g0071a0001c0001t0001g0220a0001c0001t0007g0116others(14): Show | 17 | HG00741.hp2 HG01074.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.287-19811T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163932 | ||||||
chr5:72163933
|
T | C | 1 | a0001c0005t0008g0030 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.287-19810T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163933 | ||||||
chr5:72163934
|
T | C | 6 | a0001c0001t0012g0053a0001c0001t0012g0054a0001c0001t0020g0128others(3): Show | 6 | HG02486.hp2 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-19809T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163934 | ||||||
chr5:72163935
|
T | C | 5 | a0001c0001t0001g0144a0001c0001t0015g0121a0001c0009t0007g0040others(2): Show | 5 | HG02145.hp2 HG02886.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.287-19808T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163935 | ||||||
chr5:72163939
|
T | C | 1 | a0001c0002t0003g0126 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.287-19804T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163939 | ||||||
chr5:72163987
|
A | G | 290 | a0001c0001t0001g0014a0001c0001t0001g0050a0001c0001t0001g0052others(287): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.287-19756A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163987 | ||||||
chr5:72163994
|
C | T | 243 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0063others(240): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.287-19749C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163994 | ||||||
chr5:72164168
|
T | G | 234 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0063others(231): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.287-19575T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72164168 | ||||||
chr5:72164169
|
G | T | 1 | a0001c0004t0011g0326 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.287-19574G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72164169 | ||||||
chr5:72164248
|
T | C | 2 | a0001c0006t0018g0035a0001c0006t0022g0036 | 2 | HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.287-19495T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72164248 | ||||||
chr5:72164414
|
G | A | 2 | a0001c0006t0007g0260a0001c0020t0007g0261 | 2 | HG01167.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.287-19329G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72164414 | ||||||
chr5:72164665
|
C | A | 3 | a0001c0002t0002g0203a0001c0002t0002g0205a0001c0008t0002g0110 | 3 | HG00621.hp1 HG02132.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.287-19078C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72164665 | ||||||
chr5:72164717
|
C | T | 1 | a0001c0001t0010g0007 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.287-19026C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72164717 | ||||||
chr5:72164868
|
T | G | 1 | a0001c0002t0013g0223 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.287-18875T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72164868 | ||||||
chr5:72164900
|
T | C | 2 | a0001c0006t0018g0035a0001c0006t0022g0036 | 2 | HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.287-18843T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72164900 | ||||||
chr5:72164993
|
T | C | 1 | a0001c0006t0018g0068 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.287-18750T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72164993 | ||||||
chr5:72165093
|
T | C | 1 | a0001c0002t0002g0106 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.287-18650T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72165093 | ||||||
chr5:72165151
|
T | C | 10 | a0001c0001t0001g0220a0001c0001t0009g0239a0001c0001t0009g0240others(7): Show | 10 | NA18943.hp1 NA18955.hp1 NA18973.hp1 others(7): Show |
intron_variant | MODIFIER | c.287-18592T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72165151 | ||||||
chr5:72165264
|
G | C | 1 | a0001c0002t0003g0308 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.287-18479G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72165264 | ||||||
chr5:72165267
|
C | T | 147 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0063others(144): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.287-18476C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72165267 | ||||||
chr5:72165347
|
G | A | 1 | a0001c0002t0002g0008 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.287-18396G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72165347 | ||||||
chr5:72165428
|
G | A | 2 | a0001c0009t0001g0059a0001c0009t0001g0060 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.287-18315G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72165428 | ||||||
chr5:72165642
|
T | C | 42 | a0001c0001t0001g0063a0001c0001t0001g0101a0001c0001t0001g0127others(39): Show | 42 | HG00140.hp2 HG00621.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.287-18101T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72165642 | ||||||
chr5:72165662
|
T | C | 25 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(22): Show | 26 | HG00140.hp1 HG00741.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.287-18081T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72165662 | ||||||
chr5:72165753
|
C | T | 1 | a0003c0007t0002g0119 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.287-17990C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72165753 | ||||||
chr5:72165780
|
A | T | 2 | a0001c0001t0004g0196a0001c0004t0017g0061 | 2 | HG01255.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.287-17963A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72165780 | ||||||
chr5:72165900
|
C | T | 3 | a0001c0001t0015g0121a0001c0034t0005g0033a0016c0035t0005g0044 | 3 | HG02145.hp2 HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.287-17843C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72165900 | ||||||
chr5:72165984
|
A | G | 1 | a0001c0001t0019g0238 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.287-17759A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72165984 | ||||||
chr5:72166238
|
C | T | 50 | a0001c0001t0001g0111a0001c0001t0001g0117a0001c0001t0001g0160others(47): Show | 50 | HG00099.hp1 HG00621.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.287-17505C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72166238 | ||||||
chr5:72166283
|
C | G | 11 | a0001c0001t0001g0071a0001c0001t0007g0116a0001c0002t0002g0108others(8): Show | 11 | HG01074.hp2 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.287-17460C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72166283 | ||||||
chr5:72166329
|
C | T | 1 | a0001c0002t0003g0309 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.287-17414C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72166329 | ||||||
chr5:72166518
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.287-17225C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72166518 | ||||||
chr5:72166646
|
C | T | 1 | a0001c0034t0005g0033 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.287-17097C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72166646 | ||||||
chr5:72166682
|
C | T | 2 | a0001c0001t0001g0111a0001c0001t0010g0246 | 2 | NA18941.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.287-17061C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72166682 | ||||||
chr5:72166800
|
T | G | 8 | a0001c0001t0009g0239a0001c0001t0009g0240a0001c0001t0009g0241others(5): Show | 8 | NA18943.hp1 NA18955.hp1 NA18973.hp1 others(5): Show |
intron_variant | MODIFIER | c.287-16943T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72166800 | ||||||
chr5:72166805
|
T | C | 290 | a0001c0001t0001g0014a0001c0001t0001g0050a0001c0001t0001g0052others(287): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.287-16938T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72166805 | ||||||
chr5:72166899
|
G | A | 1 | a0001c0002t0003g0175 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.287-16844G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72166899 | ||||||
chr5:72166915
|
G | A | 4 | a0001c0001t0001g0144a0001c0009t0007g0040a0001c0028t0025g0039others(1): Show | 4 | HG02886.hp2 HG03041.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-16828G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72166915 | ||||||
chr5:72166992
|
T | G | 4 | a0001c0001t0001g0188a0001c0001t0001g0311a0001c0001t0001g0312others(1): Show | 4 | HG00140.hp1 HG01106.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-16751T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72166992 | ||||||
chr5:72166996
|
T | G | 1 | a0003c0007t0002g0080 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.287-16747T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72166996 | ||||||
chr5:72167010
|
T | G | 4 | a0001c0002t0003g0087a0001c0002t0013g0018a0001c0002t0013g0226others(1): Show | 4 | HG00140.hp2 HG01255.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-16733T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72167010 | ||||||
chr5:72167016
|
C | CT | 19 | a0001c0001t0001g0220a0001c0001t0001g0319a0001c0001t0004g0213others(16): Show | 19 | HG01358.hp2 HG01433.hp1 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.287-16711dupT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72167016 | |||||
chr5:72167016
|
C | T | 5 | a0001c0001t0001g0014a0001c0001t0001g0144a0001c0009t0007g0040others(2): Show | 5 | HG00642.hp1 HG02886.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.287-16727C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72167016 | ||||||
chr5:72167016
|
