Search by Gene
| geneid | 22915 |
|---|---|
| ensemblid | ENSG00000138722.10 |
| hgncid | 7178 |
| symbol | MMRN1 |
| name | multimerin 1 |
| refseq_nuc | NM_007351.3 |
| refseq_prot | NP_031377.2 |
| ensembl_nuc | ENST00000264790.7 |
| ensembl_prot | ENSP00000264790.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 89894854 |
| end | 89954614 |
| strand | + |
| ver | v1.2 |
| region | chr4:89894854-89954614 |
| region5000 | chr4:89889854-89959614 |
| regionname0 | MMRN1_chr4_89894854_89954614 |
| regionname5000 | MMRN1_chr4_89889854_89959614 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa |
|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 1228 | 286 | 67 | 59 | 120 | 12 | 27 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0002 | 0/0 | 1228 | 45 | 0 | 1 | 41 | 0 | 3 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0003 | 0/0 | 1228 | 13 | 11 | 1 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0004 | 0/0 | 1228 | 5 | 2 | 3 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0005 | 0/0 | 1228 | 3 | 3 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0006 | 0/0 | 1228 | 3 | 3 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0007 | 0/1 | 1228 | 2 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0008 | 0/0 | 1228 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0009 | 0/0 | 1228 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0010 | 0/0 | 1228 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0011 | 0/0 | 1228 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0012 | 0/0 | 1228 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0013 | 0/0 | 1228 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0014 | 0/0 | 1228 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0015 | 0/0 | 1228 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0016 | 0/0 | 1228 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0017 | 0/0 | 1228 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0018 | 0/0 | 1228 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 3687 | 281 | 63 | 59 | 119 | 12 | 27 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| c0002 | 0/0 | 3687 | 42 | 0 | 1 | 38 | 0 | 3 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| c0003 | 0/0 | 3687 | 6 | 6 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| c0004 | 0/0 | 3687 | 4 | 1 | 3 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| c0005 | 0/0 | 3687 | 3 | 3 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| c0006 | 0/0 | 3687 | 3 | 3 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| c0007 | 0/0 | 3687 | 3 | 3 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| c0008 | 0/0 | 3687 | 2 | 2 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| c0009 | 0/0 | 3687 | 2 | 0 | 0 | 2 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| c0010 | 0/1 | 3687 | 2 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| c0011 | 0/0 | 3687 | 2 | 1 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| c0012 | 0/0 | 3687 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| c0013 | 0/0 | 3687 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| c0014 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| c0015 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| c0016 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| c0017 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| c0018 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| c0019 | 0/0 | 3687 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| c0020 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| c0021 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| c0022 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| c0023 | 0/0 | 3687 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| c0024 | 0/0 | 3687 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| c0025 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| c0026 | 0/0 | 3687 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| c0027 | 0/0 | 3687 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| c0028 | 0/0 | 3687 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| c0029 | 0/0 | 3687 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 1315 | 220 | 40 | 28 | 127 | 6 | 18 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| t0002 | 0/0 | 1315 | 52 | 13 | 12 | 19 | 2 | 6 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| t0003 | 1/0 | 1315 | 46 | 7 | 12 | 18 | 4 | 4 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| t0004 | 0/0 | 1315 | 36 | 26 | 5 | 3 | 0 | 2 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| t0005 | 0/0 | 1315 | 7 | 0 | 7 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| t0006 | 0/0 | 1315 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| t0007 | 0/0 | 1315 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| t0008 | 0/0 | 1315 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| t0009 | 0/0 | 1315 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| t0010 | 0/0 | 1315 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| t0011 | 0/0 | 1315 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| t0012 | 0/0 | 1315 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0002 | 0/0 | 7 | 0 | 5 | 0 | 1 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0005 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0007 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0009 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0011 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0015 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0026 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0033 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0239 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0286 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| achapid | ahapid | chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | a0001 | c0001 | 1/0 | 281 | 63 | 59 | 119 | 12 | 27 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0001c0005 | a0001 | c0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0001c0022 | a0001 | c0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0001c0023 | a0001 | c0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0002c0002 | a0002 | c0002 | 0/0 | 42 | 0 | 1 | 38 | 0 | 3 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0002c0009 | a0002 | c0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0002c0015 | a0002 | c0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0003c0003 | a0003 | c0003 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0003c0007 | a0003 | c0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0003c0011 | a0003 | c0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0003c0027 | a0003 | c0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0003c0029 | a0003 | c0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0004c0004 | a0004 | c0004 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0004c0012 | a0004 | c0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0005c0008 | a0005 | c0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0005c0024 | a0005 | c0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0006c0006 | a0006 | c0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0007c0010 | a0007 | c0010 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0008c0028 | a0008 | c0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0009c0013 | a0009 | c0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0010c0026 | a0010 | c0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0011c0025 | a0011 | c0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0012c0014 | a0012 | c0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0013c0021 | a0013 | c0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0014c0016 | a0014 | c0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0015c0017 | a0015 | c0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0016c0020 | a0016 | c0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0017c0019 | a0017 | c0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0018c0018 | a0018 | c0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| acthapid | ahapid | chapid | thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | actseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | a0001 | c0001 | t0001 | 0/0 | 151 | 25 | 24 | 82 | 6 | 14 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 51 | 13 | 12 | 18 | 2 | 6 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0001c0001t0003 | a0001 | c0001 | t0003 | 1/0 | 45 | 7 | 12 | 17 | 4 | 4 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 22 | 17 | 2 | 2 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0001c0001t0006 | a0001 | c0001 | t0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0001c0001t0008 | a0001 | c0001 | t0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0001c0001t0009 | a0001 | c0001 | t0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0001c0001t0010 | a0001 | c0001 | t0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0001c0001t0012 | a0001 | c0001 | t0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0001c0005t0001 | a0001 | c0005 | t0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0001c0022t0003 | a0001 | c0022 | t0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0001c0023t0004 | a0001 | c0023 | t0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0002c0002t0001 | a0002 | c0002 | t0001 | 0/0 | 39 | 0 | 1 | 36 | 0 | 2 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0002c0002t0002 | a0002 | c0002 | t0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0002c0002t0004 | a0002 | c0002 | t0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0002c0002t0007 | a0002 | c0002 | t0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0002c0009t0001 | a0002 | c0009 | t0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0002c0015t0001 | a0002 | c0015 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0003c0003t0001 | a0003 | c0003 | t0001 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0003c0007t0001 | a0003 | c0007 | t0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0003c0011t0001 | a0003 | c0011 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0003c0011t0004 | a0003 | c0011 | t0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0003c0027t0011 | a0003 | c0027 | t0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0003c0029t0001 | a0003 | c0029 | t0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0004c0004t0004 | a0004 | c0004 | t0004 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0004c0012t0004 | a0004 | c0012 | t0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0005c0008t0004 | a0005 | c0008 | t0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0005c0024t0004 | a0005 | c0024 | t0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0006c0006t0001 | a0006 | c0006 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0006c0006t0004 | a0006 | c0006 | t0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0007c0010t0001 | a0007 | c0010 | t0001 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0008c0028t0001 | a0008 | c0028 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0009c0013t0001 | a0009 | c0013 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0010c0026t0001 | a0010 | c0026 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0011c0025t0001 | a0011 | c0025 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0012c0014t0001 | a0012 | c0014 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0013c0021t0001 | a0013 | c0021 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0014c0016t0001 | a0014 | c0016 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0015c0017t0001 | a0015 | c0017 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0016c0020t0001 | a0016 | c0020 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0017c0019t0001 | a0017 | c0019 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| a0018c0018t0004 | a0018 | c0018 | t0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 | copy fasta |
| actghapid | ahapid | chapid | thapid | ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | a0001 | c0001 | t0001 | g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0002 | a0001 | c0001 | t0001 | g0002 | 0/0 | 7 | 0 | 5 | 0 | 1 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0005 | a0001 | c0001 | t0001 | g0005 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0006 | a0001 | c0001 | t0001 | g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0008 | a0001 | c0001 | t0001 | g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0009 | a0001 | c0001 | t0001 | g0009 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0012 | a0001 | c0001 | t0001 | g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0013 | a0001 | c0001 | t0001 | g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0014 | a0001 | c0001 | t0001 | g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0015 | a0001 | c0001 | t0001 | g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0016 | a0001 | c0001 | t0001 | g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0018 | a0001 | c0001 | t0001 | g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0019 | a0001 | c0001 | t0001 | g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0022 | a0001 | c0001 | t0001 | g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0037 | a0001 | c0001 | t0001 | g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0038 | a0001 | c0001 | t0001 | g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0039 | a0001 | c0001 | t0001 | g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0040 | a0001 | c0001 | t0001 | g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0043 | a0001 | c0001 | t0001 | g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0044 | a0001 | c0001 | t0001 | g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0046 | a0001 | c0001 | t0001 | g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0047 | a0001 | c0001 | t0001 | g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0048 | a0001 | c0001 | t0001 | g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0049 | a0001 | c0001 | t0001 | g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0050 | a0001 | c0001 | t0001 | g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0052 | a0001 | c0001 | t0001 | g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0053 | a0001 | c0001 | t0001 | g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0054 | a0001 | c0001 | t0001 | g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0055 | a0001 | c0001 | t0001 | g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0056 | a0001 | c0001 | t0001 | g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0057 | a0001 | c0001 | t0001 | g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0058 | a0001 | c0001 | t0001 | g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0059 | a0001 | c0001 | t0001 | g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0060 | a0001 | c0001 | t0001 | g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0061 | a0001 | c0001 | t0001 | g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0062 | a0001 | c0001 | t0001 | g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0063 | a0001 | c0001 | t0001 | g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0064 | a0001 | c0001 | t0001 | g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0065 | a0001 | c0001 | t0001 | g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0066 | a0001 | c0001 | t0001 | g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0067 | a0001 | c0001 | t0001 | g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0068 | a0001 | c0001 | t0001 | g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0069 | a0001 | c0001 | t0001 | g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0070 | a0001 | c0001 | t0001 | g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0071 | a0001 | c0001 | t0001 | g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0072 | a0001 | c0001 | t0001 | g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0075 | a0001 | c0001 | t0001 | g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0077 | a0001 | c0001 | t0001 | g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0079 | a0001 | c0001 | t0001 | g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0080 | a0001 | c0001 | t0001 | g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0081 | a0001 | c0001 | t0001 | g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0082 | a0001 | c0001 | t0001 | g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0084 | a0001 | c0001 | t0001 | g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0085 | a0001 | c0001 | t0001 | g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0087 | a0001 | c0001 | t0001 | g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0088 | a0001 | c0001 | t0001 | g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0090 | a0001 | c0001 | t0001 | g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0091 | a0001 | c0001 | t0001 | g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0092 | a0001 | c0001 | t0001 | g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0093 | a0001 | c0001 | t0001 | g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0094 | a0001 | c0001 | t0001 | g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0096 | a0001 | c0001 | t0001 | g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0097 | a0001 | c0001 | t0001 | g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0098 | a0001 | c0001 | t0001 | g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0099 | a0001 | c0001 | t0001 | g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0100 | a0001 | c0001 | t0001 | g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0101 | a0001 | c0001 | t0001 | g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0102 | a0001 | c0001 | t0001 | g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0103 | a0001 | c0001 | t0001 | g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0107 | a0001 | c0001 | t0001 | g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0108 | a0001 | c0001 | t0001 | g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0110 | a0001 | c0001 | t0001 | g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0111 | a0001 | c0001 | t0001 | g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0112 | a0001 | c0001 | t0001 | g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0113 | a0001 | c0001 | t0001 | g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0114 | a0001 | c0001 | t0001 | g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0115 | a0001 | c0001 | t0001 | g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0116 | a0001 | c0001 | t0001 | g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0117 | a0001 | c0001 | t0001 | g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0118 | a0001 | c0001 | t0001 | g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0119 | a0001 | c0001 | t0001 | g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0120 | a0001 | c0001 | t0001 | g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0121 | a0001 | c0001 | t0001 | g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0122 | a0001 | c0001 | t0001 | g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0123 | a0001 | c0001 | t0001 | g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0129 | a0001 | c0001 | t0001 | g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0130 | a0001 | c0001 | t0001 | g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0131 | a0001 | c0001 | t0001 | g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0132 | a0001 | c0001 | t0001 | g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0133 | a0001 | c0001 | t0001 | g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0134 | a0001 | c0001 | t0001 | g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0135 | a0001 | c0001 | t0001 | g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0136 | a0001 | c0001 | t0001 | g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0139 | a0001 | c0001 | t0001 | g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0140 | a0001 | c0001 | t0001 | g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0141 | a0001 | c0001 | t0001 | g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0142 | a0001 | c0001 | t0001 | g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0143 | a0001 | c0001 | t0001 | g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0144 | a0001 | c0001 | t0001 | g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0145 | a0001 | c0001 | t0001 | g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0146 | a0001 | c0001 | t0001 | g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0151 | a0001 | c0001 | t0001 | g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0156 | a0001 | c0001 | t0001 | g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0158 | a0001 | c0001 | t0001 | g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0159 | a0001 | c0001 | t0001 | g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0161 | a0001 | c0001 | t0001 | g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0162 | a0001 | c0001 | t0001 | g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0171 | a0001 | c0001 | t0001 | g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0191 | a0001 | c0001 | t0001 | g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0197 | a0001 | c0001 | t0001 | g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0200 | a0001 | c0001 | t0001 | g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0201 | a0001 | c0001 | t0001 | g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0207 | a0001 | c0001 | t0001 | g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0208 | a0001 | c0001 | t0001 | g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0209 | a0001 | c0001 | t0001 | g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0211 | a0001 | c0001 | t0001 | g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0213 | a0001 | c0001 | t0001 | g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0214 | a0001 | c0001 | t0001 | g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0215 | a0001 | c0001 | t0001 | g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0001g0217 | a0001 | c0001 | t0001 | g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0010 | a0001 | c0001 | t0002 | g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0011 | a0001 | c0001 | t0002 | g0011 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0025 | a0001 | c0001 | t0002 | g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0027 | a0001 | c0001 | t0002 | g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0028 | a0001 | c0001 | t0002 | g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0030 | a0001 | c0001 | t0002 | g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0032 | a0001 | c0001 | t0002 | g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0220 | a0001 | c0001 | t0002 | g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0221 | a0001 | c0001 | t0002 | g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0222 | a0001 | c0001 | t0002 | g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0223 | a0001 | c0001 | t0002 | g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0224 | a0001 | c0001 | t0002 | g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0227 | a0001 | c0001 | t0002 | g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0230 | a0001 | c0001 | t0002 | g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0231 | a0001 | c0001 | t0002 | g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0233 | a0001 | c0001 | t0002 | g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0237 | a0001 | c0001 | t0002 | g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0238 | a0001 | c0001 | t0002 | g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0241 | a0001 | c0001 | t0002 | g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0242 | a0001 | c0001 | t0002 | g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0243 | a0001 | c0001 | t0002 | g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0244 | a0001 | c0001 | t0002 | g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0245 | a0001 | c0001 | t0002 | g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0250 | a0001 | c0001 | t0002 | g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0251 | a0001 | c0001 | t0002 | g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0252 | a0001 | c0001 | t0002 | g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0253 | a0001 | c0001 | t0002 | g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0254 | a0001 | c0001 | t0002 | g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0256 | a0001 | c0001 | t0002 | g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0257 | a0001 | c0001 | t0002 | g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0258 | a0001 | c0001 | t0002 | g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0259 | a0001 | c0001 | t0002 | g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0266 | a0001 | c0001 | t0002 | g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0267 | a0001 | c0001 | t0002 | g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0268 | a0001 | c0001 | t0002 | g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0269 | a0001 | c0001 | t0002 | g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0270 | a0001 | c0001 | t0002 | g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0271 | a0001 | c0001 | t0002 | g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0272 | a0001 | c0001 | t0002 | g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0278 | a0001 | c0001 | t0002 | g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0279 | a0001 | c0001 | t0002 | g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0002g0300 | a0001 | c0001 | t0002 | g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0003g0003 | a0001 | c0001 | t0003 | g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0003g0023 | a0001 | c0001 | t0003 | g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0003g0024 | a0001 | c0001 | t0003 | g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0003g0026 | a0001 | c0001 | t0003 | g0026 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0003g0029 | a0001 | c0001 | t0003 | g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0003g0031 | a0001 | c0001 | t0003 | g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0003g0033 | a0001 | c0001 | t0003 | g0033 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0003g0034 | a0001 | c0001 | t0003 | g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0003g0225 | a0001 | c0001 | t0003 | g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0003g0226 | a0001 | c0001 | t0003 | g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0003g0229 | a0001 | c0001 | t0003 | g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0003g0235 | a0001 | c0001 | t0003 | g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0003g0236 | a0001 | c0001 | t0003 | g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0003g0239 | a0001 | c0001 | t0003 | g0239 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0003g0240 | a0001 | c0001 | t0003 | g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0003g0246 | a0001 | c0001 | t0003 | g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0003g0247 | a0001 | c0001 | t0003 | g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0003g0248 | a0001 | c0001 | t0003 | g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0003g0249 | a0001 | c0001 | t0003 | g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0003g0255 | a0001 | c0001 | t0003 | g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0003g0260 | a0001 | c0001 | t0003 | g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0003g0261 | a0001 | c0001 | t0003 | g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0003g0262 | a0001 | c0001 | t0003 | g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0003g0263 | a0001 | c0001 | t0003 | g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0003g0264 | a0001 | c0001 | t0003 | g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0003g0265 | a0001 | c0001 | t0003 | g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0003g0273 | a0001 | c0001 | t0003 | g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0003g0274 | a0001 | c0001 | t0003 | g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0003g0275 | a0001 | c0001 | t0003 | g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0003g0276 | a0001 | c0001 | t0003 | g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0003g0277 | a0001 | c0001 | t0003 | g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0003g0280 | a0001 | c0001 | t0003 | g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0003g0299 | a0001 | c0001 | t0003 | g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0004g0017 | a0001 | c0001 | t0004 | g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0004g0042 | a0001 | c0001 | t0004 | g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0004g0045 | a0001 | c0001 | t0004 | g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0004g0076 | a0001 | c0001 | t0004 | g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0004g0078 | a0001 | c0001 | t0004 | g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0004g0086 | a0001 | c0001 | t0004 | g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0004g0104 | a0001 | c0001 | t0004 | g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0004g0106 | a0001 | c0001 | t0004 | g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0004g0109 | a0001 | c0001 | t0004 | g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0004g0124 | a0001 | c0001 | t0004 | g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0004g0125 | a0001 | c0001 | t0004 | g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0004g0126 | a0001 | c0001 | t0004 | g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0004g0127 | a0001 | c0001 | t0004 | g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0004g0128 | a0001 | c0001 | t0004 | g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0004g0150 | a0001 | c0001 | t0004 | g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0004g0152 | a0001 | c0001 | t0004 | g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0004g0155 | a0001 | c0001 | t0004 | g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0004g0157 | a0001 | c0001 | t0004 | g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0004g0160 | a0001 | c0001 | t0004 | g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0004g0210 | a0001 | c0001 | t0004 | g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0004g0212 | a0001 | c0001 | t0004 | g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0005g0007 | a0001 | c0001 | t0005 | g0007 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0005g0228 | a0001 | c0001 | t0005 | g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0005g0232 | a0001 | c0001 | t0005 | g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0005g0234 | a0001 | c0001 | t0005 | g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0006g0095 | a0001 | c0001 | t0006 | g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0008g0298 | a0001 | c0001 | t0008 | g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0009g0297 | a0001 | c0001 | t0009 | g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0010g0089 | a0001 | c0001 | t0010 | g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0001t0012g0015 | a0001 | c0001 | t0012 | g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0005t0001g0203 | a0001 | c0005 | t0001 | g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0005t0001g0204 | a0001 | c0005 | t0001 | g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0005t0001g0205 | a0001 | c0005 | t0001 | g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0022t0003g0003 | a0001 | c0022 | t0003 | g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0001c0023t0004g0218 | a0001 | c0023 | t0004 | g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0002c0002t0001g0004 | a0002 | c0002 | t0001 | g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0002c0002t0001g0020 | a0002 | c0002 | t0001 | g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0002c0002t0001g0021 | a0002 | c0002 | t0001 | g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0002c0002t0001g0041 | a0002 | c0002 | t0001 | g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0002c0002t0001g0083 | a0002 | c0002 | t0001 | g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0002c0002t0001g0164 | a0002 | c0002 | t0001 | g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0002c0002t0001g0165 | a0002 | c0002 | t0001 | g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0002c0002t0001g0166 | a0002 | c0002 | t0001 | g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0002c0002t0001g0167 | a0002 | c0002 | t0001 | g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0002c0002t0001g0169 | a0002 | c0002 | t0001 | g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0002c0002t0001g0172 | a0002 | c0002 | t0001 | g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0002c0002t0001g0173 | a0002 | c0002 | t0001 | g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0002c0002t0001g0174 | a0002 | c0002 | t0001 | g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0002c0002t0001g0175 | a0002 | c0002 | t0001 | g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0002c0002t0001g0176 | a0002 | c0002 | t0001 | g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0002c0002t0001g0178 | a0002 | c0002 | t0001 | g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0002c0002t0001g0179 | a0002 | c0002 | t0001 | g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0002c0002t0001g0180 | a0002 | c0002 | t0001 | g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0002c0002t0001g0181 | a0002 | c0002 | t0001 | g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0002c0002t0001g0182 | a0002 | c0002 | t0001 | g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0002c0002t0001g0183 | a0002 | c0002 | t0001 | g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0002c0002t0001g0184 | a0002 | c0002 | t0001 | g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0002c0002t0001g0185 | a0002 | c0002 | t0001 | g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0002c0002t0001g0186 | a0002 | c0002 | t0001 | g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0002c0002t0001g0188 | a0002 | c0002 | t0001 | g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0002c0002t0001g0189 | a0002 | c0002 | t0001 | g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0002c0002t0001g0190 | a0002 | c0002 | t0001 | g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0002c0002t0001g0192 | a0002 | c0002 | t0001 | g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0002c0002t0001g0194 | a0002 | c0002 | t0001 | g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0002c0002t0001g0195 | a0002 | c0002 | t0001 | g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0002c0002t0001g0196 | a0002 | c0002 | t0001 | g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0002c0002t0001g0198 | a0002 | c0002 | t0001 | g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0002c0002t0001g0202 | a0002 | c0002 | t0001 | g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0002c0002t0001g0206 | a0002 | c0002 | t0001 | g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0002c0002t0002g0219 | a0002 | c0002 | t0002 | g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0002c0002t0004g0199 | a0002 | c0002 | t0004 | g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0002c0002t0007g0193 | a0002 | c0002 | t0007 | g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0002c0009t0001g0004 | a0002 | c0009 | t0001 | g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0002c0015t0001g0187 | a0002 | c0015 | t0001 | g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0003c0003t0001g0035 | a0003 | c0003 | t0001 | g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0003c0003t0001g0281 | a0003 | c0003 | t0001 | g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0003c0003t0001g0282 | a0003 | c0003 | t0001 | g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0003c0003t0001g0283 | a0003 | c0003 | t0001 | g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0003c0003t0001g0284 | a0003 | c0003 | t0001 | g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0003c0007t0001g0289 | a0003 | c0007 | t0001 | g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0003c0007t0001g0291 | a0003 | c0007 | t0001 | g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0003c0007t0001g0301 | a0003 | c0007 | t0001 | g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0003c0011t0001g0288 | a0003 | c0011 | t0001 | g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0003c0011t0004g0295 | a0003 | c0011 | t0004 | g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0003c0027t0011g0296 | a0003 | c0027 | t0011 | g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0003c0029t0001g0285 | a0003 | c0029 | t0001 | g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0004c0004t0004g0036 | a0004 | c0004 | t0004 | g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0004c0004t0004g0292 | a0004 | c0004 | t0004 | g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0004c0004t0004g0294 | a0004 | c0004 | t0004 | g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0004c0012t0004g0293 | a0004 | c0012 | t0004 | g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0005c0008t0004g0148 | a0005 | c0008 | t0004 | g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0005c0008t0004g0149 | a0005 | c0008 | t0004 | g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0005c0024t0004g0147 | a0005 | c0024 | t0004 | g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0006c0006t0001g0153 | a0006 | c0006 | t0001 | g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0006c0006t0004g0074 | a0006 | c0006 | t0004 | g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0006c0006t0004g0154 | a0006 | c0006 | t0004 | g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0007c0010t0001g0286 | a0007 | c0010 | t0001 | g0286 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0007c0010t0001g0287 | a0007 | c0010 | t0001 | g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0008c0028t0001g0290 | a0008 | c0028 | t0001 | g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0009c0013t0001g0216 | a0009 | c0013 | t0001 | g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0010c0026t0001g0073 | a0010 | c0026 | t0001 | g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0011c0025t0001g0138 | a0011 | c0025 | t0001 | g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0012c0014t0001g0168 | a0012 | c0014 | t0001 | g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0013c0021t0001g0170 | a0013 | c0021 | t0001 | g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0014c0016t0001g0177 | a0014 | c0016 | t0001 | g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0015c0017t0001g0163 | a0015 | c0017 | t0001 | g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0016c0020t0001g0137 | a0016 | c0020 | t0001 | g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0017c0019t0001g0105 | a0017 | c0019 | t0001 | g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| a0018c0018t0004g0051 | a0018 | c0018 | t0004 | g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMRN1_chr4_89889854_89959614 | MMRN1 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0230 | EUR | GBR | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0031 | EUR | GBR | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0133 | EUR | GBR | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG00408 | hp1 | a0002 | c0009 | t0001 | g0004 | EAS | CHS | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | CHS | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0189 | EAS | CHS | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG00423 | hp2 | a0002 | c0002 | t0007 | g0193 | EAS | CHS | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0176 | EAS | CHS | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0236 | EAS | CHS | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | CHS | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG00597 | hp2 | a0016 | c0020 | t0001 | g0137 | EAS | CHS | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | CHS | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG00621 | hp2 | a0002 | c0009 | t0001 | g0004 | EAS | CHS | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | CHS | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0256 | AMR | PUR | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0226 | AMR | PUR | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0273 | AMR | PUR | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | PUR | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0034 | AMR | PUR | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01099 | hp2 | a0003 | c0011 | t0001 | g0288 | AMR | PUR | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0212 | AMR | PUR | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01167 | hp1 | a0004 | c0004 | t0004 | g0292 | AMR | PUR | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0235 | AMR | PUR | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01169 | hp1 | a0004 | c0004 | t0004 | g0036 | AMR | PUR | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0023 | AMR | PUR | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01192 | hp2 | a0004 | c0004 | t0004 | g0036 | AMR | PUR | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01243 | hp1 | a0001 | c0001 | t0009 | g0297 | AMR | PUR | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01243 | hp2 | a0009 | c0013 | t0001 | g0216 | AMR | PUR | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0031 | AMR | CLM | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | CLM | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | CLM | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0228 | AMR | CLM | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0269 | AMR | CLM | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | CLM | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | CLM | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0086 | AMR | CLM | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0259 | AMR | CLM | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0275 | AMR | CLM | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01433 | hp1 | a0001 | c0001 | t0005 | g0007 | AMR | CLM | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | IBS | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0245 | EUR | IBS | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0111 | EUR | IBS | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0033 | EUR | IBS | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0033 | EUR | IBS | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0090 | EUR | IBS | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01884 | hp1 | a0004 | c0004 | t0004 | g0294 | AFR | ACB | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01884 | hp2 | a0001 | c0005 | t0001 | g0203 | AFR | ACB | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0268 | AFR | ACB | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01928 | hp2 | a0001 | c0001 | t0005 | g0234 | AMR | PEL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01934 | hp2 | a0001 | c0001 | t0006 | g0095 | AMR | PEL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01943 | hp2 | a0001 | c0001 | t0005 | g0007 | AMR | PEL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01978 | hp1 | a0001 | c0001 | t0005 | g0007 | AMR | PEL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0225 | AMR | PEL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0244 | AMR | PEL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0276 | AFR | ACB | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02055 | hp2 | a0003 | c0011 | t0004 | g0295 | AFR | ACB | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0173 | EAS | KHV | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02074 | hp2 | a0014 | c0016 | t0001 | g0177 | EAS | KHV | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | KHV | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | KHV | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0174 | EAS | KHV | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02135 | hp2 | a0001 | c0022 | t0003 | g0003 | EAS | KHV | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0278 | AFR | ACB | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0264 | AFR | ACB | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | CDX | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CDX | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CDX | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0167 | EAS | CDX | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0227 | AFR | ACB | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02273 | hp1 | a0001 | c0001 | t0005 | g0232 | AMR | PEL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02280 | hp2 | a0001 | c0001 | t0008 | g0298 | AFR | ACB | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02293 | hp2 | a0001 | c0001 | t0005 | g0007 | AMR | PEL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02300 | hp1 | a0010 | c0026 | t0001 | g0073 | AMR | PEL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0248 | AMR | PEL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0272 | AFR | ACB | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0206 | EAS | KHV | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02572 | hp1 | a0005 | c0024 | t0004 | g0147 | AFR | GWD | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02602 | hp1 | a0007 | c0010 | t0001 | g0287 | SAS | PJL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0270 | AFR | GWD | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0076 | AFR | GWD | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02630 | hp2 | a0001 | c0005 | t0001 | g0205 | AFR | GWD | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0106 | AFR | GWD | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02698 | hp1 | a0001 | c0001 | t0012 | g0015 | SAS | PJL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02717 | hp1 | a0003 | c0027 | t0011 | g0296 | AFR | GWD | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02717 | hp2 | a0001 | c0005 | t0001 | g0204 | AFR | GWD | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02723 | hp1 | a0003 | c0003 | t0001 | g0281 | AFR | GWD | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0023 | SAS | PJL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0125 | AFR | GWD | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0160 | AFR | GWD | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0104 | AFR | GWD | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02886 | hp1 | a0005 | c0008 | t0004 | g0149 | AFR | GWD | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02886 | hp2 | a0003 | c0003 | t0001 | g0282 | AFR | GWD | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0126 | AFR | GWD | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0152 | AFR | GWD | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02896 | hp2 | a0003 | c0003 | t0001 | g0035 | AFR | GWD | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02897 | hp1 | a0003 | c0003 | t0001 | g0035 | AFR | GWD | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0222 | AFR | ESN | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02965 | hp1 | a0006 | c0006 | t0004 | g0074 | AFR | ESN | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0109 | AFR | ESN | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02970 | hp2 | a0006 | c0006 | t0004 | g0154 | AFR | ESN | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0299 | SAS | PJL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03017 | hp2 | a0003 | c0029 | t0001 | g0285 | SAS | PJL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0157 | AFR | GWD | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0271 | AFR | MSL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03098 | hp2 | a0003 | c0007 | t0001 | g0289 | AFR | MSL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0300 | AFR | ESN | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0263 | AFR | ESN | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0221 | AFR | ESN | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03139 | hp2 | a0003 | c0007 | t0001 | g0301 | AFR | ESN | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | ESN | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0279 | AFR | MSL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0261 | AFR | MSL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0220 | AFR | MSL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0078 | AFR | MSL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0128 | AFR | MSL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0026 | SAS | PJL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03516 | hp1 | a0003 | c0003 | t0001 | g0283 | AFR | ESN | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03516 | hp2 | a0001 | c0023 | t0004 | g0218 | AFR | ESN | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0155 | AFR | GWD | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0127 | AFR | MSL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0223 | AFR | MSL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0083 | SAS | PJL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0241 | SAS | PJL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0172 | SAS | PJL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | BEB | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0257 | SAS | BEB | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0274 | SAS | STU | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG04115 | hp2 | a0002 | c0002 | t0004 | g0199 | SAS | STU | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG04228 | hp1 | a0001 | c0001 | t0004 | g0045 | SAS | STU | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG04228 | hp2 | a0001 | c0001 | t0010 | g0089 | SAS | STU | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | CHB | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | CHB | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHB | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0210 | EAS | CHB | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18906 | hp1 | a0005 | c0008 | t0004 | g0148 | AFR | YRI | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18906 | hp2 | a0004 | c0012 | t0004 | g0293 | AFR | YRI | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18948 | hp2 | a0012 | c0014 | t0001 | g0168 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18971 | hp1 | a0002 | c0015 | t0001 | g0187 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0175 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0265 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18995 | hp2 | a0013 | c0021 | t0001 | g0170 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19000 | hp2 | a0015 | c0017 | t0001 | g0163 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0181 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | LWK | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | LWK | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | LWK | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | LWK | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19058 | hp1 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19063 | hp2 | a0011 | c0025 | t0001 | g0138 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0165 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19072 | hp1 | a0018 | c0018 | t0004 | g0051 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0180 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19083 | hp2 | a0002 | c0002 | t0002 | g0219 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19086 | hp1 | a0002 | c0002 | t0001 | g0166 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19089 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | YRI | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0262 | AFR | YRI | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ASW | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA20129 | hp2 | a0008 | c0028 | t0001 | g0290 | AFR | ASW | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0088 | EUR | TSI | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0280 | EUR | TSI | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | GIH | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | GIH | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0198 | AMR | CLM | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02486 | hp1 | a0006 | c0006 | t0001 | g0153 | AFR | ACB | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02486 | hp2 | a0003 | c0007 | t0001 | g0291 | AFR | ACB | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02559 | hp1 | a0003 | c0003 | t0001 | g0284 | AFR | ACB | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0124 | AFR | ACB | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG06807 | hp1 | a0017 | c0019 | t0001 | g0105 | AFR | USA | MMRN1_chr4_89889854_89959614 | MMRN1 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0150 | AFR | USA | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0255 | AFR | LWK | MMRN1_chr4_89889854_89959614 | MMRN1 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0277 | AFR | LWK | MMRN1_chr4_89889854_89959614 | MMRN1 |
