Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 221938 |
|---|---|
| ensemblid | ENSG00000136297.15 |
| hgncid | 30133 |
| symbol | MMD2 |
| name | monocyte to macrophage differentiation associated 2 |
| refseq_nuc | NM_198403.4 |
| refseq_prot | NP_940685.3 |
| ensembl_nuc | ENST00000401401.8 |
| ensembl_prot | ENSP00000384141.3 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 4905998 |
| end | 4959187 |
| strand | - |
| ver | v1.2 |
| region | chr7:4905998-4959187 |
| region5000 | chr7:4900998-4964187 |
| regionname0 | MMD2_chr7_4905998_4959187 |
| regionname5000 | MMD2_chr7_4900998_4964187 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 246 | 382 | 92 | 68 | 156 | 16 | 48 | 110 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 741 | 195 | 32 | 31 | 84 | 9 | 38 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| c0002 | 0/1 | 741 | 162 | 58 | 34 | 52 | 7 | 10 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| c0003 | 0/0 | 741 | 21 | 0 | 1 | 20 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| c0004 | 0/0 | 741 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| c0005 | 0/0 | 741 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| c0006 | 0/0 | 741 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| c0007 | 0/0 | 741 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 1569 | 109 | 46 | 15 | 44 | 1 | 2 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| t0002 | 0/0 | 1569 | 59 | 5 | 17 | 14 | 8 | 15 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| t0003 | 1/0 | 1569 | 55 | 5 | 5 | 28 | 2 | 14 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| t0004 | 0/0 | 1569 | 43 | 3 | 8 | 25 | 1 | 6 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| t0005 | 0/0 | 1569 | 19 | 0 | 5 | 12 | 0 | 2 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| t0006 | 0/0 | 1569 | 17 | 9 | 6 | 0 | 2 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| t0007 | 0/0 | 1569 | 14 | 0 | 1 | 13 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| t0008 | 0/0 | 1569 | 10 | 1 | 7 | 0 | 1 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| t0009 | 0/0 | 1569 | 6 | 6 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| t0010 | 0/0 | 1569 | 5 | 0 | 0 | 5 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| t0011 | 0/0 | 1569 | 4 | 4 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| t0012 | 0/0 | 1569 | 3 | 0 | 0 | 2 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| t0013 | 0/0 | 1569 | 3 | 2 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| t0014 | 0/0 | 1575 | 3 | 2 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| t0015 | 0/0 | 1569 | 3 | 0 | 0 | 3 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| t0016 | 0/0 | 1569 | 2 | 2 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| t0017 | 0/0 | 1569 | 2 | 2 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| t0018 | 0/0 | 1569 | 2 | 2 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| t0019 | 0/0 | 1569 | 2 | 0 | 0 | 1 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| t0020 | 0/0 | 1569 | 2 | 0 | 1 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| t0021 | 0/0 | 1569 | 2 | 0 | 2 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| t0022 | 0/0 | 1557 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| t0023 | 0/0 | 1569 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| t0024 | 0/0 | 1569 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| t0025 | 0/0 | 1569 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| t0026 | 0/0 | 1569 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| t0027 | 0/0 | 1569 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| t0028 | 0/0 | 1569 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| t0029 | 0/0 | 1569 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| t0030 | 0/0 | 1569 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| t0031 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| t0032 | 0/0 | 1569 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| t0033 | 0/0 | 1569 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| t0034 | 0/0 | 1569 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| t0035 | 0/0 | 1569 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| t0036 | 0/0 | 1569 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| t0037 | 0/0 | 1575 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| t0038 | 0/0 | 1569 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0086 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0118 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0362 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0363 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0369 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 741 | 195 | 32 | 31 | 84 | 9 | 38 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0002 | 0/1 | 741 | 162 | 58 | 34 | 52 | 7 | 10 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0003 | 0/0 | 741 | 21 | 0 | 1 | 20 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0004 | 0/0 | 741 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0005 | 0/0 | 741 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0006 | 0/0 | 741 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0007 | 0/0 | 741 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2309 | 41 | 11 | 5 | 23 | 0 | 2 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0001t0002 | 0/0 | 2309 | 49 | 4 | 15 | 13 | 5 | 12 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0001t0003 | 1/0 | 2309 | 37 | 5 | 4 | 15 | 2 | 10 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0001t0004 | 0/0 | 2309 | 21 | 3 | 6 | 5 | 1 | 6 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0001t0005 | 0/0 | 2309 | 6 | 0 | 0 | 4 | 0 | 2 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0001t0007 | 0/0 | 2309 | 9 | 0 | 0 | 9 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0001t0009 | 0/0 | 2309 | 2 | 2 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0001t0010 | 0/0 | 2309 | 5 | 0 | 0 | 5 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0001t0011 | 0/0 | 2309 | 3 | 3 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0001t0012 | 0/0 | 2309 | 3 | 0 | 0 | 2 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0001t0013 | 0/0 | 2309 | 2 | 1 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0001t0015 | 0/0 | 2309 | 3 | 0 | 0 | 3 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0001t0016 | 0/0 | 2309 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0001t0017 | 0/0 | 2309 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0001t0019 | 0/0 | 2309 | 2 | 0 | 0 | 1 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0001t0020 | 0/0 | 2309 | 2 | 0 | 1 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0001t0022 | 0/0 | 2297 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0001t0024 | 0/0 | 2309 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0001t0025 | 0/0 | 2309 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0001t0026 | 0/0 | 2309 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0001t0027 | 0/0 | 2309 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0001t0030 | 0/0 | 2309 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0001t0033 | 0/0 | 2309 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0001t0034 | 0/0 | 2309 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0002t0001 | 0/1 | 2309 | 66 | 35 | 9 | 20 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0002t0002 | 0/0 | 2309 | 9 | 0 | 2 | 1 | 3 | 3 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0002t0003 | 0/0 | 2309 | 16 | 0 | 0 | 12 | 0 | 4 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0002t0004 | 0/0 | 2309 | 5 | 0 | 1 | 4 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0002t0005 | 0/0 | 2309 | 13 | 0 | 5 | 8 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0002t0006 | 0/0 | 2309 | 17 | 9 | 6 | 0 | 2 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0002t0007 | 0/0 | 2309 | 5 | 0 | 1 | 4 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0002t0008 | 0/0 | 2309 | 10 | 1 | 7 | 0 | 1 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0002t0009 | 0/0 | 2309 | 4 | 4 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0002t0011 | 0/0 | 2309 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0002t0013 | 0/0 | 2309 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0002t0014 | 0/0 | 2315 | 3 | 2 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0002t0016 | 0/0 | 2309 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0002t0017 | 0/0 | 2309 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0002t0018 | 0/0 | 2309 | 2 | 2 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0002t0021 | 0/0 | 2309 | 2 | 0 | 2 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0002t0023 | 0/0 | 2309 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0002t0031 | 0/0 | 2294 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0002t0032 | 0/0 | 2309 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0002t0035 | 0/0 | 2309 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0002t0037 | 0/0 | 2315 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0002t0038 | 0/0 | 2309 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0003t0001 | 0/0 | 2309 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0003t0003 | 0/0 | 2309 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0003t0004 | 0/0 | 2309 | 17 | 0 | 1 | 16 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0003t0029 | 0/0 | 2309 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0003t0036 | 0/0 | 2309 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0004t0002 | 0/0 | 2309 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0005t0003 | 0/0 | 2309 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0006t0001 | 0/0 | 2309 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| a0001c0007t0028 | 0/0 | 2309 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | copy fasta | chr7 | 4900998 | 4964187 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0118 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0005g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0005g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0005g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0005g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0007g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0007g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0007g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0007g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0007g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0007g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0007g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0007g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0007g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0009g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0009g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0010g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0010g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0010g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0010g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0010g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0011g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0011g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0011g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0012g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0012g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0012g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0013g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0013g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0015g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0015g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0015g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0016g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0017g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0019g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0019g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0020g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0020g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0022g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0024g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0025g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0026g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0027g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0030g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0033g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0034g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0086 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0003g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0004g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0004g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0004g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0005g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0005g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0005g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0005g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0005g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0005g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0005g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0005g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0005g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0005g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0005g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0005g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0006g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0006g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0006g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0006g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0006g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0006g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0006g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0006g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0006g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0006g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0006g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0006g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0006g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0006g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0006g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0006g0362 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0006g0363 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0007g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0007g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0007g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0007g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0007g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0008g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0008g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0008g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0008g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0008g0369 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0008g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0008g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0008g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0008g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0008g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0009g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0009g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0009g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0009g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0011g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0013g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0014g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0014g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0014g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0016g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0017g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0018g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0018g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0021g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0021g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0023g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0031g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0032g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0035g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0037g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0038g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0004g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0004g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0004g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0004g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0004g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0004g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0004g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0004g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0004g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0004g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0004g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0029g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0036g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0004t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0005t0003g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0006t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0007t0028g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0120 | EUR | GBR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00099 | hp2 | a0001 | c0002 | t0002 | g0119 | EUR | GBR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0094 | EUR | GBR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0060 | EUR | GBR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00280 | hp1 | a0001 | c0002 | t0008 | g0369 | EUR | FIN | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00280 | hp2 | a0001 | c0002 | t0002 | g0111 | EUR | FIN | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00408 | hp1 | a0001 | c0003 | t0004 | g0304 | EAS | CHS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00408 | hp2 | a0001 | c0001 | t0005 | g0080 | EAS | CHS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | CHS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | CHS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | CHS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | CHS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00544 | hp2 | a0001 | c0002 | t0005 | g0169 | EAS | CHS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00558 | hp1 | a0001 | c0002 | t0005 | g0167 | EAS | CHS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | CHS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00597 | hp1 | a0001 | c0001 | t0010 | g0338 | EAS | CHS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00609 | hp1 | a0001 | c0003 | t0004 | g0241 | EAS | CHS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00621 | hp1 | a0001 | c0002 | t0003 | g0162 | EAS | CHS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00639 | hp1 | a0001 | c0002 | t0008 | g0376 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0275 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0251 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | CHS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | CHS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0253 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00735 | hp2 | a0001 | c0002 | t0005 | g0143 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00738 | hp1 | a0001 | c0001 | t0020 | g0355 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0215 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0115 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01069 | hp1 | a0001 | c0002 | t0005 | g0142 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0134 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0129 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0252 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0222 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0218 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01081 | hp2 | a0001 | c0002 | t0006 | g0360 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0133 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0254 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0261 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0091 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01109 | hp2 | a0001 | c0002 | t0006 | g0350 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0281 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01167 | hp2 | a0001 | c0002 | t0004 | g0187 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0113 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0280 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01192 | hp2 | a0001 | c0002 | t0008 | g0366 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01243 | hp1 | a0001 | c0002 | t0007 | g0226 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0033 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0065 | AMR | CLM | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01255 | hp2 | a0001 | c0002 | t0006 | g0354 | AMR | CLM | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0114 | AMR | CLM | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01256 | hp2 | a0001 | c0002 | t0006 | g0361 | AMR | CLM | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0270 | AMR | CLM | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0112 | AMR | CLM | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0096 | AMR | CLM | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0132 | AMR | CLM | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01433 | hp2 | a0001 | c0002 | t0008 | g0374 | AMR | CLM | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01496 | hp2 | a0001 | c0005 | t0003 | g0292 | AMR | CLM | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01515 | hp1 | a0001 | c0002 | t0006 | g0363 | EUR | IBS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01515 | hp2 | a0001 | c0001 | t0022 | g0004 | EUR | IBS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0109 | EUR | IBS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0282 | EUR | IBS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01517 | hp1 | a0001 | c0002 | t0006 | g0362 | EUR | IBS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0283 | EUR | IBS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0095 | AFR | ACB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0228 | AFR | ACB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01891 | hp1 | a0001 | c0001 | t0011 | g0333 | AFR | ACB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01891 | hp2 | a0001 | c0002 | t0006 | g0349 | AFR | ACB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01928 | hp1 | a0001 | c0002 | t0021 | g0372 | AMR | PEL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01928 | hp2 | a0001 | c0002 | t0005 | g0144 | AMR | PEL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01934 | hp1 | a0001 | c0002 | t0038 | g0364 | AMR | PEL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0131 | AMR | PEL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01943 | hp1 | a0001 | c0002 | t0008 | g0370 | AMR | PEL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0276 | AMR | PEL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01975 | hp1 | a0001 | c0002 | t0006 | g0358 | AMR | PEL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01975 | hp2 | a0001 | c0002 | t0005 | g0137 | AMR | PEL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01978 | hp1 | a0001 | c0002 | t0021 | g0373 | AMR | PEL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0272 | AMR | PEL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01981 | hp1 | a0001 | c0006 | t0001 | g0217 | AMR | PEL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01981 | hp2 | a0001 | c0002 | t0008 | g0367 | AMR | PEL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02004 | hp1 | a0001 | c0003 | t0004 | g0306 | AMR | PEL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02004 | hp2 | a0001 | c0002 | t0008 | g0375 | AMR | PEL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0320 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02040 | hp1 | a0001 | c0001 | t0019 | g0051 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02055 | hp1 | a0001 | c0001 | t0011 | g0039 | AFR | ACB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02055 | hp2 | a0001 | c0004 | t0002 | g0293 | AFR | ACB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02056 | hp1 | a0001 | c0002 | t0003 | g0179 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02071 | hp1 | a0001 | c0001 | t0010 | g0340 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02071 | hp2 | a0001 | c0002 | t0005 | g0159 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02074 | hp1 | a0001 | c0001 | t0007 | g0047 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0250 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02083 | hp1 | a0001 | c0003 | t0003 | g0295 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0184 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02129 | hp2 | a0001 | c0001 | t0007 | g0074 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02132 | hp1 | a0001 | c0002 | t0007 | g0181 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02135 | hp2 | a0001 | c0001 | t0033 | g0089 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0101 | AFR | ACB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02145 | hp2 | a0001 | c0002 | t0008 | g0368 | AFR | ACB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02155 | hp1 | a0001 | c0002 | t0003 | g0180 | EAS | CDX | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | CDX | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02165 | hp1 | a0001 | c0001 | t0010 | g0337 | EAS | CDX | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0214 | EAS | CDX | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0235 | AFR | ACB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02258 | hp2 | a0001 | c0002 | t0009 | g0042 | AFR | ACB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02293 | hp1 | a0001 | c0002 | t0005 | g0141 | AMR | PEL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02293 | hp2 | a0001 | c0002 | t0006 | g0357 | AMR | PEL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02300 | hp2 | a0001 | c0002 | t0008 | g0371 | AMR | PEL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0242 | AFR | ACB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0127 | AFR | ACB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02523 | hp2 | a0001 | c0001 | t0010 | g0335 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02572 | hp1 | a0001 | c0002 | t0009 | g0038 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02572 | hp2 | a0001 | c0007 | t0028 | g0332 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02602 | hp1 | a0001 | c0001 | t0027 | g0018 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02602 | hp2 | a0001 | c0002 | t0037 | g0341 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02615 | hp2 | a0001 | c0001 | t0017 | g0123 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0126 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0243 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02647 | hp2 | a0001 | c0001 | t0009 | g0246 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0257 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02698 | hp2 | a0001 | c0001 | t0020 | g0345 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0233 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02717 | hp2 | a0001 | c0002 | t0009 | g0041 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0117 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0231 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0016 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0003 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0264 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0122 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02809 | hp2 | a0001 | c0002 | t0006 | g0351 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0329 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02818 | hp2 | a0001 | c0001 | t0030 | g0322 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0116 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0121 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0331 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0326 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02896 | hp2 | a0001 | c0002 | t0006 | g0353 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0125 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02897 | hp2 | a0001 | c0002 | t0006 | g0352 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | ESN | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | ESN | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02965 | hp1 | a0001 | c0002 | t0016 | g0157 | AFR | ESN | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02965 | hp2 | a0001 | c0002 | t0006 | g0347 | AFR | ESN | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | ESN | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ESN | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0324 | AFR | ESN | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02976 | hp2 | a0001 | c0001 | t0009 | g0245 | AFR | ESN | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0093 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03017 | hp2 | a0001 | c0002 | t0008 | g0365 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03041 | hp1 | a0001 | c0001 | t0011 | g0334 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0202 | AFR | MSL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03098 | hp2 | a0001 | c0002 | t0013 | g0176 | AFR | MSL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0008 | AFR | ESN | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03130 | hp2 | a0001 | c0002 | t0006 | g0348 | AFR | ESN | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0330 | AFR | ESN | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03139 | hp2 | a0001 | c0002 | t0006 | g0359 | AFR | ESN | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03195 | hp1 | a0001 | c0002 | t0009 | g0040 | AFR | ESN | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0197 | AFR | ESN | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0201 | AFR | MSL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0236 | AFR | MSL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03225 | hp1 | a0001 | c0002 | t0014 | g0344 | AFR | MSL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | MSL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0285 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0077 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0110 | AFR | MSL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0203 | AFR | MSL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03490 | hp1 | a0001 | c0001 | t0005 | g0288 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03490 | hp2 | a0001 | c0001 | t0024 | g0045 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0260 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0284 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0259 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03492 | hp2 | a0001 | c0001 | t0005 | g0266 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0230 | AFR | ESN | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0102 | AFR | ESN | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03540 | hp1 | a0001 | c0002 | t0014 | g0343 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0327 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | MSL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0155 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0090 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0274 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0003 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03688 | hp1 | a0001 | c0001 | t0034 | g0150 | SAS | STU | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03688 | hp2 | a0001 | c0002 | t0003 | g0136 | SAS | STU | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0022 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0076 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03831 | hp1 | a0001 | c0002 | t0032 | g0152 | SAS | BEB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0015 | SAS | BEB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0221 | SAS | BEB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03834 | hp2 | a0001 | c0001 | t0012 | g0064 | SAS | BEB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03927 | hp1 | a0001 | c0001 | t0019 | g0050 | SAS | BEB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0287 | SAS | BEB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | BEB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0262 | SAS | BEB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0265 | SAS | STU | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG04115 | hp2 | a0001 | c0002 | t0003 | g0178 | SAS | STU | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0034 | SAS | BEB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0279 | SAS | BEB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0035 | SAS | STU | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0069 | SAS | STU | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0073 | SAS | STU | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG04204 | hp2 | a0001 | c0002 | t0003 | g0151 | SAS | STU | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0010 | SAS | STU | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0156 | SAS | STU | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0128 | AFR | YRI | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0205 | AFR | YRI | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | CHB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18612 | hp2 | a0001 | c0002 | t0007 | g0194 | EAS | CHB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | CHB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18906 | hp1 | a0001 | c0002 | t0017 | g0190 | AFR | YRI | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18906 | hp2 | a0001 | c0002 | t0011 | g0147 | AFR | YRI | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18939 | hp2 | a0001 | c0001 | t0013 | g0277 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18942 | hp1 | a0001 | c0002 | t0004 | g0182 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18942 | hp2 | a0001 | c0001 | t0005 | g0075 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18946 | hp1 | a0001 | c0001 | t0015 | g0378 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18950 | hp2 | a0001 | c0003 | t0004 | g0299 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18951 | hp1 | a0001 | c0002 | t0005 | g0145 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18952 | hp1 | a0001 | c0001 | t0012 | g0071 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18952 | hp2 | a0001 | c0002 | t0004 | g0308 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18956 | hp1 | a0001 | c0001 | t0004 | g0323 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18956 | hp2 | a0001 | c0002 | t0003 | g0140 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18959 | hp1 | a0001 | c0003 | t0004 | g0300 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18962 | hp2 | a0001 | c0001 | t0007 | g0085 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18963 | hp1 | a0001 | c0003 | t0004 | g0314 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18966 | hp1 | a0001 | c0002 | t0005 | g0158 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18967 | hp2 | a0001 | c0002 | t0003 | g0183 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18968 | hp2 | a0001 | c0003 | t0004 | g0296 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18969 | hp1 | a0001 | c0003 | t0004 | g0317 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18971 | hp2 | a0001 | c0001 | t0025 | g0269 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18977 | hp2 | a0001 | c0003 | t0004 | g0321 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18980 | hp2 | a0001 | c0002 | t0003 | g0185 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18981 | hp1 | a0001 | c0001 | t0007 | g0062 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18981 | hp2 | a0001 | c0003 | t0004 | g0196 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18982 | hp2 | a0001 | c0001 | t0004 | g0311 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18983 | hp1 | a0001 | c0001 | t0007 | g0083 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18986 | hp2 | a0001 | c0003 | t0001 | g0318 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18991 | hp1 | a0001 | c0003 | t0036 | g0339 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18992 | hp2 | a0001 | c0002 | t0003 | g0174 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18994 | hp1 | a0001 | c0001 | t0007 | g0224 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18994 | hp2 | a0001 | c0003 | t0004 | g0307 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18998 | hp1 | a0001 | c0002 | t0003 | g0160 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18998 | hp2 | a0001 | c0003 | t0004 | g0301 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19000 | hp1 | a0001 | c0001 | t0026 | g0289 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19002 | hp1 | a0001 | c0001 | t0007 | g0081 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19002 | hp2 | a0001 | c0001 | t0015 | g0377 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19003 | hp2 | a0001 | c0002 | t0003 | g0148 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19007 | hp1 | a0001 | c0001 | t0010 | g0336 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19009 | hp1 | a0001 | c0002 | t0007 | g0168 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19010 | hp1 | a0001 | c0002 | t0005 | g0173 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19010 | hp2 | a0001 | c0002 | t0003 | g0186 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19011 | hp1 | a0001 | c0003 | t0029 | g0313 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19011 | hp2 | a0001 | c0002 | t0004 | g0171 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19012 | hp2 | a0001 | c0003 | t0004 | g0305 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | LWK | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0188 | AFR | LWK | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19043 | hp1 | a0001 | c0002 | t0018 | g0153 | AFR | LWK | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0103 | AFR | LWK | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19054 | hp1 | a0001 | c0002 | t0005 | g0172 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19054 | hp2 | a0001 | c0001 | t0004 | g0309 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19056 | hp1 | a0001 | c0003 | t0004 | g0297 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19057 | hp1 | a0001 | c0001 | t0007 | g0063 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19058 | hp1 | a0001 | c0002 | t0031 | g0161 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19060 | hp2 | a0001 | c0002 | t0023 | g0005 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19064 | hp1 | a0001 | c0001 | t0015 | g0379 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19064 | hp2 | a0001 | c0002 | t0003 | g0170 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19065 | hp1 | a0001 | c0002 | t0003 | g0315 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19065 | hp2 | a0001 | c0001 | t0004 | g0310 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19066 | hp1 | a0001 | c0003 | t0004 | g0298 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19066 | hp2 | a0001 | c0001 | t0005 | g0079 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19068 | hp1 | a0001 | c0003 | t0004 | g0302 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19070 | hp2 | a0001 | c0003 | t0004 | g0316 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19074 | hp1 | a0001 | c0001 | t0007 | g0061 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19080 | hp1 | a0001 | c0002 | t0004 | g0303 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19085 | hp2 | a0001 | c0001 | t0005 | g0070 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19087 | hp1 | a0001 | c0002 | t0014 | g0342 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19087 | hp2 | a0001 | c0001 | t0012 | g0227 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19090 | hp2 | a0001 | c0002 | t0007 | g0163 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19091 | hp1 | a0001 | c0002 | t0005 | g0191 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0232 | AFR | YRI | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | YRI | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0244 | AFR | ASW | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA20129 | hp2 | a0001 | c0002 | t0035 | g0199 | AFR | ASW | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0267 | EUR | TSI | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0057 | EUR | TSI | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0023 | EUR | TSI | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0200 | EUR | TSI | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA20905 | hp1 | a0001 | c0002 | t0003 | g0124 | SAS | GIH | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0294 | SAS | GIH | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02109 | hp1 | a0001 | c0002 | t0006 | g0356 | AFR | ACB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02109 | hp2 | a0001 | c0002 | t0006 | g0346 | AFR | ACB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0325 | AFR | ACB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0263 | AFR | ACB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03471 | hp1 | a0001 | c0001 | t0013 | g0229 | AFR | MSL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG06807 | hp1 | a0001 | c0001 | t0016 | g0104 | AFR | USA | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0291 | AFR | USA | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0130 | AFR | USA | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0278 | AFR | USA | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA21309 | hp1 | a0001 | c0002 | t0018 | g0154 | AFR | LWK | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0234 | AFR | LWK | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0086 | REF | REF | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0118 | REF | REF | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:4907423
|
G | A | 1 | a0001c0004 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.714C>T | p.Ser238Ser | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 884/2309 | 714/741 | 238/246 | chr7 | 4907423 | ||
| chr7:4909920
|
G | A | 1 | a0001c0006 | 1 | HG01981.hp1 | synonymous_variant | LOW | c.498C>T | p.Val166Val | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/7 | 668/2309 | 498/741 | 166/246 | chr7 | 4909920 | ||
| chr7:4911222
|
G | C | 1 | a0001c0005 | 1 | HG01496.hp2 | synonymous_variant | LOW | c.390C>G | p.Pro130Pro | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 5/7 | 560/2309 | 390/741 | 130/246 | chr7 | 4911222 | ||
| chr7:4916022
|
C | T | 1 | a0001c0003 | 21 | HG00408.hp1 HG00609.hp1 HG02004.hp1 others(18): Show |
synonymous_variant | LOW | c.348G>A | p.Ala116Ala | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/7 | 518/2309 | 348/741 | 116/246 | chr7 | 4916022 | ||
| chr7:4920176
|
G | A | 2 | a0001c0002a0001c0006 | 163 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(160): Show |
synonymous_variant | LOW | c.285C>T | p.His95His | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/7 | 455/2309 | 285/741 | 95/246 | chr7 | 4920176 | ||
| chr7:4920278
|
G | A | 1 | a0001c0007 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.183C>T | p.Asp61Asp | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/7 | 353/2309 | 183/741 | 61/246 | chr7 | 4920278 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:4906123
|
G | C | 2 | a0001c0001t0016a0001c0002t0016 | 2 | HG02965.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1273C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 1273 | chr7 | 4906123 | |||||
| chr7:4906274
|
G | A | 1 | a0001c0002t0018 | 2 | NA19043.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1122C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 1122 | chr7 | 4906274 | |||||
| chr7:4906319
|
G | A | 1 | a0001c0001t0012 | 3 | HG03834.hp2 NA18952.hp1 NA19087.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1077C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 1077 | chr7 | 4906319 | |||||
| chr7:4906486
|
G | A | 1 | a0001c0002t0032 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*910C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 910 | chr7 | 4906486 | |||||
| chr7:4906526
|
TCTCTGGA others(8): Show |
T | 1 | a0001c0002t0031 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*855_*869delTCCAAA others(9): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 855 | chr7 | 4906526 | |||||
| chr7:4906544
|
T | C | 10 | a0001c0001t0002a0001c0001t0010a0001c0001t0020others(7): Show | 71 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*852A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 852 | chr7 | 4906544 | |||||
| chr7:4906584
|
T | C | 1 | a0001c0001t0019 | 2 | HG02040.hp1 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*812A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 812 | chr7 | 4906584 | |||||
| chr7:4906595
|
T | C | 6 | a0001c0001t0004a0001c0001t0025a0001c0002t0004others(3): Show | 46 | HG00099.hp1 HG00408.hp1 HG00609.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*801A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 801 | chr7 | 4906595 | |||||
| chr7:4906656
|
C | T | 40 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(37): Show | 311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): Show |
3_prime_UTR_variant | MODIFIER | c.*740G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 740 | chr7 | 4906656 | |||||
| chr7:4906712
|
T | G | 2 | a0001c0001t0017a0001c0002t0017 | 2 | HG02615.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*684A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 684 | chr7 | 4906712 | |||||
| chr7:4906873
|
A | C | 2 | a0001c0001t0009a0001c0002t0009 | 6 | HG02258.hp2 HG02572.hp1 HG02647.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*523T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 523 | chr7 | 4906873 | |||||
| chr7:4906974
|
G | A | 5 | a0001c0001t0004a0001c0001t0025a0001c0002t0004others(2): Show | 45 | HG00099.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*422C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 422 | chr7 | 4906974 | |||||
| chr7:4907036
|
G | A | 1 | a0001c0001t0030 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*360C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 360 | chr7 | 4907036 | |||||
| chr7:4907069
|
A | G | 4 | a0001c0001t0005a0001c0002t0005a0001c0002t0021others(1): Show | 22 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*327T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 327 | chr7 | 4907069 | |||||
| chr7:4907169
|
T | C | 1 | a0001c0001t0033 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*227A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 227 | chr7 | 4907169 | |||||
| chr7:4907200
|
T | C | 1 | a0001c0001t0030 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*196A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 196 | chr7 | 4907200 | |||||
| chr7:4907229
|
G | A | 10 | a0001c0001t0005a0001c0001t0007a0001c0001t0009others(7): Show | 46 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*167C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 167 | chr7 | 4907229 | |||||
| chr7:4907233
|
G | A | 1 | a0001c0002t0035 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*163C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 163 | chr7 | 4907233 | |||||
| chr7:4907246
|
T | C | 45 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(42): Show | 317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): Show |
3_prime_UTR_variant | MODIFIER | c.*150A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 150 | chr7 | 4907246 | |||||
| chr7:4907320
|
G | A | 5 | a0001c0001t0004a0001c0001t0025a0001c0002t0004others(2): Show | 45 | HG00099.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*76C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 76 | chr7 | 4907320 | |||||
| chr7:4907330
|
G | C | 1 | a0001c0001t0025 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*66C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 66 | chr7 | 4907330 | |||||
| chr7:4907342
|
A | G | 41 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(38): Show | 312 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(309): Show |
3_prime_UTR_variant | MODIFIER | c.*54T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 54 | chr7 | 4907342 | |||||
| chr7:4907343
|
C | T | 1 | a0001c0001t0027 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*53G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 53 | chr7 | 4907343 | |||||
| chr7:4907347
|
A | T | 1 | a0001c0001t0026 | 1 | NA19000.hp1 | 3_prime_UTR_variant | MODIFIER | c.*49T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 49 | chr7 | 4907347 | |||||
| chr7:4907350
|
G | A | 2 | a0001c0001t0011a0001c0002t0011 | 4 | HG01891.hp1 HG02055.hp1 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*46C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 46 | chr7 | 4907350 | |||||
| chr7:4907352
|
G | C | 5 | a0001c0001t0004a0001c0001t0025a0001c0002t0004others(2): Show | 45 | HG00099.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*44C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 44 | chr7 | 4907352 | |||||
| chr7:4907382
|
A | G | 5 | a0001c0001t0004a0001c0001t0025a0001c0002t0004others(2): Show | 45 | HG00099.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*14T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 14 | chr7 | 4907382 | |||||
| chr7:4907393
|
A | G | 1 | a0001c0001t0024 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 3 | chr7 | 4907393 | |||||
| chr7:4959079
|
G | A | 3 | a0001c0001t0015a0001c0002t0008a0001c0002t0021 | 15 | HG00280.hp1 HG00639.hp1 HG01192.hp2 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-62C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/7 | 62 | chr7 | 4959079 | |||||
| chr7:4959082
|
G | A | 2 | a0001c0001t0010a0001c0003t0036 | 6 | HG00597.hp1 HG02071.hp1 HG02165.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-65C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/7 | 65 | chr7 | 4959082 | |||||
| chr7:4959153
|
C | G | 1 | a0001c0002t0023 | 1 | NA19060.hp2 | 5_prime_UTR_variant | MODIFIER | c.-136G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/7 | 136 | chr7 | 4959153 | |||||
| chr7:4959154
|
G | T | 1 | a0001c0002t0023 | 1 | NA19060.hp2 | 5_prime_UTR_variant | MODIFIER | c.-137C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/7 | 137 | chr7 | 4959154 | |||||
| chr7:4959154
|
GGAGCCGG others(5): Show |
G | 1 | a0001c0001t0022 | 1 | HG01515.hp2 | 5_prime_UTR_variant | MODIFIER | c.-149_-138delGGGCTC others(6): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/7 | 138 | chr7 | 4959154 | |||||
| chr7:4959160
|
G | C | 6 | a0001c0001t0015a0001c0001t0020a0001c0002t0006others(3): Show | 35 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(32): Show |
5_prime_UTR_variant | MODIFIER | c.-143C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/7 | 143 | chr7 | 4959160 | |||||
| chr7:4959160
|
G | GGAGCCC | 2 | a0001c0002t0014a0001c0002t0037 | 4 | HG02602.hp2 HG03225.hp1 HG03540.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-149_-144dupGGGCTC | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/7 | 144 | chr7 | 4959160 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:4907616
|
G | T | 2 | a0001c0001t0002g0026a0001c0004t0002g0293 | 2 | HG02055.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.538-17C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4907616 | ||||||
| chr7:4907651
|
C | G | 2 | a0001c0001t0004g0329a0001c0001t0004g0330 | 2 | HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.538-52G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4907651 | ||||||
| chr7:4907728
|
G | C | 6 | a0001c0002t0001g0101a0001c0002t0001g0102a0001c0002t0001g0103others(3): Show | 6 | HG01891.hp2 HG02145.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.538-129C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4907728 | ||||||
| chr7:4907736
|
A | G | 2 | a0001c0001t0002g0258a0001c0002t0002g0214 | 2 | HG02165.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.538-137T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4907736 | ||||||
| chr7:4907768
|
A | C | 95 | a0001c0001t0001g0032a0001c0001t0001g0092a0001c0001t0001g0105others(92): Show | 96 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.538-169T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4907768 | ||||||
| chr7:4907853
|
C | T | 46 | a0001c0001t0005g0070a0001c0001t0005g0075a0001c0001t0005g0079others(43): Show | 46 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.538-254G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4907853 | ||||||
| chr7:4907854
|
G | A | 2 | a0001c0001t0011g0039a0001c0002t0011g0147 | 2 | HG02055.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.538-255C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4907854 | ||||||
| chr7:4907874
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.538-275C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4907874 | ||||||
| chr7:4907883
|
T | C | 1 | a0001c0002t0035g0199 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.538-284A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4907883 | ||||||
| chr7:4907970
|
G | A | 14 | a0001c0001t0001g0108a0001c0002t0006g0356a0001c0002t0006g0357others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.538-371C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4907970 | ||||||
| chr7:4908002
|
A | G | 4 | a0001c0001t0002g0001a0001c0001t0002g0253a0001c0001t0002g0254others(1): Show | 5 | HG00735.hp1 HG00741.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.538-403T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908002 | ||||||
| chr7:4908059
|
C | T | 1 | a0001c0007t0028g0332 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.538-460G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908059 | ||||||
| chr7:4908105
|
C | T | 2 | a0001c0001t0001g0328a0001c0002t0006g0360 | 2 | HG01081.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.538-506G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908105 | ||||||
| chr7:4908147
|
G | GT | 76 | a0001c0001t0001g0007a0001c0001t0001g0105a0001c0001t0001g0108others(73): Show | 76 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.538-549dupA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908147 | ||||||
| chr7:4908147
|
G | T | 1 | a0001c0002t0014g0343 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.538-548C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908147 | ||||||
| chr7:4908148
|
T | C | 2 | a0001c0001t0001g0247a0001c0002t0001g0188 | 2 | NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.538-549A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908148 | ||||||
| chr7:4908186
|
G | C | 1 | a0001c0001t0013g0229 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.538-587C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908186 | ||||||
| chr7:4908213
|
T | C | 45 | a0001c0001t0003g0264a0001c0001t0004g0003a0001c0001t0004g0120others(42): Show | 46 | HG00099.hp1 HG00408.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.538-614A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908213 | ||||||
| chr7:4908219
|
G | C | 45 | a0001c0001t0003g0264a0001c0001t0004g0003a0001c0001t0004g0120others(42): Show | 46 | HG00099.hp1 HG00408.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.538-620C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908219 | ||||||
| chr7:4908255
|
C | A | 6 | a0001c0002t0003g0148a0001c0002t0003g0160a0001c0002t0003g0170others(3): Show | 6 | NA18992.hp2 NA18998.hp1 NA19003.hp2 others(3): Show |
intron_variant | MODIFIER | c.538-656G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908255 | ||||||
| chr7:4908266
|
C | T | 2 | a0001c0002t0006g0362a0001c0002t0006g0363 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.538-667G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908266 | ||||||
| chr7:4908267
|
G | A | 3 | a0001c0001t0001g0139a0001c0001t0001g0193a0001c0001t0001g0225 | 3 | NA18747.hp2 NA18939.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.538-668C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908267 | ||||||
| chr7:4908276
|
G | T | 1 | a0001c0002t0001g0220 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.538-677C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908276 | ||||||
| chr7:4908288
|
T | C | 205 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0046others(202): Show | 207 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.538-689A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908288 | ||||||
| chr7:4908303
|
G | A | 1 | a0001c0003t0001g0318 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.538-704C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908303 | ||||||
| chr7:4908340
|
C | T | 1 | a0001c0001t0030g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.538-741G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908340 | ||||||
| chr7:4908412
|
G | C | 22 | a0001c0001t0001g0007a0001c0001t0002g0001a0001c0001t0002g0011others(19): Show | 23 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.538-813C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908412 | ||||||
| chr7:4908431
|
T | C | 165 | a0001c0001t0001g0007a0001c0001t0001g0059a0001c0001t0001g0105others(162): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.538-832A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908431 | ||||||
| chr7:4908471
|
C | T | 1 | a0001c0001t0030g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.538-872G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908471 | ||||||
| chr7:4908530
|
T | C | 1 | a0001c0001t0001g0249 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.538-931A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908530 | ||||||
| chr7:4908609
|
T | C | 6 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0106others(3): Show | 6 | HG01496.hp1 HG02055.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.538-1010A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908609 | ||||||
| chr7:4908627
|
C | T | 151 | a0001c0001t0001g0020a0001c0001t0001g0046a0001c0001t0001g0068others(148): Show | 152 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.538-1028G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908627 | ||||||
| chr7:4908661
|
G | A | 3 | a0001c0001t0001g0108a0001c0001t0030g0322a0001c0007t0028g0332 | 3 | HG02559.hp1 HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.538-1062C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908661 | ||||||
| chr7:4908673
|
C | T | 4 | a0001c0002t0001g0006a0001c0002t0001g0008a0001c0002t0001g0127others(1): Show | 4 | HG02451.hp2 HG02970.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.538-1074G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908673 | ||||||
| chr7:4908680
|
C | T | 2 | a0001c0001t0004g0270a0001c0001t0004g0272 | 2 | HG01257.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.538-1081G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908680 | ||||||
| chr7:4908688
|
G | C | 1 | a0001c0001t0002g0012 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.538-1089C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908688 | ||||||
| chr7:4908694
|
C | G | 1 | a0001c0001t0003g0095 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.538-1095G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908694 | ||||||
| chr7:4908694
|
C | T | 5 | a0001c0001t0003g0065a0001c0002t0003g0148a0001c0002t0003g0170others(2): Show | 5 | HG01255.hp1 NA18992.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.538-1095G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908694 | ||||||
| chr7:4908702
|
G | T | 1 | a0001c0002t0006g0358 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.538-1103C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908702 | ||||||
| chr7:4908724
|
C | T | 1 | a0001c0002t0035g0199 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.538-1125G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908724 | ||||||
| chr7:4908736
|
A | C | 3 | a0001c0002t0001g0131a0001c0002t0001g0132a0001c0002t0001g0133 | 3 | HG01099.hp1 HG01433.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.538-1137T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908736 | ||||||
| chr7:4908745
|
T | A | 6 | a0001c0002t0006g0347a0001c0002t0006g0348a0001c0002t0006g0350others(3): Show | 6 | HG01109.hp2 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.537+1136A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908745 | ||||||
| chr7:4908745
|
T | C | 251 | a0001c0001t0001g0007a0001c0001t0001g0059a0001c0001t0001g0068others(248): Show | 253 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.537+1136A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908745 | ||||||
| chr7:4908754
|
G | T | 1 | a0001c0001t0013g0277 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.537+1127C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908754 | ||||||
| chr7:4908756
|
G | A | 1 | a0001c0002t0001g0231 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.537+1125C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908756 | ||||||
| chr7:4908766
|
A | G | 1 | a0001c0002t0003g0136 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.537+1115T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908766 | ||||||
| chr7:4908770
|
G | A | 1 | a0001c0002t0003g0136 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.537+1111C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908770 | ||||||
| chr7:4908833
|
G | T | 1 | a0001c0001t0030g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.537+1048C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908833 | ||||||
| chr7:4908841
|
A | G | 1 | a0001c0001t0002g0257 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.537+1040T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908841 | ||||||
| chr7:4908846
|
G | A | 1 | a0001c0004t0002g0293 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.537+1035C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908846 | ||||||
| chr7:4908874
|
G | C | 1 | a0001c0001t0003g0287 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.537+1007C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908874 | ||||||
| chr7:4908896
|
C | CA | 9 | a0001c0001t0001g0100a0001c0001t0001g0106a0001c0001t0001g0286others(6): Show | 9 | HG01109.hp1 HG02056.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.537+984dupT | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908896 | ||||||
| chr7:4908896
|
CA | C | 56 | a0001c0001t0001g0225a0001c0001t0001g0328a0001c0001t0002g0012others(53): Show | 57 | HG00099.hp1 HG00408.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.537+984delT | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908896 | ||||||
| chr7:4908987
|
G | A | 1 | a0001c0002t0001g0102 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.537+894C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908987 | ||||||
| chr7:4909070
|
T | G | 7 | a0001c0001t0001g0249a0001c0002t0001g0002a0001c0002t0001g0197others(4): Show | 8 | HG02451.hp1 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.537+811A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4909070 | ||||||
| chr7:4909203
|
T | C | 15 | a0001c0001t0001g0007a0001c0001t0001g0099a0001c0001t0001g0100others(12): Show | 15 | HG01496.hp1 HG02559.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.537+678A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4909203 | ||||||
| chr7:4909208
|
G | A | 2 | a0001c0001t0011g0333a0001c0001t0011g0334 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.537+673C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4909208 | ||||||
| chr7:4909241
|
C | A | 1 | a0001c0001t0030g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.537+640G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4909241 | ||||||
| chr7:4909363
|