CT | C | 6 | a0001c0001t0007g0270a0001c0002t0002g0276a0001c0005t0008g0038others(3): Show | 6 | HG00741.hp2 HG03130.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.287-16711delT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72167016 | |||||
chr5:72167016
|
CTT | C | 113 | a0001c0001t0001g0071a0001c0001t0001g0083a0001c0001t0001g0129others(110): Show | 114 | HG00140.hp1 HG00408.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.287-16712_287-1671 others(6): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72167016 | |||||
chr5:72167029
|
T | C | 3 | a0001c0004t0007g0140a0001c0006t0007g0260a0001c0020t0007g0261 | 3 | HG01167.hp2 HG01243.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.287-16714T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72167029 | ||||||
chr5:72167322
|
A | G | 1 | a0001c0002t0002g0315 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.287-16421A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72167322 | ||||||
chr5:72167440
|
T | C | 11 | a0001c0001t0001g0071a0001c0001t0007g0116a0001c0002t0002g0108others(8): Show | 11 | HG01074.hp2 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.287-16303T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72167440 | ||||||
chr5:72167668
|
C | T | 8 | a0001c0001t0009g0239a0001c0001t0009g0240a0001c0001t0009g0241others(5): Show | 8 | NA18943.hp1 NA18955.hp1 NA18973.hp1 others(5): Show |
intron_variant | MODIFIER | c.287-16075C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72167668 | ||||||
chr5:72167711
|
A | G | 1 | a0013c0031t0003g0046 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.287-16032A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72167711 | ||||||
chr5:72167774
|
AC | A | 7 | a0001c0001t0001g0014a0001c0001t0001g0144a0001c0005t0005g0155others(4): Show | 7 | HG00642.hp1 HG02451.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.287-15966delC | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72167774 | |||||
chr5:72167909
|
C | G | 2 | a0001c0006t0007g0260a0001c0020t0007g0261 | 2 | HG01167.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.287-15834C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72167909 | ||||||
chr5:72167910
|
A | G | 1 | a0001c0002t0003g0173 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.287-15833A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72167910 | ||||||
chr5:72168006
|
C | T | 1 | a0001c0001t0019g0247 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.287-15737C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72168006 | ||||||
chr5:72168010
|
C | T | 9 | a0001c0002t0002g0092a0002c0003t0006g0142a0002c0003t0006g0143others(6): Show | 9 | HG00735.hp1 HG00738.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.287-15733C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72168010 | ||||||
chr5:72168060
|
G | C | 2 | a0001c0001t0001g0164a0001c0001t0005g0156 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.287-15683G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72168060 | ||||||
chr5:72168353
|
C | T | 11 | a0001c0001t0001g0071a0001c0001t0007g0116a0001c0002t0002g0108others(8): Show | 11 | HG01074.hp2 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.287-15390C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72168353 | ||||||
chr5:72168417
|
G | A | 11 | a0001c0001t0001g0071a0001c0001t0007g0116a0001c0002t0002g0108others(8): Show | 11 | HG01074.hp2 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.287-15326G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72168417 | ||||||
chr5:72168441
|
T | C | 121 | a0001c0001t0001g0071a0001c0001t0001g0083a0001c0001t0001g0129others(118): Show | 122 | HG00140.hp1 HG00408.hp2 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.287-15302T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72168441 | ||||||
chr5:72168483
|
C | T | 1 | a0001c0001t0015g0113 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.287-15260C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72168483 | ||||||
chr5:72168587
|
C | T | 1 | a0001c0002t0002g0169 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.287-15156C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72168587 | ||||||
chr5:72168640
|
G | A | 74 | a0001c0001t0001g0083a0001c0001t0001g0164a0001c0001t0001g0182others(71): Show | 74 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.287-15103G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72168640 | ||||||
chr5:72169027
|
G | C | 143 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0083others(140): Show | 144 | HG00140.hp1 HG00408.hp2 HG00558.hp2 others(141): Show |
intron_variant | MODIFIER | c.287-14716G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72169027 | ||||||
chr5:72169150
|
C | T | 4 | a0001c0001t0012g0053a0001c0001t0012g0054a0001c0001t0020g0128others(1): Show | 4 | HG02486.hp2 HG02559.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-14593C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72169150 | ||||||
chr5:72169344
|
C | G | 74 | a0001c0001t0001g0083a0001c0001t0001g0164a0001c0001t0001g0182others(71): Show | 74 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.287-14399C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72169344 | ||||||
chr5:72169513
|
A | C | 1 | a0001c0001t0020g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.287-14230A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72169513 | ||||||
chr5:72169534
|
T | A | 119 | a0001c0001t0001g0071a0001c0001t0001g0083a0001c0001t0001g0129others(116): Show | 120 | HG00140.hp1 HG00408.hp2 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.287-14209T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72169534 | ||||||
chr5:72169834
|
T | C | 1 | a0001c0001t0012g0314 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.287-13909T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72169834 | ||||||
chr5:72169907
|
A | G | 23 | a0001c0001t0001g0014a0001c0001t0001g0144a0001c0001t0001g0220others(20): Show | 23 | HG00642.hp1 HG00741.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.287-13836A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72169907 | ||||||
chr5:72170028
|
T | G | 1 | a0001c0002t0003g0084 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.287-13715T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72170028 | ||||||
chr5:72170094
|
G | T | 27 | a0001c0001t0001g0014a0001c0001t0001g0041a0001c0001t0001g0144others(24): Show | 27 | HG00642.hp1 HG00741.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.287-13649G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72170094 | ||||||
chr5:72170231
|
CAAGGGCC others(1): Show |
C | 22 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(19): Show | 23 | HG00140.hp1 HG01106.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.287-13511_287-1350 others(12): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72170231 | ||||||
chr5:72170366
|
G | T | 1 | a0001c0001t0012g0314 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.287-13377G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72170366 | ||||||
chr5:72170449
|
C | A | 3 | a0001c0001t0012g0053a0001c0001t0012g0054a0001c0039t0018g0013 | 3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.287-13294C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72170449 | ||||||
chr5:72170802
|
C | G | 3 | a0001c0005t0008g0038a0007c0013t0001g0123a0007c0013t0029g0124 | 3 | HG00741.hp2 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.287-12941C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72170802 | ||||||
chr5:72170806
|
A | G | 143 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0083others(140): Show | 144 | HG00140.hp1 HG00408.hp2 HG00558.hp2 others(141): Show |
intron_variant | MODIFIER | c.287-12937A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72170806 | ||||||
chr5:72170875
|
A | AG | 74 | a0001c0001t0001g0083a0001c0001t0001g0164a0001c0001t0001g0182others(71): Show | 74 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.287-12866dupG | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72170875 | |||||
chr5:72170942
|
C | T | 3 | a0001c0001t0015g0121a0001c0034t0005g0033a0016c0035t0005g0044 | 3 | HG02145.hp2 HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.287-12801C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72170942 | ||||||
chr5:72171176
|
T | C | 24 | a0001c0001t0001g0014a0001c0001t0001g0144a0001c0001t0001g0220others(21): Show | 24 | HG00642.hp1 HG00741.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.287-12567T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72171176 | ||||||
chr5:72171243
|
G | A | 18 | a0001c0001t0001g0111a0001c0001t0001g0183a0001c0001t0001g0313others(15): Show | 18 | HG00621.hp1 HG00673.hp1 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.287-12500G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72171243 | ||||||
chr5:72171292
|
T | A | 1 | a0004c0010t0005g0133 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.287-12451T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72171292 | ||||||
chr5:72171352
|
C | T | 119 | a0001c0001t0001g0071a0001c0001t0001g0083a0001c0001t0001g0129others(116): Show | 120 | HG00140.hp1 HG00408.hp2 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.287-12391C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72171352 | ||||||
chr5:72171372
|
G | A | 18 | a0001c0001t0001g0014a0001c0001t0001g0144a0001c0001t0001g0220others(15): Show | 18 | HG00642.hp1 HG00741.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.287-12371G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72171372 | ||||||
chr5:72171505
|
A | G | 144 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0083others(141): Show | 145 | HG00140.hp1 HG00408.hp2 HG00558.hp2 others(142): Show |
