Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 57787 |
|---|---|
| ensemblid | ENSG00000007047.16 |
| hgncid | 13538 |
| symbol | MARK4 |
| name | microtubule affinity regulating kinase 4 |
| refseq_nuc | NM_001199867.2 |
| refseq_prot | NP_001186796.1 |
| ensembl_nuc | ENST00000262891.9 |
| ensembl_prot | ENSP00000262891.3 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 45251271 |
| end | 45305284 |
| strand | + |
| ver | v1.2 |
| region | chr19:45251271-45305284 |
| region5000 | chr19:45246271-45310284 |
| regionname0 | MARK4_chr19_45251271_45305284 |
| regionname5000 | MARK4_chr19_45246271_45310284 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 752 | 256 | 89 | 49 | 67 | 14 | 35 | 45 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0002 | 0/0 | 752 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0003 | 0/0 | 752 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0004 | 0/0 | 752 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0005 | 0/0 | 752 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 2259 | 242 | 81 | 48 | 66 | 14 | 32 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| c0002 | 0/0 | 2259 | 7 | 6 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| c0003 | 0/0 | 2259 | 2 | 0 | 0 | 0 | 0 | 2 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| c0004 | 1/0 | 2259 | 2 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| c0005 | 0/0 | 2259 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| c0006 | 0/0 | 2259 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| c0007 | 0/0 | 2259 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| c0008 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| c0009 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| c0010 | 0/0 | 2259 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| c0011 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2893 | 51 | 6 | 16 | 20 | 4 | 5 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| t0002 | 0/0 | 2893 | 37 | 22 | 2 | 11 | 0 | 2 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| t0003 | 0/0 | 2894 | 25 | 2 | 5 | 12 | 0 | 6 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| t0004 | 0/0 | 2894 | 22 | 12 | 1 | 4 | 0 | 5 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| t0005 | 0/0 | 2893 | 21 | 2 | 4 | 11 | 2 | 2 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| t0006 | 0/0 | 2893 | 19 | 17 | 2 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| t0007 | 0/1 | 2894 | 12 | 0 | 2 | 6 | 1 | 2 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| t0008 | 0/0 | 2892 | 11 | 0 | 5 | 0 | 1 | 5 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| t0009 | 0/0 | 2893 | 8 | 0 | 3 | 0 | 2 | 3 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| t0010 | 0/0 | 2894 | 7 | 2 | 3 | 0 | 0 | 2 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| t0011 | 0/0 | 2889 | 6 | 6 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| t0012 | 0/0 | 2893 | 4 | 4 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| t0013 | 0/0 | 2896 | 2 | 2 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| t0014 | 0/0 | 2893 | 2 | 0 | 0 | 1 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| t0015 | 0/0 | 2893 | 2 | 0 | 1 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| t0016 | 0/0 | 2893 | 2 | 0 | 0 | 0 | 1 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| t0017 | 0/0 | 2893 | 2 | 0 | 1 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| t0018 | 0/0 | 2893 | 2 | 2 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| t0019 | 0/0 | 2893 | 2 | 2 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| t0020 | 0/0 | 2894 | 2 | 2 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| t0021 | 0/0 | 2894 | 2 | 2 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| t0022 | 1/0 | 2893 | 2 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| t0023 | 0/0 | 2897 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| t0024 | 0/0 | 2893 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| t0025 | 0/0 | 2893 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| t0026 | 0/0 | 2893 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| t0027 | 0/0 | 2892 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| t0028 | 0/0 | 2893 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| t0029 | 0/0 | 2893 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| t0030 | 0/0 | 2893 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| t0031 | 0/0 | 2893 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| t0032 | 0/0 | 2893 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| t0033 | 0/0 | 2893 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| t0034 | 0/0 | 2893 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| t0035 | 0/0 | 2893 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| t0036 | 0/0 | 2894 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| t0037 | 0/0 | 2894 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| t0038 | 0/0 | 2894 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| t0039 | 0/0 | 2893 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0050 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0155 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2259 | 242 | 81 | 48 | 66 | 14 | 32 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0002 | 0/0 | 2259 | 7 | 6 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0003 | 0/0 | 2259 | 2 | 0 | 0 | 0 | 0 | 2 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0004 | 1/0 | 2259 | 2 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0008 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0009 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0010 | 0/0 | 2259 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0002c0011 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0003c0005 | 0/0 | 2259 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0004c0007 | 0/0 | 2259 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0005c0006 | 0/0 | 2259 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5151 | 50 | 6 | 16 | 19 | 4 | 5 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0001t0002 | 0/0 | 5151 | 35 | 22 | 2 | 10 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0001t0003 | 0/0 | 5152 | 23 | 2 | 4 | 12 | 0 | 5 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0001t0004 | 0/0 | 5152 | 21 | 12 | 1 | 4 | 0 | 4 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0001t0005 | 0/0 | 5151 | 21 | 2 | 4 | 11 | 2 | 2 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0001t0006 | 0/0 | 5151 | 17 | 15 | 2 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0001t0007 | 0/1 | 5152 | 12 | 0 | 2 | 6 | 1 | 2 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0001t0008 | 0/0 | 5150 | 11 | 0 | 5 | 0 | 1 | 5 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0001t0009 | 0/0 | 5151 | 8 | 0 | 3 | 0 | 2 | 3 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0001t0010 | 0/0 | 5152 | 6 | 1 | 3 | 0 | 0 | 2 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0001t0011 | 0/0 | 5147 | 6 | 6 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0001t0013 | 0/0 | 5154 | 2 | 2 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0001t0014 | 0/0 | 5151 | 2 | 0 | 0 | 1 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0001t0015 | 0/0 | 5151 | 2 | 0 | 1 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0001t0016 | 0/0 | 5151 | 2 | 0 | 0 | 0 | 1 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0001t0017 | 0/0 | 5151 | 2 | 0 | 1 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0001t0018 | 0/0 | 5151 | 2 | 2 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0001t0019 | 0/0 | 5151 | 2 | 2 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0001t0020 | 0/0 | 5152 | 2 | 2 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0001t0023 | 0/0 | 5155 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0001t0024 | 0/0 | 5151 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0001t0025 | 0/0 | 5151 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0001t0026 | 0/0 | 5151 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0001t0027 | 0/0 | 5150 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0001t0028 | 0/0 | 5151 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0001t0029 | 0/0 | 5151 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0001t0030 | 0/0 | 5151 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0001t0031 | 0/0 | 5151 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0001t0032 | 0/0 | 5151 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0001t0033 | 0/0 | 5151 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0001t0034 | 0/0 | 5151 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0001t0035 | 0/0 | 5151 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0001t0036 | 0/0 | 5152 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0001t0037 | 0/0 | 5152 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0001t0038 | 0/0 | 5152 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0002t0012 | 0/0 | 5151 | 4 | 4 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0002t0021 | 0/0 | 5152 | 2 | 2 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0002t0039 | 0/0 | 5151 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0003t0002 | 0/0 | 5151 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0003t0004 | 0/0 | 5152 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0004t0022 | 1/0 | 5151 | 2 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0008t0006 | 0/0 | 5151 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0009t0010 | 0/0 | 5152 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0001c0010t0001 | 0/0 | 5151 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0002c0011t0006 | 0/0 | 5151 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0003c0005t0003 | 0/0 | 5152 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0004c0007t0003 | 0/0 | 5152 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| a0005c0006t0002 | 0/0 | 5151 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | copy fasta | chr19 | 45246271 | 45310284 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0005g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0006g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0006g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0006g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0006g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0006g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0006g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0006g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0006g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0006g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0006g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0006g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0006g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0006g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0006g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0006g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0006g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0006g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0007g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0007g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0007g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0007g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0007g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0007g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0007g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0007g0050 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0007g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0007g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0007g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0007g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0008g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0008g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0008g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0008g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0008g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0008g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0008g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0008g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0008g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0008g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0008g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0009g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0009g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0009g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0009g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0009g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0009g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0009g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0009g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0010g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0010g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0010g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0010g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0010g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0010g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0011g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0011g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0011g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0011g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0011g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0011g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0013g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0013g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0014g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0014g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0015g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0015g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0016g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0016g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0017g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0017g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0018g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0018g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0019g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0019g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0020g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0020g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0023g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0024g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0025g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0026g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0027g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0028g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0029g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0030g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0031g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0032g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0033g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0034g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0035g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0036g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0037g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0001t0038g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0002t0012g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0002t0012g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0002t0012g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0002t0012g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0002t0021g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0002t0021g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0002t0039g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0003t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0003t0004g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0004t0022g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0004t0022g0155 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0008t0006g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0009t0010g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0001c0010t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0002c0011t0006g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0003c0005t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0004c0007t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| a0005c0006t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0137 | EUR | GBR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG00099 | hp2 | a0001 | c0001 | t0015 | g0129 | EUR | GBR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG00140 | hp1 | a0001 | c0001 | t0016 | g0119 | EUR | GBR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG00140 | hp2 | a0001 | c0001 | t0009 | g0075 | EUR | GBR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG00280 | hp1 | a0001 | c0001 | t0017 | g0229 | EUR | FIN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG00280 | hp2 | a0001 | c0001 | t0008 | g0251 | EUR | FIN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG00323 | hp1 | a0001 | c0001 | t0024 | g0141 | EUR | FIN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG00323 | hp2 | a0001 | c0001 | t0005 | g0043 | EUR | FIN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG00609 | hp2 | a0001 | c0001 | t0005 | g0056 | EAS | CHS | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0207 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG00639 | hp2 | a0001 | c0001 | t0008 | g0254 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG00642 | hp2 | a0001 | c0001 | t0030 | g0241 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0128 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG00735 | hp2 | a0001 | c0001 | t0010 | g0049 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0214 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0067 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0186 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01074 | hp1 | a0001 | c0002 | t0039 | g0019 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01081 | hp1 | a0001 | c0001 | t0008 | g0068 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0046 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01099 | hp1 | a0001 | c0001 | t0038 | g0127 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01099 | hp2 | a0001 | c0001 | t0008 | g0113 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01106 | hp2 | a0001 | c0001 | t0015 | g0037 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01109 | hp1 | a0004 | c0007 | t0003 | g0158 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01109 | hp2 | a0001 | c0001 | t0007 | g0074 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01167 | hp1 | a0001 | c0001 | t0006 | g0187 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01167 | hp2 | a0001 | c0001 | t0005 | g0072 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01169 | hp1 | a0001 | c0001 | t0006 | g0188 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01192 | hp1 | a0001 | c0001 | t0036 | g0160 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01192 | hp2 | a0001 | c0001 | t0017 | g0228 | AMR | PUR | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01256 | hp1 | a0001 | c0001 | t0005 | g0071 | AMR | CLM | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01257 | hp2 | a0001 | c0001 | t0009 | g0256 | AMR | CLM | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01258 | hp1 | a0001 | c0001 | t0008 | g0255 | AMR | CLM | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01261 | hp1 | a0001 | c0001 | t0010 | g0197 | AMR | CLM | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0144 | AMR | CLM | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01346 | hp1 | a0001 | c0001 | t0007 | g0032 | AMR | CLM | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01358 | hp1 | a0001 | c0001 | t0008 | g0085 | AMR | CLM | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01358 | hp2 | a0001 | c0001 | t0027 | g0253 | AMR | CLM | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01433 | hp1 | a0001 | c0001 | t0010 | g0172 | AMR | CLM | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01433 | hp2 | a0001 | c0001 | t0009 | g0242 | AMR | CLM | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | IBS | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01516 | hp2 | a0001 | c0001 | t0007 | g0041 | EUR | IBS | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01517 | hp1 | a0001 | c0001 | t0005 | g0073 | EUR | IBS | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0109 | EUR | IBS | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01884 | hp1 | a0001 | c0001 | t0013 | g0020 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0007 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0003 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0177 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01934 | hp1 | a0001 | c0001 | t0009 | g0245 | AMR | PEL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0097 | AMR | PEL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0162 | AMR | PEL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | KHV | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0211 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0179 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02071 | hp1 | a0001 | c0001 | t0004 | g0209 | EAS | KHV | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | KHV | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | KHV | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | KHV | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | KHV | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | KHV | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | KHV | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02129 | hp2 | a0001 | c0001 | t0005 | g0057 | EAS | KHV | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | KHV | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0132 | EAS | KHV | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0078 | EAS | KHV | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02145 | hp1 | a0001 | c0002 | t0021 | g0013 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0234 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0227 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0217 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02258 | hp1 | a0001 | c0002 | t0021 | g0016 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0208 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0199 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0058 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0102 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02602 | hp1 | a0001 | c0001 | t0016 | g0140 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02602 | hp2 | a0001 | c0001 | t0014 | g0081 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02615 | hp1 | a0001 | c0001 | t0006 | g0170 