A | G | 1 | a0001c0002t0004g0187 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.537+518T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4909363 | ||||||
| chr7:4909432
|
C | CA | 13 | a0001c0001t0001g0007a0001c0001t0002g0028a0001c0001t0002g0031others(10): Show | 13 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(10): Show |
intron_variant | MODIFIER | c.537+448dupT | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4909432 | ||||||
| chr7:4909432
|
C | CAA | 227 | a0001c0001t0001g0046a0001c0001t0001g0052a0001c0001t0001g0078others(224): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.537+447_537+448dup others(2): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4909432 | ||||||
| chr7:4909432
|
C | CAAA | 6 | a0001c0001t0003g0264a0001c0002t0003g0170a0001c0002t0004g0182others(3): Show | 6 | HG02738.hp2 NA18942.hp1 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.537+446_537+448dup others(3): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4909432 | ||||||
| chr7:4909438
|
A | C | 1 | a0001c0001t0017g0123 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.537+443T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4909438 | ||||||
| chr7:4909491
|
G | A | 8 | a0001c0001t0001g0273a0001c0002t0001g0146a0001c0002t0001g0208others(5): Show | 8 | HG02083.hp2 NA18951.hp2 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.537+390C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4909491 | ||||||
| chr7:4909502
|
G | A | 179 | a0001c0001t0001g0046a0001c0001t0001g0052a0001c0001t0001g0078others(176): Show | 180 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.537+379C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4909502 | ||||||
| chr7:4909512
|
G | A | 179 | a0001c0001t0001g0046a0001c0001t0001g0052a0001c0001t0001g0078others(176): Show | 180 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.537+369C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4909512 | ||||||
| chr7:4909582
|
A | G | 51 | a0001c0001t0001g0189a0001c0001t0001g0312a0001c0001t0001g0328others(48): Show | 52 | HG00408.hp1 HG00609.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.537+299T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4909582 | ||||||
| chr7:4909600
|
T | G | 1 | a0001c0001t0017g0123 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.537+281A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4909600 | ||||||
| chr7:4909659
|
T | C | 16 | a0001c0001t0001g0007a0001c0001t0001g0099a0001c0001t0001g0100others(13): Show | 16 | HG01496.hp1 HG02559.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.537+222A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4909659 | ||||||
| chr7:4910034
|
G | A | 1 | a0001c0001t0001g0007 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.468-84C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 5/6 | chr7 | 4910034 | ||||||
| chr7:4910092
|
T | G | 1 | a0001c0002t0003g0183 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.468-142A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 5/6 | chr7 | 4910092 | ||||||
| chr7:4910129
|
G | A | 1 | a0001c0001t0011g0039 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.468-179C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 5/6 | chr7 | 4910129 | ||||||
| chr7:4910180
|
C | T | 236 | a0001c0001t0001g0007a0001c0001t0001g0046a0001c0001t0001g0052others(233): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.468-230G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 5/6 | chr7 | 4910180 | ||||||
| chr7:4910287
|
T | C | 1 | a0001c0001t0001g0007 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.468-337A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 5/6 | chr7 | 4910287 | ||||||
| chr7:4910318
|
A | G | 1 | a0001c0002t0001g0212 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.468-368T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 5/6 | chr7 | 4910318 | ||||||
| chr7:4910382
|
T | A | 3 | a0001c0001t0001g0247a0001c0001t0009g0245a0001c0001t0009g0246 | 3 | HG02647.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.468-432A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 5/6 | chr7 | 4910382 | ||||||
| chr7:4910575
|
AC | A | 4 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(1): Show | 4 | HG01496.hp1 HG02886.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.467+569delG | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 5/6 | chr7 | 4910575 | ||||||
| chr7:4910590
|
C | G | 1 | a0001c0002t0002g0214 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.467+555G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 5/6 | chr7 | 4910590 | ||||||
| chr7:4910599
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.467+546C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 5/6 | chr7 | 4910599 | ||||||
| chr7:4910659
|
T | C | 287 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0046others(284): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.467+486A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 5/6 | chr7 | 4910659 | ||||||
| chr7:4910681
|
C | T | 7 | a0001c0002t0001g0230a0001c0002t0001g0231a0001c0002t0001g0232others(4): Show | 7 | HG02258.hp1 HG02717.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.467+464G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 5/6 | chr7 | 4910681 | ||||||
| chr7:4910687
|
G | A | 3 | a0001c0001t0001g0247a0001c0001t0009g0245a0001c0001t0009g0246 | 3 | HG02647.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.467+458C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 5/6 | chr7 | 4910687 | ||||||
| chr7:4910721
|
C | T | 1 | a0001c0001t0033g0089 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.467+424G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 5/6 | chr7 | 4910721 | ||||||
| chr7:4910780
|
C | T | 6 | a0001c0002t0001g0200a0001c0002t0001g0201a0001c0002t0001g0202others(3): Show | 6 | HG03098.hp1 HG03209.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.467+365G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 5/6 | chr7 | 4910780 | ||||||
| chr7:4910843
|
G | C | 3 | a0001c0002t0001g0101a0001c0002t0001g0102a0001c0002t0001g0103 | 3 | HG02145.hp1 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.467+302C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 5/6 | chr7 | 4910843 | ||||||
| chr7:4910968
|
G | C | 6 | a0001c0002t0006g0347a0001c0002t0006g0348a0001c0002t0006g0350others(3): Show | 6 | HG01109.hp2 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.467+177C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 5/6 | chr7 | 4910968 | ||||||
| chr7:4910981
|
T | A | 4 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0239others(1): Show | 4 | NA18980.hp1 NA19007.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.467+164A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 5/6 | chr7 | 4910981 | ||||||
| chr7:4911380
|
C | T | 1 | a0001c0001t0002g0011 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.366-134G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4911380 | ||||||
| chr7:4911414
|
G | C | 3 | a0001c0001t0001g0247a0001c0001t0009g0245a0001c0001t0009g0246 | 3 | HG02647.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.366-168C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4911414 | ||||||
| chr7:4911502
|
T | A | 183 | a0001c0001t0001g0007a0001c0001t0001g0046a0001c0001t0001g0052others(180): Show | 184 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.366-256A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4911502 | ||||||
| chr7:4911502
|
T | C | 14 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(11): Show | 14 | HG01496.hp1 HG02559.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.366-256A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4911502 | ||||||
| chr7:4911570
|
C | T | 1 | a0001c0002t0002g0109 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.366-324G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4911570 | ||||||
| chr7:4911571
|
G | A | 3 | a0001c0003t0003g0295a0001c0003t0004g0301a0001c0003t0004g0302 | 3 | HG02083.hp1 NA18998.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.366-325C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4911571 | ||||||
| chr7:4911584
|
A | G | 287 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0046others(284): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.366-338T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4911584 | ||||||
| chr7:4911598
|
G | GTTTTA | 287 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0046others(284): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.366-357_366-353dup others(5): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4911598 | ||||||
| chr7:4911630
|
T | G | 1 | a0001c0002t0005g0159 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.366-384A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4911630 | ||||||
| chr7:4911705
|
G | A | 1 | a0001c0002t0009g0040 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.366-459C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4911705 | ||||||
| chr7:4911734
|
C | T | 10 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0149others(7): Show | 10 | HG02056.hp2 HG02135.hp1 NA18747.hp2 others(7): Show |
intron_variant | MODIFIER | c.366-488G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4911734 | ||||||
| chr7:4911961
|
A | C | 1 | a0001c0002t0006g0361 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.366-715T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4911961 | ||||||
| chr7:4911987
|
T | C | 1 | a0001c0001t0002g0257 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.366-741A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4911987 | ||||||
| chr7:4912153
|
G | T | 2 | a0001c0001t0001g0189a0001c0001t0001g0328 | 2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.366-907C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4912153 | ||||||
| chr7:4912199
|
G | A | 1 | a0001c0002t0001g0220 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.366-953C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4912199 | ||||||
| chr7:4912297
|
G | A | 1 | a0001c0001t0002g0012 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.366-1051C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4912297 | ||||||
| chr7:4912362
|
T | C | 2 | a0001c0001t0002g0082a0001c0001t0020g0355 | 2 | HG00642.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.366-1116A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4912362 | ||||||
| chr7:4912425
|
G | A | 87 | a0001c0001t0001g0020a0001c0001t0001g0189a0001c0001t0001g0273others(84): Show | 88 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.366-1179C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4912425 | ||||||
| chr7:4912479
|
G | A | 3 | a0001c0002t0002g0155a0001c0002t0002g0156a0001c0002t0003g0136 | 3 | HG03654.hp1 HG03688.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.366-1233C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4912479 | ||||||
| chr7:4912488
|
G | A | 6 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0247others(3): Show | 6 | HG02559.hp1 HG02647.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.366-1242C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4912488 | ||||||
| chr7:4912519
|
G | A | 2 | a0001c0001t0011g0333a0001c0001t0011g0334 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.366-1273C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4912519 | ||||||
| chr7:4912561
|
C | CA | 7 | a0001c0001t0001g0138a0001c0001t0002g0256a0001c0002t0001g0014others(4): Show | 7 | HG01981.hp1 NA18983.hp2 NA18995.hp1 others(4): Show |
intron_variant | MODIFIER | c.366-1316dupT | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4912561 | ||||||
| chr7:4912651
|
A | G | 285 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0046others(282): Show | 287 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.366-1405T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4912651 | ||||||
| chr7:4912674
|
G | C | 78 | a0001c0001t0001g0020a0001c0001t0001g0273a0001c0001t0001g0290others(75): Show | 79 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.366-1428C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4912674 | ||||||
| chr7:4912677
|
T | C | 1 | a0001c0002t0001g0218 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.366-1431A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4912677 | ||||||
| chr7:4912882
|
G | A | 1 | a0001c0002t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.366-1636C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4912882 | ||||||
| chr7:4912959
|
C | A | 2 | a0001c0002t0001g0006a0001c0002t0001g0008 | 2 | HG02970.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.366-1713G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4912959 | ||||||
| chr7:4912983
|
C | T | 2 | a0001c0002t0007g0163a0001c0002t0007g0168 | 2 | NA19009.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.366-1737G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4912983 | ||||||
| chr7:4913000
|
G | T | 2 | a0001c0001t0011g0333a0001c0001t0011g0334 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.366-1754C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913000 | ||||||
| chr7:4913028
|
G | C | 1 | a0001c0001t0003g0010 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.366-1782C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913028 | ||||||
| chr7:4913199
|
G | A | 1 | a0001c0001t0013g0229 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.366-1953C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913199 | ||||||
| chr7:4913265
|
A | C | 2 | a0001c0001t0011g0333a0001c0001t0011g0334 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.366-2019T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913265 | ||||||
| chr7:4913334
|
C | A | 7 | a0001c0002t0001g0200a0001c0002t0001g0201a0001c0002t0001g0202others(4): Show | 7 | HG02109.hp2 HG03098.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.366-2088G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913334 | ||||||
| chr7:4913341
|
T | G | 1 | a0001c0001t0017g0123 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.366-2095A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913341 | ||||||
| chr7:4913385
|
G | A | 7 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0247others(4): Show | 7 | HG02559.hp1 HG02615.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.366-2139C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913385 | ||||||
| chr7:4913443
|
G | A | 269 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0046others(266): Show | 271 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.366-2197C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913443 | ||||||
| chr7:4913448
|
G | A | 1 | a0001c0001t0030g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.366-2202C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913448 | ||||||
| chr7:4913549
|
C | A | 1 | a0001c0001t0003g0037 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.366-2303G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913549 | ||||||
| chr7:4913567
|
A | G | 1 | a0001c0003t0003g0295 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.366-2321T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913567 | ||||||
| chr7:4913653
|
G | A | 1 | a0001c0002t0006g0356 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.365+2352C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913653 | ||||||
| chr7:4913721
|
C | CA | 31 | a0001c0001t0001g0032a0001c0001t0001g0055a0001c0001t0001g0059others(28): Show | 31 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.365+2283dupT | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913721 | ||||||
| chr7:4913721
|
CA | C | 219 | a0001c0001t0001g0007a0001c0001t0001g0046a0001c0001t0001g0078others(216): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.365+2283delT | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913721 | ||||||
| chr7:4913721
|
CAA | C | 8 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(5): Show | 8 | HG01496.hp1 HG02572.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.365+2282_365+2283d others(4): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913721 | ||||||
| chr7:4913721
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0022g0004 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.365+2273_365+2283d others(13): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913721 | ||||||
| chr7:4913766
|
A | G | 265 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0046others(262): Show | 267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.365+2239T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913766 | ||||||
| chr7:4913792
|
G | T | 5 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(2): Show | 5 | HG01496.hp1 HG02886.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.365+2213C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913792 | ||||||
| chr7:4913810
|
T | C | 3 | a0001c0001t0001g0189a0001c0001t0001g0328a0001c0001t0010g0338 | 3 | HG00597.hp1 HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.365+2195A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913810 | ||||||
| chr7:4913822
|
C | T | 12 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(9): Show | 12 | HG01496.hp1 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.365+2183G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913822 | ||||||
| chr7:4913851
|
C | T | 1 | a0001c0001t0010g0336 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.365+2154G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913851 | ||||||
| chr7:4914013
|
C | A | 281 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0099others(278): Show | 283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.365+1992G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4914013 | ||||||
| chr7:4914052
|
C | G | 2 | a0001c0002t0001g0211a0001c0002t0001g0213 | 2 | NA18977.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.365+1953G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4914052 | ||||||
| chr7:4914070
|
T | C | 374 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0046others(371): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.365+1935A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4914070 | ||||||
| chr7:4914090
|
G | A | 283 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0046others(280): Show | 285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.365+1915C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4914090 | ||||||
| chr7:4914254
|
T | C | 2 | a0001c0002t0001g0117a0001c0002t0001g0122 | 2 | HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.365+1751A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4914254 | ||||||
| chr7:4914264
|
G | A | 3 | a0001c0002t0001g0192a0001c0002t0005g0191a0001c0002t0023g0005 | 3 | NA19060.hp2 NA19074.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.365+1741C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4914264 | ||||||
| chr7:4914315
|
A | G | 180 | a0001c0001t0001g0007a0001c0001t0001g0046a0001c0001t0001g0052others(177): Show | 181 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.365+1690T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4914315 | ||||||
| chr7:4914502
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.365+1503A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4914502 | ||||||
| chr7:4914566
|
C | A | 1 | a0001c0001t0030g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.365+1439G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4914566 | ||||||
| chr7:4914657
|
A | G | 285 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0046others(282): Show | 287 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.365+1348T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4914657 | ||||||
| chr7:4914667
|
G | A | 7 | a0001c0002t0001g0200a0001c0002t0001g0201a0001c0002t0001g0202others(4): Show | 7 | HG02109.hp2 HG03098.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.365+1338C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4914667 | ||||||
| chr7:4914895
|
C | T | 1 | a0001c0002t0008g0365 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.365+1110G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4914895 | ||||||
| chr7:4915063
|
A | C | 89 | a0001c0001t0001g0020a0001c0001t0001g0189a0001c0001t0001g0273others(86): Show | 90 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.365+942T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4915063 | ||||||
| chr7:4915114
|
T | C | 1 | a0001c0007t0028g0332 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.365+891A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4915114 | ||||||
| chr7:4915119
|
A | G | 2 | a0001c0001t0002g0026a0001c0004t0002g0293 | 2 | HG02055.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.365+886T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4915119 | ||||||
| chr7:4915129
|
A | C | 10 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(7): Show | 11 | HG01069.hp2 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.365+876T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4915129 | ||||||
| chr7:4915176
|
T | C | 283 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0046others(280): Show | 285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.365+829A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4915176 | ||||||
| chr7:4915339
|
G | C | 1 | a0001c0001t0017g0123 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.365+666C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4915339 | ||||||
| chr7:4915459
|
G | A | 2 | a0001c0002t0006g0359a0001c0002t0006g0360 | 2 | HG01081.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.365+546C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4915459 | ||||||
| chr7:4915530
|
A | G | 2 | a0001c0001t0002g0259a0001c0001t0002g0260 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.365+475T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4915530 | ||||||
| chr7:4915633
|
G | C | 1 | a0001c0001t0013g0229 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.365+372C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4915633 | ||||||
| chr7:4915640
|
A | T | 1 | a0001c0007t0028g0332 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.365+365T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4915640 | ||||||
| chr7:4915659
|
C | G | 283 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0046others(280): Show | 285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.365+346G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4915659 | ||||||
| chr7:4915750
|
G | GA | 25 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(22): Show | 25 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.365+254dupT | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4915750 | ||||||
| chr7:4915779
|
T | TTTTTCTG others(26): Show |
97 | a0001c0001t0001g0020a0001c0001t0001g0139a0001c0001t0001g0149others(94): Show | 98 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.365+193_365+225dup others(33): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4915779 | ||||||
| chr7:4915779
|
T | TTTTTCTG others(59): Show |
1 | a0001c0001t0004g0309 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.365+225_365+226ins others(66): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4915779 | ||||||
| chr7:4915804
|
A | AGTGAGTT others(26): Show |
3 | a0001c0001t0001g0138a0001c0001t0001g0193a0001c0001t0001g0195 | 3 | HG02135.hp1 NA18967.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.365+200_365+201ins others(33): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4915804 | ||||||
| chr7:4915845
|
A | G | 1 | a0001c0001t0004g0320 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.365+160T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4915845 | ||||||
| chr7:4915867
|
GAA | G | 4 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(1): Show | 4 | HG01496.hp1 HG02886.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.365+136_365+137del others(2): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4915867 | ||||||
| chr7:4915976
|
G | C | 1 | a0001c0001t0001g0068 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.365+29C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4915976 | ||||||
| chr7:4915990
|
C | T | 5 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(2): Show | 5 | HG01496.hp1 HG02886.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.365+15G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4915990 | ||||||
| chr7:4916086
|
C | T | 2 | a0001c0001t0013g0229a0001c0002t0004g0187 | 2 | HG01167.hp2 HG03471.hp1 |
splice_region_variant&intron_variant | LOW | c.291-7G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4916086 | ||||||
| chr7:4916174
|
A | G | 14 | a0001c0001t0003g0264a0001c0001t0004g0003a0001c0001t0004g0120others(11): Show | 15 | HG00099.hp1 HG00639.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.291-95T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4916174 | ||||||
| chr7:4916258
|
T | A | 1 | a0001c0001t0003g0035 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.291-179A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4916258 | ||||||
| chr7:4916371
|
C | CT | 17 | a0001c0001t0001g0240a0001c0001t0002g0034a0001c0001t0002g0091others(14): Show | 17 | HG00408.hp2 HG01109.hp1 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.291-293dupA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4916371 | ||||||
| chr7:4916371
|
CT | C | 171 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0138others(168): Show | 171 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.291-293delA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4916371 | ||||||
| chr7:4916371
|
CTT | C | 67 | a0001c0001t0001g0046a0001c0001t0001g0052a0001c0001t0001g0078others(64): Show | 68 | HG00099.hp2 HG00597.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.291-294_291-293del others(2): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4916371 | ||||||
| chr7:4916371
|
CTTT | C | 7 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0247others(4): Show | 7 | HG01074.hp2 HG02559.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.291-295_291-293del others(3): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4916371 | ||||||
| chr7:4916371
|
CTTTTTTT others(7): Show |
C | 5 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(2): Show | 5 | HG01496.hp1 HG02886.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.291-306_291-293del others(14): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4916371 | ||||||
| chr7:4916434
|
G | A | 4 | a0001c0001t0001g0059a0001c0001t0005g0070a0001c0001t0005g0075others(1): Show | 4 | HG00408.hp2 NA18942.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.291-355C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4916434 | ||||||
| chr7:4916572
|
G | A | 5 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(2): Show | 5 | HG01496.hp1 HG02886.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.291-493C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4916572 | ||||||
| chr7:4916672
|
C | T | 7 | a0001c0002t0001g0200a0001c0002t0001g0201a0001c0002t0001g0202others(4): Show | 7 | HG02109.hp2 HG03098.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.291-593G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4916672 | ||||||
| chr7:4916777
|
A | G | 1 | a0001c0007t0028g0332 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.291-698T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4916777 | ||||||
| chr7:4916939
|
G | C | 5 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(2): Show | 5 | HG01496.hp1 HG02886.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.291-860C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4916939 | ||||||
| chr7:4917045
|
C | A | 1 | a0001c0002t0003g0178 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.291-966G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4917045 | ||||||
| chr7:4917191
|
T | A | 1 | a0001c0001t0002g0098 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.291-1112A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4917191 | ||||||
| chr7:4917281
|
G | A | 1 | a0001c0001t0002g0098 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.291-1202C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4917281 | ||||||
| chr7:4917342
|
C | T | 140 | a0001c0001t0001g0046a0001c0001t0001g0052a0001c0001t0001g0078others(137): Show | 141 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(138): Show |
intron_variant | MODIFIER | c.291-1263G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4917342 | ||||||
| chr7:4917386
|
G | C | 7 | a0001c0002t0001g0200a0001c0002t0001g0201a0001c0002t0001g0202others(4): Show | 7 | HG02109.hp2 HG03098.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.291-1307C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4917386 | ||||||
| chr7:4917498
|
C | T | 2 | a0001c0001t0002g0082a0001c0001t0020g0355 | 2 | HG00642.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.291-1419G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4917498 | ||||||
| chr7:4917549
|
G | A | 7 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0247others(4): Show | 7 | HG02559.hp1 HG02615.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.291-1470C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4917549 | ||||||
| chr7:4917664
|
C | T | 149 | a0001c0001t0001g0046a0001c0001t0001g0052a0001c0001t0001g0078others(146): Show | 150 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(147): Show |
intron_variant | MODIFIER | c.291-1585G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4917664 | ||||||
| chr7:4917702
|
AT | A | 4 | a0001c0001t0001g0149a0001c0001t0001g0198a0001c0001t0003g0327others(1): Show | 4 | HG03540.hp2 NA18946.hp2 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.291-1624delA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4917702 | ||||||
| chr7:4917703
|
T | A | 101 | a0001c0001t0001g0020a0001c0001t0001g0138a0001c0001t0001g0139others(98): Show | 102 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.291-1624A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4917703 | ||||||
| chr7:4917704
|
A | T | 1 | a0001c0001t0003g0060 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.291-1625T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4917704 | ||||||
| chr7:4917779
|
C | T | 6 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0247others(3): Show | 6 | HG02559.hp1 HG02647.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.291-1700G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4917779 | ||||||
| chr7:4917785
|
C | T | 1 | a0001c0001t0001g0189 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.291-1706G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4917785 | ||||||
| chr7:4917835
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.291-1756C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4917835 | ||||||
| chr7:4918428
|
G | C | 154 | a0001c0001t0001g0046a0001c0001t0001g0052a0001c0001t0001g0078others(151): Show | 155 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.290+1743C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4918428 | ||||||
| chr7:4918446
|
G | A | 1 | a0001c0002t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.290+1725C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4918446 | ||||||
| chr7:4918483
|
C | CT | 14 | a0001c0001t0001g0059a0001c0001t0001g0238a0001c0001t0001g0328others(11): Show | 14 | HG01516.hp2 HG01517.hp2 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.290+1687dupA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4918483 | ||||||
| chr7:4918483
|
CT | C | 10 | a0001c0001t0001g0198a0001c0001t0003g0016a0001c0001t0003g0250others(7): Show | 10 | HG01515.hp1 HG01975.hp1 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.290+1687delA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4918483 | ||||||
| chr7:4918483
|
CTTT | C | 139 | a0001c0001t0001g0046a0001c0001t0001g0052a0001c0001t0001g0078others(136): Show | 140 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(137): Show |
intron_variant | MODIFIER | c.290+1685_290+1687d others(5): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4918483 | ||||||
| chr7:4918483
|
CTTTT | C | 15 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(12): Show | 15 | HG01496.hp1 HG01891.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.290+1684_290+1687d others(6): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4918483 | ||||||
| chr7:4918494
|
