Search by Gene
| geneid | 55700 |
|---|---|
| ensemblid | ENSG00000116871.16 |
| hgncid | 25514 |
| symbol | MAP7D1 |
| name | MAP7 domain containing 1 |
| refseq_nuc | NM_001388490.1 |
| refseq_prot | NP_001375419.1 |
| ensembl_nuc | ENST00000474796.2 |
| ensembl_prot | ENSP00000507044.1 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 36156160 |
| end | 36180849 |
| strand | + |
| ver | v1.2 |
| region | chr1:36156160-36180849 |
| region5000 | chr1:36151160-36185849 |
| regionname0 | MAP7D1_chr1_36156160_36180849 |
| regionname5000 | MAP7D1_chr1_36151160_36185849 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| 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 | regionname | genename | aa |
|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 840 | 251 | 56 | 44 | 103 | 13 | 33 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0002 | 0/0 | 839 | 33 | 0 | 7 | 24 | 1 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0003 | 0/0 | 840 | 30 | 2 | 3 | 24 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0004 | 0/0 | 840 | 18 | 15 | 3 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0005 | 0/0 | 840 | 10 | 0 | 9 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0006 | 0/0 | 386 | 10 | 1 | 2 | 6 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0007 | 0/0 | 840 | 5 | 4 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0008 | 0/0 | 840 | 5 | 0 | 0 | 4 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0009 | 0/0 | 840 | 3 | 0 | 2 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0010 | 0/0 | 840 | 3 | 0 | 0 | 3 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0011 | 0/0 | 840 | 2 | 0 | 2 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0012 | 0/0 | 840 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0013 | 0/0 | 386 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0014 | 0/0 | 845 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0015 | 0/0 | 840 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0016 | 0/0 | 840 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0017 | 0/0 | 840 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0018 | 0/0 | 840 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0019 | 0/0 | 386 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 2523 | 150 | 30 | 19 | 78 | 6 | 17 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| c0002 | 1/1 | 2523 | 71 | 9 | 21 | 16 | 7 | 16 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| c0003 | 0/0 | 2520 | 33 | 0 | 7 | 24 | 1 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| c0004 | 0/0 | 2523 | 24 | 1 | 0 | 23 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| c0005 | 0/0 | 2523 | 15 | 12 | 3 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| c0006 | 0/0 | 2523 | 12 | 11 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| c0007 | 0/0 | 2523 | 10 | 0 | 9 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| c0008 | 0/0 | 2523 | 7 | 0 | 0 | 7 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| c0009 | 0/0 | 2524 | 6 | 0 | 2 | 3 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| c0010 | 0/0 | 2523 | 5 | 4 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| c0011 | 0/0 | 2523 | 5 | 0 | 3 | 1 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| c0012 | 0/0 | 2523 | 5 | 0 | 0 | 4 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| c0013 | 0/0 | 2523 | 3 | 0 | 2 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| c0014 | 0/0 | 2523 | 3 | 3 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| c0015 | 0/0 | 2523 | 3 | 1 | 2 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| c0016 | 0/0 | 2523 | 3 | 3 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| c0017 | 0/0 | 2523 | 3 | 0 | 0 | 3 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| c0018 | 0/0 | 2523 | 2 | 0 | 2 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| c0019 | 0/0 | 2524 | 2 | 0 | 0 | 2 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| c0020 | 0/0 | 2523 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| c0021 | 0/0 | 2524 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| c0022 | 0/0 | 2523 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| c0023 | 0/0 | 2524 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| c0024 | 0/0 | 2523 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| c0025 | 0/0 | 2523 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| c0026 | 0/0 | 2524 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| c0027 | 0/0 | 2524 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| c0028 | 0/0 | 2523 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| c0029 | 0/0 | 2538 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| c0030 | 0/0 | 2523 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| c0031 | 0/0 | 2523 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| c0032 | 0/0 | 2523 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| c0033 | 0/0 | 2523 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| c0034 | 0/0 | 2523 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| c0035 | 0/0 | 2523 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| thapid | 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
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 850 | 288 | 72 | 60 | 109 | 13 | 32 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| t0002 | 0/0 | 850 | 73 | 6 | 16 | 45 | 0 | 6 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| t0003 | 0/0 | 850 | 5 | 0 | 0 | 5 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| t0004 | 0/0 | 850 | 2 | 0 | 0 | 2 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| t0005 | 0/0 | 850 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| t0006 | 0/0 | 850 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| t0007 | 0/0 | 845 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| t0008 | 0/0 | 850 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| t0009 | 0/0 | 850 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| t0010 | 0/0 | 850 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| t0011 | 0/0 | 850 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| t0012 | 0/0 | 845 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| t0013 | 0/0 | 850 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| t0014 | 0/0 | 845 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| 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 |
|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 22 | 0 | 6 | 16 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0002 | 0/0 | 19 | 1 | 3 | 11 | 0 | 4 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0003 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0004 | 1/0 | 6 | 0 | 1 | 1 | 2 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0005 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0006 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0007 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0008 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0009 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0011 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0015 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0017 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0039 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0040 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0042 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0210 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| achapid | ahapid | 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 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | a0001 | c0001 | 0/0 | 150 | 30 | 19 | 78 | 6 | 17 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0001c0002 | a0001 | c0002 | 1/1 | 71 | 9 | 21 | 16 | 7 | 16 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0001c0006 | a0001 | c0006 | 0/0 | 12 | 11 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0001c0008 | a0001 | c0008 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0001c0014 | a0001 | c0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0001c0015 | a0001 | c0015 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0001c0020 | a0001 | c0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0001c0024 | a0001 | c0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0001c0030 | a0001 | c0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0001c0033 | a0001 | c0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0001c0034 | a0001 | c0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0002c0003 | a0002 | c0003 | 0/0 | 33 | 0 | 7 | 24 | 1 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0003c0004 | a0003 | c0004 | 0/0 | 24 | 1 | 0 | 23 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0003c0011 | a0003 | c0011 | 0/0 | 5 | 0 | 3 | 1 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0003c0032 | a0003 | c0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0004c0005 | a0004 | c0005 | 0/0 | 15 | 12 | 3 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0004c0016 | a0004 | c0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0005c0007 | a0005 | c0007 | 0/0 | 10 | 0 | 9 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0006c0009 | a0006 | c0009 | 0/0 | 6 | 0 | 2 | 3 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0006c0019 | a0006 | c0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0006c0026 | a0006 | c0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0006c0027 | a0006 | c0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0007c0010 | a0007 | c0010 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0008c0012 | a0008 | c0012 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0009c0013 | a0009 | c0013 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0010c0017 | a0010 | c0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0011c0018 | a0011 | c0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0012c0022 | a0012 | c0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0013c0023 | a0013 | c0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0014c0029 | a0014 | c0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0015c0031 | a0015 | c0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0016c0028 | a0016 | c0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0017c0025 | a0017 | c0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0018c0035 | a0018 | c0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0019c0021 | a0019 | c0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| acthapid | ahapid | chapid | thapid | 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 | actseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | a0001 | c0001 | t0001 | 0/0 | 90 | 22 | 17 | 34 | 6 | 11 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 53 | 6 | 2 | 39 | 0 | 6 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0001c0001t0006 | a0001 | c0001 | t0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0001c0001t0008 | a0001 | c0001 | t0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0001c0001t0010 | a0001 | c0001 | t0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0001c0001t0013 | a0001 | c0001 | t0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0001c0001t0014 | a0001 | c0001 | t0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0001c0002t0001 | a0001 | c0002 | t0001 | 1/1 | 69 | 9 | 21 | 15 | 6 | 16 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0001c0002t0005 | a0001 | c0002 | t0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0001c0002t0009 | a0001 | c0002 | t0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0001c0006t0001 | a0001 | c0006 | t0001 | 0/0 | 12 | 11 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0001c0008t0001 | a0001 | c0008 | t0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0001c0014t0001 | a0001 | c0014 | t0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0001c0015t0001 | a0001 | c0015 | t0001 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0001c0020t0001 | a0001 | c0020 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0001c0024t0002 | a0001 | c0024 | t0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0001c0030t0001 | a0001 | c0030 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0001c0033t0012 | a0001 | c0033 | t0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0001c0034t0001 | a0001 | c0034 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0002c0003t0001 | a0002 | c0003 | t0001 | 0/0 | 32 | 0 | 7 | 23 | 1 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0002c0003t0002 | a0002 | c0003 | t0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0003c0004t0001 | a0003 | c0004 | t0001 | 0/0 | 19 | 1 | 0 | 18 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0003c0004t0003 | a0003 | c0004 | t0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0003c0004t0011 | a0003 | c0004 | t0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0003c0011t0001 | a0003 | c0011 | t0001 | 0/0 | 5 | 0 | 3 | 1 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0003c0032t0001 | a0003 | c0032 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0004c0005t0001 | a0004 | c0005 | t0001 | 0/0 | 15 | 12 | 3 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0004c0016t0001 | a0004 | c0016 | t0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0005c0007t0002 | a0005 | c0007 | t0002 | 0/0 | 10 | 0 | 9 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0006c0009t0001 | a0006 | c0009 | t0001 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0006c0009t0002 | a0006 | c0009 | t0002 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0006c0009t0007 | a0006 | c0009 | t0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0006c0019t0001 | a0006 | c0019 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0006c0019t0003 | a0006 | c0019 | t0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0006c0026t0001 | a0006 | c0026 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0006c0027t0001 | a0006 | c0027 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0007c0010t0001 | a0007 | c0010 | t0001 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0008c0012t0001 | a0008 | c0012 | t0001 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0009c0013t0002 | a0009 | c0013 | t0002 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0010c0017t0001 | a0010 | c0017 | t0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0011c0018t0001 | a0011 | c0018 | t0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0012c0022t0001 | a0012 | c0022 | t0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0013c0023t0002 | a0013 | c0023 | t0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0014c0029t0001 | a0014 | c0029 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0015c0031t0001 | a0015 | c0031 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0016c0028t0001 | a0016 | c0028 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0017c0025t0001 | a0017 | c0025 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0018c0035t0001 | a0018 | c0035 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| a0019c0021t0002 | a0019 | c0021 | t0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 | copy fasta |
| actghapid | ahapid | chapid | thapid | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | a0001 | c0001 | t0001 | g0002 | 0/0 | 14 | 1 | 2 | 8 | 0 | 3 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0005 | a0001 | c0001 | t0001 | g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0014 | a0001 | c0001 | t0001 | g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0016 | a0001 | c0001 | t0001 | g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0020 | a0001 | c0001 | t0001 | g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0025 | a0001 | c0001 | t0001 | g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0028 | a0001 | c0001 | t0001 | g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0029 | a0001 | c0001 | t0001 | g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0030 | a0001 | c0001 | t0001 | g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0032 | a0001 | c0001 | t0001 | g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0035 | a0001 | c0001 | t0001 | g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0036 | a0001 | c0001 | t0001 | g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0045 | a0001 | c0001 | t0001 | g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0046 | a0001 | c0001 | t0001 | g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0047 | a0001 | c0001 | t0001 | g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0068 | a0001 | c0001 | t0001 | g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0080 | a0001 | c0001 | t0001 | g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0081 | a0001 | c0001 | t0001 | g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0082 | a0001 | c0001 | t0001 | g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0083 | a0001 | c0001 | t0001 | g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0084 | a0001 | c0001 | t0001 | g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0086 | a0001 | c0001 | t0001 | g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0089 | a0001 | c0001 | t0001 | g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0094 | a0001 | c0001 | t0001 | g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0095 | a0001 | c0001 | t0001 | g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0097 | a0001 | c0001 | t0001 | g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0105 | a0001 | c0001 | t0001 | g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0106 | a0001 | c0001 | t0001 | g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0107 | a0001 | c0001 | t0001 | g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0108 | a0001 | c0001 | t0001 | g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0109 | a0001 | c0001 | t0001 | g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0110 | a0001 | c0001 | t0001 | g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0111 | a0001 | c0001 | t0001 | g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0112 | a0001 | c0001 | t0001 | g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0113 | a0001 | c0001 | t0001 | g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0114 | a0001 | c0001 | t0001 | g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0115 | a0001 | c0001 | t0001 | g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0117 | a0001 | c0001 | t0001 | g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0118 | a0001 | c0001 | t0001 | g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0119 | a0001 | c0001 | t0001 | g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0120 | a0001 | c0001 | t0001 | g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0121 | a0001 | c0001 | t0001 | g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0123 | a0001 | c0001 | t0001 | g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0124 | a0001 | c0001 | t0001 | g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0125 | a0001 | c0001 | t0001 | g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0127 | a0001 | c0001 | t0001 | g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0129 | a0001 | c0001 | t0001 | g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0130 | a0001 | c0001 | t0001 | g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0131 | a0001 | c0001 | t0001 | g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0132 | a0001 | c0001 | t0001 | g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0133 | a0001 | c0001 | t0001 | g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0135 | a0001 | c0001 | t0001 | g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0136 | a0001 | c0001 | t0001 | g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0137 | a0001 | c0001 | t0001 | g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0138 | a0001 | c0001 | t0001 | g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0139 | a0001 | c0001 | t0001 | g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0140 | a0001 | c0001 | t0001 | g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0141 | a0001 | c0001 | t0001 | g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0142 | a0001 | c0001 | t0001 | g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0147 | a0001 | c0001 | t0001 | g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0148 | a0001 | c0001 | t0001 | g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0149 | a0001 | c0001 | t0001 | g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0161 | a0001 | c0001 | t0001 | g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0170 | a0001 | c0001 | t0001 | g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0178 | a0001 | c0001 | t0001 | g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0257 | a0001 | c0001 | t0001 | g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0260 | a0001 | c0001 | t0001 | g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0001g0263 | a0001 | c0001 | t0001 | g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0002g0001 | a0001 | c0001 | t0002 | g0001 | 0/0 | 13 | 0 | 0 | 13 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0002g0006 | a0001 | c0001 | t0002 | g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0002g0008 | a0001 | c0001 | t0002 | g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0002g0009 | a0001 | c0001 | t0002 | g0009 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0002g0019 | a0001 | c0001 | t0002 | g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0002g0039 | a0001 | c0001 | t0002 | g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0002g0040 | a0001 | c0001 | t0002 | g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0002g0213 | a0001 | c0001 | t0002 | g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0002g0214 | a0001 | c0001 | t0002 | g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0002g0215 | a0001 | c0001 | t0002 | g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0002g0216 | a0001 | c0001 | t0002 | g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0002g0217 | a0001 | c0001 | t0002 | g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0002g0219 | a0001 | c0001 | t0002 | g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0002g0220 | a0001 | c0001 | t0002 | g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0002g0221 | a0001 | c0001 | t0002 | g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0002g0223 | a0001 | c0001 | t0002 | g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0002g0225 | a0001 | c0001 | t0002 | g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0002g0228 | a0001 | c0001 | t0002 | g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0002g0229 | a0001 | c0001 | t0002 | g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0002g0230 | a0001 | c0001 | t0002 | g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0002g0231 | a0001 | c0001 | t0002 | g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0002g0232 | a0001 | c0001 | t0002 | g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0002g0233 | a0001 | c0001 | t0002 | g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0002g0234 | a0001 | c0001 | t0002 | g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0002g0235 | a0001 | c0001 | t0002 | g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0002g0236 | a0001 | c0001 | t0002 | g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0002g0238 | a0001 | c0001 | t0002 | g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0002g0239 | a0001 | c0001 | t0002 | g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0002g0240 | a0001 | c0001 | t0002 | g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0002g0241 | a0001 | c0001 | t0002 | g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0002g0242 | a0001 | c0001 | t0002 | g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0002g0243 | a0001 | c0001 | t0002 | g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0002g0264 | a0001 | c0001 | t0002 | g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0004g0001 | a0001 | c0001 | t0004 | g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0004g0039 | a0001 | c0001 | t0004 | g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0006g0227 | a0001 | c0001 | t0006 | g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0008g0163 | a0001 | c0001 | t0008 | g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0010g0245 | a0001 | c0001 | t0010 | g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0013g0179 | a0001 | c0001 | t0013 | g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0001t0014g0088 | a0001 | c0001 | t0014 | g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0004 | a0001 | c0002 | t0001 | g0004 | 1/0 | 5 | 0 | 1 | 1 | 1 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0011 | a0001 | c0002 | t0001 | g0011 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0015 | a0001 | c0002 | t0001 | g0015 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0017 | a0001 | c0002 | t0001 | g0017 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0021 | a0001 | c0002 | t0001 | g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0022 | a0001 | c0002 | t0001 | g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0031 | a0001 | c0002 | t0001 | g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0037 | a0001 | c0002 | t0001 | g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0038 | a0001 | c0002 | t0001 | g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0048 | a0001 | c0002 | t0001 | g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0049 | a0001 | c0002 | t0001 | g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0051 | a0001 | c0002 | t0001 | g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0053 | a0001 | c0002 | t0001 | g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0054 | a0001 | c0002 | t0001 | g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0055 | a0001 | c0002 | t0001 | g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0056 | a0001 | c0002 | t0001 | g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0057 | a0001 | c0002 | t0001 | g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0059 | a0001 | c0002 | t0001 | g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0060 | a0001 | c0002 | t0001 | g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0061 | a0001 | c0002 | t0001 | g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0062 | a0001 | c0002 | t0001 | g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0063 | a0001 | c0002 | t0001 | g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0064 | a0001 | c0002 | t0001 | g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0065 | a0001 | c0002 | t0001 | g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0066 | a0001 | c0002 | t0001 | g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0067 | a0001 | c0002 | t0001 | g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0128 | a0001 | c0002 | t0001 | g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0145 | a0001 | c0002 | t0001 | g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0169 | a0001 | c0002 | t0001 | g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0180 | a0001 | c0002 | t0001 | g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0181 | a0001 | c0002 | t0001 | g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0182 | a0001 | c0002 | t0001 | g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0183 | a0001 | c0002 | t0001 | g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0184 | a0001 | c0002 | t0001 | g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0185 | a0001 | c0002 | t0001 | g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0186 | a0001 | c0002 | t0001 | g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0189 | a0001 | c0002 | t0001 | g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0190 | a0001 | c0002 | t0001 | g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0191 | a0001 | c0002 | t0001 | g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0193 | a0001 | c0002 | t0001 | g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0195 | a0001 | c0002 | t0001 | g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0196 | a0001 | c0002 | t0001 | g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0197 | a0001 | c0002 | t0001 | g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0198 | a0001 | c0002 | t0001 | g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0199 | a0001 | c0002 | t0001 | g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0200 | a0001 | c0002 | t0001 | g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0201 | a0001 | c0002 | t0001 | g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0202 | a0001 | c0002 | t0001 | g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0203 | a0001 | c0002 | t0001 | g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0204 | a0001 | c0002 | t0001 | g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0205 | a0001 | c0002 | t0001 | g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0206 | a0001 | c0002 | t0001 | g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0208 | a0001 | c0002 | t0001 | g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0210 | a0001 | c0002 | t0001 | g0210 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0211 | a0001 | c0002 | t0001 | g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0001g0212 | a0001 | c0002 | t0001 | g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0005g0187 | a0001 | c0002 | t0005 | g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0002t0009g0004 | a0001 | c0002 | t0009 | g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0006t0001g0012 | a0001 | c0006 | t0001 | g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0006t0001g0013 | a0001 | c0006 | t0001 | g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0006t0001g0073 | a0001 | c0006 | t0001 | g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0006t0001g0074 | a0001 | c0006 | t0001 | g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0006t0001g0076 | a0001 | c0006 | t0001 | g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0006t0001g0077 | a0001 | c0006 | t0001 | g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0006t0001g0078 | a0001 | c0006 | t0001 | g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0006t0001g0079 | a0001 | c0006 | t0001 | g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0008t0001g0018 | a0001 | c0008 | t0001 | g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0008t0001g0188 | a0001 | c0008 | t0001 | g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0008t0001g0192 | a0001 | c0008 | t0001 | g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0008t0001g0194 | a0001 | c0008 | t0001 | g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0008t0001g0209 | a0001 | c0008 | t0001 | g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0014t0001g0010 | a0001 | c0014 | t0001 | g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0014t0001g0058 | a0001 | c0014 | t0001 | g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0015t0001g0024 | a0001 | c0015 | t0001 | g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0015t0001g0085 | a0001 | c0015 | t0001 | g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0020t0001g0002 | a0001 | c0020 | t0001 | g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0024t0002g0222 | a0001 | c0024 | t0002 | g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0030t0001g0075 | a0001 | c0030 | t0001 | g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0033t0012g0037 | a0001 | c0033 | t0012 | g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0001c0034t0001g0152 | a0001 | c0034 | t0001 | g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0002c0003t0001g0002 | a0002 | c0003 | t0001 | g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0002c0003t0001g0029 | a0002 | c0003 | t0001 | g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0002c0003t0001g0042 | a0002 | c0003 | t0001 | g0042 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0002c0003t0001g0043 | a0002 | c0003 | t0001 | g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0002c0003t0001g0044 | a0002 | c0003 | t0001 | g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0002c0003t0001g0099 | a0002 | c0003 | t0001 | g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0002c0003t0001g0100 | a0002 | c0003 | t0001 | g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0002c0003t0001g0101 | a0002 | c0003 | t0001 | g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0002c0003t0001g0102 | a0002 | c0003 | t0001 | g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0002c0003t0001g0103 | a0002 | c0003 | t0001 | g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0002c0003t0001g0104 | a0002 | c0003 | t0001 | g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0002c0003t0001g0122 | a0002 | c0003 | t0001 | g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0002c0003t0001g0126 | a0002 | c0003 | t0001 | g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0002c0003t0001g0144 | a0002 | c0003 | t0001 | g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0002c0003t0001g0244 | a0002 | c0003 | t0001 | g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0002c0003t0001g0246 | a0002 | c0003 | t0001 | g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0002c0003t0001g0247 | a0002 | c0003 | t0001 | g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0002c0003t0001g0248 | a0002 | c0003 | t0001 | g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0002c0003t0001g0249 | a0002 | c0003 | t0001 | g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0002c0003t0001g0250 | a0002 | c0003 | t0001 | g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0002c0003t0001g0251 | a0002 | c0003 | t0001 | g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0002c0003t0001g0252 | a0002 | c0003 | t0001 | g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0002c0003t0001g0253 | a0002 | c0003 | t0001 | g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0002c0003t0001g0254 | a0002 | c0003 | t0001 | g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0002c0003t0001g0255 | a0002 | c0003 | t0001 | g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0002c0003t0001g0256 | a0002 | c0003 | t0001 | g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0002c0003t0001g0258 | a0002 | c0003 | t0001 | g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0002c0003t0001g0259 | a0002 | c0003 | t0001 | g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0002c0003t0002g0096 | a0002 | c0003 | t0002 | g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0003c0004t0001g0003 | a0003 | c0004 | t0001 | g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0003c0004t0001g0026 | a0003 | c0004 | t0001 | g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0003c0004t0001g0027 | a0003 | c0004 | t0001 | g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0003c0004t0001g0033 | a0003 | c0004 | t0001 | g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0003c0004t0001g0087 | a0003 | c0004 | t0001 | g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0003c0004t0001g0090 | a0003 | c0004 | t0001 | g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0003c0004t0001g0092 | a0003 | c0004 | t0001 | g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0003c0004t0001g0093 | a0003 | c0004 | t0001 | g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0003c0004t0001g0153 | a0003 | c0004 | t0001 | g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0003c0004t0001g0154 | a0003 | c0004 | t0001 | g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0003c0004t0001g0156 | a0003 | c0004 | t0001 | g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0003c0004t0001g0157 | a0003 | c0004 | t0001 | g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0003c0004t0001g0159 | a0003 | c0004 | t0001 | g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0003c0004t0003g0003 | a0003 | c0004 | t0003 | g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0003c0004t0011g0003 | a0003 | c0004 | t0011 | g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0003c0011t0001g0007 | a0003 | c0011 | t0001 | g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0003c0011t0001g0158 | a0003 | c0011 | t0001 | g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0003c0011t0001g0160 | a0003 | c0011 | t0001 | g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0003c0032t0001g0262 | a0003 | c0032 | t0001 | g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0004c0005t0001g0005 | a0004 | c0005 | t0001 | g0005 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0004c0005t0001g0016 | a0004 | c0005 | t0001 | g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0004c0005t0001g0034 | a0004 | c0005 | t0001 | g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0004c0005t0001g0035 | a0004 | c0005 | t0001 | g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0004c0005t0001g0150 | a0004 | c0005 | t0001 | g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0004c0005t0001g0151 | a0004 | c0005 | t0001 | g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0004c0005t0001g0164 | a0004 | c0005 | t0001 | g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0004c0005t0001g0171 | a0004 | c0005 | t0001 | g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0004c0005t0001g0173 | a0004 | c0005 | t0001 | g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0004c0005t0001g0174 | a0004 | c0005 | t0001 | g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0004c0005t0001g0175 | a0004 | c0005 | t0001 | g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0004c0005t0001g0176 | a0004 | c0005 | t0001 | g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0004c0016t0001g0005 | a0004 | c0016 | t0001 | g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0004c0016t0001g0172 | a0004 | c0016 | t0001 | g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0004c0016t0001g0177 | a0004 | c0016 | t0001 | g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0005c0007t0002g0001 | a0005 | c0007 | t0002 | g0001 | 0/0 | 6 | 0 | 5 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0005c0007t0002g0006 | a0005 | c0007 | t0002 | g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0005c0007t0002g0008 | a0005 | c0007 | t0002 | g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0005c0007t0002g0218 | a0005 | c0007 | t0002 | g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0005c0007t0002g0226 | a0005 | c0007 | t0002 | g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0006c0009t0001g0116 | a0006 | c0009 | t0001 | g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0006c0009t0001g0143 | a0006 | c0009 | t0001 | g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0006c0009t0002g0019 | a0006 | c0009 | t0002 | g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0006c0009t0002g0041 | a0006 | c0009 | t0002 | g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0006c0009t0002g0237 | a0006 | c0009 | t0002 | g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0006c0009t0007g0041 | a0006 | c0009 | t0007 | g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0006c0019t0001g0091 | a0006 | c0019 | t0001 | g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0006c0019t0003g0155 | a0006 | c0019 | t0003 | g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0006c0026t0001g0207 | a0006 | c0026 | t0001 | g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0006c0027t0001g0010 | a0006 | c0027 | t0001 | g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0007c0010t0001g0023 | a0007 | c0010 | t0001 | g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0007c0010t0001g0069 | a0007 | c0010 | t0001 | g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0007c0010t0001g0070 | a0007 | c0010 | t0001 | g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0007c0010t0001g0071 | a0007 | c0010 | t0001 | g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0008c0012t0001g0162 | a0008 | c0012 | t0001 | g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0008c0012t0001g0165 | a0008 | c0012 | t0001 | g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0008c0012t0001g0166 | a0008 | c0012 | t0001 | g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0008c0012t0001g0167 | a0008 | c0012 | t0001 | g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0008c0012t0001g0168 | a0008 | c0012 | t0001 | g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0009c0013t0002g0001 | a0009 | c0013 | t0002 | g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0009c0013t0002g0006 | a0009 | c0013 | t0002 | g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0009c0013t0002g0040 | a0009 | c0013 | t0002 | g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0010c0017t0001g0022 | a0010 | c0017 | t0001 | g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0010c0017t0001g0050 | a0010 | c0017 | t0001 | g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0010c0017t0001g0052 | a0010 | c0017 | t0001 | g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0011c0018t0001g0134 | a0011 | c0018 | t0001 | g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0011c0018t0001g0146 | a0011 | c0018 | t0001 | g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0012c0022t0001g0002 | a0012 | c0022 | t0001 | g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0013c0023t0002g0224 | a0013 | c0023 | t0002 | g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0014c0029t0001g0072 | a0014 | c0029 | t0001 | g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0015c0031t0001g0098 | a0015 | c0031 | t0001 | g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0016c0028t0001g0002 | a0016 | c0028 | t0001 | g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0017c0025t0001g0007 | a0017 | c0025 | t0001 | g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0018c0035t0001g0261 | a0018 | c0035 | t0001 | g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| a0019c0021t0002g0001 | a0019 | c0021 | t0002 | g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0257 | EUR | GBR | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0030 | EUR | GBR | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0111 | EUR | FIN | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0063 | EUR | FIN | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0066 | EUR | FIN | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG00323 | hp2 | a0002 | c0003 | t0001 | g0122 | EUR | FIN | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | CHS | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | CHS | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | CHS | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG00544 | hp2 | a0003 | c0004 | t0003 | g0003 | EAS | CHS | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG00558 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | CHS | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | CHS | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG00597 | hp1 | a0002 | c0003 | t0001 | g0249 | EAS | CHS | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG00597 | hp2 | a0003 | c0004 | t0001 | g0027 | EAS | CHS | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG00621 | hp1 | a0015 | c0031 | t0001 | g0098 | EAS | CHS | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG00642 | hp1 | a0002 | c0003 | t0001 | g0104 | AMR | PUR | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0128 | AMR | PUR | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG00673 | hp1 | a0001 | c0001 | t0010 | g0245 | EAS | CHS | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0145 | AMR | PUR | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG00735 | hp1 | a0002 | c0003 | t0001 | g0042 | AMR | PUR | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG00741 | hp1 | a0013 | c0023 | t0002 | g0224 | AMR | PUR | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0031 | AMR | PUR | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01069 | hp1 | a0007 | c0010 | t0001 | g0023 | AMR | PUR | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01069 | hp2 | a0004 | c0005 | t0001 | g0164 | AMR | PUR | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0031 | AMR | PUR | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01071 | hp2 | a0004 | c0005 | t0001 | g0034 | AMR | PUR | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0022 | AMR | PUR | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0198 | AMR | PUR | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0021 | AMR | PUR | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0197 | AMR | PUR | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0021 | AMR | PUR | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01109 | hp2 | a0006 | c0009 | t0002 | g0237 | AMR | PUR | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01167 | hp1 | a0001 | c0015 | t0001 | g0024 | AMR | PUR | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01168 | hp2 | a0002 | c0003 | t0001 | g0102 | AMR | PUR | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01169 | hp2 | a0001 | c0015 | t0001 | g0024 | AMR | PUR | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0203 | AMR | PUR | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01175 | hp2 | a0004 | c0005 | t0001 | g0005 | AMR | PUR | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0208 | AMR | PUR | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0056 | AMR | CLM | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0206 | AMR | CLM | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01257 | hp2 | a0001 | c0020 | t0001 | g0002 | AMR | CLM | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0204 | AMR | CLM | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01261 | hp1 | a0006 | c0009 | t0001 | g0116 | AMR | CLM | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01261 | hp2 | a0005 | c0007 | t0002 | g0001 | AMR | CLM | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0202 | AMR | CLM | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0015 | AMR | CLM | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01358 | hp1 | a0009 | c0013 | t0002 | g0006 | AMR | CLM | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | CLM | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0185 | AMR | CLM | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01361 | hp2 | a0002 | c0003 | t0001 | g0246 | AMR | CLM | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01433 | hp1 | a0002 | c0003 | t0001 | g0101 | AMR | CLM | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01433 | hp2 | a0005 | c0007 | t0002 | g0001 | AMR | CLM | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0015 | EUR | IBS | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0195 | EUR | IBS | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0004 | EUR | IBS | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0015 | EUR | IBS | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01884 | hp1 | a0006 | c0027 | t0001 | g0010 | AFR | ACB | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01884 | hp2 | a0001 | c0006 | t0001 | g0013 | AFR | ACB | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01928 | hp1 | a0005 | c0007 | t0002 | g0226 | AMR | PEL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01934 | hp1 | a0001 | c0006 | t0001 | g0077 | AMR | PEL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01934 | hp2 | a0019 | c0021 | t0002 | g0001 | AMR | PEL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01943 | hp1 | a0011 | c0018 | t0001 | g0146 | AMR | PEL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01943 | hp2 | a0003 | c0011 | t0001 | g0007 | AMR | PEL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01952 | hp1 | a0005 | c0007 | t0002 | g0218 | AMR | PEL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01975 | hp1 | a0005 | c0007 | t0002 | g0001 | AMR | PEL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01975 | hp2 | a0017 | c0025 | t0001 | g0007 | AMR | PEL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01978 | hp1 | a0002 | c0003 | t0001 | g0099 | AMR | PEL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0180 | AMR | PEL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01993 | hp1 | a0005 | c0007 | t0002 | g0001 | AMR | PEL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01993 | hp2 | a0003 | c0011 | t0001 | g0007 | AMR | PEL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02004 | hp1 | a0003 | c0011 | t0001 | g0007 | AMR | PEL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02027 | hp1 | a0008 | c0012 | t0001 | g0166 | EAS | KHV | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02027 | hp2 | a0003 | c0004 | t0001 | g0159 | EAS | KHV | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02040 | hp1 | a0003 | c0004 | t0003 | g0003 | EAS | KHV | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02055 | hp1 | a0001 | c0014 | t0001 | g0058 | AFR | ACB | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02055 | hp2 | a0001 | c0006 | t0001 | g0078 | AFR | ACB | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | KHV | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02083 | hp2 | a0003 | c0004 | t0001 | g0026 | EAS | KHV | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02132 | hp1 | a0003 | c0004 | t0003 | g0003 | EAS | KHV | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02135 | hp2 | a0006 | c0019 | t0001 | g0091 | EAS | KHV | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02145 | hp1 | a0004 | c0005 | t0001 | g0171 | AFR | ACB | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02145 | hp2 | a0003 | c0004 | t0001 | g0087 | AFR | ACB | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02148 | hp2 | a0005 | c0007 | t0002 | g0006 | AMR | PEL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02257 | hp1 | a0001 | c0006 | t0001 | g0013 | AFR | ACB | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02257 | hp2 | a0004 | c0005 | t0001 | g0016 | AFR | ACB | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02258 | hp2 | a0004 | c0005 | t0001 | g0035 | AFR | ACB | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02273 | hp2 | a0005 | c0007 | t0002 | g0008 | AMR | PEL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0231 | AFR | ACB | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02280 | hp2 | a0007 | c0010 | t0001 | g0071 | AFR | ACB | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02300 | hp1 | a0005 | c0007 | t0002 | g0001 | AMR | PEL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02300 | hp2 | a0002 | c0003 | t0001 | g0100 | AMR | PEL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0215 | AFR | ACB | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02451 | hp2 | a0001 | c0006 | t0001 | g0012 | AFR | ACB | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02572 | hp1 | a0007 | c0010 | t0001 | g0070 | AFR | GWD | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02572 | hp2 | a0004 | c0016 | t0001 | g0172 | AFR | GWD | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0223 | SAS | PJL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0017 | SAS | PJL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | GWD | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02615 | hp2 | a0004 | c0016 | t0001 | g0177 | AFR | GWD | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02622 | hp1 | a0004 | c0005 | t0001 | g0005 | AFR | GWD | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02647 | hp1 | a0004 | c0016 | t0001 | g0005 | AFR | GWD | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02647 | hp2 | a0001 | c0034 | t0001 | g0152 | AFR | GWD | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02683 | hp2 | a0008 | c0012 | t0001 | g0162 | SAS | PJL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02717 | hp1 | a0001 | c0006 | t0001 | g0012 | AFR | GWD | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0211 | AFR | GWD | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02723 | hp2 | a0018 | c0035 | t0001 | g0261 | AFR | GWD | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02738 | hp1 | a0006 | c0009 | t0001 | g0143 | SAS | PJL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0201 | SAS | PJL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02809 | hp2 | a0001 | c0006 | t0001 | g0073 | AFR | GWD | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02818 | hp1 | a0004 | c0005 | t0001 | g0175 | AFR | GWD | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02896 | hp1 | a0007 | c0010 | t0001 | g0023 | AFR | GWD | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02896 | hp2 | a0001 | c0014 | t0001 | g0010 | AFR | GWD | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02897 | hp1 | a0001 | c0014 | t0001 | g0010 | AFR | GWD | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02897 | hp2 | a0001 | c0030 | t0001 | g0075 | AFR | GWD | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02922 | hp1 | a0004 | c0005 | t0001 | g0034 | AFR | ESN | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02970 | hp1 | a0001 | c0001 | t0014 | g0088 | AFR | ESN | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02976 | hp1 | a0001 | c0006 | t0001 | g0013 | AFR | ESN | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0011 | SAS | PJL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03041 | hp1 | a0014 | c0029 | t0001 | g0072 | AFR | GWD | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0067 | AFR | GWD | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0233 | AFR | MSL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0228 | AFR | MSL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03195 | hp1 | a0001 | c0006 | t0001 | g0074 | AFR | ESN | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03225 | hp1 | a0004 | c0005 | t0001 | g0173 | AFR | MSL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0038 | AFR | MSL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03239 | hp1 | a0002 | c0003 | t0001 | g0103 | SAS | PJL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0169 | AFR | MSL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03486 | hp1 | a0001 | c0015 | t0001 | g0085 | AFR | MSL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0059 | AFR | MSL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03490 | hp1 | a0012 | c0022 | t0001 | g0002 | SAS | PJL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03490 | hp2 | a0003 | c0011 | t0001 | g0158 | SAS | PJL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0062 | SAS | PJL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03516 | hp2 | a0001 | c0006 | t0001 | g0076 | AFR | ESN | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03540 | hp1 | a0001 | c0006 | t0001 | g0012 | AFR | GWD | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03579 | hp1 | a0004 | c0005 | t0001 | g0150 | AFR | MSL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0060 | AFR | MSL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0017 | SAS | PJL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0212 | SAS | STU | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0229 | SAS | STU | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0061 | SAS | PJL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0196 | SAS | PJL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0064 | SAS | PJL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0199 | SAS | PJL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0217 | SAS | BEB | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0193 | SAS | BEB | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0186 | SAS | BEB | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0039 | SAS | STU | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | STU | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0205 | SAS | BEB | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0200 | SAS | STU | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | STU | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | STU | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | STU | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18522 | hp2 | a0004 | c0005 | t0001 | g0174 | AFR | YRI | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | CHB | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18747 | hp1 | a0003 | c0004 | t0001 | g0027 | EAS | CHB | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18939 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18940 | hp2 | a0010 | c0017 | t0001 | g0050 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18942 | hp2 | a0010 | c0017 | t0001 | g0022 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18943 | hp1 | a0001 | c0008 | t0001 | g0188 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18943 | hp2 | a0002 | c0003 | t0001 | g0126 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18945 | hp2 | a0001 | c0008 | t0001 | g0018 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18947 | hp2 | a0003 | c0004 | t0001 | g0154 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18948 | hp2 | a0003 | c0004 | t0001 | g0156 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18950 | hp2 | a0006 | c0019 | t0003 | g0155 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18952 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18957 | hp1 | a0008 | c0012 | t0001 | g0168 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18960 | hp1 | a0001 | c0001 | t0006 | g0227 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18960 | hp2 | a0002 | c0003 | t0001 | g0252 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18961 | hp1 | a0003 | c0004 | t0001 | g0033 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18961 | hp2 | a0006 | c0009 | t0002 | g0019 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18962 | hp2 | a0002 | c0003 | t0001 | g0044 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18963 | hp1 | a0006 | c0009 | t0007 | g0041 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18963 | hp2 | a0016 | c0028 | t0001 | g0002 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18966 | hp2 | a0003 | c0004 | t0001 | g0026 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18967 | hp1 | a0006 | c0009 | t0002 | g0041 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18968 | hp1 | a0001 | c0033 | t0012 | g0037 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18968 | hp2 | a0003 | c0011 | t0001 | g0160 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18969 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18969 | hp2 | a0002 | c0003 | t0001 | g0043 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18973 | hp1 | a0003 | c0004 | t0003 | g0003 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18974 | hp2 | a0002 | c0003 | t0001 | g0044 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18977 | hp2 | a0008 | c0012 | t0001 | g0165 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18978 | hp2 | a0003 | c0004 | t0001 | g0157 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18979 | hp1 | a0010 | c0017 | t0001 | g0052 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0191 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18980 | hp2 | a0003 | c0004 | t0001 | g0092 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18982 | hp2 | a0001 | c0024 | t0002 | g0222 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18983 | hp2 | a0009 | c0013 | t0002 | g0001 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18985 | hp1 | a0003 | c0004 | t0001 | g0093 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18985 | hp2 | a0002 | c0003 | t0002 | g0096 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18988 | hp1 | a0002 | c0003 | t0001 | g0247 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18989 | hp1 | a0002 | c0003 | t0001 | g0254 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18989 | hp2 | a0001 | c0008 | t0001 | g0192 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18991 | hp2 | a0006 | c0026 | t0001 | g0207 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18993 | hp2 | a0002 | c0003 | t0001 | g0259 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18994 | hp2 | a0001 | c0008 | t0001 | g0209 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18998 | hp2 | a0002 | c0003 | t0001 | g0253 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19000 | hp1 | a0008 | c0012 | t0001 | g0167 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19000 | hp2 | a0001 | c0001 | t0008 | g0163 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19002 | hp1 | a0003 | c0004 | t0001 | g0033 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19007 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0190 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19055 | hp1 | a0002 | c0003 | t0001 | g0244 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19056 | hp2 | a0002 | c0003 | t0001 | g0251 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19058 | hp1 | a0003 | c0004 | t0011 | g0003 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19058 | hp2 | a0002 | c0003 | t0001 | g0255 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19064 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19064 | hp2 | a0001 | c0008 | t0001 | g0018 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19066 | hp1 | a0001 | c0008 | t0001 | g0018 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19066 | hp2 | a0002 | c0003 | t0001 | g0256 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19070 | hp1 | a0002 | c0003 | t0001 | g0144 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19080 | hp1 | a0002 | c0003 | t0001 | g0248 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19081 | hp1 | a0003 | c0004 | t0001 | g0153 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19081 | hp2 | a0001 | c0002 | t0005 | g0187 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19082 | hp1 | a0005 | c0007 | t0002 | g0001 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19083 | hp2 | a0002 | c0003 | t0001 | g0042 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19084 | hp2 | a0002 | c0003 | t0001 | g0250 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19087 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19087 | hp2 | a0003 | c0004 | t0001 | g0090 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19088 | hp1 | a0002 | c0003 | t0001 | g0043 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19089 | hp2 | a0002 | c0003 | t0001 | g0029 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19090 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19090 | hp2 | a0002 | c0003 | t0001 | g0258 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19240 | hp1 | a0004 | c0005 | t0001 | g0005 | AFR | YRI | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0057 | AFR | YRI | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0038 | AFR | ASW | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA20129 | hp2 | a0004 | c0005 | t0001 | g0151 | AFR | ASW | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | TSI | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0136 | EUR | TSI | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | TSI | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA20805 | hp2 | a0001 | c0002 | t0009 | g0004 | EUR | TSI | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0065 | SAS | GIH | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0238 | SAS | GIH | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01123 | hp1 | a0011 | c0018 | t0001 | g0134 | AMR | CLM | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG01123 | hp2 | a0009 | c0013 | t0002 | g0040 | AMR | CLM | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02486 | hp2 | a0007 | c0010 | t0001 | g0069 | AFR | ACB | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG02559 | hp2 | a0004 | c0005 | t0001 | g0176 | AFR | ACB | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03471 | hp1 | a0001 | c0006 | t0001 | g0079 | AFR | MSL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG03471 | hp2 | a0003 | c0032 | t0001 | g0262 | AFR | MSL | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | USA | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0055 | AFR | USA | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18955 | hp1 | a0001 | c0008 | t0001 | g0194 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | USA | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0240 | AFR | USA | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | LWK | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| NA21309 | hp2 | a0001 | c0001 | t0013 | g0179 | AFR | LWK | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0210 | REF | REF | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0004 | REF | REF | MAP7D1_chr1_36151160_36185849 | MAP7D1 |
| chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:36171234
|
C | T | 2 | a0008a0010 | 8 | HG02027.hp1 HG02683.hp2 NA18940.hp2 others(5): Show |
missense_variant | MODERATE | c.310C>T | p.Arg104Trp | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 2/17 | 568/3372 | 310/2523 | 104/840 | chr1 | 36171234 | ||
| chr1:36171253
|
G | A | 1 | a0011 | 2 | HG01123.hp1 HG01943.hp1 |
missense_variant | MODERATE | c.329G>A | p.Arg110Gln | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 2/17 | 587/3372 | 329/2523 | 110/840 | chr1 | 36171253 | ||
| chr1:36171294
|
G | A | 1 | a0019 | 1 | HG01934.hp2 | missense_variant | MODERATE | c.370G>A | p.Asp124Asn | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 2/17 | 628/3372 | 370/2523 | 124/840 | chr1 | 36171294 | ||
| chr1:36172542
|
G | A | 1 | a0012 | 1 | HG03490.hp1 | missense_variant | MODERATE | c.539G>A | p.Arg180His | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 4/17 | 797/3372 | 539/2523 | 180/840 | chr1 | 36172542 | ||
| chr1:36172545
|
G | A | 1 | a0009 | 3 | HG01123.hp2 HG01358.hp1 NA18983.hp2 |
missense_variant | MODERATE | c.542G>A | p.Arg181Gln | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 4/17 | 800/3372 | 542/2523 | 181/840 | chr1 | 36172545 | ||
| chr1:36172605
|
G | A | 3 | a0005a0013a0019 | 12 | HG00741.hp1 HG01261.hp2 HG01433.hp2 others(9): Show |
missense_variant | MODERATE | c.602G>A | p.Arg201Gln | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 4/17 | 860/3372 | 602/2523 | 201/840 | chr1 | 36172605 | ||
| chr1:36176384
|
G | A | 1 | a0007 | 5 | HG01069.hp1 HG02280.hp2 HG02486.hp2 others(2): Show |
missense_variant | MODERATE | c.1036G>A | p.Gly346Arg | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 7/17 | 1294/3372 | 1036/2523 | 346/840 | chr1 | 36176384 | ||
| chr1:36176495
|
G | GC | 3 | a0006a0013a0019 | 12 | HG00741.hp1 HG01109.hp2 HG01261.hp1 others(9): Show |
frameshift_variant | HIGH | c.1152dupC | p.Ala385fs | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 7/17 | 1411/3372 | 1153/2523 | 385/840 | INFO_REALIGN_3_PRIME | chr1 | 36176495 | |
| chr1:36176573
|
G | T | 1 | a0018 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1225G>T | p.Ala409Ser | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 7/17 | 1483/3372 | 1225/2523 | 409/840 | chr1 | 36176573 | ||
| chr1:36176760
|
C | T | 1 | a0004 | 18 | HG01069.hp2 HG01071.hp2 HG01175.hp2 others(15): Show |
missense_variant | MODERATE | c.1297C>T | p.Arg433Trp | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 8/17 | 1555/3372 | 1297/2523 | 433/840 | chr1 | 36176760 | ||
| chr1:36176833
|
C | T | 1 | a0010 | 3 | NA18940.hp2 NA18942.hp2 NA18979.hp1 |
missense_variant | MODERATE | c.1370C>T | p.Ser457Phe | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 8/17 | 1628/3372 | 1370/2523 | 457/840 | chr1 | 36176833 | ||
| chr1:36177886
|
G | A | 1 | a0017 | 1 | HG01975.hp2 | missense_variant | MODERATE | c.1393G>A | p.Ala465Thr | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 9/17 | 1651/3372 | 1393/2523 | 465/840 | chr1 | 36177886 | ||
| chr1:36178057
|
G | A | 1 | a0016 | 1 | NA18963.hp2 | missense_variant | MODERATE | c.1564G>A | p.Gly522Arg | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 9/17 | 1822/3372 | 1564/2523 | 522/840 | chr1 | 36178057 | ||
| chr1:36178084
|
C | A | 3 | a0003a0006a0017 | 33 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(30): Show |
missense_variant | MODERATE | c.1591C>A | p.Arg531Ser | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 9/17 | 1849/3372 | 1591/2523 | 531/840 | chr1 | 36178084 | ||
| chr1:36178099
|
GAGA | G | 1 | a0002 | 33 | HG00323.hp2 HG00597.hp1 HG00642.hp1 others(30): Show |
conservative_inframe_deletion | MODERATE | c.1609_1611delAAG | p.Lys537del | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 9/17 | 1867/3372 | 1609/2523 | 537/840 | INFO_REALIGN_3_PRIME | chr1 | 36178099 | |
| chr1:36178741
|
C | T | 1 | a0018 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1943C>T | p.Ala648Val | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 11/17 | 2201/3372 | 1943/2523 | 648/840 | chr1 | 36178741 | ||
| chr1:36178921
|
A | G | 1 | a0014 | 1 | HG03041.hp1 | missense_variant&splice_region_variant | MODERATE | c.2026A>G | p.Lys676Glu | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/17 | 2284/3372 | 2026/2523 | 676/840 | chr1 | 36178921 | ||
| chr1:36178966
|
C | G | 1 | a0014 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.2071C>G | p.Arg691Gly | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/17 | 2329/3372 | 2071/2523 | 691/840 | chr1 | 36178966 | ||
| chr1:36178967
|
G | A | 1 | a0014 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.2072G>A | p.Arg691His | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/17 | 2330/3372 | 2072/2523 | 691/840 | chr1 | 36178967 | ||
| chr1:36178980
|
A | C | 1 | a0014 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.2085A>C | p.Glu695Asp | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/17 | 2343/3372 | 2085/2523 | 695/840 | chr1 | 36178980 | ||
| chr1:36178990
|
C | A | 1 | a0014 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.2095C>A | p.Gln699Lys | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/17 | 2353/3372 | 2095/2523 | 699/840 | chr1 | 36178990 | ||
| chr1:36179003
|
A | C | 1 | a0014 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.2108A>C | p.Gln703Pro | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/17 | 2366/3372 | 2108/2523 | 703/840 | chr1 | 36179003 | ||
| chr1:36179004
|
A | T | 1 | a0014 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.2109A>T | p.Gln703His | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/17 | 2367/3372 | 2109/2523 | 703/840 | chr1 | 36179004 | ||
| chr1:36179005
|
G | A | 1 | a0014 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.2110G>A | p.Glu704Lys | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/17 | 2368/3372 | 2110/2523 | 704/840 | chr1 | 36179005 | ||
| chr1:36179006
|
A | G | 1 | a0014 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.2111A>G | p.Glu704Gly | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/17 | 2369/3372 | 2111/2523 | 704/840 | chr1 | 36179006 | ||
| chr1:36179023
|
A | G | 1 | a0014 | 1 | HG03041.hp1 | missense_variant&splice_region_variant | MODERATE | c.2128A>G | p.Lys710Glu | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/17 | 2386/3372 | 2128/2523 | 710/840 | chr1 | 36179023 | ||
| chr1:36179281
|
A | T | 1 | a0014 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.2150A>T | p.Lys717Met | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 13/17 | 2408/3372 | 2150/2523 | 717/840 | chr1 | 36179281 | ||
| chr1:36179287
|
C | CTCGGAGG others(8): Show |
1 | a0014 | 1 | HG03041.hp1 | disruptive_inframe_insertion | MODERATE | c.2161_2162insGGACAG others(9): Show |
p.Arg720_Lys721insAr others(13): Show |
MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 13/17 | 2420/3372 | 2162/2523 | 721/840 | INFO_REALIGN_3_PRIME | chr1 | 36179287 | |
| chr1:36179310
|
A | T | 1 | a0014 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.2179A>T | p.Thr727Ser | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 13/17 | 2437/3372 | 2179/2523 | 727/840 | chr1 | 36179310 | ||
| chr1:36179533
|
G | T | 1 | a0015 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.2203G>T | p.Ala735Ser | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 14/17 | 2461/3372 | 2203/2523 | 735/840 | chr1 | 36179533 |
| chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:36171071
|
G | A | 1 | a0001c0020 | 1 | HG01257.hp2 | synonymous_variant | LOW | c.147G>A | p.Pro49Pro | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 2/17 | 405/3372 | 147/2523 | 49/840 | chr1 | 36171071 | ||
| chr1:36173369
|