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02622 | hp2 | a0002 | c0011 | t0006 | g0006 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0001 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02647 | hp2 | a0001 | c0001 | t0019 | g0175 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02683 | hp2 | a0001 | c0001 | t0008 | g0249 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0196 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02723 | hp1 | a0001 | c0008 | t0006 | g0165 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02723 | hp2 | a0001 | c0001 | t0031 | g0026 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02735 | hp1 | a0001 | c0001 | t0005 | g0059 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0076 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0083 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02809 | hp1 | a0001 | c0001 | t0011 | g0051 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0200 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0238 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02818 | hp2 | a0001 | c0001 | t0033 | g0023 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02895 | hp1 | a0001 | c0001 | t0020 | g0192 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02895 | hp2 | a0001 | c0001 | t0035 | g0161 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0203 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0236 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0198 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02897 | hp2 | a0001 | c0001 | t0026 | g0190 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0082 | AFR | ESN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | ESN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0011 | AFR | ESN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0194 | AFR | ESN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0223 | AFR | ESN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | ESN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0230 | AFR | ESN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0168 | AFR | ESN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03041 | hp1 | a0001 | c0001 | t0018 | g0025 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03041 | hp2 | a0001 | c0001 | t0011 | g0052 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03098 | hp1 | a0001 | c0001 | t0011 | g0033 | AFR | MSL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0235 | AFR | MSL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0259 | AFR | ESN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03130 | hp2 | a0001 | c0002 | t0012 | g0017 | AFR | ESN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0178 | AFR | ESN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0224 | AFR | ESN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03195 | hp2 | a0001 | c0002 | t0012 | g0018 | AFR | ESN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0222 | AFR | MSL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0174 | AFR | MSL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03225 | hp1 | a0001 | c0001 | t0034 | g0012 | AFR | MSL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03225 | hp2 | a0001 | c0002 | t0012 | g0014 | AFR | MSL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03239 | hp1 | a0001 | c0001 | t0009 | g0257 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0048 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0173 | AFR | MSL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0210 | AFR | MSL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0237 | AFR | MSL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | MSL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03490 | hp2 | a0001 | c0003 | t0002 | g0212 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03491 | hp1 | a0001 | c0001 | t0008 | g0246 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03491 | hp2 | a0003 | c0005 | t0003 | g0157 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03492 | hp1 | a0001 | c0001 | t0008 | g0243 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0139 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03516 | hp1 | a0001 | c0001 | t0020 | g0191 | AFR | ESN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03516 | hp2 | a0001 | c0001 | t0011 | g0002 | AFR | ESN | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03540 | hp1 | a0001 | c0001 | t0018 | g0024 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0225 | AFR | GWD | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03579 | hp1 | a0001 | c0001 | t0032 | g0005 | AFR | MSL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03579 | hp2 | a0001 | c0009 | t0010 | g0166 | AFR | MSL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03654 | hp1 | a0001 | c0001 | t0007 | g0031 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03669 | hp1 | a0001 | c0001 | t0037 | g0111 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0184 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0114 | SAS | STU | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0183 | SAS | STU | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03704 | hp1 | a0001 | c0004 | t0022 | g0154 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0147 | SAS | PJL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03831 | hp1 | a0001 | c0001 | t0010 | g0169 | SAS | BEB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0095 | SAS | BEB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0115 | SAS | BEB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03834 | hp2 | a0001 | c0001 | t0008 | g0247 | SAS | BEB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03942 | hp1 | a0001 | c0001 | t0010 | g0030 | SAS | BEB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03942 | hp2 | a0001 | c0001 | t0007 | g0107 | SAS | BEB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG04184 | hp1 | a0001 | c0001 | t0009 | g0027 | SAS | BEB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0220 | SAS | BEB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG04199 | hp1 | a0001 | c0001 | t0008 | g0248 | SAS | STU | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | STU | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG04228 | hp1 | a0001 | c0003 | t0004 | g0216 | SAS | STU | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG04228 | hp2 | a0001 | c0001 | t0009 | g0244 | SAS | STU | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18522 | hp1 | a0001 | c0002 | t0012 | g0015 | AFR | YRI | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0201 | AFR | YRI | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | CHB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | CHB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0010 | AFR | YRI | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18906 | hp2 | a0001 | c0001 | t0013 | g0021 | AFR | YRI | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18942 | hp1 | a0001 | c0001 | t0005 | g0054 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18942 | hp2 | a0005 | c0006 | t0002 | g0226 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18950 | hp1 | a0001 | c0001 | t0005 | g0066 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18962 | hp1 | a0001 | c0001 | t0005 | g0061 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18963 | hp1 | a0001 | c0001 | t0025 | g0185 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18963 | hp2 | a0001 | c0001 | t0007 | g0042 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18966 | hp2 | a0001 | c0001 | t0014 | g0086 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18974 | hp1 | a0001 | c0001 | t0029 | g0145 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18983 | hp2 | a0001 | c0001 | t0005 | g0055 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18994 | hp1 | a0001 | c0001 | t0005 | g0062 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19000 | hp1 | a0001 | c0001 | t0005 | g0044 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19043 | hp1 | a0001 | c0001 | t0019 | g0239 | AFR | LWK | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19043 | hp2 | a0001 | c0001 | t0011 | g0053 | AFR | LWK | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19054 | hp1 | a0001 | c0001 | t0028 | g0151 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19054 | hp2 | a0001 | c0001 | t0007 | g0039 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19056 | hp2 | a0001 | c0001 | t0005 | g0045 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19068 | hp2 | a0001 | c0001 | t0007 | g0035 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19074 | hp1 | a0001 | c0001 | t0007 | g0064 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19074 | hp2 | a0001 | c0010 | t0001 | g0150 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19082 | hp1 | a0001 | c0001 | t0004 | g0182 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19085 | hp1 | a0001 | c0001 | t0007 | g0036 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19087 | hp1 | a0001 | c0001 | t0005 | g0029 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19089 | hp1 | a0001 | c0001 | t0005 | g0040 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19089 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19091 | hp1 | a0001 | c0001 | t0007 | g0135 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0118 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0008 | AFR | ASW | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA20129 | hp2 | a0001 | c0001 | t0023 | g0022 | AFR | ASW | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0221 | EUR | TSI | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA20805 | hp2 | a0001 | c0001 | t0009 | g0250 | EUR | TSI | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02109 | hp1 | a0001 | c0001 | t0011 | g0047 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0004 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0176 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0038 | AFR | ACB | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0204 | AFR | MSL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0167 | AFR | MSL | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | USA | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| HG06807 | hp2 | a0001 | c0001 | t0010 | g0171 | AFR | USA | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0205 | EAS | JPT | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0240 | AFR | USA | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0202 | AFR | USA | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0105 | AFR | LWK | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | LWK | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0007 | g0050 | REF | REF | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| homoSapiens_grch38 | hp1 | a0001 | c0004 | t0022 | g0155 | REF | REF | MARK4_chr19_45246271_45310284 | MARK4 | chr19 | 45246271 | 45310284 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:45297684
|
C | G | 1 | a0002 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.1607C>G | p.Thr536Ser | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/17 | 1925/5151 | 1607/2259 | 536/752 | chr19 | 45297684 | ||
| chr19:45297807
|
G | A | 1 | a0003 | 1 | HG03491.hp2 | missense_variant | MODERATE | c.1730G>A | p.Arg577Gln | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/17 | 2048/5151 | 1730/2259 | 577/752 | chr19 | 45297807 | ||
| chr19:45297893
|
G | A | 1 | a0005 | 1 | NA18942.hp2 | missense_variant | MODERATE | c.1816G>A | p.Ala606Thr | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/17 | 2134/5151 | 1816/2259 | 606/752 | chr19 | 45297893 | ||
| chr19:45302385
|
C | T | 1 | a0004 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.1934C>T | p.Pro645Leu | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 2252/5151 | 1934/2259 | 645/752 | chr19 | 45302385 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:45271582
|
A | G | 1 | a0002c0011 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.660A>G | p.Pro220Pro | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/17 | 978/5151 | 660/2259 | 220/752 | chr19 | 45271582 | ||
| chr19:45271600
|
G | A | 1 | a0001c0002 | 7 | HG01074.hp1 HG02145.hp1 HG02258.hp1 others(4): Show |
synonymous_variant | LOW | c.678G>A | p.Leu226Leu | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/17 | 996/5151 | 678/2259 | 226/752 | chr19 | 45271600 | ||
| chr19:45277928
|
G | C | 1 | a0001c0003 | 2 | HG03490.hp2 HG04228.hp1 |
synonymous_variant | LOW | c.792G>C | p.Leu264Leu | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 9/17 | 1110/5151 | 792/2259 | 264/752 | chr19 | 45277928 | ||
| chr19:45280589
|
G | T | 1 | a0001c0010 | 1 | NA19074.hp2 | synonymous_variant | LOW | c.1131G>T | p.Arg377Arg | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/17 | 1449/5151 | 1131/2259 | 377/752 | chr19 | 45280589 | ||
| chr19:45287553
|
C | T | 1 | a0001c0009 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.1383C>T | p.Thr461Thr | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/17 | 1701/5151 | 1383/2259 | 461/752 | chr19 | 45287553 | ||
| chr19:45294420
|
C | T | 1 | a0001c0008 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.1566C>T | p.Arg522Arg | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/17 | 1884/5151 | 1566/2259 | 522/752 | chr19 | 45294420 | ||
| chr19:45297760
|
T | C | 10 | a0001c0001a0001c0002a0001c0003others(7): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
synonymous_variant | LOW | c.1683T>C | p.Arg561Arg | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/17 | 2001/5151 | 1683/2259 | 561/752 | chr19 | 45297760 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:45251300
|
T | TCCG | 2 | a0001c0001t0013a0001c0001t0023 | 3 | HG01884.hp1 NA18906.hp2 NA20129.hp2 |
5_prime_UTR_variant | MODIFIER | c.-281_-279dupCGC | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/17 | 278 | INFO_REALIGN_3_PRIME | chr19 | 45251300 | ||||
| chr19:45251311
|
T | C | 47 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(44): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-278T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/17 | chr19 | 45251311 | ||||||
| chr19:45251363
|
G | A | 1 | a0001c0001t0024 | 1 | HG00323.hp1 | 5_prime_UTR_variant | MODIFIER | c.-226G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/17 | 226 | chr19 | 45251363 | |||||
| chr19:45251386
|
C | G | 3 | a0001c0002t0012a0001c0002t0021a0001c0002t0039 | 7 | HG01074.hp1 HG02145.hp1 HG02258.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-203C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/17 | 203 | chr19 | 45251386 | |||||
| chr19:45251545
|
G | C | 3 | a0001c0001t0014a0001c0001t0025a0001c0001t0026 | 4 | HG02602.hp2 HG02897.hp2 NA18963.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-44G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/17 | 44 | chr19 | 45251545 | |||||
| chr19:45251545
|
G | GC | 15 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(12): Show | 82 | HG00140.hp2 HG00735.hp1 HG00735.hp2 others(79): Show |
5_prime_UTR_variant | MODIFIER | c.-36dupC | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/17 | 35 | INFO_REALIGN_3_PRIME | chr19 | 45251545 | ||||
| chr19:45302904
|
CG | C | 3 | a0001c0001t0008a0001c0001t0009a0001c0001t0027 | 20 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*200delG | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 200 | INFO_REALIGN_3_PRIME | chr19 | 45302904 | ||||
| chr19:45303264
|
C | T | 3 | a0001c0001t0034a0001c0001t0035a0001c0001t0038 | 3 | HG01099.hp1 HG02895.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*554C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 554 | chr19 | 45303264 | |||||
| chr19:45303351
|
A | G | 36 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(33): Show | 173 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*641A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 641 | chr19 | 45303351 | |||||
| chr19:45303467
|
C | T | 3 | a0001c0001t0019a0001c0001t0020a0001c0001t0026 | 5 | HG02647.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*757C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 757 | chr19 | 45303467 | |||||
| chr19:45303539
|
G | A | 2 | a0001c0001t0015a0001c0001t0036 | 3 | HG00099.hp2 HG01106.hp2 HG01192.hp1 |
3_prime_UTR_variant | MODIFIER | c.*829G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 829 | chr19 | 45303539 | |||||
| chr19:45303643
|
C | A | 1 | a0001c0001t0030 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*933C>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 933 | chr19 | 45303643 | |||||
| chr19:45303692
|
C | G | 1 | a0001c0001t0033 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*982C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 982 | chr19 | 45303692 | |||||
| chr19:45303728
|
CTCTG | C | 1 | a0001c0001t0011 | 6 | HG02109.hp1 HG02809.hp1 HG03041.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1024_*1027delCTGT | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 1024 | INFO_REALIGN_3_PRIME | chr19 | 45303728 | ||||
| chr19:45303901
|
C | G | 1 | a0001c0001t0011 | 6 | HG02109.hp1 HG02809.hp1 HG03041.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1191C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 1191 | chr19 | 45303901 | |||||
| chr19:45303968
|
C | T | 1 | a0001c0001t0032 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1258C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 1258 | chr19 | 45303968 | |||||
| chr19:45304130
|
G | A | 1 | a0001c0001t0017 | 2 | HG00280.hp1 HG01192.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1420G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 1420 | chr19 | 45304130 | |||||
| chr19:45304470
|
C | T | 1 | a0001c0001t0031 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1760C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 1760 | chr19 | 45304470 | |||||
| chr19:45304577
|
A | T | 1 | a0001c0002t0039 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1867A>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 1867 | chr19 | 45304577 | |||||
| chr19:45304588
|
C | G | 1 | a0001c0001t0031 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1878C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 1878 | chr19 | 45304588 | |||||
| chr19:45304673
|
T | C | 14 | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(11): Show | 87 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*1963T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 1963 | chr19 | 45304673 | |||||
| chr19:45304687
|
G | A | 3 | a0001c0001t0005a0001c0001t0007a0001c0001t0024 | 34 | HG00323.hp1 HG00323.hp2 HG00609.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1977G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 1977 | chr19 | 45304687 | |||||
| chr19:45304860
|
T | A | 1 | a0001c0001t0027 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2150T>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 2150 | chr19 | 45304860 | |||||
| chr19:45304884
|
T | C | 1 | a0001c0001t0028 | 1 | NA19054.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2174T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 2174 | chr19 | 45304884 | |||||
| chr19:45304884
|
T | G | 35 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(32): Show | 172 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
3_prime_UTR_variant | MODIFIER | c.*2174T>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 2174 | chr19 | 45304884 | |||||
| chr19:45305171
|
A | C | 1 | a0001c0001t0029 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2461A>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 17/17 | 2461 | chr19 | 45305171 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:45251732
|
C | T | 1 | a0001c0001t0002g0259 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.51+93C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45251732 | ||||||
| chr19:45251757
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.51+118C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45251757 | ||||||
| chr19:45252034
|
C | T | 1 | a0001c0001t0009g0257 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.51+395C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45252034 | ||||||
| chr19:45252110
|
G | T | 19 | a0001c0001t0001g0252a0001c0001t0002g0240a0001c0001t0008g0243others(16): Show | 19 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.51+471G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45252110 | ||||||
| chr19:45252203
|
G | A | 1 | a0001c0001t0011g0002 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.51+564G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45252203 | ||||||
| chr19:45252374
|
T | C | 25 | a0001c0001t0002g0001a0001c0001t0004g0001a0001c0001t0006g0003others(22): Show | 25 | HG01074.hp1 HG01884.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.51+735T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45252374 | ||||||
| chr19:45252449
|
G | A | 1 | a0001c0001t0031g0026 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.51+810G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45252449 | ||||||
| chr19:45252948
|
T | C | 1 | a0001c0001t0019g0239 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.51+1309T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45252948 | ||||||
| chr19:45252997
|
C | T | 2 | a0001c0001t0018g0024a0001c0001t0018g0025 | 2 | HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.51+1358C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45252997 | ||||||
| chr19:45253033
|
A | G | 5 | a0001c0001t0002g0237a0001c0001t0002g0238a0001c0001t0004g0234others(2): Show | 5 | HG02145.hp2 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.51+1394A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45253033 | ||||||
| chr19:45253118
|
G | C | 82 | a0001c0001t0001g0028a0001c0001t0001g0065a0001c0001t0001g0069others(79): Show | 82 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.51+1479G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45253118 | ||||||
| chr19:45253178
|
G | A | 2 | a0001c0001t0003g0076a0001c0001t0009g0075 | 2 | HG00140.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.51+1539G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45253178 | ||||||
| chr19:45253190
|
C | G | 1 | a0001c0001t0001g0233 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.51+1551C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45253190 | ||||||
| chr19:45253191
|
A | C | 64 | a0001c0001t0001g0028a0001c0001t0001g0065a0001c0001t0001g0069others(61): Show | 64 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.51+1552A>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45253191 | ||||||
| chr19:45253192
|
C | CA | 52 | a0001c0001t0001g0028a0001c0001t0001g0065a0001c0001t0001g0069others(49): Show | 52 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.51+1554dupA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr19 | 45253192 | |||||
| chr19:45253192
|
C | CCA | 8 | a0001c0001t0005g0071a0001c0001t0005g0072a0001c0001t0005g0073others(5): Show | 8 | HG01109.hp2 HG01167.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.51+1553_51+1554ins others(2): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45253192 | ||||||