T | C | 1 | a0001c0001t0004g0263 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.290+1677A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4918494 | ||||||
| chr7:4918628
|
T | C | 2 | a0001c0001t0004g0280a0001c0001t0004g0281 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.290+1543A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4918628 | ||||||
| chr7:4918792
|
A | AT | 11 | a0001c0001t0002g0082a0001c0002t0001g0188a0001c0002t0001g0200others(8): Show | 11 | HG00642.hp2 HG02109.hp2 HG03098.hp1 others(8): Show |
intron_variant | MODIFIER | c.290+1378dupA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4918792 | ||||||
| chr7:4919047
|
C | T | 107 | a0001c0001t0001g0020a0001c0001t0001g0138a0001c0001t0001g0139others(104): Show | 108 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.290+1124G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4919047 | ||||||
| chr7:4919068
|
C | T | 1 | a0001c0001t0001g0007 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.290+1103G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4919068 | ||||||
| chr7:4919115
|
C | A | 1 | a0001c0001t0030g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.290+1056G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4919115 | ||||||
| chr7:4919156
|
A | T | 3 | a0001c0001t0001g0247a0001c0001t0009g0245a0001c0001t0009g0246 | 3 | HG02647.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.290+1015T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4919156 | ||||||
| chr7:4919168
|
A | G | 1 | a0001c0001t0002g0267 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.290+1003T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4919168 | ||||||
| chr7:4919405
|
C | T | 72 | a0001c0002t0001g0006a0001c0002t0001g0008a0001c0002t0001g0097others(69): Show | 72 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.290+766G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4919405 | ||||||
| chr7:4919406
|
A | G | 1 | a0001c0002t0004g0182 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.290+765T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4919406 | ||||||
| chr7:4919519
|
G | C | 1 | a0001c0007t0028g0332 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.290+652C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4919519 | ||||||
| chr7:4919561
|
C | G | 2 | a0001c0001t0011g0333a0001c0001t0011g0334 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.290+610G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4919561 | ||||||
| chr7:4919664
|
C | T | 2 | a0001c0002t0011g0147a0001c0002t0016g0157 | 2 | HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.290+507G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4919664 | ||||||
| chr7:4919715
|
A | G | 3 | a0001c0001t0001g0032a0001c0001t0001g0092a0001c0001t0022g0004 | 3 | HG01106.hp2 HG01515.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.290+456T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4919715 | ||||||
| chr7:4919950
|
G | A | 179 | a0001c0001t0001g0007a0001c0001t0001g0099a0001c0001t0001g0100others(176): Show | 180 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.290+221C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4919950 | ||||||
| chr7:4919953
|
G | C | 7 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0247others(4): Show | 7 | HG02559.hp1 HG02615.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.290+218C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4919953 | ||||||
| chr7:4919959
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.290+212G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4919959 | ||||||
| chr7:4919971
|
A | G | 162 | a0001c0002t0001g0002a0001c0002t0001g0006a0001c0002t0001g0008others(159): Show | 163 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.290+200T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4919971 | ||||||
| chr7:4920158
|
G | A | 162 | a0001c0002t0001g0002a0001c0002t0001g0006a0001c0002t0001g0008others(159): Show | 163 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.290+13C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4920158 | ||||||
| chr7:4920420
|
G | A | 6 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0247others(3): Show | 6 | HG02559.hp1 HG02647.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.130-89C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4920420 | ||||||
| chr7:4920498
|
G | A | 2 | a0001c0002t0001g0188a0001c0002t0017g0190 | 2 | NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.130-167C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4920498 | ||||||
| chr7:4920522
|
T | C | 1 | a0001c0001t0017g0123 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.130-191A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4920522 | ||||||
| chr7:4920638
|
C | A | 1 | a0001c0002t0006g0346 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.130-307G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4920638 | ||||||
| chr7:4920668
|
C | T | 1 | a0001c0001t0017g0123 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.130-337G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4920668 | ||||||
| chr7:4920688
|
TCCTCCCT others(1): Show |
T | 269 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0100others(266): Show | 271 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.130-365_130-358del others(8): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4920688 | ||||||
| chr7:4920688
|
TCCTCCCT others(5): Show |
T | 1 | a0001c0001t0001g0248 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.130-369_130-358del others(12): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4920688 | ||||||
| chr7:4920785
|
G | A | 270 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0100others(267): Show | 272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.130-454C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4920785 | ||||||
| chr7:4920837
|
G | C | 284 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0099others(281): Show | 286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.130-506C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4920837 | ||||||
| chr7:4920865
|
C | A | 257 | a0001c0001t0001g0020a0001c0001t0001g0138a0001c0001t0001g0139others(254): Show | 259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.130-534G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4920865 | ||||||
| chr7:4920996
|
C | A | 11 | a0001c0001t0002g0028a0001c0001t0002g0031a0001c0001t0002g0034others(8): Show | 11 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(8): Show |
intron_variant | MODIFIER | c.130-665G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4920996 | ||||||
| chr7:4921016
|
C | A | 2 | a0001c0001t0003g0087a0001c0001t0003g0088 | 2 | HG00558.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.130-685G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4921016 | ||||||
| chr7:4921072
|
C | A | 1 | a0001c0001t0017g0123 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.130-741G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4921072 | ||||||
| chr7:4921103
|
G | C | 52 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0029others(49): Show | 53 | HG00738.hp2 HG01074.hp2 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.130-772C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4921103 | ||||||
| chr7:4921417
|
G | A | 1 | a0001c0002t0003g0178 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.130-1086C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4921417 | ||||||
| chr7:4921447
|
C | T | 1 | a0001c0002t0001g0006 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.130-1116G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4921447 | ||||||
| chr7:4921485
|
G | A | 1 | a0001c0001t0002g0021 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.130-1154C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4921485 | ||||||
| chr7:4921494
|
A | G | 257 | a0001c0001t0001g0020a0001c0001t0001g0138a0001c0001t0001g0139others(254): Show | 259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.130-1163T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4921494 | ||||||
| chr7:4921576
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.130-1245C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4921576 | ||||||
| chr7:4921577
|
C | T | 235 | a0001c0001t0001g0020a0001c0001t0001g0138a0001c0001t0001g0139others(232): Show | 237 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.130-1246G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4921577 | ||||||
| chr7:4921620
|
C | CA | 17 | a0001c0001t0001g0223a0001c0001t0001g0249a0001c0001t0002g0319others(14): Show | 17 | HG00544.hp1 HG02109.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.130-1290dupT | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4921620 | ||||||
| chr7:4921620
|
CA | C | 27 | a0001c0001t0001g0007a0001c0001t0001g0099a0001c0001t0001g0100others(24): Show | 27 | HG01069.hp1 HG01256.hp1 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.130-1290delT | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4921620 | ||||||
| chr7:4921742
|
G | A | 2 | a0001c0002t0001g0200a0001c0002t0001g0202 | 2 | HG03098.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.130-1411C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4921742 | ||||||
| chr7:4921749
|
G | A | 1 | a0001c0001t0003g0043 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.130-1418C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4921749 | ||||||
| chr7:4921777
|
G | A | 95 | a0001c0001t0001g0020a0001c0001t0001g0138a0001c0001t0001g0139others(92): Show | 96 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.130-1446C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4921777 | ||||||
| chr7:4922099
|
G | A | 1 | a0001c0001t0002g0036 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.130-1768C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4922099 | ||||||
| chr7:4922192
|
C | T | 48 | a0001c0001t0001g0046a0001c0001t0001g0052a0001c0001t0001g0053others(45): Show | 48 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.130-1861G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4922192 | ||||||
| chr7:4922269
|
A | T | 253 | a0001c0001t0001g0020a0001c0001t0001g0138a0001c0001t0001g0139others(250): Show | 255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.130-1938T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4922269 | ||||||
| chr7:4922341
|
A | G | 253 | a0001c0001t0001g0020a0001c0001t0001g0138a0001c0001t0001g0139others(250): Show | 255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.130-2010T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4922341 | ||||||
| chr7:4922350
|
C | A | 231 | a0001c0001t0001g0020a0001c0001t0001g0138a0001c0001t0001g0139others(228): Show | 233 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.130-2019G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4922350 | ||||||
| chr7:4922350
|
C | T | 1 | a0001c0001t0002g0036 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.130-2019G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4922350 | ||||||
| chr7:4922425
|
C | T | 1 | a0001c0001t0009g0245 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.130-2094G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4922425 | ||||||
| chr7:4922439
|
G | A | 2 | a0001c0002t0001g0121a0001c0002t0001g0125 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.130-2108C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4922439 | ||||||
| chr7:4922475
|
A | T | 1 | a0001c0001t0004g0330 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.130-2144T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4922475 | ||||||
| chr7:4922587
|
T | G | 253 | a0001c0001t0001g0020a0001c0001t0001g0138a0001c0001t0001g0139others(250): Show | 255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.130-2256A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4922587 | ||||||
| chr7:4922617
|
C | A | 1 | a0001c0001t0011g0039 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.130-2286G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4922617 | ||||||
| chr7:4922695
|
C | A | 1 | a0001c0002t0001g0117 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.130-2364G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4922695 | ||||||
| chr7:4922732
|
G | A | 253 | a0001c0001t0001g0020a0001c0001t0001g0138a0001c0001t0001g0139others(250): Show | 255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.130-2401C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4922732 | ||||||
| chr7:4922759
|
C | T | 97 | a0001c0002t0001g0006a0001c0002t0001g0008a0001c0002t0001g0033others(94): Show | 97 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.130-2428G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4922759 | ||||||
| chr7:4922761
|
A | G | 7 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0247others(4): Show | 7 | HG02559.hp1 HG02615.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.130-2430T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4922761 | ||||||
| chr7:4922839
|
T | C | 14 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(11): Show | 14 | HG01496.hp1 HG02559.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.130-2508A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4922839 | ||||||
| chr7:4922877
|
C | T | 1 | a0001c0002t0001g0110 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.130-2546G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4922877 | ||||||
| chr7:4923001
|
C | A | 6 | a0001c0002t0002g0155a0001c0002t0002g0156a0001c0002t0003g0136others(3): Show | 6 | HG01243.hp1 HG03654.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.129+2450G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4923001 | ||||||
| chr7:4923052
|
C | A | 5 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(2): Show | 5 | HG01496.hp1 HG02886.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.129+2399G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4923052 | ||||||
| chr7:4923057
|
G | A | 231 | a0001c0001t0001g0020a0001c0001t0001g0138a0001c0001t0001g0139others(228): Show | 233 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.129+2394C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4923057 | ||||||
| chr7:4923101
|
C | CT | 18 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0247others(15): Show | 18 | HG01891.hp1 HG01978.hp1 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.129+2349dupA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4923101 | ||||||
| chr7:4923316
|
C | G | 2 | a0001c0001t0011g0333a0001c0001t0011g0334 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.129+2135G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4923316 | ||||||
| chr7:4923330
|
C | T | 1 | a0001c0001t0017g0123 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.129+2121G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4923330 | ||||||
| chr7:4923564
|
C | G | 1 | a0001c0007t0028g0332 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.129+1887G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4923564 | ||||||
| chr7:4923617
|
A | AC | 248 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0100others(245): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.129+1833_129+1834i others(3): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4923617 | ||||||
| chr7:4923639
|
T | G | 2 | a0001c0001t0011g0333a0001c0001t0011g0334 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.129+1812A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4923639 | ||||||
| chr7:4923674
|
T | A | 232 | a0001c0001t0001g0020a0001c0001t0001g0138a0001c0001t0001g0139others(229): Show | 234 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.129+1777A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4923674 | ||||||
| chr7:4923707
|
A | T | 1 | a0001c0002t0009g0038 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.129+1744T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4923707 | ||||||
| chr7:4923717
|
A | G | 279 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0099others(276): Show | 281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.129+1734T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4923717 | ||||||
| chr7:4923931
|
A | G | 18 | a0001c0002t0006g0354a0001c0002t0006g0357a0001c0002t0006g0358others(15): Show | 18 | HG00280.hp1 HG00639.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.129+1520T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4923931 | ||||||
| chr7:4923997
|
T | C | 3 | a0001c0002t0001g0202a0001c0002t0009g0042a0001c0003t0004g0306 | 3 | HG02004.hp1 HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.129+1454A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4923997 | ||||||
| chr7:4924008
|
C | T | 1 | a0001c0002t0001g0116 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.129+1443G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4924008 | ||||||
| chr7:4924053
|
T | G | 7 | a0001c0002t0001g0200a0001c0002t0001g0201a0001c0002t0001g0202others(4): Show | 7 | HG02109.hp2 HG03098.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.129+1398A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4924053 | ||||||
| chr7:4924064
|
C | T | 1 | a0001c0001t0002g0093 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.129+1387G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4924064 | ||||||
| chr7:4924109
|
A | G | 6 | a0001c0001t0002g0026a0001c0001t0011g0333a0001c0001t0011g0334others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.129+1342T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4924109 | ||||||
| chr7:4924149
|
A | G | 243 | a0001c0001t0001g0020a0001c0001t0001g0138a0001c0001t0001g0139others(240): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.129+1302T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4924149 | ||||||
| chr7:4924185
|
T | C | 241 | a0001c0001t0001g0020a0001c0001t0001g0107a0001c0001t0001g0108others(238): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.129+1266A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4924185 | ||||||
| chr7:4924309
|
T | C | 1 | a0001c0002t0003g0179 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.129+1142A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4924309 | ||||||
| chr7:4924371
|
G | A | 232 | a0001c0001t0001g0020a0001c0001t0001g0138a0001c0001t0001g0139others(229): Show | 234 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.129+1080C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4924371 | ||||||
| chr7:4924421
|
C | A | 4 | a0001c0002t0001g0002a0001c0002t0001g0242a0001c0002t0001g0243others(1): Show | 5 | HG02451.hp1 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.129+1030G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4924421 | ||||||
| chr7:4924582
|
G | T | 6 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0247others(3): Show | 6 | HG02559.hp1 HG02647.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.129+869C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4924582 | ||||||
| chr7:4924583
|
A | C | 6 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0247others(3): Show | 6 | HG02559.hp1 HG02647.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.129+868T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4924583 | ||||||
| chr7:4924603
|
T | C | 6 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(3): Show | 6 | HG01496.hp1 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.129+848A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4924603 | ||||||
| chr7:4924639
|
G | C | 1 | a0001c0001t0001g0248 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.129+812C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4924639 | ||||||
| chr7:4924726
|
T | C | 1 | a0001c0001t0001g0248 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.129+725A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4924726 | ||||||
| chr7:4924749
|
G | A | 245 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0100others(242): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.129+702C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4924749 | ||||||
| chr7:4924865
|
C | T | 1 | a0001c0001t0033g0089 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.129+586G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4924865 | ||||||
| chr7:4924866
|
G | A | 11 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(8): Show | 12 | HG01069.hp2 HG01070.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.129+585C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4924866 | ||||||
| chr7:4925106
|
G | C | 1 | a0001c0001t0002g0284 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.129+345C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4925106 | ||||||
| chr7:4925227
|
G | A | 2 | a0001c0001t0005g0266a0001c0001t0005g0288 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.129+224C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4925227 | ||||||
| chr7:4925236
|
G | T | 81 | a0001c0001t0001g0020a0001c0001t0001g0249a0001c0001t0001g0273others(78): Show | 82 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.129+215C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4925236 | ||||||
| chr7:4925260
|
A | G | 1 | a0001c0001t0030g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.129+191T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4925260 | ||||||
| chr7:4925310
|
GCCA | G | 92 | a0001c0001t0001g0020a0001c0001t0001g0249a0001c0001t0001g0273others(89): Show | 93 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.129+138_129+140del others(3): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4925310 | ||||||
| chr7:4925316
|
G | C | 92 | a0001c0001t0001g0020a0001c0001t0001g0249a0001c0001t0001g0273others(89): Show | 93 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.129+135C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4925316 | ||||||
| chr7:4925318
|
G | C | 92 | a0001c0001t0001g0020a0001c0001t0001g0249a0001c0001t0001g0273others(89): Show | 93 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.129+133C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4925318 | ||||||
| chr7:4925320
|
C | CT | 92 | a0001c0001t0001g0020a0001c0001t0001g0249a0001c0001t0001g0273others(89): Show | 93 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.129+130_129+131ins others(1): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4925320 | ||||||
| chr7:4925323
|
TCC | T | 92 | a0001c0001t0001g0020a0001c0001t0001g0249a0001c0001t0001g0273others(89): Show | 93 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.129+126_129+127del others(2): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4925323 | ||||||
| chr7:4925564
|
C | T | 81 | a0001c0001t0001g0020a0001c0001t0001g0249a0001c0001t0001g0273others(78): Show | 82 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.48-32G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4925564 | ||||||
| chr7:4925632
|
G | T | 1 | a0001c0001t0002g0098 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.48-100C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4925632 | ||||||
| chr7:4925702
|
T | C | 98 | a0001c0001t0001g0020a0001c0001t0001g0237a0001c0001t0001g0238others(95): Show | 99 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.48-170A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4925702 | ||||||
| chr7:4925707
|
G | A | 6 | a0001c0001t0011g0333a0001c0001t0011g0334a0001c0002t0008g0366others(3): Show | 6 | HG00280.hp1 HG01192.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.48-175C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4925707 | ||||||
| chr7:4925834
|
A | C | 7 | a0001c0002t0001g0200a0001c0002t0001g0201a0001c0002t0001g0202others(4): Show | 7 | HG02109.hp2 HG03098.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.48-302T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4925834 | ||||||
| chr7:4925948
|
G | A | 90 | a0001c0001t0001g0020a0001c0001t0001g0248a0001c0001t0001g0249others(87): Show | 91 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.48-416C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4925948 | ||||||
| chr7:4925951
|
G | A | 1 | a0001c0001t0017g0123 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.48-419C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4925951 | ||||||
| chr7:4926104
|
C | CT | 11 | a0001c0001t0001g0248a0001c0001t0002g0256a0001c0001t0004g0262others(8): Show | 11 | HG01109.hp2 HG01934.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.48-573dupA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4926104 | ||||||
| chr7:4926114
|
C | T | 244 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0100others(241): Show | 246 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.48-582G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4926114 | ||||||
| chr7:4926209
|
C | T | 1 | a0001c0001t0017g0123 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.48-677G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4926209 | ||||||
| chr7:4926287
|
G | C | 3 | a0001c0001t0001g0247a0001c0001t0009g0245a0001c0001t0009g0246 | 3 | HG02647.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.48-755C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4926287 | ||||||
| chr7:4926498
|
C | A | 80 | a0001c0001t0001g0249a0001c0001t0001g0273a0001c0001t0001g0290others(77): Show | 81 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.48-966G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4926498 | ||||||
| chr7:4926508
|
G | A | 2 | a0001c0001t0011g0333a0001c0001t0011g0334 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.48-976C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4926508 | ||||||
| chr7:4926572
|
C | G | 4 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(1): Show | 4 | HG01496.hp1 HG02886.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.48-1040G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4926572 | ||||||
| chr7:4926696
|
C | T | 2 | a0001c0001t0002g0259a0001c0001t0002g0260 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.48-1164G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4926696 | ||||||
| chr7:4926716
|
G | C | 1 | a0001c0002t0003g0183 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.48-1184C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4926716 | ||||||
| chr7:4926821
|
A | T | 84 | a0001c0001t0001g0249a0001c0001t0001g0268a0001c0001t0001g0273others(81): Show | 85 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.48-1289T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4926821 | ||||||
| chr7:4926824
|
A | G | 2 | a0001c0002t0001g0002a0001c0002t0001g0242 | 3 | HG02451.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.48-1292T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4926824 | ||||||
| chr7:4926846
|
G | A | 11 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(8): Show | 12 | HG01069.hp2 HG01070.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.48-1314C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4926846 | ||||||
| chr7:4926858
|
C | G | 83 | a0001c0001t0001g0249a0001c0001t0001g0268a0001c0001t0001g0273others(80): Show | 84 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.48-1326G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4926858 | ||||||
| chr7:4926859
|
C | G | 1 | a0001c0002t0005g0172 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.48-1327G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4926859 | ||||||
| chr7:4926898
|
T | C | 1 | a0001c0001t0004g0309 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.48-1366A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4926898 | ||||||
| chr7:4926942
|
C | T | 1 | a0001c0001t0013g0229 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.48-1410G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4926942 | ||||||
| chr7:4926969
|
T | C | 271 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(268): Show | 273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.48-1437A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4926969 | ||||||
| chr7:4926993
|
C | G | 1 | a0001c0001t0003g0250 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.48-1461G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4926993 | ||||||
| chr7:4927034
|
G | A | 86 | a0001c0001t0001g0249a0001c0001t0001g0268a0001c0001t0001g0273others(83): Show | 87 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.48-1502C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4927034 | ||||||
| chr7:4927303
|
A | G | 1 | a0001c0001t0001g0138 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.48-1771T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4927303 | ||||||
| chr7:4927304
|
A | G | 1 | a0001c0001t0001g0138 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.48-1772T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4927304 | ||||||
| chr7:4927307
|
G | C | 128 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0032others(125): Show | 129 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.48-1775C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4927307 | ||||||
| chr7:4927337
|
G | C | 32 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0011others(29): Show | 33 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.48-1805C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4927337 | ||||||
| chr7:4927351
|
C | T | 1 | a0001c0001t0030g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.48-1819G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4927351 | ||||||
| chr7:4927496
|
G | A | 8 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0247others(5): Show | 8 | HG01891.hp1 HG02559.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.48-1964C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4927496 | ||||||
| chr7:4927638
|
C | T | 1 | a0001c0001t0003g0056 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.48-2106G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4927638 | ||||||
| chr7:4927656
|
G | A | 1 | a0001c0001t0013g0229 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.48-2124C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4927656 | ||||||
| chr7:4927724
|
A | C | 1 | a0001c0002t0003g0178 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.48-2192T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4927724 | ||||||
| chr7:4927943
|
C | T | 6 | a0001c0002t0006g0347a0001c0002t0006g0348a0001c0002t0006g0350others(3): Show | 6 | HG01109.hp2 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.48-2411G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4927943 | ||||||
| chr7:4928032
|
G | A | 65 | a0001c0001t0001g0032a0001c0001t0001g0046a0001c0001t0001g0052others(62): Show | 65 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.48-2500C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4928032 | ||||||
| chr7:4928234
|
G | C | 2 | a0001c0001t0003g0073a0001c0001t0003g0077 | 2 | HG03239.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.48-2702C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4928234 | ||||||
| chr7:4928288
|
T | C | 1 | a0001c0002t0007g0226 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.48-2756A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4928288 | ||||||
| chr7:4928351
|
G | A | 1 | a0001c0001t0003g0044 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.48-2819C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4928351 | ||||||
| chr7:4928412
|
G | T | 1 | a0001c0002t0014g0344 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.48-2880C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4928412 | ||||||
| chr7:4928494
|
C | A | 86 | a0001c0001t0001g0249a0001c0001t0001g0268a0001c0001t0001g0273others(83): Show | 87 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.48-2962G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4928494 | ||||||
| chr7:4928540
|
C | T | 1 | a0001c0007t0028g0332 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.48-3008G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4928540 | ||||||
| chr7:4928549
|
C | T | 4 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(1): Show | 4 | HG01496.hp1 HG02886.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.48-3017G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4928549 | ||||||
| chr7:4928689
|
G | C | 86 | a0001c0001t0001g0249a0001c0001t0001g0268a0001c0001t0001g0273others(83): Show | 87 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.48-3157C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4928689 | ||||||
| chr7:4928739
|
C | A | 1 | a0001c0001t0003g0077 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.48-3207G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4928739 | ||||||
| chr7:4928760
|