| homoSapiens_chm13v2 | hp1 | a0007 | c0010 | t0001 | g0286 | REF | REF | MMRN1_chr4_89889854_89959614 | MMRN1 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0239 | REF | REF | MMRN1_chr4_89889854_89959614 | MMRN1 |
| chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:89895101
|
G | A | 1 | a0004 | 5 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(2): Show |
missense_variant | MODERATE | c.130G>A | p.Val44Ile | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/8 | 248/5001 | 130/3687 | 44/1228 | chr4 | 89895101 | ||
| chr4:89895143
|
A | G | 4 | a0003a0004a0007others(1): Show | 21 | HG01099.hp2 HG01167.hp1 HG01169.hp1 others(18): Show |
missense_variant | MODERATE | c.172A>G | p.Thr58Ala | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/8 | 290/5001 | 172/3687 | 58/1228 | chr4 | 89895143 | ||
| chr4:89895147
|
G | A | 1 | a0009 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.176G>A | p.Arg59Gln | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/8 | 294/5001 | 176/3687 | 59/1228 | chr4 | 89895147 | ||
| chr4:89895174
|
C | T | 1 | a0010 | 1 | HG02300.hp1 | missense_variant | MODERATE | c.203C>T | p.Thr68Ile | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/8 | 321/5001 | 203/3687 | 68/1228 | chr4 | 89895174 | ||
| chr4:89909334
|
G | T | 1 | a0011 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.682G>T | p.Val228Phe | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/8 | 800/5001 | 682/3687 | 228/1228 | chr4 | 89909334 | ||
| chr4:89912033
|
C | T | 2 | a0004a0005 | 8 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(5): Show |
missense_variant | MODERATE | c.833C>T | p.Pro278Leu | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/8 | 951/5001 | 833/3687 | 278/1228 | chr4 | 89912033 | ||
| chr4:89934920
|
T | C | 1 | a0012 | 1 | NA18948.hp2 | missense_variant | MODERATE | c.1240T>C | p.Ser414Pro | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/8 | 1358/5001 | 1240/3687 | 414/1228 | chr4 | 89934920 | ||
| chr4:89935413
|
C | G | 1 | a0008 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.1733C>G | p.Thr578Ser | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/8 | 1851/5001 | 1733/3687 | 578/1228 | chr4 | 89935413 | ||
| chr4:89935824
|
G | A | 1 | a0006 | 3 | HG02486.hp1 HG02965.hp1 HG02970.hp2 |
missense_variant | MODERATE | c.2144G>A | p.Arg715Lys | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/8 | 2262/5001 | 2144/3687 | 715/1228 | chr4 | 89935824 | ||
| chr4:89936093
|
A | G | 1 | a0013 | 1 | NA18995.hp2 | missense_variant | MODERATE | c.2413A>G | p.Thr805Ala | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/8 | 2531/5001 | 2413/3687 | 805/1228 | chr4 | 89936093 | ||
| chr4:89936328
|
G | A | 7 | a0002a0007a0011others(4): Show | 52 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(49): Show |
missense_variant | MODERATE | c.2648G>A | p.Gly883Asp | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/8 | 2766/5001 | 2648/3687 | 883/1228 | chr4 | 89936328 | ||
| chr4:89936546
|
A | G | 1 | a0015 | 1 | NA19000.hp2 | missense_variant | MODERATE | c.2866A>G | p.Ile956Val | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/8 | 2984/5001 | 2866/3687 | 956/1228 | chr4 | 89936546 | ||
| chr4:89936571
|
C | G | 1 | a0016 | 1 | HG00597.hp2 | missense_variant | MODERATE | c.2891C>G | p.Thr964Arg | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/8 | 3009/5001 | 2891/3687 | 964/1228 | chr4 | 89936571 | ||
| chr4:89936634
|
G | A | 1 | a0018 | 1 | NA19072.hp1 | missense_variant | MODERATE | c.2954G>A | p.Cys985Tyr | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/8 | 3072/5001 | 2954/3687 | 985/1228 | chr4 | 89936634 | ||
| chr4:89953114
|
C | G | 1 | a0014 | 1 | HG02074.hp2 | missense_variant | MODERATE | c.3383C>G | p.Ala1128Gly | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 8/8 | 3501/5001 | 3383/3687 | 1128/1228 | chr4 | 89953114 | ||
| chr4:89953261
|
T | C | 1 | a0017 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.3530T>C | p.Ile1177Thr | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 8/8 | 3648/5001 | 3530/3687 | 1177/1228 | chr4 | 89953261 |
| chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:89895430
|
A | G | 2 | a0003c0003a0003c0029 | 7 | HG02559.hp1 HG02723.hp1 HG02886.hp2 others(4): Show |
synonymous_variant | LOW | c.459A>G | p.Ala153Ala | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/8 | 577/5001 | 459/3687 | 153/1228 | chr4 | 89895430 | ||
| chr4:89895490
|
C | T | 2 | a0003c0007a0008c0028 | 4 | HG02486.hp2 HG03098.hp2 HG03139.hp2 others(1): Show |
synonymous_variant | LOW | c.519C>T | p.Gly173Gly | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/8 | 637/5001 | 519/3687 | 173/1228 | chr4 | 89895490 | ||
| chr4:89909322
|
T | C | 2 | a0004c0004a0004c0012 | 5 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(2): Show |
synonymous_variant | LOW | c.670T>C | p.Leu224Leu | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/8 | 788/5001 | 670/3687 | 224/1228 | chr4 | 89909322 | ||
| chr4:89911980
|
A | G | 1 | a0002c0009 | 2 | HG00408.hp1 HG00621.hp2 |
synonymous_variant | LOW | c.780A>G | p.Gln260Gln | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/8 | 898/5001 | 780/3687 | 260/1228 | chr4 | 89911980 | ||
| chr4:89927892
|
T | C | 1 | a0005c0024 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.1053T>C | p.Asp351Asp | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/8 | 1171/5001 | 1053/3687 | 351/1228 | chr4 | 89927892 | ||
| chr4:89934812
|
C | T | 1 | a0001c0023 | 1 | HG03516.hp2 | splice_region_variant&synonymous_variant | LOW | c.1132C>T | p.Leu378Leu | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/8 | 1250/5001 | 1132/3687 | 378/1228 | chr4 | 89934812 | ||
| chr4:89934940
|
C | T | 1 | a0003c0029 | 1 | HG03017.hp2 | synonymous_variant | LOW | c.1260C>T | p.Leu420Leu | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/8 | 1378/5001 | 1260/3687 | 420/1228 | chr4 | 89934940 | ||
| chr4:89934997
|
C | T | 1 | a0001c0022 | 1 | HG02135.hp2 | synonymous_variant | LOW | c.1317C>T | p.Ala439Ala | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/8 | 1435/5001 | 1317/3687 | 439/1228 | chr4 | 89934997 | ||
| chr4:89935075
|
T | C | 1 | a0001c0005 | 3 | HG01884.hp2 HG02630.hp2 HG02717.hp2 |
synonymous_variant | LOW | c.1395T>C | p.Asn465Asn | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/8 | 1513/5001 | 1395/3687 | 465/1228 | chr4 | 89935075 | ||
| chr4:89935381
|
G | A | 1 | a0002c0015 | 1 | NA18971.hp1 | synonymous_variant | LOW | c.1701G>A | p.Leu567Leu | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/8 | 1819/5001 | 1701/3687 | 567/1228 | chr4 | 89935381 | ||
| chr4:89935978
|
C | T | 1 | a0003c0029 | 1 | HG03017.hp2 | synonymous_variant | LOW | c.2298C>T | p.Thr766Thr | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/8 | 2416/5001 | 2298/3687 | 766/1228 | chr4 | 89935978 | ||
| chr4:89936311
|
T | C | 1 | a0004c0012 | 1 | NA18906.hp2 | synonymous_variant | LOW | c.2631T>C | p.Tyr877Tyr | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/8 | 2749/5001 | 2631/3687 | 877/1228 | chr4 | 89936311 | ||
| chr4:89953160
|
A | G | 1 | a0003c0027 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.3429A>G | p.Gly1143Gly | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 8/8 | 3547/5001 | 3429/3687 | 1143/1228 | chr4 | 89953160 |
| chr:pos | ref | alt | # # of thapid:transcript level
|
thapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:89894872
|
A | G | 38 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(35): Show | 263 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(260): Show |
5_prime_UTR_variant | MODIFIER | c.-100A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/8 | 100 | chr4 | 89894872 | |||||
| chr4:89953488
|
C | T | 1 | a0001c0001t0012 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*70C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 8/8 | 70 | chr4 | 89953488 | |||||
| chr4:89953668
|
A | C | 1 | a0003c0027t0011 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*250A>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 8/8 | 250 | chr4 | 89953668 | |||||
| chr4:89953728
|
T | C | 28 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(25): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*310T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 8/8 | 310 | chr4 | 89953728 | |||||
| chr4:89953776
|
C | G | 2 | a0001c0001t0008a0001c0001t0009 | 2 | HG01243.hp1 HG02280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*358C>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 8/8 | 358 | chr4 | 89953776 | |||||
| chr4:89953798
|
A | T | 2 | a0001c0001t0008a0001c0001t0009 | 2 | HG01243.hp1 HG02280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*380A>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 8/8 | 380 | chr4 | 89953798 | |||||
| chr4:89953929
|
C | G | 1 | a0003c0027t0011 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*511C>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 8/8 | 511 | chr4 | 89953929 | |||||
| chr4:89953984
|
T | C | 1 | a0001c0001t0006 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*566T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 8/8 | 566 | chr4 | 89953984 | |||||
| chr4:89954350
|
C | A | 1 | a0001c0001t0008 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*932C>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 8/8 | 932 | chr4 | 89954350 | |||||
| chr4:89954356
|
C | T | 1 | a0003c0027t0011 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*938C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 8/8 | 938 | chr4 | 89954356 | |||||
| chr4:89954477
|
T | C | 1 | a0002c0002t0007 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1059T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 8/8 | 1059 | chr4 | 89954477 | |||||
| chr4:89954611
|
A | T | 2 | a0001c0001t0005a0001c0001t0010 | 8 | HG01261.hp1 HG01433.hp1 HG01928.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1193A>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 8/8 | 1193 | chr4 | 89954611 |
| chr:pos | ref | alt | # # of ghapid:genebody level
|
ghapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:89895637
|
G | T | 1 | a0003c0007t0001g0301 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.623+43G>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89895637 | ||||||
| chr4:89895639
|
T | A | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(120): Show | 151 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.623+45T>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89895639 | ||||||
| chr4:89895777
|
A | G | 1 | a0001c0001t0002g0300 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.623+183A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89895777 | ||||||
| chr4:89895935
|
T | G | 1 | a0001c0001t0001g0037 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.623+341T>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89895935 | ||||||
| chr4:89895968
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.623+374A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89895968 | ||||||
| chr4:89896012
|
T | C | 3 | a0005c0008t0004g0148a0005c0008t0004g0149a0005c0024t0004g0147 | 3 | HG02572.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.623+418T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89896012 | ||||||
| chr4:89896108
|
G | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(130): Show | 161 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.623+514G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89896108 | ||||||
| chr4:89896150
|
G | T | 1 | a0001c0001t0003g0299 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.623+556G>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89896150 | ||||||
| chr4:89896160
|
A | G | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(131): Show | 162 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(159): Show |
intron_variant | MODIFIER | c.623+566A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89896160 | ||||||
| chr4:89896243
|
C | T | 3 | a0001c0001t0001g0012a0001c0001t0008g0298a0001c0001t0009g0297 | 5 | HG01243.hp1 HG02280.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.623+649C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89896243 | ||||||
| chr4:89896697
|
A | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(153): Show | 186 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(183): Show |
intron_variant | MODIFIER | c.623+1103A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89896697 | ||||||
| chr4:89896830
|
T | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(52): Show | 71 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.623+1236T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89896830 | ||||||
| chr4:89896840
|
C | T | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(131): Show | 162 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(159): Show |
intron_variant | MODIFIER | c.623+1246C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89896840 | ||||||
| chr4:89896858
|
C | T | 1 | a0001c0001t0001g0084 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.623+1264C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89896858 | ||||||
| chr4:89897044
|
A | G | 1 | a0005c0008t0004g0149 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.623+1450A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89897044 | ||||||
| chr4:89897065
|
C | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(153): Show | 186 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(183): Show |
intron_variant | MODIFIER | c.623+1471C>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89897065 | ||||||
| chr4:89897214
|
A | AT | 8 | a0001c0001t0001g0038a0001c0001t0003g0280a0003c0003t0001g0035others(5): Show | 9 | HG01975.hp1 HG02559.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.623+1633dupT | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 89897214 | |||||
| chr4:89897214
|
A | ATT | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(146): Show | 178 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.623+1632_623+1633d others(4): Show |
MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 89897214 | |||||
| chr4:89897277
|
C | G | 13 | a0003c0007t0001g0289a0003c0007t0001g0291a0003c0007t0001g0301others(10): Show | 14 | HG01099.hp2 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.623+1683C>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89897277 | ||||||
| chr4:89897289
|
AT | A | 2 | a0003c0003t0001g0035a0003c0003t0001g0281 | 3 | HG02723.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.623+1696delT | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89897289 | ||||||
| chr4:89897292
|
T | C | 2 | a0003c0003t0001g0035a0003c0003t0001g0281 | 3 | HG02723.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.623+1698T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89897292 | ||||||
| chr4:89897311
|
C | T | 6 | a0003c0003t0001g0035a0003c0003t0001g0281a0003c0003t0001g0282others(3): Show | 7 | HG02559.hp1 HG02723.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.623+1717C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89897311 | ||||||
| chr4:89897363
|
T | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(134): Show | 165 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.623+1769T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89897363 | ||||||
| chr4:89897462
|
C | T | 2 | a0001c0001t0002g0278a0001c0001t0002g0279 | 2 | HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.623+1868C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89897462 | ||||||
| chr4:89897476
|
G | T | 13 | a0003c0007t0001g0289a0003c0007t0001g0291a0003c0007t0001g0301others(10): Show | 14 | HG01099.hp2 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.623+1882G>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89897476 | ||||||
| chr4:89897488
|
G | A | 13 | a0003c0007t0001g0289a0003c0007t0001g0291a0003c0007t0001g0301others(10): Show | 14 | HG01099.hp2 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.623+1894G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89897488 | ||||||
| chr4:89897706
|
T | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(52): Show | 71 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.623+2112T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89897706 | ||||||
| chr4:89897825
|
T | C | 1 | a0001c0001t0004g0150 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.623+2231T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89897825 | ||||||
| chr4:89897875
|
T | A | 1 | a0001c0001t0001g0161 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.623+2281T>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89897875 | ||||||
| chr4:89897875
|
T | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(134): Show | 165 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.623+2281T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89897875 | ||||||
| chr4:89897942
|
T | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(220): Show | 263 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.623+2348T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89897942 | ||||||
| chr4:89898003
|
T | C | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(153): Show | 186 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(183): Show |
intron_variant | MODIFIER | c.623+2409T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89898003 | ||||||
| chr4:89898044
|
C | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(134): Show | 165 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.623+2450C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89898044 | ||||||
| chr4:89898240
|
A | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(134): Show | 165 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.623+2646A>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89898240 | ||||||
| chr4:89898256
|
C | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(134): Show | 165 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.623+2662C>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89898256 | ||||||
| chr4:89898418
|
T | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(134): Show | 165 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.623+2824T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89898418 | ||||||
| chr4:89898523
|
A | G | 67 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0022others(64): Show | 77 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.623+2929A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89898523 | ||||||
| chr4:89898599
|
C | T | 5 | a0001c0001t0001g0161a0001c0001t0001g0215a0001c0001t0001g0217others(2): Show | 5 | HG01167.hp2 HG01243.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.623+3005C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89898599 | ||||||
| chr4:89898626
|
C | T | 4 | a0003c0003t0001g0282a0003c0003t0001g0283a0003c0003t0001g0284others(1): Show | 4 | HG02559.hp1 HG02886.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.623+3032C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89898626 | ||||||
| chr4:89898635
|
C | G | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(120): Show | 151 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.623+3041C>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89898635 | ||||||
| chr4:89898678
|
T | G | 14 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0158others(11): Show | 14 | HG01891.hp1 HG02257.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.623+3084T>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89898678 | ||||||
| chr4:89898810
|
T | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 260 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(257): Show |
intron_variant | MODIFIER | c.623+3216T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89898810 | ||||||
| chr4:89898838
|
C | G | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | NA18961.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.623+3244C>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89898838 | ||||||
| chr4:89898850
|
C | A | 1 | a0001c0001t0001g0039 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.623+3256C>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89898850 | ||||||
| chr4:89899013
|
G | T | 2 | a0003c0011t0004g0295a0003c0027t0011g0296 | 2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.623+3419G>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89899013 | ||||||
| chr4:89899095
|
C | A | 1 | a0001c0001t0001g0151 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.623+3501C>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89899095 | ||||||
| chr4:89899109
|
A | G | 4 | a0004c0004t0004g0036a0004c0004t0004g0292a0004c0004t0004g0294others(1): Show | 5 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.623+3515A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89899109 | ||||||
| chr4:89899127
|
C | A | 3 | a0005c0008t0004g0148a0005c0008t0004g0149a0005c0024t0004g0147 | 3 | HG02572.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.623+3533C>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89899127 | ||||||
| chr4:89899156
|
T | A | 3 | a0003c0011t0001g0288a0007c0010t0001g0286a0007c0010t0001g0287 | 3 | HG01099.hp2 HG02602.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.623+3562T>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89899156 | ||||||
| chr4:89899210
|
C | CT | 18 | a0001c0001t0001g0018a0001c0001t0001g0037a0001c0001t0001g0131others(15): Show | 19 | HG00140.hp2 HG00597.hp2 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.623+3627dupT | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 89899210 | |||||
| chr4:89899359
|
A | C | 1 | a0001c0001t0004g0160 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.623+3765A>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89899359 | ||||||
| chr4:89899483
|
G | T | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0145 | 3 | HG02698.hp2 HG03491.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.623+3889G>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89899483 | ||||||
| chr4:89899642
|
G | A | 79 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0022others(76): Show | 89 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.623+4048G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89899642 | ||||||
| chr4:89899657
|
C | T | 7 | a0001c0001t0003g0033a0001c0001t0003g0034a0001c0001t0003g0273others(4): Show | 9 | HG01081.hp1 HG01081.hp2 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.623+4063C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89899657 | ||||||
| chr4:89899658
|
C | T | 7 | a0001c0001t0003g0033a0001c0001t0003g0034a0001c0001t0003g0273others(4): Show | 9 | HG01081.hp1 HG01081.hp2 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.623+4064C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89899658 | ||||||
| chr4:89899683
|
A | G | 3 | a0005c0008t0004g0148a0005c0008t0004g0149a0005c0024t0004g0147 | 3 | HG02572.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.623+4089A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89899683 | ||||||
| chr4:89899742
|
G | T | 1 | a0001c0001t0004g0128 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.623+4148G>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89899742 | ||||||
| chr4:89899758
|
T | C | 3 | a0005c0008t0004g0148a0005c0008t0004g0149a0005c0024t0004g0147 | 3 | HG02572.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.623+4164T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89899758 | ||||||
| chr4:89899864
|
C | G | 3 | a0001c0001t0001g0040a0001c0001t0001g0215a0009c0013t0001g0216 | 3 | HG01243.hp2 HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.623+4270C>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89899864 | ||||||
| chr4:89899908
|
A | G | 1 | a0001c0001t0004g0150 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.623+4314A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89899908 | ||||||
| chr4:89899945
|
A | G | 3 | a0003c0003t0001g0283a0003c0003t0001g0284a0003c0029t0001g0285 | 3 | HG02559.hp1 HG03017.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.623+4351A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89899945 | ||||||
| chr4:89900182
|
C | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0162 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.623+4588C>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89900182 | ||||||
| chr4:89900191
|
G | A | 61 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0022others(58): Show | 71 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.623+4597G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89900191 | ||||||
| chr4:89900230
|
A | G | 93 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0022others(90): Show | 104 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.623+4636A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89900230 | ||||||
| chr4:89900292
|
T | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0043a0001c0001t0004g0042 | 5 | NA18747.hp1 NA18968.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.623+4698T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89900292 | ||||||
| chr4:89900301
|
C | G | 1 | a0001c0001t0002g0272 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.623+4707C>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89900301 | ||||||
| chr4:89900309
|
A | G | 3 | a0005c0008t0004g0148a0005c0008t0004g0149a0005c0024t0004g0147 | 3 | HG02572.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.623+4715A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89900309 | ||||||
| chr4:89900471
|
C | T | 3 | a0001c0001t0001g0037a0001c0001t0001g0082a0001c0001t0001g0142 | 3 | HG00621.hp1 NA19060.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.623+4877C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89900471 | ||||||
| chr4:89900505
|
C | T | 3 | a0005c0008t0004g0148a0005c0008t0004g0149a0005c0024t0004g0147 | 3 | HG02572.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.623+4911C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89900505 | ||||||
| chr4:89900548
|
T | C | 7 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0152others(4): Show | 7 | HG02486.hp1 HG02818.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.623+4954T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89900548 | ||||||
| chr4:89900732
|