| chr19:45253193
|
AC | A | 3 | a0001c0001t0018g0024a0001c0001t0018g0025a0001c0001t0034g0012 | 3 | HG03041.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.51+1555delC | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45253193 | ||||||
| chr19:45253236
|
C | T | 5 | a0001c0001t0006g0007a0001c0001t0006g0008a0001c0001t0006g0009others(2): Show | 5 | HG01884.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.51+1597C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45253236 | ||||||
| chr19:45253298
|
T | G | 1 | a0001c0001t0002g0077 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.51+1659T>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45253298 | ||||||
| chr19:45253495
|
A | G | 63 | a0001c0001t0001g0028a0001c0001t0001g0065a0001c0001t0001g0069others(60): Show | 63 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.51+1856A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45253495 | ||||||
| chr19:45253505
|
C | T | 63 | a0001c0001t0001g0028a0001c0001t0001g0065a0001c0001t0001g0069others(60): Show | 63 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.51+1866C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45253505 | ||||||
| chr19:45253856
|
G | A | 4 | a0001c0001t0001g0080a0001c0001t0003g0078a0001c0001t0003g0079others(1): Show | 4 | HG02080.hp1 HG02135.hp2 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+2217G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45253856 | ||||||
| chr19:45254117
|
T | G | 1 | a0001c0001t0006g0082 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.51+2478T>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45254117 | ||||||
| chr19:45254139
|
C | T | 3 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0008g0068 | 3 | HG01081.hp1 HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.51+2500C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45254139 | ||||||
| chr19:45254192
|
G | A | 1 | a0001c0001t0002g0083 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.51+2553G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45254192 | ||||||
| chr19:45254215
|
G | A | 1 | a0001c0001t0034g0012 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.51+2576G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45254215 | ||||||
| chr19:45254754
|
A | G | 1 | a0001c0001t0003g0231 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.51+3115A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45254754 | ||||||
| chr19:45255030
|
A | G | 1 | a0001c0001t0002g0230 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.51+3391A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45255030 | ||||||
| chr19:45255106
|
A | G | 169 | a0001c0001t0001g0028a0001c0001t0001g0065a0001c0001t0001g0069others(166): Show | 169 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.51+3467A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45255106 | ||||||
| chr19:45255180
|
G | A | 60 | a0001c0001t0001g0028a0001c0001t0001g0065a0001c0001t0001g0069others(57): Show | 60 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.51+3541G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45255180 | ||||||
| chr19:45255202
|
C | CA | 6 | a0001c0001t0001g0084a0001c0001t0002g0164a0001c0001t0006g0003others(3): Show | 6 | HG01358.hp1 HG01891.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.51+3577dupA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr19 | 45255202 | |||||
| chr19:45255336
|
A | G | 96 | a0001c0001t0001g0028a0001c0001t0001g0065a0001c0001t0001g0069others(93): Show | 96 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.52-3653A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45255336 | ||||||
| chr19:45255342
|
C | G | 1 | a0001c0001t0001g0163 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.52-3647C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45255342 | ||||||
| chr19:45255413
|
T | C | 1 | a0001c0008t0006g0165 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.52-3576T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45255413 | ||||||
| chr19:45255433
|
C | T | 1 | a0001c0001t0003g0162 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.52-3556C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45255433 | ||||||
| chr19:45255559
|
C | CA | 70 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(67): Show | 70 | HG00642.hp1 HG01071.hp1 HG01081.hp1 others(67): Show |
intron_variant | MODIFIER | c.52-3406dupA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr19 | 45255559 | |||||
| chr19:45255559
|
C | CAA | 10 | a0001c0001t0001g0084a0001c0001t0001g0087a0001c0001t0002g0077others(7): Show | 10 | HG00408.hp2 HG00642.hp2 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.52-3407_52-3406dup others(2): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr19 | 45255559 | |||||
| chr19:45255559
|
CA | C | 15 | a0001c0001t0001g0159a0001c0001t0002g0001a0001c0001t0002g0222others(12): Show | 15 | HG01192.hp1 HG02602.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.52-3406delA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr19 | 45255559 | |||||
| chr19:45255559
|
CAAAAAAA others(4): Show |
C | 17 | a0001c0001t0001g0252a0001c0001t0008g0243a0001c0001t0008g0246others(14): Show | 17 | HG00280.hp2 HG00639.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.52-3416_52-3406del others(11): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr19 | 45255559 | |||||
| chr19:45255613
|
G | A | 2 | a0001c0001t0018g0024a0001c0001t0018g0025 | 2 | HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.52-3376G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45255613 | ||||||
| chr19:45255798
|
C | T | 2 | a0001c0001t0006g0007a0001c0001t0006g0011 | 2 | HG01884.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.52-3191C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45255798 | ||||||
| chr19:45255822
|
C | A | 2 | a0001c0001t0006g0003a0001c0001t0006g0004 | 2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.52-3167C>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45255822 | ||||||
| chr19:45255869
|
G | A | 3 | a0001c0001t0002g0001a0001c0001t0004g0001a0002c0011t0006g0006 | 3 | HG02615.hp2 HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.52-3120G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45255869 | ||||||
| chr19:45255897
|
G | GAC | 83 | a0001c0001t0001g0028a0001c0001t0001g0065a0001c0001t0001g0069others(80): Show | 83 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.52-3090_52-3089dup others(2): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr19 | 45255897 | |||||
| chr19:45256086
|
G | A | 83 | a0001c0001t0001g0028a0001c0001t0001g0065a0001c0001t0001g0069others(80): Show | 83 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.52-2903G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45256086 | ||||||
| chr19:45256203
|
C | T | 2 | a0001c0001t0017g0228a0001c0001t0017g0229 | 2 | HG00280.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.52-2786C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45256203 | ||||||
| chr19:45256291
|
A | G | 86 | a0001c0001t0001g0028a0001c0001t0001g0065a0001c0001t0001g0069others(83): Show | 86 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.52-2698A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45256291 | ||||||
| chr19:45256342
|
G | A | 2 | a0001c0001t0017g0228a0001c0001t0017g0229 | 2 | HG00280.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.52-2647G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45256342 | ||||||
| chr19:45256352
|
C | T | 2 | a0001c0001t0006g0003a0001c0001t0006g0004 | 2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.52-2637C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45256352 | ||||||
| chr19:45256353
|
G | C | 51 | a0001c0001t0001g0028a0001c0001t0001g0065a0001c0001t0001g0069others(48): Show | 51 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.52-2636G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45256353 | ||||||
| chr19:45256384
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.52-2605G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45256384 | ||||||
| chr19:45256429
|
C | T | 1 | a0005c0006t0002g0226 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.52-2560C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45256429 | ||||||
| chr19:45256636
|
C | T | 1 | a0001c0001t0001g0221 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.52-2353C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45256636 | ||||||
| chr19:45256930
|
T | C | 1 | a0001c0001t0006g0008 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.52-2059T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45256930 | ||||||
| chr19:45256959
|
T | C | 2 | a0001c0001t0006g0003a0001c0001t0006g0004 | 2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.52-2030T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45256959 | ||||||
| chr19:45256960
|
CT | C | 17 | a0001c0001t0001g0189a0001c0001t0001g0221a0001c0001t0005g0040others(14): Show | 17 | HG01167.hp1 HG01169.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.52-2019delT | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr19 | 45256960 | |||||
| chr19:45257158
|
C | T | 1 | a0001c0001t0006g0174 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.52-1831C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45257158 | ||||||
| chr19:45257162
|
T | C | 4 | a0001c0001t0019g0175a0001c0001t0020g0191a0001c0001t0020g0192others(1): Show | 4 | HG02647.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.52-1827T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45257162 | ||||||
| chr19:45257290
|
A | G | 48 | a0001c0001t0001g0028a0001c0001t0001g0065a0001c0001t0001g0069others(45): Show | 48 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.52-1699A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45257290 | ||||||
| chr19:45257352
|
G | A | 83 | a0001c0001t0001g0028a0001c0001t0001g0065a0001c0001t0001g0069others(80): Show | 83 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.52-1637G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45257352 | ||||||
| chr19:45257383
|
C | CT | 42 | a0001c0001t0001g0252a0001c0001t0002g0083a0001c0001t0002g0186others(39): Show | 42 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.52-1588dupT | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr19 | 45257383 | |||||
| chr19:45257383
|
C | CTT | 48 | a0001c0001t0001g0028a0001c0001t0001g0065a0001c0001t0001g0069others(45): Show | 48 | HG00408.hp1 HG00609.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.52-1589_52-1588dup others(2): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr19 | 45257383 | |||||
| chr19:45257383
|
CT | C | 43 | a0001c0001t0001g0087a0001c0001t0001g0089a0001c0001t0001g0090others(40): Show | 43 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(40): Show |
intron_variant | MODIFIER | c.52-1588delT | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr19 | 45257383 | |||||
| chr19:45257530
|
C | T | 1 | a0001c0001t0008g0254 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.52-1459C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45257530 | ||||||
| chr19:45257572
|
C | T | 1 | a0001c0001t0005g0067 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.52-1417C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45257572 | ||||||
| chr19:45257573
|
G | A | 6 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0112others(3): Show | 6 | HG01099.hp2 HG01255.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.52-1416G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45257573 | ||||||
| chr19:45257607
|
C | T | 2 | a0001c0001t0002g0001a0001c0001t0004g0001 | 2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.52-1382C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45257607 | ||||||
| chr19:45257662
|
C | T | 20 | a0001c0001t0001g0252a0001c0001t0002g0240a0001c0001t0008g0243others(17): Show | 20 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.52-1327C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45257662 | ||||||
| chr19:45257675
|
G | A | 83 | a0001c0001t0001g0028a0001c0001t0001g0065a0001c0001t0001g0069others(80): Show | 83 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.52-1314G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45257675 | ||||||
| chr19:45257688
|
TA | T | 23 | a0001c0001t0001g0252a0001c0001t0002g0240a0001c0001t0008g0243others(20): Show | 23 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.52-1300delA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45257688 | ||||||
| chr19:45257689
|
A | AT | 29 | a0001c0001t0001g0094a0001c0001t0001g0106a0001c0001t0002g0083others(26): Show | 29 | HG00738.hp1 HG02074.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.52-1282dupT | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr19 | 45257689 | |||||
| chr19:45257689
|
A | T | 1 | a0001c0001t0009g0027 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.52-1300A>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45257689 | ||||||
| chr19:45257689
|
AT | A | 6 | a0001c0001t0001g0159a0001c0001t0002g0195a0001c0001t0002g0196others(3): Show | 6 | HG01109.hp2 HG01891.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.52-1282delT | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr19 | 45257689 | |||||
| chr19:45257689
|
ATT | A | 57 | a0001c0001t0001g0028a0001c0001t0001g0065a0001c0001t0001g0069others(54): Show | 57 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.52-1283_52-1282del others(2): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr19 | 45257689 | |||||
| chr19:45257693
|
T | A | 1 | a0001c0001t0001g0028 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.52-1296T>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45257693 | ||||||
| chr19:45257720
|
C | T | 1 | a0001c0001t0006g0173 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.52-1269C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45257720 | ||||||
| chr19:45257753
|
G | C | 1 | a0001c0001t0002g0240 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.52-1236G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45257753 | ||||||
| chr19:45257835
|
G | A | 2 | a0001c0001t0005g0044a0001c0001t0010g0197 | 2 | HG01261.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.52-1154G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45257835 | ||||||
| chr19:45257958
|
G | C | 15 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0198others(12): Show | 15 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.52-1031G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45257958 | ||||||
| chr19:45257988
|
C | CT | 23 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0198others(20): Show | 23 | HG01433.hp1 HG01517.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.52-985dupT | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr19 | 45257988 | |||||
| chr19:45257988
|
CT | C | 25 | a0001c0001t0001g0252a0001c0001t0002g0240a0001c0001t0005g0045others(22): Show | 25 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.52-985delT | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr19 | 45257988 | |||||
| chr19:45258103
|
A | T | 1 | a0001c0001t0005g0038 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.52-886A>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45258103 | ||||||
| chr19:45258179
|
T | G | 82 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(79): Show | 82 | HG00280.hp2 HG00323.hp2 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.52-810T>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45258179 | ||||||
| chr19:45258199
|
C | T | 3 | a0001c0001t0002g0001a0001c0001t0004g0001a0002c0011t0006g0006 | 3 | HG02615.hp2 HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.52-790C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45258199 | ||||||
| chr19:45258231
|
C | T | 2 | a0001c0001t0017g0228a0001c0001t0017g0229 | 2 | HG00280.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.52-758C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45258231 | ||||||
| chr19:45258235
|
T | A | 82 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(79): Show | 82 | HG00280.hp2 HG00323.hp2 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.52-754T>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45258235 | ||||||
| chr19:45258321
|
A | G | 1 | a0001c0001t0003g0108 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.52-668A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45258321 | ||||||
| chr19:45258368
|
G | A | 1 | a0001c0001t0005g0046 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.52-621G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45258368 | ||||||
| chr19:45258478
|
A | G | 82 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(79): Show | 82 | HG00280.hp2 HG00323.hp2 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.52-511A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45258478 | ||||||
| chr19:45258493
|
G | A | 82 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(79): Show | 82 | HG00280.hp2 HG00323.hp2 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.52-496G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45258493 | ||||||
| chr19:45258831
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.52-158T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 1/16 | chr19 | 45258831 | ||||||
| chr19:45259245
|
G | A | 3 | a0001c0001t0018g0024a0001c0001t0018g0025a0001c0001t0034g0012 | 3 | HG03041.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.252+56G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45259245 | ||||||
| chr19:45259245
|
G | T | 1 | a0001c0001t0001g0094 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.252+56G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45259245 | ||||||
| chr19:45259360
|
A | G | 82 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(79): Show | 82 | HG00280.hp2 HG00323.hp2 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.252+171A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45259360 | ||||||
| chr19:45259383
|
T | C | 87 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(84): Show | 87 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.252+194T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45259383 | ||||||
| chr19:45259434
|
G | A | 1 | a0001c0008t0006g0165 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.252+245G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45259434 | ||||||
| chr19:45259436
|
G | A | 51 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(48): Show | 51 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.252+247G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45259436 | ||||||
| chr19:45259490
|
A | G | 1 | a0001c0001t0004g0234 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.252+301A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45259490 | ||||||
| chr19:45259501
|
C | T | 5 | a0001c0001t0006g0007a0001c0001t0006g0008a0001c0001t0006g0009others(2): Show | 5 | HG01884.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.252+312C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45259501 | ||||||
| chr19:45259628
|
A | G | 20 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0112others(17): Show | 20 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.252+439A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45259628 | ||||||
| chr19:45259689
|
C | T | 2 | a0001c0001t0017g0228a0001c0001t0017g0229 | 2 | HG00280.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.252+500C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45259689 | ||||||
| chr19:45259715
|
C | T | 1 | a0001c0001t0015g0037 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.252+526C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45259715 | ||||||
| chr19:45259885
|
G | A | 1 | a0001c0001t0010g0197 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.252+696G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45259885 | ||||||
| chr19:45259923
|
T | C | 87 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(84): Show | 87 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.252+734T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45259923 | ||||||
| chr19:45260053
|
C | T | 1 | a0001c0001t0010g0197 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.252+864C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45260053 | ||||||
| chr19:45260246
|
T | C | 51 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(48): Show | 51 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.252+1057T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45260246 | ||||||
| chr19:45260360
|
G | A | 82 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(79): Show | 82 | HG00280.hp2 HG00323.hp2 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.252+1171G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45260360 | ||||||
| chr19:45260389
|
C | CA | 82 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(79): Show | 82 | HG00280.hp2 HG00323.hp2 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.252+1218dupA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr19 | 45260389 | |||||
| chr19:45260413
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.252+1224C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45260413 | ||||||
| chr19:45260540
|
T | A | 2 | a0001c0001t0003g0078a0001c0001t0003g0079 | 2 | HG02080.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.252+1351T>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45260540 | ||||||
| chr19:45260542
|
C | CTGAAAAA | 3 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0032g0005 | 3 | HG01891.hp1 HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.252+1353_252+1354i others(9): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45260542 | ||||||
| chr19:45260636
|
G | A | 2 | a0001c0001t0006g0187a0001c0001t0006g0188 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.252+1447G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45260636 | ||||||
| chr19:45260678
|
C | G | 1 | a0001c0001t0032g0005 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.252+1489C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45260678 | ||||||
| chr19:45260692
|
C | G | 5 | a0001c0001t0006g0007a0001c0001t0006g0008a0001c0001t0006g0009others(2): Show | 5 | HG01884.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.252+1503C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45260692 | ||||||
| chr19:45260697
|
AAAATAAA others(1): Show |
A | 82 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(79): Show | 82 | HG00280.hp2 HG00323.hp2 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.252+1526_252+1533d others(10): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr19 | 45260697 | |||||
| chr19:45261056
|
C | A | 1 | a0001c0001t0001g0233 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.252+1867C>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45261056 | ||||||
| chr19:45261093
|
C | G | 1 | a0001c0001t0002g0204 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.252+1904C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45261093 | ||||||
| chr19:45261396
|
C | T | 1 | a0001c0001t0006g0227 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.253-1717C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45261396 | ||||||