C | T | 1 | a0004c0016 | 3 | HG02572.hp2 HG02615.hp2 HG02647.hp1 |
synonymous_variant | LOW | c.630C>T | p.Arg210Arg | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 5/17 | 888/3372 | 630/2523 | 210/840 | chr1 | 36173369 | ||
| chr1:36173384
|
C | T | 1 | a0001c0008 | 7 | NA18943.hp1 NA18945.hp2 NA18955.hp1 others(4): Show |
synonymous_variant | LOW | c.645C>T | p.Ile215Ile | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 5/17 | 903/3372 | 645/2523 | 215/840 | chr1 | 36173384 | ||
| chr1:36174920
|
G | A | 1 | a0001c0024 | 1 | NA18982.hp2 | synonymous_variant | LOW | c.762G>A | p.Ser254Ser | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 6/17 | 1020/3372 | 762/2523 | 254/840 | chr1 | 36174920 | ||
| chr1:36174941
|
C | T | 1 | a0001c0015 | 3 | HG01167.hp1 HG01169.hp2 HG03486.hp1 |
synonymous_variant | LOW | c.783C>T | p.His261His | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 6/17 | 1041/3372 | 783/2523 | 261/840 | chr1 | 36174941 | ||
| chr1:36176464
|
G | A | 4 | a0003c0004a0003c0011a0006c0019others(1): Show | 32 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(29): Show |
synonymous_variant | LOW | c.1116G>A | p.Pro372Pro | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 7/17 | 1374/3372 | 1116/2523 | 372/840 | chr1 | 36176464 | ||
| chr1:36176548
|
C | T | 2 | a0003c0011a0017c0025 | 6 | HG01943.hp2 HG01975.hp2 HG01993.hp2 others(3): Show |
synonymous_variant | LOW | c.1200C>T | p.Pro400Pro | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 7/17 | 1458/3372 | 1200/2523 | 400/840 | chr1 | 36176548 | ||
| chr1:36176798
|
C | T | 1 | a0001c0034 | 1 | HG02647.hp2 | synonymous_variant | LOW | c.1335C>T | p.Ala445Ala | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 8/17 | 1593/3372 | 1335/2523 | 445/840 | chr1 | 36176798 | ||
| chr1:36176819
|
T | C | 28 | a0001c0001a0001c0006a0001c0015others(25): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
synonymous_variant | LOW | c.1356T>C | p.Ser452Ser | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 8/17 | 1614/3372 | 1356/2523 | 452/840 | chr1 | 36176819 | ||
| chr1:36177906
|
C | T | 1 | a0003c0032 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.1413C>T | p.Ser471Ser | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 9/17 | 1671/3372 | 1413/2523 | 471/840 | chr1 | 36177906 | ||
| chr1:36178128
|
G | C | 2 | a0001c0006a0014c0029 | 13 | HG01884.hp2 HG01934.hp1 HG02055.hp2 others(10): Show |
synonymous_variant | LOW | c.1635G>C | p.Pro545Pro | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 9/17 | 1893/3372 | 1635/2523 | 545/840 | chr1 | 36178128 | ||
| chr1:36178182
|
C | T | 5 | a0003c0004a0003c0011a0003c0032others(2): Show | 33 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(30): Show |
synonymous_variant | LOW | c.1689C>T | p.Pro563Pro | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 9/17 | 1947/3372 | 1689/2523 | 563/840 | chr1 | 36178182 | ||
| chr1:36178727
|
G | C | 1 | a0014c0029 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.1929G>C | p.Arg643Arg | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 11/17 | 2187/3372 | 1929/2523 | 643/840 | chr1 | 36178727 | ||
| chr1:36179019
|
C | G | 1 | a0014c0029 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.2124C>G | p.Arg708Arg | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/17 | 2382/3372 | 2124/2523 | 708/840 | chr1 | 36179019 | ||
| chr1:36179283
|
A | C | 1 | a0014c0029 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.2152A>C | p.Arg718Arg | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 13/17 | 2410/3372 | 2152/2523 | 718/840 | chr1 | 36179283 | ||
| chr1:36179297
|
A | C | 1 | a0014c0029 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.2166A>C | p.Ser722Ser | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 13/17 | 2424/3372 | 2166/2523 | 722/840 | chr1 | 36179297 | ||
| chr1:36179898
|
G | A | 1 | a0001c0033 | 1 | NA18968.hp1 | synonymous_variant | LOW | c.2343G>A | p.Ala781Ala | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 16/17 | 2601/3372 | 2343/2523 | 781/840 | chr1 | 36179898 | ||
| chr1:36179901
|
C | T | 1 | a0001c0030 | 1 | HG02897.hp2 | synonymous_variant | LOW | c.2346C>T | p.Ser782Ser | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 16/17 | 2604/3372 | 2346/2523 | 782/840 | chr1 | 36179901 | ||
| chr1:36179925
|
C | G | 2 | a0001c0014a0006c0027 | 4 | HG01884.hp1 HG02055.hp1 HG02896.hp2 others(1): Show |
synonymous_variant | LOW | c.2370C>G | p.Leu790Leu | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 16/17 | 2628/3372 | 2370/2523 | 790/840 | chr1 | 36179925 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:36156213
|
C | A | 1 | a0001c0002t0005 | 1 | NA19081.hp2 | 5_prime_UTR_variant | MODIFIER | c.-205C>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/17 | 205 | chr1 | 36156213 | |||||
| chr1:36156229
|
C | T | 2 | a0001c0001t0013a0001c0001t0014 | 2 | HG02970.hp1 NA21309.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-189C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/17 | chr1 | 36156229 | ||||||
| chr1:36156243
|
C | T | 2 | a0003c0004t0003a0006c0019t0003 | 5 | HG00544.hp2 HG02040.hp1 HG02132.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-175C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/17 | 175 | chr1 | 36156243 | |||||
| chr1:36156308
|
TGCCGG | T | 3 | a0001c0001t0014a0001c0033t0012a0006c0009t0007 | 3 | HG02970.hp1 NA18963.hp1 NA18968.hp1 |
5_prime_UTR_variant | MODIFIER | c.-92_-88delCGGGC | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/17 | 88 | INFO_REALIGN_3_PRIME | chr1 | 36156308 | ||||
| chr1:36156309
|
G | C | 10 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(7): Show | 76 | HG00423.hp2 HG00438.hp2 HG00735.hp2 others(73): Show |
5_prime_UTR_variant | MODIFIER | c.-109G>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/17 | 109 | chr1 | 36156309 | |||||
| chr1:36156314
|
G | C | 1 | a0006c0009t0007 | 1 | NA18963.hp1 | 5_prime_UTR_variant | MODIFIER | c.-104G>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/17 | 104 | chr1 | 36156314 | |||||
| chr1:36180372
|
G | A | 1 | a0001c0001t0008 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*114G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 17/17 | 114 | chr1 | 36180372 | |||||
| chr1:36180448
|
G | A | 1 | a0001c0002t0009 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*190G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 17/17 | 190 | chr1 | 36180448 | |||||
| chr1:36180501
|
T | C | 2 | a0001c0001t0006a0001c0001t0010 | 2 | HG00673.hp1 NA18960.hp1 |
3_prime_UTR_variant | MODIFIER | c.*243T>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 17/17 | 243 | chr1 | 36180501 | |||||
| chr1:36180532
|
G | T | 1 | a0003c0004t0011 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*274G>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 17/17 | 274 | chr1 | 36180532 | |||||
| chr1:36180771
|
C | G | 1 | a0001c0001t0004 | 2 | NA18969.hp1 NA19090.hp1 |
3_prime_UTR_variant | MODIFIER | c.*513C>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 17/17 | 513 | chr1 | 36180771 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:36156484
|
A | G | 1 | a0001c0001t0002g0264 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.46+21A>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36156484 | ||||||
| chr1:36156568
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.46+105C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36156568 | ||||||
| chr1:36156570
|
C | G | 1 | a0003c0032t0001g0262 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.46+107C>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36156570 | ||||||
| chr1:36156578
|
A | G | 2 | a0001c0001t0001g0260a0018c0035t0001g0261 | 2 | HG02723.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.46+115A>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36156578 | ||||||
| chr1:36156602
|
TGCG | T | 19 | a0001c0001t0001g0257a0001c0001t0010g0245a0002c0003t0001g0042others(16): Show | 22 | HG00140.hp1 HG00597.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.46+151_46+153delGG others(1): Show |
MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 36156602 | |||||
| chr1:36156649
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.46+186C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36156649 | ||||||
| chr1:36156672
|
G | C | 3 | a0001c0001t0001g0020a0001c0001t0001g0045a0001c0001t0001g0046 | 4 | HG00673.hp2 HG02129.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.46+209G>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36156672 | ||||||
| chr1:36156789
|
C | G | 1 | a0001c0001t0001g0263 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.46+326C>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36156789 | ||||||
| chr1:36156843
|
C | T | 51 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0008others(48): Show | 76 | HG00423.hp2 HG00438.hp2 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.46+380C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36156843 | ||||||
| chr1:36156915
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.46+452G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36156915 | ||||||
| chr1:36157101
|
G | C | 1 | a0001c0001t0002g0213 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.46+638G>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36157101 | ||||||
| chr1:36157129
|
T | C | 251 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(248): Show | 329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.46+666T>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36157129 | ||||||
| chr1:36157269
|
C | G | 225 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(222): Show | 299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.46+806C>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36157269 | ||||||
| chr1:36157302
|
A | G | 144 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(141): Show | 186 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.46+839A>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36157302 | ||||||
| chr1:36157362
|
C | G | 1 | a0001c0002t0001g0212 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.46+899C>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36157362 | ||||||
| chr1:36157877
|
G | A | 6 | a0003c0004t0001g0026a0003c0004t0001g0027a0003c0004t0001g0090others(3): Show | 8 | HG00597.hp2 HG02083.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.46+1414G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36157877 | ||||||
| chr1:36157977
|
C | T | 2 | a0001c0002t0001g0038a0001c0002t0001g0211 | 3 | HG02717.hp2 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.46+1514C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36157977 | ||||||
| chr1:36158002
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.46+1539T>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36158002 | ||||||
| chr1:36158142
|
AG | A | 91 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0020others(88): Show | 117 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.46+1685delG | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 36158142 | |||||
| chr1:36158149
|
A | C | 1 | a0001c0002t0001g0067 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.46+1686A>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36158149 | ||||||
| chr1:36158161
|
C | T | 6 | a0001c0001t0001g0025a0001c0001t0001g0068a0001c0001t0001g0089others(3): Show | 7 | HG02809.hp1 HG02818.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.46+1698C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36158161 | ||||||
| chr1:36158403
|
T | C | 2 | a0004c0005t0001g0150a0004c0005t0001g0151 | 2 | HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.46+1940T>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36158403 | ||||||
| chr1:36158494
|
G | A | 4 | a0007c0010t0001g0023a0007c0010t0001g0069a0007c0010t0001g0070others(1): Show | 5 | HG01069.hp1 HG02280.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.46+2031G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36158494 | ||||||
| chr1:36158633
|
G | C | 21 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(18): Show | 26 | HG01069.hp1 HG01255.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.46+2170G>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36158633 | ||||||
| chr1:36158665
|
A | C | 1 | a0001c0002t0001g0210 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.46+2202A>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36158665 | ||||||
| chr1:36158795
|
T | G | 1 | a0001c0001t0001g0094 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.46+2332T>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36158795 | ||||||
| chr1:36158816
|
AT | A | 21 | a0001c0001t0002g0214a0003c0004t0001g0003a0003c0004t0001g0026others(18): Show | 32 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.46+2357delT | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 36158816 | |||||
| chr1:36158822
|
G | A | 1 | a0001c0002t0001g0181 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.46+2359G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36158822 | ||||||
| chr1:36158884
|
A | T | 1 | a0001c0001t0002g0243 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.46+2421A>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36158884 | ||||||
| chr1:36158888
|
T | G | 2 | a0001c0002t0001g0048a0001c0002t0001g0049 | 2 | NA18994.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.46+2425T>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36158888 | ||||||
| chr1:36158909
|
T | C | 1 | a0001c0015t0001g0085 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.46+2446T>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36158909 | ||||||
| chr1:36158970
|
G | T | 11 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(8): Show | 12 | HG01069.hp1 HG01255.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.46+2507G>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36158970 | ||||||
| chr1:36158993
|
G | C | 1 | a0001c0001t0013g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.46+2530G>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36158993 | ||||||
| chr1:36159035
|
G | GTTAT | 103 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0016others(100): Show | 129 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.46+2607_46+2610dup others(4): Show |
MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 36159035 | |||||
| chr1:36159035
|
G | GTTATTTA others(1): Show |
27 | a0001c0001t0001g0097a0001c0001t0001g0170a0001c0001t0008g0163others(24): Show | 30 | HG00597.hp1 HG00621.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.46+2603_46+2610dup others(8): Show |
MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 36159035 | |||||
| chr1:36159035
|
G | GTTATTTA others(5): Show |
12 | a0001c0001t0001g0014a0001c0001t0001g0095a0001c0001t0001g0161others(9): Show | 16 | HG00673.hp1 HG00735.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.46+2599_46+2610dup others(12): Show |
MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 36159035 | |||||
| chr1:36159035
|
GTTAT | G | 3 | a0001c0001t0002g0240a0001c0001t0002g0241a0003c0004t0001g0087 | 3 | HG00735.hp2 HG02145.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.46+2607_46+2610del others(4): Show |
MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 36159035 | |||||
| chr1:36159035
|
GTTATTTA others(1): Show |
G | 3 | a0001c0001t0001g0025a0001c0001t0001g0089a0001c0001t0002g0242 | 4 | HG02809.hp1 HG02818.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.46+2603_46+2610del others(8): Show |
MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 36159035 | |||||
| chr1:36159203
|
G | C | 11 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(8): Show | 12 | HG01069.hp1 HG01255.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.46+2740G>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36159203 | ||||||
| chr1:36159214
|
C | T | 1 | a0001c0008t0001g0209 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.46+2751C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36159214 | ||||||
| chr1:36159291
|
C | T | 1 | a0001c0002t0001g0211 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.46+2828C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36159291 | ||||||
| chr1:36159321
|
G | T | 1 | a0001c0001t0001g0263 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.46+2858G>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36159321 | ||||||
| chr1:36159452
|
C | T | 6 | a0001c0001t0001g0084a0001c0001t0001g0263a0007c0010t0001g0023others(3): Show | 7 | HG01069.hp1 HG01255.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.46+2989C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36159452 | ||||||
| chr1:36159501
|
G | T | 103 | a0001c0001t0001g0025a0001c0001t0001g0047a0001c0001t0001g0068others(100): Show | 146 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.46+3038G>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36159501 | ||||||
| chr1:36159680
|
G | A | 1 | a0001c0001t0002g0215 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.46+3217G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36159680 | ||||||
| chr1:36159681
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.46+3218C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36159681 | ||||||
| chr1:36159684
|
C | T | 1 | a0001c0001t0001g0147 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.46+3221C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36159684 | ||||||
| chr1:36159825
|
C | T | 3 | a0003c0004t0001g0027a0003c0004t0001g0092a0003c0004t0001g0093 | 4 | HG00597.hp2 NA18747.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.46+3362C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36159825 | ||||||
| chr1:36159829
|
G | C | 20 | a0003c0004t0001g0003a0003c0004t0001g0026a0003c0004t0001g0027others(17): Show | 31 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.46+3366G>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36159829 | ||||||
| chr1:36159921
|
A | G | 9 | a0001c0002t0001g0011a0001c0002t0001g0056a0001c0002t0001g0061others(6): Show | 11 | HG00280.hp2 HG00323.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.46+3458A>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36159921 | ||||||