T | C | 1 | a0001c0001t0001g0162 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.623+5138T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89900732 | ||||||
| chr4:89900836
|
T | G | 3 | a0005c0008t0004g0148a0005c0008t0004g0149a0005c0024t0004g0147 | 3 | HG02572.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.623+5242T>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89900836 | ||||||
| chr4:89900900
|
T | C | 93 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0022others(90): Show | 104 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.623+5306T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89900900 | ||||||
| chr4:89900907
|
T | A | 3 | a0005c0008t0004g0148a0005c0008t0004g0149a0005c0024t0004g0147 | 3 | HG02572.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.623+5313T>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89900907 | ||||||
| chr4:89901030
|
T | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0162 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.623+5436T>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89901030 | ||||||
| chr4:89901049
|
A | G | 1 | a0001c0001t0001g0043 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.623+5455A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89901049 | ||||||
| chr4:89901154
|
G | GA | 20 | a0001c0001t0001g0044a0001c0001t0001g0085a0001c0001t0001g0087others(17): Show | 21 | HG00741.hp2 HG01167.hp1 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.623+5578dupA | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 89901154 | |||||
| chr4:89901154
|
GA | G | 66 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0081others(63): Show | 77 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.623+5578delA | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 89901154 | |||||
| chr4:89901154
|
GAA | G | 9 | a0001c0001t0001g0022a0001c0001t0001g0207a0001c0001t0001g0208others(6): Show | 11 | HG02055.hp2 HG02083.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.623+5577_623+5578d others(4): Show |
MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 89901154 | |||||
| chr4:89901370
|
AATT | A | 3 | a0005c0008t0004g0148a0005c0008t0004g0149a0005c0024t0004g0147 | 3 | HG02572.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.623+5783_623+5785d others(5): Show |
MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 89901370 | |||||
| chr4:89901377
|
A | G | 3 | a0005c0008t0004g0148a0005c0008t0004g0149a0005c0024t0004g0147 | 3 | HG02572.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.623+5783A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89901377 | ||||||
| chr4:89901464
|
G | A | 3 | a0005c0008t0004g0148a0005c0008t0004g0149a0005c0024t0004g0147 | 3 | HG02572.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.623+5870G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89901464 | ||||||
| chr4:89901489
|
G | T | 3 | a0003c0011t0001g0288a0007c0010t0001g0286a0007c0010t0001g0287 | 3 | HG01099.hp2 HG02602.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.623+5895G>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89901489 | ||||||
| chr4:89901522
|
A | G | 3 | a0005c0008t0004g0148a0005c0008t0004g0149a0005c0024t0004g0147 | 3 | HG02572.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.623+5928A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89901522 | ||||||
| chr4:89901650
|
A | G | 7 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0152others(4): Show | 7 | HG02486.hp1 HG02818.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.623+6056A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89901650 | ||||||
| chr4:89901848
|
T | C | 3 | a0005c0008t0004g0148a0005c0008t0004g0149a0005c0024t0004g0147 | 3 | HG02572.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.623+6254T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89901848 | ||||||
| chr4:89901866
|
G | A | 17 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0158others(14): Show | 17 | HG01109.hp1 HG01891.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.623+6272G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89901866 | ||||||
| chr4:89901919
|
G | T | 10 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0079others(7): Show | 10 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.623+6325G>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89901919 | ||||||
| chr4:89901952
|
C | T | 3 | a0005c0008t0004g0148a0005c0008t0004g0149a0005c0024t0004g0147 | 3 | HG02572.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.623+6358C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89901952 | ||||||
| chr4:89901961
|
G | A | 3 | a0005c0008t0004g0148a0005c0008t0004g0149a0005c0024t0004g0147 | 3 | HG02572.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.623+6367G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89901961 | ||||||
| chr4:89901986
|
C | T | 3 | a0005c0008t0004g0148a0005c0008t0004g0149a0005c0024t0004g0147 | 3 | HG02572.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.623+6392C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89901986 | ||||||
| chr4:89902029
|
C | A | 1 | a0001c0001t0001g0131 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.623+6435C>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89902029 | ||||||
| chr4:89902055
|
C | T | 3 | a0005c0008t0004g0148a0005c0008t0004g0149a0005c0024t0004g0147 | 3 | HG02572.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.623+6461C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89902055 | ||||||
| chr4:89902060
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0162 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.623+6466G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89902060 | ||||||
| chr4:89902121
|
A | AATAAAAC | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(228): Show | 272 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(269): Show |
intron_variant | MODIFIER | c.623+6528_623+6529i others(9): Show |
MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 89902121 | |||||
| chr4:89902124
|
G | A | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(228): Show | 272 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(269): Show |
intron_variant | MODIFIER | c.623+6530G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89902124 | ||||||
| chr4:89902125
|
A | T | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(228): Show | 272 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(269): Show |
intron_variant | MODIFIER | c.623+6531A>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89902125 | ||||||
| chr4:89902126
|
G | T | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(228): Show | 272 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(269): Show |
intron_variant | MODIFIER | c.623+6532G>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89902126 | ||||||
| chr4:89902176
|
T | C | 1 | a0001c0001t0005g0228 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.623+6582T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89902176 | ||||||
| chr4:89902177
|
G | A | 2 | a0001c0001t0001g0043a0001c0001t0004g0042 | 2 | NA18986.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.623+6583G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89902177 | ||||||
| chr4:89902182
|
A | T | 2 | a0001c0001t0002g0270a0001c0001t0002g0271 | 2 | HG02615.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.623+6588A>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89902182 | ||||||
| chr4:89902326
|
TA | T | 20 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0158others(17): Show | 20 | HG01109.hp1 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.623+6740delA | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 89902326 | |||||
| chr4:89902335
|
T | A | 1 | a0003c0007t0001g0289 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.623+6741T>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89902335 | ||||||
| chr4:89902357
|
GA | G | 70 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0022others(67): Show | 80 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.623+6771delA | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 89902357 | |||||
| chr4:89902418
|
T | A | 52 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0171others(49): Show | 60 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.623+6824T>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89902418 | ||||||
| chr4:89902560
|
C | T | 1 | a0002c0002t0001g0202 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.624-6716C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89902560 | ||||||
| chr4:89902582
|
A | G | 1 | a0003c0029t0001g0285 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.624-6694A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89902582 | ||||||
| chr4:89902718
|
A | C | 1 | a0001c0001t0004g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.624-6558A>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89902718 | ||||||
| chr4:89902899
|
T | G | 9 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0152others(6): Show | 9 | HG02055.hp2 HG02486.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.624-6377T>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89902899 | ||||||
| chr4:89902927
|
A | G | 3 | a0003c0011t0001g0288a0007c0010t0001g0286a0007c0010t0001g0287 | 3 | HG01099.hp2 HG02602.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.624-6349A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89902927 | ||||||
| chr4:89903199
|
A | G | 1 | a0001c0001t0003g0265 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.624-6077A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89903199 | ||||||
| chr4:89903251
|
T | C | 1 | a0015c0017t0001g0163 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.624-6025T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89903251 | ||||||
| chr4:89903279
|
C | T | 93 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0022others(90): Show | 104 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.624-5997C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89903279 | ||||||
| chr4:89903424
|
T | C | 43 | a0001c0001t0001g0019a0001c0001t0001g0171a0001c0001t0001g0191others(40): Show | 50 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.624-5852T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89903424 | ||||||
| chr4:89903667
|
T | C | 2 | a0001c0001t0001g0085a0001c0001t0001g0162 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.624-5609T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89903667 | ||||||
| chr4:89903730
|
A | G | 61 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0022others(58): Show | 71 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.624-5546A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89903730 | ||||||
| chr4:89903787
|
C | T | 1 | a0001c0001t0002g0300 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.624-5489C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89903787 | ||||||
| chr4:89903790
|
C | T | 1 | a0008c0028t0001g0290 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.624-5486C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89903790 | ||||||
| chr4:89903839
|
T | C | 1 | a0003c0003t0001g0283 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.624-5437T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89903839 | ||||||
| chr4:89903851
|
A | G | 93 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0022others(90): Show | 104 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.624-5425A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89903851 | ||||||
| chr4:89903897
|
G | GA | 125 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(122): Show | 148 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.624-5363dupA | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 89903897 | |||||
| chr4:89903897
|
G | GAA | 61 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0016others(58): Show | 73 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.624-5364_624-5363d others(4): Show |
MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 89903897 | |||||
| chr4:89903916
|
C | A | 3 | a0003c0003t0001g0283a0003c0003t0001g0284a0003c0029t0001g0285 | 3 | HG02559.hp1 HG03017.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.624-5360C>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89903916 | ||||||
| chr4:89903983
|
C | A | 3 | a0001c0005t0001g0203a0001c0005t0001g0204a0001c0005t0001g0205 | 3 | HG01884.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.624-5293C>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89903983 | ||||||
| chr4:89904008
|
A | T | 1 | a0001c0001t0001g0140 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.624-5268A>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89904008 | ||||||
| chr4:89904074
|
G | A | 61 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0022others(58): Show | 71 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.624-5202G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89904074 | ||||||
| chr4:89904312
|
G | A | 5 | a0001c0001t0002g0233a0001c0001t0005g0007a0001c0001t0005g0228others(2): Show | 8 | HG01261.hp1 HG01346.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.624-4964G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89904312 | ||||||
| chr4:89904347
|
T | G | 2 | a0002c0002t0001g0164a0002c0002t0001g0178 | 2 | NA18943.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.624-4929T>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89904347 | ||||||
| chr4:89904389
|
C | A | 1 | a0001c0001t0004g0150 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.624-4887C>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89904389 | ||||||
| chr4:89904439
|
C | T | 1 | a0014c0016t0001g0177 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.624-4837C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89904439 | ||||||
| chr4:89904471
|
AC | A | 58 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0022others(55): Show | 68 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.624-4803delC | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 89904471 | |||||
| chr4:89904611
|
A | G | 1 | a0003c0003t0001g0282 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.624-4665A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89904611 | ||||||
| chr4:89904648
|
G | T | 2 | a0001c0001t0004g0109a0001c0001t0004g0128 | 2 | HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.624-4628G>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89904648 | ||||||
| chr4:89904672
|
C | G | 58 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0022others(55): Show | 68 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.624-4604C>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89904672 | ||||||
| chr4:89904747
|
C | T | 1 | a0001c0001t0002g0231 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.624-4529C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89904747 | ||||||
| chr4:89904781
|
A | G | 2 | a0001c0001t0008g0298a0001c0001t0009g0297 | 2 | HG01243.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.624-4495A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89904781 | ||||||
| chr4:89904965
|
T | G | 3 | a0001c0001t0001g0012a0001c0001t0008g0298a0001c0001t0009g0297 | 5 | HG01243.hp1 HG02280.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.624-4311T>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89904965 | ||||||
| chr4:89904968
|
T | C | 9 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0152others(6): Show | 9 | HG02055.hp2 HG02486.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.624-4308T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89904968 | ||||||
| chr4:89905017
|
G | C | 1 | a0001c0001t0004g0086 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.624-4259G>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89905017 | ||||||
| chr4:89905126
|
A | G | 4 | a0001c0001t0003g0261a0001c0001t0003g0262a0001c0001t0003g0263others(1): Show | 4 | HG02145.hp2 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.624-4150A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89905126 | ||||||
| chr4:89905181
|
A | G | 17 | a0001c0001t0001g0009a0001c0001t0001g0068a0001c0001t0001g0069others(14): Show | 19 | HG01109.hp2 HG01433.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.624-4095A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89905181 | ||||||
| chr4:89905245
|
T | C | 1 | a0001c0001t0001g0197 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.624-4031T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89905245 | ||||||
| chr4:89905269
|
T | A | 7 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0152others(4): Show | 7 | HG02486.hp1 HG02818.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.624-4007T>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89905269 | ||||||
| chr4:89905353
|
A | C | 3 | a0003c0003t0001g0283a0003c0003t0001g0284a0003c0029t0001g0285 | 3 | HG02559.hp1 HG03017.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.624-3923A>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89905353 | ||||||
| chr4:89905530
|
C | G | 2 | a0002c0002t0001g0195a0002c0002t0001g0196 | 2 | NA18962.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.624-3746C>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89905530 | ||||||
| chr4:89905585
|
G | T | 1 | a0001c0001t0002g0011 | 3 | HG00639.hp2 HG02738.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.624-3691G>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89905585 | ||||||
| chr4:89905609
|
A | G | 78 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0022others(75): Show | 88 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.624-3667A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89905609 | ||||||
| chr4:89905840
|
C | G | 2 | a0001c0001t0001g0085a0001c0001t0001g0162 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.624-3436C>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89905840 | ||||||
| chr4:89905941
|
A | G | 3 | a0001c0001t0001g0151a0001c0001t0001g0158a0001c0001t0001g0159 | 3 | HG01891.hp1 HG02257.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.624-3335A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89905941 | ||||||
| chr4:89905971
|
T | C | 3 | a0003c0003t0001g0283a0003c0003t0001g0284a0003c0029t0001g0285 | 3 | HG02559.hp1 HG03017.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.624-3305T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89905971 | ||||||
| chr4:89906269
|
A | T | 3 | a0005c0008t0004g0148a0005c0008t0004g0149a0005c0024t0004g0147 | 3 | HG02572.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.624-3007A>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89906269 | ||||||
| chr4:89906315
|
A | C | 64 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0022others(61): Show | 74 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.624-2961A>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89906315 | ||||||
| chr4:89906932
|
C | T | 3 | a0003c0003t0001g0283a0003c0003t0001g0284a0003c0029t0001g0285 | 3 | HG02559.hp1 HG03017.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.624-2344C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89906932 | ||||||
| chr4:89906956
|
T | C | 3 | a0003c0003t0001g0283a0003c0003t0001g0284a0003c0029t0001g0285 | 3 | HG02559.hp1 HG03017.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.624-2320T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89906956 | ||||||
| chr4:89907078
|
A | T | 1 | a0001c0001t0002g0269 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.624-2198A>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89907078 | ||||||
| chr4:89907109
|
T | C | 3 | a0004c0004t0004g0036a0004c0004t0004g0292a0004c0004t0004g0294 | 4 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.624-2167T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89907109 | ||||||
| chr4:89907117
|
G | T | 3 | a0005c0008t0004g0148a0005c0008t0004g0149a0005c0024t0004g0147 | 3 | HG02572.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.624-2159G>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89907117 | ||||||
| chr4:89907146
|
A | G | 2 | a0001c0001t0001g0085a0001c0001t0001g0162 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.624-2130A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89907146 | ||||||
| chr4:89907246
|
G | A | 3 | a0005c0008t0004g0148a0005c0008t0004g0149a0005c0024t0004g0147 | 3 | HG02572.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.624-2030G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89907246 | ||||||
| chr4:89907376
|
G | A | 3 | a0003c0011t0001g0288a0007c0010t0001g0286a0007c0010t0001g0287 | 3 | HG01099.hp2 HG02602.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.624-1900G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89907376 | ||||||
| chr4:89907546
|
T | C | 3 | a0005c0008t0004g0148a0005c0008t0004g0149a0005c0024t0004g0147 | 3 | HG02572.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.624-1730T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89907546 | ||||||
| chr4:89907550
|
C | T | 4 | a0004c0004t0004g0036a0004c0004t0004g0292a0004c0004t0004g0294others(1): Show | 5 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.624-1726C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89907550 | ||||||
| chr4:89907740
|
A | G | 3 | a0003c0011t0001g0288a0007c0010t0001g0286a0007c0010t0001g0287 | 3 | HG01099.hp2 HG02602.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.624-1536A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89907740 | ||||||
| chr4:89907817
|
G | T | 3 | a0003c0003t0001g0283a0003c0003t0001g0284a0003c0029t0001g0285 | 3 | HG02559.hp1 HG03017.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.624-1459G>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89907817 | ||||||
| chr4:89907829
|
G | GT | 144 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(141): Show | 171 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.624-1435dupT | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 89907829 | |||||
| chr4:89907830
|
T | G | 1 | a0003c0007t0001g0289 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.624-1446T>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89907830 | ||||||
| chr4:89907834
|
T | TG | 3 | a0003c0011t0001g0288a0007c0010t0001g0286a0007c0010t0001g0287 | 3 | HG01099.hp2 HG02602.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.624-1442_624-1441i others(3): Show |
MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89907834 | ||||||
| chr4:89907845
|
T | C | 2 | a0001c0001t0001g0085a0001c0001t0001g0162 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.624-1431T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89907845 | ||||||
| chr4:89908005
|
C | A | 2 | a0001c0001t0003g0024a0001c0001t0003g0235 | 3 | HG01074.hp1 HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.624-1271C>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89908005 | ||||||
| chr4:89908454
|
G | A | 52 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0171others(49): Show | 60 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.624-822G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89908454 | ||||||
| chr4:89908466
|
G | A | 58 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0022others(55): Show | 68 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.624-810G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89908466 | ||||||
| chr4:89908467
|
A | C | 58 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0022others(55): Show | 68 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.624-809A>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89908467 | ||||||
| chr4:89908534
|
A | G | 3 | a0005c0008t0004g0148a0005c0008t0004g0149a0005c0024t0004g0147 | 3 | HG02572.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.624-742A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89908534 | ||||||
| chr4:89908598
|
T | C | 2 | a0002c0002t0001g0195a0002c0002t0001g0196 | 2 | NA18962.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.624-678T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89908598 | ||||||
| chr4:89908820
|
A | G | 2 | a0001c0001t0001g0022a0001c0001t0001g0208 | 3 | HG02622.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.624-456A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89908820 | ||||||
| chr4:89908886
|
T | A | 3 | a0005c0008t0004g0148a0005c0008t0004g0149a0005c0024t0004g0147 | 3 | HG02572.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.624-390T>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89908886 | ||||||
| chr4:89908907
|
C | A | 3 | a0001c0001t0001g0049a0001c0001t0001g0050a0018c0018t0004g0051 | 3 | NA18990.hp1 NA18995.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.624-369C>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89908907 | ||||||
| chr4:89909086
|
C | T | 6 | a0001c0001t0004g0017a0001c0001t0004g0104a0001c0001t0004g0106others(3): Show | 7 | HG02559.hp2 HG02647.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.624-190C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89909086 | ||||||
| chr4:89909089
|
T | C | 58 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0022others(55): Show | 68 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.624-187T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89909089 | ||||||
| chr4:89909092
|
G | A | 1 | a0001c0001t0003g0229 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.624-184G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89909092 | ||||||
| chr4:89909136
|
T | C | 1 | a0001c0001t0004g0104 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.624-140T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89909136 | ||||||
| chr4:89909156
|
C | A | 5 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0222others(2): Show | 5 | HG02922.hp1 HG03139.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.624-120C>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 1/7 | chr4 | 89909156 | ||||||
| chr4:89909402
|
A | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0162 | 2 | HG02109.hp1 HG02451.hp2 |
splice_region_variant&intron_variant | LOW | c.743+7A>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/7 | chr4 | 89909402 | ||||||
| chr4:89909452
|
G | T | 3 | a0003c0011t0001g0288a0007c0010t0001g0286a0007c0010t0001g0287 | 3 | HG01099.hp2 HG02602.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.743+57G>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/7 | chr4 | 89909452 | ||||||
| chr4:89909454
|
G | A | 1 | a0001c0001t0002g0270 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.743+59G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/7 | chr4 | 89909454 | ||||||
| chr4:89909472
|