| chr19:45261542
|
C | T | 1 | a0001c0001t0001g0084 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.253-1571C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45261542 | ||||||
| chr19:45261662
|
G | A | 1 | a0001c0001t0003g0114 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.253-1451G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45261662 | ||||||
| chr19:45261794
|
A | G | 97 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(94): Show | 97 | HG00280.hp2 HG00323.hp2 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.253-1319A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45261794 | ||||||
| chr19:45261874
|
G | A | 1 | a0001c0001t0003g0132 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.253-1239G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45261874 | ||||||
| chr19:45261887
|
T | C | 97 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(94): Show | 97 | HG00280.hp2 HG00323.hp2 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.253-1226T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45261887 | ||||||
| chr19:45261933
|
CA | C | 39 | a0001c0001t0001g0189a0001c0001t0001g0221a0001c0001t0001g0252others(36): Show | 39 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.253-1167delA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr19 | 45261933 | |||||
| chr19:45262037
|
T | A | 1 | a0001c0001t0002g0164 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.253-1076T>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45262037 | ||||||
| chr19:45262050
|
C | T | 1 | a0001c0001t0010g0197 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.253-1063C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45262050 | ||||||
| chr19:45262074
|
C | G | 2 | a0001c0001t0006g0003a0001c0001t0006g0004 | 2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.253-1039C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45262074 | ||||||
| chr19:45262140
|
C | T | 1 | a0001c0001t0003g0211 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.253-973C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45262140 | ||||||
| chr19:45262197
|
T | C | 3 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0032g0005 | 3 | HG01891.hp1 HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.253-916T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45262197 | ||||||
| chr19:45262298
|
A | C | 1 | a0001c0001t0005g0040 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.253-815A>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45262298 | ||||||
| chr19:45262299
|
C | G | 2 | a0001c0001t0017g0228a0001c0001t0017g0229 | 2 | HG00280.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.253-814C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45262299 | ||||||
| chr19:45262299
|
C | T | 1 | a0001c0001t0005g0040 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.253-814C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45262299 | ||||||
| chr19:45262353
|
C | CG | 24 | a0001c0001t0001g0065a0001c0001t0001g0089a0001c0001t0001g0109others(21): Show | 24 | HG00408.hp1 HG00609.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.253-753dupG | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr19 | 45262353 | |||||
| chr19:45262449
|
A | G | 2 | a0001c0001t0017g0228a0001c0001t0017g0229 | 2 | HG00280.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.253-664A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45262449 | ||||||
| chr19:45262584
|
A | G | 1 | a0001c0001t0032g0005 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.253-529A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45262584 | ||||||
| chr19:45262741
|
C | T | 59 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(56): Show | 59 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.253-372C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45262741 | ||||||
| chr19:45262791
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.253-322G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45262791 | ||||||
| chr19:45262868
|
G | A | 1 | a0001c0001t0003g0095 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.253-245G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45262868 | ||||||
| chr19:45262964
|
C | T | 1 | a0001c0001t0008g0113 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.253-149C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45262964 | ||||||
| chr19:45263010
|
C | G | 4 | a0001c0001t0005g0029a0001c0001t0005g0044a0001c0001t0007g0036others(1): Show | 4 | NA19000.hp1 NA19074.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.253-103C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45263010 | ||||||
| chr19:45263011
|
C | G | 4 | a0001c0001t0005g0029a0001c0001t0005g0044a0001c0001t0007g0036others(1): Show | 4 | NA19000.hp1 NA19074.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.253-102C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45263011 | ||||||
| chr19:45263012
|
G | A | 3 | a0001c0001t0018g0024a0001c0001t0018g0025a0001c0001t0034g0012 | 3 | HG03041.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.253-101G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 2/16 | chr19 | 45263012 | ||||||
| chr19:45263177
|
G | T | 1 | a0001c0001t0002g0230 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.306+11G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 3/16 | chr19 | 45263177 | ||||||
| chr19:45263249
|
C | T | 2 | a0001c0001t0005g0062a0001c0001t0007g0035 | 2 | NA18994.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.307-70C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 3/16 | chr19 | 45263249 | ||||||
| chr19:45263267
|
C | T | 5 | a0001c0001t0006g0007a0001c0001t0006g0008a0001c0001t0006g0009others(2): Show | 5 | HG01884.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.307-52C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 3/16 | chr19 | 45263267 | ||||||
| chr19:45263468
|
G | A | 1 | a0001c0001t0014g0081 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.355+101G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 4/16 | chr19 | 45263468 | ||||||
| chr19:45263471
|
G | A | 20 | a0001c0001t0001g0252a0001c0001t0002g0240a0001c0001t0008g0085others(17): Show | 20 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.355+104G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 4/16 | chr19 | 45263471 | ||||||
| chr19:45263634
|
C | T | 3 | a0001c0001t0002g0001a0001c0001t0004g0001a0002c0011t0006g0006 | 3 | HG02615.hp2 HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.355+267C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 4/16 | chr19 | 45263634 | ||||||
| chr19:45263741
|
CA | C | 6 | a0001c0001t0001g0089a0001c0001t0001g0221a0001c0001t0002g0203others(3): Show | 6 | HG01167.hp1 HG01361.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.355+390delA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr19 | 45263741 | |||||
| chr19:45263956
|
G | A | 100 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(97): Show | 100 | HG00280.hp2 HG00323.hp2 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.355+589G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 4/16 | chr19 | 45263956 | ||||||
| chr19:45264037
|
G | A | 1 | a0001c0001t0009g0244 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.356-647G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 4/16 | chr19 | 45264037 | ||||||
| chr19:45264119
|
G | A | 1 | a0001c0001t0002g0259 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.356-565G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 4/16 | chr19 | 45264119 | ||||||
| chr19:45264146
|
C | T | 1 | a0001c0001t0003g0078 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.356-538C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 4/16 | chr19 | 45264146 | ||||||
| chr19:45264177
|
C | T | 1 | a0001c0001t0004g0220 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.356-507C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 4/16 | chr19 | 45264177 | ||||||
| chr19:45264281
|
G | C | 64 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(61): Show | 64 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.356-403G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 4/16 | chr19 | 45264281 | ||||||
| chr19:45264288
|
G | A | 3 | a0001c0001t0018g0024a0001c0001t0018g0025a0001c0001t0034g0012 | 3 | HG03041.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.356-396G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 4/16 | chr19 | 45264288 | ||||||
| chr19:45264290
|
T | C | 2 | a0001c0001t0002g0195a0001c0001t0002g0196 | 2 | HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.356-394T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 4/16 | chr19 | 45264290 | ||||||
| chr19:45264490
|
C | CA | 41 | a0001c0001t0001g0065a0001c0001t0001g0080a0001c0001t0001g0084others(38): Show | 41 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(38): Show |
intron_variant | MODIFIER | c.356-182dupA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr19 | 45264490 | |||||
| chr19:45264612
|
G | T | 5 | a0001c0001t0010g0197a0001c0001t0019g0175a0001c0001t0020g0191others(2): Show | 5 | HG01261.hp1 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.356-72G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 4/16 | chr19 | 45264612 | ||||||
| chr19:45265110
|
C | T | 2 | a0001c0001t0023g0022a0001c0001t0032g0005 | 2 | HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.492+200C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 6/16 | chr19 | 45265110 | ||||||
| chr19:45265113
|
T | A | 1 | a0001c0001t0009g0245 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.492+203T>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 6/16 | chr19 | 45265113 | ||||||
| chr19:45265145
|
C | T | 1 | a0001c0001t0005g0061 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.492+235C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 6/16 | chr19 | 45265145 | ||||||
| chr19:45265203
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.492+293G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 6/16 | chr19 | 45265203 | ||||||
| chr19:45265213
|
TGGG | T | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0024others(2): Show | 5 | HG01891.hp1 HG02109.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.492+306_492+308del others(3): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr19 | 45265213 | |||||
| chr19:45265218
|
G | A | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0024others(2): Show | 5 | HG01891.hp1 HG02109.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.492+308G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 6/16 | chr19 | 45265218 | ||||||
| chr19:45265428
|
G | A | 1 | a0001c0001t0031g0026 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.492+518G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 6/16 | chr19 | 45265428 | ||||||
| chr19:45265604
|
T | TATGTGCA others(193): Show |
1 | a0001c0001t0003g0099 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.493-599_493-400dup others(200): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr19 | 45265604 | |||||
| chr19:45265688
|
T | C | 61 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(58): Show | 61 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.493-537T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 6/16 | chr19 | 45265688 | ||||||
| chr19:45265784
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.493-441C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 6/16 | chr19 | 45265784 | ||||||
| chr19:45265884
|
T | C | 1 | a0001c0001t0004g0184 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.493-341T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 6/16 | chr19 | 45265884 | ||||||
| chr19:45265886
|
C | T | 1 | a0001c0001t0004g0184 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.493-339C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 6/16 | chr19 | 45265886 | ||||||
| chr19:45265897
|
G | C | 1 | a0001c0001t0004g0184 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.493-328G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 6/16 | chr19 | 45265897 | ||||||
| chr19:45265923
|
G | A | 55 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(52): Show | 55 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.493-302G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 6/16 | chr19 | 45265923 | ||||||
| chr19:45265961
|
G | A | 5 | a0001c0001t0006g0007a0001c0001t0006g0008a0001c0001t0006g0009others(2): Show | 5 | HG01884.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.493-264G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 6/16 | chr19 | 45265961 | ||||||
| chr19:45266043
|
A | G | 70 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(67): Show | 70 | HG00280.hp1 HG00323.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.493-182A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 6/16 | chr19 | 45266043 | ||||||
| chr19:45266066
|
G | T | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0024others(2): Show | 5 | HG01891.hp1 HG02109.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.493-159G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 6/16 | chr19 | 45266066 | ||||||
| chr19:45266128
|
G | C | 55 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(52): Show | 55 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.493-97G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 6/16 | chr19 | 45266128 | ||||||
| chr19:45266317
|
G | A | 70 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(67): Show | 70 | HG00280.hp1 HG00323.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.549+36G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45266317 | ||||||
| chr19:45266484
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.549+203G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45266484 | ||||||
| chr19:45266488
|
G | C | 1 | a0001c0001t0014g0086 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.549+207G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45266488 | ||||||
| chr19:45266491
|
G | A | 93 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(90): Show | 93 | HG00280.hp1 HG00323.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.549+210G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45266491 | ||||||
| chr19:45266511
|
A | G | 1 | a0001c0001t0025g0185 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.549+230A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45266511 | ||||||
| chr19:45266603
|
G | A | 1 | a0001c0001t0004g0214 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.549+322G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45266603 | ||||||
| chr19:45266730
|
C | CT | 73 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(70): Show | 73 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.549+469dupT | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr19 | 45266730 | |||||
| chr19:45266730
|
C | CTT | 6 | a0001c0001t0005g0038a0001c0001t0005g0044a0001c0001t0005g0067others(3): Show | 6 | HG00738.hp2 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.549+468_549+469dup others(2): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr19 | 45266730 | |||||
| chr19:45266730
|
CT | C | 5 | a0001c0001t0001g0221a0001c0001t0003g0136a0001c0001t0004g0234others(2): Show | 5 | HG01074.hp1 HG02145.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.549+469delT | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr19 | 45266730 | |||||
| chr19:45266796
|
G | A | 2 | a0001c0001t0002g0001a0001c0001t0004g0001 | 2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.549+515G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45266796 | ||||||
| chr19:45266802
|
C | G | 7 | a0001c0002t0012g0014a0001c0002t0012g0015a0001c0002t0012g0017others(4): Show | 7 | HG01074.hp1 HG02145.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.549+521C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45266802 | ||||||
| chr19:45266819
|
G | T | 7 | a0001c0002t0012g0014a0001c0002t0012g0015a0001c0002t0012g0017others(4): Show | 7 | HG01074.hp1 HG02145.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.549+538G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45266819 | ||||||
| chr19:45266820
|
C | A | 7 | a0001c0002t0012g0014a0001c0002t0012g0015a0001c0002t0012g0017others(4): Show | 7 | HG01074.hp1 HG02145.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.549+539C>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45266820 | ||||||
| chr19:45266825
|
T | C | 7 | a0001c0002t0012g0014a0001c0002t0012g0015a0001c0002t0012g0017others(4): Show | 7 | HG01074.hp1 HG02145.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.549+544T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45266825 | ||||||
| chr19:45266893
|
C | T | 1 | a0001c0001t0004g0205 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.549+612C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45266893 | ||||||
| chr19:45266978
|
C | T | 1 | a0001c0001t0009g0244 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.549+697C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45266978 | ||||||
| chr19:45267008
|
A | G | 4 | a0001c0001t0019g0175a0001c0001t0020g0191a0001c0001t0020g0192others(1): Show | 4 | HG02647.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.549+727A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45267008 | ||||||
| chr19:45267042
|
G | C | 7 | a0001c0002t0012g0014a0001c0002t0012g0015a0001c0002t0012g0017others(4): Show | 7 | HG01074.hp1 HG02145.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.549+761G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45267042 | ||||||
| chr19:45267048
|
A | G | 56 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(53): Show | 56 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.549+767A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45267048 | ||||||
| chr19:45267179
|
C | T | 46 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(43): Show | 46 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.549+898C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45267179 | ||||||
| chr19:45267192
|
G | T | 2 | a0001c0001t0017g0228a0001c0001t0017g0229 | 2 | HG00280.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.549+911G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45267192 | ||||||
| chr19:45267256
|
C | T | 2 | a0001c0001t0001g0112a0001c0001t0008g0113 | 2 | HG01099.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.549+975C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45267256 | ||||||
| chr19:45267310
|
C | T | 1 | a0001c0008t0006g0165 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.549+1029C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45267310 | ||||||
| chr19:45267476
|
T | C | 1 | a0001c0001t0010g0049 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.549+1195T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45267476 | ||||||
| chr19:45267505
|
C | T | 7 | a0001c0001t0002g0001a0001c0001t0004g0001a0001c0001t0010g0197others(4): Show | 7 | HG01261.hp1 HG02615.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.549+1224C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45267505 | ||||||
| chr19:45267600
|
G | A | 1 | a0001c0001t0013g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.549+1319G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45267600 | ||||||
| chr19:45267835
|
G | GT | 46 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(43): Show | 46 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.549+1560dupT | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr19 | 45267835 | |||||
| chr19:45268009
|
T | C | 1 | a0001c0001t0006g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.549+1728T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45268009 | ||||||
| chr19:45268029
|
T | C | 48 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(45): Show | 48 | HG00280.hp1 HG00323.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.549+1748T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45268029 | ||||||
| chr19:45268300
|
A | G | 15 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0198others(12): Show | 15 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.549+2019A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45268300 | ||||||
| chr19:45268364
|
A | G | 1 | a0001c0001t0008g0251 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.549+2083A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45268364 | ||||||
| chr19:45268453
|
G | A | 1 | a0001c0001t0002g0225 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.549+2172G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45268453 | ||||||
| chr19:45268575
|
C | T | 1 | a0002c0011t0006g0006 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.549+2294C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45268575 | ||||||
| chr19:45268650
|
C | G | 1 | a0001c0001t0001g0093 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.549+2369C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45268650 | ||||||
| chr19:45268982
|
C | T | 48 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(45): Show | 48 | HG00280.hp1 HG00323.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.550-2490C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45268982 | ||||||
| chr19:45269059
|
G | A | 1 | a0001c0001t0002g0215 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.550-2413G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45269059 | ||||||
| chr19:45269269
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.550-2203C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45269269 | ||||||
| chr19:45269433
|
C | T | 46 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(43): Show | 46 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.550-2039C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45269433 | ||||||
| chr19:45269456
|
G | A | 1 | a0001c0001t0002g0206 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.550-2016G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45269456 | ||||||
| chr19:45269608
|
C | T | 2 | a0001c0001t0017g0228a0001c0001t0017g0229 | 2 | HG00280.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.550-1864C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45269608 | ||||||
| chr19:45269710
|
C | G | 45 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(42): Show | 45 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.550-1762C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45269710 | ||||||
| chr19:45269888
|
G | A | 4 | a0001c0001t0013g0020a0001c0001t0013g0021a0001c0001t0023g0022others(1): Show | 4 | HG01884.hp1 HG02818.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.550-1584G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45269888 | ||||||
| chr19:45269931
|
C | T | 1 | a0001c0001t0003g0114 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.550-1541C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45269931 | ||||||
| chr19:45270041
|
T | C | 1 | a0001c0001t0014g0081 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.550-1431T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45270041 | ||||||
| chr19:45270050
|
