Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 641700 |
|---|---|
| ensemblid | ENSG00000249751.4 |
| hgncid | 35454 |
| symbol | ECSCR |
| name | endothelial cell surface expressed chemotaxis and apoptosis regulator |
| refseq_nuc | NM_001077693.4 |
| refseq_prot | NP_001071161.1 |
| ensembl_nuc | ENST00000618155.3 |
| ensembl_prot | ENSP00000479243.1 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 139448560 |
| end | 139462743 |
| strand | - |
| ver | v1.2 |
| region | chr5:139448560-139462743 |
| region5000 | chr5:139443560-139467743 |
| regionname0 | ECSCR_chr5_139448560_139462743 |
| regionname5000 | ECSCR_chr5_139443560_139467743 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 205 | 368 | 84 | 70 | 163 | 16 | 34 | 123 | ECSCR_chr5_139443560_139467743 | ECSCR | copy fasta | chr5 | 139443560 | 139467743 |
| a0002 | 0/0 | 205 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | copy fasta | chr5 | 139443560 | 139467743 |
| 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 | 618 | 368 | 84 | 70 | 163 | 16 | 34 | ECSCR_chr5_139443560_139467743 | ECSCR | copy fasta | chr5 | 139443560 | 139467743 |
| c0002 | 0/0 | 618 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | copy fasta | chr5 | 139443560 | 139467743 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 414 | 368 | 84 | 70 | 164 | 16 | 33 | ECSCR_chr5_139443560_139467743 | ECSCR | copy fasta | chr5 | 139443560 | 139467743 |
| t0002 | 0/0 | 414 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | copy fasta | chr5 | 139443560 | 139467743 |
| 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 | 0/1 | 58 | 3 | 14 | 33 | 5 | 2 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0002 | 0/0 | 51 | 9 | 6 | 29 | 4 | 3 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0003 | 0/0 | 18 | 1 | 2 | 13 | 0 | 2 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0004 | 0/0 | 15 | 1 | 6 | 6 | 1 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0005 | 0/0 | 12 | 0 | 4 | 6 | 1 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0006 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0007 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0008 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0012 | 0/0 | 4 | 1 | 1 | 1 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0013 | 0/0 | 4 | 1 | 0 | 2 | 1 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0014 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0018 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0019 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0032 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0034 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| 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 | 618 | 368 | 84 | 70 | 163 | 16 | 34 | ECSCR_chr5_139443560_139467743 | ECSCR | copy fasta | chr5 | 139443560 | 139467743 |
| a0002c0002 | 0/0 | 618 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | copy fasta | chr5 | 139443560 | 139467743 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1031 | 367 | 84 | 70 | 163 | 16 | 33 | ECSCR_chr5_139443560_139467743 | ECSCR | copy fasta | chr5 | 139443560 | 139467743 |
| a0001c0001t0002 | 0/0 | 1031 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | copy fasta | chr5 | 139443560 | 139467743 |
| a0002c0002t0001 | 0/0 | 1031 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | copy fasta | chr5 | 139443560 | 139467743 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/1 | 58 | 3 | 14 | 33 | 5 | 2 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0002 | 0/0 | 51 | 9 | 6 | 29 | 4 | 3 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0003 | 0/0 | 18 | 1 | 2 | 13 | 0 | 2 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0004 | 0/0 | 15 | 1 | 6 | 6 | 1 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0005 | 0/0 | 12 | 0 | 4 | 6 | 1 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0006 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0012 | 0/0 | 4 | 1 | 1 | 1 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0013 | 0/0 | 4 | 1 | 0 | 2 | 1 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0032 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0034 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | GBR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0070 | EUR | FIN | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0104 | EUR | IBS | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CDX | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0079 | SAS | PJL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | STU | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | STU | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | BEB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | BEB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | BEB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | STU | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | STU | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | STU | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | YRI | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | YRI | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | YRI | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | LWK | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | LWK | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | LWK | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | LWK | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | YRI | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ASW | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ASW | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0151 | EUR | TSI | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | GIH | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | USA | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | USA | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | USA | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | ECSCR_chr5_139443560_139467743 | ECSCR | chr5 | 139443560 | 139467743 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:139449093
|
A | T | 1 | a0002 | 1 | NA18974.hp2 | missense_variant | MODERATE | c.594T>A | p.Ser198Arg | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 9/10 | 667/1031 | 594/618 | 198/205 | chr5 | 139449093 |
| 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 |
|---|
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:139448634
|
G | C | 1 | a0001c0001t0002 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*266C>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 10/10 | 266 | chr5 | 139448634 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:139448957
|
A | G | 19 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0016others(16): Show | 30 | HG01243.hp2 HG02129.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.610-49T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 9/9 | chr5 | 139448957 | ||||||
| chr5:139449297
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.513-123A>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139449297 | ||||||
| chr5:139449351
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.513-177T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139449351 | ||||||
| chr5:139449430
|
C | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0149 | 3 | HG01081.hp1 HG01934.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.513-256G>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139449430 | ||||||
| chr5:139449441
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.513-267C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139449441 | ||||||
| chr5:139449459
|
T | C | 1 | a0001c0001t0001g0144 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.513-285A>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139449459 | ||||||
| chr5:139449703
|
C | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.513-529G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139449703 | ||||||
| chr5:139449876
|
C | A | 42 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(39): Show | 129 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.513-702G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139449876 | ||||||
| chr5:139449895
|
AT | A | 5 | a0001c0001t0001g0027a0001c0001t0001g0075a0001c0001t0001g0080others(2): Show | 6 | HG01517.hp2 HG02015.hp2 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.513-722delA | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139449895 | ||||||
| chr5:139449907
|
T | C | 1 | a0001c0001t0001g0080 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.513-733A>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139449907 | ||||||
| chr5:139450033
|
T | A | 1 | a0001c0001t0001g0082 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.513-859A>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139450033 | ||||||
| chr5:139450236
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.513-1062G>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139450236 | ||||||
| chr5:139450335
|
T | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG02895.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.513-1161A>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139450335 | ||||||
| chr5:139450337
|
T | G | 1 | a0001c0001t0001g0151 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.513-1163A>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139450337 | ||||||
| chr5:139450434
|
G | A | 3 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0155 | 3 | HG00639.hp2 HG00733.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.513-1260C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139450434 | ||||||
| chr5:139450464
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.513-1290C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139450464 | ||||||
| chr5:139450478
|
T | TA | 5 | a0001c0001t0001g0012a0001c0001t0001g0049a0001c0001t0001g0088others(2): Show | 8 | HG01261.hp1 HG02630.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.513-1305dupT | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139450478 | ||||||
| chr5:139450478
|
TA | T | 6 | a0001c0001t0001g0028a0001c0001t0001g0060a0001c0001t0001g0092others(3): Show | 7 | HG00408.hp1 HG01192.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.513-1305delT | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139450478 | ||||||
| chr5:139450478
|
TAA | T | 41 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(38): Show | 127 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.513-1306_513-1305d others(4): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139450478 | ||||||
| chr5:139450551
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.513-1377C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139450551 | ||||||
| chr5:139450669
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.513-1495C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139450669 | ||||||
| chr5:139450740
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.513-1566G>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139450740 | ||||||
| chr5:139450906
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.513-1732C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139450906 | ||||||
| chr5:139451009
|
G | T | 2 | a0001c0001t0001g0091a0001c0001t0001g0101 | 2 | HG00621.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.513-1835C>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139451009 | ||||||
| chr5:139451111
|
G | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0111 | 3 | NA18985.hp2 NA19010.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.513-1937C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139451111 | ||||||
| chr5:139451354
|
T | G | 42 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(39): Show | 129 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.513-2180A>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139451354 | ||||||
| chr5:139451368
|
G | A | 1 | a0001c0001t0001g0144 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.513-2194C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139451368 | ||||||
| chr5:139451430
|
T | G | 3 | a0001c0001t0001g0020a0001c0001t0001g0062a0001c0001t0001g0123 | 5 | HG02622.hp2 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.513-2256A>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139451430 | ||||||
| chr5:139451488
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.513-2314C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139451488 | ||||||
| chr5:139451744
|
G | C | 10 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0024others(7): Show | 18 | HG01243.hp2 HG02145.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.513-2570C>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139451744 | ||||||
| chr5:139451901
|
T | C | 1 | a0001c0001t0001g0120 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.512+2701A>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139451901 | ||||||
| chr5:139451941
|
T | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+2661A>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139451941 | ||||||
| chr5:139451943
|
A | G | 2 | a0001c0001t0001g0078a0001c0001t0001g0084 | 2 | HG03490.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.512+2659T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139451943 | ||||||
| chr5:139452163
|
T | A | 1 | a0001c0001t0001g0107 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.512+2439A>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452163 | ||||||
| chr5:139452226
|
G | C | 1 | a0001c0001t0001g0083 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.512+2376C>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452226 | ||||||
| chr5:139452272
|
T | C | 1 | a0001c0001t0001g0037 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.512+2330A>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452272 | ||||||
| chr5:139452335
|
G | T | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.512+2267C>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452335 | ||||||
| chr5:139452659
|
GNNNNNNN others(690): Show |
G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1246_512+1942d others(2): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452659 | ||||||
| chr5:139452659
|
GNNNNNNN others(730): Show |
G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1206_512+1942d others(2): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452659 | ||||||
| chr5:139452659
|
GNNNNNNN others(738): Show |
G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1198_512+1942d others(2): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452659 | ||||||
| chr5:139452660
|
N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1942G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452660 | ||||||
| chr5:139452661
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1941T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452661 | ||||||
| chr5:139452662
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1940T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452662 | ||||||
| chr5:139452663
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1939T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452663 | ||||||
| chr5:139452664
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1938T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452664 | ||||||
| chr5:139452665
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1937T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452665 | ||||||
| chr5:139452666
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1936T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452666 | ||||||
| chr5:139452667
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1935T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452667 | ||||||
| chr5:139452668
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1934T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452668 | ||||||
| chr5:139452669