| chr1:36159936
|
C | G | 1 | a0001c0002t0001g0210 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.46+3473C>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36159936 | ||||||
| chr1:36159946
|
C | T | 1 | a0011c0018t0001g0146 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.46+3483C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36159946 | ||||||
| chr1:36159955
|
A | G | 22 | a0001c0001t0001g0032a0001c0001t0001g0080a0001c0001t0001g0081others(19): Show | 28 | HG01069.hp1 HG01255.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.46+3492A>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36159955 | ||||||
| chr1:36160063
|
T | C | 1 | a0001c0002t0001g0061 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.46+3600T>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36160063 | ||||||
| chr1:36160279
|
C | G | 1 | a0001c0001t0002g0239 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.46+3816C>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36160279 | ||||||
| chr1:36160314
|
C | T | 1 | a0003c0032t0001g0262 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.46+3851C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36160314 | ||||||
| chr1:36160405
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.46+3942G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36160405 | ||||||
| chr1:36160422
|
C | G | 1 | a0001c0002t0001g0145 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.46+3959C>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36160422 | ||||||
| chr1:36160455
|
T | G | 1 | a0001c0001t0001g0105 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.46+3992T>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36160455 | ||||||
| chr1:36160501
|
G | A | 2 | a0001c0001t0001g0086a0001c0002t0001g0056 | 2 | HG01255.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.46+4038G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36160501 | ||||||
| chr1:36160508
|
G | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0260 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.46+4045G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36160508 | ||||||
| chr1:36160528
|
C | T | 52 | a0001c0001t0001g0047a0001c0001t0002g0001a0001c0001t0002g0006others(49): Show | 77 | HG00423.hp2 HG00438.hp2 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.46+4065C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36160528 | ||||||
| chr1:36160785
|
T | C | 3 | a0003c0004t0001g0033a0003c0004t0001g0153a0003c0004t0001g0154 | 4 | NA18947.hp2 NA18961.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.46+4322T>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36160785 | ||||||
| chr1:36160866
|
C | G | 1 | a0001c0001t0001g0047 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.46+4403C>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36160866 | ||||||
| chr1:36160909
|
G | T | 1 | a0001c0002t0001g0210 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.46+4446G>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36160909 | ||||||
| chr1:36160910
|
G | C | 1 | a0001c0001t0001g0106 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.46+4447G>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36160910 | ||||||
| chr1:36161191
|
C | T | 1 | a0001c0002t0001g0208 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.46+4728C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36161191 | ||||||
| chr1:36161310
|
A | T | 1 | a0003c0032t0001g0262 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.46+4847A>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36161310 | ||||||
| chr1:36161497
|
T | C | 1 | a0001c0002t0001g0145 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.46+5034T>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36161497 | ||||||
| chr1:36161510
|
T | G | 17 | a0001c0002t0001g0017a0001c0002t0001g0037a0001c0002t0001g0182others(14): Show | 21 | HG00558.hp2 HG02602.hp2 HG03654.hp1 others(18): Show |
intron_variant | MODIFIER | c.46+5047T>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36161510 | ||||||
| chr1:36161590
|
T | C | 225 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(222): Show | 299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.46+5127T>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36161590 | ||||||
| chr1:36161655
|
T | C | 1 | a0001c0002t0001g0057 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.46+5192T>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36161655 | ||||||
| chr1:36161715
|
C | T | 1 | a0001c0001t0002g0214 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.46+5252C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36161715 | ||||||
| chr1:36161745
|
T | C | 1 | a0001c0001t0001g0260 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.46+5282T>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36161745 | ||||||
| chr1:36161829
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.46+5366G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36161829 | ||||||
| chr1:36161842
|
C | G | 6 | a0001c0001t0001g0025a0001c0001t0001g0068a0001c0001t0001g0089others(3): Show | 7 | HG02809.hp1 HG02818.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.46+5379C>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36161842 | ||||||
| chr1:36161844
|
G | T | 27 | a0001c0001t0001g0257a0001c0001t0010g0245a0002c0003t0001g0042others(24): Show | 30 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.46+5381G>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36161844 | ||||||
| chr1:36161863
|
A | ATGTGTGT others(1): Show |
41 | a0001c0001t0001g0047a0001c0001t0002g0001a0001c0001t0002g0006others(38): Show | 66 | HG00423.hp2 HG00438.hp2 HG00741.hp1 others(63): Show |
intron_variant | MODIFIER | c.46+5406_46+5413dup others(8): Show |
MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 36161863 | |||||
| chr1:36161875
|
G | GTGTGTGT others(3): Show |
5 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(2): Show | 5 | HG00735.hp2 HG01109.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.46+5413_46+5414ins others(10): Show |
MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 36161875 | |||||
| chr1:36161877
|
A | ATG | 12 | a0001c0002t0001g0055a0001c0002t0001g0204a0001c0002t0001g0205others(9): Show | 14 | HG01192.hp1 HG01256.hp1 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.46+5447_46+5448dup others(2): Show |
MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 36161877 | |||||
| chr1:36161877
|
A | ATGTGTGT others(5): Show |
1 | a0003c0004t0001g0087 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.46+5437_46+5448dup others(12): Show |
MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 36161877 | |||||
| chr1:36161877
|
A | G | 13 | a0001c0001t0001g0025a0001c0001t0001g0089a0001c0001t0002g0217others(10): Show | 14 | HG00735.hp2 HG01109.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.46+5414A>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36161877 | ||||||
| chr1:36161877
|
ATG | A | 130 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(127): Show | 164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.46+5447_46+5448del others(2): Show |
MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 36161877 | |||||
| chr1:36161877
|
ATGTG | A | 7 | a0001c0001t0001g0068a0001c0001t0001g0107a0001c0001t0001g0260others(4): Show | 7 | HG02080.hp1 HG02723.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.46+5445_46+5448del others(4): Show |
MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 36161877 | |||||
| chr1:36161879
|
G | GTGTGTA | 5 | a0001c0001t0002g0217a0001c0001t0002g0219a0001c0001t0002g0239others(2): Show | 5 | HG01952.hp1 HG03834.hp1 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.46+5421_46+5422ins others(6): Show |
MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 36161879 | |||||
| chr1:36161910
|
T | A | 7 | a0001c0001t0001g0108a0001c0001t0002g0216a0001c0002t0005g0187others(4): Show | 8 | HG00597.hp1 HG00733.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.46+5447T>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36161910 | ||||||
| chr1:36161910
|
T | TGA | 3 | a0001c0001t0001g0080a0001c0015t0001g0024a0001c0015t0001g0085 | 4 | HG01167.hp1 HG01169.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.46+5457_46+5458dup others(2): Show |
MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 36161910 | |||||
| chr1:36161910
|
T | TGTGA | 5 | a0001c0001t0001g0084a0007c0010t0001g0023a0007c0010t0001g0069others(2): Show | 6 | HG01069.hp1 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.46+5448_46+5449ins others(4): Show |
MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 36161910 | |||||
| chr1:36161910
|
T | TGTGTGTG others(3): Show |
3 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083 | 3 | HG02922.hp2 HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.46+5448_46+5449ins others(10): Show |
MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 36161910 | |||||
| chr1:36161912
|
A | T | 1 | a0001c0001t0001g0086 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.46+5449A>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36161912 | ||||||
| chr1:36161931
|
T | A | 1 | a0001c0001t0001g0084 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.46+5468T>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36161931 | ||||||
| chr1:36161941
|
C | T | 120 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(117): Show | 151 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.46+5478C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36161941 | ||||||
| chr1:36162313
|
G | T | 1 | a0003c0011t0001g0160 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.46+5850G>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36162313 | ||||||
| chr1:36162413
|
C | T | 1 | a0001c0015t0001g0085 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.46+5950C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36162413 | ||||||
| chr1:36162432
|
G | A | 141 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(138): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.46+5969G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36162432 | ||||||
| chr1:36162439
|
T | C | 1 | a0001c0001t0014g0088 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.46+5976T>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36162439 | ||||||
| chr1:36162458
|
C | T | 104 | a0001c0001t0001g0025a0001c0001t0001g0047a0001c0001t0001g0068others(101): Show | 147 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(144): Show |
intron_variant | MODIFIER | c.46+5995C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36162458 | ||||||
| chr1:36162494
|
G | C | 4 | a0001c0001t0001g0068a0001c0001t0001g0260a0001c0001t0013g0179others(1): Show | 4 | HG02970.hp1 HG03139.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.46+6031G>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36162494 | ||||||
| chr1:36162550
|
T | C | 21 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(18): Show | 26 | HG01069.hp1 HG01255.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.46+6087T>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36162550 | ||||||
| chr1:36162640
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.46+6177G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36162640 | ||||||
| chr1:36162686
|
A | T | 1 | a0001c0002t0001g0186 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.46+6223A>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36162686 | ||||||
| chr1:36162700
|
A | G | 4 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(1): Show | 4 | HG01928.hp2 HG01952.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.46+6237A>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36162700 | ||||||
| chr1:36162794
|
T | C | 1 | a0003c0032t0001g0262 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.46+6331T>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36162794 | ||||||
| chr1:36163002
|
A | C | 3 | a0001c0001t0002g0232a0001c0001t0002g0233a0006c0009t0002g0237 | 3 | HG01109.hp2 HG02615.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.46+6539A>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36163002 | ||||||
| chr1:36163065
|
G | A | 20 | a0003c0004t0001g0003a0003c0004t0001g0026a0003c0004t0001g0027others(17): Show | 31 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.46+6602G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36163065 | ||||||
| chr1:36163102
|
G | C | 1 | a0003c0032t0001g0262 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.46+6639G>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36163102 | ||||||
| chr1:36163132
|
TG | T | 5 | a0001c0001t0001g0032a0001c0001t0001g0136a0001c0001t0001g0137others(2): Show | 6 | HG01257.hp1 HG01258.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.46+6670delG | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36163132 | ||||||
| chr1:36163143
|
C | T | 2 | a0001c0001t0001g0170a0001c0002t0001g0169 | 2 | HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.46+6680C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36163143 | ||||||
| chr1:36163393
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.46+6930C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36163393 | ||||||
| chr1:36163711
|
C | T | 4 | a0001c0001t0002g0231a0001c0001t0002g0232a0001c0001t0002g0233others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.46+7248C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36163711 | ||||||
| chr1:36163712
|
T | G | 1 | a0001c0002t0001g0182 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.46+7249T>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36163712 | ||||||
| chr1:36163783
|
G | T | 2 | a0001c0001t0002g0219a0001c0001t0002g0239 | 2 | NA19054.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.47-7188G>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36163783 | ||||||
| chr1:36163785
|
TATAAGTT others(25): Show |
T | 2 | a0001c0001t0002g0219a0001c0001t0002g0239 | 2 | NA19054.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.47-7185_47-7154del others(32): Show |
MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36163785 | ||||||
| chr1:36163817
|
C | CT | 51 | a0001c0001t0001g0047a0001c0001t0001g0086a0001c0001t0001g0260others(48): Show | 73 | HG00438.hp2 HG00735.hp2 HG00741.hp1 others(70): Show |
intron_variant | MODIFIER | c.47-7127dupT | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 36163817 | |||||
| chr1:36163817
|
C | CTT | 11 | a0001c0001t0001g0068a0001c0001t0002g0009a0001c0001t0002g0216others(8): Show | 14 | HG00423.hp2 HG02071.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.47-7128_47-7127dup others(2): Show |
MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 36163817 | |||||
| chr1:36163817
|
CT | C | 33 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0263others(30): Show | 45 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.47-7127delT | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 36163817 | |||||
| chr1:36163817
|
CTT | C | 5 | a0003c0004t0001g0156a0003c0011t0001g0007a0003c0011t0001g0158others(2): Show | 7 | HG01943.hp2 HG01975.hp2 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.47-7128_47-7127del others(2): Show |
MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 36163817 | |||||
| chr1:36163817
|
CTTTTTTT | C | 109 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(106): Show | 140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.47-7133_47-7127del others(7): Show |
MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 36163817 | |||||
| chr1:36163823
|
T | C | 1 | a0001c0001t0002g0239 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.47-7148T>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36163823 | ||||||
| chr1:36163828
|
T | C | 1 | a0006c0019t0003g0155 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.47-7143T>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36163828 | ||||||
| chr1:36163866
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.47-7105C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36163866 | ||||||
| chr1:36164301
|
C | T | 11 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(8): Show | 12 | HG01069.hp1 HG01255.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.47-6670C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36164301 | ||||||
| chr1:36164556
|
G | A | 1 | a0010c0017t0001g0050 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.47-6415G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36164556 | ||||||
| chr1:36164606
|
A | G | 1 | a0001c0001t0002g0229 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.47-6365A>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36164606 | ||||||
| chr1:36164648
|
G | A | 1 | a0003c0032t0001g0262 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.47-6323G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36164648 | ||||||
| chr1:36164781
|
G | T | 1 | a0001c0001t0001g0046 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.47-6190G>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36164781 | ||||||
| chr1:36164854
|
G | A | 1 | a0001c0002t0001g0202 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.47-6117G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36164854 | ||||||
| chr1:36165170
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.47-5801C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36165170 | ||||||
| chr1:36165193
|
C | A | 10 | a0001c0006t0001g0012a0001c0006t0001g0013a0001c0006t0001g0073others(7): Show | 14 | HG01884.hp2 HG01934.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.47-5778C>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36165193 | ||||||
| chr1:36165252
|
T | C | 1 | a0003c0004t0001g0092 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.47-5719T>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36165252 | ||||||
| chr1:36165272
|
C | T | 2 | a0001c0002t0001g0189a0001c0002t0001g0190 | 2 | NA18990.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.47-5699C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36165272 | ||||||
| chr1:36165406
|
AGCCACCT others(1): Show |