A | C | 1 | a0001c0001t0003g0231 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.550-1422A>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45270050 | ||||||
| chr19:45270090
|
A | G | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0024others(2): Show | 5 | HG01891.hp1 HG02109.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.550-1382A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45270090 | ||||||
| chr19:45270118
|
G | T | 2 | a0001c0001t0018g0024a0001c0001t0018g0025 | 2 | HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.550-1354G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45270118 | ||||||
| chr19:45270123
|
C | T | 46 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(43): Show | 46 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.550-1349C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45270123 | ||||||
| chr19:45270164
|
G | C | 5 | a0001c0001t0006g0007a0001c0001t0006g0008a0001c0001t0006g0009others(2): Show | 5 | HG01884.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.550-1308G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45270164 | ||||||
| chr19:45270216
|
C | T | 1 | a0001c0001t0006g0105 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.550-1256C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45270216 | ||||||
| chr19:45270641
|
T | C | 46 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(43): Show | 46 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.550-831T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45270641 | ||||||
| chr19:45270848
|
G | A | 3 | a0001c0001t0013g0020a0001c0001t0013g0021a0001c0001t0023g0022 | 3 | HG01884.hp1 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.550-624G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45270848 | ||||||
| chr19:45270895
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.550-577C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45270895 | ||||||
| chr19:45270896
|
G | A | 1 | a0001c0001t0003g0115 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.550-576G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45270896 | ||||||
| chr19:45270927
|
C | T | 1 | a0001c0002t0039g0019 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.550-545C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45270927 | ||||||
| chr19:45271098
|
G | T | 1 | a0001c0001t0032g0005 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.550-374G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45271098 | ||||||
| chr19:45271119
|
C | T | 46 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(43): Show | 46 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.550-353C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45271119 | ||||||
| chr19:45271210
|
C | A | 4 | a0001c0001t0019g0175a0001c0001t0020g0191a0001c0001t0020g0192others(1): Show | 4 | HG02647.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.550-262C>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45271210 | ||||||
| chr19:45271251
|
G | A | 2 | a0001c0001t0002g0001a0001c0001t0004g0001 | 2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.550-221G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45271251 | ||||||
| chr19:45271311
|
A | G | 1 | a0001c0001t0002g0186 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.550-161A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45271311 | ||||||
| chr19:45271422
|
A | G | 46 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(43): Show | 46 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.550-50A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 7/16 | chr19 | 45271422 | ||||||
| chr19:45271772
|
C | A | 1 | a0001c0003t0004g0216 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.786+64C>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45271772 | ||||||
| chr19:45271814
|
A | G | 2 | a0001c0001t0006g0003a0001c0001t0006g0004 | 2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.786+106A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45271814 | ||||||
| chr19:45272032
|
A | G | 3 | a0001c0001t0002g0001a0001c0001t0004g0001a0001c0001t0010g0197 | 3 | HG01261.hp1 HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.786+324A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45272032 | ||||||
| chr19:45272049
|
TG | T | 46 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(43): Show | 46 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.786+343delG | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr19 | 45272049 | |||||
| chr19:45272097
|
G | A | 258 | a0001c0001t0001g0028a0001c0001t0001g0065a0001c0001t0001g0069others(255): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.786+389G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45272097 | ||||||
| chr19:45272315
|
G | A | 2 | a0001c0001t0017g0228a0001c0001t0017g0229 | 2 | HG00280.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.786+607G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45272315 | ||||||
| chr19:45272331
|
C | T | 46 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(43): Show | 46 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.786+623C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45272331 | ||||||
| chr19:45272364
|
G | A | 5 | a0001c0001t0001g0100a0001c0001t0001g0104a0001c0001t0003g0101others(2): Show | 5 | HG00642.hp1 HG01109.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.786+656G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45272364 | ||||||
| chr19:45272431
|
C | T | 1 | a0001c0001t0003g0132 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.786+723C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45272431 | ||||||
| chr19:45272524
|
G | A | 2 | a0001c0001t0017g0228a0001c0001t0017g0229 | 2 | HG00280.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.786+816G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45272524 | ||||||
| chr19:45272606
|
T | A | 1 | a0001c0001t0007g0050 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.786+898T>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45272606 | ||||||
| chr19:45272650
|
G | A | 1 | a0001c0001t0027g0253 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.786+942G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45272650 | ||||||
| chr19:45272700
|
CA | C | 5 | a0001c0001t0006g0007a0001c0001t0006g0008a0001c0001t0006g0009others(2): Show | 5 | HG01884.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+994delA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr19 | 45272700 | |||||
| chr19:45272842
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.786+1134T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45272842 | ||||||
| chr19:45272875
|
G | A | 2 | a0001c0001t0002g0001a0001c0001t0004g0001 | 2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.786+1167G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45272875 | ||||||
| chr19:45272883
|
G | A | 1 | a0001c0001t0009g0245 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.786+1175G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45272883 | ||||||
| chr19:45272934
|
C | T | 3 | a0001c0002t0012g0014a0001c0002t0012g0017a0001c0002t0012g0018 | 3 | HG03130.hp2 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.786+1226C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45272934 | ||||||
| chr19:45273242
|
C | A | 3 | a0001c0001t0018g0024a0001c0001t0018g0025a0001c0001t0034g0012 | 3 | HG03041.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.786+1534C>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45273242 | ||||||
| chr19:45273250
|
T | G | 1 | a0001c0001t0018g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.786+1542T>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45273250 | ||||||
| chr19:45273317
|
G | A | 1 | a0001c0001t0003g0115 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.786+1609G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45273317 | ||||||
| chr19:45273323
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.786+1615T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45273323 | ||||||
| chr19:45273367
|
G | C | 14 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0017g0228others(11): Show | 14 | HG00280.hp1 HG01074.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.786+1659G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45273367 | ||||||
| chr19:45273369
|
G | C | 39 | a0001c0001t0001g0189a0001c0001t0001g0221a0001c0001t0006g0003others(36): Show | 39 | HG00280.hp1 HG01074.hp1 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.786+1661G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45273369 | ||||||
| chr19:45273519
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.786+1811T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45273519 | ||||||
| chr19:45273702
|
C | T | 1 | a0001c0001t0002g0206 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.786+1994C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45273702 | ||||||
| chr19:45273722
|
T | C | 45 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(42): Show | 45 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.786+2014T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45273722 | ||||||
| chr19:45273772
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.786+2064C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45273772 | ||||||
| chr19:45273843
|
C | G | 20 | a0001c0001t0001g0189a0001c0001t0001g0221a0001c0001t0006g0082others(17): Show | 20 | HG01167.hp1 HG01169.hp1 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.786+2135C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45273843 | ||||||
| chr19:45273973
|
G | C | 3 | a0001c0001t0018g0024a0001c0001t0018g0025a0001c0001t0034g0012 | 3 | HG03041.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.786+2265G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45273973 | ||||||
| chr19:45273987
|
C | T | 46 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(43): Show | 46 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.786+2279C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45273987 | ||||||
| chr19:45274010
|
G | T | 2 | a0001c0001t0017g0228a0001c0001t0017g0229 | 2 | HG00280.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.786+2302G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45274010 | ||||||
| chr19:45274044
|
G | T | 5 | a0001c0001t0006g0007a0001c0001t0006g0008a0001c0001t0006g0009others(2): Show | 5 | HG01884.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+2336G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45274044 | ||||||
| chr19:45274064
|
A | G | 15 | a0001c0001t0001g0189a0001c0001t0001g0221a0001c0001t0006g0082others(12): Show | 15 | HG01167.hp1 HG01169.hp1 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.786+2356A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45274064 | ||||||
| chr19:45274249
|
AAAAC | A | 5 | a0001c0001t0001g0094a0001c0001t0002g0034a0001c0001t0002g0060others(2): Show | 5 | NA18974.hp1 NA18974.hp2 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.786+2553_786+2556d others(6): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr19 | 45274249 | |||||
| chr19:45274583
|
A | G | 1 | a0001c0001t0015g0129 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.786+2875A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45274583 | ||||||
| chr19:45274676
|
C | A | 5 | a0001c0001t0001g0100a0001c0001t0001g0104a0001c0001t0003g0101others(2): Show | 5 | HG00642.hp1 HG01109.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.786+2968C>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45274676 | ||||||
| chr19:45274822
|
C | A | 1 | a0001c0001t0003g0099 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.787-3101C>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45274822 | ||||||
| chr19:45275087
|
C | A | 1 | a0001c0001t0019g0239 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.787-2836C>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45275087 | ||||||
| chr19:45275126
|
C | T | 4 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0002g0225others(1): Show | 4 | HG02970.hp1 HG03195.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.787-2797C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45275126 | ||||||
| chr19:45275142
|
T | G | 1 | a0001c0001t0001g0106 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.787-2781T>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45275142 | ||||||
| chr19:45275297
|
C | T | 1 | a0001c0001t0035g0161 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.787-2626C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45275297 | ||||||
| chr19:45275487
|
TA | T | 58 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(55): Show | 58 | HG00280.hp1 HG00323.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.787-2423delA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr19 | 45275487 | |||||
| chr19:45275591
|
G | A | 1 | a0001c0001t0004g0183 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.787-2332G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45275591 | ||||||
| chr19:45275630
|
G | A | 3 | a0001c0001t0013g0020a0001c0001t0013g0021a0001c0001t0023g0022 | 3 | HG01884.hp1 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.787-2293G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45275630 | ||||||
| chr19:45275683
|
T | C | 7 | a0001c0001t0006g0007a0001c0001t0006g0008a0001c0001t0006g0009others(4): Show | 7 | HG00280.hp1 HG01192.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.787-2240T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45275683 | ||||||
| chr19:45275814
|
G | A | 3 | a0001c0001t0004g0183a0001c0003t0002g0212a0001c0003t0004g0216 | 3 | HG03490.hp2 HG03688.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.787-2109G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45275814 | ||||||
| chr19:45275986
|
G | T | 1 | a0001c0001t0002g0210 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.787-1937G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45275986 | ||||||
| chr19:45276057
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.787-1866G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45276057 | ||||||
| chr19:45276170
|
G | C | 1 | a0001c0001t0002g0195 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.787-1753G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45276170 | ||||||
| chr19:45276336
|
T | C | 1 | a0001c0001t0002g0206 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.787-1587T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45276336 | ||||||
| chr19:45276377
|
T | C | 108 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(105): Show | 108 | HG00280.hp1 HG00323.hp2 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.787-1546T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45276377 | ||||||
| chr19:45276397
|
C | T | 1 | a0001c0001t0004g0183 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.787-1526C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45276397 | ||||||
| chr19:45276518
|
C | T | 1 | a0001c0001t0003g0108 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.787-1405C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45276518 | ||||||
| chr19:45276519
|
G | A | 1 | a0001c0001t0013g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.787-1404G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45276519 | ||||||
| chr19:45276558
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.787-1365G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45276558 | ||||||
| chr19:45276622
|
A | AT | 15 | a0001c0001t0001g0121a0001c0001t0001g0130a0001c0001t0001g0143others(12): Show | 15 | HG00735.hp1 HG01361.hp1 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.787-1280dupT | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr19 | 45276622 | |||||
| chr19:45276622
|
AT | A | 29 | a0001c0001t0001g0080a0001c0001t0001g0109a0001c0001t0001g0123others(26): Show | 29 | HG00639.hp1 HG01074.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.787-1280delT | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr19 | 45276622 | |||||
| chr19:45276800
|
A | AT | 6 | a0001c0001t0006g0007a0001c0001t0006g0008a0001c0001t0006g0009others(3): Show | 6 | HG01884.hp2 HG02451.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.787-1109dupT | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr19 | 45276800 | |||||
| chr19:45276823
|
TG | T | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0024others(2): Show | 5 | HG01891.hp1 HG02109.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.787-1096delG | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr19 | 45276823 | |||||
| chr19:45277107
|
G | A | 1 | a0001c0001t0034g0012 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.787-816G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45277107 | ||||||
| chr19:45277329
|
C | T | 37 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0005g0029others(34): Show | 37 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.787-594C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45277329 | ||||||
| chr19:45277423
|
T | A | 1 | a0001c0001t0027g0253 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.787-500T>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45277423 | ||||||
| chr19:45277433
|
A | AT | 34 | a0001c0001t0001g0120a0001c0001t0001g0156a0001c0001t0002g0186others(31): Show | 34 | HG01071.hp1 HG01071.hp2 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.787-471dupT | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr19 | 45277433 | |||||
| chr19:45277433
|
A | ATT | 23 | a0001c0001t0001g0189a0001c0001t0001g0221a0001c0001t0006g0082others(20): Show | 23 | HG01074.hp1 HG01167.hp1 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.787-472_787-471dup others(2): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr19 | 45277433 | |||||
| chr19:45277526
|
A | G | 5 | a0001c0001t0006g0007a0001c0001t0006g0008a0001c0001t0006g0009others(2): Show | 5 | HG01884.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.787-397A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45277526 | ||||||
| chr19:45277555
|
A | G | 7 | a0001c0001t0002g0001a0001c0001t0004g0001a0001c0001t0010g0197others(4): Show | 7 | HG01261.hp1 HG02615.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.787-368A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45277555 | ||||||
| chr19:45277693
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.787-230C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45277693 | ||||||
| chr19:45277694
|
G | A | 1 | a0001c0001t0004g0199 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.787-229G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45277694 | ||||||
| chr19:45277775
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.787-148T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45277775 | ||||||
| chr19:45277823
|
T | TTG | 16 | a0001c0001t0001g0152a0001c0001t0001g0252a0001c0001t0002g0196others(13): Show | 16 | HG00280.hp2 HG00639.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.787-54_787-53dupGT | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr19 | 45277823 | |||||
| chr19:45277823
|
T | TTGTG | 2 | a0001c0001t0002g0195a0001c0001t0005g0061 | 2 | HG02970.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.787-56_787-53dupGT others(2): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr19 | 45277823 | |||||
| chr19:45277823
|
TTG | T | 110 | a0001c0001t0001g0028a0001c0001t0001g0065a0001c0001t0001g0069others(107): Show | 110 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.787-54_787-53delGT | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr19 | 45277823 | |||||
| chr19:45277823
|
TTGTG | T | 26 | a0001c0001t0001g0088a0001c0001t0001g0100a0001c0001t0001g0142others(23): Show | 26 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.787-56_787-53delGT others(2): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr19 | 45277823 | |||||
| chr19:45277823
|
TTGTGTG | T | 27 | a0001c0001t0001g0092a0001c0001t0001g0138a0001c0001t0001g0193others(24): Show | 27 | HG01884.hp1 HG01891.hp2 HG02135.hp2 others(24): Show |
intron_variant | MODIFIER | c.787-58_787-53delGT others(4): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr19 | 45277823 | |||||
| chr19:45277823
|
TTGTGTGT others(1): Show |
T | 18 | a0001c0001t0001g0221a0001c0001t0006g0167a0001c0001t0006g0173others(15): Show | 18 | HG01074.hp1 HG01167.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.787-60_787-53delGT others(6): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr19 | 45277823 | |||||
| chr19:45277823
|
TTGTGTGT others(3): Show |
T | 8 | a0001c0001t0001g0189a0001c0001t0006g0082a0001c0001t0006g0170others(5): Show | 8 | HG01433.hp1 HG02145.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.787-62_787-53delGT others(8): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr19 | 45277823 | |||||
| chr19:45277823
|
TTGTGTGT others(7): Show |
T | 5 | a0001c0001t0006g0007a0001c0001t0006g0008a0001c0001t0006g0009others(2): Show | 5 | HG01884.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.787-66_787-53delGT others(12): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr19 | 45277823 | |||||
| chr19:45277823
|
TTGTGTGT others(9): Show |
T | 2 | a0001c0001t0017g0228a0001c0001t0017g0229 | 2 | HG00280.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.787-68_787-53delGT others(14): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr19 | 45277823 | |||||
| chr19:45277867
|
G | A | 6 | a0001c0001t0006g0167a0001c0001t0006g0168a0001c0001t0006g0173others(3): Show | 6 | HG01433.hp1 HG02976.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.787-56G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45277867 | ||||||
| chr19:45277868
|
T | A | 6 | a0001c0001t0006g0167a0001c0001t0006g0168a0001c0001t0006g0173others(3): Show | 6 | HG01433.hp1 HG02976.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.787-55T>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45277868 | ||||||
| chr19:45277886
|
G | A | 1 | a0001c0001t0002g0207 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.787-37G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 8/16 | chr19 | 45277886 | ||||||
| chr19:45278279
|
G | T | 1 | a0001c0001t0008g0249 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.906+237G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 9/16 | chr19 | 45278279 | ||||||
| chr19:45278434
|
G | A | 1 | a0001c0009t0010g0166 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.907-82G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 9/16 | chr19 | 45278434 | ||||||
| chr19:45278658
|
C | A | 17 | a0001c0001t0001g0189a0001c0001t0001g0221a0001c0001t0006g0082others(14): Show | 17 | HG01167.hp1 HG01169.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.1006+43C>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 10/16 | chr19 | 45278658 | ||||||
| chr19:45278777
|
T | C | 1 | a0001c0001t0002g0240 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1006+162T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 10/16 | chr19 | 45278777 | ||||||
| chr19:45278906
|
A | T | 45 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(42): Show | 45 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.1006+291A>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 10/16 | chr19 | 45278906 | ||||||
| chr19:45278911
|