A | G | 3 | a0003c0003t0001g0283a0003c0003t0001g0284a0003c0029t0001g0285 | 3 | HG02559.hp1 HG03017.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.743+77A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/7 | chr4 | 89909472 | ||||||
| chr4:89909482
|
C | T | 2 | a0002c0002t0001g0175a0002c0002t0001g0176 | 2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.743+87C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/7 | chr4 | 89909482 | ||||||
| chr4:89909608
|
T | G | 2 | a0001c0001t0001g0088a0001c0001t0001g0146 | 2 | HG03942.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.743+213T>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/7 | chr4 | 89909608 | ||||||
| chr4:89909632
|
A | G | 69 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0022others(66): Show | 79 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.743+237A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/7 | chr4 | 89909632 | ||||||
| chr4:89909660
|
C | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0162 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.743+265C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/7 | chr4 | 89909660 | ||||||
| chr4:89909698
|
A | G | 2 | a0002c0002t0001g0164a0002c0002t0001g0178 | 2 | NA18943.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.743+303A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/7 | chr4 | 89909698 | ||||||
| chr4:89909720
|
C | CT | 61 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0022others(58): Show | 71 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.743+327dupT | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 89909720 | |||||
| chr4:89909893
|
T | C | 1 | a0002c0002t0001g0180 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.743+498T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/7 | chr4 | 89909893 | ||||||
| chr4:89910171
|
C | T | 3 | a0001c0001t0001g0161a0001c0001t0001g0217a0001c0023t0004g0218 | 3 | HG01167.hp2 HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.743+776C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/7 | chr4 | 89910171 | ||||||
| chr4:89910335
|
A | C | 65 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0022others(62): Show | 76 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.743+940A>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/7 | chr4 | 89910335 | ||||||
| chr4:89910449
|
C | A | 1 | a0001c0001t0003g0273 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.743+1054C>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/7 | chr4 | 89910449 | ||||||
| chr4:89910480
|
T | C | 1 | a0001c0001t0010g0089 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.743+1085T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/7 | chr4 | 89910480 | ||||||
| chr4:89910499
|
G | A | 2 | a0001c0001t0001g0018a0001c0001t0003g0274 | 3 | HG04115.hp1 NA18961.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.743+1104G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/7 | chr4 | 89910499 | ||||||
| chr4:89910567
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0162 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.743+1172G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/7 | chr4 | 89910567 | ||||||
| chr4:89910654
|
T | C | 58 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0022others(55): Show | 68 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.743+1259T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/7 | chr4 | 89910654 | ||||||
| chr4:89910666
|
A | G | 2 | a0001c0001t0001g0044a0001c0001t0001g0067 | 2 | HG03239.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.743+1271A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/7 | chr4 | 89910666 | ||||||
| chr4:89910780
|
T | G | 1 | a0001c0001t0003g0236 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.744-1164T>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/7 | chr4 | 89910780 | ||||||
| chr4:89910850
|
T | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 260 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(257): Show |
intron_variant | MODIFIER | c.744-1094T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/7 | chr4 | 89910850 | ||||||
| chr4:89910872
|
T | G | 2 | a0003c0011t0004g0295a0003c0027t0011g0296 | 2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.744-1072T>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/7 | chr4 | 89910872 | ||||||
| chr4:89910893
|
C | G | 82 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0022others(79): Show | 93 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.744-1051C>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/7 | chr4 | 89910893 | ||||||
| chr4:89910931
|
T | C | 58 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0022others(55): Show | 68 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.744-1013T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/7 | chr4 | 89910931 | ||||||
| chr4:89910944
|
C | T | 1 | a0002c0002t0001g0194 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.744-1000C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/7 | chr4 | 89910944 | ||||||
| chr4:89911068
|
G | A | 1 | a0001c0001t0002g0237 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.744-876G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/7 | chr4 | 89911068 | ||||||
| chr4:89911076
|
G | A | 1 | a0001c0001t0002g0238 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.744-868G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/7 | chr4 | 89911076 | ||||||
| chr4:89911153
|
G | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0162 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.744-791G>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/7 | chr4 | 89911153 | ||||||
| chr4:89911314
|
G | C | 58 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0022others(55): Show | 68 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.744-630G>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/7 | chr4 | 89911314 | ||||||
| chr4:89911425
|
C | A | 6 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0158others(3): Show | 6 | HG01891.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.744-519C>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/7 | chr4 | 89911425 | ||||||
| chr4:89911457
|
C | A | 68 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0022others(65): Show | 79 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.744-487C>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/7 | chr4 | 89911457 | ||||||
| chr4:89911550
|
G | A | 4 | a0004c0004t0004g0036a0004c0004t0004g0292a0004c0004t0004g0294others(1): Show | 5 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.744-394G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/7 | chr4 | 89911550 | ||||||
| chr4:89911551
|
A | G | 1 | a0001c0001t0004g0212 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.744-393A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/7 | chr4 | 89911551 | ||||||
| chr4:89911710
|
G | C | 1 | a0001c0005t0001g0203 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.744-234G>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/7 | chr4 | 89911710 | ||||||
| chr4:89911862
|
A | G | 7 | a0001c0001t0001g0006a0001c0001t0001g0100a0001c0001t0001g0101others(4): Show | 10 | NA18943.hp1 NA18946.hp2 NA18953.hp1 others(7): Show |
intron_variant | MODIFIER | c.744-82A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/7 | chr4 | 89911862 | ||||||
| chr4:89911885
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0162 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.744-59G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/7 | chr4 | 89911885 | ||||||
| chr4:89911893
|
A | C | 1 | a0001c0001t0004g0150 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.744-51A>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/7 | chr4 | 89911893 | ||||||
| chr4:89911915
|
G | A | 3 | a0001c0005t0001g0203a0001c0005t0001g0204a0001c0005t0001g0205 | 3 | HG01884.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.744-29G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/7 | chr4 | 89911915 | ||||||
| chr4:89911915
|
G | T | 1 | a0001c0001t0002g0032 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.744-29G>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 2/7 | chr4 | 89911915 | ||||||
| chr4:89912058
|
C | T | 1 | a0002c0002t0001g0083 | 1 | HG03654.hp1 | splice_region_variant&intron_variant | LOW | c.850+8C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89912058 | ||||||
| chr4:89912127
|
C | T | 1 | a0001c0001t0003g0260 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.850+77C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89912127 | ||||||
| chr4:89912155
|
G | A | 3 | a0003c0011t0001g0288a0007c0010t0001g0286a0007c0010t0001g0287 | 3 | HG01099.hp2 HG02602.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.850+105G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89912155 | ||||||
| chr4:89912186
|
G | A | 1 | a0002c0002t0001g0166 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.850+136G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89912186 | ||||||
| chr4:89912221
|
A | G | 222 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(219): Show | 261 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(258): Show |
intron_variant | MODIFIER | c.850+171A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89912221 | ||||||
| chr4:89912270
|
A | G | 56 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0016others(53): Show | 68 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.850+220A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89912270 | ||||||
| chr4:89912305
|
T | C | 1 | a0003c0003t0001g0282 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.850+255T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89912305 | ||||||
| chr4:89912338
|
C | G | 3 | a0005c0008t0004g0148a0005c0008t0004g0149a0005c0024t0004g0147 | 3 | HG02572.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.850+288C>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89912338 | ||||||
| chr4:89912377
|
A | G | 2 | a0001c0001t0001g0085a0001c0001t0001g0162 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.850+327A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89912377 | ||||||
| chr4:89912496
|
G | A | 7 | a0004c0004t0004g0036a0004c0004t0004g0292a0004c0004t0004g0294others(4): Show | 8 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.850+446G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89912496 | ||||||
| chr4:89912885
|
A | T | 1 | a0001c0001t0005g0228 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.850+835A>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89912885 | ||||||
| chr4:89913107
|
A | G | 3 | a0003c0003t0001g0283a0003c0003t0001g0284a0003c0029t0001g0285 | 3 | HG02559.hp1 HG03017.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.850+1057A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89913107 | ||||||
| chr4:89913209
|
A | G | 1 | a0001c0001t0003g0274 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.850+1159A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89913209 | ||||||
| chr4:89913340
|
T | C | 1 | a0001c0001t0004g0212 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.850+1290T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89913340 | ||||||
| chr4:89913446
|
G | A | 1 | a0001c0001t0001g0113 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.850+1396G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89913446 | ||||||
| chr4:89913649
|
G | A | 7 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0152others(4): Show | 7 | HG02486.hp1 HG02818.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.850+1599G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89913649 | ||||||
| chr4:89913745
|
A | C | 3 | a0001c0001t0004g0160a0006c0006t0001g0153a0006c0006t0004g0154 | 3 | HG02486.hp1 HG02818.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.850+1695A>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89913745 | ||||||
| chr4:89913771
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.850+1721A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89913771 | ||||||
| chr4:89913778
|
G | A | 1 | a0001c0001t0004g0150 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.850+1728G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89913778 | ||||||
| chr4:89913855
|
C | T | 1 | a0002c0002t0007g0193 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.850+1805C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89913855 | ||||||
| chr4:89913995
|
A | C | 1 | a0001c0001t0002g0300 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.850+1945A>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89913995 | ||||||
| chr4:89914035
|
A | G | 2 | a0001c0001t0001g0201a0001c0001t0001g0207 | 2 | HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.850+1985A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89914035 | ||||||
| chr4:89914075
|
T | C | 3 | a0003c0011t0001g0288a0007c0010t0001g0286a0007c0010t0001g0287 | 3 | HG01099.hp2 HG02602.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.850+2025T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89914075 | ||||||
| chr4:89914101
|
A | G | 1 | a0001c0001t0004g0128 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.850+2051A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89914101 | ||||||
| chr4:89914245
|
C | T | 1 | a0001c0005t0001g0203 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.850+2195C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89914245 | ||||||
| chr4:89914251
|
C | G | 1 | a0003c0011t0001g0288 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.850+2201C>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89914251 | ||||||
| chr4:89914403
|
C | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0162 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.850+2353C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89914403 | ||||||
| chr4:89914407
|
C | T | 2 | a0001c0001t0002g0010a0001c0001t0003g0031 | 5 | HG00140.hp1 HG01192.hp1 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+2357C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89914407 | ||||||
| chr4:89914550
|
T | C | 222 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(219): Show | 261 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(258): Show |
intron_variant | MODIFIER | c.850+2500T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89914550 | ||||||
| chr4:89914751
|
T | C | 4 | a0004c0004t0004g0036a0004c0004t0004g0292a0004c0004t0004g0294others(1): Show | 5 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+2701T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89914751 | ||||||
| chr4:89914999
|
C | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0162 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.850+2949C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89914999 | ||||||
| chr4:89915368
|
A | C | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(128): Show | 159 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.850+3318A>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89915368 | ||||||
| chr4:89915422
|
T | C | 4 | a0004c0004t0004g0036a0004c0004t0004g0292a0004c0004t0004g0294others(1): Show | 5 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+3372T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89915422 | ||||||
| chr4:89915473
|
G | T | 1 | a0018c0018t0004g0051 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.850+3423G>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89915473 | ||||||
| chr4:89915511
|
T | G | 1 | a0001c0001t0003g0299 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.850+3461T>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89915511 | ||||||
| chr4:89915551
|
AG | A | 3 | a0005c0008t0004g0148a0005c0008t0004g0149a0005c0024t0004g0147 | 3 | HG02572.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.850+3503delG | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 89915551 | |||||
| chr4:89915612
|
A | G | 2 | a0001c0001t0001g0156a0001c0001t0004g0157 | 2 | HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.850+3562A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89915612 | ||||||
| chr4:89915772
|
C | T | 4 | a0004c0004t0004g0036a0004c0004t0004g0292a0004c0004t0004g0294others(1): Show | 5 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+3722C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89915772 | ||||||
| chr4:89915855
|
G | A | 1 | a0001c0001t0004g0212 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.850+3805G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89915855 | ||||||
| chr4:89915951
|
C | G | 2 | a0001c0001t0001g0085a0001c0001t0001g0162 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.850+3901C>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89915951 | ||||||
| chr4:89915954
|
A | G | 3 | a0003c0011t0001g0288a0007c0010t0001g0286a0007c0010t0001g0287 | 3 | HG01099.hp2 HG02602.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.850+3904A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89915954 | ||||||
| chr4:89915976
|
A | G | 76 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0040others(73): Show | 84 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.850+3926A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89915976 | ||||||
| chr4:89916038
|
A | T | 1 | a0001c0001t0002g0258 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.850+3988A>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89916038 | ||||||
| chr4:89916152
|
ACTC | A | 55 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0040others(52): Show | 63 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.850+4104_850+4106d others(5): Show |
MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 89916152 | |||||
| chr4:89916187
|
A | G | 1 | a0009c0013t0001g0216 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.850+4137A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89916187 | ||||||
| chr4:89916255
|
G | A | 3 | a0003c0003t0001g0283a0003c0003t0001g0284a0003c0029t0001g0285 | 3 | HG02559.hp1 HG03017.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.850+4205G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89916255 | ||||||
| chr4:89916261
|
C | T | 1 | a0004c0012t0004g0293 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.850+4211C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89916261 | ||||||
| chr4:89916364
|
GA | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.850+4326delA | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 89916364 | |||||
| chr4:89916373
|
A | C | 8 | a0001c0001t0001g0088a0001c0001t0001g0099a0001c0001t0001g0146others(5): Show | 8 | HG01358.hp2 HG02486.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.850+4323A>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89916373 | ||||||
| chr4:89916373
|
AAAAC | A | 9 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0152others(6): Show | 9 | HG02486.hp1 HG02559.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.850+4338_850+4341d others(6): Show |
MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 89916373 | |||||
| chr4:89916376
|
AC | A | 50 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0040others(47): Show | 58 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.850+4327delC | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89916376 | ||||||
| chr4:89916377
|
C | A | 9 | a0002c0002t0001g0083a0002c0002t0001g0181a0002c0002t0001g0182others(6): Show | 10 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.850+4327C>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89916377 | ||||||
| chr4:89916381
|
C | A | 76 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0040others(73): Show | 85 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.850+4331C>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89916381 | ||||||
| chr4:89916385
|
C | A | 4 | a0004c0004t0004g0036a0004c0004t0004g0292a0004c0004t0004g0294others(1): Show | 5 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+4335C>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89916385 | ||||||
| chr4:89916490
|
G | T | 78 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0040others(75): Show | 87 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.850+4440G>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89916490 | ||||||
| chr4:89916551
|
T | C | 1 | a0001c0001t0001g0214 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.850+4501T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89916551 | ||||||
| chr4:89916722
|
CCTT | C | 3 | a0004c0004t0004g0036a0004c0004t0004g0292a0004c0004t0004g0294 | 4 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.850+4678_850+4680d others(5): Show |
MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 89916722 | |||||
| chr4:89916740
|
T | G | 1 | a0002c0002t0001g0195 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.850+4690T>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89916740 | ||||||
| chr4:89916793
|
C | T | 74 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0040others(71): Show | 83 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.850+4743C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89916793 | ||||||
| chr4:89916808
|
A | C | 8 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0152others(5): Show | 8 | HG02486.hp1 HG02818.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.850+4758A>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89916808 | ||||||
| chr4:89916829
|
A | G | 78 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0040others(75): Show | 87 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.850+4779A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89916829 | ||||||
| chr4:89916846
|
A | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0162 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.850+4796A>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89916846 | ||||||
| chr4:89916957
|
T | C | 1 | a0005c0008t0004g0149 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.850+4907T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89916957 | ||||||
| chr4:89916985
|
T | A | 1 | a0001c0001t0001g0053 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.850+4935T>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89916985 | ||||||
| chr4:89917006
|
C | T | 3 | a0005c0008t0004g0148a0005c0008t0004g0149a0005c0024t0004g0147 | 3 | HG02572.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.850+4956C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89917006 | ||||||
| chr4:89917007
|
G | A | 78 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0040others(75): Show | 87 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.850+4957G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89917007 | ||||||
| chr4:89917050
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.850+5000A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89917050 | ||||||
| chr4:89917090
|
CGTGTGTG others(7): Show |
C | 1 | a0001c0001t0004g0212 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.850+5051_850+5064d others(16): Show |
MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 89917090 | |||||
| chr4:89917108
|
T | G | 1 | a0002c0002t0001g0167 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.850+5058T>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89917108 | ||||||
| chr4:89917362
|
T | G | 1 | a0001c0001t0004g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.850+5312T>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89917362 | ||||||
| chr4:89917475
|
A | G | 1 | a0002c0002t0001g0183 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.850+5425A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89917475 | ||||||
| chr4:89917492
|
C | T | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(123): Show | 154 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.850+5442C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89917492 | ||||||
| chr4:89917544
|
C | A | 3 | a0001c0005t0001g0203a0001c0005t0001g0204a0001c0005t0001g0205 | 3 | HG01884.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.850+5494C>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89917544 | ||||||
| chr4:89917546
|
A | G | 3 | a0005c0008t0004g0148a0005c0008t0004g0149a0005c0024t0004g0147 | 3 | HG02572.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.850+5496A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89917546 | ||||||
| chr4:89917640
|
G | C | 1 | a0001c0001t0002g0227 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.851-5528G>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89917640 | ||||||
| chr4:89917703
|
T | C | 4 | a0002c0002t0001g0083a0003c0011t0001g0288a0007c0010t0001g0286others(1): Show | 4 | HG01099.hp2 HG02602.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.851-5465T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89917703 | ||||||
| chr4:89917707
|
G | C | 55 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0040others(52): Show | 63 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.851-5461G>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89917707 | ||||||
| chr4:89917762
|
A | G | 3 | a0005c0008t0004g0148a0005c0008t0004g0149a0005c0024t0004g0147 | 3 | HG02572.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.851-5406A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89917762 | ||||||
| chr4:89917796
|
C | T | 1 | a0001c0001t0001g0103 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.851-5372C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89917796 | ||||||
| chr4:89917871
|
T | C | 78 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0040others(75): Show | 87 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.851-5297T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89917871 | ||||||
| chr4:89917916
|
A | G | 1 | a0001c0005t0001g0203 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.851-5252A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89917916 | ||||||
| chr4:89917984
|
C | T | 11 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0152others(8): Show | 11 | HG02486.hp1 HG02559.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.851-5184C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89917984 | ||||||
| chr4:89918098
|
C | T | 78 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0040others(75): Show | 87 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.851-5070C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89918098 | ||||||
| chr4:89918207
|
T | A | 2 | a0001c0001t0002g0266a0001c0001t0002g0267 | 2 | HG00408.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.851-4961T>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89918207 | ||||||
| chr4:89918357
|