intron_variant | MODIFIER | c.287-12238A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72171505 | ||||||
chr5:72171597
|
A | T | 3 | a0001c0001t0003g0325a0001c0001t0004g0025a0001c0001t0004g0324 | 3 | HG01934.hp2 HG03579.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.287-12146A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72171597 | ||||||
chr5:72171635
|
A | G | 1 | a0001c0004t0015g0186 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.287-12108A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72171635 | ||||||
chr5:72171689
|
T | G | 2 | a0001c0005t0001g0005a0001c0005t0001g0271 | 2 | HG01884.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.287-12054T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72171689 | ||||||
chr5:72171820
|
G | A | 1 | a0001c0002t0003g0175 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.287-11923G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72171820 | ||||||
chr5:72171843
|
T | C | 74 | a0001c0001t0001g0083a0001c0001t0001g0164a0001c0001t0001g0182others(71): Show | 74 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.287-11900T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72171843 | ||||||
chr5:72171871
|
C | T | 1 | a0001c0004t0017g0191 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.287-11872C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72171871 | ||||||
chr5:72172109
|
C | T | 8 | a0001c0001t0001g0336a0001c0001t0012g0053a0001c0001t0012g0054others(5): Show | 8 | HG02145.hp2 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.287-11634C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72172109 | ||||||
chr5:72172135
|
G | T | 1 | a0002c0003t0006g0047 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.287-11608G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72172135 | ||||||
chr5:72172233
|
C | A | 1 | a0001c0002t0002g0002 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.287-11510C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72172233 | ||||||
chr5:72172279
|
C | T | 2 | a0007c0013t0001g0123a0007c0013t0029g0124 | 2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.287-11464C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72172279 | ||||||
chr5:72172522
|
T | C | 1 | a0001c0001t0001g0211 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.287-11221T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72172522 | ||||||
chr5:72172769
|
T | C | 1 | a0001c0004t0015g0272 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.287-10974T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72172769 | ||||||
chr5:72172841
|
C | T | 18 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(15): Show | 19 | HG00140.hp1 HG01106.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.287-10902C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72172841 | ||||||
chr5:72172974
|
T | C | 23 | a0001c0001t0001g0220a0001c0001t0001g0338a0001c0001t0009g0239others(20): Show | 23 | HG00741.hp1 HG02055.hp2 HG02559.hp1 others(20): Show |
intron_variant | MODIFIER | c.287-10769T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72172974 | ||||||
chr5:72173067
|
C | T | 1 | a0001c0001t0014g0091 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.287-10676C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72173067 | ||||||
chr5:72173183
|
T | C | 1 | a0001c0004t0017g0165 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.287-10560T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72173183 | ||||||
chr5:72173209
|
C | T | 1 | a0001c0002t0003g0118 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.287-10534C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72173209 | ||||||
chr5:72173312
|
G | A | 3 | a0001c0002t0011g0154a0001c0002t0014g0001a0001c0002t0016g0153 | 4 | HG01884.hp1 HG02922.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-10431G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72173312 | ||||||
chr5:72173629
|
C | A | 4 | a0001c0001t0015g0121a0001c0002t0003g0204a0001c0034t0005g0033others(1): Show | 4 | HG02015.hp1 HG02145.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-10114C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72173629 | ||||||
chr5:72173818
|
C | T | 2 | a0001c0006t0007g0260a0001c0020t0007g0261 | 2 | HG01167.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.287-9925C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72173818 | ||||||
chr5:72173819
|
C | G | 2 | a0001c0006t0007g0260a0001c0020t0007g0261 | 2 | HG01167.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.287-9924C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72173819 | ||||||
chr5:72173954
|
C | A | 216 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0041others(213): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.287-9789C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72173954 | ||||||
chr5:72173964
|
C | T | 22 | a0001c0001t0001g0093a0001c0001t0001g0115a0001c0001t0001g0120others(19): Show | 23 | HG00609.hp2 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.287-9779C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72173964 | ||||||
chr5:72174054
|
C | T | 22 | a0001c0001t0001g0093a0001c0001t0001g0115a0001c0001t0001g0120others(19): Show | 23 | HG00609.hp2 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.287-9689C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72174054 | ||||||
chr5:72174072
|
G | T | 208 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0041others(205): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.287-9671G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72174072 | ||||||
chr5:72174306
|
A | G | 2 | a0001c0001t0007g0116a0001c0005t0008g0107 | 2 | HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.287-9437A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72174306 | ||||||
chr5:72174335
|
T | C | 1 | a0001c0002t0003g0058 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.287-9408T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72174335 | ||||||
chr5:72174366
|
C | G | 221 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0041others(218): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.287-9377C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72174366 | ||||||
chr5:72174438
|
C | T | 1 | a0001c0002t0003g0058 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.287-9305C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72174438 | ||||||
chr5:72174595
|
C | G | 223 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0041others(220): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.287-9148C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72174595 | ||||||
chr5:72174621
|
C | T | 5 | a0001c0001t0012g0031a0001c0001t0012g0053a0001c0001t0012g0054others(2): Show | 5 | HG02559.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.287-9122C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72174621 | ||||||
chr5:72174663
|
C | T | 1 | a0016c0035t0005g0044 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.287-9080C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72174663 | ||||||
chr5:72174783
|
C | T | 2 | a0001c0006t0007g0260a0001c0020t0007g0261 | 2 | HG01167.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.287-8960C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72174783 | ||||||
chr5:72174875
|
T | TCTTC | 219 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0041others(216): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.287-8850_287-8847d others(6): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72174875 | |||||
chr5:72174875
|
TCTTCCTT others(1): Show |
T | 3 | a0001c0001t0015g0121a0001c0034t0005g0033a0016c0035t0005g0044 | 3 | HG02145.hp2 HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.287-8854_287-8847d others(10): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72174875 | |||||
chr5:72174897
|
C | T | 1 | a0001c0002t0003g0290 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.287-8846C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72174897 | ||||||
chr5:72174996
|
TCCTTCCT others(10): Show |
T | 1 | a0001c0001t0001g0146 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.287-8726_287-8710d others(19): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72174996 | |||||
chr5:72175013
|
CCCTT | C | 9 | a0001c0001t0001g0220a0001c0001t0009g0239a0001c0001t0009g0240others(6): Show | 9 | NA18943.hp1 NA18955.hp1 NA18973.hp1 others(6): Show |
intron_variant | MODIFIER | c.287-8723_287-8720d others(6): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72175013 | |||||
chr5:72175017
|
TCCTTCCC others(10): Show |
T | 1 | a0001c0001t0012g0314 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.287-8707_287-8691d others(19): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72175017 | |||||
chr5:72175038
|
T | C | 3 | a0001c0001t0015g0121a0001c0034t0005g0033a0016c0035t0005g0044 | 3 | HG02145.hp2 HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.287-8705T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72175038 | ||||||
chr5:72175086
|
A | G | 9 | a0001c0001t0001g0338a0001c0001t0012g0031a0001c0001t0012g0053others(6): Show | 9 | HG00741.hp1 HG02055.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.287-8657A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72175086 | ||||||
chr5:72175134
|
G | A | 9 | a0001c0001t0001g0338a0001c0001t0012g0031a0001c0001t0012g0053others(6): Show | 9 | HG00741.hp1 HG02055.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.287-8609G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72175134 | ||||||
chr5:72175135
|
G | A | 1 | a0001c0009t0007g0040 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.287-8608G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72175135 | ||||||