C | T | 8 | a0001c0001t0002g0001a0001c0001t0002g0259a0001c0001t0004g0001others(5): Show | 8 | HG01261.hp1 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1006+296C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 10/16 | chr19 | 45278911 | ||||||
| chr19:45278955
|
A | C | 1 | a0001c0001t0002g0219 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1006+340A>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 10/16 | chr19 | 45278955 | ||||||
| chr19:45279042
|
G | A | 2 | a0001c0001t0008g0243a0001c0001t0008g0246 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1006+427G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 10/16 | chr19 | 45279042 | ||||||
| chr19:45279330
|
A | C | 2 | a0001c0001t0017g0228a0001c0001t0017g0229 | 2 | HG00280.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1006+715A>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 10/16 | chr19 | 45279330 | ||||||
| chr19:45279336
|
A | G | 9 | a0001c0001t0002g0001a0001c0001t0002g0259a0001c0001t0004g0001others(6): Show | 9 | HG01261.hp1 HG02257.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1006+721A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 10/16 | chr19 | 45279336 | ||||||
| chr19:45279664
|
A | G | 2 | a0001c0001t0017g0228a0001c0001t0017g0229 | 2 | HG00280.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1007-710A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 10/16 | chr19 | 45279664 | ||||||
| chr19:45279863
|
T | C | 1 | a0001c0001t0004g0184 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1007-511T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 10/16 | chr19 | 45279863 | ||||||
| chr19:45279904
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1007-470G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 10/16 | chr19 | 45279904 | ||||||
| chr19:45280169
|
C | A | 1 | a0001c0009t0010g0166 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1007-205C>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 10/16 | chr19 | 45280169 | ||||||
| chr19:45280234
|
C | T | 5 | a0001c0001t0006g0007a0001c0001t0006g0008a0001c0001t0006g0009others(2): Show | 5 | HG01884.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1007-140C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 10/16 | chr19 | 45280234 | ||||||
| chr19:45280789
|
T | TA | 5 | a0001c0001t0006g0007a0001c0001t0006g0008a0001c0001t0006g0009others(2): Show | 5 | HG01884.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1276+56dupA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr19 | 45280789 | |||||
| chr19:45280890
|
G | A | 3 | a0001c0001t0018g0024a0001c0001t0018g0025a0001c0001t0034g0012 | 3 | HG03041.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1276+156G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45280890 | ||||||
| chr19:45280939
|
G | A | 4 | a0001c0001t0001g0189a0001c0001t0001g0221a0001c0001t0010g0030others(1): Show | 4 | HG03654.hp2 HG03831.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1276+205G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45280939 | ||||||
| chr19:45280983
|
C | T | 1 | a0001c0001t0028g0151 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1276+249C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45280983 | ||||||
| chr19:45280995
|
G | A | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0024others(2): Show | 5 | HG01891.hp1 HG02109.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1276+261G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45280995 | ||||||
| chr19:45281174
|
T | C | 4 | a0001c0001t0013g0020a0001c0001t0013g0021a0001c0001t0023g0022others(1): Show | 4 | HG01884.hp1 HG02818.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1276+440T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45281174 | ||||||
| chr19:45281300
|
C | T | 1 | a0001c0001t0004g0178 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1276+566C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45281300 | ||||||
| chr19:45281367
|
C | CTTTTTT | 9 | a0001c0001t0006g0009a0001c0002t0012g0014a0001c0002t0012g0015others(6): Show | 9 | HG01074.hp1 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1276+639_1276+644d others(8): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr19 | 45281367 | |||||
| chr19:45281367
|
C | CTTTTTTT | 90 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0070others(87): Show | 90 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(87): Show |
intron_variant | MODIFIER | c.1276+638_1276+644d others(9): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr19 | 45281367 | |||||
| chr19:45281367
|
C | CTTTTTTT others(1): Show |
7 | a0001c0001t0001g0189a0001c0001t0002g0177a0001c0001t0006g0007others(4): Show | 7 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1276+637_1276+644d others(10): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr19 | 45281367 | |||||
| chr19:45281444
|
T | C | 1 | a0001c0001t0002g0225 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1276+710T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45281444 | ||||||
| chr19:45281592
|
C | T | 1 | a0001c0001t0009g0027 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1276+858C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45281592 | ||||||
| chr19:45281859
|
G | T | 1 | a0001c0001t0010g0169 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1276+1125G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45281859 | ||||||
| chr19:45281935
|
G | A | 15 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0198others(12): Show | 15 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1276+1201G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45281935 | ||||||
| chr19:45281974
|
A | C | 1 | a0001c0001t0003g0231 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1276+1240A>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45281974 | ||||||
| chr19:45282028
|
G | A | 15 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0198others(12): Show | 15 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1276+1294G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45282028 | ||||||
| chr19:45282041
|
T | C | 2 | a0001c0001t0008g0247a0001c0001t0009g0027 | 2 | HG03834.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1276+1307T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45282041 | ||||||
| chr19:45282178
|
A | G | 2 | a0001c0001t0006g0187a0001c0001t0006g0188 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1276+1444A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45282178 | ||||||
| chr19:45282229
|
TA | T | 5 | a0001c0001t0001g0142a0001c0001t0001g0193a0001c0001t0002g0198others(2): Show | 5 | HG00323.hp1 HG02451.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1276+1511delA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr19 | 45282229 | |||||
| chr19:45282245
|
A | AT | 4 | a0001c0001t0005g0029a0001c0001t0005g0044a0001c0001t0007g0036others(1): Show | 4 | NA19000.hp1 NA19074.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.1276+1511_1276+151 others(5): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45282245 | ||||||
| chr19:45282260
|
A | G | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1276+1526A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45282260 | ||||||
| chr19:45282337
|
A | T | 1 | a0001c0001t0010g0049 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1276+1603A>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45282337 | ||||||
| chr19:45282413
|
C | T | 1 | a0001c0001t0034g0012 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1276+1679C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45282413 | ||||||
| chr19:45282590
|
A | G | 258 | a0001c0001t0001g0028a0001c0001t0001g0065a0001c0001t0001g0069others(255): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1276+1856A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45282590 | ||||||
| chr19:45282654
|
T | C | 1 | a0001c0001t0003g0079 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1276+1920T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45282654 | ||||||
| chr19:45282723
|
G | A | 1 | a0001c0001t0034g0012 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1276+1989G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45282723 | ||||||
| chr19:45282833
|
T | C | 2 | a0001c0001t0019g0239a0001c0001t0034g0012 | 2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1276+2099T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45282833 | ||||||
| chr19:45282946
|
C | T | 7 | a0001c0001t0006g0227a0001c0001t0011g0002a0001c0001t0011g0033others(4): Show | 7 | HG02109.hp1 HG02257.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1276+2212C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45282946 | ||||||
| chr19:45283207
|
C | T | 36 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0005g0029others(33): Show | 36 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.1276+2473C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45283207 | ||||||
| chr19:45283297
|
T | C | 79 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0060others(76): Show | 79 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.1276+2563T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45283297 | ||||||
| chr19:45283409
|
C | CA | 15 | a0001c0001t0001g0094a0001c0001t0001g0103a0001c0001t0001g0159others(12): Show | 15 | HG01109.hp1 HG01258.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.1276+2702dupA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr19 | 45283409 | |||||
| chr19:45283409
|
CA | C | 15 | a0001c0001t0001g0142a0001c0001t0001g0252a0001c0001t0001g0258others(12): Show | 15 | HG01099.hp1 HG01168.hp1 HG02602.hp1 others(12): Show |
intron_variant | MODIFIER | c.1276+2702delA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr19 | 45283409 | |||||
| chr19:45283409
|
CAAAAAAA | C | 39 | a0001c0001t0001g0189a0001c0001t0001g0221a0001c0001t0002g0237others(36): Show | 39 | HG00738.hp1 HG01074.hp1 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.1276+2696_1276+270 others(11): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr19 | 45283409 | |||||
| chr19:45283409
|
CAAAAAAA others(1): Show |
C | 34 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0005g0029others(31): Show | 34 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.1276+2695_1276+270 others(12): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr19 | 45283409 | |||||
| chr19:45283409
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0019g0239 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1276+2691_1276+270 others(16): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr19 | 45283409 | |||||
| chr19:45283743
|
C | T | 1 | a0001c0001t0019g0239 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1276+3009C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45283743 | ||||||
| chr19:45283744
|
G | A | 73 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0189others(70): Show | 73 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.1276+3010G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45283744 | ||||||
| chr19:45283788
|
G | A | 168 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0189others(165): Show | 168 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.1276+3054G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45283788 | ||||||
| chr19:45283824
|
T | C | 167 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0189others(164): Show | 167 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1276+3090T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45283824 | ||||||
| chr19:45283900
|
A | G | 1 | a0001c0001t0014g0081 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1276+3166A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45283900 | ||||||
| chr19:45284150
|
A | G | 2 | a0001c0001t0019g0239a0001c0001t0034g0012 | 2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1277-3297A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45284150 | ||||||
| chr19:45284308
|
A | G | 163 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0189others(160): Show | 163 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.1277-3139A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45284308 | ||||||
| chr19:45284311
|
C | G | 1 | a0001c0001t0019g0239 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1277-3136C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45284311 | ||||||
| chr19:45284325
|
C | CT | 15 | a0001c0001t0006g0007a0001c0001t0006g0008a0001c0001t0006g0009others(12): Show | 15 | HG01099.hp1 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1277-3108dupT | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr19 | 45284325 | |||||
| chr19:45284349
|
G | A | 34 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0005g0029others(31): Show | 34 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.1277-3098G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45284349 | ||||||
| chr19:45284350
|
T | C | 1 | a0001c0001t0019g0239 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1277-3097T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45284350 | ||||||
| chr19:45284618
|
G | A | 2 | a0001c0001t0008g0249a0001c0001t0009g0244 | 2 | HG02683.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1277-2829G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45284618 | ||||||
| chr19:45284629
|
G | A | 5 | a0001c0001t0006g0007a0001c0001t0006g0008a0001c0001t0006g0009others(2): Show | 5 | HG01884.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1277-2818G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45284629 | ||||||
| chr19:45284647
|
T | G | 9 | a0001c0001t0006g0227a0001c0001t0011g0002a0001c0001t0011g0033others(6): Show | 9 | HG02109.hp1 HG02257.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1277-2800T>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45284647 | ||||||
| chr19:45284840
|
C | T | 1 | a0001c0001t0034g0012 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1277-2607C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45284840 | ||||||
| chr19:45285191
|
C | T | 4 | a0001c0001t0019g0175a0001c0001t0020g0191a0001c0001t0020g0192others(1): Show | 4 | HG02647.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1277-2256C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45285191 | ||||||
| chr19:45285261
|
C | CA | 40 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0121others(37): Show | 40 | HG00323.hp2 HG00735.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.1277-2162dupA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr19 | 45285261 | |||||
| chr19:45285261
|
CA | C | 20 | a0001c0001t0001g0065a0001c0001t0001g0087a0001c0001t0001g0093others(17): Show | 20 | HG00408.hp1 HG00408.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1277-2162delA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr19 | 45285261 | |||||
| chr19:45285261
|
CAAAAA | C | 5 | a0001c0001t0006g0007a0001c0001t0006g0008a0001c0001t0006g0009others(2): Show | 5 | HG01884.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1277-2166_1277-216 others(9): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr19 | 45285261 | |||||
| chr19:45285261
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0019g0239 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1277-2174_1277-216 others(17): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr19 | 45285261 | |||||
| chr19:45285354
|
T | C | 81 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0189others(78): Show | 81 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1277-2093T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45285354 | ||||||
| chr19:45285511
|
G | A | 3 | a0001c0001t0001g0090a0001c0001t0003g0099a0001c0001t0029g0145 | 3 | HG02027.hp2 NA18974.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1277-1936G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45285511 | ||||||
| chr19:45285659
|
G | A | 2 | a0001c0001t0019g0239a0001c0001t0034g0012 | 2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1277-1788G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45285659 | ||||||
| chr19:45285659
|
G | GTATCATA others(18): Show |
6 | a0001c0001t0011g0002a0001c0001t0011g0033a0001c0001t0011g0047others(3): Show | 6 | HG02109.hp1 HG02809.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1277-1787_1277-178 others(29): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr19 | 45285659 | |||||
| chr19:45285665
|
A | T | 6 | a0001c0001t0011g0002a0001c0001t0011g0033a0001c0001t0011g0047others(3): Show | 6 | HG02109.hp1 HG02809.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1277-1782A>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45285665 | ||||||
| chr19:45285666
|
C | CATATG | 6 | a0001c0001t0011g0002a0001c0001t0011g0033a0001c0001t0011g0047others(3): Show | 6 | HG02109.hp1 HG02809.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1277-1781_1277-178 others(9): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45285666 | ||||||
| chr19:45285667
|
C | G | 6 | a0001c0001t0011g0002a0001c0001t0011g0033a0001c0001t0011g0047others(3): Show | 6 | HG02109.hp1 HG02809.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1277-1780C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45285667 | ||||||
| chr19:45285791
|
A | G | 6 | a0001c0001t0002g0237a0001c0001t0002g0238a0001c0001t0004g0214others(3): Show | 6 | HG00738.hp1 HG02257.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1277-1656A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45285791 | ||||||
| chr19:45285895
|
T | A | 2 | a0001c0001t0019g0239a0001c0001t0034g0012 | 2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1277-1552T>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45285895 | ||||||
| chr19:45286212
|
T | C | 2 | a0001c0001t0019g0239a0001c0001t0034g0012 | 2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1277-1235T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45286212 | ||||||
| chr19:45286252
|
T | C | 1 | a0001c0001t0014g0086 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1277-1195T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45286252 | ||||||
| chr19:45286253
|
G | A | 1 | a0001c0001t0014g0086 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1277-1194G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45286253 | ||||||
| chr19:45286278
|
T | A | 1 | a0001c0001t0002g0240 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1277-1169T>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45286278 | ||||||
| chr19:45286289
|
T | C | 1 | a0001c0001t0019g0239 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1277-1158T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45286289 | ||||||
| chr19:45286743
|
T | A | 168 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0189others(165): Show | 168 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.1277-704T>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45286743 | ||||||
| chr19:45286774
|
T | C | 1 | a0001c0001t0010g0169 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1277-673T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45286774 | ||||||
| chr19:45286856
|
A | C | 1 | a0001c0001t0019g0239 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1277-591A>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45286856 | ||||||
| chr19:45286856
|
A | G | 7 | a0001c0001t0006g0227a0001c0001t0011g0002a0001c0001t0011g0033others(4): Show | 7 | HG02109.hp1 HG02257.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1277-591A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45286856 | ||||||
| chr19:45286870
|
G | T | 1 | a0001c0001t0004g0214 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1277-577G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45286870 | ||||||
| chr19:45286916
|
G | T | 1 | a0001c0001t0034g0012 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1277-531G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45286916 | ||||||
| chr19:45286963
|
A | C | 1 | a0001c0001t0005g0072 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1277-484A>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45286963 | ||||||
| chr19:45287042
|
C | T | 1 | a0001c0001t0008g0248 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1277-405C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45287042 | ||||||
| chr19:45287095
|
T | G | 9 | a0001c0001t0002g0177a0001c0001t0002g0198a0001c0001t0002g0202others(6): Show | 9 | HG01891.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1277-352T>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45287095 | ||||||
| chr19:45287129
|
A | G | 1 | a0001c0001t0034g0012 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1277-318A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45287129 | ||||||
| chr19:45287181
|
C | T | 3 | a0001c0001t0002g0077a0001c0001t0002g0213a0001c0001t0004g0209 | 3 | HG02071.hp1 HG02080.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.1277-266C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | chr19 | 45287181 | ||||||
| chr19:45287202
|
C | CA | 20 | a0001c0001t0001g0189a0001c0001t0001g0221a0001c0001t0002g0238others(17): Show | 20 | HG00738.hp1 HG01167.hp1 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.1277-225dupA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr19 | 45287202 | |||||
| chr19:45287202
|
CA | C | 12 | a0001c0001t0001g0070a0001c0001t0001g0093a0001c0001t0001g0123others(9): Show | 12 | HG00280.hp2 HG01074.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.1277-225delA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr19 | 45287202 | |||||
| chr19:45287433
|
A | AC | 5 | a0001c0001t0002g0083a0001c0001t0002g0222a0001c0001t0003g0108others(2): Show | 5 | HG02074.hp1 HG02145.hp1 HG02738.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.1277-9dupC | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr19 | 45287433 | |||||
| chr19:45287749
|
C | T | 1 | a0001c0001t0009g0257 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1494+85C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45287749 | ||||||
| chr19:45287750
|
G | T | 1 | a0001c0001t0034g0012 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1494+86G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45287750 | ||||||
| chr19:45287870
|
A | G | 1 | a0001c0008t0006g0165 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1494+206A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45287870 | ||||||
| chr19:45287910
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1494+246G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45287910 | ||||||
| chr19:45287945
|
A | G | 1 | a0001c0001t0034g0012 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1494+281A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45287945 | ||||||
| chr19:45288267
|
A | C | 1 | a0001c0008t0006g0165 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1494+603A>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45288267 | ||||||
| chr19:45288279
|
A | G | 3 | a0001c0001t0034g0012a0001c0001t0035g0161a0001c0001t0038g0127 | 3 | HG01099.hp1 HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1494+615A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45288279 | ||||||
| chr19:45288421
|