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1933T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452669 | ||||||
| chr5:139452670
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1932T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452670 | ||||||
| chr5:139452671
|
N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1931G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452671 | ||||||
| chr5:139452672
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1930T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452672 | ||||||
| chr5:139452673
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1929T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452673 | ||||||
| chr5:139452674
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1928T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452674 | ||||||
| chr5:139452675
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1927T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452675 | ||||||
| chr5:139452676
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1926T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452676 | ||||||
| chr5:139452677
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1925T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452677 | ||||||
| chr5:139452678
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1924T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452678 | ||||||
| chr5:139452679
|
N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1923G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452679 | ||||||
| chr5:139452680
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1922T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452680 | ||||||
| chr5:139452681
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1921T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452681 | ||||||
| chr5:139452682
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1920T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452682 | ||||||
| chr5:139452683
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1919T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452683 | ||||||
| chr5:139452684
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1918T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452684 | ||||||
| chr5:139452685
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1917T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452685 | ||||||
| chr5:139452686
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1916T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452686 | ||||||
| chr5:139452687
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1915T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452687 | ||||||
| chr5:139452688
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1914T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452688 | ||||||
| chr5:139452689
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1913T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452689 | ||||||
| chr5:139452690
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1912T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452690 | ||||||
| chr5:139452691
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1911T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452691 | ||||||
| chr5:139452692
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1910T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452692 | ||||||
| chr5:139452693
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1909T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452693 | ||||||
| chr5:139452694
|
N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1908G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452694 | ||||||
| chr5:139452695
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1907T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452695 | ||||||
| chr5:139452696
|
N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1906G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452696 | ||||||
| chr5:139452697
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1905T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452697 | ||||||
| chr5:139452698
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1904T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452698 | ||||||
| chr5:139452699
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1903T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452699 | ||||||
| chr5:139452700
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1902T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452700 | ||||||
| chr5:139452701
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1901T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452701 | ||||||
| chr5:139452702
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1900T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452702 | ||||||
| chr5:139452703
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1899T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452703 | ||||||
| chr5:139452704
|
N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1898G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452704 | ||||||
| chr5:139452705
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1897T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452705 | ||||||
| chr5:139452706
|
N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1896G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452706 | ||||||
| chr5:139452707
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1895T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452707 | ||||||
| chr5:139452708
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1894T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452708 | ||||||
| chr5:139452709
|
N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1893G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452709 | ||||||
| chr5:139452710
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1892T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452710 | ||||||
| chr5:139452711
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1891T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452711 | ||||||
| chr5:139452712
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1890T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452712 | ||||||
| chr5:139452713
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1889T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452713 | ||||||
| chr5:139452714
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1888T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452714 | ||||||
| chr5:139452715
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1887T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452715 | ||||||
| chr5:139452716
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1886T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452716 | ||||||
| chr5:139452717
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1885T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452717 | ||||||
| chr5:139452718
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1884T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452718 | ||||||
| chr5:139452719
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1883T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452719 | ||||||
| chr5:139452720
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1882T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452720 | ||||||
| chr5:139452721
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1881T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452721 | ||||||
| chr5:139452722
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1880T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452722 | ||||||
| chr5:139452723
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1879T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452723 | ||||||
| chr5:139452724
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1878T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452724 | ||||||
| chr5:139452725
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1877T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452725 | ||||||
| chr5:139452726
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1876T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452726 | ||||||
| chr5:139452727
|
N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1875G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452727 | ||||||
| chr5:139452728
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1874T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452728 | ||||||
| chr5:139452729
|
N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1873G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452729 | ||||||
| chr5:139452730
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1872T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452730 | ||||||
| chr5:139452731
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1871T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452731 | ||||||
| chr5:139452732
|
N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1870G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452732 | ||||||
| chr5:139452733
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1869T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452733 | ||||||
| chr5:139452734
|
N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1868G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452734 | ||||||
| chr5:139452735
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1867T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452735 | ||||||
| chr5:139452736
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1866T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452736 | ||||||
| chr5:139452737
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1865T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452737 | ||||||
| chr5:139452738
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1864T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452738 | ||||||
| chr5:139452739
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1863T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452739 | ||||||
| chr5:139452740
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1862T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452740 | ||||||
| chr5:139452741
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1861T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452741 | ||||||
| chr5:139452742
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1860T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452742 | ||||||
| chr5:139452743
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1859T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452743 | ||||||
| chr5:139452744
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1858T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452744 | ||||||
| chr5:139452745
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1857T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452745 | ||||||
| chr5:139452746
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1856T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452746 | ||||||
| chr5:139452747
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1855T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452747 | ||||||
| chr5:139452748
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1854T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452748 | ||||||
| chr5:139452749
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1853T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452749 | ||||||
| chr5:139452750
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1852T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452750 | ||||||
| chr5:139452751
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1851T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452751 | ||||||
| chr5:139452752
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1850T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452752 | ||||||
| chr5:139452753
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1849T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452753 | ||||||
| chr5:139452754
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1848T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452754 | ||||||
| chr5:139452755
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1847T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452755 | ||||||
| chr5:139452756
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1846T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452756 | ||||||
| chr5:139452757
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1845T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452757 | ||||||
| chr5:139452758
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1844T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452758 | ||||||
| chr5:139452759
|
N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1843G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452759 | ||||||
| chr5:139452760
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1842T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452760 | ||||||
| chr5:139452761
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1841T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452761 | ||||||
| chr5:139452762
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1840T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452762 | ||||||
| chr5:139452763
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1839T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452763 | ||||||
| chr5:139452764
|
N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1838G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452764 | ||||||
| chr5:139452765
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1837T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452765 | ||||||
| chr5:139452766
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1836T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452766 | ||||||
| chr5:139452767
|
N | C | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1835T>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452767 | ||||||
| chr5:139452768
|
N | C | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1834T>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452768 | ||||||
| chr5:139452769
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1833T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452769 | ||||||
| chr5:139452770
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1832T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452770 | ||||||
| chr5:139452771
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1831T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452771 | ||||||
| chr5:139452772
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1830T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452772 | ||||||
| chr5:139452773
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1829T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452773 | ||||||
| chr5:139452774
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1828T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452774 | ||||||
| chr5:139452775
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1827T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452775 | ||||||
| chr5:139452776
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1826T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452776 | ||||||
| chr5:139452777
|
N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1825G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452777 | ||||||
| chr5:139452778
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1824T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452778 | ||||||
| chr5:139452779
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1823T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452779 | ||||||