A | C | 1 | a0001c0002t0005g0167 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.48-3228T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4928760 | ||||||
| chr7:4928787
|
A | G | 1 | a0001c0001t0002g0098 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.48-3255T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4928787 | ||||||
| chr7:4928813
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.48-3281G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4928813 | ||||||
| chr7:4928846
|
G | A | 24 | a0001c0002t0001g0006a0001c0002t0001g0008a0001c0002t0001g0101others(21): Show | 24 | HG00099.hp2 HG00741.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.48-3314C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4928846 | ||||||
| chr7:4928928
|
G | T | 2 | a0001c0001t0001g0273a0001c0001t0003g0250 | 2 | HG02074.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.48-3396C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4928928 | ||||||
| chr7:4929007
|
A | G | 87 | a0001c0001t0001g0249a0001c0001t0001g0268a0001c0001t0001g0273others(84): Show | 88 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.48-3475T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929007 | ||||||
| chr7:4929061
|
C | T | 1 | a0001c0002t0006g0359 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.48-3529G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929061 | ||||||
| chr7:4929114
|
G | C | 24 | a0001c0002t0001g0006a0001c0002t0001g0008a0001c0002t0001g0101others(21): Show | 24 | HG00099.hp2 HG00741.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.48-3582C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929114 | ||||||
| chr7:4929161
|
T | A | 1 | a0001c0001t0001g0248 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.48-3629A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929161 | ||||||
| chr7:4929226
|
G | C | 1 | a0001c0001t0004g0285 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.48-3694C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929226 | ||||||
| chr7:4929235
|
G | A | 1 | a0001c0003t0004g0307 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.48-3703C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929235 | ||||||
| chr7:4929245
|
G | A | 1 | a0001c0001t0030g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.48-3713C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929245 | ||||||
| chr7:4929252
|
G | A | 5 | a0001c0001t0002g0048a0001c0001t0002g0206a0001c0001t0003g0087others(2): Show | 5 | HG00558.hp2 HG00673.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.48-3720C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929252 | ||||||
| chr7:4929300
|
A | T | 1 | a0001c0002t0006g0351 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.48-3768T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929300 | ||||||
| chr7:4929312
|
A | G | 236 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0032others(233): Show | 238 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(235): Show |
intron_variant | MODIFIER | c.48-3780T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929312 | ||||||
| chr7:4929414
|
C | G | 1 | a0001c0001t0017g0123 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.48-3882G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929414 | ||||||
| chr7:4929415
|
C | A | 1 | a0001c0001t0004g0323 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.48-3883G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929415 | ||||||
| chr7:4929476
|
C | T | 118 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(115): Show | 119 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(116): Show |
intron_variant | MODIFIER | c.48-3944G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929476 | ||||||
| chr7:4929481
|
G | A | 118 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(115): Show | 119 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(116): Show |
intron_variant | MODIFIER | c.48-3949C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929481 | ||||||
| chr7:4929564
|
G | A | 1 | a0001c0001t0013g0229 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.48-4032C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929564 | ||||||
| chr7:4929574
|
G | A | 323 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0032others(320): Show | 326 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.48-4042C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929574 | ||||||
| chr7:4929596
|
C | T | 2 | a0001c0001t0011g0333a0001c0001t0011g0334 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.48-4064G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929596 | ||||||
| chr7:4929607
|
C | G | 1 | a0001c0002t0007g0226 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.48-4075G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929607 | ||||||
| chr7:4929610
|
T | C | 1 | a0001c0001t0003g0058 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.48-4078A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929610 | ||||||
| chr7:4929617
|
C | T | 1 | a0001c0001t0017g0123 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.48-4085G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929617 | ||||||
| chr7:4929643
|
G | A | 1 | a0001c0001t0030g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.48-4111C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929643 | ||||||
| chr7:4929673
|
C | T | 2 | a0001c0003t0004g0296a0001c0003t0004g0297 | 2 | NA18968.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.48-4141G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929673 | ||||||
| chr7:4929825
|
G | C | 1 | a0001c0001t0017g0123 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.48-4293C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929825 | ||||||
| chr7:4929881
|
G | C | 84 | a0001c0001t0001g0249a0001c0001t0001g0268a0001c0001t0001g0273others(81): Show | 85 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.48-4349C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929881 | ||||||
| chr7:4929985
|
C | G | 8 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0247others(5): Show | 8 | HG02559.hp1 HG02647.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.48-4453G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929985 | ||||||
| chr7:4930026
|
T | G | 37 | a0001c0001t0001g0268a0001c0001t0001g0273a0001c0001t0001g0290others(34): Show | 37 | HG00597.hp1 HG00642.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.48-4494A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930026 | ||||||
| chr7:4930057
|
C | G | 1 | a0001c0001t0007g0062 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.48-4525G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930057 | ||||||
| chr7:4930080
|
T | C | 1 | a0001c0001t0003g0015 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.48-4548A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930080 | ||||||
| chr7:4930271
|
C | CA | 82 | a0001c0001t0007g0063a0001c0001t0011g0039a0001c0001t0011g0333others(79): Show | 83 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.48-4740dupT | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930271 | ||||||
| chr7:4930271
|
C | CAAA | 27 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0175others(24): Show | 27 | HG01167.hp2 HG01884.hp2 HG02056.hp1 others(24): Show |
intron_variant | MODIFIER | c.48-4742_48-4740dup others(3): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930271 | ||||||
| chr7:4930271
|
CA | C | 6 | a0001c0001t0002g0009a0001c0001t0003g0016a0001c0001t0003g0114others(3): Show | 6 | HG01256.hp1 HG02735.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.48-4740delT | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930271 | ||||||
| chr7:4930357
|
A | G | 1 | a0001c0002t0005g0167 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.48-4825T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930357 | ||||||
| chr7:4930362
|
G | A | 1 | a0001c0001t0003g0076 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.48-4830C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930362 | ||||||
| chr7:4930452
|
T | C | 318 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0032others(315): Show | 321 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.48-4920A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930452 | ||||||
| chr7:4930474
|
T | C | 2 | a0001c0002t0001g0006a0001c0002t0001g0008 | 2 | HG02970.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.48-4942A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930474 | ||||||
| chr7:4930505
|
G | A | 2 | a0001c0001t0002g0082a0001c0001t0020g0355 | 2 | HG00642.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.48-4973C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930505 | ||||||
| chr7:4930516
|
C | T | 89 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0249others(86): Show | 90 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.48-4984G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930516 | ||||||
| chr7:4930531
|
C | T | 10 | a0001c0001t0001g0007a0001c0001t0001g0189a0001c0001t0001g0328others(7): Show | 10 | HG02486.hp1 HG02559.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.48-4999G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930531 | ||||||
| chr7:4930536
|
C | T | 10 | a0001c0001t0001g0007a0001c0001t0001g0189a0001c0001t0001g0328others(7): Show | 10 | HG02486.hp1 HG02559.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.48-5004G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930536 | ||||||
| chr7:4930569
|
G | A | 1 | a0001c0001t0003g0060 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.48-5037C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930569 | ||||||
| chr7:4930577
|
G | A | 4 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(1): Show | 4 | HG01496.hp1 HG02886.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.48-5045C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930577 | ||||||
| chr7:4930632
|
G | A | 10 | a0001c0001t0001g0007a0001c0001t0001g0189a0001c0001t0001g0328others(7): Show | 10 | HG02486.hp1 HG02559.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.48-5100C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930632 | ||||||
| chr7:4930645
|
C | CAAAAAAA others(2): Show |
111 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0032others(108): Show | 112 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.48-5122_48-5114dup others(9): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930645 | ||||||
| chr7:4930645
|
C | CAAAAAAA others(3): Show |
117 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(114): Show | 118 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.48-5123_48-5114dup others(10): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930645 | ||||||
| chr7:4930645
|
C | CAAAAAAA others(4): Show |
7 | a0001c0001t0001g0149a0001c0002t0001g0209a0001c0002t0001g0244others(4): Show | 7 | HG01981.hp1 HG02572.hp1 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.48-5114_48-5113ins others(11): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930645 | ||||||
| chr7:4930658
|
G | C | 237 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0032others(234): Show | 239 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(236): Show |
intron_variant | MODIFIER | c.48-5126C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930658 | ||||||
| chr7:4930659
|
G | A | 1 | a0001c0001t0003g0066 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.48-5127C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930659 | ||||||
| chr7:4930703
|
G | A | 1 | a0001c0002t0001g0203 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.48-5171C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930703 | ||||||
| chr7:4930708
|
C | T | 2 | a0001c0001t0011g0333a0001c0001t0011g0334 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.48-5176G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930708 | ||||||
| chr7:4930722
|
C | T | 2 | a0001c0003t0001g0318a0001c0003t0036g0339 | 2 | NA18986.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.48-5190G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930722 | ||||||
| chr7:4930748
|
C | A | 55 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0149others(52): Show | 56 | HG00738.hp2 HG01074.hp2 HG01081.hp1 others(53): Show |
intron_variant | MODIFIER | c.48-5216G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930748 | ||||||
| chr7:4930764
|
T | G | 237 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0032others(234): Show | 239 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(236): Show |
intron_variant | MODIFIER | c.48-5232A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930764 | ||||||
| chr7:4930920
|
G | A | 3 | a0001c0001t0001g0249a0001c0002t0014g0343a0001c0002t0014g0344 | 3 | HG02647.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.48-5388C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930920 | ||||||
| chr7:4930956
|
C | T | 236 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0046others(233): Show | 238 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(235): Show |
intron_variant | MODIFIER | c.48-5424G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930956 | ||||||
| chr7:4931119
|
G | A | 1 | a0001c0002t0014g0344 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.48-5587C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4931119 | ||||||
| chr7:4931165
|
T | C | 3 | a0001c0001t0001g0249a0001c0002t0014g0343a0001c0002t0014g0344 | 3 | HG02647.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.48-5633A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4931165 | ||||||
| chr7:4931444
|
C | T | 3 | a0001c0001t0001g0247a0001c0001t0009g0245a0001c0001t0009g0246 | 3 | HG02647.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.48-5912G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4931444 | ||||||
| chr7:4931445
|
G | A | 5 | a0001c0001t0001g0249a0001c0001t0013g0229a0001c0001t0030g0322others(2): Show | 5 | HG02647.hp1 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.48-5913C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4931445 | ||||||
| chr7:4931898
|
A | G | 1 | a0001c0001t0017g0123 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.48-6366T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4931898 | ||||||
| chr7:4931942
|
G | C | 1 | a0001c0001t0002g0098 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.48-6410C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4931942 | ||||||
| chr7:4931952
|
C | T | 2 | a0001c0001t0012g0064a0001c0001t0012g0227 | 2 | HG03834.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.48-6420G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4931952 | ||||||
| chr7:4932054
|
G | A | 3 | a0001c0001t0001g0247a0001c0001t0009g0245a0001c0001t0009g0246 | 3 | HG02647.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.48-6522C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4932054 | ||||||
| chr7:4932117
|
G | C | 1 | a0001c0002t0001g0126 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.48-6585C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4932117 | ||||||
| chr7:4932149
|
C | A | 1 | a0001c0002t0006g0356 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.48-6617G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4932149 | ||||||
| chr7:4932311
|
C | T | 1 | a0001c0001t0002g0090 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.48-6779G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4932311 | ||||||
| chr7:4932312
|
G | A | 113 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(110): Show | 114 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(111): Show |
intron_variant | MODIFIER | c.48-6780C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4932312 | ||||||
| chr7:4932417
|
T | C | 1 | a0001c0001t0007g0081 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.48-6885A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4932417 | ||||||
| chr7:4932474
|
C | T | 4 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(1): Show | 4 | HG01496.hp1 HG02886.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.48-6942G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4932474 | ||||||
| chr7:4932485
|
G | A | 1 | a0001c0001t0003g0087 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.48-6953C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4932485 | ||||||
| chr7:4932501
|
C | T | 3 | a0001c0002t0001g0101a0001c0002t0001g0102a0001c0002t0001g0103 | 3 | HG02145.hp1 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.48-6969G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4932501 | ||||||
| chr7:4932620
|
GTGCATTT others(1013): Show |
G | 1 | a0001c0001t0017g0123 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.48-8108_48-7089del | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4932620 | ||||||
| chr7:4932624
|
AT | A | 198 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0032others(195): Show | 200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.48-7093delA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4932624 | ||||||
| chr7:4932957
|
T | G | 1 | a0001c0002t0005g0167 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.48-7425A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4932957 | ||||||
| chr7:4932981
|
CT | C | 87 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0268others(84): Show | 88 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.48-7450delA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4932981 | ||||||
| chr7:4933104
|
G | T | 1 | a0001c0002t0003g0183 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.48-7572C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4933104 | ||||||
| chr7:4933124
|
C | T | 1 | a0001c0003t0004g0321 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.48-7592G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4933124 | ||||||
| chr7:4933190
|
G | A | 3 | a0001c0002t0001g0101a0001c0002t0001g0102a0001c0002t0001g0103 | 3 | HG02145.hp1 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.48-7658C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4933190 | ||||||
| chr7:4933342
|
G | A | 248 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0032others(245): Show | 250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.48-7810C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4933342 | ||||||
| chr7:4933427
|
T | C | 1 | a0001c0001t0003g0056 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.48-7895A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4933427 | ||||||
| chr7:4933471
|
G | A | 87 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0268others(84): Show | 88 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.48-7939C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4933471 | ||||||
| chr7:4933569
|
T | C | 351 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0046others(348): Show | 354 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(351): Show |
intron_variant | MODIFIER | c.48-8037A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4933569 | ||||||
| chr7:4933640
|
A | T | 83 | a0001c0001t0001g0248a0001c0001t0001g0268a0001c0001t0001g0273others(80): Show | 84 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.48-8108T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4933640 | ||||||
| chr7:4933644
|
AT | A | 10 | a0001c0001t0001g0052a0001c0001t0002g0271a0001c0001t0003g0037others(7): Show | 10 | HG00423.hp1 HG00621.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.48-8113delA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4933644 | ||||||
| chr7:4933725
|
G | A | 129 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(126): Show | 130 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.48-8193C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4933725 | ||||||
| chr7:4933791
|
C | A | 1 | a0001c0002t0003g0178 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.48-8259G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4933791 | ||||||
| chr7:4933940
|
C | CT | 54 | a0001c0001t0001g0107a0001c0001t0001g0138a0001c0001t0001g0139others(51): Show | 55 | HG00738.hp2 HG01074.hp2 HG01081.hp1 others(52): Show |
intron_variant | MODIFIER | c.48-8409dupA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4933940 | ||||||
| chr7:4933940
|
CT | C | 75 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0046others(72): Show | 76 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.48-8409delA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4933940 | ||||||
| chr7:4933940
|
CTT | C | 23 | a0001c0001t0001g0053a0001c0001t0001g0068a0001c0001t0001g0238others(20): Show | 23 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(20): Show |
intron_variant | MODIFIER | c.48-8410_48-8409del others(2): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4933940 | ||||||
| chr7:4933940
|
CTTTT | C | 47 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(44): Show | 47 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.48-8412_48-8409del others(4): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4933940 | ||||||
| chr7:4933940
|
CTTTTT | C | 83 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0268others(80): Show | 84 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.48-8413_48-8409del others(5): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4933940 | ||||||
| chr7:4933972
|
T | C | 2 | a0001c0002t0006g0362a0001c0002t0006g0363 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.48-8440A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4933972 | ||||||
| chr7:4934023
|
A | G | 352 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0046others(349): Show | 355 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(352): Show |
intron_variant | MODIFIER | c.48-8491T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4934023 | ||||||
| chr7:4934042
|
G | A | 1 | a0001c0005t0003g0292 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.48-8510C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4934042 | ||||||
| chr7:4934078
|
C | T | 1 | a0001c0002t0013g0176 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.48-8546G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4934078 | ||||||
| chr7:4934182
|
G | A | 7 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(4): Show | 7 | HG01496.hp1 HG02647.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.48-8650C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4934182 | ||||||
| chr7:4934210
|
G | A | 1 | a0001c0001t0013g0229 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.48-8678C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4934210 | ||||||
| chr7:4934269
|
T | C | 1 | a0001c0001t0026g0289 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.48-8737A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4934269 | ||||||
| chr7:4934294
|
GGGTTTTG others(1): Show |
G | 31 | a0001c0001t0015g0377a0001c0001t0015g0378a0001c0001t0015g0379others(28): Show | 31 | HG00280.hp1 HG00639.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.48-8770_48-8763del others(8): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4934294 | ||||||
| chr7:4934304
|
A | C | 31 | a0001c0001t0015g0377a0001c0001t0015g0378a0001c0001t0015g0379others(28): Show | 31 | HG00280.hp1 HG00639.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.48-8772T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4934304 | ||||||
| chr7:4934325
|
A | C | 3 | a0001c0001t0001g0249a0001c0002t0014g0343a0001c0002t0014g0344 | 3 | HG02647.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.48-8793T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4934325 | ||||||
| chr7:4934334
|
T | C | 350 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0046others(347): Show | 353 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(350): Show |
intron_variant | MODIFIER | c.48-8802A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4934334 | ||||||
| chr7:4934350
|
C | T | 40 | a0001c0001t0001g0189a0001c0001t0001g0328a0001c0001t0002g0098others(37): Show | 40 | HG00280.hp1 HG00639.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.48-8818G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4934350 | ||||||
| chr7:4934429
|
C | A | 8 | a0001c0001t0001g0189a0001c0001t0001g0328a0001c0001t0003g0324others(5): Show | 8 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.48-8897G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4934429 | ||||||
| chr7:4934468
|
G | T | 1 | a0001c0001t0002g0057 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.48-8936C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4934468 | ||||||
| chr7:4934497
|
C | G | 105 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0149others(102): Show | 106 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.48-8965G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4934497 | ||||||
| chr7:4934570
|
C | T | 1 | a0001c0001t0013g0229 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.48-9038G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4934570 | ||||||
| chr7:4934854
|
A | G | 238 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0149others(235): Show | 240 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(237): Show |
intron_variant | MODIFIER | c.48-9322T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4934854 | ||||||
| chr7:4934872
|
A | T | 96 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0046others(93): Show | 97 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.48-9340T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4934872 | ||||||
| chr7:4935064
|
T | C | 130 | a0001c0001t0001g0189a0001c0001t0001g0248a0001c0001t0001g0249others(127): Show | 131 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.48-9532A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4935064 | ||||||
| chr7:4935161
|
G | A | 1 | a0001c0001t0007g0074 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.48-9629C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4935161 | ||||||
| chr7:4935193
|
GA | G | 27 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0149others(24): Show | 27 | HG00642.hp2 HG00738.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.48-9662delT | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4935193 | ||||||
| chr7:4935285
|
G | A | 87 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0268others(84): Show | 88 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.48-9753C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4935285 | ||||||
| chr7:4935288
|
G | A | 40 | a0001c0001t0001g0189a0001c0001t0001g0328a0001c0001t0002g0098others(37): Show | 40 | HG00280.hp1 HG00639.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.48-9756C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4935288 | ||||||
| chr7:4935379
|
G | A | 111 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0149others(108): Show | 112 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(109): Show |
intron_variant | MODIFIER | c.48-9847C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4935379 | ||||||
| chr7:4935398
|
C | T | 1 | a0001c0002t0007g0226 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.48-9866G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4935398 | ||||||
| chr7:4935473
|
A | G | 1 | a0001c0001t0017g0123 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.48-9941T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4935473 | ||||||
| chr7:4935677
|
C | CA | 29 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0106others(26): Show | 29 | HG00423.hp2 HG01496.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.48-10146dupT | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4935677 | ||||||
| chr7:4935677
|
CA | C | 119 | a0001c0001t0001g0189a0001c0001t0001g0249a0001c0001t0001g0268others(116): Show | 120 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(117): Show |
intron_variant | MODIFIER | c.48-10146delT | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4935677 | ||||||
| chr7:4935677
|
CAA | C | 52 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0175others(49): Show | 53 | HG00738.hp2 HG01074.hp2 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.48-10147_48-10146d others(4): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4935677 | ||||||
| chr7:4935696
|
AAC | A | 28 | a0001c0002t0001g0164a0001c0002t0001g0165a0001c0002t0001g0166others(25): Show | 28 | HG00558.hp1 HG02258.hp1 HG02258.hp2 others(25): Show |
intron_variant | MODIFIER | c.48-10166_48-10165d others(4): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4935696 | ||||||
| chr7:4935697
|
A | C | 1 | a0001c0002t0006g0358 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.48-10165T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4935697 | ||||||
| chr7:4935697
|
AC | A | 19 | a0001c0001t0011g0039a0001c0002t0001g0192a0001c0002t0001g0230others(16): Show | 19 | HG00544.hp2 HG00621.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.48-10166delG | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4935697 | ||||||
| chr7:4935698
|
C | A | 2 | a0001c0002t0003g0148a0001c0007t0028g0332 | 2 | HG02572.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.48-10166G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4935698 | ||||||
| chr7:4935699
|
C | A | 1 | a0001c0002t0005g0159 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.48-10167G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4935699 | ||||||
| chr7:4935904
|
G | C | 1 | a0001c0001t0003g0324 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.48-10372C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4935904 | ||||||
| chr7:4935950
|
C | T | 111 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0149others(108): Show | 112 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(109): Show |
intron_variant | MODIFIER | c.48-10418G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4935950 | ||||||
| chr7:4936110
|
G | A | 1 | a0001c0002t0014g0342 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.48-10578C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4936110 | ||||||
| chr7:4936112
|
G | A | 1 | a0001c0001t0002g0021 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.48-10580C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4936112 | ||||||
| chr7:4936177
|
C | A | 1 | a0001c0001t0030g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.48-10645G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4936177 | ||||||
| chr7:4936185
|
CA | C | 117 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0149others(114): Show | 118 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.48-10654delT | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4936185 | ||||||
| chr7:4936246
|
C | A | 80 | a0001c0001t0001g0268a0001c0001t0001g0273a0001c0001t0001g0286others(77): Show | 81 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.48-10714G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4936246 | ||||||
| chr7:4936325
|
C | A | 83 | a0001c0001t0001g0248a0001c0001t0001g0268a0001c0001t0001g0273others(80): Show | 84 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.48-10793G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4936325 | ||||||
| chr7:4936359
|
G | C | 1 | a0001c0001t0004g0320 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.48-10827C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4936359 | ||||||
| chr7:4936400
|
T | C | 4 | a0001c0003t0004g0298a0001c0003t0004g0314a0001c0003t0004g0316others(1): Show | 4 | NA18963.hp1 NA18969.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.48-10868A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4936400 | ||||||
| chr7:4936605
|
C | G | 1 | a0001c0001t0030g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.48-11073G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4936605 | ||||||
| chr7:4936702
|
C | A | 1 | a0001c0001t0010g0337 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.48-11170G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4936702 | ||||||
| chr7:4936795
|
C | T | 40 | a0001c0001t0001g0189a0001c0001t0001g0328a0001c0001t0002g0098others(37): Show | 40 | HG00280.hp1 HG00639.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.48-11263G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4936795 | ||||||
| chr7:4936809
|
A | G | 114 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0138others(111): Show | 115 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(112): Show |
intron_variant | MODIFIER | c.48-11277T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4936809 | ||||||
| chr7:4936820
|