C | T | 22 | a0001c0001t0001g0189a0001c0001t0001g0221a0001c0001t0002g0237others(19): Show | 22 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.1494+757C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45288421 | ||||||
| chr19:45288432
|
A | G | 5 | a0001c0001t0006g0007a0001c0001t0006g0008a0001c0001t0006g0009others(2): Show | 5 | HG01884.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1494+768A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45288432 | ||||||
| chr19:45288543
|
A | G | 2 | a0001c0001t0002g0001a0001c0001t0004g0001 | 2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1494+879A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45288543 | ||||||
| chr19:45288552
|
CA | C | 80 | a0001c0001t0001g0070a0001c0001t0001g0088a0001c0001t0001g0189others(77): Show | 80 | HG00280.hp2 HG00323.hp2 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.1494+905delA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr19 | 45288552 | |||||
| chr19:45288578
|
C | T | 2 | a0001c0001t0002g0001a0001c0001t0004g0001 | 2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1494+914C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45288578 | ||||||
| chr19:45288580
|
A | C | 80 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0060others(77): Show | 80 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.1494+916A>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45288580 | ||||||
| chr19:45288774
|
C | T | 6 | a0001c0001t0011g0002a0001c0001t0011g0033a0001c0001t0011g0047others(3): Show | 6 | HG02109.hp1 HG02809.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1494+1110C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45288774 | ||||||
| chr19:45288849
|
C | CA | 5 | a0001c0001t0002g0203a0001c0001t0003g0115a0001c0001t0006g0227others(2): Show | 5 | HG01099.hp2 HG02257.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1494+1203dupA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr19 | 45288849 | |||||
| chr19:45288849
|
C | CAA | 109 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0002g0001others(106): Show | 109 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.1494+1202_1494+120 others(6): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr19 | 45288849 | |||||
| chr19:45288849
|
C | CAAA | 25 | a0001c0001t0002g0164a0001c0001t0002g0225a0001c0001t0004g0182others(22): Show | 25 | HG00735.hp2 HG01099.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.1494+1201_1494+120 others(7): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr19 | 45288849 | |||||
| chr19:45288849
|
C | CAAAAAA | 22 | a0001c0001t0001g0189a0001c0001t0001g0221a0001c0001t0002g0237others(19): Show | 22 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.1494+1198_1494+120 others(10): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr19 | 45288849 | |||||
| chr19:45288868
|
G | A | 1 | a0001c0001t0006g0227 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1494+1204G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45288868 | ||||||
| chr19:45288869
|
T | A | 1 | a0001c0001t0006g0227 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1494+1205T>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45288869 | ||||||
| chr19:45288870
|
C | A | 1 | a0001c0001t0006g0227 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1494+1206C>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45288870 | ||||||
| chr19:45288913
|
G | A | 1 | a0001c0001t0006g0227 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1494+1249G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45288913 | ||||||
| chr19:45288919
|
A | G | 2 | a0001c0001t0006g0003a0001c0001t0006g0004 | 2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1494+1255A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45288919 | ||||||
| chr19:45289021
|
C | T | 1 | a0001c0001t0006g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1494+1357C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45289021 | ||||||
| chr19:45289118
|
G | A | 4 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0003g0095others(1): Show | 4 | HG00140.hp1 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1494+1454G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45289118 | ||||||
| chr19:45289317
|
G | A | 2 | a0001c0001t0006g0227a0001c0008t0006g0165 | 2 | HG02257.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1494+1653G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45289317 | ||||||
| chr19:45289341
|
C | T | 2 | a0001c0001t0002g0146a0001c0001t0004g0102 | 2 | HG02572.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1494+1677C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45289341 | ||||||
| chr19:45289385
|
C | CA | 52 | a0001c0001t0001g0028a0001c0001t0001g0159a0001c0001t0002g0180others(49): Show | 52 | HG00738.hp1 HG01074.hp1 HG01167.hp1 others(49): Show |
intron_variant | MODIFIER | c.1494+1744dupA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr19 | 45289385 | |||||
| chr19:45289385
|
CA | C | 11 | a0001c0001t0001g0131a0001c0001t0001g0134a0001c0001t0001g0258others(8): Show | 11 | HG00140.hp2 HG00280.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.1494+1744delA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr19 | 45289385 | |||||
| chr19:45289385
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0004g0205 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1494+1734_1494+174 others(15): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr19 | 45289385 | |||||
| chr19:45289447
|
G | A | 51 | a0001c0001t0005g0029a0001c0001t0005g0038a0001c0001t0005g0040others(48): Show | 51 | HG00280.hp1 HG00323.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.1494+1783G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45289447 | ||||||
| chr19:45289506
|
C | T | 33 | a0001c0001t0005g0029a0001c0001t0005g0038a0001c0001t0005g0040others(30): Show | 33 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.1494+1842C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45289506 | ||||||
| chr19:45289560
|
G | A | 4 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0003g0095others(1): Show | 4 | HG00140.hp1 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1494+1896G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45289560 | ||||||
| chr19:45289640
|
C | T | 1 | a0003c0005t0003g0157 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1494+1976C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45289640 | ||||||
| chr19:45289648
|
T | TA | 3 | a0001c0001t0034g0012a0001c0001t0035g0161a0001c0001t0038g0127 | 3 | HG01099.hp1 HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1494+1986dupA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr19 | 45289648 | |||||
| chr19:45289712
|
G | A | 7 | a0001c0002t0012g0014a0001c0002t0012g0015a0001c0002t0012g0017others(4): Show | 7 | HG01074.hp1 HG02145.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1494+2048G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45289712 | ||||||
| chr19:45289718
|
C | T | 3 | a0001c0001t0034g0012a0001c0001t0035g0161a0001c0001t0038g0127 | 3 | HG01099.hp1 HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1494+2054C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45289718 | ||||||
| chr19:45289856
|
C | T | 2 | a0001c0003t0002g0212a0001c0003t0004g0216 | 2 | HG03490.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1494+2192C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45289856 | ||||||
| chr19:45289857
|
A | G | 165 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0060others(162): Show | 165 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.1494+2193A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45289857 | ||||||
| chr19:45289864
|
A | C | 1 | a0001c0001t0001g0116 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1494+2200A>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45289864 | ||||||
| chr19:45289955
|
G | A | 1 | a0001c0001t0032g0005 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1494+2291G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45289955 | ||||||
| chr19:45289971
|
G | A | 7 | a0001c0002t0012g0014a0001c0002t0012g0015a0001c0002t0012g0017others(4): Show | 7 | HG01074.hp1 HG02145.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1494+2307G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45289971 | ||||||
| chr19:45290144
|
G | T | 6 | a0001c0001t0011g0002a0001c0001t0011g0033a0001c0001t0011g0047others(3): Show | 6 | HG02109.hp1 HG02809.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1494+2480G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45290144 | ||||||
| chr19:45290449
|
G | T | 77 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0060others(74): Show | 77 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.1494+2785G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45290449 | ||||||
| chr19:45290570
|
T | C | 20 | a0001c0001t0002g0237a0001c0001t0002g0238a0001c0001t0004g0214others(17): Show | 20 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.1494+2906T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45290570 | ||||||
| chr19:45290574
|
A | T | 42 | a0001c0001t0005g0029a0001c0001t0005g0038a0001c0001t0005g0040others(39): Show | 42 | HG00280.hp1 HG00323.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.1494+2910A>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45290574 | ||||||
| chr19:45290581
|
G | A | 1 | a0001c0001t0002g0259 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1494+2917G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45290581 | ||||||
| chr19:45290658
|
G | C | 1 | a0001c0001t0028g0151 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1494+2994G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45290658 | ||||||
| chr19:45290715
|
G | A | 1 | a0001c0001t0004g0200 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1494+3051G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45290715 | ||||||
| chr19:45290786
|
G | C | 20 | a0001c0001t0002g0237a0001c0001t0002g0238a0001c0001t0004g0214others(17): Show | 20 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.1494+3122G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45290786 | ||||||
| chr19:45290786
|
G | T | 4 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0002g0225others(1): Show | 4 | HG02970.hp1 HG03195.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1494+3122G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45290786 | ||||||
| chr19:45290790
|
C | T | 2 | a0001c0001t0004g0179a0001c0001t0004g0234 | 2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1494+3126C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45290790 | ||||||
| chr19:45290851
|
G | A | 1 | a0001c0001t0027g0253 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1494+3187G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45290851 | ||||||
| chr19:45290894
|
C | T | 1 | a0001c0001t0003g0076 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1494+3230C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45290894 | ||||||
| chr19:45291110
|
A | G | 5 | a0001c0001t0006g0007a0001c0001t0006g0008a0001c0001t0006g0009others(2): Show | 5 | HG01884.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1495-3239A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45291110 | ||||||
| chr19:45291141
|
T | G | 1 | a0001c0008t0006g0165 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1495-3208T>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45291141 | ||||||
| chr19:45291245
|
C | T | 6 | a0001c0001t0011g0002a0001c0001t0011g0033a0001c0001t0011g0047others(3): Show | 6 | HG02109.hp1 HG02809.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1495-3104C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45291245 | ||||||
| chr19:45291463
|
TGGCAAAA others(128): Show |
T | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1495-2883_1495-274 others(4): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr19 | 45291463 | |||||
| chr19:45291511
|
G | A | 1 | a0001c0001t0007g0107 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1495-2838G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45291511 | ||||||
| chr19:45291554
|
G | A | 2 | a0001c0001t0006g0173a0001c0001t0019g0239 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1495-2795G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45291554 | ||||||
| chr19:45291607
|
C | G | 1 | a0001c0001t0009g0257 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1495-2742C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45291607 | ||||||
| chr19:45291612
|
C | T | 1 | a0001c0001t0008g0248 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1495-2737C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45291612 | ||||||
| chr19:45291675
|
G | A | 2 | a0001c0001t0017g0228a0001c0001t0017g0229 | 2 | HG00280.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1495-2674G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45291675 | ||||||
| chr19:45291795
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1495-2554A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45291795 | ||||||
| chr19:45291880
|
G | A | 2 | a0001c0001t0035g0161a0001c0001t0038g0127 | 2 | HG01099.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1495-2469G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45291880 | ||||||
| chr19:45291928
|
G | T | 7 | a0001c0001t0006g0007a0001c0001t0006g0008a0001c0001t0006g0009others(4): Show | 7 | HG01261.hp1 HG01884.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1495-2421G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45291928 | ||||||
| chr19:45292028
|
A | C | 9 | a0001c0001t0002g0259a0001c0001t0006g0003a0001c0001t0006g0004others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1495-2321A>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45292028 | ||||||
| chr19:45292357
|
C | T | 3 | a0001c0001t0034g0012a0001c0001t0035g0161a0001c0001t0038g0127 | 3 | HG01099.hp1 HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1495-1992C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45292357 | ||||||
| chr19:45292381
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1495-1968C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45292381 | ||||||
| chr19:45292694
|
T | G | 3 | a0001c0001t0001g0100a0001c0001t0001g0104a0004c0007t0003g0158 | 3 | HG00642.hp1 HG01109.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1495-1655T>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45292694 | ||||||
| chr19:45292804
|
C | T | 6 | a0001c0001t0011g0002a0001c0001t0011g0033a0001c0001t0011g0047others(3): Show | 6 | HG02109.hp1 HG02809.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1495-1545C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45292804 | ||||||
| chr19:45292850
|
C | T | 4 | a0001c0001t0019g0175a0001c0001t0020g0191a0001c0001t0020g0192others(1): Show | 4 | HG02647.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1495-1499C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45292850 | ||||||
| chr19:45292972
|
G | T | 3 | a0001c0001t0002g0034a0001c0001t0002g0060a0001c0001t0002g0063 | 3 | NA18974.hp2 NA18975.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1495-1377G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45292972 | ||||||
| chr19:45292994
|
G | A | 6 | a0001c0001t0011g0002a0001c0001t0011g0033a0001c0001t0011g0047others(3): Show | 6 | HG02109.hp1 HG02809.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1495-1355G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45292994 | ||||||
| chr19:45293162
|
G | A | 76 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0060others(73): Show | 76 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.1495-1187G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45293162 | ||||||
| chr19:45293188
|
T | C | 41 | a0001c0001t0005g0029a0001c0001t0005g0038a0001c0001t0005g0040others(38): Show | 41 | HG00280.hp1 HG00323.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.1495-1161T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45293188 | ||||||
| chr19:45293269
|
A | T | 4 | a0001c0001t0001g0103a0001c0001t0001g0131a0001c0001t0001g0134others(1): Show | 4 | HG02027.hp1 NA18983.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.1495-1080A>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45293269 | ||||||
| chr19:45293363
|
A | G | 1 | a0001c0001t0004g0235 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1495-986A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45293363 | ||||||
| chr19:45293441
|
A | G | 1 | a0001c0001t0027g0253 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1495-908A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45293441 | ||||||
| chr19:45293507
|
C | G | 3 | a0001c0001t0008g0243a0001c0001t0008g0246a0001c0001t0009g0245 | 3 | HG01934.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1495-842C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45293507 | ||||||
| chr19:45293534
|
G | T | 1 | a0001c0001t0006g0227 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1495-815G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45293534 | ||||||
| chr19:45293545
|
C | T | 1 | a0001c0004t0022g0154 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1495-804C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45293545 | ||||||
| chr19:45293617
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1495-732A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45293617 | ||||||
| chr19:45293777
|
T | C | 5 | a0001c0001t0002g0259a0001c0001t0019g0175a0001c0001t0020g0191others(2): Show | 5 | HG02647.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1495-572T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45293777 | ||||||
| chr19:45293834
|
A | C | 41 | a0001c0001t0005g0029a0001c0001t0005g0038a0001c0001t0005g0040others(38): Show | 41 | HG00280.hp1 HG00323.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.1495-515A>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45293834 | ||||||
| chr19:45293973
|
T | G | 41 | a0001c0001t0005g0029a0001c0001t0005g0038a0001c0001t0005g0040others(38): Show | 41 | HG00280.hp1 HG00323.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.1495-376T>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45293973 | ||||||
| chr19:45294122
|
C | A | 1 | a0001c0001t0001g0252 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1495-227C>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45294122 | ||||||
| chr19:45294135
|
G | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1495-214G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45294135 | ||||||
| chr19:45294335
|
T | C | 39 | a0001c0001t0005g0029a0001c0001t0005g0038a0001c0001t0005g0040others(36): Show | 39 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.1495-14T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 13/16 | chr19 | 45294335 | ||||||
| chr19:45294476
|
T | G | 2 | a0001c0001t0023g0022a0001c0001t0033g0023 | 2 | HG02818.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1598+24T>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45294476 | ||||||
| chr19:45294734
|
A | C | 3 | a0001c0001t0008g0251a0001c0001t0009g0242a0001c0001t0009g0250 | 3 | HG00280.hp2 HG01433.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1598+282A>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45294734 | ||||||
| chr19:45294834
|
G | A | 39 | a0001c0001t0005g0029a0001c0001t0005g0038a0001c0001t0005g0040others(36): Show | 39 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.1598+382G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45294834 | ||||||
| chr19:45294937
|
C | T | 77 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0060others(74): Show | 77 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.1598+485C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45294937 | ||||||
| chr19:45295120
|
C | T | 1 | a0001c0001t0006g0227 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1598+668C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45295120 | ||||||
| chr19:45295121
|
A | G | 165 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0060others(162): Show | 165 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.1598+669A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45295121 | ||||||
| chr19:45295134
|
A | T | 33 | a0001c0001t0005g0029a0001c0001t0005g0038a0001c0001t0005g0040others(30): Show | 33 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.1598+682A>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45295134 | ||||||
| chr19:45295194
|
CA | C | 12 | a0001c0001t0001g0258a0001c0001t0010g0169a0001c0001t0019g0239others(9): Show | 12 | HG01074.hp1 HG01168.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1598+757delA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr19 | 45295194 | |||||
| chr19:45295227
|
T | C | 165 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0060others(162): Show | 165 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.1598+775T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45295227 | ||||||
| chr19:45295375
|
G | A | 2 | a0001c0001t0004g0205a0001c0001t0006g0174 | 2 | HG03209.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.1598+923G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45295375 | ||||||
| chr19:45295407
|
C | T | 39 | a0001c0001t0005g0029a0001c0001t0005g0038a0001c0001t0005g0040others(36): Show | 39 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.1598+955C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45295407 | ||||||
| chr19:45295438
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1598+986G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45295438 | ||||||
| chr19:45295441
|
C | T | 4 | a0001c0001t0019g0175a0001c0001t0020g0191a0001c0001t0020g0192others(1): Show | 4 | HG02647.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1598+989C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45295441 | ||||||
| chr19:45295442
|
G | A | 1 | a0001c0001t0003g0078 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1598+990G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45295442 | ||||||
| chr19:45295496
|
C | G | 3 | a0001c0001t0034g0012a0001c0001t0035g0161a0001c0001t0038g0127 | 3 | HG01099.hp1 HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1598+1044C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45295496 | ||||||
| chr19:45295541
|
G | A | 39 | a0001c0001t0005g0029a0001c0001t0005g0038a0001c0001t0005g0040others(36): Show | 39 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.1598+1089G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45295541 | ||||||
| chr19:45295715
|
G | A | 4 | a0001c0001t0019g0175a0001c0001t0020g0191a0001c0001t0020g0192others(1): Show | 4 | HG02647.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1598+1263G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45295715 | ||||||
| chr19:45295773
|
C | T | 20 | a0001c0001t0002g0237a0001c0001t0002g0238a0001c0001t0004g0214others(17): Show | 20 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.1598+1321C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45295773 | ||||||
| chr19:45295820
|
A | G | 7 | a0001c0002t0012g0014a0001c0002t0012g0015a0001c0002t0012g0017others(4): Show | 7 | HG01074.hp1 HG02145.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1598+1368A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45295820 | ||||||
| chr19:45296023
|