| chr5:139452780
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1822T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452780 | ||||||
| chr5:139452781
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1821T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452781 | ||||||
| chr5:139452782
|
N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1820G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452782 | ||||||
| chr5:139452783
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1819T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452783 | ||||||
| chr5:139452784
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1818T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452784 | ||||||
| chr5:139452785
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1817T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452785 | ||||||
| chr5:139452786
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1816T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452786 | ||||||
| chr5:139452787
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1815T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452787 | ||||||
| chr5:139452788
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1814T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452788 | ||||||
| chr5:139452789
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1813T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452789 | ||||||
| chr5:139452790
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1812T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452790 | ||||||
| chr5:139452791
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1811T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452791 | ||||||
| chr5:139452792
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1810T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452792 | ||||||
| chr5:139452793
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1809T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452793 | ||||||
| chr5:139452794
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1808T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452794 | ||||||
| chr5:139452795
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1807T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452795 | ||||||
| chr5:139452796
|
N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1806G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452796 | ||||||
| chr5:139452797
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1805T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452797 | ||||||
| chr5:139452798
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1804T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452798 | ||||||
| chr5:139452799
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1803T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452799 | ||||||
| chr5:139452800
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1802T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452800 | ||||||
| chr5:139452801
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1801T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452801 | ||||||
| chr5:139452802
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1800T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452802 | ||||||
| chr5:139452803
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1799T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452803 | ||||||
| chr5:139452804
|
N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1798G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452804 | ||||||
| chr5:139452805
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1797T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452805 | ||||||
| chr5:139452806
|
N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1796G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452806 | ||||||
| chr5:139452807
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1795T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452807 | ||||||
| chr5:139452808
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1794T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452808 | ||||||
| chr5:139452809
|
N | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1793G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452809 | ||||||
| chr5:139452810
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1792T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452810 | ||||||
| chr5:139452811
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1791T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452811 | ||||||
| chr5:139452812
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1790T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452812 | ||||||
| chr5:139452813
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1789T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452813 | ||||||
| chr5:139452814
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1788T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452814 | ||||||
| chr5:139452815
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1787T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452815 | ||||||
| chr5:139452816
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1786T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452816 | ||||||
| chr5:139452817
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1785T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452817 | ||||||
| chr5:139452818
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1784T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452818 | ||||||
| chr5:139452819
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1783T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452819 | ||||||
| chr5:139452820
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1782T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452820 | ||||||
| chr5:139452821
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1781T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452821 | ||||||
| chr5:139452822
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1780T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452822 | ||||||
| chr5:139452823
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1779T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452823 | ||||||
| chr5:139452824
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1778T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452824 | ||||||
| chr5:139452825
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1777T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452825 | ||||||
| chr5:139452826
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1776T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452826 | ||||||
| chr5:139452827
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1775T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452827 | ||||||
| chr5:139452828
|
N | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1774T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452828 | ||||||
| chr5:139452829
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1773T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452829 | ||||||
| chr5:139452830
|
N | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+1772T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452830 | ||||||
| chr5:139452831
|
NNNNNNNN others(839): Show |
N | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+926_512+1771de others(1): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139452831 | ||||||
| chr5:139453357
|
N | A | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1245G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453357 | ||||||
| chr5:139453358
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1244T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453358 | ||||||
| chr5:139453359
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1243T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453359 | ||||||
| chr5:139453360
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1242T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453360 | ||||||
| chr5:139453361
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1241T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453361 | ||||||
| chr5:139453362
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1240T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453362 | ||||||
| chr5:139453363
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1239T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453363 | ||||||
| chr5:139453364
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1238T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453364 | ||||||
| chr5:139453365
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1237T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453365 | ||||||
| chr5:139453366
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1236T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453366 | ||||||
| chr5:139453367
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1235T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453367 | ||||||
| chr5:139453368
|
N | A | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1234G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453368 | ||||||
| chr5:139453369
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1233T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453369 | ||||||
| chr5:139453370
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1232T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453370 | ||||||
| chr5:139453371
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1231T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453371 | ||||||
| chr5:139453372
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1230T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453372 | ||||||
| chr5:139453373
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1229T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453373 | ||||||
| chr5:139453374
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1228T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453374 | ||||||
| chr5:139453375
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1227T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453375 | ||||||
| chr5:139453376
|
N | A | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1226G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453376 | ||||||
| chr5:139453377
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1225T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453377 | ||||||
| chr5:139453378
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1224T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453378 | ||||||
| chr5:139453379
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1223T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453379 | ||||||
| chr5:139453380
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1222T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453380 | ||||||
| chr5:139453381
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1221T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453381 | ||||||
| chr5:139453382
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1220T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453382 | ||||||
| chr5:139453383
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1219T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453383 | ||||||
| chr5:139453384
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1218T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453384 | ||||||
| chr5:139453385
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1217T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453385 | ||||||
| chr5:139453386
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1216T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453386 | ||||||
| chr5:139453387
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1215T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453387 | ||||||
| chr5:139453388
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1214T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453388 | ||||||
| chr5:139453389
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1213T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453389 | ||||||
| chr5:139453390
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1212T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453390 | ||||||
| chr5:139453391
|
N | A | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1211G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453391 | ||||||
| chr5:139453392
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1210T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453392 | ||||||
| chr5:139453393
|
N | A | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1209G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453393 | ||||||
| chr5:139453394
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1208T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453394 | ||||||
| chr5:139453395
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1207T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453395 | ||||||
| chr5:139453396
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1206T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453396 | ||||||
| chr5:139453397
|
N | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1205G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453397 | ||||||
| chr5:139453397
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1205T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453397 | ||||||
| chr5:139453398
|
N | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1204T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453398 | ||||||
| chr5:139453398
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1204T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453398 | ||||||
| chr5:139453399
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1203T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453399 | ||||||
| chr5:139453400
|
N | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1202T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453400 | ||||||
| chr5:139453400
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1202T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453400 | ||||||
| chr5:139453401
|
N | A | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1201G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453401 | ||||||
| chr5:139453401
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1201T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453401 | ||||||
| chr5:139453402
|
N | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1200T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453402 | ||||||
| chr5:139453402
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1200T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453402 | ||||||
| chr5:139453403
|
N | A | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1199G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453403 | ||||||
| chr5:139453403
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1199T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453403 | ||||||
| chr5:139453404
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1198T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453404 | ||||||
| chr5:139453405
|
N | A | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1197G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453405 | ||||||
| chr5:139453405
|
N | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1197T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453405 | ||||||
| chr5:139453405
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1197T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453405 | ||||||
| chr5:139453406
|