T | A | 1 | a0001c0001t0005g0232 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.851-4811T>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89918357 | ||||||
| chr4:89918358
|
A | T | 1 | a0001c0001t0001g0201 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.851-4810A>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89918358 | ||||||
| chr4:89918543
|
C | T | 4 | a0001c0001t0003g0261a0001c0001t0003g0262a0001c0001t0003g0263others(1): Show | 4 | HG02145.hp2 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.851-4625C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89918543 | ||||||
| chr4:89918563
|
G | A | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG01168.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.851-4605G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89918563 | ||||||
| chr4:89918732
|
C | T | 1 | a0003c0029t0001g0285 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.851-4436C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89918732 | ||||||
| chr4:89918766
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.851-4402T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89918766 | ||||||
| chr4:89918974
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.851-4194T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89918974 | ||||||
| chr4:89919095
|
C | T | 72 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0040others(69): Show | 81 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.851-4073C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89919095 | ||||||
| chr4:89919099
|
A | T | 1 | a0001c0001t0003g0277 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.851-4069A>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89919099 | ||||||
| chr4:89919528
|
A | C | 1 | a0004c0012t0004g0293 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.851-3640A>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89919528 | ||||||
| chr4:89919550
|
G | A | 1 | a0001c0001t0004g0155 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.851-3618G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89919550 | ||||||
| chr4:89919677
|
G | T | 1 | a0002c0002t0001g0194 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.851-3491G>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89919677 | ||||||
| chr4:89920013
|
A | T | 1 | a0001c0001t0002g0256 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.851-3155A>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89920013 | ||||||
| chr4:89920036
|
T | A | 1 | a0001c0001t0004g0104 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.851-3132T>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89920036 | ||||||
| chr4:89920120
|
T | A | 3 | a0005c0008t0004g0148a0005c0008t0004g0149a0005c0024t0004g0147 | 3 | HG02572.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.851-3048T>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89920120 | ||||||
| chr4:89920203
|
T | C | 1 | a0002c0002t0001g0167 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.851-2965T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89920203 | ||||||
| chr4:89920229
|
C | A | 3 | a0001c0001t0001g0012a0001c0001t0008g0298a0001c0001t0009g0297 | 5 | HG01243.hp1 HG02280.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.851-2939C>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89920229 | ||||||
| chr4:89920280
|
T | G | 1 | a0001c0001t0002g0231 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.851-2888T>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89920280 | ||||||
| chr4:89920413
|
A | C | 1 | a0003c0011t0001g0288 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.851-2755A>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89920413 | ||||||
| chr4:89920501
|
A | G | 1 | a0001c0001t0001g0037 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.851-2667A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89920501 | ||||||
| chr4:89920636
|
G | A | 78 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0040others(75): Show | 87 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.851-2532G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89920636 | ||||||
| chr4:89920787
|
G | C | 1 | a0001c0001t0001g0162 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.851-2381G>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89920787 | ||||||
| chr4:89920816
|
G | T | 3 | a0002c0002t0001g0083a0007c0010t0001g0286a0007c0010t0001g0287 | 3 | HG02602.hp1 HG03654.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.851-2352G>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89920816 | ||||||
| chr4:89920828
|
T | G | 9 | a0001c0001t0001g0012a0001c0001t0001g0151a0001c0001t0001g0156others(6): Show | 11 | HG01243.hp1 HG01891.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.851-2340T>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89920828 | ||||||
| chr4:89920846
|
C | T | 1 | a0001c0001t0002g0272 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.851-2322C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89920846 | ||||||
| chr4:89921159
|
CT | C | 76 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0040others(73): Show | 85 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.851-2000delT | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 89921159 | |||||
| chr4:89921262
|
A | G | 5 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0066others(2): Show | 5 | HG02056.hp1 NA18990.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.851-1906A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89921262 | ||||||
| chr4:89921563
|
TAGA | T | 3 | a0001c0001t0004g0017a0001c0001t0004g0106a0001c0001t0004g0125 | 4 | HG02647.hp2 HG02809.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.851-1598_851-1596d others(5): Show |
MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 89921563 | |||||
| chr4:89921664
|
T | C | 1 | a0001c0001t0001g0082 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.851-1504T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89921664 | ||||||
| chr4:89921689
|
A | G | 78 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0040others(75): Show | 87 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.851-1479A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89921689 | ||||||
| chr4:89921763
|
C | T | 2 | a0001c0001t0001g0044a0001c0001t0001g0067 | 2 | HG03239.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.851-1405C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89921763 | ||||||
| chr4:89921811
|
A | G | 1 | a0002c0002t0001g0174 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.851-1357A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89921811 | ||||||
| chr4:89921820
|
A | C | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(123): Show | 154 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.851-1348A>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89921820 | ||||||
| chr4:89921869
|
A | G | 1 | a0002c0002t0002g0219 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.851-1299A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89921869 | ||||||
| chr4:89921944
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.851-1224C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89921944 | ||||||
| chr4:89922010
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.851-1158T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89922010 | ||||||
| chr4:89922068
|
A | G | 4 | a0002c0002t0001g0083a0003c0011t0001g0288a0007c0010t0001g0286others(1): Show | 4 | HG01099.hp2 HG02602.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.851-1100A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89922068 | ||||||
| chr4:89922098
|
TATTG | T | 11 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(8): Show | 11 | HG00408.hp2 HG01109.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.851-1045_851-1042d others(6): Show |
MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 89922098 | |||||
| chr4:89922167
|
C | T | 1 | a0001c0001t0002g0272 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.851-1001C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89922167 | ||||||
| chr4:89922266
|
C | T | 1 | a0002c0002t0002g0219 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.851-902C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89922266 | ||||||
| chr4:89922297
|
G | T | 72 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0040others(69): Show | 81 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.851-871G>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89922297 | ||||||
| chr4:89922358
|
A | G | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(214): Show | 256 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.851-810A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89922358 | ||||||
| chr4:89922396
|
G | A | 1 | a0001c0001t0002g0238 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.851-772G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89922396 | ||||||
| chr4:89922499
|
T | A | 76 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0040others(73): Show | 85 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.851-669T>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89922499 | ||||||
| chr4:89922592
|
A | C | 8 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0152others(5): Show | 8 | HG02486.hp1 HG02818.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.851-576A>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89922592 | ||||||
| chr4:89922722
|
T | C | 1 | a0002c0002t0001g0184 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.851-446T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89922722 | ||||||
| chr4:89922946
|
AT | A | 17 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0152others(14): Show | 17 | HG01099.hp2 HG02055.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.851-213delT | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 89922946 | |||||
| chr4:89922998
|
G | T | 1 | a0001c0001t0004g0150 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.851-170G>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89922998 | ||||||
| chr4:89923011
|
A | G | 2 | a0001c0001t0001g0085a0001c0001t0001g0162 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.851-157A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89923011 | ||||||
| chr4:89923132
|
C | T | 2 | a0001c0001t0001g0052a0001c0001t0001g0065 | 2 | HG02074.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.851-36C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 3/7 | chr4 | 89923132 | ||||||
| chr4:89923370
|
A | T | 1 | a0001c0001t0006g0095 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.955+98A>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89923370 | ||||||
| chr4:89923432
|
G | T | 1 | a0001c0001t0002g0300 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.955+160G>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89923432 | ||||||
| chr4:89923550
|
A | C | 1 | a0001c0001t0001g0102 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.955+278A>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89923550 | ||||||
| chr4:89923583
|
T | C | 23 | a0001c0001t0001g0085a0001c0001t0001g0162a0001c0001t0004g0126others(20): Show | 24 | HG01099.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.955+311T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89923583 | ||||||
| chr4:89923685
|
G | C | 3 | a0005c0008t0004g0148a0005c0008t0004g0149a0005c0024t0004g0147 | 3 | HG02572.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.955+413G>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89923685 | ||||||
| chr4:89923697
|
A | G | 55 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0040others(52): Show | 63 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.955+425A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89923697 | ||||||
| chr4:89923813
|
T | C | 303 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(300): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.955+541T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89923813 | ||||||
| chr4:89923870
|
A | G | 11 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0038others(8): Show | 16 | HG01106.hp1 HG01255.hp1 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.955+598A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89923870 | ||||||
| chr4:89924161
|
A | G | 1 | a0001c0001t0001g0112 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.955+889A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89924161 | ||||||
| chr4:89924167
|
A | C | 2 | a0001c0001t0001g0085a0001c0001t0001g0162 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.955+895A>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89924167 | ||||||
| chr4:89924184
|
A | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0162 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.955+912A>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89924184 | ||||||
| chr4:89924193
|
G | A | 2 | a0001c0001t0004g0126a0001c0001t0004g0127 | 2 | HG02895.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.955+921G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89924193 | ||||||
| chr4:89924265
|
C | T | 1 | a0001c0001t0004g0150 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.955+993C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89924265 | ||||||
| chr4:89924298
|
CTT | C | 19 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0152others(16): Show | 20 | HG01099.hp2 HG01167.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.955+1028_955+1029d others(4): Show |
MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 89924298 | |||||
| chr4:89924398
|
G | C | 55 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0040others(52): Show | 63 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.955+1126G>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89924398 | ||||||
| chr4:89924423
|
C | T | 19 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0152others(16): Show | 20 | HG01099.hp2 HG01167.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.955+1151C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89924423 | ||||||
| chr4:89924489
|
A | G | 20 | a0001c0001t0001g0009a0001c0001t0001g0068a0001c0001t0001g0069others(17): Show | 22 | HG01109.hp2 HG01433.hp2 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.955+1217A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89924489 | ||||||
| chr4:89924549
|
T | A | 8 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0152others(5): Show | 8 | HG02486.hp1 HG02818.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.955+1277T>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89924549 | ||||||
| chr4:89924580
|
T | C | 78 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0040others(75): Show | 87 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.955+1308T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89924580 | ||||||
| chr4:89924597
|
C | G | 1 | a0001c0001t0004g0150 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.955+1325C>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89924597 | ||||||
| chr4:89924610
|
C | T | 19 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0152others(16): Show | 20 | HG01099.hp2 HG01167.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.955+1338C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89924610 | ||||||
| chr4:89924640
|
C | T | 4 | a0004c0004t0004g0036a0004c0004t0004g0292a0004c0004t0004g0294others(1): Show | 5 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.955+1368C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89924640 | ||||||
| chr4:89924704
|
C | T | 1 | a0001c0001t0003g0255 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.955+1432C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89924704 | ||||||
| chr4:89924829
|
C | T | 1 | a0001c0001t0004g0128 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.955+1557C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89924829 | ||||||
| chr4:89924915
|
G | A | 4 | a0002c0002t0001g0083a0003c0011t0001g0288a0007c0010t0001g0286others(1): Show | 4 | HG01099.hp2 HG02602.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.955+1643G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89924915 | ||||||
| chr4:89924960
|
A | G | 1 | a0004c0012t0004g0293 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.955+1688A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89924960 | ||||||
| chr4:89924964
|
T | C | 3 | a0001c0001t0001g0151a0001c0001t0001g0158a0001c0001t0001g0159 | 3 | HG01891.hp1 HG02257.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.955+1692T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89924964 | ||||||
| chr4:89925014
|
C | A | 1 | a0002c0002t0001g0185 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.955+1742C>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89925014 | ||||||
| chr4:89925015
|
A | C | 1 | a0002c0002t0001g0185 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.955+1743A>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89925015 | ||||||
| chr4:89925165
|
A | G | 1 | a0001c0023t0004g0218 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.955+1893A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89925165 | ||||||
| chr4:89925224
|
T | A | 1 | a0001c0001t0003g0273 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.955+1952T>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89925224 | ||||||
| chr4:89925258
|
C | T | 2 | a0001c0001t0004g0126a0001c0001t0004g0127 | 2 | HG02895.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.955+1986C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89925258 | ||||||
| chr4:89925285
|
C | G | 229 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(226): Show | 272 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(269): Show |
intron_variant | MODIFIER | c.955+2013C>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89925285 | ||||||
| chr4:89925302
|
A | AT | 49 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0043others(46): Show | 52 | HG00621.hp1 HG00741.hp1 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.955+2056dupT | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 89925302 | |||||
| chr4:89925302
|
A | ATT | 8 | a0001c0001t0001g0080a0001c0001t0002g0254a0001c0001t0002g0271others(5): Show | 8 | HG01099.hp2 HG02615.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.955+2055_955+2056d others(4): Show |
MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 89925302 | |||||
| chr4:89925302
|
A | ATTT | 7 | a0001c0001t0004g0127a0001c0001t0004g0155a0001c0001t0004g0160others(4): Show | 7 | HG02486.hp1 HG02602.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.955+2054_955+2056d others(5): Show |
MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 89925302 | |||||
| chr4:89925302
|
AT | A | 33 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(30): Show | 43 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.955+2056delT | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 89925302 | |||||
| chr4:89925302
|
ATT | A | 48 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0171others(45): Show | 56 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.955+2055_955+2056d others(4): Show |
MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 89925302 | |||||
| chr4:89925336
|
C | T | 1 | a0003c0007t0001g0301 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.955+2064C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89925336 | ||||||
| chr4:89925488
|
T | A | 3 | a0003c0003t0001g0283a0003c0003t0001g0284a0003c0029t0001g0285 | 3 | HG02559.hp1 HG03017.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.955+2216T>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89925488 | ||||||
| chr4:89925501
|
AAT | A | 81 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0040others(78): Show | 90 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.955+2244_955+2245d others(4): Show |
MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 89925501 | |||||
| chr4:89925559
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.956-2236T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89925559 | ||||||
| chr4:89925570
|
G | A | 3 | a0005c0008t0004g0148a0005c0008t0004g0149a0005c0024t0004g0147 | 3 | HG02572.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.956-2225G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89925570 | ||||||
| chr4:89925893
|
C | T | 20 | a0001c0001t0001g0085a0001c0001t0001g0162a0001c0001t0004g0126others(17): Show | 21 | HG01099.hp2 HG01167.hp1 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.956-1902C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89925893 | ||||||
| chr4:89926166
|
A | G | 8 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0152others(5): Show | 8 | HG02486.hp1 HG02818.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.956-1629A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89926166 | ||||||
| chr4:89926303
|
C | T | 84 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0040others(81): Show | 93 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.956-1492C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89926303 | ||||||
| chr4:89926373
|
TG | T | 58 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0040others(55): Show | 66 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.956-1421delG | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89926373 | ||||||
| chr4:89926398
|
T | A | 1 | a0001c0001t0004g0150 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.956-1397T>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89926398 | ||||||
| chr4:89926577
|
G | C | 3 | a0003c0003t0001g0283a0003c0003t0001g0284a0003c0029t0001g0285 | 3 | HG02559.hp1 HG03017.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.956-1218G>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89926577 | ||||||
| chr4:89926612
|
G | T | 1 | a0001c0001t0001g0151 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.956-1183G>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89926612 | ||||||
| chr4:89926644
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.956-1151T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89926644 | ||||||
| chr4:89926670
|
G | C | 4 | a0004c0004t0004g0036a0004c0004t0004g0292a0004c0004t0004g0294others(1): Show | 5 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.956-1125G>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89926670 | ||||||
| chr4:89926706
|
G | A | 3 | a0001c0001t0003g0261a0001c0001t0003g0262a0001c0001t0003g0264 | 3 | HG02145.hp2 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.956-1089G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89926706 | ||||||
| chr4:89926708
|
C | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(63): Show | 80 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.956-1087C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89926708 | ||||||
| chr4:89926786
|
C | A | 1 | a0001c0001t0004g0155 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.956-1009C>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89926786 | ||||||
| chr4:89926962
|
C | A | 58 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0040others(55): Show | 66 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.956-833C>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89926962 | ||||||
| chr4:89926972
|
C | T | 1 | a0001c0001t0002g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.956-823C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89926972 | ||||||
| chr4:89927002
|
G | A | 1 | a0001c0001t0003g0255 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.956-793G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89927002 | ||||||
| chr4:89927124
|
T | G | 3 | a0001c0001t0003g0033a0001c0001t0003g0034a0001c0001t0003g0275 | 5 | HG01081.hp2 HG01099.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.956-671T>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89927124 | ||||||
| chr4:89927148
|
AT | A | 15 | a0001c0001t0001g0012a0001c0001t0001g0151a0001c0001t0001g0156others(12): Show | 18 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.956-636delT | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 89927148 | |||||
| chr4:89927179
|
C | G | 3 | a0001c0001t0004g0109a0001c0001t0004g0128a0001c0023t0004g0218 | 3 | HG02970.hp1 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.956-616C>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89927179 | ||||||
| chr4:89927201
|
G | A | 7 | a0001c0001t0001g0012a0001c0001t0001g0156a0001c0001t0001g0158others(4): Show | 9 | HG01243.hp1 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.956-594G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89927201 | ||||||
| chr4:89927206
|
G | C | 16 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0152others(13): Show | 17 | HG01099.hp2 HG01167.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.956-589G>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89927206 | ||||||
| chr4:89927261
|
A | G | 11 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0152others(8): Show | 11 | HG02486.hp1 HG02559.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.956-534A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89927261 | ||||||
| chr4:89927273
|
G | A | 1 | a0001c0001t0001g0213 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.956-522G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89927273 | ||||||
| chr4:89927492
|
A | G | 58 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0040others(55): Show | 66 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.956-303A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89927492 | ||||||
| chr4:89927721
|
C | T | 4 | a0001c0001t0001g0197a0001c0001t0001g0200a0001c0001t0001g0201others(1): Show | 4 | HG02280.hp1 HG02622.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.956-74C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 4/7 | chr4 | 89927721 | ||||||
| chr4:89927996
|
A | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0162 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1129+28A>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89927996 | ||||||
| chr4:89928049
|
G | A | 2 | a0001c0001t0001g0040a0001c0001t0001g0215 | 2 | HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1129+81G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89928049 | ||||||
| chr4:89928096
|
TTTTAATG others(5): Show |
T | 8 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0152others(5): Show | 8 | HG02486.hp1 HG02818.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1129+130_1129+141d others(14): Show |
MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 89928096 | |||||
| chr4:89928174
|