chr5:72175196
|
C | G | 1 | a0001c0028t0025g0039 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.287-8547C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72175196 | ||||||
chr5:72175258
|
T | A | 1 | a0001c0002t0002g0187 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.287-8485T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72175258 | ||||||
chr5:72175436
|
C | A | 2 | a0001c0001t0004g0025a0001c0001t0004g0324 | 2 | HG01934.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.287-8307C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72175436 | ||||||
chr5:72175487
|
T | C | 50 | a0001c0001t0001g0006a0001c0001t0001g0111a0001c0001t0001g0117others(47): Show | 50 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.287-8256T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72175487 | ||||||
chr5:72175502
|
C | T | 198 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0041others(195): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.287-8241C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72175502 | ||||||
chr5:72175601
|
T | C | 3 | a0001c0005t0008g0038a0007c0013t0001g0123a0007c0013t0029g0124 | 3 | HG00741.hp2 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.287-8142T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72175601 | ||||||
chr5:72175736
|
G | GCACATGG others(3): Show |
1 | a0001c0001t0002g0210 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.287-8006_287-7997d others(12): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72175736 | |||||
chr5:72175742
|
G | A | 1 | a0001c0001t0012g0145 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.287-8001G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72175742 | ||||||
chr5:72175797
|
C | A | 7 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0004g0048others(4): Show | 7 | HG01070.hp1 HG01123.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.287-7946C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72175797 | ||||||
chr5:72175886
|
T | C | 66 | a0001c0001t0001g0006a0001c0001t0001g0111a0001c0001t0001g0117others(63): Show | 66 | HG00621.hp1 HG00639.hp1 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.287-7857T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72175886 | ||||||
chr5:72176191
|
CCACACAC others(11): Show |
C | 1 | a0002c0003t0006g0195 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.287-7550_287-7533d others(20): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72176191 | |||||
chr5:72176193
|
A | G | 65 | a0001c0001t0001g0006a0001c0001t0001g0111a0001c0001t0001g0117others(62): Show | 65 | HG00621.hp1 HG00639.hp1 HG00673.hp1 others(62): Show |
intron_variant | MODIFIER | c.287-7550A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72176193 | ||||||
chr5:72176328
|
A | C | 3 | a0001c0004t0007g0140a0001c0006t0007g0260a0001c0020t0007g0261 | 3 | HG01167.hp2 HG01243.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.287-7415A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72176328 | ||||||
chr5:72176331
|
T | G | 1 | a0001c0005t0008g0030 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.287-7412T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72176331 | ||||||
chr5:72176393
|
G | A | 6 | a0001c0001t0001g0291a0001c0002t0002g0181a0001c0002t0003g0308others(3): Show | 6 | HG02056.hp2 HG02074.hp2 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-7350G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72176393 | ||||||
chr5:72176422
|
C | G | 1 | a0001c0001t0012g0314 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.287-7321C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72176422 | ||||||
chr5:72176466
|
C | G | 1 | a0001c0001t0019g0238 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.287-7277C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72176466 | ||||||
chr5:72176471
|
G | A | 1 | a0001c0001t0002g0069 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.287-7272G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72176471 | ||||||
chr5:72176561
|
G | A | 3 | a0001c0002t0011g0154a0001c0002t0014g0001a0001c0002t0016g0153 | 4 | HG01884.hp1 HG02922.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-7182G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72176561 | ||||||
chr5:72176588
|
A | G | 2 | a0001c0001t0004g0025a0001c0001t0004g0324 | 2 | HG01934.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.287-7155A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72176588 | ||||||
chr5:72176622
|
T | C | 1 | a0001c0001t0001g0336 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.287-7121T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72176622 | ||||||
chr5:72176638
|
A | G | 3 | a0001c0004t0001g0337a0001c0005t0008g0335a0004c0010t0005g0334 | 3 | HG02630.hp2 HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.287-7105A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72176638 | ||||||
chr5:72176697
|
G | A | 1 | a0002c0003t0006g0047 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.287-7046G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72176697 | ||||||
chr5:72176705
|
G | T | 14 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(11): Show | 14 | HG00140.hp1 HG01106.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.287-7038G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72176705 | ||||||
chr5:72176756
|
C | T | 3 | a0001c0001t0002g0189a0002c0015t0016g0016a0002c0015t0016g0206 | 3 | HG00609.hp1 HG02523.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.287-6987C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72176756 | ||||||
chr5:72176758
|
C | T | 1 | a0014c0033t0009g0234 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.287-6985C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72176758 | ||||||
chr5:72176869
|
C | T | 3 | a0001c0004t0001g0337a0001c0005t0008g0335a0004c0010t0005g0334 | 3 | HG02630.hp2 HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.287-6874C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72176869 | ||||||
chr5:72177009
|
G | A | 6 | a0001c0001t0012g0031a0001c0001t0012g0053a0001c0001t0012g0054others(3): Show | 6 | HG02559.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.287-6734G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72177009 | ||||||
chr5:72177077
|
C | A | 10 | a0001c0001t0001g0071a0001c0001t0007g0116a0001c0002t0002g0108others(7): Show | 10 | HG01074.hp2 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.287-6666C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72177077 | ||||||
chr5:72177294
|
C | T | 1 | a0001c0005t0008g0038 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.287-6449C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72177294 | ||||||
chr5:72177350
|
T | C | 1 | a0002c0003t0023g0243 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.287-6393T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72177350 | ||||||
chr5:72177358
|
T | TAGAAATG others(324): Show |
1 | a0001c0001t0012g0145 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.287-6368_287-6367i others(333): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72177358 | |||||
chr5:72177358
|
T | TAGAAATG others(323): Show |
5 | a0001c0001t0012g0031a0001c0001t0012g0053a0001c0001t0012g0054others(2): Show | 5 | HG02895.hp1 HG02897.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.287-6368_287-6367i others(332): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72177358 | |||||
chr5:72177580
|
G | A | 3 | a0001c0001t0001g0264a0001c0002t0002g0217a0001c0002t0002g0268 | 3 | HG01099.hp1 HG02622.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.287-6163G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72177580 | ||||||
chr5:72177898
|
A | T | 2 | a0001c0001t0002g0147a0001c0002t0002g0010 | 2 | HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.287-5845A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72177898 | ||||||
chr5:72178025
|
C | T | 1 | a0001c0002t0001g0015 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.287-5718C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72178025 | ||||||
chr5:72178054
|
G | C | 1 | a0001c0001t0001g0114 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.287-5689G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72178054 | ||||||
chr5:72178078
|
C | T | 6 | a0001c0001t0012g0031a0001c0001t0012g0053a0001c0001t0012g0054others(3): Show | 6 | HG02559.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.287-5665C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72178078 | ||||||
chr5:72178121
|
G | T | 3 | a0001c0001t0001g0144a0004c0010t0005g0133a0004c0010t0005g0332 | 3 | HG02647.hp1 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.287-5622G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72178121 | ||||||
chr5:72178232
|
A | G | 1 | a0001c0001t0020g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.287-5511A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72178232 | ||||||
chr5:72178245
|
C | T | 2 | a0001c0002t0002g0298a0001c0002t0003g0288 | 2 | NA18977.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.287-5498C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72178245 | ||||||
chr5:72178246
|
A | G | 3 | a0001c0002t0002g0029a0001c0002t0002g0298a0001c0002t0003g0288 | 3 | NA18955.hp1 NA18977.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.287-5497A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72178246 | ||||||
chr5:72178268
|
C | G | 1 | a0001c0004t0017g0191 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.287-5475C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72178268 | ||||||
chr5:72178314
|