N | A | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1196G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453406 | ||||||
| chr5:139453406
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1196T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453406 | ||||||
| chr5:139453407
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1195T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453407 | ||||||
| chr5:139453407
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1195T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453407 | ||||||
| chr5:139453408
|
N | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1194G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453408 | ||||||
| chr5:139453408
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1194T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453408 | ||||||
| chr5:139453409
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1193T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453409 | ||||||
| chr5:139453409
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1193T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453409 | ||||||
| chr5:139453410
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1192T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453410 | ||||||
| chr5:139453410
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1192T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453410 | ||||||
| chr5:139453411
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1191T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453411 | ||||||
| chr5:139453411
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1191T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453411 | ||||||
| chr5:139453412
|
N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1190T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453412 | ||||||
| chr5:139453412
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1190T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453412 | ||||||
| chr5:139453413
|
N | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+1189T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453413 | ||||||
| chr5:139453414
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1188T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453414 | ||||||
| chr5:139453414
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1188T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453414 | ||||||
| chr5:139453415
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1187T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453415 | ||||||
| chr5:139453415
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1187T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453415 | ||||||
| chr5:139453416
|
N | A | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1186G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453416 | ||||||
| chr5:139453416
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1186T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453416 | ||||||
| chr5:139453417
|
N | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+1185T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453417 | ||||||
| chr5:139453418
|
N | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1184T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453418 | ||||||
| chr5:139453418
|
N | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1184T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453418 | ||||||
| chr5:139453419
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1183T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453419 | ||||||
| chr5:139453419
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1183T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453419 | ||||||
| chr5:139453420
|
N | T | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+1182T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453420 | ||||||
| chr5:139453421
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1181T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453421 | ||||||
| chr5:139453421
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1181T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453421 | ||||||
| chr5:139453422
|
N | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+1180T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453422 | ||||||
| chr5:139453423
|
N | T | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+1179T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453423 | ||||||
| chr5:139453424
|
N | A | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1178G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453424 | ||||||
| chr5:139453424
|
N | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1178T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453424 | ||||||
| chr5:139453425
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1177T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453425 | ||||||
| chr5:139453425
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1177T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453425 | ||||||
| chr5:139453426
|
N | A | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1176G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453426 | ||||||
| chr5:139453426
|
N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1176T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453426 | ||||||
| chr5:139453426
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1176T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453426 | ||||||
| chr5:139453427
|
N | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1175T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453427 | ||||||
| chr5:139453427
|
N | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1175T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453427 | ||||||
| chr5:139453428
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1174T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453428 | ||||||
| chr5:139453428
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1174T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453428 | ||||||
| chr5:139453429
|
N | A | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1173G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453429 | ||||||
| chr5:139453429
|
N | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1173T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453429 | ||||||
| chr5:139453429
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1173T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453429 | ||||||
| chr5:139453430
|
N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1172T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453430 | ||||||
| chr5:139453430
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1172T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453430 | ||||||
| chr5:139453431
|
N | A | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1171G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453431 | ||||||
| chr5:139453431
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1171T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453431 | ||||||
| chr5:139453432
|
N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1170T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453432 | ||||||
| chr5:139453432
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1170T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453432 | ||||||
| chr5:139453433
|
N | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1169G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453433 | ||||||
| chr5:139453433
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1169T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453433 | ||||||
| chr5:139453434
|
N | T | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+1168T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453434 | ||||||
| chr5:139453435
|
N | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+1167T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453435 | ||||||
| chr5:139453436
|
N | T | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+1166T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453436 | ||||||
| chr5:139453437
|
N | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+1165T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453437 | ||||||
| chr5:139453438
|
N | T | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+1164T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453438 | ||||||
| chr5:139453439
|
N | A | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1163G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453439 | ||||||
| chr5:139453439
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1163T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453439 | ||||||
| chr5:139453440
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1162T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453440 | ||||||
| chr5:139453440
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1162T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453440 | ||||||
| chr5:139453441
|
N | A | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1161G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453441 | ||||||
| chr5:139453441
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1161T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453441 | ||||||
| chr5:139453442
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1160T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453442 | ||||||
| chr5:139453442
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1160T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453442 | ||||||
| chr5:139453443
|
N | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1159G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453443 | ||||||
| chr5:139453443
|
N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1159T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453443 | ||||||
| chr5:139453443
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1159T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453443 | ||||||
| chr5:139453444
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1158T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453444 | ||||||
| chr5:139453444
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1158T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453444 | ||||||
| chr5:139453445
|
N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1157T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453445 | ||||||
| chr5:139453445
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1157T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453445 | ||||||
| chr5:139453446
|
N | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1156G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453446 | ||||||
| chr5:139453446
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1156T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453446 | ||||||
| chr5:139453446
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1156T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453446 | ||||||
| chr5:139453447
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1155T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453447 | ||||||
| chr5:139453447
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1155T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453447 | ||||||
| chr5:139453448
|
N | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1154T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453448 | ||||||
| chr5:139453448
|
N | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1154T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453448 | ||||||
| chr5:139453449
|
N | A | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1153G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453449 | ||||||
| chr5:139453449
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1153T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453449 | ||||||
| chr5:139453450
|
N | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1152T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453450 | ||||||
| chr5:139453450
|
N | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1152T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453450 | ||||||
| chr5:139453451
|
N | A | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1151G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453451 | ||||||
| chr5:139453451
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1151T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453451 | ||||||
| chr5:139453452
|
N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1150T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453452 | ||||||
| chr5:139453452
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1150T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453452 | ||||||
| chr5:139453453
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1149T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453453 | ||||||
| chr5:139453453
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1149T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453453 | ||||||
| chr5:139453454
|
N | A | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1148G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453454 | ||||||
| chr5:139453454
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1148T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453454 | ||||||
| chr5:139453455
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1147T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453455 | ||||||
| chr5:139453455
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1147T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453455 | ||||||
| chr5:139453456
|
N | A | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1146G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453456 | ||||||
| chr5:139453456
|
N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1146T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453456 | ||||||
| chr5:139453456
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1146T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453456 | ||||||
| chr5:139453457
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1145T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453457 | ||||||
| chr5:139453457
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1145T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453457 | ||||||
| chr5:139453458
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1144T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453458 | ||||||
| chr5:139453458
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1144T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453458 | ||||||
| chr5:139453459
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1143T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453459 | ||||||
| chr5:139453459
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1143T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453459 | ||||||
| chr5:139453460
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1142T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453460 | ||||||
| chr5:139453460
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1142T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453460 | ||||||
| chr5:139453461
|
N | A | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1141G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453461 | ||||||
| chr5:139453461
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1141T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453461 | ||||||
| chr5:139453462
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1140T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453462 | ||||||
| chr5:139453462
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1140T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453462 | ||||||
| chr5:139453463