C | G | 1 | a0001c0001t0010g0169 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1598+1571C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45296023 | ||||||
| chr19:45296051
|
A | C | 1 | a0001c0001t0010g0169 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1598+1599A>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45296051 | ||||||
| chr19:45296184
|
T | C | 167 | a0001c0001t0001g0093a0001c0001t0002g0001a0001c0001t0002g0034others(164): Show | 167 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1599-1492T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45296184 | ||||||
| chr19:45296435
|
T | A | 1 | a0001c0001t0001g0117 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1599-1241T>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45296435 | ||||||
| chr19:45296446
|
G | C | 166 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0060others(163): Show | 166 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.1599-1230G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45296446 | ||||||
| chr19:45296494
|
C | T | 6 | a0001c0001t0011g0002a0001c0001t0011g0033a0001c0001t0011g0047others(3): Show | 6 | HG02109.hp1 HG02809.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1599-1182C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45296494 | ||||||
| chr19:45296534
|
C | T | 3 | a0001c0001t0034g0012a0001c0001t0035g0161a0001c0001t0038g0127 | 3 | HG01099.hp1 HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1599-1142C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45296534 | ||||||
| chr19:45296565
|
C | T | 1 | a0001c0001t0003g0231 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1599-1111C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45296565 | ||||||
| chr19:45296652
|
C | T | 2 | a0001c0001t0001g0089a0001c0001t0001g0137 | 2 | HG00099.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1599-1024C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45296652 | ||||||
| chr19:45296717
|
G | C | 146 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0060others(143): Show | 146 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.1599-959G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45296717 | ||||||
| chr19:45296776
|
G | A | 1 | a0001c0001t0005g0058 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1599-900G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45296776 | ||||||
| chr19:45296832
|
C | T | 2 | a0001c0001t0006g0003a0001c0001t0006g0004 | 2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1599-844C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45296832 | ||||||
| chr19:45297048
|
C | CA | 91 | a0001c0001t0001g0028a0001c0001t0001g0193a0001c0001t0002g0001others(88): Show | 91 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.1599-608dupA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr19 | 45297048 | |||||
| chr19:45297048
|
CA | C | 10 | a0001c0001t0003g0149a0001c0001t0007g0041a0001c0001t0007g0135others(7): Show | 10 | HG01074.hp1 HG01516.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1599-608delA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr19 | 45297048 | |||||
| chr19:45297133
|
G | A | 4 | a0001c0001t0005g0043a0001c0001t0005g0071a0001c0001t0005g0072others(1): Show | 4 | HG00323.hp2 HG01167.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.1599-543G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45297133 | ||||||
| chr19:45297181
|
G | A | 2 | a0001c0001t0006g0003a0001c0001t0006g0004 | 2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1599-495G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45297181 | ||||||
| chr19:45297327
|
T | G | 1 | a0001c0008t0006g0165 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1599-349T>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45297327 | ||||||
| chr19:45297438
|
C | T | 19 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0007others(16): Show | 19 | HG00280.hp1 HG01192.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.1599-238C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 14/16 | chr19 | 45297438 | ||||||
| chr19:45297965
|
C | A | 4 | a0001c0001t0019g0175a0001c0001t0020g0191a0001c0001t0020g0192others(1): Show | 4 | HG02647.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1877+11C>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45297965 | ||||||
| chr19:45298074
|
C | G | 1 | a0001c0001t0005g0057 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1877+120C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45298074 | ||||||
| chr19:45298076
|
C | T | 1 | a0001c0001t0005g0057 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1877+122C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45298076 | ||||||
| chr19:45298077
|
G | T | 1 | a0001c0001t0005g0057 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1877+123G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45298077 | ||||||
| chr19:45298078
|
T | C | 1 | a0001c0001t0005g0057 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1877+124T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45298078 | ||||||
| chr19:45298079
|
T | C | 1 | a0001c0001t0005g0057 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1877+125T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45298079 | ||||||
| chr19:45298079
|
T | TTCC | 32 | a0001c0001t0005g0029a0001c0001t0005g0038a0001c0001t0005g0040others(29): Show | 32 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.1877+142_1877+144d others(5): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr19 | 45298079 | |||||
| chr19:45298179
|
C | T | 1 | a0001c0010t0001g0150 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1877+225C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45298179 | ||||||
| chr19:45298292
|
G | A | 1 | a0001c0001t0011g0033 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1877+338G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45298292 | ||||||
| chr19:45298321
|
GGGTCTGT others(4): Show |
G | 108 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0060others(105): Show | 108 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.1877+370_1877+380d others(13): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr19 | 45298321 | |||||
| chr19:45298376
|
G | A | 1 | a0001c0001t0003g0091 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1877+422G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45298376 | ||||||
| chr19:45298470
|
G | T | 20 | a0001c0001t0008g0068a0001c0001t0008g0085a0001c0001t0008g0113others(17): Show | 20 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.1877+516G>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45298470 | ||||||
| chr19:45298527
|
G | A | 1 | a0001c0001t0004g0118 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1877+573G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45298527 | ||||||
| chr19:45298651
|
G | A | 1 | a0001c0008t0006g0165 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1877+697G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45298651 | ||||||
| chr19:45298693
|
C | T | 70 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0060others(67): Show | 70 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.1877+739C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45298693 | ||||||
| chr19:45298764
|
C | T | 34 | a0001c0001t0002g0077a0001c0001t0002g0186a0001c0001t0002g0195others(31): Show | 34 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.1877+810C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45298764 | ||||||
| chr19:45298891
|
C | T | 1 | a0001c0001t0007g0074 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1878-920C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45298891 | ||||||
| chr19:45298920
|
T | C | 1 | a0001c0001t0032g0005 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1878-891T>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45298920 | ||||||
| chr19:45299000
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1878-811C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45299000 | ||||||
| chr19:45299041
|
G | A | 4 | a0001c0001t0001g0065a0001c0001t0001g0088a0001c0001t0001g0133others(1): Show | 4 | HG00408.hp1 HG00609.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.1878-770G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45299041 | ||||||
| chr19:45299064
|
T | TA | 6 | a0001c0001t0001g0065a0001c0001t0001g0109a0001c0001t0001g0110others(3): Show | 6 | HG00323.hp1 HG00408.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.1878-721dupA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr19 | 45299064 | |||||
| chr19:45299064
|
TA | T | 31 | a0001c0001t0001g0028a0001c0001t0001g0070a0001c0001t0001g0080others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.1878-721delA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr19 | 45299064 | |||||
| chr19:45299064
|
TAA | T | 96 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0060others(93): Show | 96 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1878-722_1878-721d others(4): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr19 | 45299064 | |||||
| chr19:45299064
|
TAAA | T | 11 | a0001c0001t0002g0198a0001c0001t0002g0203a0001c0001t0002g0218others(8): Show | 11 | HG02896.hp1 HG02896.hp2 HG02897.hp1 others(8): Show |
intron_variant | MODIFIER | c.1878-723_1878-721d others(5): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr19 | 45299064 | |||||
| chr19:45299064
|
TAAAAA | T | 5 | a0001c0001t0019g0175a0001c0001t0020g0191a0001c0001t0020g0192others(2): Show | 5 | HG02647.hp2 HG02723.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1878-725_1878-721d others(7): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr19 | 45299064 | |||||
| chr19:45299064
|
TAAAAAAA others(2): Show |
T | 30 | a0001c0001t0005g0029a0001c0001t0005g0038a0001c0001t0005g0043others(27): Show | 30 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1878-729_1878-721d others(11): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr19 | 45299064 | |||||
| chr19:45299064
|
TAAAAAAA others(3): Show |
T | 3 | a0001c0001t0005g0040a0001c0001t0005g0057a0001c0001t0007g0074 | 3 | HG01109.hp2 HG02129.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1878-730_1878-721d others(12): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr19 | 45299064 | |||||
| chr19:45299152
|
G | C | 9 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0011g0002others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1878-659G>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45299152 | ||||||
| chr19:45299296
|
C | T | 1 | a0001c0001t0005g0056 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1878-515C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45299296 | ||||||
| chr19:45299333
|
A | G | 7 | a0001c0002t0012g0014a0001c0002t0012g0015a0001c0002t0012g0017others(4): Show | 7 | HG01074.hp1 HG02145.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1878-478A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45299333 | ||||||
| chr19:45299380
|
C | T | 4 | a0001c0001t0001g0028a0001c0001t0001g0193a0001c0001t0003g0208others(1): Show | 4 | HG02055.hp1 HG02280.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1878-431C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45299380 | ||||||
| chr19:45299407
|
T | A | 9 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0011g0002others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1878-404T>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45299407 | ||||||
| chr19:45299562
|
T | A | 2 | a0001c0003t0002g0212a0001c0003t0004g0216 | 2 | HG03490.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1878-249T>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45299562 | ||||||
| chr19:45299605
|
A | G | 33 | a0001c0001t0005g0029a0001c0001t0005g0038a0001c0001t0005g0040others(30): Show | 33 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.1878-206A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45299605 | ||||||
| chr19:45299750
|
G | A | 21 | a0001c0001t0002g0237a0001c0001t0002g0238a0001c0001t0004g0214others(18): Show | 21 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.1878-61G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 15/16 | chr19 | 45299750 | ||||||
| chr19:45300273
|
A | G | 1 | a0001c0010t0001g0150 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1922+418A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | chr19 | 45300273 | ||||||
| chr19:45300344
|
G | GAAA | 42 | a0001c0001t0001g0028a0001c0001t0001g0065a0001c0001t0001g0080others(39): Show | 42 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(39): Show |
intron_variant | MODIFIER | c.1922+513_1922+515d others(5): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45300344 | |||||
| chr19:45300344
|
G | GAAAA | 46 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0088others(43): Show | 46 | HG00099.hp1 HG00140.hp1 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.1922+512_1922+515d others(6): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45300344 | |||||
| chr19:45300344
|
G | GAAAAA | 8 | a0001c0001t0001g0087a0001c0001t0001g0106a0001c0001t0001g0121others(5): Show | 8 | HG00408.hp2 HG00735.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1922+511_1922+515d others(7): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45300344 | |||||
| chr19:45300344
|
G | GAAAAAA | 6 | a0001c0001t0001g0143a0001c0001t0003g0076a0001c0001t0004g0236others(3): Show | 6 | HG01361.hp1 HG02723.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1922+510_1922+515d others(8): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45300344 | |||||
| chr19:45300344
|
G | GAAAAAAA | 11 | a0001c0001t0002g0237a0001c0001t0002g0238a0001c0001t0004g0214others(8): Show | 11 | HG00738.hp1 HG01169.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.1922+509_1922+515d others(9): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45300344 | |||||
| chr19:45300344
|
G | GAAAAAAA others(1): Show |
18 | a0001c0001t0005g0038a0001c0001t0005g0040a0001c0001t0005g0046others(15): Show | 18 | HG00735.hp2 HG01081.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.1922+508_1922+515d others(10): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45300344 | |||||
| chr19:45300344
|
G | GAAAAAAA others(2): Show |
15 | a0001c0001t0004g0235a0001c0001t0005g0029a0001c0001t0005g0043others(12): Show | 15 | HG00323.hp2 HG01109.hp2 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.1922+507_1922+515d others(11): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45300344 | |||||
| chr19:45300344
|
G | GAAAAAAA others(3): Show |
8 | a0001c0001t0005g0044a0001c0001t0005g0045a0001c0001t0005g0054others(5): Show | 8 | HG00609.hp2 HG00738.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1922+506_1922+515d others(12): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45300344 | |||||
| chr19:45300344
|
G | GAAAAAAA others(4): Show |
2 | a0001c0001t0035g0161a0001c0001t0038g0127 | 2 | HG01099.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1922+505_1922+515d others(13): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45300344 | |||||
| chr19:45300344
|
G | GAAAAAAA others(5): Show |
5 | a0001c0001t0002g0215a0001c0001t0002g0219a0001c0001t0004g0205others(2): Show | 5 | HG02129.hp1 NA18942.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.1922+504_1922+515d others(14): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45300344 | |||||
| chr19:45300344
|
G | GAAAAAAA others(6): Show |
3 | a0001c0001t0002g0180a0001c0001t0002g0218a0001c0001t0017g0229 | 3 | HG00280.hp1 HG02074.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.1922+503_1922+515d others(15): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45300344 | |||||
| chr19:45300344
|
G | GAAAAAAA others(7): Show |
1 | a0001c0001t0017g0228 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1922+502_1922+515d others(16): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45300344 | |||||
| chr19:45300344
|
GAAAA | G | 5 | a0001c0001t0002g0222a0001c0001t0004g0102a0001c0001t0004g0179others(2): Show | 5 | HG02055.hp2 HG02145.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1922+512_1922+515d others(6): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45300344 | |||||
| chr19:45300344
|
GAAAAA | G | 62 | a0001c0001t0002g0034a0001c0001t0002g0060a0001c0001t0002g0063others(59): Show | 62 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.1922+511_1922+515d others(7): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45300344 | |||||
| chr19:45300344
|
GAAAAAA | G | 9 | a0001c0001t0004g0147a0001c0001t0020g0192a0001c0002t0012g0014others(6): Show | 9 | HG01074.hp1 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1922+510_1922+515d others(8): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45300344 | |||||
| chr19:45300344
|
GAAAAAAA others(6): Show |
G | 9 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0011g0002others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1922+503_1922+515d others(15): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45300344 | |||||
| chr19:45300621
|
A | C | 1 | a0001c0008t0006g0165 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1922+766A>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | chr19 | 45300621 | ||||||
| chr19:45300751
|
A | G | 2 | a0001c0001t0002g0146a0001c0001t0004g0102 | 2 | HG02572.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1922+896A>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | chr19 | 45300751 | ||||||
| chr19:45300865
|
C | T | 2 | a0001c0003t0002g0212a0001c0003t0004g0216 | 2 | HG03490.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1922+1010C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | chr19 | 45300865 | ||||||
| chr19:45301049
|
T | A | 168 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0060others(165): Show | 168 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.1922+1194T>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | chr19 | 45301049 | ||||||
| chr19:45301106
|
A | C | 70 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0060others(67): Show | 70 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.1922+1251A>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | chr19 | 45301106 | ||||||
| chr19:45301424
|
C | G | 2 | a0001c0001t0002g0001a0001c0001t0004g0001 | 2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1923-950C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | chr19 | 45301424 | ||||||
| chr19:45301557
|
C | CA | 48 | a0001c0001t0001g0106a0001c0001t0001g0122a0001c0001t0001g0142others(45): Show | 48 | HG00099.hp2 HG00738.hp1 HG01106.hp2 others(45): Show |
intron_variant | MODIFIER | c.1923-795dupA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45301557 | |||||
| chr19:45301557
|
C | CAA | 41 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0063others(38): Show | 41 | HG00280.hp1 HG00642.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.1923-796_1923-795d others(4): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45301557 | |||||
| chr19:45301557
|
C | CAAA | 31 | a0001c0001t0002g0164a0001c0001t0002g0177a0001c0001t0002g0194others(28): Show | 31 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.1923-797_1923-795d others(5): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45301557 | |||||
| chr19:45301557
|
C | CAAAA | 9 | a0001c0001t0008g0085a0001c0001t0008g0251a0001c0001t0009g0242others(6): Show | 9 | HG00280.hp2 HG01257.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.1923-798_1923-795d others(6): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45301557 | |||||
| chr19:45301557
|
C | CAAAAAA | 29 | a0001c0001t0005g0029a0001c0001t0005g0038a0001c0001t0005g0043others(26): Show | 29 | HG00323.hp1 HG00323.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.1923-800_1923-795d others(8): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45301557 | |||||
| chr19:45301557
|
C | CAAAAAAA | 6 | a0001c0001t0005g0040a0001c0001t0005g0044a0001c0001t0005g0058others(3): Show | 6 | HG02572.hp1 HG03654.hp1 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.1923-801_1923-795d others(9): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45301557 | |||||
| chr19:45301634
|
G | A | 1 | a0001c0001t0004g0209 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1923-740G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | chr19 | 45301634 | ||||||
| chr19:45301676
|
C | G | 1 | a0001c0001t0001g0233 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1923-698C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | chr19 | 45301676 | ||||||
| chr19:45301692
|
C | T | 10 | a0001c0001t0002g0180a0001c0001t0002g0215a0001c0001t0002g0218others(7): Show | 10 | HG01099.hp1 HG02074.hp2 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.1923-682C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | chr19 | 45301692 | ||||||
| chr19:45301749
|
C | G | 3 | a0001c0001t0006g0167a0001c0001t0006g0173a0001c0001t0010g0172 | 3 | HG01433.hp1 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1923-625C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | chr19 | 45301749 | ||||||
| chr19:45301779
|
C | T | 35 | a0001c0001t0005g0029a0001c0001t0005g0038a0001c0001t0005g0040others(32): Show | 35 | HG00323.hp1 HG00323.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.1923-595C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | chr19 | 45301779 | ||||||
| chr19:45301790
|
A | C | 2 | a0001c0001t0017g0228a0001c0001t0017g0229 | 2 | HG00280.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1923-584A>C | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | chr19 | 45301790 | ||||||
| chr19:45301859
|
C | A | 1 | a0001c0001t0002g0164 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1923-515C>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | chr19 | 45301859 | ||||||
| chr19:45301861
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1923-513G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | chr19 | 45301861 | ||||||
| chr19:45301865
|
CA | C | 80 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0060others(77): Show | 80 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.1923-492delA | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45301865 | |||||
| chr19:45301865
|
CAA | C | 85 | a0001c0001t0002g0180a0001c0001t0002g0215a0001c0001t0002g0218others(82): Show | 85 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.1923-493_1923-492d others(4): Show |
MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr19 | 45301865 | |||||
| chr19:45301889
|
G | A | 168 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0060others(165): Show | 168 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.1923-485G>A | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | chr19 | 45301889 | ||||||
| chr19:45301908
|
C | G | 1 | a0001c0001t0001g0148 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1923-466C>G | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | chr19 | 45301908 | ||||||
| chr19:45302290
|
C | T | 8 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0011g0002others(5): Show | 8 | HG01891.hp1 HG02109.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1923-84C>T | MARK4 | ENSG00000007047.16 | transcript | ENST00000262891.9 | protein_coding | 16/16 | chr19 | 45302290 |