A | 2 | a0001c0001t0002g0019a0006c0009t0002g0019 | 3 | NA18961.hp2 NA18993.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.47-5561_47-5554del others(8): Show |
MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 36165406 | |||||
| chr1:36165438
|
T | G | 1 | a0001c0001t0013g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.47-5533T>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36165438 | ||||||
| chr1:36165451
|
T | C | 1 | a0001c0001t0013g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.47-5520T>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36165451 | ||||||
| chr1:36165654
|
G | C | 1 | a0001c0001t0014g0088 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.47-5317G>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36165654 | ||||||
| chr1:36165664
|
G | A | 4 | a0001c0001t0001g0028a0001c0001t0001g0109a0001c0001t0001g0110others(1): Show | 5 | NA18942.hp1 NA18970.hp1 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.47-5307G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36165664 | ||||||
| chr1:36165729
|
C | CT | 149 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(146): Show | 188 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.47-5224dupT | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 36165729 | |||||
| chr1:36165729
|
C | CTT | 14 | a0001c0001t0001g0080a0001c0001t0001g0127a0001c0001t0001g0129others(11): Show | 14 | HG00642.hp1 HG00642.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.47-5225_47-5224dup others(2): Show |
MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 36165729 | |||||
| chr1:36165729
|
C | CTTT | 19 | a0003c0004t0001g0003a0003c0004t0001g0026a0003c0004t0001g0027others(16): Show | 30 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.47-5226_47-5224dup others(3): Show |
MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 36165729 | |||||
| chr1:36165793
|
C | G | 1 | a0001c0001t0002g0216 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.47-5178C>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36165793 | ||||||
| chr1:36165927
|
G | A | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083 | 3 | HG02922.hp2 HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.47-5044G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36165927 | ||||||
| chr1:36165962
|
T | C | 58 | a0001c0001t0001g0025a0001c0001t0001g0047a0001c0001t0001g0068others(55): Show | 84 | HG00423.hp2 HG00438.hp2 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.47-5009T>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36165962 | ||||||
| chr1:36166019
|
C | T | 1 | a0001c0006t0001g0076 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.47-4952C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36166019 | ||||||
| chr1:36166248
|
C | G | 1 | a0001c0006t0001g0079 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.47-4723C>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36166248 | ||||||
| chr1:36166294
|
A | T | 1 | a0001c0001t0002g0239 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.47-4677A>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36166294 | ||||||
| chr1:36166312
|
A | G | 1 | a0003c0032t0001g0262 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.47-4659A>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36166312 | ||||||
| chr1:36166389
|
C | CT | 30 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(27): Show | 32 | HG00438.hp2 HG01175.hp1 HG01928.hp2 others(29): Show |
intron_variant | MODIFIER | c.47-4564dupT | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 36166389 | |||||
| chr1:36166389
|
CT | C | 15 | a0001c0001t0001g0005a0001c0001t0001g0131a0001c0001t0013g0179others(12): Show | 17 | HG01069.hp2 HG01175.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.47-4564delT | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 36166389 | |||||
| chr1:36166418
|
C | G | 1 | a0001c0001t0002g0216 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.47-4553C>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36166418 | ||||||
| chr1:36166450
|
C | T | 120 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(117): Show | 151 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.47-4521C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36166450 | ||||||
| chr1:36166668
|
C | T | 1 | a0003c0032t0001g0262 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.47-4303C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36166668 | ||||||
| chr1:36166970
|
A | C | 1 | a0001c0002t0001g0055 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.47-4001A>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36166970 | ||||||
| chr1:36167123
|
A | C | 2 | a0001c0001t0001g0025a0001c0001t0001g0089 | 3 | HG02809.hp1 HG02818.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.47-3848A>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36167123 | ||||||
| chr1:36167256
|
A | T | 2 | a0003c0004t0001g0087a0003c0032t0001g0262 | 2 | HG02145.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.47-3715A>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36167256 | ||||||
| chr1:36167445
|
A | G | 1 | a0008c0012t0001g0167 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.47-3526A>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36167445 | ||||||
| chr1:36167665
|
C | T | 4 | a0001c0001t0001g0068a0001c0001t0001g0260a0001c0001t0013g0179others(1): Show | 4 | HG02970.hp1 HG03139.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.47-3306C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36167665 | ||||||
| chr1:36167707
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.47-3264C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36167707 | ||||||
| chr1:36167757
|
ACTC | A | 120 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(117): Show | 151 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.47-3210_47-3208del others(3): Show |
MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 36167757 | |||||
| chr1:36168051
|
CTTTGGGA others(7): Show |
C | 1 | a0001c0002t0001g0051 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.47-2919_47-2906del others(14): Show |
MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36168051 | ||||||
| chr1:36168053
|
T | G | 1 | a0001c0001t0001g0127 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.47-2918T>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36168053 | ||||||
| chr1:36168222
|
G | C | 1 | a0001c0001t0001g0080 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.47-2749G>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36168222 | ||||||
| chr1:36168273
|
A | G | 104 | a0001c0001t0001g0025a0001c0001t0001g0047a0001c0001t0001g0068others(101): Show | 147 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(144): Show |
intron_variant | MODIFIER | c.47-2698A>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36168273 | ||||||
| chr1:36168296
|
G | GA | 167 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(164): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.47-2660dupA | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 36168296 | |||||
| chr1:36168296
|
G | GAA | 18 | a0001c0001t0001g0086a0001c0001t0001g0109a0001c0001t0001g0114others(15): Show | 18 | HG00597.hp1 HG00673.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.47-2661_47-2660dup others(2): Show |
MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 36168296 | |||||
| chr1:36168463
|
A | C | 10 | a0001c0006t0001g0012a0001c0006t0001g0013a0001c0006t0001g0073others(7): Show | 14 | HG01884.hp2 HG01934.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.47-2508A>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36168463 | ||||||
| chr1:36168530
|
G | A | 1 | a0001c0002t0001g0064 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.47-2441G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36168530 | ||||||
| chr1:36168813
|
G | A | 225 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(222): Show | 299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.47-2158G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36168813 | ||||||
| chr1:36168958
|
A | G | 1 | a0001c0001t0013g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.47-2013A>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36168958 | ||||||
| chr1:36169136
|
C | T | 3 | a0001c0001t0001g0124a0001c0001t0001g0125a0006c0009t0001g0116 | 3 | HG00639.hp2 HG01256.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.47-1835C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36169136 | ||||||
| chr1:36169207
|
G | A | 20 | a0003c0004t0001g0003a0003c0004t0001g0026a0003c0004t0001g0027others(17): Show | 31 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.47-1764G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36169207 | ||||||
| chr1:36169252
|
G | GA | 11 | a0001c0001t0001g0084a0001c0001t0001g0117a0001c0001t0002g0232others(8): Show | 11 | HG01261.hp1 HG02027.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.47-1704dupA | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 36169252 | |||||
| chr1:36169276
|
G | A | 1 | a0003c0004t0001g0087 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.47-1695G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36169276 | ||||||
| chr1:36169294
|
C | T | 1 | a0003c0032t0001g0262 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.47-1677C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36169294 | ||||||
| chr1:36169314
|
C | T | 121 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(118): Show | 152 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.47-1657C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36169314 | ||||||
| chr1:36169403
|
A | C | 7 | a0001c0001t0001g0084a0001c0001t0001g0263a0001c0034t0001g0152others(4): Show | 8 | HG01069.hp1 HG01255.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.47-1568A>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36169403 | ||||||
| chr1:36169555
|
CA | C | 6 | a0001c0001t0001g0123a0001c0001t0001g0131a0001c0001t0002g0243others(3): Show | 6 | HG02970.hp1 HG03491.hp1 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.47-1401delA | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 36169555 | |||||
| chr1:36169567
|
A | G | 1 | a0002c0003t0001g0103 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.47-1404A>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36169567 | ||||||
| chr1:36169608
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.47-1363C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36169608 | ||||||
| chr1:36169666
|
G | A | 3 | a0008c0012t0001g0165a0008c0012t0001g0166a0008c0012t0001g0168 | 3 | HG02027.hp1 NA18957.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.47-1305G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36169666 | ||||||
| chr1:36169759
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.47-1212G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36169759 | ||||||
| chr1:36170048
|
GAAACA | G | 2 | a0001c0001t0001g0025a0001c0001t0001g0089 | 3 | HG02809.hp1 HG02818.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.47-904_47-900delCA others(3): Show |
MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 36170048 | |||||
| chr1:36170209
|
G | A | 1 | a0002c0003t0001g0251 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.47-762G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36170209 | ||||||
| chr1:36170339
|
T | A | 2 | a0001c0001t0001g0114a0001c0001t0001g0118 | 2 | HG00423.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.47-632T>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36170339 | ||||||
| chr1:36170494
|
C | CA | 256 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(253): Show | 335 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.47-475dupA | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 36170494 | |||||
| chr1:36170765
|
G | C | 1 | a0003c0004t0001g0087 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.47-206G>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36170765 | ||||||
| chr1:36170869
|
A | G | 1 | a0001c0001t0001g0045 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47-102A>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 1/16 | chr1 | 36170869 | ||||||
| chr1:36171333
|
G | A | 11 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(8): Show | 12 | HG01069.hp1 HG01255.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.391+18G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 2/16 | chr1 | 36171333 | ||||||
| chr1:36171614
|
A | G | 4 | a0004c0005t0001g0150a0004c0005t0001g0151a0004c0005t0001g0175others(1): Show | 4 | HG02559.hp2 HG02818.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.460+33A>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 3/16 | chr1 | 36171614 | ||||||
| chr1:36171746
|
A | G | 1 | a0005c0007t0002g0226 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.460+165A>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 3/16 | chr1 | 36171746 | ||||||
| chr1:36171830
|
A | G | 1 | a0001c0002t0001g0182 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.460+249A>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 3/16 | chr1 | 36171830 | ||||||
| chr1:36171841
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.460+260G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 3/16 | chr1 | 36171841 | ||||||
| chr1:36171916
|
A | C | 11 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(8): Show | 12 | HG01069.hp1 HG01255.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.460+335A>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 3/16 | chr1 | 36171916 | ||||||
| chr1:36171929
|
C | T | 1 | a0003c0032t0001g0262 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.460+348C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 3/16 | chr1 | 36171929 | ||||||
| chr1:36171934
|
C | CA | 51 | a0001c0001t0001g0036a0001c0001t0001g0080a0001c0001t0001g0081others(48): Show | 63 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.460+377dupA | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 36171934 | |||||
| chr1:36171934
|
C | CAA | 127 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(124): Show | 180 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.460+376_460+377dup others(2): Show |
MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 36171934 | |||||
| chr1:36171934
|
C | CAAA | 44 | a0001c0001t0001g0029a0001c0001t0001g0035a0001c0001t0001g0106others(41): Show | 48 | HG00438.hp1 HG00735.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.460+375_460+377dup others(3): Show |
MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 36171934 | |||||
| chr1:36171950
|
A | C | 1 | a0001c0002t0001g0060 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.460+369A>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 3/16 | chr1 | 36171950 | ||||||
| chr1:36171963
|
C | T | 1 | a0001c0001t0002g0216 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.460+382C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 3/16 | chr1 | 36171963 | ||||||
| chr1:36172107
|
A | G | 133 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(130): Show | 166 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.461-357A>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 3/16 | chr1 | 36172107 | ||||||
| chr1:36172172
|
G | C | 2 | a0001c0001t0001g0025a0001c0001t0001g0089 | 3 | HG02809.hp1 HG02818.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.461-292G>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 3/16 | chr1 | 36172172 | ||||||
| chr1:36172388
|
C | T | 1 | a0001c0006t0001g0077 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.461-76C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 3/16 | chr1 | 36172388 | ||||||
| chr1:36172414
|
G | A | 1 | a0001c0001t0014g0088 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.461-50G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 3/16 | chr1 | 36172414 | ||||||
| chr1:36173015
|
C | T | 2 | a0002c0003t0001g0043a0002c0003t0001g0251 | 3 | NA18969.hp2 NA19056.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.625-349C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 4/16 | chr1 | 36173015 | ||||||
| chr1:36173348
|
C | G | 21 | a0003c0004t0001g0003a0003c0004t0001g0026a0003c0004t0001g0027others(18): Show | 32 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.625-16C>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 4/16 | chr1 | 36173348 | ||||||
| chr1:36173584
|
G | A | 2 | a0004c0005t0001g0171a0004c0005t0001g0173 | 2 | HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.739+106G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 5/16 | chr1 | 36173584 | ||||||
| chr1:36173623
|
T | G | 1 | a0001c0001t0001g0097 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.739+145T>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 5/16 | chr1 | 36173623 | ||||||
| chr1:36173643
|
C | G | 1 | a0001c0001t0001g0125 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.739+165C>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 5/16 | chr1 | 36173643 | ||||||
| chr1:36173712
|
T | A | 21 | a0003c0004t0001g0003a0003c0004t0001g0026a0003c0004t0001g0027others(18): Show | 32 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.739+234T>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 5/16 | chr1 | 36173712 | ||||||
| chr1:36173822
|
C | T | 1 | a0001c0006t0001g0077 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.739+344C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 5/16 | chr1 | 36173822 | ||||||
| chr1:36173823
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.739+345G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 5/16 | chr1 | 36173823 | ||||||
| chr1:36173980
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.739+502T>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 5/16 | chr1 | 36173980 | ||||||
| chr1:36174098
|
G | A | 44 | a0001c0001t0001g0047a0001c0001t0002g0001a0001c0001t0002g0006others(41): Show | 69 | HG00423.hp2 HG00438.hp2 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.739+620G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 5/16 | chr1 | 36174098 | ||||||
| chr1:36174129
|