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1139T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453463 | ||||||
| chr5:139453463
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1139T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453463 | ||||||
| chr5:139453464
|
N | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1138G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453464 | ||||||
| chr5:139453464
|
N | C | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1138T>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453464 | ||||||
| chr5:139453464
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1138T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453464 | ||||||
| chr5:139453465
|
N | C | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1137T>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453465 | ||||||
| chr5:139453465
|
N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1137T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453465 | ||||||
| chr5:139453465
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1137T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453465 | ||||||
| chr5:139453466
|
N | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1136G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453466 | ||||||
| chr5:139453466
|
N | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1136T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453466 | ||||||
| chr5:139453467
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1135T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453467 | ||||||
| chr5:139453467
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1135T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453467 | ||||||
| chr5:139453468
|
N | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1134T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453468 | ||||||
| chr5:139453468
|
N | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1134T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453468 | ||||||
| chr5:139453469
|
N | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1133G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453469 | ||||||
| chr5:139453469
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1133T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453469 | ||||||
| chr5:139453470
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1132T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453470 | ||||||
| chr5:139453470
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1132T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453470 | ||||||
| chr5:139453471
|
N | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1131G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453471 | ||||||
| chr5:139453471
|
N | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1131T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453471 | ||||||
| chr5:139453472
|
N | A | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1130G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453472 | ||||||
| chr5:139453472
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1130T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453472 | ||||||
| chr5:139453472
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1130T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453472 | ||||||
| chr5:139453473
|
N | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1129T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453473 | ||||||
| chr5:139453473
|
N | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1129T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453473 | ||||||
| chr5:139453474
|
N | A | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1128G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453474 | ||||||
| chr5:139453474
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1128T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453474 | ||||||
| chr5:139453475
|
N | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1127T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453475 | ||||||
| chr5:139453475
|
N | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1127T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453475 | ||||||
| chr5:139453476
|
N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1126T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453476 | ||||||
| chr5:139453476
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1126T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453476 | ||||||
| chr5:139453477
|
N | A | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1125G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453477 | ||||||
| chr5:139453477
|
N | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1125T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453477 | ||||||
| chr5:139453477
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1125T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453477 | ||||||
| chr5:139453478
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1124T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453478 | ||||||
| chr5:139453478
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1124T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453478 | ||||||
| chr5:139453479
|
N | A | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1123G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453479 | ||||||
| chr5:139453479
|
N | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1123T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453479 | ||||||
| chr5:139453480
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1122T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453480 | ||||||
| chr5:139453480
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1122T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453480 | ||||||
| chr5:139453481
|
N | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+1121T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453481 | ||||||
| chr5:139453482
|
N | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1120T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453482 | ||||||
| chr5:139453482
|
N | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1120T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453482 | ||||||
| chr5:139453483
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1119T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453483 | ||||||
| chr5:139453483
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1119T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453483 | ||||||
| chr5:139453484
|
N | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1118T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453484 | ||||||
| chr5:139453484
|
N | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1118T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453484 | ||||||
| chr5:139453485
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1117T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453485 | ||||||
| chr5:139453485
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1117T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453485 | ||||||
| chr5:139453486
|
N | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1116T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453486 | ||||||
| chr5:139453486
|
N | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1116T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453486 | ||||||
| chr5:139453487
|
N | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+1115T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453487 | ||||||
| chr5:139453488
|
N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1114T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453488 | ||||||
| chr5:139453488
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1114T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453488 | ||||||
| chr5:139453489
|
N | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+1113T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453489 | ||||||
| chr5:139453490
|
N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1112T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453490 | ||||||
| chr5:139453490
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1112T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453490 | ||||||
| chr5:139453491
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1111T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453491 | ||||||
| chr5:139453491
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1111T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453491 | ||||||
| chr5:139453492
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1110T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453492 | ||||||
| chr5:139453492
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1110T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453492 | ||||||
| chr5:139453493
|
N | A | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1109G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453493 | ||||||
| chr5:139453493
|
N | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1109T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453493 | ||||||
| chr5:139453493
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1109T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453493 | ||||||
| chr5:139453494
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1108T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453494 | ||||||
| chr5:139453494
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1108T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453494 | ||||||
| chr5:139453495
|
N | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+1107T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453495 | ||||||
| chr5:139453496
|
N | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1106G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453496 | ||||||
| chr5:139453496
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1106T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453496 | ||||||
| chr5:139453496
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1106T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453496 | ||||||
| chr5:139453497
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1105T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453497 | ||||||
| chr5:139453497
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1105T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453497 | ||||||
| chr5:139453498
|
N | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1104T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453498 | ||||||
| chr5:139453498
|
N | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1104T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453498 | ||||||
| chr5:139453499
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1103T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453499 | ||||||
| chr5:139453499
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1103T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453499 | ||||||
| chr5:139453500
|
N | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1102T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453500 | ||||||
| chr5:139453500
|
N | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1102T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453500 | ||||||
| chr5:139453501
|
N | A | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1101G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453501 | ||||||
| chr5:139453501
|
N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1101T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453501 | ||||||
| chr5:139453502
|
N | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1100T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453502 | ||||||
| chr5:139453502
|
N | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1100T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453502 | ||||||
| chr5:139453503
|
N | A | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1099G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453503 | ||||||
| chr5:139453503
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1099T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453503 | ||||||
| chr5:139453504
|
N | A | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1098G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453504 | ||||||
| chr5:139453504
|
N | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1098T>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453504 | ||||||
| chr5:139453504
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1098T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453504 | ||||||
| chr5:139453505
|
N | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1097T>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453505 | ||||||
| chr5:139453505
|
N | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1097T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453505 | ||||||
| chr5:139453506
|
N | A | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1096G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453506 | ||||||
| chr5:139453506
|
N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1096T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453506 | ||||||
| chr5:139453506
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1096T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453506 | ||||||
| chr5:139453507
|
N | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1095T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453507 | ||||||
| chr5:139453507
|
N | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1095T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453507 | ||||||
| chr5:139453508
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1094T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453508 | ||||||
| chr5:139453508
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1094T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453508 | ||||||
| chr5:139453509
|
N | A | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1093G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453509 | ||||||
| chr5:139453509
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1093T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453509 | ||||||
| chr5:139453510
|
N | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+1092T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453510 | ||||||
| chr5:139453511
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1091T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453511 | ||||||
| chr5:139453511
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1091T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453511 | ||||||
| chr5:139453512
|
N | C | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1090T>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453512 | ||||||
| chr5:139453512
|
N | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1090T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453512 | ||||||
| chr5:139453512
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1090T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453512 | ||||||
| chr5:139453513
|
N | C | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1089T>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453513 | ||||||
| chr5:139453513
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1089T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453513 | ||||||
| chr5:139453513
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1089T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453513 | ||||||
| chr5:139453514
|
N | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1088G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453514 | ||||||
| chr5:139453514
|
N | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1088T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453514 | ||||||