CG | C | 3 | a0001c0001t0001g0247a0001c0001t0009g0245a0001c0001t0009g0246 | 3 | HG02647.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.48-11289delC | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4936820 | ||||||
| chr7:4936863
|
T | A | 53 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0149others(50): Show | 54 | HG00738.hp2 HG01074.hp2 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.48-11331A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4936863 | ||||||
| chr7:4936880
|
G | T | 22 | a0001c0001t0015g0377a0001c0001t0015g0378a0001c0001t0015g0379others(19): Show | 22 | HG00280.hp1 HG00639.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.48-11348C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4936880 | ||||||
| chr7:4936924
|
C | T | 1 | a0001c0001t0002g0256 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.48-11392G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4936924 | ||||||
| chr7:4936988
|
G | A | 1 | a0001c0002t0006g0361 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.48-11456C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4936988 | ||||||
| chr7:4937168
|
G | C | 115 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0046others(112): Show | 116 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.48-11636C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937168 | ||||||
| chr7:4937233
|
C | A | 1 | a0001c0001t0030g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.48-11701G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937233 | ||||||
| chr7:4937346
|
G | A | 1 | a0001c0001t0013g0229 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.48-11814C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937346 | ||||||
| chr7:4937432
|
A | G | 1 | a0001c0002t0001g0197 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.48-11900T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937432 | ||||||
| chr7:4937463
|
A | G | 2 | a0001c0002t0014g0343a0001c0002t0014g0344 | 2 | HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.48-11931T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937463 | ||||||
| chr7:4937478
|
A | T | 108 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0149others(105): Show | 109 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.48-11946T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937478 | ||||||
| chr7:4937506
|
T | C | 1 | a0001c0001t0001g0248 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.48-11974A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937506 | ||||||
| chr7:4937561
|
C | T | 1 | a0001c0001t0002g0258 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.48-12029G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937561 | ||||||
| chr7:4937617
|
T | C | 2 | a0001c0001t0011g0333a0001c0001t0011g0334 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.48-12085A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937617 | ||||||
| chr7:4937653
|
C | T | 3 | a0001c0001t0002g0252a0001c0001t0002g0253a0001c0001t0002g0254 | 3 | HG00735.hp1 HG01074.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.48-12121G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937653 | ||||||
| chr7:4937715
|
C | G | 85 | a0001c0001t0001g0268a0001c0001t0001g0273a0001c0001t0001g0286others(82): Show | 86 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.48-12183G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937715 | ||||||
| chr7:4937731
|
C | G | 85 | a0001c0001t0001g0268a0001c0001t0001g0273a0001c0001t0001g0286others(82): Show | 86 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.48-12199G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937731 | ||||||
| chr7:4937874
|
C | T | 1 | a0001c0001t0030g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.48-12342G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937874 | ||||||
| chr7:4937880
|
C | T | 4 | a0001c0001t0001g0249a0001c0002t0001g0101a0001c0002t0001g0102others(1): Show | 4 | HG02145.hp1 HG02647.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.48-12348G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937880 | ||||||
| chr7:4937957
|
A | G | 1 | a0001c0001t0007g0074 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.48-12425T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937957 | ||||||
| chr7:4937969
|
C | CTTTTTCT others(3): Show |
1 | a0001c0001t0001g0149 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.48-12447_48-12438d others(12): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937969 | ||||||
| chr7:4937969
|
C | CTTTTTCT others(4): Show |
48 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0175others(45): Show | 49 | HG00738.hp2 HG01074.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.48-12448_48-12438d others(13): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937969 | ||||||
| chr7:4937978
|
T | C | 2 | a0001c0002t0014g0343a0001c0002t0014g0344 | 2 | HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.48-12446A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937978 | ||||||
| chr7:4937990
|
T | TTTTTTTT others(9): Show |
1 | a0001c0002t0001g0207 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.48-12459_48-12458i others(18): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937990 | ||||||
| chr7:4937994
|
C | T | 2 | a0001c0001t0001g0225a0001c0002t0004g0182 | 2 | NA18939.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.48-12462G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937994 | ||||||
| chr7:4938002
|
C | CT | 86 | a0001c0001t0001g0020a0001c0001t0001g0052a0001c0001t0001g0053others(83): Show | 87 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.48-12471dupA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4938002 | ||||||
| chr7:4938002
|
C | CTT | 21 | a0001c0001t0001g0046a0001c0001t0001g0055a0001c0001t0002g0023others(18): Show | 21 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.48-12472_48-12471d others(4): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4938002 | ||||||
| chr7:4938002
|
C | T | 1 | a0001c0002t0001g0207 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.48-12470G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4938002 | ||||||
| chr7:4938002
|
CT | C | 81 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0149others(78): Show | 82 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.48-12471delA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4938002 | ||||||
| chr7:4938002
|
CTT | C | 32 | a0001c0001t0001g0328a0001c0001t0002g0098a0001c0001t0003g0324others(29): Show | 32 | HG00280.hp1 HG00639.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.48-12472_48-12471d others(4): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4938002 | ||||||
| chr7:4938002
|
CTTTT | C | 66 | a0001c0001t0001g0273a0001c0001t0001g0286a0001c0001t0001g0290others(63): Show | 67 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.48-12474_48-12471d others(6): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4938002 | ||||||
| chr7:4938002
|
CTTTTT | C | 13 | a0001c0001t0001g0268a0001c0001t0002g0276a0001c0001t0004g0280others(10): Show | 13 | HG00741.hp1 HG01169.hp2 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.48-12475_48-12471d others(7): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4938002 | ||||||
| chr7:4938105
|
G | A | 126 | a0001c0001t0001g0189a0001c0001t0001g0248a0001c0001t0001g0268others(123): Show | 127 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(124): Show |
intron_variant | MODIFIER | c.48-12573C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4938105 | ||||||
| chr7:4938114
|
G | C | 2 | a0001c0001t0011g0333a0001c0001t0011g0334 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.48-12582C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4938114 | ||||||
| chr7:4938200
|
G | T | 83 | a0001c0001t0001g0248a0001c0001t0001g0268a0001c0001t0001g0273others(80): Show | 84 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.48-12668C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4938200 | ||||||
| chr7:4938292
|
A | G | 112 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0046others(109): Show | 113 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.48-12760T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4938292 | ||||||
| chr7:4938304
|
C | T | 1 | a0001c0002t0001g0243 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.48-12772G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4938304 | ||||||
| chr7:4938353
|
A | G | 111 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0149others(108): Show | 112 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(109): Show |
intron_variant | MODIFIER | c.48-12821T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4938353 | ||||||
| chr7:4938400
|
G | C | 3 | a0001c0001t0001g0247a0001c0001t0009g0245a0001c0001t0009g0246 | 3 | HG02647.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.48-12868C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4938400 | ||||||
| chr7:4938446
|
A | G | 2 | a0001c0001t0004g0280a0001c0001t0004g0281 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.48-12914T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4938446 | ||||||
| chr7:4938508
|
G | A | 2 | a0001c0003t0004g0301a0001c0003t0029g0313 | 2 | NA18998.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.48-12976C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4938508 | ||||||
| chr7:4938509
|
C | A | 125 | a0001c0001t0001g0189a0001c0001t0001g0248a0001c0001t0001g0268others(122): Show | 126 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(123): Show |
intron_variant | MODIFIER | c.48-12977G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4938509 | ||||||
| chr7:4938660
|
T | C | 1 | a0001c0002t0013g0176 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.48-13128A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4938660 | ||||||
| chr7:4938808
|
C | G | 1 | a0001c0001t0007g0074 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.48-13276G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4938808 | ||||||
| chr7:4939004
|
T | G | 1 | a0001c0002t0002g0221 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.48-13472A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939004 | ||||||
| chr7:4939029
|
G | A | 1 | a0001c0002t0005g0141 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.48-13497C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939029 | ||||||
| chr7:4939035
|
C | G | 88 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0239others(85): Show | 89 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.48-13503G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939035 | ||||||
| chr7:4939188
|
C | A | 10 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(7): Show | 10 | HG01496.hp1 HG02559.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.48-13656G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939188 | ||||||
| chr7:4939196
|
C | T | 1 | a0001c0003t0004g0302 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.48-13664G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939196 | ||||||
| chr7:4939274
|
G | A | 2 | a0001c0001t0013g0229a0001c0002t0001g0228 | 2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.48-13742C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939274 | ||||||
| chr7:4939359
|
C | A | 1 | a0001c0002t0009g0042 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.48-13827G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939359 | ||||||
| chr7:4939446
|
G | C | 1 | a0001c0002t0009g0042 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.48-13914C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939446 | ||||||
| chr7:4939474
|
T | C | 1 | a0001c0001t0022g0004 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.48-13942A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939474 | ||||||
| chr7:4939521
|
C | T | 45 | a0001c0001t0011g0039a0001c0002t0001g0164a0001c0002t0001g0165others(42): Show | 45 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.48-13989G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939521 | ||||||
| chr7:4939628
|
T | C | 108 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0149others(105): Show | 109 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.48-14096A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939628 | ||||||
| chr7:4939705
|
C | T | 142 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(139): Show | 143 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(140): Show |
intron_variant | MODIFIER | c.48-14173G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939705 | ||||||
| chr7:4939742
|
CT | C | 198 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0138others(195): Show | 200 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(197): Show |
intron_variant | MODIFIER | c.48-14211delA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939742 | ||||||
| chr7:4939746
|
T | C | 93 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0046others(90): Show | 94 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.48-14214A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939746 | ||||||
| chr7:4939747
|
T | C | 51 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0149others(48): Show | 52 | HG00738.hp2 HG01074.hp2 HG01081.hp1 others(49): Show |
intron_variant | MODIFIER | c.48-14215A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939747 | ||||||
| chr7:4939748
|
T | C | 1 | a0001c0002t0001g0213 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.48-14216A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939748 | ||||||
| chr7:4939752
|
T | A | 1 | a0001c0002t0001g0197 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.48-14220A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939752 | ||||||
| chr7:4939767
|
G | C | 1 | a0001c0001t0001g0248 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.48-14235C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939767 | ||||||
| chr7:4939793
|
T | A | 108 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0149others(105): Show | 109 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.48-14261A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939793 | ||||||
| chr7:4939823
|
C | T | 5 | a0001c0001t0001g0249a0001c0001t0030g0322a0001c0002t0001g0101others(2): Show | 5 | HG02145.hp1 HG02647.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.48-14291G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939823 | ||||||
| chr7:4939883
|
G | A | 108 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0149others(105): Show | 109 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.48-14351C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939883 | ||||||
| chr7:4940007
|
G | A | 45 | a0001c0001t0011g0039a0001c0002t0001g0164a0001c0002t0001g0165others(42): Show | 45 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.48-14475C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4940007 | ||||||
| chr7:4940158
|
G | A | 2 | a0001c0001t0011g0333a0001c0001t0011g0334 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.48-14626C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4940158 | ||||||
| chr7:4940201
|
G | A | 1 | a0001c0001t0030g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.48-14669C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4940201 | ||||||
| chr7:4940220
|
C | T | 8 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(5): Show | 8 | HG01496.hp1 HG02145.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.48-14688G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4940220 | ||||||
| chr7:4940230
|
G | C | 350 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0046others(347): Show | 353 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.48-14698C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4940230 | ||||||
| chr7:4940546
|
G | C | 2 | a0001c0001t0011g0333a0001c0001t0011g0334 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.48-15014C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4940546 | ||||||
| chr7:4940565
|
C | G | 1 | a0001c0002t0014g0344 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.48-15033G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4940565 | ||||||
| chr7:4940583
|
C | T | 1 | a0001c0002t0003g0178 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.48-15051G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4940583 | ||||||
| chr7:4940734
|
G | A | 1 | a0001c0002t0017g0190 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.48-15202C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4940734 | ||||||
| chr7:4940775
|
C | T | 1 | a0001c0001t0002g0021 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.48-15243G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4940775 | ||||||
| chr7:4940811
|
A | G | 1 | a0001c0001t0003g0056 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.48-15279T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4940811 | ||||||
| chr7:4940843
|
A | T | 1 | a0001c0001t0002g0021 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.48-15311T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4940843 | ||||||
| chr7:4940908
|
C | G | 14 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(11): Show | 14 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.48-15376G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4940908 | ||||||
| chr7:4940998
|
C | A | 1 | a0001c0002t0001g0130 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.48-15466G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4940998 | ||||||
| chr7:4941100
|
G | A | 1 | a0001c0001t0002g0009 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.48-15568C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4941100 | ||||||
| chr7:4941430
|
G | C | 1 | a0001c0001t0003g0287 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.48-15898C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4941430 | ||||||
| chr7:4941459
|
G | A | 1 | a0001c0002t0001g0216 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.48-15927C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4941459 | ||||||
| chr7:4941467
|
T | G | 1 | a0001c0002t0038g0364 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.48-15935A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4941467 | ||||||
| chr7:4941495
|
T | G | 1 | a0001c0001t0003g0037 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.48-15963A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4941495 | ||||||
| chr7:4941629
|
CA | C | 129 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0149others(126): Show | 129 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.48-16098delT | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4941629 | ||||||
| chr7:4941629
|
CAA | C | 195 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0046others(192): Show | 197 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.48-16099_48-16098d others(4): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4941629 | ||||||
| chr7:4941721
|
G | A | 108 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0149others(105): Show | 109 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.48-16189C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4941721 | ||||||
| chr7:4941749
|
T | C | 1 | a0001c0001t0030g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.48-16217A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4941749 | ||||||
| chr7:4941859
|
A | G | 1 | a0001c0001t0030g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.48-16327T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4941859 | ||||||
| chr7:4941865
|
C | T | 4 | a0001c0001t0001g0189a0001c0002t0001g0188a0001c0002t0009g0038others(1): Show | 4 | HG02572.hp1 NA18906.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.48-16333G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4941865 | ||||||
| chr7:4941927
|
T | A | 241 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0046others(238): Show | 243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.48-16395A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4941927 | ||||||
| chr7:4941927
|
T | C | 1 | a0001c0002t0001g0220 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.48-16395A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4941927 | ||||||
| chr7:4941951
|
T | A | 2 | a0001c0001t0003g0087a0001c0001t0003g0088 | 2 | HG00558.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.48-16419A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4941951 | ||||||
| chr7:4941984
|
C | T | 1 | a0001c0001t0002g0057 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.48-16452G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4941984 | ||||||
| chr7:4941985
|
G | A | 1 | a0001c0001t0004g0120 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.48-16453C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4941985 | ||||||
| chr7:4942286
|
G | T | 1 | a0001c0002t0001g0146 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.47+16685C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4942286 | ||||||
| chr7:4942346
|
C | T | 1 | a0001c0001t0002g0284 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.47+16625G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4942346 | ||||||
| chr7:4942386
|
C | T | 1 | a0001c0001t0002g0028 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.47+16585G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4942386 | ||||||
| chr7:4942415
|
AT | A | 132 | a0001c0001t0001g0007a0001c0001t0001g0099a0001c0001t0001g0100others(129): Show | 133 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(130): Show |
intron_variant | MODIFIER | c.47+16555delA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4942415 | ||||||
| chr7:4942415
|
ATT | A | 234 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0046others(231): Show | 236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.47+16554_47+16555d others(4): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4942415 | ||||||
| chr7:4942435
|
A | T | 1 | a0001c0001t0002g0258 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.47+16536T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4942435 | ||||||
| chr7:4942441
|
T | C | 1 | a0001c0001t0002g0284 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.47+16530A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4942441 | ||||||
| chr7:4942442
|
T | A | 2 | a0001c0001t0002g0259a0001c0001t0002g0260 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.47+16529A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4942442 | ||||||
| chr7:4942524
|
T | C | 17 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(14): Show | 17 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.47+16447A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4942524 | ||||||
| chr7:4942562
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.47+16409G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4942562 | ||||||
| chr7:4942617
|
CT | C | 94 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0046others(91): Show | 95 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.47+16353delA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4942617 | ||||||
| chr7:4942704
|
G | C | 374 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0032others(371): Show | 377 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(374): Show |
intron_variant | MODIFIER | c.47+16267C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4942704 | ||||||
| chr7:4942730
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.47+16241G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4942730 | ||||||
| chr7:4942777
|
G | A | 30 | a0001c0002t0001g0164a0001c0002t0001g0165a0001c0002t0001g0166others(27): Show | 30 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.47+16194C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4942777 | ||||||
| chr7:4942779
|
C | G | 1 | a0001c0001t0030g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.47+16192G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4942779 | ||||||
| chr7:4942822
|
A | C | 2 | a0001c0001t0007g0061a0001c0001t0007g0062 | 2 | NA18981.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.47+16149T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4942822 | ||||||
| chr7:4942906
|
G | A | 40 | a0001c0001t0001g0328a0001c0001t0002g0098a0001c0001t0003g0324others(37): Show | 40 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.47+16065C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4942906 | ||||||
| chr7:4943004
|
C | CT | 8 | a0001c0001t0003g0324a0001c0001t0003g0325a0001c0001t0003g0327others(5): Show | 8 | HG00741.hp2 HG01109.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.47+15966dupA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4943004 | ||||||
| chr7:4943004
|
CT | C | 102 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(99): Show | 103 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.47+15966delA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4943004 | ||||||
| chr7:4943004
|
CTT | C | 94 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0046others(91): Show | 95 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.47+15965_47+15966d others(4): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4943004 | ||||||
| chr7:4943009
|
T | C | 1 | a0001c0001t0001g0248 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.47+15962A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4943009 | ||||||
| chr7:4943027
|
T | G | 1 | a0001c0001t0017g0123 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.47+15944A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4943027 | ||||||
| chr7:4943168
|
C | T | 14 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(11): Show | 14 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.47+15803G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4943168 | ||||||
| chr7:4943228
|
C | A | 2 | a0001c0001t0003g0112a0001c0001t0003g0114 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.47+15743G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4943228 | ||||||
| chr7:4943299
|
G | A | 1 | a0001c0002t0003g0180 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.47+15672C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4943299 | ||||||
| chr7:4943364
|
C | T | 2 | a0001c0002t0001g0002a0001c0002t0001g0242 | 3 | HG02451.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.47+15607G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4943364 | ||||||
| chr7:4943428
|
C | G | 1 | a0001c0001t0003g0327 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.47+15543G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4943428 | ||||||
| chr7:4943515
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.47+15456C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4943515 | ||||||
| chr7:4943622
|
A | G | 9 | a0001c0001t0013g0229a0001c0002t0001g0228a0001c0002t0001g0230others(6): Show | 9 | HG01884.hp2 HG02258.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.47+15349T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4943622 | ||||||
| chr7:4943638
|
G | A | 1 | a0001c0001t0030g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.47+15333C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4943638 | ||||||
| chr7:4943834
|
C | T | 17 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(14): Show | 17 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.47+15137G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4943834 | ||||||
| chr7:4943853
|
G | A | 1 | a0001c0001t0003g0043 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.47+15118C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4943853 | ||||||
| chr7:4943950
|
C | T | 40 | a0001c0001t0001g0328a0001c0001t0002g0098a0001c0001t0003g0324others(37): Show | 40 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.47+15021G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4943950 | ||||||
| chr7:4943978
|
T | C | 17 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(14): Show | 17 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.47+14993A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4943978 | ||||||
| chr7:4944059
|
A | C | 1 | a0001c0001t0002g0082 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.47+14912T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944059 | ||||||
| chr7:4944244
|
C | A | 4 | a0001c0001t0003g0069a0001c0001t0003g0073a0001c0001t0003g0077others(1): Show | 4 | HG01346.hp2 HG03239.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.47+14727G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944244 | ||||||
| chr7:4944443
|
G | A | 1 | a0001c0001t0030g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.47+14528C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944443 | ||||||
| chr7:4944515
|
CTCAGCAC others(30): Show |
C | 1 | a0001c0001t0012g0227 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.47+14419_47+14455d others(39): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944515 | ||||||
| chr7:4944530
|
A | G | 1 | a0001c0002t0003g0183 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.47+14441T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944530 | ||||||
| chr7:4944617
|
G | T | 2 | a0001c0001t0013g0229a0001c0002t0001g0228 | 2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.47+14354C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944617 | ||||||
| chr7:4944700
|
T | C | 2 | a0001c0001t0011g0333a0001c0001t0011g0334 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.47+14271A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944700 | ||||||
| chr7:4944745
|
C | T | 3 | a0001c0001t0011g0333a0001c0001t0011g0334a0001c0002t0003g0148 | 3 | HG01891.hp1 HG03041.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.47+14226G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944745 | ||||||
| chr7:4944760
|
C | CT | 38 | a0001c0001t0001g0053a0001c0001t0001g0092a0001c0001t0001g0247others(35): Show | 38 | HG01256.hp2 HG01433.hp2 HG01517.hp1 others(35): Show |
intron_variant | MODIFIER | c.47+14210dupA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944760 | ||||||
| chr7:4944760
|
CT | C | 96 | a0001c0001t0001g0032a0001c0001t0001g0059a0001c0001t0001g0099others(93): Show | 97 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.47+14210delA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944760 | ||||||
| chr7:4944760
|
CTT | C | 71 | a0001c0001t0001g0020a0001c0001t0001g0175a0001c0001t0002g0012others(68): Show | 72 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.47+14209_47+14210d others(4): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944760 | ||||||
| chr7:4944760
|
CTTT | C | 6 | a0001c0002t0001g0230a0001c0002t0001g0231a0001c0002t0001g0232others(3): Show | 6 | HG00735.hp2 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.47+14208_47+14210d others(5): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944760 | ||||||
| chr7:4944762
|
T | TC | 4 | a0001c0002t0001g0207a0001c0002t0003g0148a0001c0002t0013g0176others(1): Show | 4 | HG03098.hp2 HG03540.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.47+14208_47+14209i others(3): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944762 | ||||||
| chr7:4944763
|
T | C | 2 | a0001c0002t0001g0211a0001c0002t0014g0344 | 2 | HG03225.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.47+14208A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944763 | ||||||
| chr7:4944764
|
T | A | 4 | a0001c0001t0001g0189a0001c0002t0001g0188a0001c0002t0009g0038others(1): Show | 4 | HG02572.hp1 NA18906.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.47+14207A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944764 | ||||||
| chr7:4944764
|
T | C | 25 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0149others(22): Show | 25 | HG01167.hp2 HG01981.hp1 HG02056.hp1 others(22): Show |
intron_variant | MODIFIER | c.47+14207A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944764 | ||||||
| chr7:4944765
|
T | C | 25 | a0001c0001t0001g0175a0001c0002t0001g0002a0001c0002t0001g0086others(22): Show | 26 | HG00738.hp2 HG01074.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.47+14206A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944765 | ||||||
| chr7:4944801
|
T | C | 2 | a0001c0002t0014g0343a0001c0002t0014g0344 | 2 | HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.47+14170A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944801 | ||||||
| chr7:4944804
|
G | A | 3 | a0001c0002t0001g0101a0001c0002t0001g0102a0001c0002t0001g0103 | 3 | HG02145.hp1 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.47+14167C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944804 | ||||||