C | T | 3 | a0001c0002t0011g0154a0001c0002t0014g0001a0001c0002t0016g0153 | 4 | HG01884.hp1 HG02922.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-5429C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72178314 | ||||||
chr5:72178371
|
T | G | 7 | a0001c0002t0002g0108a0001c0004t0001g0337a0001c0009t0007g0040others(4): Show | 7 | HG01074.hp2 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.287-5372T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72178371 | ||||||
chr5:72178388
|
G | A | 1 | a0016c0035t0005g0044 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.287-5355G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72178388 | ||||||
chr5:72178447
|
C | T | 63 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0041others(60): Show | 64 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.287-5296C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72178447 | ||||||
chr5:72178460
|
C | T | 199 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0024others(196): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.287-5283C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72178460 | ||||||
chr5:72178725
|
G | GGT | 69 | a0001c0001t0001g0052a0001c0001t0001g0083a0001c0001t0001g0144others(66): Show | 70 | HG00558.hp1 HG00609.hp2 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.287-4973_287-4972d others(4): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72178725 | |||||
chr5:72178725
|
G | GGTGT | 25 | a0001c0001t0001g0041a0001c0001t0001g0146a0001c0001t0001g0267others(22): Show | 25 | HG00621.hp1 HG00621.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.287-4975_287-4972d others(6): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72178725 | |||||
chr5:72178725
|
G | GGTGTGT | 7 | a0001c0001t0001g0014a0001c0001t0002g0112a0001c0001t0010g0232others(4): Show | 7 | HG00642.hp1 HG02080.hp2 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.287-4977_287-4972d others(8): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72178725 | |||||
chr5:72178725
|
G | GT | 3 | a0001c0002t0002g0181a0001c0002t0002g0214a0001c0017t0003g0070 | 3 | NA18944.hp1 NA18983.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.287-5018_287-5017i others(3): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72178725 | ||||||
chr5:72178725
|
G | T | 1 | a0001c0002t0003g0175 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.287-5018G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72178725 | ||||||
chr5:72178725
|
GGT | G | 99 | a0001c0001t0001g0006a0001c0001t0001g0050a0001c0001t0001g0115others(96): Show | 101 | HG00408.hp1 HG00609.hp1 HG00642.hp2 others(98): Show |
intron_variant | MODIFIER | c.287-4973_287-4972d others(4): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72178725 | |||||
chr5:72178725
|
GGTGT | G | 14 | a0001c0001t0001g0188a0001c0001t0004g0081a0001c0001t0012g0031others(11): Show | 15 | HG00099.hp2 HG00735.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.287-4975_287-4972d others(6): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72178725 | |||||
chr5:72178725
|
GGTGTGTG others(3): Show |
G | 1 | a0001c0001t0012g0145 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.287-4981_287-4972d others(12): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72178725 | |||||
chr5:72178725
|
GGTGTGTG others(19): Show |
G | 1 | a0001c0004t0001g0337 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.287-4997_287-4972d others(28): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72178725 | |||||
chr5:72178727
|
T | G | 17 | a0001c0001t0001g0111a0001c0001t0001g0183a0001c0001t0001g0319others(14): Show | 17 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.287-5016T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72178727 | ||||||
chr5:72178729
|
T | G | 2 | a0001c0004t0007g0140a0001c0005t0008g0335 | 2 | HG02630.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.287-5014T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72178729 | ||||||
chr5:72179038
|
C | T | 3 | a0007c0013t0001g0123a0007c0013t0001g0265a0007c0013t0029g0124 | 3 | HG03130.hp1 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.287-4705C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72179038 | ||||||
chr5:72179105
|
C | T | 1 | a0001c0028t0025g0039 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.287-4638C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72179105 | ||||||
chr5:72179106
|
G | A | 1 | a0001c0004t0017g0191 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.287-4637G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72179106 | ||||||
chr5:72179129
|
A | G | 37 | a0001c0001t0001g0006a0001c0001t0001g0041a0001c0001t0001g0052others(34): Show | 37 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.287-4614A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72179129 | ||||||
chr5:72179318
|
G | A | 1 | a0002c0015t0016g0206 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.287-4425G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72179318 | ||||||
chr5:72179599
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.287-4144G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72179599 | ||||||
chr5:72179601
|
G | A | 9 | a0001c0001t0005g0139a0001c0001t0007g0270a0001c0005t0008g0030others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.287-4142G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72179601 | ||||||
chr5:72179785
|
C | A | 1 | a0001c0002t0002g0108 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.287-3958C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72179785 | ||||||
chr5:72179859
|
T | C | 1 | a0001c0002t0003g0118 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.287-3884T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72179859 | ||||||
chr5:72179948
|
C | G | 165 | a0001c0001t0001g0006a0001c0001t0001g0041a0001c0001t0001g0050others(162): Show | 167 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(164): Show |
intron_variant | MODIFIER | c.287-3795C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72179948 | ||||||
chr5:72180015
|
G | A | 2 | a0008c0016t0001g0262a0008c0016t0001g0333 | 2 | HG00741.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.287-3728G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72180015 | ||||||
chr5:72180024
|
C | A | 28 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(25): Show | 29 | HG00642.hp2 HG00733.hp2 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.287-3719C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72180024 | ||||||
chr5:72180268
|
C | T | 1 | a0001c0005t0008g0107 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.287-3475C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72180268 | ||||||
chr5:72180459
|
T | C | 1 | a0001c0005t0008g0335 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.287-3284T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72180459 | ||||||
chr5:72180904
|
T | C | 1 | a0001c0001t0001g0160 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.287-2839T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72180904 | ||||||
chr5:72180965
|
G | A | 1 | a0001c0001t0001g0257 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.287-2778G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72180965 | ||||||
chr5:72181078
|
C | T | 44 | a0001c0001t0001g0006a0001c0001t0001g0083a0001c0001t0001g0093others(41): Show | 45 | HG00099.hp2 HG00621.hp1 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.287-2665C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72181078 | ||||||
chr5:72181124
|
T | C | 10 | a0001c0001t0021g0269a0001c0002t0013g0226a0001c0004t0001g0337others(7): Show | 10 | HG01167.hp2 HG01255.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.287-2619T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72181124 | ||||||
chr5:72181130
|
G | A | 221 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0063others(218): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.287-2613G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72181130 | ||||||
chr5:72181288
|
G | A | 166 | a0001c0001t0001g0050a0001c0001t0001g0129a0001c0001t0001g0131others(163): Show | 166 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(163): Show |
intron_variant | MODIFIER | c.287-2455G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72181288 | ||||||
chr5:72181482
|
G | C | 1 | a0001c0002t0002g0002 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.287-2261G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72181482 | ||||||
chr5:72181723
|
A | AT | 172 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0041others(169): Show | 174 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(171): Show |
intron_variant | MODIFIER | c.287-2004dupT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72181723 | |||||
chr5:72181723
|
A | ATT | 83 | a0001c0001t0001g0006a0001c0001t0002g0069a0001c0001t0002g0076others(80): Show | 83 | HG00408.hp1 HG00642.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.287-2005_287-2004d others(4): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72181723 | |||||
chr5:72181755
|
A | G | 1 | a0001c0004t0005g0104 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.287-1988A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72181755 | ||||||
chr5:72181823
|
G | A | 12 | a0001c0002t0014g0001a0001c0002t0016g0153a0001c0005t0001g0307others(9): Show | 13 | HG01167.hp2 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.287-1920G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72181823 | ||||||
chr5:72181824
|
C | T | 12 | a0001c0002t0002g0108a0001c0005t0008g0030a0001c0005t0008g0032others(9): Show | 12 | HG02145.hp1 HG02280.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.287-1919C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72181824 | ||||||