| chr5:139453515
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1087T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453515 | ||||||
| chr5:139453515
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1087T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453515 | ||||||
| chr5:139453516
|
N | T | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+1086T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453516 | ||||||
| chr5:139453517
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1085T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453517 | ||||||
| chr5:139453517
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1085T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453517 | ||||||
| chr5:139453518
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1084T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453518 | ||||||
| chr5:139453518
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1084T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453518 | ||||||
| chr5:139453519
|
N | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1083G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453519 | ||||||
| chr5:139453519
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1083T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453519 | ||||||
| chr5:139453519
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1083T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453519 | ||||||
| chr5:139453520
|
N | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+1082T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453520 | ||||||
| chr5:139453521
|
N | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1081T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453521 | ||||||
| chr5:139453521
|
N | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1081T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453521 | ||||||
| chr5:139453522
|
N | A | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1080G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453522 | ||||||
| chr5:139453522
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1080T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453522 | ||||||
| chr5:139453523
|
N | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1079T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453523 | ||||||
| chr5:139453523
|
N | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1079T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453523 | ||||||
| chr5:139453524
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1078T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453524 | ||||||
| chr5:139453524
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1078T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453524 | ||||||
| chr5:139453525
|
N | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1077T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453525 | ||||||
| chr5:139453525
|
N | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1077T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453525 | ||||||
| chr5:139453526
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1076T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453526 | ||||||
| chr5:139453526
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1076T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453526 | ||||||
| chr5:139453527
|
N | A | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1075G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453527 | ||||||
| chr5:139453527
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1075T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453527 | ||||||
| chr5:139453528
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1074T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453528 | ||||||
| chr5:139453528
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1074T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453528 | ||||||
| chr5:139453529
|
N | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+1073T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453529 | ||||||
| chr5:139453530
|
N | T | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+1072T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453530 | ||||||
| chr5:139453531
|
N | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+1071T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453531 | ||||||
| chr5:139453532
|
N | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1070T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453532 | ||||||
| chr5:139453532
|
N | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1070T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453532 | ||||||
| chr5:139453533
|
N | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1069G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453533 | ||||||
| chr5:139453533
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1069T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453533 | ||||||
| chr5:139453534
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1068T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453534 | ||||||
| chr5:139453534
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1068T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453534 | ||||||
| chr5:139453535
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1067T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453535 | ||||||
| chr5:139453535
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1067T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453535 | ||||||
| chr5:139453536
|
N | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1066T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453536 | ||||||
| chr5:139453536
|
N | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1066T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453536 | ||||||
| chr5:139453537
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1065T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453537 | ||||||
| chr5:139453537
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1065T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453537 | ||||||
| chr5:139453538
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1064T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453538 | ||||||
| chr5:139453538
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1064T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453538 | ||||||
| chr5:139453539
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1063T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453539 | ||||||
| chr5:139453539
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1063T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453539 | ||||||
| chr5:139453540
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1062T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453540 | ||||||
| chr5:139453540
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1062T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453540 | ||||||
| chr5:139453541
|
N | A | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1061G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453541 | ||||||
| chr5:139453541
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1061T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453541 | ||||||
| chr5:139453542
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1060T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453542 | ||||||
| chr5:139453542
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1060T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453542 | ||||||
| chr5:139453543
|
N | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1059G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453543 | ||||||
| chr5:139453543
|
N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1059T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453543 | ||||||
| chr5:139453543
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1059T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453543 | ||||||
| chr5:139453544
|
N | A | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1058G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453544 | ||||||
| chr5:139453544
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1058T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453544 | ||||||
| chr5:139453545
|
N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1057T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453545 | ||||||
| chr5:139453545
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1057T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453545 | ||||||
| chr5:139453546
|
N | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1056G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453546 | ||||||
| chr5:139453546
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1056T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453546 | ||||||
| chr5:139453546
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1056T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453546 | ||||||
| chr5:139453547
|
N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1055T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453547 | ||||||
| chr5:139453547
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1055T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453547 | ||||||
| chr5:139453548
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1054T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453548 | ||||||
| chr5:139453548
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1054T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453548 | ||||||
| chr5:139453549
|
N | A | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1053G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453549 | ||||||
| chr5:139453549
|
N | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1053T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453549 | ||||||
| chr5:139453549
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1053T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453549 | ||||||
| chr5:139453550
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1052T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453550 | ||||||
| chr5:139453550
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1052T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453550 | ||||||
| chr5:139453551
|
N | A | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1051G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453551 | ||||||
| chr5:139453551
|
N | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1051T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453551 | ||||||
| chr5:139453551
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1051T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453551 | ||||||
| chr5:139453552
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1050T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453552 | ||||||
| chr5:139453552
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1050T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453552 | ||||||
| chr5:139453553
|
N | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1049T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453553 | ||||||
| chr5:139453553
|
N | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1049T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453553 | ||||||
| chr5:139453554
|
N | A | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1048G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453554 | ||||||
| chr5:139453554
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1048T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453554 | ||||||
| chr5:139453555
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1047T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453555 | ||||||
| chr5:139453555
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1047T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453555 | ||||||
| chr5:139453556
|
N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1046T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453556 | ||||||
| chr5:139453556
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1046T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453556 | ||||||
| chr5:139453557
|
N | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+1045T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453557 | ||||||
| chr5:139453558
|
N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1044T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453558 | ||||||
| chr5:139453558
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1044T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453558 | ||||||
| chr5:139453559
|
N | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+1043T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453559 | ||||||
| chr5:139453560
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1042T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453560 | ||||||
| chr5:139453560
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1042T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453560 | ||||||
| chr5:139453561
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1041T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453561 | ||||||
| chr5:139453561
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1041T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453561 | ||||||
| chr5:139453562
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1040T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453562 | ||||||
| chr5:139453562
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1040T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453562 | ||||||
| chr5:139453563
|
N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1039T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453563 | ||||||
| chr5:139453563
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1039T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453563 | ||||||
| chr5:139453564
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1038T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453564 | ||||||
| chr5:139453564
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1038T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453564 | ||||||
| chr5:139453565
|
N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1037T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453565 | ||||||
| chr5:139453565
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1037T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453565 | ||||||
| chr5:139453566
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1036T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453566 | ||||||
| chr5:139453566
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1036T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453566 | ||||||
| chr5:139453567
|
N | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+1035T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453567 | ||||||
| chr5:139453568
|
N | A | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1034G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453568 | ||||||
| chr5:139453568
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1034T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453568 | ||||||
| chr5:139453569
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1033T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453569 | ||||||
| chr5:139453569
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1033T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453569 | ||||||
| chr5:139453570
|
N | T | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+1032T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453570 | ||||||
| chr5:139453571
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1031T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453571 | ||||||