G | C | 1 | a0001c0001t0001g0091 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1129+206G>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89928174 | ||||||
| chr4:89928247
|
T | C | 2 | a0003c0011t0004g0295a0003c0027t0011g0296 | 2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1129+279T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89928247 | ||||||
| chr4:89928295
|
A | G | 235 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(232): Show | 276 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(273): Show |
intron_variant | MODIFIER | c.1129+327A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89928295 | ||||||
| chr4:89928298
|
G | A | 1 | a0001c0001t0002g0278 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1129+330G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89928298 | ||||||
| chr4:89928381
|
A | G | 8 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0152others(5): Show | 8 | HG02486.hp1 HG02818.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1129+413A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89928381 | ||||||
| chr4:89928879
|
G | A | 16 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0152others(13): Show | 17 | HG01099.hp2 HG01167.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.1129+911G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89928879 | ||||||
| chr4:89929169
|
C | G | 1 | a0001c0001t0001g0121 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1129+1201C>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89929169 | ||||||
| chr4:89929181
|
C | A | 1 | a0003c0007t0001g0291 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1129+1213C>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89929181 | ||||||
| chr4:89929419
|
A | G | 6 | a0001c0001t0002g0300a0003c0007t0001g0289a0003c0007t0001g0301others(3): Show | 6 | HG02572.hp1 HG02886.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1129+1451A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89929419 | ||||||
| chr4:89929480
|
C | G | 1 | a0001c0001t0001g0214 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1129+1512C>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89929480 | ||||||
| chr4:89929709
|
G | A | 1 | a0002c0002t0001g0172 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1129+1741G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89929709 | ||||||
| chr4:89930038
|
C | G | 1 | a0003c0011t0001g0288 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1129+2070C>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89930038 | ||||||
| chr4:89930223
|
C | G | 1 | a0001c0001t0001g0071 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1129+2255C>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89930223 | ||||||
| chr4:89930236
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0162 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1129+2268G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89930236 | ||||||
| chr4:89930244
|
A | G | 1 | a0001c0001t0004g0150 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1129+2276A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89930244 | ||||||
| chr4:89930457
|
T | C | 1 | a0002c0002t0001g0186 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1129+2489T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89930457 | ||||||
| chr4:89930525
|
C | T | 95 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0022others(92): Show | 106 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.1129+2557C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89930525 | ||||||
| chr4:89930529
|
A | C | 1 | a0004c0012t0004g0293 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1129+2561A>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89930529 | ||||||
| chr4:89930541
|
C | CT | 95 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0022others(92): Show | 106 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.1129+2576dupT | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 89930541 | |||||
| chr4:89930564
|
G | A | 1 | a0001c0001t0003g0240 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1129+2596G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89930564 | ||||||
| chr4:89930806
|
A | G | 2 | a0003c0011t0004g0295a0003c0027t0011g0296 | 2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1129+2838A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89930806 | ||||||
| chr4:89930875
|
T | C | 6 | a0001c0001t0002g0300a0003c0007t0001g0289a0003c0007t0001g0301others(3): Show | 6 | HG02572.hp1 HG02886.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1129+2907T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89930875 | ||||||
| chr4:89931054
|
G | T | 2 | a0003c0011t0004g0295a0003c0027t0011g0296 | 2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1129+3086G>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89931054 | ||||||
| chr4:89931071
|
A | G | 1 | a0004c0012t0004g0293 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1129+3103A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89931071 | ||||||
| chr4:89931271
|
G | A | 1 | a0002c0002t0007g0193 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1129+3303G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89931271 | ||||||
| chr4:89931377
|
G | A | 2 | a0001c0001t0002g0270a0001c0001t0002g0271 | 2 | HG02615.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1129+3409G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89931377 | ||||||
| chr4:89931449
|
C | A | 2 | a0003c0011t0004g0295a0003c0027t0011g0296 | 2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1130-3361C>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89931449 | ||||||
| chr4:89931486
|
GTATTGTG others(25): Show |
G | 2 | a0001c0001t0001g0085a0001c0001t0001g0162 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1130-3315_1130-328 others(36): Show |
MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 89931486 | |||||
| chr4:89931664
|
A | C | 4 | a0001c0001t0002g0027a0001c0001t0002g0030a0001c0001t0002g0250others(1): Show | 6 | HG00609.hp1 NA18955.hp1 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.1130-3146A>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89931664 | ||||||
| chr4:89931895
|
G | A | 1 | a0001c0001t0001g0103 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1130-2915G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89931895 | ||||||
| chr4:89932022
|
G | C | 1 | a0001c0001t0001g0214 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1130-2788G>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89932022 | ||||||
| chr4:89932064
|
T | C | 3 | a0001c0001t0004g0017a0001c0001t0004g0106a0001c0001t0004g0125 | 4 | HG02647.hp2 HG02809.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1130-2746T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89932064 | ||||||
| chr4:89932165
|
A | G | 1 | a0001c0001t0002g0010 | 3 | HG01192.hp1 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1130-2645A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89932165 | ||||||
| chr4:89932171
|
G | A | 1 | a0001c0001t0001g0214 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1130-2639G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89932171 | ||||||
| chr4:89932201
|
C | T | 1 | a0001c0001t0001g0050 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1130-2609C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89932201 | ||||||
| chr4:89932252
|
G | A | 2 | a0003c0003t0001g0035a0003c0003t0001g0281 | 3 | HG02723.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1130-2558G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89932252 | ||||||
| chr4:89932382
|
G | A | 2 | a0001c0001t0001g0022a0001c0001t0001g0208 | 3 | HG02622.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1130-2428G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89932382 | ||||||
| chr4:89932515
|
G | T | 1 | a0003c0029t0001g0285 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1130-2295G>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89932515 | ||||||
| chr4:89932537
|
C | T | 1 | a0001c0001t0009g0297 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1130-2273C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89932537 | ||||||
| chr4:89932601
|
A | G | 3 | a0001c0001t0001g0085a0001c0001t0001g0162a0003c0011t0001g0288 | 3 | HG01099.hp2 HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1130-2209A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89932601 | ||||||
| chr4:89932719
|
A | G | 2 | a0001c0001t0002g0270a0001c0001t0002g0271 | 2 | HG02615.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1130-2091A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89932719 | ||||||
| chr4:89932945
|
T | C | 1 | a0001c0001t0003g0280 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1130-1865T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89932945 | ||||||
| chr4:89932951
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1130-1859C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89932951 | ||||||
| chr4:89933014
|
C | G | 1 | a0001c0001t0003g0280 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1130-1796C>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89933014 | ||||||
| chr4:89933081
|
T | C | 3 | a0001c0001t0001g0085a0001c0001t0001g0162a0003c0011t0001g0288 | 3 | HG01099.hp2 HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1130-1729T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89933081 | ||||||
| chr4:89933268
|
C | T | 2 | a0002c0002t0001g0182a0002c0002t0001g0190 | 2 | NA18974.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1130-1542C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89933268 | ||||||
| chr4:89933355
|
A | G | 5 | a0003c0029t0001g0285a0004c0004t0004g0036a0004c0004t0004g0292others(2): Show | 6 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1130-1455A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89933355 | ||||||
| chr4:89933385
|
C | T | 2 | a0003c0011t0004g0295a0003c0027t0011g0296 | 2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1130-1425C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89933385 | ||||||
| chr4:89933415
|
T | C | 1 | a0001c0001t0001g0048 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1130-1395T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89933415 | ||||||
| chr4:89933507
|
G | A | 14 | a0001c0001t0002g0300a0001c0001t0004g0126a0001c0001t0004g0127others(11): Show | 14 | HG02486.hp1 HG02572.hp1 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.1130-1303G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89933507 | ||||||
| chr4:89933557
|
G | A | 5 | a0003c0029t0001g0285a0004c0004t0004g0036a0004c0004t0004g0292others(2): Show | 6 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1130-1253G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89933557 | ||||||
| chr4:89933561
|
G | A | 1 | a0008c0028t0001g0290 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1130-1249G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89933561 | ||||||
| chr4:89933722
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1130-1088C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89933722 | ||||||
| chr4:89933790
|
A | G | 2 | a0003c0011t0004g0295a0003c0027t0011g0296 | 2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1130-1020A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89933790 | ||||||
| chr4:89934201
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1130-609C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89934201 | ||||||
| chr4:89934282
|
A | G | 1 | a0001c0001t0001g0100 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1130-528A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89934282 | ||||||
| chr4:89934435
|
T | C | 1 | a0001c0001t0003g0255 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1130-375T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89934435 | ||||||
| chr4:89934479
|
A | G | 1 | a0003c0029t0001g0285 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1130-331A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89934479 | ||||||
| chr4:89934515
|
T | C | 2 | a0001c0001t0002g0241a0001c0001t0010g0089 | 2 | HG03704.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1130-295T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89934515 | ||||||
| chr4:89934684
|
A | C | 2 | a0003c0011t0004g0295a0003c0027t0011g0296 | 2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1130-126A>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89934684 | ||||||
| chr4:89934781
|
T | C | 91 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(88): Show | 109 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.1130-29T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 5/7 | chr4 | 89934781 | ||||||
| chr4:89936845
|
A | G | 1 | a0001c0001t0004g0045 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3118+47A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89936845 | ||||||
| chr4:89936979
|
C | A | 4 | a0001c0001t0005g0007a0001c0001t0005g0228a0001c0001t0005g0232others(1): Show | 7 | HG01261.hp1 HG01433.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.3118+181C>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89936979 | ||||||
| chr4:89936979
|
C | T | 4 | a0001c0001t0002g0227a0001c0001t0002g0233a0001c0001t0002g0268others(1): Show | 4 | HG01261.hp2 HG01346.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.3118+181C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89936979 | ||||||
| chr4:89937289
|
TG | T | 3 | a0001c0001t0001g0085a0001c0001t0001g0162a0003c0011t0001g0288 | 3 | HG01099.hp2 HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.3118+492delG | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89937289 | ||||||
| chr4:89937298
|
A | T | 1 | a0016c0020t0001g0137 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3118+500A>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89937298 | ||||||
| chr4:89937494
|
G | A | 3 | a0001c0001t0001g0085a0001c0001t0001g0162a0003c0011t0001g0288 | 3 | HG01099.hp2 HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.3118+696G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89937494 | ||||||
| chr4:89937594
|
A | G | 8 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0152others(5): Show | 8 | HG02486.hp1 HG02818.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.3118+796A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89937594 | ||||||
| chr4:89937698
|
T | A | 5 | a0003c0029t0001g0285a0004c0004t0004g0036a0004c0004t0004g0292others(2): Show | 6 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.3118+900T>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89937698 | ||||||
| chr4:89937866
|
G | A | 14 | a0001c0001t0002g0300a0001c0001t0004g0126a0001c0001t0004g0127others(11): Show | 14 | HG02486.hp1 HG02572.hp1 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.3118+1068G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89937866 | ||||||
| chr4:89938043
|
C | G | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3118+1245C>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89938043 | ||||||
| chr4:89938061
|
G | T | 12 | a0001c0001t0002g0300a0001c0001t0004g0126a0001c0001t0004g0127others(9): Show | 12 | HG02486.hp1 HG02572.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.3118+1263G>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89938061 | ||||||
| chr4:89938128
|
G | A | 8 | a0001c0001t0002g0011a0001c0001t0002g0027a0001c0001t0002g0030others(5): Show | 12 | HG00609.hp1 HG00639.hp2 HG02738.hp2 others(9): Show |
intron_variant | MODIFIER | c.3118+1330G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89938128 | ||||||
| chr4:89938136
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3118+1338G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89938136 | ||||||
| chr4:89938283
|
C | T | 2 | a0001c0001t0004g0152a0001c0001t0004g0155 | 2 | HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3118+1485C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89938283 | ||||||
| chr4:89938384
|
T | A | 1 | a0001c0001t0001g0072 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3118+1586T>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89938384 | ||||||
| chr4:89938476
|
C | CAT | 11 | a0001c0001t0001g0048a0001c0001t0002g0250a0001c0001t0002g0272others(8): Show | 12 | HG00609.hp1 HG01243.hp2 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.3118+1713_3118+171 others(6): Show |
MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 89938476 | |||||
| chr4:89938476
|
C | CATAT | 4 | a0001c0001t0001g0215a0001c0001t0002g0243a0001c0001t0003g0280others(1): Show | 4 | HG02155.hp1 HG03041.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.3118+1711_3118+171 others(8): Show |
MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 89938476 | |||||
| chr4:89938476
|
C | CATATATA others(3): Show |
1 | a0001c0001t0003g0274 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3118+1705_3118+171 others(14): Show |
MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 89938476 | |||||
| chr4:89938476
|
C | CATATATA others(9): Show |
1 | a0001c0001t0001g0040 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3118+1699_3118+171 others(20): Show |
MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 89938476 | |||||
| chr4:89938476
|
CAT | C | 40 | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0001g0217others(37): Show | 57 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.3118+1713_3118+171 others(6): Show |
MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 89938476 | |||||
| chr4:89938476
|
CATAT | C | 16 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0062others(13): Show | 18 | HG01346.hp1 HG02155.hp2 HG02698.hp1 others(15): Show |
intron_variant | MODIFIER | c.3118+1711_3118+171 others(8): Show |
MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 89938476 | |||||
| chr4:89938476
|
CATATAT | C | 29 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0038others(26): Show | 39 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.3118+1709_3118+171 others(10): Show |
MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 89938476 | |||||
| chr4:89938497
|
A | T | 4 | a0004c0004t0004g0036a0004c0004t0004g0292a0004c0004t0004g0294others(1): Show | 5 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.3118+1699A>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89938497 | ||||||
| chr4:89938499
|
A | T | 4 | a0001c0001t0001g0012a0001c0001t0001g0162a0001c0001t0008g0298others(1): Show | 6 | HG01243.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.3118+1701A>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89938499 | ||||||
| chr4:89938499
|
ATATATAT others(7): Show |
A | 4 | a0004c0004t0004g0036a0004c0004t0004g0292a0004c0004t0004g0294others(1): Show | 5 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.3118+1704_3118+171 others(18): Show |
MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 89938499 | |||||
| chr4:89938501
|
A | T | 8 | a0001c0001t0001g0085a0001c0001t0001g0131a0001c0001t0001g0145others(5): Show | 8 | HG01934.hp2 HG02109.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.3118+1703A>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89938501 | ||||||
| chr4:89938501
|
ATATATAT others(5): Show |
A | 4 | a0001c0001t0001g0012a0001c0001t0001g0162a0001c0001t0008g0298others(1): Show | 6 | HG01243.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.3118+1706_3118+171 others(16): Show |
MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 89938501 | |||||
| chr4:89938503
|
A | T | 57 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(54): Show | 72 | HG00099.hp2 HG00140.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.3118+1705A>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89938503 | ||||||
| chr4:89938503
|
ATATATAT others(3): Show |
A | 8 | a0001c0001t0001g0085a0001c0001t0001g0131a0001c0001t0001g0145others(5): Show | 8 | HG01934.hp2 HG02109.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.3118+1708_3118+171 others(14): Show |
MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 89938503 | |||||
| chr4:89938505
|
A | T | 15 | a0001c0001t0001g0092a0001c0001t0001g0101a0001c0001t0001g0103others(12): Show | 15 | HG00597.hp2 HG01256.hp2 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.3118+1707A>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89938505 | ||||||
| chr4:89938505
|
ATATATAT others(1): Show |
A | 57 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(54): Show | 72 | HG00099.hp2 HG00140.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.3118+1710_3118+171 others(12): Show |
MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 89938505 | |||||
| chr4:89938507
|
A | T | 27 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0068others(24): Show | 30 | HG01109.hp2 HG01433.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.3118+1709A>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89938507 | ||||||
| chr4:89938507
|
ATATATT | A | 15 | a0001c0001t0001g0092a0001c0001t0001g0101a0001c0001t0001g0103others(12): Show | 15 | HG00597.hp2 HG01256.hp2 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.3118+1712_3118+171 others(10): Show |
MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 89938507 | |||||
| chr4:89938509
|
A | T | 8 | a0001c0001t0001g0022a0001c0001t0001g0098a0001c0001t0001g0107others(5): Show | 9 | HG00423.hp1 HG01928.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.3118+1711A>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89938509 | ||||||
| chr4:89938509
|
ATAT | A | 4 | a0001c0001t0001g0054a0001c0001t0002g0278a0001c0001t0003g0247others(1): Show | 4 | HG00558.hp2 HG02145.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.3118+1713_3118+171 others(7): Show |
MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 89938509 | |||||
| chr4:89938509
|
ATATT | A | 28 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0068others(25): Show | 31 | HG01109.hp2 HG01433.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.3118+1714_3118+171 others(8): Show |
MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 89938509 | |||||
| chr4:89938511
|
A | T | 37 | a0001c0001t0001g0075a0001c0001t0001g0079a0001c0001t0001g0197others(34): Show | 43 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.3118+1713A>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89938511 | ||||||
| chr4:89938511
|
ATT | A | 8 | a0001c0001t0001g0022a0001c0001t0001g0098a0001c0001t0001g0107others(5): Show | 9 | HG00423.hp1 HG01928.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.3118+1715_3118+171 others(6): Show |
MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 89938511 | |||||
| chr4:89938513
|
T | A | 37 | a0001c0001t0001g0075a0001c0001t0001g0079a0001c0001t0001g0197others(34): Show | 43 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.3118+1715T>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89938513 | ||||||
| chr4:89938514
|
T | A | 160 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(157): Show | 188 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.3118+1716T>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89938514 | ||||||
| chr4:89938517
|
A | AAT | 25 | a0001c0001t0001g0040a0001c0001t0001g0201a0001c0001t0001g0215others(22): Show | 26 | HG01123.hp2 HG01243.hp2 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.3118+1728_3118+172 others(6): Show |
MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 89938517 | |||||
| chr4:89938517
|
A | T | 160 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(157): Show | 188 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.3118+1719A>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89938517 | ||||||
| chr4:89938560
|
G | C | 60 | a0001c0001t0001g0022a0001c0001t0001g0040a0001c0001t0001g0197others(57): Show | 68 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.3118+1762G>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89938560 | ||||||
| chr4:89938935
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0162 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.3118+2137G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89938935 | ||||||
| chr4:89938971
|
G | A | 3 | a0001c0001t0001g0085a0001c0001t0001g0162a0003c0011t0001g0288 | 3 | HG01099.hp2 HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.3118+2173G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89938971 | ||||||
| chr4:89938972
|
T | G | 122 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(119): Show | 136 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.3118+2174T>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89938972 | ||||||
| chr4:89938978
|
A | T | 1 | a0001c0001t0001g0162 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3118+2180A>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89938978 | ||||||
| chr4:89939024
|
A | G | 1 | a0003c0011t0001g0288 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.3118+2226A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89939024 | ||||||
| chr4:89939084
|
G | A | 1 | a0001c0001t0001g0049 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.3118+2286G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89939084 | ||||||
| chr4:89939187
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.3118+2389G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89939187 | ||||||
| chr4:89939305
|
C | T | 1 | a0002c0002t0001g0188 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.3118+2507C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89939305 | ||||||
| chr4:89939365
|
A | T | 88 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0022others(85): Show | 99 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.3118+2567A>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89939365 | ||||||
| chr4:89939438
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3118+2640C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89939438 | ||||||
| chr4:89939522
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3118+2724C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89939522 | ||||||
| chr4:89939573
|
G | A | 4 | a0001c0001t0004g0160a0006c0006t0001g0153a0006c0006t0004g0074others(1): Show | 4 | HG02486.hp1 HG02818.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.3118+2775G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89939573 | ||||||
| chr4:89939622
|
T | C | 1 | a0001c0001t0001g0118 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.3118+2824T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89939622 | ||||||
| chr4:89939678
|
A | G | 7 | a0003c0011t0004g0295a0003c0027t0011g0296a0003c0029t0001g0285others(4): Show | 8 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.3118+2880A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89939678 | ||||||
| chr4:89939755
|