chr5:72181842
|
A | G | 3 | a0001c0005t0005g0125a0001c0005t0005g0155a0001c0005t0005g0258 | 3 | HG02257.hp1 HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.287-1901A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72181842 | ||||||
chr5:72182023
|
C | CT | 35 | a0001c0001t0001g0146a0001c0001t0035g0303a0001c0002t0002g0108others(32): Show | 36 | HG00558.hp1 HG00738.hp2 HG01168.hp2 others(33): Show |
intron_variant | MODIFIER | c.287-1699dupT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72182023 | |||||
chr5:72182023
|
C | CTT | 13 | a0001c0001t0001g0083a0001c0001t0001g0127a0001c0001t0001g0211others(10): Show | 13 | HG02015.hp2 HG02135.hp2 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.287-1700_287-1699d others(4): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72182023 | |||||
chr5:72182023
|
C | CTTT | 73 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0041others(70): Show | 73 | HG00140.hp1 HG00609.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.287-1701_287-1699d others(5): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72182023 | |||||
chr5:72182023
|
C | CTTTT | 17 | a0001c0001t0001g0024a0001c0001t0001g0250a0001c0001t0001g0278others(14): Show | 17 | HG00673.hp1 HG01192.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.287-1702_287-1699d others(6): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72182023 | |||||
chr5:72182023
|
CT | C | 8 | a0001c0001t0001g0220a0001c0001t0004g0048a0001c0001t0004g0081others(5): Show | 8 | HG00735.hp2 HG01168.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.287-1699delT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72182023 | |||||
chr5:72182023
|
CTT | C | 44 | a0001c0001t0002g0069a0001c0001t0002g0076a0001c0001t0002g0112others(41): Show | 44 | HG00408.hp1 HG00642.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.287-1700_287-1699d others(4): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72182023 | |||||
chr5:72182023
|
CTTT | C | 10 | a0001c0005t0001g0307a0001c0006t0005g0064a0001c0006t0007g0260others(7): Show | 10 | HG01167.hp2 HG01243.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.287-1701_287-1699d others(5): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72182023 | |||||
chr5:72182023
|
CTTTTTT | C | 55 | a0001c0001t0001g0063a0001c0001t0001g0093a0001c0001t0001g0111others(52): Show | 56 | HG00558.hp2 HG00621.hp1 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.287-1704_287-1699d others(8): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72182023 | |||||
chr5:72182050
|
C | A | 18 | a0001c0001t0001g0273a0001c0001t0001g0275a0001c0001t0001g0277others(15): Show | 18 | HG00609.hp2 HG02056.hp2 NA18942.hp1 others(15): Show |
intron_variant | MODIFIER | c.287-1693C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72182050 | ||||||
chr5:72182185
|
A | G | 2 | a0001c0004t0022g0034a0001c0028t0025g0039 | 2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.287-1558A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72182185 | ||||||
chr5:72182195
|
C | T | 3 | a0001c0002t0013g0018a0001c0002t0013g0226a0001c0002t0013g0227 | 3 | HG01255.hp2 HG01346.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.287-1548C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72182195 | ||||||
chr5:72182438
|
C | T | 6 | a0001c0001t0001g0063a0001c0001t0001g0111a0001c0002t0002g0029others(3): Show | 6 | NA18941.hp1 NA18943.hp2 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-1305C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72182438 | ||||||
chr5:72182726
|
A | G | 1 | a0001c0002t0003g0012 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.287-1017A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72182726 | ||||||
chr5:72182768
|
A | G | 15 | a0001c0001t0001g0257a0001c0004t0005g0104a0001c0005t0001g0307others(12): Show | 15 | HG00733.hp2 HG01167.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.287-975A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72182768 | ||||||
chr5:72182912
|
A | C | 1 | a0001c0001t0012g0009 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.287-831A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72182912 | ||||||
chr5:72182996
|
A | G | 10 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(7): Show | 10 | HG01891.hp2 HG02055.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.287-747A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72182996 | ||||||
chr5:72183108
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.287-635A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72183108 | ||||||
chr5:72183694
|
C | T | 1 | a0001c0002t0009g0228 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.287-49C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72183694 | ||||||
chr5:72184010
|
T | C | 1 | a0001c0001t0001g0338 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.369+185T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72184010 | ||||||
chr5:72184217
|
A | C | 3 | a0001c0004t0001g0190a0001c0004t0001g0330a0001c0004t0001g0337 | 3 | HG02717.hp2 HG03041.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.369+392A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72184217 | ||||||
chr5:72184588
|
G | A | 1 | a0001c0002t0003g0058 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.369+763G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72184588 | ||||||
chr5:72184969
|
G | A | 4 | a0001c0002t0003g0174a0001c0002t0003g0177a0001c0002t0004g0003others(1): Show | 5 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.369+1144G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72184969 | ||||||
chr5:72185027
|
T | A | 1 | a0016c0035t0005g0044 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.369+1202T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72185027 | ||||||
chr5:72185072
|
G | A | 3 | a0007c0013t0001g0123a0007c0013t0001g0265a0007c0013t0029g0124 | 3 | HG03130.hp1 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.369+1247G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72185072 | ||||||
chr5:72185118
|
G | A | 2 | a0001c0002t0001g0074a0001c0002t0010g0225 | 2 | HG00408.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.369+1293G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72185118 | ||||||
chr5:72185210
|
C | G | 3 | a0007c0013t0001g0123a0007c0013t0001g0265a0007c0013t0029g0124 | 3 | HG03130.hp1 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.369+1385C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72185210 | ||||||
chr5:72185227
|
C | T | 4 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(1): Show | 4 | HG02622.hp2 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.370-1387C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72185227 | ||||||
chr5:72185235
|
C | A | 4 | a0006c0011t0001g0254a0006c0011t0011g0136a0006c0011t0011g0137others(1): Show | 4 | HG01074.hp2 HG02965.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.370-1379C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72185235 | ||||||
chr5:72185423
|
G | T | 1 | a0001c0008t0003g0184 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.370-1191G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72185423 | ||||||
chr5:72185438
|
A | C | 2 | a0001c0004t0007g0140a0011c0032t0033g0222 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.370-1176A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72185438 | ||||||
chr5:72185545
|
G | A | 4 | a0004c0010t0005g0133a0004c0010t0005g0256a0004c0010t0005g0332others(1): Show | 4 | HG02647.hp1 HG02922.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.370-1069G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72185545 | ||||||
chr5:72185576
|
G | T | 2 | a0003c0007t0002g0095a0003c0007t0002g0096 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.370-1038G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72185576 | ||||||
chr5:72185608
|
GA | G | 293 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0024others(290): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.370-990delA | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr5 | 72185608 | |||||
chr5:72185608
|
GAA | G | 12 | a0001c0001t0001g0185a0001c0004t0002g0180a0001c0004t0007g0327others(9): Show | 12 | HG00558.hp1 HG00738.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.370-991_370-990del others(2): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr5 | 72185608 | |||||
chr5:72185974
|
C | T | 1 | a0001c0001t0001g0282 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.370-640C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72185974 | ||||||
chr5:72185980
|
C | T | 1 | a0001c0002t0002g0108 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.370-634C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72185980 | ||||||
chr5:72186060
|
C | T | 311 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0024others(308): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.370-554C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72186060 | ||||||
chr5:72186131
|
G | A | 1 | a0001c0006t0007g0263 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.370-483G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72186131 | ||||||
chr5:72186218
|
C | T | 2 | a0003c0007t0002g0095a0003c0007t0002g0096 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.370-396C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72186218 | ||||||
chr5:72186340
|
AC | A | 3 | a0001c0005t0005g0125a0001c0005t0005g0155a0001c0005t0005g0258 | 3 | HG02257.hp1 HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.370-273delC | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72186340 | ||||||