T | C | 1 | a0001c0002t0001g0065 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.739+651T>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 5/16 | chr1 | 36174129 | ||||||
| chr1:36174178
|
A | G | 14 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(11): Show | 16 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.739+700A>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 5/16 | chr1 | 36174178 | ||||||
| chr1:36174628
|
G | A | 1 | a0001c0002t0001g0200 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.740-270G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 5/16 | chr1 | 36174628 | ||||||
| chr1:36174666
|
A | C | 1 | a0001c0001t0001g0136 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.740-232A>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 5/16 | chr1 | 36174666 | ||||||
| chr1:36174732
|
C | T | 1 | a0001c0001t0002g0233 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.740-166C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 5/16 | chr1 | 36174732 | ||||||
| chr1:36174849
|
C | G | 1 | a0001c0001t0001g0047 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.740-49C>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 5/16 | chr1 | 36174849 | ||||||
| chr1:36175086
|
C | T | 2 | a0001c0015t0001g0024a0001c0015t0001g0085 | 3 | HG01167.hp1 HG01169.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.850+78C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 6/16 | chr1 | 36175086 | ||||||
| chr1:36175087
|
ACCAGGTC others(19): Show |
A | 53 | a0001c0001t0001g0047a0001c0001t0002g0001a0001c0001t0002g0006others(50): Show | 78 | HG00423.hp2 HG00438.hp2 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.850+89_850+114delT others(25): Show |
MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr1 | 36175087 | |||||
| chr1:36175508
|
G | C | 4 | a0001c0001t0001g0068a0001c0001t0001g0260a0001c0001t0013g0179others(1): Show | 4 | HG02970.hp1 HG03139.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.850+500G>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 6/16 | chr1 | 36175508 | ||||||
| chr1:36175544
|
C | T | 1 | a0001c0001t0001g0036 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.850+536C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 6/16 | chr1 | 36175544 | ||||||
| chr1:36175673
|
T | TAAAAATA others(974): Show |
1 | a0003c0004t0001g0153 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.851-509_851-508ins others(981): Show |
MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr1 | 36175673 | |||||
| chr1:36175765
|
G | A | 3 | a0001c0002t0001g0037a0001c0002t0001g0191a0001c0033t0012g0037 | 3 | HG00558.hp2 NA18968.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.851-434G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 6/16 | chr1 | 36175765 | ||||||
| chr1:36175779
|
G | C | 1 | a0001c0001t0001g0030 | 2 | HG00140.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.851-420G>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 6/16 | chr1 | 36175779 | ||||||
| chr1:36175903
|
T | C | 21 | a0003c0004t0001g0003a0003c0004t0001g0026a0003c0004t0001g0027others(18): Show | 32 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.851-296T>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 6/16 | chr1 | 36175903 | ||||||
| chr1:36176128
|
C | T | 115 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(112): Show | 143 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.851-71C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 6/16 | chr1 | 36176128 | ||||||
| chr1:36176130
|
G | T | 1 | a0001c0001t0002g0240 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.851-69G>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 6/16 | chr1 | 36176130 | ||||||
| chr1:36176610
|
G | A | 3 | a0001c0001t0001g0086a0001c0015t0001g0024a0001c0015t0001g0085 | 4 | HG01167.hp1 HG01169.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1233+29G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 7/16 | chr1 | 36176610 | ||||||
| chr1:36176642
|
G | C | 14 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(11): Show | 16 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.1234-55G>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 7/16 | chr1 | 36176642 | ||||||
| chr1:36176668
|
C | T | 1 | a0001c0002t0001g0059 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1234-29C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 7/16 | chr1 | 36176668 | ||||||
| chr1:36176849
|
G | C | 1 | a0003c0032t0001g0262 | 1 | HG03471.hp2 | splice_region_variant&intron_variant | LOW | c.1379+7G>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 8/16 | chr1 | 36176849 | ||||||
| chr1:36176935
|
A | G | 14 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(11): Show | 16 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.1379+93A>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 8/16 | chr1 | 36176935 | ||||||
| chr1:36177087
|
G | A | 250 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(247): Show | 326 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.1379+245G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 8/16 | chr1 | 36177087 | ||||||
| chr1:36177139
|
G | A | 1 | a0004c0005t0001g0174 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1379+297G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 8/16 | chr1 | 36177139 | ||||||
| chr1:36177257
|
C | T | 115 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(112): Show | 143 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.1379+415C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 8/16 | chr1 | 36177257 | ||||||
| chr1:36177275
|
G | A | 1 | a0001c0001t0013g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1379+433G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 8/16 | chr1 | 36177275 | ||||||
| chr1:36177318
|
C | A | 2 | a0001c0002t0001g0186a0001c0002t0001g0193 | 2 | HG03942.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1379+476C>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 8/16 | chr1 | 36177318 | ||||||
| chr1:36177382
|
G | T | 1 | a0001c0014t0001g0058 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1380-491G>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 8/16 | chr1 | 36177382 | ||||||
| chr1:36177390
|
C | T | 115 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(112): Show | 143 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.1380-483C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 8/16 | chr1 | 36177390 | ||||||
| chr1:36177485
|
C | T | 1 | a0001c0002t0001g0049 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1380-388C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 8/16 | chr1 | 36177485 | ||||||
| chr1:36177504
|
T | A | 4 | a0003c0011t0001g0007a0003c0011t0001g0158a0003c0011t0001g0160others(1): Show | 6 | HG01943.hp2 HG01975.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.1380-369T>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 8/16 | chr1 | 36177504 | ||||||
| chr1:36177524
|
A | AAAC | 4 | a0001c0001t0001g0106a0001c0001t0001g0119a0001c0001t0001g0121others(1): Show | 4 | HG00621.hp2 NA18947.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.1380-328_1380-326d others(5): Show |
MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr1 | 36177524 | |||||
| chr1:36177758
|
C | CG | 11 | a0001c0001t0001g0115a0001c0001t0001g0120a0001c0001t0001g0263others(8): Show | 11 | HG00438.hp2 HG00741.hp1 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.1380-109dupG | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr1 | 36177758 | |||||
| chr1:36177792
|
G | A | 9 | a0001c0006t0001g0012a0001c0006t0001g0013a0001c0006t0001g0073others(6): Show | 13 | HG01884.hp2 HG01934.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1380-81G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 8/16 | chr1 | 36177792 | ||||||
| chr1:36177807
|
A | T | 2 | a0001c0015t0001g0024a0001c0015t0001g0085 | 3 | HG01167.hp1 HG01169.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1380-66A>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 8/16 | chr1 | 36177807 | ||||||
| chr1:36178219
|
G | A | 1 | a0001c0006t0001g0077 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1708+18G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 9/16 | chr1 | 36178219 | ||||||
| chr1:36178372
|
G | A | 1 | a0007c0010t0001g0069 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1709-47G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 9/16 | chr1 | 36178372 | ||||||
| chr1:36178653
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1887-32G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 10/16 | chr1 | 36178653 | ||||||
| chr1:36178831
|
C | CGGCG | 102 | a0001c0001t0001g0025a0001c0001t0001g0047a0001c0001t0001g0068others(99): Show | 145 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(142): Show |
intron_variant | MODIFIER | c.2025+15_2025+18dup others(4): Show |
MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr1 | 36178831 | |||||
| chr1:36178838
|
C | G | 5 | a0001c0008t0001g0018a0001c0008t0001g0188a0001c0008t0001g0192others(2): Show | 7 | NA18943.hp1 NA18945.hp2 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.2025+15C>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 11/16 | chr1 | 36178838 | ||||||
| chr1:36178868
|
C | T | 9 | a0001c0006t0001g0012a0001c0006t0001g0013a0001c0006t0001g0073others(6): Show | 13 | HG01884.hp2 HG01934.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.2025+45C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 11/16 | chr1 | 36178868 | ||||||
| chr1:36178890
|
A | C | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2026-31A>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 11/16 | chr1 | 36178890 | ||||||
| chr1:36178892
|
T | A | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2026-29T>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 11/16 | chr1 | 36178892 | ||||||
| chr1:36178895
|
C | A | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2026-26C>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 11/16 | chr1 | 36178895 | ||||||
| chr1:36178897
|
C | A | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2026-24C>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 11/16 | chr1 | 36178897 | ||||||
| chr1:36178899
|
C | G | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2026-22C>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 11/16 | chr1 | 36178899 | ||||||
| chr1:36178901
|
C | G | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2026-20C>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 11/16 | chr1 | 36178901 | ||||||
| chr1:36178902
|
T | G | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2026-19T>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 11/16 | chr1 | 36178902 | ||||||
| chr1:36178905
|
T | G | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2026-16T>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 11/16 | chr1 | 36178905 | ||||||
| chr1:36178907
|
G | A | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2026-14G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 11/16 | chr1 | 36178907 | ||||||
| chr1:36178913
|
T | C | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | splice_region_variant&intron_variant | LOW | c.2026-8T>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 11/16 | chr1 | 36178913 | ||||||
| chr1:36179027
|
T | G | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | splice_donor_variant&intron_variant | HIGH | c.2130+2T>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/16 | chr1 | 36179027 | ||||||
| chr1:36179059
|
G | C | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2130+34G>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/16 | chr1 | 36179059 | ||||||
| chr1:36179060
|
C | T | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2130+35C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/16 | chr1 | 36179060 | ||||||
| chr1:36179061
|
C | G | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2130+36C>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/16 | chr1 | 36179061 | ||||||
| chr1:36179072
|
G | C | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2130+47G>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/16 | chr1 | 36179072 | ||||||
| chr1:36179073
|
G | T | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2130+48G>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/16 | chr1 | 36179073 | ||||||
| chr1:36179075
|
C | G | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2130+50C>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/16 | chr1 | 36179075 | ||||||
| chr1:36179075
|
C | T | 1 | a0001c0001t0014g0088 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2130+50C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/16 | chr1 | 36179075 | ||||||
| chr1:36179077
|
A | G | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2130+52A>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/16 | chr1 | 36179077 | ||||||
| chr1:36179078
|
G | T | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2130+53G>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/16 | chr1 | 36179078 | ||||||
| chr1:36179156
|
T | A | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2131-106T>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/16 | chr1 | 36179156 | ||||||
| chr1:36179161
|
T | A | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2131-101T>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/16 | chr1 | 36179161 | ||||||
| chr1:36179182
|
T | C | 2 | a0003c0011t0001g0007a0017c0025t0001g0007 | 4 | HG01943.hp2 HG01975.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.2131-80T>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/16 | chr1 | 36179182 | ||||||
| chr1:36179185
|
G | T | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2131-77G>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/16 | chr1 | 36179185 | ||||||
| chr1:36179186
|
A | G | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2131-76A>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/16 | chr1 | 36179186 | ||||||
| chr1:36179188
|
G | A | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2131-74G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/16 | chr1 | 36179188 | ||||||
| chr1:36179190
|
C | G | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2131-72C>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/16 | chr1 | 36179190 | ||||||
| chr1:36179198
|
G | T | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2131-64G>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/16 | chr1 | 36179198 | ||||||
| chr1:36179205
|
G | C | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2131-57G>C | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/16 | chr1 | 36179205 | ||||||
| chr1:36179207
|
A | T | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2131-55A>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/16 | chr1 | 36179207 | ||||||
| chr1:36179210
|
T | A | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2131-52T>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/16 | chr1 | 36179210 | ||||||
| chr1:36179218
|
T | G | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2131-44T>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/16 | chr1 | 36179218 | ||||||
| chr1:36179219
|
A | T | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2131-43A>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/16 | chr1 | 36179219 | ||||||
| chr1:36179220
|
G | A | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2131-42G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/16 | chr1 | 36179220 | ||||||
| chr1:36179223
|
G | T | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2131-39G>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/16 | chr1 | 36179223 | ||||||
| chr1:36179224
|
C | T | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2131-38C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/16 | chr1 | 36179224 | ||||||
| chr1:36179225
|
G | A | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2131-37G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/16 | chr1 | 36179225 | ||||||
| chr1:36179231
|
C | A | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2131-31C>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/16 | chr1 | 36179231 | ||||||
| chr1:36179232
|
G | T | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2131-30G>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/16 | chr1 | 36179232 | ||||||
| chr1:36179233
|
A | G | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2131-29A>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/16 | chr1 | 36179233 | ||||||
| chr1:36179235
|
C | G | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2131-27C>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/16 | chr1 | 36179235 | ||||||
| chr1:36179239
|
A | G | 1 | a0014c0029t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2131-23A>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 12/16 | chr1 | 36179239 | ||||||
| chr1:36179376
|
C | T | 2 | a0001c0001t0001g0086a0001c0001t0002g0223 | 2 | HG02602.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2184+61C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 13/16 | chr1 | 36179376 | ||||||
| chr1:36179428
|
G | A | 1 | a0001c0002t0001g0197 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2185-87G>A | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 13/16 | chr1 | 36179428 | ||||||
| chr1:36179577
|
C | T | 7 | a0001c0001t0001g0084a0001c0001t0001g0263a0001c0034t0001g0152others(4): Show | 8 | HG01069.hp1 HG01255.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2227+20C>T | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 14/16 | chr1 | 36179577 | ||||||
| chr1:36180123
|
C | G | 53 | a0001c0001t0001g0047a0001c0001t0002g0001a0001c0001t0002g0006others(50): Show | 78 | HG00423.hp2 HG00438.hp2 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.2512+56C>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 16/16 | chr1 | 36180123 | ||||||
| chr1:36180210
|
T | G | 11 | a0001c0001t0001g0135a0001c0002t0001g0011a0001c0002t0001g0056others(8): Show | 13 | HG00280.hp2 HG00323.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.2513-38T>G | MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 16/16 | chr1 | 36180210 |