| chr7:4944888
|
C | T | 87 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0239others(84): Show | 88 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.47+14083G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944888 | ||||||
| chr7:4944902
|
G | A | 1 | a0001c0001t0002g0274 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.47+14069C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944902 | ||||||
| chr7:4944923
|
A | G | 1 | a0001c0001t0002g0009 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.47+14048T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944923 | ||||||
| chr7:4945078
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.47+13893G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945078 | ||||||
| chr7:4945184
|
C | CCTTCTT | 4 | a0001c0001t0001g0053a0001c0002t0005g0141a0001c0002t0011g0147others(1): Show | 4 | HG02293.hp1 HG02300.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.47+13786_47+13787i others(8): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945184 | ||||||
| chr7:4945184
|
C | CCTTCTTC others(2): Show |
4 | a0001c0002t0003g0136a0001c0002t0005g0167a0001c0002t0005g0173others(1): Show | 4 | HG00558.hp1 HG03688.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.47+13786_47+13787i others(11): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945184 | ||||||
| chr7:4945184
|
C | CCTTCTTC others(5): Show |
7 | a0001c0002t0003g0148a0001c0002t0003g0162a0001c0002t0003g0174others(4): Show | 7 | HG00621.hp1 HG01975.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.47+13786_47+13787i others(14): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945184 | ||||||
| chr7:4945184
|
C | CCTTCTTC others(8): Show |
9 | a0001c0002t0001g0166a0001c0002t0001g0230a0001c0002t0001g0236others(6): Show | 9 | HG01928.hp2 HG03209.hp2 HG03516.hp1 others(6): Show |
intron_variant | MODIFIER | c.47+13786_47+13787i others(17): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945184 | ||||||
| chr7:4945184
|
C | CCTTCTTC others(11): Show |
7 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0002t0001g0165others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.47+13786_47+13787i others(20): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945184 | ||||||
| chr7:4945184
|
C | CCTTCTTC others(14): Show |
4 | a0001c0002t0001g0164a0001c0002t0001g0232a0001c0002t0003g0160others(1): Show | 4 | HG00544.hp2 NA18990.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.47+13786_47+13787i others(23): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945184 | ||||||
| chr7:4945184
|
C | CCTTCTTC others(17): Show |
4 | a0001c0002t0001g0231a0001c0002t0003g0315a0001c0002t0007g0168others(1): Show | 4 | HG02723.hp2 NA19009.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.47+13786_47+13787i others(26): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945184 | ||||||
| chr7:4945184
|
C | CCTTCTTC others(23): Show |
1 | a0001c0002t0007g0163 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.47+13786_47+13787i others(32): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945184 | ||||||
| chr7:4945184
|
C | CCTTCTTC others(35): Show |
1 | a0001c0002t0005g0159 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.47+13786_47+13787i others(44): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945184 | ||||||
| chr7:4945185
|
T | C | 46 | a0001c0001t0001g0053a0001c0001t0002g0024a0001c0001t0002g0025others(43): Show | 46 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.47+13786A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | ||||||
| chr7:4945185
|
T | TCTTCTTC others(6): Show |
1 | a0001c0002t0007g0226 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.47+13785_47+13786i others(15): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | ||||||
| chr7:4945185
|
T | TCTTCTTC others(36): Show |
1 | a0001c0001t0004g0311 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.47+13785_47+13786i others(45): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | ||||||
| chr7:4945185
|
T | TTCTTCCT others(15): Show |
1 | a0001c0002t0001g0207 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.47+13785_47+13786i others(24): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | ||||||
| chr7:4945185
|
T | TTCTTCTT others(4): Show |
2 | a0001c0001t0002g0319a0001c0003t0036g0339 | 2 | NA18991.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.47+13785_47+13786i others(13): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | ||||||
| chr7:4945185
|
T | TTCTTCTT others(37): Show |
1 | a0001c0003t0004g0196 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.47+13785_47+13786i others(46): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | ||||||
| chr7:4945185
|
T | TTTC | 13 | a0001c0001t0002g0031a0001c0001t0003g0037a0001c0001t0003g0043others(10): Show | 13 | HG00140.hp2 HG00423.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.47+13783_47+13785d others(5): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | ||||||
| chr7:4945185
|
T | TTTCTTC | 18 | a0001c0001t0001g0032a0001c0001t0001g0238a0001c0001t0001g0239others(15): Show | 18 | HG00609.hp1 HG01070.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.47+13780_47+13785d others(8): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | ||||||
| chr7:4945185
|
T | TTTCTTCT others(2): Show |
28 | a0001c0001t0001g0055a0001c0001t0001g0059a0001c0001t0001g0237others(25): Show | 29 | HG00099.hp2 HG00438.hp2 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.47+13777_47+13785d others(11): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | ||||||
| chr7:4945185
|
T | TTTCTTCT others(5): Show |
31 | a0001c0001t0001g0020a0001c0001t0001g0068a0001c0001t0001g0107others(28): Show | 31 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.47+13774_47+13785d others(14): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | ||||||
| chr7:4945185
|
T | TTTCTTCT others(23): Show |
1 | a0001c0001t0030g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.47+13785_47+13786i others(32): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | ||||||
| chr7:4945185
|
T | TTTCTTCT others(8): Show |
51 | a0001c0001t0001g0007a0001c0001t0001g0149a0001c0001t0001g0198others(48): Show | 52 | HG00408.hp1 HG00639.hp1 HG01074.hp1 others(49): Show |
intron_variant | MODIFIER | c.47+13771_47+13785d others(17): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | ||||||
| chr7:4945185
|
T | TTTCTTCT others(11): Show |
37 | a0001c0001t0001g0052a0001c0001t0001g0177a0001c0001t0001g0193others(34): Show | 37 | HG00280.hp1 HG00423.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.47+13768_47+13785d others(20): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | ||||||
| chr7:4945185
|
T | TTTCTTCT others(14): Show |
43 | a0001c0001t0001g0175a0001c0001t0001g0189a0001c0001t0001g0223others(40): Show | 43 | HG00408.hp2 HG00639.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.47+13765_47+13785d others(23): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | ||||||
| chr7:4945185
|
T | TTTCTTCT others(17): Show |
24 | a0001c0001t0001g0078a0001c0001t0002g0009a0001c0001t0002g0023others(21): Show | 24 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.47+13762_47+13785d others(26): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | ||||||
| chr7:4945185
|
T | TTTCTTCT others(20): Show |
15 | a0001c0001t0001g0046a0001c0001t0001g0092a0001c0001t0001g0195others(12): Show | 15 | HG00558.hp2 HG00597.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.47+13759_47+13785d others(29): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | ||||||
| chr7:4945185
|
T | TTTCTTCT others(23): Show |
10 | a0001c0001t0002g0093a0001c0001t0002g0278a0001c0001t0003g0016others(7): Show | 10 | HG01978.hp2 HG02486.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.47+13756_47+13785d others(32): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | ||||||
| chr7:4945185
|
T | TTTCTTCT others(26): Show |
6 | a0001c0001t0001g0138a0001c0001t0003g0264a0001c0001t0004g0279others(3): Show | 6 | HG01169.hp2 HG02055.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.47+13753_47+13785d others(35): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | ||||||
| chr7:4945185
|
T | TTTCTTCT others(29): Show |
6 | a0001c0001t0001g0312a0001c0001t0002g0282a0001c0001t0002g0283others(3): Show | 6 | HG01167.hp1 HG01516.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.47+13750_47+13785d others(38): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | ||||||
| chr7:4945185
|
T | TTTCTTCT others(32): Show |
5 | a0001c0001t0002g0251a0001c0001t0003g0088a0001c0001t0004g0270others(2): Show | 5 | HG00642.hp1 HG00673.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.47+13747_47+13785d others(41): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | ||||||
| chr7:4945185
|
T | TTTCTTCT others(35): Show |
1 | a0001c0001t0002g0256 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.47+13744_47+13785d others(44): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | ||||||
| chr7:4945185
|
T | TTTCTTCT others(38): Show |
1 | a0001c0001t0002g0284 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.47+13741_47+13785d others(47): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | ||||||
| chr7:4945185
|
T | TTTCTTCT others(41): Show |
3 | a0001c0001t0004g0285a0001c0001t0004g0310a0001c0002t0008g0365 | 3 | HG03017.hp2 HG03239.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.47+13738_47+13785d others(50): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | ||||||
| chr7:4945185
|
T | TTTCTTCT others(44): Show |
2 | a0001c0001t0005g0266a0001c0001t0005g0288 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.47+13735_47+13785d others(53): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | ||||||
| chr7:4945185
|
T | TTTCTTCT others(47): Show |
1 | a0001c0002t0002g0214 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.47+13732_47+13785d others(56): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | ||||||
| chr7:4945185
|
T | TTTCTTCT others(50): Show |
2 | a0001c0001t0001g0247a0001c0002t0001g0097 | 2 | NA18990.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.47+13785_47+13786i others(59): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | ||||||
| chr7:4945185
|
T | TTTCTTCT others(56): Show |
1 | a0001c0001t0001g0286 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.47+13785_47+13786i others(65): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | ||||||
| chr7:4945185
|
T | TTTCTTCT others(59): Show |
1 | a0001c0001t0004g0003 | 2 | HG02735.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.47+13785_47+13786i others(68): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | ||||||
| chr7:4945185
|
T | TTTCTTCT others(65): Show |
2 | a0001c0001t0002g0255a0001c0002t0004g0303 | 2 | NA19080.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.47+13785_47+13786i others(74): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | ||||||
| chr7:4945185
|
T | TTTCTTCT others(32): Show |
1 | a0001c0002t0014g0343 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.47+13785_47+13786i others(41): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | ||||||
| chr7:4945185
|
T | TTTCTTCT others(44): Show |
1 | a0001c0002t0014g0344 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.47+13785_47+13786i others(53): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | ||||||
| chr7:4945185
|
TTTC | T | 5 | a0001c0001t0001g0099a0001c0001t0001g0105a0001c0002t0002g0111others(2): Show | 5 | HG00280.hp2 HG01168.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.47+13783_47+13785d others(5): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | ||||||
| chr7:4945198
|
T | G | 1 | a0001c0001t0030g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.47+13773A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945198 | ||||||
| chr7:4945203
|
C | CTTCTTCT others(7): Show |
2 | a0001c0002t0006g0362a0001c0002t0006g0363 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.47+13754_47+13767d others(16): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945203 | ||||||
| chr7:4945206
|
C | CTTCTTCT others(31): Show |
1 | a0001c0001t0013g0229 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.47+13764_47+13765i others(40): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945206 | ||||||
| chr7:4945206
|
C | CTTCTTCT others(34): Show |
1 | a0001c0002t0001g0228 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.47+13764_47+13765i others(43): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945206 | ||||||
| chr7:4945237
|
T | TTCTTCTT others(22): Show |
1 | a0001c0001t0001g0290 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.47+13733_47+13734i others(31): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945237 | ||||||
| chr7:4945240
|
C | T | 3 | a0001c0001t0002g0013a0001c0001t0002g0027a0001c0002t0001g0207 | 3 | HG01168.hp1 HG01169.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.47+13731G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945240 | ||||||
| chr7:4945250
|
T | C | 1 | a0001c0002t0017g0190 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.47+13721A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945250 | ||||||
| chr7:4945263
|
C | T | 40 | a0001c0001t0001g0328a0001c0001t0002g0098a0001c0001t0003g0324others(37): Show | 40 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.47+13708G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945263 | ||||||
| chr7:4945378
|
C | G | 2 | a0001c0001t0013g0229a0001c0002t0001g0228 | 2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.47+13593G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945378 | ||||||
| chr7:4945409
|
C | CAGGTGCC others(8): Show |
1 | a0001c0002t0006g0362 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.47+13547_47+13561d others(17): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945409 | ||||||
| chr7:4945493
|
C | T | 32 | a0001c0001t0015g0377a0001c0001t0015g0378a0001c0001t0015g0379others(29): Show | 32 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.47+13478G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945493 | ||||||
| chr7:4945543
|
G | A | 1 | a0001c0001t0001g0312 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.47+13428C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945543 | ||||||
| chr7:4945553
|
G | C | 18 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(15): Show | 18 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.47+13418C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945553 | ||||||
| chr7:4945630
|
A | AGTGGCGC others(32): Show |
1 | a0001c0001t0012g0227 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.47+13302_47+13340d others(41): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945630 | ||||||
| chr7:4945635
|
C | T | 38 | a0001c0001t0001g0053a0001c0001t0011g0039a0001c0002t0001g0164others(35): Show | 38 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.47+13336G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945635 | ||||||
| chr7:4945775
|
ATGT | A | 40 | a0001c0001t0001g0328a0001c0001t0002g0098a0001c0001t0003g0324others(37): Show | 40 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.47+13193_47+13195d others(5): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945775 | ||||||
| chr7:4945917
|
A | C | 2 | a0001c0002t0018g0153a0001c0002t0018g0154 | 2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.47+13054T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945917 | ||||||
| chr7:4946030
|
T | C | 2 | a0001c0001t0004g0329a0001c0001t0004g0330 | 2 | HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.47+12941A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4946030 | ||||||
| chr7:4946093
|
A | G | 1 | a0001c0001t0003g0094 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.47+12878T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4946093 | ||||||
| chr7:4946095
|
A | G | 41 | a0001c0001t0001g0328a0001c0001t0002g0098a0001c0001t0003g0324others(38): Show | 41 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.47+12876T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4946095 | ||||||
| chr7:4946102
|
T | C | 94 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0046others(91): Show | 95 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.47+12869A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4946102 | ||||||
| chr7:4946115
|
A | G | 83 | a0001c0001t0001g0268a0001c0001t0001g0273a0001c0001t0001g0286others(80): Show | 84 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.47+12856T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4946115 | ||||||
| chr7:4946181
|
A | G | 13 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(10): Show | 13 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.47+12790T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4946181 | ||||||
| chr7:4946183
|
A | G | 148 | a0001c0001t0001g0020a0001c0001t0001g0052a0001c0001t0001g0107others(145): Show | 150 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(147): Show |
intron_variant | MODIFIER | c.47+12788T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4946183 | ||||||
| chr7:4946226
|
TACACGCA others(3): Show |
T | 2 | a0001c0001t0002g0255a0001c0002t0004g0303 | 2 | NA19080.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.47+12735_47+12744d others(12): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4946226 | ||||||
| chr7:4946397
|
A | G | 1 | a0001c0001t0003g0060 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.47+12574T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4946397 | ||||||
| chr7:4946546
|
T | A | 3 | a0001c0001t0001g0249a0001c0002t0014g0343a0001c0002t0014g0344 | 3 | HG02647.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.47+12425A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4946546 | ||||||
| chr7:4946834
|
G | A | 2 | a0001c0001t0013g0229a0001c0002t0001g0228 | 2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.47+12137C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4946834 | ||||||
| chr7:4946884
|
G | T | 19 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0002g0001others(16): Show | 20 | HG01069.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.47+12087C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4946884 | ||||||
| chr7:4947000
|
G | A | 2 | a0001c0002t0001g0215a0001c0002t0002g0221 | 2 | HG00738.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.47+11971C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947000 | ||||||
| chr7:4947014
|
C | T | 5 | a0001c0002t0001g0164a0001c0002t0001g0165a0001c0002t0001g0166others(2): Show | 5 | HG00558.hp1 HG00621.hp1 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.47+11957G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947014 | ||||||
| chr7:4947133
|
G | A | 4 | a0001c0003t0003g0295a0001c0003t0004g0301a0001c0003t0004g0302others(1): Show | 4 | HG02083.hp1 NA18998.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.47+11838C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947133 | ||||||
| chr7:4947164
|
C | T | 16 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(13): Show | 17 | HG01496.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.47+11807G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947164 | ||||||
| chr7:4947171
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.47+11800C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947171 | ||||||
| chr7:4947177
|
C | T | 1 | a0001c0001t0002g0271 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+11794G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947177 | ||||||
| chr7:4947203
|
G | A | 3 | a0001c0001t0002g0012a0001c0001t0002g0090a0001c0001t0002g0093 | 3 | HG01070.hp1 HG03017.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.47+11768C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947203 | ||||||
| chr7:4947253
|
A | G | 1 | a0001c0001t0001g0223 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.47+11718T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947253 | ||||||
| chr7:4947280
|
C | T | 20 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(17): Show | 21 | HG01496.hp1 HG02145.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.47+11691G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947280 | ||||||
| chr7:4947311
|
T | G | 82 | a0001c0001t0001g0268a0001c0001t0001g0273a0001c0001t0001g0286others(79): Show | 83 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.47+11660A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947311 | ||||||
| chr7:4947398
|
C | CT | 329 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0046others(326): Show | 332 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.47+11572dupA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947398 | ||||||
| chr7:4947398
|
C | CTT | 11 | a0001c0001t0001g0059a0001c0001t0001g0328a0001c0001t0003g0324others(8): Show | 11 | HG02486.hp1 HG02818.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.47+11571_47+11572d others(4): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947398 | ||||||
| chr7:4947518
|
C | T | 1 | a0001c0001t0005g0080 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.47+11453G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947518 | ||||||
| chr7:4947539
|
G | A | 1 | a0001c0001t0005g0079 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.47+11432C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947539 | ||||||
| chr7:4947567
|
G | A | 107 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0138others(104): Show | 107 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.47+11404C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947567 | ||||||
| chr7:4947628
|
G | A | 1 | a0001c0001t0017g0123 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.47+11343C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947628 | ||||||
| chr7:4947692
|
C | CT | 6 | a0001c0001t0004g0329a0001c0002t0006g0346a0001c0002t0006g0362others(3): Show | 6 | HG01517.hp1 HG01978.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.47+11278dupA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947692 | ||||||
| chr7:4947692
|
CT | C | 112 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0046others(109): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.47+11278delA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947692 | ||||||
| chr7:4947692
|
CTT | C | 166 | a0001c0001t0001g0138a0001c0001t0001g0247a0001c0001t0001g0248others(163): Show | 168 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.47+11277_47+11278d others(4): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947692 | ||||||
| chr7:4947692
|
CTTT | C | 31 | a0001c0001t0001g0139a0001c0001t0001g0149a0001c0001t0001g0175others(28): Show | 31 | HG00609.hp1 HG01070.hp2 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.47+11276_47+11278d others(5): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947692 | ||||||
| chr7:4947692
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0002g0098 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.47+11267_47+11278d others(14): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947692 | ||||||
| chr7:4947692
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0003t0004g0297 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.47+11264_47+11278d others(17): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947692 | ||||||
| chr7:4947753
|
A | G | 129 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(126): Show | 130 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(127): Show |
intron_variant | MODIFIER | c.47+11218T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947753 | ||||||
| chr7:4947758
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.47+11213C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947758 | ||||||
| chr7:4947764
|
A | G | 2 | a0001c0001t0003g0087a0001c0001t0003g0088 | 2 | HG00558.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.47+11207T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947764 | ||||||
| chr7:4948121
|
C | A | 1 | a0001c0001t0002g0271 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10850G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948121 | ||||||
| chr7:4948122
|
A | T | 1 | a0001c0001t0002g0271 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10849T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948122 | ||||||
| chr7:4948124
|
C | G | 1 | a0001c0001t0002g0271 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10847G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948124 | ||||||
| chr7:4948125
|
C | G | 1 | a0001c0001t0002g0271 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10846G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948125 | ||||||
| chr7:4948127
|
A | T | 1 | a0001c0001t0002g0271 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10844T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948127 | ||||||
| chr7:4948136
|
A | G | 1 | a0001c0001t0002g0271 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10835T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948136 | ||||||
| chr7:4948139
|
A | T | 1 | a0001c0001t0002g0271 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10832T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948139 | ||||||
| chr7:4948141
|
A | T | 1 | a0001c0001t0002g0271 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10830T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948141 | ||||||
| chr7:4948142
|
A | C | 1 | a0001c0001t0002g0271 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10829T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948142 | ||||||
| chr7:4948143
|
C | A | 1 | a0001c0001t0002g0271 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10828G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948143 | ||||||
| chr7:4948154
|
A | G | 1 | a0001c0001t0002g0271 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10817T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948154 | ||||||
| chr7:4948157
|
G | T | 1 | a0001c0001t0002g0271 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10814C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948157 | ||||||
| chr7:4948158
|
G | A | 1 | a0001c0001t0002g0271 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10813C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948158 | ||||||
| chr7:4948160
|
G | C | 1 | a0001c0001t0002g0271 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10811C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948160 | ||||||
| chr7:4948171
|
G | T | 1 | a0001c0001t0002g0271 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10800C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948171 | ||||||
| chr7:4948173
|
T | C | 2 | a0001c0001t0013g0229a0001c0002t0001g0228 | 2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.47+10798A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948173 | ||||||
| chr7:4948176
|
A | C | 1 | a0001c0001t0002g0271 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10795T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948176 | ||||||
| chr7:4948178
|
A | C | 1 | a0001c0001t0002g0271 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10793T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948178 | ||||||
| chr7:4948180
|
C | T | 1 | a0001c0001t0002g0271 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10791G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948180 | ||||||
| chr7:4948181
|
A | T | 1 | a0001c0001t0002g0271 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10790T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948181 | ||||||
| chr7:4948182
|
T | G | 1 | a0001c0001t0002g0271 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10789A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948182 | ||||||
| chr7:4948183
|
A | G | 1 | a0001c0001t0002g0271 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10788T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948183 | ||||||
| chr7:4948185
|
C | T | 1 | a0001c0001t0002g0271 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10786G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948185 | ||||||
| chr7:4948186
|
A | G | 1 | a0001c0001t0002g0271 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10785T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948186 | ||||||
| chr7:4948188
|
A | G | 1 | a0001c0001t0002g0271 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10783T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948188 | ||||||
| chr7:4948203
|
T | A | 1 | a0001c0001t0002g0271 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10768A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948203 | ||||||
| chr7:4948208
|
A | G | 1 | a0001c0001t0002g0271 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10763T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948208 | ||||||
| chr7:4948209
|
C | T | 1 | a0001c0001t0002g0271 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10762G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948209 | ||||||
| chr7:4948215
|
G | C | 1 | a0001c0001t0002g0271 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10756C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948215 | ||||||
| chr7:4948217
|
T | A | 1 | a0001c0001t0002g0271 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10754A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948217 | ||||||
| chr7:4948233
|
T | G | 1 | a0001c0001t0002g0271 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10738A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948233 | ||||||
| chr7:4948236
|
A | T | 1 | a0001c0001t0002g0271 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10735T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948236 | ||||||
| chr7:4948254
|
T | C | 1 | a0001c0001t0002g0271 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10717A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948254 | ||||||
| chr7:4948290
|
A | G | 1 | a0001c0001t0002g0271 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10681T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948290 | ||||||
| chr7:4948305
|
T | A | 1 | a0001c0001t0002g0028 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.47+10666A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948305 | ||||||
| chr7:4948440
|
T | A | 1 | a0001c0002t0003g0124 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.47+10531A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948440 | ||||||
| chr7:4948478
|
G | A | 1 | a0001c0001t0017g0123 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.47+10493C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948478 | ||||||
| chr7:4948527
|
GA | G | 6 | a0001c0001t0001g0328a0001c0001t0002g0291a0001c0001t0003g0324others(3): Show | 6 | HG02486.hp1 HG02896.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.47+10443delT | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948527 | ||||||
| chr7:4948716
|
G | A | 1 | a0001c0001t0007g0081 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.47+10255C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948716 | ||||||
| chr7:4948746
|
A | C | 2 | a0001c0001t0011g0333a0001c0001t0011g0334 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.47+10225T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948746 | ||||||
| chr7:4949057
|
A | G | 1 | a0001c0001t0030g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.47+9914T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4949057 | ||||||
| chr7:4949071
|
G | A | 2 | a0001c0001t0003g0094a0001c0001t0003g0095 | 2 | HG00140.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.47+9900C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4949071 | ||||||
| chr7:4949085
|
C | G | 2 | a0001c0001t0004g0270a0001c0001t0004g0272 | 2 | HG01257.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.47+9886G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4949085 | ||||||
| chr7:4949146
|
G | T | 1 | a0001c0002t0003g0178 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.47+9825C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4949146 | ||||||
| chr7:4949159
|
G | A | 82 | a0001c0001t0001g0268a0001c0001t0001g0273a0001c0001t0001g0286others(79): Show | 83 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.47+9812C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4949159 | ||||||
| chr7:4949207
|
C | A | 21 | a0001c0002t0001g0086a0001c0002t0001g0146a0001c0002t0001g0207others(18): Show | 21 | HG00738.hp2 HG01074.hp2 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.47+9764G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4949207 | ||||||