chr5:72186354
|
C | T | 1 | a0001c0006t0018g0215 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.370-260C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72186354 | ||||||
chr5:72186768
|
T | C | 1 | a0002c0003t0023g0243 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.510+14T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72186768 | ||||||
chr5:72186853
|
C | T | 5 | a0001c0001t0012g0031a0001c0001t0012g0053a0001c0001t0012g0054others(2): Show | 5 | HG02258.hp2 HG02559.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.510+99C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72186853 | ||||||
chr5:72187070
|
G | A | 1 | a0001c0002t0002g0037 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.510+316G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72187070 | ||||||
chr5:72187329
|
T | G | 1 | a0001c0004t0017g0061 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.510+575T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72187329 | ||||||
chr5:72187379
|
G | T | 1 | a0001c0002t0002g0072 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.510+625G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72187379 | ||||||
chr5:72187386
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.510+632G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72187386 | ||||||
chr5:72187624
|
G | A | 98 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0024others(95): Show | 98 | HG00140.hp1 HG00609.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.510+870G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72187624 | ||||||
chr5:72187660
|
A | G | 3 | a0001c0004t0001g0190a0001c0004t0001g0337a0011c0032t0033g0222 | 3 | HG02717.hp2 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.510+906A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72187660 | ||||||
chr5:72187914
|
G | A | 98 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0024others(95): Show | 98 | HG00140.hp1 HG00609.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.510+1160G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72187914 | ||||||
chr5:72188217
|
G | A | 9 | a0001c0006t0005g0064a0001c0006t0007g0260a0001c0006t0007g0263others(6): Show | 9 | HG01167.hp2 HG01243.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.510+1463G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72188217 | ||||||
chr5:72188285
|
A | G | 105 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0024others(102): Show | 105 | HG00140.hp1 HG00609.hp2 HG00639.hp2 others(102): Show |
intron_variant | MODIFIER | c.510+1531A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72188285 | ||||||
chr5:72188336
|
A | G | 1 | a0001c0001t0001g0291 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.510+1582A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72188336 | ||||||
chr5:72188570
|
G | A | 1 | a0001c0001t0019g0247 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.510+1816G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72188570 | ||||||
chr5:72188605
|
C | T | 1 | a0001c0004t0005g0104 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.510+1851C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72188605 | ||||||
chr5:72188986
|
A | G | 3 | a0007c0013t0001g0123a0007c0013t0001g0265a0007c0013t0029g0124 | 3 | HG03130.hp1 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.510+2232A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72188986 | ||||||
chr5:72188991
|
T | G | 312 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0024others(309): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.510+2237T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72188991 | ||||||
chr5:72189038
|
C | A | 2 | a0001c0006t0005g0064a0001c0006t0018g0068 | 2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.510+2284C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72189038 | ||||||
chr5:72189508
|
G | C | 2 | a0001c0002t0002g0037a0001c0002t0002g0161 | 2 | HG01109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.510+2754G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72189508 | ||||||
chr5:72189556
|
G | A | 2 | a0001c0001t0001g0063a0001c0001t0001g0111 | 2 | NA18941.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.510+2802G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72189556 | ||||||
chr5:72189694
|
T | TA | 16 | a0001c0001t0007g0116a0001c0001t0007g0255a0001c0001t0007g0270others(13): Show | 16 | HG00621.hp2 HG01891.hp1 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.510+2953dupA | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr5 | 72189694 | |||||
chr5:72189694
|
TA | T | 8 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0006t0005g0064others(5): Show | 8 | HG01074.hp2 HG02109.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.510+2953delA | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr5 | 72189694 | |||||
chr5:72189884
|
A | G | 1 | a0001c0005t0008g0134 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.510+3130A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72189884 | ||||||
chr5:72189950
|
A | T | 1 | a0001c0001t0001g0182 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.510+3196A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72189950 | ||||||
chr5:72190100
|
T | C | 1 | a0011c0032t0033g0222 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.510+3346T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72190100 | ||||||
chr5:72190401
|
C | T | 36 | a0001c0001t0002g0069a0001c0001t0002g0076a0001c0001t0002g0112others(33): Show | 36 | HG00408.hp1 HG00642.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.511-3465C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72190401 | ||||||
chr5:72190472
|
T | C | 1 | a0001c0002t0002g0152 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.511-3394T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72190472 | ||||||
chr5:72190474
|
G | A | 1 | a0001c0004t0002g0180 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.511-3392G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72190474 | ||||||
chr5:72190807
|
A | T | 1 | a0002c0003t0006g0151 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.511-3059A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72190807 | ||||||
chr5:72190819
|
T | C | 5 | a0001c0001t0001g0071a0001c0001t0001g0267a0001c0001t0007g0116others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.511-3047T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72190819 | ||||||
chr5:72190885
|
G | A | 19 | a0001c0001t0001g0146a0001c0005t0005g0043a0001c0005t0005g0125others(16): Show | 19 | HG00741.hp2 HG01243.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.511-2981G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72190885 | ||||||
chr5:72190958
|
C | T | 155 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0024others(152): Show | 155 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(152): Show |
intron_variant | MODIFIER | c.511-2908C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72190958 | ||||||
chr5:72191036
|
G | C | 1 | a0001c0002t0001g0089 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.511-2830G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72191036 | ||||||
chr5:72191059
|
TAAGAACC others(14): Show |
T | 1 | a0010c0023t0006g0166 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.511-2806_511-2786d others(23): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72191059 | ||||||
chr5:72191517
|
G | A | 4 | a0006c0011t0001g0254a0006c0011t0011g0136a0006c0011t0011g0137others(1): Show | 4 | HG01074.hp2 HG02965.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.511-2349G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72191517 | ||||||
chr5:72191519
|
A | G | 1 | a0010c0023t0006g0166 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.511-2347A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72191519 | ||||||
chr5:72191526
|
G | A | 3 | a0001c0002t0002g0008a0001c0002t0002g0051a0001c0002t0023g0141 | 3 | HG01070.hp1 HG03831.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.511-2340G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72191526 | ||||||
chr5:72191974
|
C | T | 312 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0024others(309): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.511-1892C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72191974 | ||||||
chr5:72192236
|
T | C | 1 | a0001c0006t0007g0260 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.511-1630T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72192236 | ||||||
chr5:72193074
|
G | A | 4 | a0004c0010t0005g0133a0004c0010t0005g0256a0004c0010t0005g0332others(1): Show | 4 | HG02647.hp1 HG02922.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.511-792G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72193074 | ||||||
chr5:72193077
|
C | T | 43 | a0001c0001t0002g0069a0001c0001t0002g0076a0001c0001t0002g0112others(40): Show | 43 | HG00408.hp1 HG00642.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.511-789C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72193077 | ||||||
chr5:72193094
|
A | G | 2 | a0001c0005t0008g0335a0001c0036t0008g0122 | 2 | HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.511-772A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72193094 | ||||||
chr5:72193164
|
A | G | 1 | a0001c0001t0004g0065 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.511-702A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72193164 | ||||||
chr5:72193172
|
G | A | 1 | a0002c0003t0023g0243 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.511-694G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72193172 | ||||||
chr5:72193238
|