G | C | 2 | a0001c0001t0001g0085a0001c0001t0001g0162 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.3118+2957G>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89939755 | ||||||
| chr4:89939786
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3118+2988C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89939786 | ||||||
| chr4:89939808
|
T | C | 1 | a0001c0001t0003g0031 | 2 | HG00140.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.3118+3010T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89939808 | ||||||
| chr4:89939924
|
A | C | 2 | a0003c0011t0004g0295a0003c0027t0011g0296 | 2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.3118+3126A>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89939924 | ||||||
| chr4:89939954
|
G | A | 14 | a0001c0001t0002g0300a0001c0001t0004g0126a0001c0001t0004g0127others(11): Show | 14 | HG02486.hp1 HG02572.hp1 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.3118+3156G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89939954 | ||||||
| chr4:89939993
|
C | T | 1 | a0001c0001t0004g0150 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3118+3195C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89939993 | ||||||
| chr4:89940282
|
A | G | 2 | a0003c0011t0004g0295a0003c0027t0011g0296 | 2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.3118+3484A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89940282 | ||||||
| chr4:89940495
|
A | C | 1 | a0001c0001t0001g0136 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.3118+3697A>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89940495 | ||||||
| chr4:89940977
|
A | T | 1 | a0001c0001t0001g0107 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3118+4179A>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89940977 | ||||||
| chr4:89941101
|
T | C | 14 | a0001c0001t0002g0300a0001c0001t0004g0126a0001c0001t0004g0127others(11): Show | 14 | HG02486.hp1 HG02572.hp1 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.3118+4303T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89941101 | ||||||
| chr4:89941116
|
C | G | 1 | a0002c0002t0001g0167 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3118+4318C>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89941116 | ||||||
| chr4:89941138
|
C | T | 1 | a0001c0001t0002g0242 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.3118+4340C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89941138 | ||||||
| chr4:89941167
|
C | A | 14 | a0001c0001t0002g0300a0001c0001t0004g0126a0001c0001t0004g0127others(11): Show | 14 | HG02486.hp1 HG02572.hp1 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.3118+4369C>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89941167 | ||||||
| chr4:89941221
|
G | A | 61 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(58): Show | 76 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.3118+4423G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89941221 | ||||||
| chr4:89941277
|
G | A | 2 | a0003c0003t0001g0035a0003c0003t0001g0281 | 3 | HG02723.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3118+4479G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89941277 | ||||||
| chr4:89941524
|
C | T | 185 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(182): Show | 214 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.3118+4726C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89941524 | ||||||
| chr4:89941565
|
C | T | 4 | a0004c0004t0004g0036a0004c0004t0004g0292a0004c0004t0004g0294others(1): Show | 5 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.3118+4767C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89941565 | ||||||
| chr4:89941792
|
A | G | 16 | a0001c0001t0002g0300a0001c0001t0004g0126a0001c0001t0004g0127others(13): Show | 16 | HG02055.hp2 HG02486.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.3118+4994A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89941792 | ||||||
| chr4:89941821
|
C | T | 2 | a0001c0001t0002g0241a0001c0001t0010g0089 | 2 | HG03704.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3118+5023C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89941821 | ||||||
| chr4:89941856
|
A | G | 10 | a0002c0002t0001g0020a0002c0002t0001g0041a0002c0002t0001g0179others(7): Show | 11 | NA18947.hp2 NA18966.hp2 NA18969.hp2 others(8): Show |
intron_variant | MODIFIER | c.3118+5058A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89941856 | ||||||
| chr4:89941940
|
A | T | 1 | a0003c0007t0001g0301 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3118+5142A>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89941940 | ||||||
| chr4:89942019
|
T | C | 58 | a0001c0001t0001g0022a0001c0001t0001g0040a0001c0001t0001g0197others(55): Show | 66 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.3118+5221T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89942019 | ||||||
| chr4:89942051
|
C | T | 3 | a0001c0001t0001g0085a0001c0001t0001g0162a0003c0011t0001g0288 | 3 | HG01099.hp2 HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.3118+5253C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89942051 | ||||||
| chr4:89942155
|
T | G | 3 | a0001c0001t0001g0085a0001c0001t0001g0162a0003c0011t0001g0288 | 3 | HG01099.hp2 HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.3118+5357T>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89942155 | ||||||
| chr4:89942311
|
C | T | 3 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0213 | 3 | NA18952.hp1 NA19010.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.3118+5513C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89942311 | ||||||
| chr4:89942789
|
T | C | 1 | a0003c0011t0001g0288 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.3118+5991T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89942789 | ||||||
| chr4:89942808
|
G | T | 58 | a0001c0001t0001g0022a0001c0001t0001g0040a0001c0001t0001g0197others(55): Show | 66 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.3118+6010G>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89942808 | ||||||
| chr4:89943020
|
G | T | 1 | a0003c0029t0001g0285 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3118+6222G>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89943020 | ||||||
| chr4:89943051
|
G | C | 4 | a0004c0004t0004g0036a0004c0004t0004g0292a0004c0004t0004g0294others(1): Show | 5 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.3118+6253G>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89943051 | ||||||
| chr4:89943284
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3118+6486A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89943284 | ||||||
| chr4:89943296
|
T | C | 1 | a0001c0001t0002g0221 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3118+6498T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89943296 | ||||||
| chr4:89943545
|
T | C | 2 | a0001c0001t0004g0126a0001c0001t0004g0127 | 2 | HG02895.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3118+6747T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89943545 | ||||||
| chr4:89943656
|
C | A | 1 | a0001c0001t0002g0252 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3118+6858C>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89943656 | ||||||
| chr4:89943733
|
T | C | 3 | a0001c0001t0001g0197a0001c0001t0001g0200a0001c0001t0001g0201 | 3 | HG02280.hp1 HG02723.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.3118+6935T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89943733 | ||||||
| chr4:89943742
|
C | A | 1 | a0003c0011t0001g0288 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.3118+6944C>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89943742 | ||||||
| chr4:89943777
|
G | A | 1 | a0001c0001t0008g0298 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3118+6979G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89943777 | ||||||
| chr4:89943787
|
C | T | 1 | a0003c0011t0001g0288 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.3118+6989C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89943787 | ||||||
| chr4:89943936
|
C | G | 1 | a0001c0001t0002g0256 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3118+7138C>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89943936 | ||||||
| chr4:89943981
|
C | CA | 7 | a0001c0001t0001g0075a0001c0001t0001g0079a0001c0001t0002g0220others(4): Show | 7 | HG02451.hp1 HG02922.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.3118+7196dupA | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 89943981 | |||||
| chr4:89943981
|
C | CAA | 15 | a0001c0001t0002g0300a0001c0001t0004g0126a0001c0001t0004g0127others(12): Show | 15 | HG02055.hp2 HG02486.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.3118+7195_3118+719 others(6): Show |
MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 89943981 | |||||
| chr4:89944038
|
A | G | 9 | a0001c0001t0001g0012a0001c0001t0001g0151a0001c0001t0001g0156others(6): Show | 11 | HG01243.hp1 HG01891.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.3118+7240A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89944038 | ||||||
| chr4:89944044
|
T | C | 1 | a0001c0001t0003g0274 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3118+7246T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89944044 | ||||||
| chr4:89944158
|
A | G | 5 | a0003c0029t0001g0285a0004c0004t0004g0036a0004c0004t0004g0292others(2): Show | 6 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.3118+7360A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89944158 | ||||||
| chr4:89944430
|
C | T | 15 | a0001c0001t0002g0300a0001c0001t0004g0126a0001c0001t0004g0127others(12): Show | 15 | HG02055.hp2 HG02486.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.3119-7175C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89944430 | ||||||
| chr4:89944440
|
G | A | 1 | a0001c0001t0003g0260 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.3119-7165G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89944440 | ||||||
| chr4:89944621
|
G | A | 15 | a0001c0001t0002g0300a0001c0001t0004g0126a0001c0001t0004g0127others(12): Show | 15 | HG02055.hp2 HG02486.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.3119-6984G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89944621 | ||||||
| chr4:89944623
|
G | A | 5 | a0001c0001t0004g0210a0004c0004t0004g0036a0004c0004t0004g0292others(2): Show | 6 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.3119-6982G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89944623 | ||||||
| chr4:89944638
|
A | G | 15 | a0001c0001t0002g0300a0001c0001t0004g0126a0001c0001t0004g0127others(12): Show | 15 | HG02055.hp2 HG02486.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.3119-6967A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89944638 | ||||||
| chr4:89944729
|
G | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0059 | 2 | NA18949.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.3119-6876G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89944729 | ||||||
| chr4:89944847
|
G | A | 1 | a0003c0029t0001g0285 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3119-6758G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89944847 | ||||||
| chr4:89945077
|
T | C | 1 | a0001c0001t0001g0093 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.3119-6528T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89945077 | ||||||
| chr4:89945118
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3119-6487G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89945118 | ||||||
| chr4:89945168
|
C | G | 4 | a0004c0004t0004g0036a0004c0004t0004g0292a0004c0004t0004g0294others(1): Show | 5 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.3119-6437C>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89945168 | ||||||
| chr4:89945189
|
T | C | 1 | a0001c0001t0002g0300 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3119-6416T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89945189 | ||||||
| chr4:89945197
|
A | T | 4 | a0001c0001t0002g0010a0001c0001t0003g0024a0001c0001t0003g0031others(1): Show | 8 | HG00140.hp1 HG01074.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.3119-6408A>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89945197 | ||||||
| chr4:89945314
|
T | C | 1 | a0001c0001t0003g0273 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3119-6291T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89945314 | ||||||
| chr4:89945390
|
T | C | 5 | a0003c0029t0001g0285a0004c0004t0004g0036a0004c0004t0004g0292others(2): Show | 6 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.3119-6215T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89945390 | ||||||
| chr4:89945505
|
A | T | 1 | a0001c0001t0001g0062 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.3119-6100A>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89945505 | ||||||
| chr4:89945525
|
T | C | 1 | a0005c0024t0004g0147 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3119-6080T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89945525 | ||||||
| chr4:89945622
|
C | A | 2 | a0003c0029t0001g0285a0004c0012t0004g0293 | 2 | HG03017.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3119-5983C>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89945622 | ||||||
| chr4:89945668
|
C | T | 91 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0040others(88): Show | 102 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.3119-5937C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89945668 | ||||||
| chr4:89945676
|
C | G | 1 | a0001c0001t0001g0070 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.3119-5929C>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89945676 | ||||||
| chr4:89945985
|
G | A | 2 | a0003c0011t0004g0295a0003c0027t0011g0296 | 2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.3119-5620G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89945985 | ||||||
| chr4:89946021
|
G | A | 20 | a0001c0001t0002g0300a0001c0001t0004g0126a0001c0001t0004g0127others(17): Show | 21 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.3119-5584G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89946021 | ||||||
| chr4:89946140
|
C | G | 303 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(300): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.3119-5465C>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89946140 | ||||||
| chr4:89946216
|
G | C | 1 | a0001c0001t0001g0071 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.3119-5389G>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89946216 | ||||||
| chr4:89946233
|
G | A | 1 | a0001c0001t0003g0280 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3119-5372G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89946233 | ||||||
| chr4:89946317
|
G | A | 1 | a0001c0001t0003g0225 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3119-5288G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89946317 | ||||||
| chr4:89946390
|
T | G | 15 | a0001c0001t0002g0300a0001c0001t0004g0126a0001c0001t0004g0127others(12): Show | 15 | HG02055.hp2 HG02486.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.3119-5215T>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89946390 | ||||||
| chr4:89946848
|
G | A | 5 | a0003c0029t0001g0285a0004c0004t0004g0036a0004c0004t0004g0292others(2): Show | 6 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.3119-4757G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89946848 | ||||||
| chr4:89946994
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0162 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.3119-4611G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89946994 | ||||||
| chr4:89947145
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3119-4460G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89947145 | ||||||
| chr4:89947204
|
T | C | 303 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(300): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.3119-4401T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89947204 | ||||||
| chr4:89947332
|
T | A | 5 | a0003c0029t0001g0285a0004c0004t0004g0036a0004c0004t0004g0292others(2): Show | 6 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.3119-4273T>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89947332 | ||||||
| chr4:89947686
|
T | A | 96 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0040others(93): Show | 107 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.3119-3919T>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89947686 | ||||||
| chr4:89947698
|
T | C | 61 | a0001c0001t0001g0022a0001c0001t0001g0058a0001c0001t0001g0060others(58): Show | 70 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.3119-3907T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89947698 | ||||||
| chr4:89947977
|
G | C | 15 | a0001c0001t0002g0300a0001c0001t0004g0126a0001c0001t0004g0127others(12): Show | 15 | HG02055.hp2 HG02486.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.3119-3628G>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89947977 | ||||||
| chr4:89948000
|
A | C | 1 | a0001c0001t0001g0108 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.3119-3605A>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89948000 | ||||||
| chr4:89948012
|
C | T | 1 | a0001c0001t0001g0101 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.3119-3593C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89948012 | ||||||
| chr4:89948121
|
G | A | 1 | a0001c0001t0002g0244 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.3119-3484G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89948121 | ||||||
| chr4:89948349
|
T | C | 45 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0067others(42): Show | 49 | HG01099.hp2 HG01243.hp1 HG01433.hp2 others(46): Show |
intron_variant | MODIFIER | c.3119-3256T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89948349 | ||||||
| chr4:89948379
|
A | G | 1 | a0003c0029t0001g0285 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3119-3226A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89948379 | ||||||
| chr4:89948731
|
T | C | 2 | a0001c0001t0003g0236a0001c0001t0003g0248 | 2 | HG00558.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.3119-2874T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89948731 | ||||||
| chr4:89949159
|
A | G | 1 | a0001c0001t0001g0044 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3119-2446A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89949159 | ||||||
| chr4:89949189
|
T | G | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(230): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.3119-2416T>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89949189 | ||||||
| chr4:89949208
|
G | A | 232 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(229): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.3119-2397G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89949208 | ||||||
| chr4:89949285
|
T | A | 1 | a0001c0001t0001g0067 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3119-2320T>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89949285 | ||||||
| chr4:89949382
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3119-2223T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89949382 | ||||||
| chr4:89949504
|
T | C | 1 | a0009c0013t0001g0216 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3119-2101T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89949504 | ||||||
| chr4:89949660
|
A | G | 1 | a0003c0007t0001g0301 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3119-1945A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89949660 | ||||||
| chr4:89949776
|
T | A | 2 | a0001c0001t0001g0061a0001c0001t0001g0065 | 2 | HG03831.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.3119-1829T>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89949776 | ||||||
| chr4:89949796
|
C | T | 2 | a0001c0001t0004g0106a0001c0001t0004g0125 | 2 | HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.3119-1809C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89949796 | ||||||
| chr4:89949841
|
CA | C | 3 | a0002c0002t0001g0166a0012c0014t0001g0168a0015c0017t0001g0163 | 3 | NA18948.hp2 NA19000.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.3119-1760delA | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 89949841 | |||||
| chr4:89949858
|
T | C | 3 | a0004c0004t0004g0036a0004c0004t0004g0292a0004c0004t0004g0294 | 4 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.3119-1747T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89949858 | ||||||
| chr4:89950176
|
C | T | 1 | a0002c0002t0001g0175 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.3119-1429C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89950176 | ||||||
| chr4:89950261
|
T | C | 6 | a0001c0001t0003g0261a0001c0001t0003g0262a0001c0001t0003g0263others(3): Show | 6 | HG02145.hp2 HG03041.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.3119-1344T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89950261 | ||||||
| chr4:89950288
|
A | G | 3 | a0001c0001t0004g0078a0001c0001t0004g0109a0001c0023t0004g0218 | 3 | HG02970.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3119-1317A>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89950288 | ||||||
| chr4:89950324
|
TG | T | 3 | a0001c0001t0001g0088a0001c0001t0001g0146a0001c0001t0002g0259 | 3 | HG01358.hp2 HG03942.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.3119-1279delG | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 89950324 | |||||
| chr4:89950349
|
T | C | 2 | a0001c0001t0002g0251a0001c0001t0002g0253 | 2 | NA18979.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.3119-1256T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89950349 | ||||||
| chr4:89950410
|
C | T | 78 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(75): Show | 95 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.3119-1195C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89950410 | ||||||
| chr4:89950411
|
G | A | 2 | a0001c0001t0002g0254a0003c0029t0001g0285 | 2 | HG03017.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.3119-1194G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89950411 | ||||||
| chr4:89950511
|
C | T | 81 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(78): Show | 98 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.3119-1094C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89950511 | ||||||
| chr4:89950529
|
G | T | 6 | a0001c0001t0003g0255a0001c0001t0004g0017a0001c0001t0004g0086others(3): Show | 7 | HG01358.hp1 HG02559.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.3119-1076G>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89950529 | ||||||
| chr4:89950663
|
C | A | 3 | a0001c0001t0004g0078a0001c0001t0004g0109a0001c0023t0004g0218 | 3 | HG02970.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3119-942C>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89950663 | ||||||
| chr4:89950727
|
T | A | 1 | a0002c0002t0001g0180 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.3119-878T>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89950727 | ||||||
| chr4:89950762
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3119-843C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89950762 | ||||||
| chr4:89950773
|
G | T | 1 | a0003c0029t0001g0285 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3119-832G>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89950773 | ||||||
| chr4:89950814
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.3119-791C>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89950814 | ||||||
| chr4:89950829
|
G | A | 3 | a0001c0001t0001g0077a0001c0001t0001g0080a0017c0019t0001g0105 | 3 | HG02615.hp2 HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3119-776G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89950829 | ||||||
| chr4:89950831
|
T | C | 1 | a0001c0001t0003g0240 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3119-774T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89950831 | ||||||
| chr4:89951012
|
T | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(152): Show | 185 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.3119-593T>G | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89951012 | ||||||
| chr4:89951133
|
T | C | 4 | a0003c0027t0011g0296a0004c0004t0004g0036a0004c0004t0004g0292others(1): Show | 5 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.3119-472T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89951133 | ||||||
| chr4:89951158
|
GT | G | 6 | a0001c0001t0003g0255a0001c0001t0004g0017a0001c0001t0004g0086others(3): Show | 7 | HG01358.hp1 HG02559.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.3119-440delT | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 89951158 | |||||
| chr4:89951312
|
G | A | 1 | a0001c0001t0008g0298 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3119-293G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89951312 | ||||||
| chr4:89951350
|
A | T | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0145 | 3 | HG02698.hp2 HG03491.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.3119-255A>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89951350 | ||||||
| chr4:89951429
|
G | A | 1 | a0001c0023t0004g0218 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3119-176G>A | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 6/7 | chr4 | 89951429 | ||||||
| chr4:89952270
|
T | C | 76 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(73): Show | 93 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.3265+519T>C | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 7/7 | chr4 | 89952270 | ||||||
| chr4:89952366
|
GTTAT | G | 6 | a0001c0001t0004g0017a0001c0001t0004g0076a0001c0001t0004g0104others(3): Show | 7 | HG02559.hp2 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.3265+619_3265+622d others(6): Show |
MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 89952366 | |||||
| chr4:89952381
|
CA | C | 3 | a0004c0004t0004g0036a0004c0004t0004g0292a0004c0004t0004g0294 | 4 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.3266-609delA | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 89952381 | |||||
| chr4:89952431
|
G | T | 1 | a0001c0001t0001g0067 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3266-566G>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 7/7 | chr4 | 89952431 | ||||||
| chr4:89952851
|
A | T | 1 | a0003c0007t0001g0291 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3266-146A>T | MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 7/7 | chr4 | 89952851 | ||||||
| chr4:89952944
|
A | AC | 246 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(243): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.3266-53_3266-52ins others(1): Show |
MMRN1 | ENSG00000138722.10 | transcript | ENST00000264790.7 | protein_coding | 7/7 | chr4 | 89952944 |