| chr5:139453571
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1031T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453571 | ||||||
| chr5:139453572
|
N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1030T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453572 | ||||||
| chr5:139453572
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1030T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453572 | ||||||
| chr5:139453573
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1029T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453573 | ||||||
| chr5:139453573
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1029T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453573 | ||||||
| chr5:139453574
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1028T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453574 | ||||||
| chr5:139453574
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1028T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453574 | ||||||
| chr5:139453575
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1027T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453575 | ||||||
| chr5:139453575
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1027T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453575 | ||||||
| chr5:139453576
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1026T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453576 | ||||||
| chr5:139453576
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1026T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453576 | ||||||
| chr5:139453577
|
N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1025T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453577 | ||||||
| chr5:139453577
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1025T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453577 | ||||||
| chr5:139453578
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1024T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453578 | ||||||
| chr5:139453578
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1024T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453578 | ||||||
| chr5:139453579
|
N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1023T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453579 | ||||||
| chr5:139453579
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1023T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453579 | ||||||
| chr5:139453580
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1022T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453580 | ||||||
| chr5:139453580
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1022T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453580 | ||||||
| chr5:139453581
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1021T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453581 | ||||||
| chr5:139453581
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1021T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453581 | ||||||
| chr5:139453582
|
N | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+1020T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453582 | ||||||
| chr5:139453583
|
N | A | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1019G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453583 | ||||||
| chr5:139453583
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1019T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453583 | ||||||
| chr5:139453584
|
N | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1018G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453584 | ||||||
| chr5:139453584
|
N | C | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1018T>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453584 | ||||||
| chr5:139453584
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1018T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453584 | ||||||
| chr5:139453585
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1017T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453585 | ||||||
| chr5:139453585
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1017T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453585 | ||||||
| chr5:139453586
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1016T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453586 | ||||||
| chr5:139453586
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1016T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453586 | ||||||
| chr5:139453587
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1015T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453587 | ||||||
| chr5:139453587
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1015T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453587 | ||||||
| chr5:139453588
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1014T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453588 | ||||||
| chr5:139453588
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1014T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453588 | ||||||
| chr5:139453589
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1013T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453589 | ||||||
| chr5:139453589
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1013T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453589 | ||||||
| chr5:139453590
|
N | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+1012T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453590 | ||||||
| chr5:139453591
|
N | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1011T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453591 | ||||||
| chr5:139453591
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1011T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453591 | ||||||
| chr5:139453592
|
N | A | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1010G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453592 | ||||||
| chr5:139453592
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1010T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453592 | ||||||
| chr5:139453593
|
N | T | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+1009T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453593 | ||||||
| chr5:139453594
|
N | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1008G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453594 | ||||||
| chr5:139453594
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1008T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453594 | ||||||
| chr5:139453595
|
N | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1007T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453595 | ||||||
| chr5:139453595
|
N | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1007T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453595 | ||||||
| chr5:139453596
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1006T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453596 | ||||||
| chr5:139453596
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1006T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453596 | ||||||
| chr5:139453597
|
N | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1005T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453597 | ||||||
| chr5:139453597
|
N | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1005T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453597 | ||||||
| chr5:139453598
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1004T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453598 | ||||||
| chr5:139453598
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1004T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453598 | ||||||
| chr5:139453599
|
N | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1003T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453599 | ||||||
| chr5:139453599
|
N | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+1003T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453599 | ||||||
| chr5:139453600
|
N | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+1002T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453600 | ||||||
| chr5:139453601
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+1001T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453601 | ||||||
| chr5:139453601
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1001T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453601 | ||||||
| chr5:139453602
|
N | A | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+1000G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453602 | ||||||
| chr5:139453602
|
N | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+1000T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453602 | ||||||
| chr5:139453602
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+1000T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453602 | ||||||
| chr5:139453603
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+999T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453603 | ||||||
| chr5:139453603
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+999T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453603 | ||||||
| chr5:139453604
|
N | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+998T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453604 | ||||||
| chr5:139453604
|
N | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+998T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453604 | ||||||
| chr5:139453605
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+997T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453605 | ||||||
| chr5:139453605
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+997T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453605 | ||||||
| chr5:139453606
|
N | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+996T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453606 | ||||||
| chr5:139453606
|
N | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+996T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453606 | ||||||
| chr5:139453607
|
N | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+995T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453607 | ||||||
| chr5:139453608
|
N | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+994G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453608 | ||||||
| chr5:139453608
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+994T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453608 | ||||||
| chr5:139453609
|
N | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+993T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453609 | ||||||
| chr5:139453610
|
N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+992T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453610 | ||||||
| chr5:139453610
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+992T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453610 | ||||||
| chr5:139453611
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+991T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453611 | ||||||
| chr5:139453611
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+991T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453611 | ||||||
| chr5:139453612
|
N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+990T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453612 | ||||||
| chr5:139453612
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+990T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453612 | ||||||
| chr5:139453613
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+989T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453613 | ||||||
| chr5:139453613
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+989T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453613 | ||||||
| chr5:139453614
|
N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+988T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453614 | ||||||
| chr5:139453614
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+988T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453614 | ||||||
| chr5:139453615
|
N | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+987T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453615 | ||||||
| chr5:139453616
|
N | A | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+986G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453616 | ||||||
| chr5:139453616
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+986T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453616 | ||||||
| chr5:139453617
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+985T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453617 | ||||||
| chr5:139453617
|
N | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+985T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453617 | ||||||
| chr5:139453618
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+984T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453618 | ||||||
| chr5:139453618
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+984T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453618 | ||||||
| chr5:139453619
|
N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+983T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453619 | ||||||
| chr5:139453619
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+983T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453619 | ||||||
| chr5:139453620
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+982T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453620 | ||||||
| chr5:139453620
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+982T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453620 | ||||||
| chr5:139453621
|
N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+981T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453621 | ||||||
| chr5:139453621
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+981T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453621 | ||||||
| chr5:139453622
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+980T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453622 | ||||||
| chr5:139453622
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+980T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453622 | ||||||
| chr5:139453623
|
N | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+979G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453623 | ||||||
| chr5:139453623
|
N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+979T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453623 | ||||||
| chr5:139453623
|
N | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.512+979T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453623 | ||||||
| chr5:139453624
|
N | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.512+978T>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453624 | ||||||
| chr5:139453624
|
N | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0118 | 2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.512+978T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453624 | ||||||
| chr5:139453625
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+977T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453625 | ||||||
| chr5:139453625
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+977T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453625 | ||||||
| chr5:139453626
|
N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+976T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453626 | ||||||
| chr5:139453626
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+976T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453626 | ||||||
| chr5:139453627
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+975T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453627 | ||||||
| chr5:139453627
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+975T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453627 | ||||||