| chr7:4949322
|
C | A | 3 | a0001c0002t0001g0014a0001c0002t0001g0029a0001c0002t0001g0030 | 3 | NA18983.hp2 NA18995.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.47+9649G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4949322 | ||||||
| chr7:4949374
|
G | A | 376 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0032others(373): Show | 379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.47+9597C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4949374 | ||||||
| chr7:4949390
|
C | T | 350 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0046others(347): Show | 353 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.47+9581G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4949390 | ||||||
| chr7:4949531
|
T | A | 1 | a0001c0002t0003g0124 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.47+9440A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4949531 | ||||||
| chr7:4949696
|
G | A | 11 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(8): Show | 11 | HG01496.hp1 HG02145.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.47+9275C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4949696 | ||||||
| chr7:4949712
|
A | C | 2 | a0001c0001t0019g0050a0001c0001t0019g0051 | 2 | HG02040.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.47+9259T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4949712 | ||||||
| chr7:4949727
|
G | T | 100 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0138others(97): Show | 100 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.47+9244C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4949727 | ||||||
| chr7:4949749
|
G | A | 100 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0138others(97): Show | 100 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.47+9222C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4949749 | ||||||
| chr7:4949811
|
G | C | 1 | a0001c0001t0030g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.47+9160C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4949811 | ||||||
| chr7:4949966
|
G | A | 80 | a0001c0001t0001g0268a0001c0001t0001g0273a0001c0001t0001g0286others(77): Show | 81 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.47+9005C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4949966 | ||||||
| chr7:4949998
|
G | A | 9 | a0001c0001t0013g0229a0001c0002t0001g0228a0001c0002t0001g0230others(6): Show | 9 | HG01884.hp2 HG02258.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.47+8973C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4949998 | ||||||
| chr7:4950007
|
C | T | 2 | a0001c0002t0011g0147a0001c0002t0016g0157 | 2 | HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.47+8964G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4950007 | ||||||
| chr7:4950079
|
T | TTG | 5 | a0001c0002t0001g0006a0001c0002t0001g0008a0001c0002t0001g0131others(2): Show | 5 | HG01099.hp1 HG01433.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.47+8890_47+8891dup others(2): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4950079 | ||||||
| chr7:4950079
|
TTG | T | 9 | a0001c0001t0001g0177a0001c0001t0001g0248a0001c0001t0002g0031others(6): Show | 9 | HG01884.hp1 HG02615.hp1 HG03831.hp2 others(6): Show |
intron_variant | MODIFIER | c.47+8890_47+8891del others(2): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4950079 | ||||||
| chr7:4950079
|
TTGTG | T | 338 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0046others(335): Show | 341 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.47+8888_47+8891del others(4): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4950079 | ||||||
| chr7:4950112
|
G | T | 4 | a0001c0001t0003g0324a0001c0001t0003g0325a0001c0001t0003g0326others(1): Show | 4 | HG02486.hp1 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.47+8859C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4950112 | ||||||
| chr7:4950117
|
A | T | 1 | a0001c0002t0003g0140 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.47+8854T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4950117 | ||||||
| chr7:4950247
|
C | T | 2 | a0001c0001t0002g0048a0001c0001t0003g0049 | 2 | NA18993.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.47+8724G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4950247 | ||||||
| chr7:4950297
|
C | T | 7 | a0001c0001t0001g0328a0001c0001t0003g0324a0001c0001t0003g0325others(4): Show | 7 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.47+8674G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4950297 | ||||||
| chr7:4950300
|
G | T | 1 | a0001c0003t0004g0298 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.47+8671C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4950300 | ||||||
| chr7:4950378
|
G | C | 5 | a0001c0002t0001g0002a0001c0002t0001g0242a0001c0002t0001g0243others(2): Show | 6 | HG02451.hp1 HG02622.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.47+8593C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4950378 | ||||||
| chr7:4950380
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.47+8591C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4950380 | ||||||
| chr7:4950420
|
C | A | 102 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0138others(99): Show | 102 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.47+8551G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4950420 | ||||||
| chr7:4950499
|
T | A | 2 | a0001c0002t0001g0218a0001c0006t0001g0217 | 2 | HG01081.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.47+8472A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4950499 | ||||||
| chr7:4950607
|
C | T | 2 | a0001c0003t0004g0299a0001c0003t0004g0300 | 2 | NA18950.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.47+8364G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4950607 | ||||||
| chr7:4950665
|
G | A | 1 | a0001c0002t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.47+8306C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4950665 | ||||||
| chr7:4950709
|
C | T | 13 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0189others(10): Show | 13 | HG02559.hp1 HG02572.hp1 HG03098.hp1 others(10): Show |
intron_variant | MODIFIER | c.47+8262G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4950709 | ||||||
| chr7:4950712
|
CT | C | 202 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0046others(199): Show | 205 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.47+8258delA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4950712 | ||||||
| chr7:4950771
|
T | G | 1 | a0001c0002t0001g0197 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.47+8200A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4950771 | ||||||
| chr7:4951009
|
G | A | 25 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0002g0001others(22): Show | 26 | HG00423.hp2 HG01069.hp2 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.47+7962C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4951009 | ||||||
| chr7:4951087
|
A | C | 1 | a0001c0001t0001g0175 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.47+7884T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4951087 | ||||||
| chr7:4951088
|
C | A | 1 | a0001c0001t0001g0175 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.47+7883G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4951088 | ||||||
| chr7:4951089
|
A | C | 1 | a0001c0001t0001g0175 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.47+7882T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4951089 | ||||||
| chr7:4951249
|
TC | T | 3 | a0001c0001t0001g0175a0001c0001t0003g0326a0001c0001t0005g0288 | 3 | HG02896.hp1 HG03490.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.47+7721delG | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4951249 | ||||||
| chr7:4951342
|
C | T | 238 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0046others(235): Show | 241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.47+7629G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4951342 | ||||||
| chr7:4951388
|
C | T | 6 | a0001c0001t0001g0248a0001c0002t0001g0002a0001c0002t0001g0242others(3): Show | 7 | HG02451.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.47+7583G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4951388 | ||||||
| chr7:4951418
|
C | A | 1 | a0001c0001t0001g0175 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.47+7553G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4951418 | ||||||
| chr7:4951446
|
C | G | 1 | a0001c0001t0001g0046 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.47+7525G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4951446 | ||||||
| chr7:4951494
|
A | G | 4 | a0001c0001t0001g0189a0001c0002t0001g0188a0001c0002t0001g0205others(1): Show | 4 | HG02572.hp1 NA18522.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.47+7477T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4951494 | ||||||
| chr7:4951628
|
C | A | 61 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(58): Show | 62 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.47+7343G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4951628 | ||||||
| chr7:4951771
|
T | A | 1 | a0001c0001t0001g0175 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.47+7200A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4951771 | ||||||
| chr7:4951774
|
A | T | 1 | a0001c0001t0001g0175 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.47+7197T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4951774 | ||||||
| chr7:4951811
|
A | T | 1 | a0001c0001t0001g0100 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.47+7160T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4951811 | ||||||
| chr7:4951945
|
C | T | 1 | a0001c0001t0003g0016 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.47+7026G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4951945 | ||||||
| chr7:4951986
|
T | G | 1 | a0001c0001t0002g0012 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.47+6985A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4951986 | ||||||
| chr7:4952028
|
G | C | 8 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(5): Show | 8 | HG01496.hp1 HG02145.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.47+6943C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4952028 | ||||||
| chr7:4952182
|
G | A | 1 | a0001c0001t0001g0175 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.47+6789C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4952182 | ||||||
| chr7:4952262
|
C | G | 11 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(8): Show | 11 | HG01496.hp1 HG02145.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.47+6709G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4952262 | ||||||
| chr7:4952640
|
C | G | 1 | a0001c0001t0025g0269 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.47+6331G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4952640 | ||||||
| chr7:4952655
|
C | T | 90 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0046others(87): Show | 91 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.47+6316G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4952655 | ||||||
| chr7:4952675
|
G | A | 74 | a0001c0001t0001g0273a0001c0001t0001g0286a0001c0001t0001g0312others(71): Show | 75 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.47+6296C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4952675 | ||||||
| chr7:4952689
|
A | AT | 19 | a0001c0001t0001g0177a0001c0001t0001g0193a0001c0001t0001g0225others(16): Show | 19 | HG00741.hp2 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.47+6281dupA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4952689 | ||||||
| chr7:4952689
|
AT | A | 214 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0046others(211): Show | 217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.47+6281delA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4952689 | ||||||
| chr7:4952714
|
CAG | C | 29 | a0001c0002t0001g0097a0001c0002t0001g0164a0001c0002t0001g0165others(26): Show | 29 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.47+6255_47+6256del others(2): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4952714 | ||||||
| chr7:4952797
|
T | G | 2 | a0001c0003t0004g0296a0001c0003t0004g0297 | 2 | NA18968.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.47+6174A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4952797 | ||||||
| chr7:4952898
|
C | T | 87 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0239others(84): Show | 88 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.47+6073G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4952898 | ||||||
| chr7:4952995
|
G | GT | 64 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0149others(61): Show | 64 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.47+5975dupA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4952995 | ||||||
| chr7:4953001
|
T | C | 1 | a0001c0001t0030g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.47+5970A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4953001 | ||||||
| chr7:4953006
|
T | G | 1 | a0001c0002t0001g0205 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.47+5965A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4953006 | ||||||
| chr7:4953023
|
A | G | 1 | a0001c0001t0001g0175 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.47+5948T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4953023 | ||||||
| chr7:4953247
|
C | T | 1 | a0001c0002t0005g0158 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.47+5724G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4953247 | ||||||
| chr7:4953321
|
C | T | 94 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0046others(91): Show | 95 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.47+5650G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4953321 | ||||||
| chr7:4953455
|
A | G | 1 | a0001c0001t0003g0325 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.47+5516T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4953455 | ||||||
| chr7:4953475
|
CT | C | 98 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0046others(95): Show | 99 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.47+5495delA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4953475 | ||||||
| chr7:4953584
|
C | T | 98 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0149others(95): Show | 98 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.47+5387G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4953584 | ||||||
| chr7:4953748
|
G | A | 1 | a0001c0007t0028g0332 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.47+5223C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4953748 | ||||||
| chr7:4953761
|
G | A | 13 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(10): Show | 13 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.47+5210C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4953761 | ||||||
| chr7:4953796
|
T | A | 1 | a0001c0001t0001g0175 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.47+5175A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4953796 | ||||||
| chr7:4953808
|
A | T | 1 | a0001c0001t0001g0175 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.47+5163T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4953808 | ||||||
| chr7:4953822
|
T | A | 4 | a0001c0002t0001g0200a0001c0002t0001g0201a0001c0002t0001g0202others(1): Show | 4 | HG03098.hp1 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.47+5149A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4953822 | ||||||
| chr7:4953869
|
G | A | 2 | a0001c0001t0002g0034a0001c0002t0001g0220 | 2 | HG04184.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.47+5102C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4953869 | ||||||
| chr7:4953998
|
G | A | 25 | a0001c0002t0001g0097a0001c0002t0001g0164a0001c0002t0001g0165others(22): Show | 25 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.47+4973C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4953998 | ||||||
| chr7:4954106
|
A | G | 1 | a0001c0001t0001g0248 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.47+4865T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4954106 | ||||||
| chr7:4954125
|
C | T | 85 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0239others(82): Show | 86 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.47+4846G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4954125 | ||||||
| chr7:4954418
|
A | AT | 94 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0046others(91): Show | 95 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.47+4552dupA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4954418 | ||||||
| chr7:4954444
|
G | T | 2 | a0001c0001t0002g0319a0001c0003t0001g0318 | 2 | NA18986.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.47+4527C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4954444 | ||||||
| chr7:4954451
|
T | G | 1 | a0001c0002t0001g0203 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.47+4520A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4954451 | ||||||
| chr7:4954520
|
C | A | 20 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(17): Show | 21 | HG01496.hp1 HG02145.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.47+4451G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4954520 | ||||||
| chr7:4954542
|
T | C | 1 | a0001c0001t0001g0248 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.47+4429A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4954542 | ||||||
| chr7:4954619
|
A | G | 39 | a0001c0001t0011g0039a0001c0002t0001g0097a0001c0002t0001g0164others(36): Show | 39 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.47+4352T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4954619 | ||||||
| chr7:4954621
|
G | A | 3 | a0001c0001t0001g0189a0001c0002t0001g0188a0001c0002t0017g0190 | 3 | NA18906.hp1 NA19030.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.47+4350C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4954621 | ||||||
| chr7:4954647
|
G | A | 9 | a0001c0001t0013g0229a0001c0002t0001g0228a0001c0002t0001g0230others(6): Show | 9 | HG01884.hp2 HG02258.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.47+4324C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4954647 | ||||||
| chr7:4954671
|
G | A | 81 | a0001c0001t0001g0268a0001c0001t0001g0273a0001c0001t0001g0286others(78): Show | 82 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.47+4300C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4954671 | ||||||
| chr7:4954685
|
T | C | 2 | a0001c0001t0002g0319a0001c0003t0001g0318 | 2 | NA18986.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.47+4286A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4954685 | ||||||
| chr7:4954859
|
A | T | 1 | a0001c0001t0003g0037 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.47+4112T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4954859 | ||||||
| chr7:4954906
|
G | C | 13 | a0001c0001t0001g0092a0001c0001t0002g0009a0001c0001t0002g0090others(10): Show | 13 | HG00140.hp1 HG00558.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.47+4065C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4954906 | ||||||
| chr7:4954920
|
A | G | 1 | a0001c0001t0002g0036 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.47+4051T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4954920 | ||||||
| chr7:4954937
|
T | A | 1 | a0001c0001t0030g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.47+4034A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4954937 | ||||||
| chr7:4954941
|
T | C | 2 | a0001c0001t0013g0229a0001c0002t0001g0228 | 2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.47+4030A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4954941 | ||||||
| chr7:4955132
|
C | T | 296 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0046others(293): Show | 298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.47+3839G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4955132 | ||||||
| chr7:4955189
|
G | A | 1 | a0001c0001t0034g0150 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.47+3782C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4955189 | ||||||
| chr7:4955351
|
G | A | 1 | a0001c0001t0030g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.47+3620C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4955351 | ||||||
| chr7:4955461
|
A | T | 1 | a0001c0001t0034g0150 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.47+3510T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4955461 | ||||||
| chr7:4955548
|
T | C | 1 | a0001c0002t0002g0221 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.47+3423A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4955548 | ||||||
| chr7:4955607
|
T | C | 8 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0193others(5): Show | 8 | HG02135.hp1 NA18612.hp2 NA18747.hp2 others(5): Show |
intron_variant | MODIFIER | c.47+3364A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4955607 | ||||||
| chr7:4955957
|
G | A | 1 | a0001c0002t0001g0197 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.47+3014C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4955957 | ||||||
| chr7:4955968
|
G | A | 22 | a0001c0001t0002g0206a0001c0001t0003g0204a0001c0002t0001g0146others(19): Show | 22 | HG00738.hp2 HG01074.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.47+3003C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4955968 | ||||||
| chr7:4956013
|
A | G | 14 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(11): Show | 14 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.47+2958T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4956013 | ||||||
| chr7:4956014
|
T | C | 5 | a0001c0002t0001g0002a0001c0002t0001g0242a0001c0002t0001g0243others(2): Show | 6 | HG02451.hp1 HG02622.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.47+2957A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4956014 | ||||||
| chr7:4956119
|
A | G | 2 | a0001c0001t0010g0335a0001c0001t0030g0322 | 2 | HG02523.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.47+2852T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4956119 | ||||||
| chr7:4956162
|
C | T | 1 | a0001c0001t0010g0336 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.47+2809G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4956162 | ||||||
| chr7:4956216
|
T | C | 350 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0046others(347): Show | 353 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.47+2755A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4956216 | ||||||
| chr7:4956247
|
A | G | 1 | a0001c0002t0005g0141 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.47+2724T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4956247 | ||||||
| chr7:4956252
|
A | G | 7 | a0001c0002t0001g0230a0001c0002t0001g0231a0001c0002t0001g0232others(4): Show | 7 | HG02258.hp1 HG02717.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.47+2719T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4956252 | ||||||
| chr7:4956362
|
G | C | 1 | a0001c0002t0001g0222 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.47+2609C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4956362 | ||||||
| chr7:4956425
|
TA | T | 28 | a0001c0001t0001g0149a0001c0001t0002g0011a0001c0001t0002g0098others(25): Show | 28 | HG01517.hp1 HG01884.hp2 HG01943.hp1 others(25): Show |
intron_variant | MODIFIER | c.47+2545delT | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4956425 | ||||||
| chr7:4956678
|
T | C | 1 | a0001c0001t0001g0198 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.47+2293A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4956678 | ||||||
| chr7:4956781
|
G | C | 1 | a0001c0001t0003g0096 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.47+2190C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4956781 | ||||||
| chr7:4956816
|
G | A | 1 | a0001c0007t0028g0332 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.47+2155C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4956816 | ||||||
| chr7:4956918
|
C | G | 1 | a0001c0001t0001g0248 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.47+2053G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4956918 | ||||||
| chr7:4957091
|
G | A | 1 | a0001c0001t0030g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.47+1880C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957091 | ||||||
| chr7:4957163
|
C | CAA | 8 | a0001c0001t0002g0098a0001c0002t0001g0230a0001c0002t0001g0231others(5): Show | 8 | HG02258.hp1 HG02717.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.47+1806_47+1807dup others(2): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957163 | ||||||
| chr7:4957163
|
CAA | C | 100 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0237others(97): Show | 102 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.47+1806_47+1807del others(2): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957163 | ||||||
| chr7:4957173
|
A | AT | 4 | a0001c0001t0003g0112a0001c0001t0003g0114a0001c0002t0002g0111others(1): Show | 4 | HG00280.hp2 HG01168.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.47+1797_47+1798ins others(1): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957173 | ||||||
| chr7:4957173
|
A | T | 16 | a0001c0001t0002g0251a0001c0001t0002g0252a0001c0001t0002g0253others(13): Show | 16 | HG00642.hp1 HG00735.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.47+1798T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957173 | ||||||
| chr7:4957173
|
AAT | A | 73 | a0001c0001t0001g0046a0001c0001t0001g0052a0001c0001t0001g0053others(70): Show | 73 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.47+1796_47+1797del others(2): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957173 | ||||||
| chr7:4957174
|
AT | A | 50 | a0001c0001t0001g0100a0001c0001t0001g0105a0001c0001t0001g0106others(47): Show | 50 | HG00735.hp2 HG00738.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.47+1796delA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957174 | ||||||
| chr7:4957175
|
T | A | 93 | a0001c0001t0001g0149a0001c0001t0001g0175a0001c0001t0001g0177others(90): Show | 93 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.47+1796A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957175 | ||||||
| chr7:4957177
|
T | A | 38 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0223others(35): Show | 38 | HG00738.hp2 HG01074.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.47+1794A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957177 | ||||||
| chr7:4957179
|
T | A | 1 | a0001c0002t0014g0342 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.47+1792A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957179 | ||||||
| chr7:4957310
|
A | C | 7 | a0001c0001t0001g0328a0001c0001t0003g0324a0001c0001t0003g0325others(4): Show | 7 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.47+1661T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957310 | ||||||
| chr7:4957375
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.47+1596C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957375 | ||||||
| chr7:4957469
|
A | G | 1 | a0001c0003t0004g0321 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.47+1502T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957469 | ||||||
| chr7:4957471
|
AC | A | 317 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0046others(314): Show | 319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.47+1499delG | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957471 | ||||||
| chr7:4957472
|
C | A | 1 | a0001c0003t0004g0321 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.47+1499G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957472 | ||||||
| chr7:4957499
|
A | G | 41 | a0001c0001t0001g0328a0001c0001t0002g0098a0001c0001t0003g0324others(38): Show | 41 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.47+1472T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957499 | ||||||
| chr7:4957526
|
G | A | 41 | a0001c0001t0001g0328a0001c0001t0002g0098a0001c0001t0003g0324others(38): Show | 41 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.47+1445C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957526 | ||||||
| chr7:4957542
|
G | C | 7 | a0001c0002t0001g0230a0001c0002t0001g0231a0001c0002t0001g0232others(4): Show | 7 | HG02258.hp1 HG02717.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.47+1429C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957542 | ||||||
| chr7:4957563
|
C | A | 1 | a0001c0004t0002g0293 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.47+1408G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957563 | ||||||
| chr7:4957633
|
G | C | 2 | a0001c0002t0006g0362a0001c0002t0006g0363 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.47+1338C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957633 | ||||||
| chr7:4957636
|
C | A | 1 | a0001c0001t0002g0294 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.47+1335G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957636 | ||||||
| chr7:4957651
|
G | GA | 97 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0046others(94): Show | 98 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.47+1319dupT | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957651 | ||||||
| chr7:4957682
|
A | C | 1 | a0001c0002t0008g0365 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.47+1289T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957682 | ||||||
| chr7:4957918
|
C | G | 22 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0105others(19): Show | 23 | HG01496.hp1 HG02145.hp1 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.47+1053G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957918 | ||||||
| chr7:4958173
|
T | C | 9 | a0001c0001t0013g0229a0001c0002t0001g0228a0001c0002t0001g0230others(6): Show | 9 | HG01884.hp2 HG02258.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.47+798A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4958173 | ||||||
| chr7:4958217
|
G | A | 32 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0239others(29): Show | 32 | HG00408.hp1 HG00609.hp1 HG02004.hp1 others(29): Show |
intron_variant | MODIFIER | c.47+754C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4958217 | ||||||
| chr7:4958261
|
C | T | 41 | a0001c0001t0001g0328a0001c0001t0002g0098a0001c0001t0003g0324others(38): Show | 41 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.47+710G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4958261 | ||||||
| chr7:4958395
|
G | C | 90 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249others(87): Show | 92 | HG00408.hp1 HG00597.hp1 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.47+576C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4958395 | ||||||
| chr7:4958512
|
C | T | 93 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0046others(90): Show | 94 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.47+459G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4958512 | ||||||
| chr7:4958515
|
C | T | 3 | a0001c0001t0001g0007a0001c0002t0001g0006a0001c0002t0001g0008 | 3 | HG02559.hp2 HG02970.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.47+456G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4958515 | ||||||
| chr7:4958601
|
G | A | 1 | a0001c0001t0030g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.47+370C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4958601 | ||||||
| chr7:4958693
|
CGCATAAC others(9): Show |
C | 1 | a0001c0001t0004g0323 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.47+262_47+277delAA others(14): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4958693 | ||||||
| chr7:4958809
|
C | A | 8 | a0001c0001t0001g0328a0001c0001t0003g0324a0001c0001t0003g0325others(5): Show | 8 | HG02486.hp1 HG02818.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.47+162G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4958809 | ||||||
| chr7:4958892
|
G | C | 3 | a0001c0001t0011g0333a0001c0001t0011g0334a0001c0007t0028g0332 | 3 | HG01891.hp1 HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.47+79C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4958892 | ||||||
| chr7:4958912
|
G | C | 1 | a0001c0002t0023g0005 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.47+59C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4958912 | ||||||
| chr7:4958915
|
C | CCCGCCGC others(40): Show |
1 | a0001c0002t0008g0365 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.47+9_47+55dupCGGCC others(42): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4958915 |