G | A | 1 | a0001c0001t0015g0121 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.511-628G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72193238 | ||||||
chr5:72193255
|
G | GT | 271 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0024others(268): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.511-605dupT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr5 | 72193255 | |||||
chr5:72193342
|
C | CT | 35 | a0001c0001t0002g0069a0001c0001t0002g0076a0001c0001t0002g0147others(32): Show | 35 | HG00408.hp1 HG00642.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-506dupT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr5 | 72193342 | |||||
chr5:72193342
|
CT | C | 250 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0024others(247): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.511-506delT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr5 | 72193342 | |||||
chr5:72193348
|
T | A | 3 | a0007c0013t0001g0123a0007c0013t0001g0265a0007c0013t0029g0124 | 3 | HG03130.hp1 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.511-518T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72193348 | ||||||
chr5:72193459
|
ATC | A | 2 | a0001c0002t0014g0001a0001c0002t0016g0153 | 3 | HG01884.hp1 HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.511-405_511-404del others(2): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr5 | 72193459 | |||||
chr5:72193478
|
G | T | 97 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0024others(94): Show | 97 | HG00140.hp1 HG00609.hp2 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.511-388G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72193478 | ||||||
chr5:72193677
|
G | A | 1 | a0001c0002t0011g0266 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.511-189G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72193677 | ||||||
chr5:72193833
|
TTTTCTTT others(5): Show |
T | 1 | a0001c0002t0003g0288 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.511-21_511-10delCT others(10): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr5 | 72193833 | |||||
chr5:72200441
|
T | C | 1 | a0001c0001t0004g0196 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.7012+74T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72200441 | ||||||
chr5:72200466
|
A | C | 1 | a0001c0001t0001g0024 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.7012+99A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72200466 | ||||||
chr5:72200513
|
C | T | 1 | a0001c0005t0001g0307 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.7012+146C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72200513 | ||||||
chr5:72200592
|
A | G | 49 | a0001c0001t0001g0188a0001c0001t0002g0028a0001c0001t0002g0069others(46): Show | 50 | HG00099.hp1 HG00408.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.7012+225A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72200592 | ||||||
chr5:72200702
|
C | T | 1 | a0016c0035t0005g0044 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.7012+335C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72200702 | ||||||
chr5:72200831
|
A | T | 4 | a0006c0011t0001g0254a0006c0011t0011g0136a0006c0011t0011g0137others(1): Show | 4 | HG01074.hp2 HG02965.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.7012+464A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72200831 | ||||||
chr5:72200838
|
A | T | 3 | a0001c0004t0007g0140a0001c0004t0034g0216a0011c0032t0033g0222 | 3 | HG02738.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.7012+471A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72200838 | ||||||
chr5:72200839
|
T | A | 1 | a0001c0001t0001g0117 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.7012+472T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72200839 | ||||||
chr5:72200988
|
A | G | 1 | a0009c0021t0036g0042 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.7012+621A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72200988 | ||||||
chr5:72201077
|
G | T | 41 | a0001c0001t0007g0049a0001c0001t0020g0128a0001c0004t0001g0190others(38): Show | 41 | HG00733.hp2 HG00741.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.7012+710G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72201077 | ||||||
chr5:72201199
|
C | CA | 6 | a0001c0004t0001g0190a0001c0004t0001g0330a0001c0004t0001g0337others(3): Show | 6 | HG02717.hp2 HG02738.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.7012+845dupA | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr5 | 72201199 | |||||
chr5:72201218
|
TTTAATTA others(21): Show |
T | 109 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0024others(106): Show | 109 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.7012+855_7012+882d others(30): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr5 | 72201218 | |||||
chr5:72201247
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.7012+880T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72201247 | ||||||
chr5:72201432
|
G | A | 1 | a0001c0002t0003g0173 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.7012+1065G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72201432 | ||||||
chr5:72201449
|
GT | G | 197 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0024others(194): Show | 198 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.7012+1087delT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr5 | 72201449 | |||||
chr5:72201492
|
A | T | 1 | a0002c0003t0006g0218 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.7012+1125A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72201492 | ||||||
chr5:72202110
|
A | T | 1 | a0001c0004t0017g0191 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.7013-1453A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72202110 | ||||||
chr5:72202112
|
G | A | 8 | a0001c0001t0002g0189a0001c0002t0002g0023a0001c0002t0002g0056others(5): Show | 8 | HG00621.hp1 HG02523.hp1 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.7013-1451G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72202112 | ||||||
chr5:72202245
|
G | A | 1 | a0001c0002t0001g0149 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.7013-1318G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72202245 | ||||||
chr5:72202284
|
C | T | 1 | a0001c0002t0030g0067 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.7013-1279C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72202284 | ||||||
chr5:72202556
|
G | A | 16 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0115others(13): Show | 16 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.7013-1007G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72202556 | ||||||
chr5:72202574
|
G | T | 1 | a0001c0001t0001g0220 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.7013-989G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72202574 | ||||||
chr5:72202593
|
A | G | 3 | a0006c0011t0011g0136a0006c0011t0011g0137a0006c0011t0011g0138 | 3 | HG01074.hp2 HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.7013-970A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72202593 | ||||||
chr5:72202840
|
G | A | 110 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0024others(107): Show | 110 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.7013-723G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72202840 | ||||||
chr5:72203020
|
T | G | 1 | a0002c0003t0006g0294 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.7013-543T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72203020 | ||||||
chr5:72203254
|
G | T | 1 | a0008c0016t0001g0333 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.7013-309G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72203254 | ||||||
chr5:72203488
|
G | A | 4 | a0001c0001t0001g0063a0001c0001t0001g0111a0001c0001t0001g0114others(1): Show | 4 | NA18941.hp1 NA18943.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.7013-75G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72203488 | ||||||
chr5:72203548
|
G | GTC | 4 | a0004c0010t0005g0133a0004c0010t0005g0256a0004c0010t0005g0332others(1): Show | 4 | HG02647.hp1 HG02922.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.7013-14_7013-13ins others(2): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr5 | 72203548 | |||||
chr5:72204347
|
T | G | 2 | a0001c0001t0020g0128a0001c0005t0020g0259 | 2 | HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.7251+546T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 6/6 | chr5 | 72204347 | ||||||
chr5:72204801
|
T | C | 2 | a0001c0001t0007g0116a0001c0001t0007g0255 | 2 | HG01891.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.7252-283T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 6/6 | chr5 | 72204801 | ||||||
chr5:72204932
|
T | C | 2 | a0001c0002t0014g0001a0001c0002t0016g0153 | 3 | HG01884.hp1 HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.7252-152T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 6/6 | chr5 | 72204932 | ||||||
chr5:72204981
|
T | C | 1 | a0001c0002t0002g0002 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.7252-103T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 6/6 | chr5 | 72204981 | ||||||
chr5:72204985
|
CCTT | C | 4 | a0001c0001t0001g0071a0001c0001t0001g0267a0001c0005t0001g0005others(1): Show | 4 | HG01884.hp2 HG02109.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.7252-91_7252-89del others(3): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr5 | 72204985 | |||||
chr5:72204998
|
G | C | 17 | a0001c0001t0007g0049a0001c0001t0007g0116a0001c0001t0007g0255others(14): Show | 17 | HG01167.hp2 HG01243.hp2 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.7252-86G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 6/6 | chr5 | 72204998 |