| chr5:139453628
|
N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+974T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453628 | ||||||
| chr5:139453628
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+974T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453628 | ||||||
| chr5:139453629
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+973T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453629 | ||||||
| chr5:139453629
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+973T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453629 | ||||||
| chr5:139453630
|
N | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+972T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453630 | ||||||
| chr5:139453631
|
N | A | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+971G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453631 | ||||||
| chr5:139453631
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+971T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453631 | ||||||
| chr5:139453632
|
N | C | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+970T>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453632 | ||||||
| chr5:139453632
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+970T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453632 | ||||||
| chr5:139453633
|
N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+969T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453633 | ||||||
| chr5:139453633
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+969T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453633 | ||||||
| chr5:139453634
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+968T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453634 | ||||||
| chr5:139453634
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+968T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453634 | ||||||
| chr5:139453635
|
N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+967T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453635 | ||||||
| chr5:139453635
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+967T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453635 | ||||||
| chr5:139453636
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+966T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453636 | ||||||
| chr5:139453636
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+966T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453636 | ||||||
| chr5:139453637
|
N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+965T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453637 | ||||||
| chr5:139453637
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+965T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453637 | ||||||
| chr5:139453638
|
N | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+964T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453638 | ||||||
| chr5:139453639
|
N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+963T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453639 | ||||||
| chr5:139453639
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+963T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453639 | ||||||
| chr5:139453640
|
N | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+962T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453640 | ||||||
| chr5:139453641
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+961T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453641 | ||||||
| chr5:139453641
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+961T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453641 | ||||||
| chr5:139453642
|
N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+960T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453642 | ||||||
| chr5:139453642
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+960T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453642 | ||||||
| chr5:139453643
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+959T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453643 | ||||||
| chr5:139453643
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+959T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453643 | ||||||
| chr5:139453644
|
N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+958T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453644 | ||||||
| chr5:139453644
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+958T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453644 | ||||||
| chr5:139453645
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+957T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453645 | ||||||
| chr5:139453645
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+957T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453645 | ||||||
| chr5:139453646
|
N | G | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+956T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453646 | ||||||
| chr5:139453646
|
N | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+956T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453646 | ||||||
| chr5:139453647
|
N | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.512+955T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453647 | ||||||
| chr5:139453647
|
N | T | 1 | a0001c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.512+955T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453647 | ||||||
| chr5:139453648
|
N | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+954T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453648 | ||||||
| chr5:139453649
|
N | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+953T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453649 | ||||||
| chr5:139453650
|
N | T | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+952T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453650 | ||||||
| chr5:139453651
|
N | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+951T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453651 | ||||||
| chr5:139453652
|
N | T | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+950T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453652 | ||||||
| chr5:139453653
|
N | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+949T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453653 | ||||||
| chr5:139453654
|
N | T | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+948T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453654 | ||||||
| chr5:139453655
|
N | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+947T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453655 | ||||||
| chr5:139453656
|
N | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+946T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453656 | ||||||
| chr5:139453657
|
N | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+945T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453657 | ||||||
| chr5:139453658
|
N | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+944T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453658 | ||||||
| chr5:139453659
|
N | T | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.512+943T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453659 | ||||||
| chr5:139453680
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+922T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453680 | ||||||
| chr5:139453684
|
G | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+918C>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453684 | ||||||
| chr5:139453687
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.512+915C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453687 | ||||||
| chr5:139453690
|
T | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+912A>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453690 | ||||||
| chr5:139453697
|
T | A | 1 | a0001c0001t0001g0077 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.512+905A>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453697 | ||||||
| chr5:139453700
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.512+902C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453700 | ||||||
| chr5:139453703
|
A | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+899T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453703 | ||||||
| chr5:139453704
|
T | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+898A>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453704 | ||||||
| chr5:139453725
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+877T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453725 | ||||||
| chr5:139453730
|
T | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+872A>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453730 | ||||||
| chr5:139453731
|
A | C | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+871T>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453731 | ||||||
| chr5:139453731
|
A | T | 1 | a0001c0001t0001g0077 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.512+871T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453731 | ||||||
| chr5:139453737
|
G | T | 1 | a0001c0001t0001g0077 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.512+865C>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453737 | ||||||
| chr5:139453744
|
G | C | 1 | a0001c0001t0001g0077 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.512+858C>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453744 | ||||||
| chr5:139453744
|
G | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+858C>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453744 | ||||||
| chr5:139453745
|
G | T | 1 | a0001c0001t0001g0077 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.512+857C>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453745 | ||||||
| chr5:139453746
|
G | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+856C>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453746 | ||||||
| chr5:139453747
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+855T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453747 | ||||||
| chr5:139453756
|
T | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+846A>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453756 | ||||||
| chr5:139453759
|
T | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+843A>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453759 | ||||||
| chr5:139453763
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.512+839C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453763 | ||||||
| chr5:139453765
|
T | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+837A>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453765 | ||||||
| chr5:139453773
|
T | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+829A>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453773 | ||||||
| chr5:139453775
|
T | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+827A>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453775 | ||||||
| chr5:139453776
|
G | C | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+826C>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453776 | ||||||
| chr5:139453777
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+825C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453777 | ||||||
| chr5:139453789
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+813G>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453789 | ||||||
| chr5:139453790
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+812T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453790 | ||||||
| chr5:139453799
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.512+803C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453799 | ||||||
| chr5:139453846
|
T | G | 1 | a0001c0001t0001g0077 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.512+756A>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453846 | ||||||
| chr5:139453847
|
A | T | 1 | a0001c0001t0001g0077 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.512+755T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453847 | ||||||
| chr5:139453853
|
G | T | 1 | a0001c0001t0001g0077 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.512+749C>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453853 | ||||||
| chr5:139453865
|
TGTGGTGT others(7): Show |
T | 1 | a0001c0001t0001g0077 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.512+723_512+736del others(14): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139453865 | ||||||
| chr5:139454064
|
G | A | 1 | a0001c0001t0001g0151 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.512+538C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139454064 | ||||||
| chr5:139454239
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.512+363G>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139454239 | ||||||
| chr5:139454259
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.512+343G>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139454259 | ||||||
| chr5:139454378
|
T | A | 1 | a0001c0001t0001g0098 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.512+224A>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139454378 | ||||||
| chr5:139454418
|
G | A | 1 | a0001c0001t0001g0144 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.512+184C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139454418 | ||||||
| chr5:139454544
|
G | T | 2 | a0001c0001t0001g0138a0001c0001t0001g0142 | 2 | HG01891.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.512+58C>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139454544 | ||||||
| chr5:139454593
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.512+9G>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 8/9 | chr5 | 139454593 | ||||||
| chr5:139454929
|
C | G | 1 | a0001c0001t0001g0100 | 1 | HG03239.hp2 | splice_region_variant&intron_variant | LOW | c.377-6G>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 6/9 | chr5 | 139454929 | ||||||
| chr5:139454978
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.377-55T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 6/9 | chr5 | 139454978 | ||||||
| chr5:139454988
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.377-65G>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 6/9 | chr5 | 139454988 | ||||||
| chr5:139455079
|
GC | G | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(154): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.377-157delG | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 6/9 | chr5 | 139455079 | ||||||
| chr5:139455184
|
T | TC | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(154): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.376+138dupG | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 6/9 | chr5 | 139455184 | ||||||
| chr5:139455201
|
T | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(154): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.376+122A>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 6/9 | chr5 | 139455201 | ||||||
| chr5:139455250
|
T | TC | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(154): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.376+72dupG | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 6/9 | chr5 | 139455250 | ||||||
| chr5:139455269
|
T | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(154): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.376+54A>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 6/9 | chr5 | 139455269 | ||||||
| chr5:139455286
|
G | T | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(154): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.376+37C>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 6/9 | chr5 | 139455286 | ||||||
| chr5:139455288
|
T | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(154): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.376+35A>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 6/9 | chr5 | 139455288 | ||||||
| chr5:139455312
|
T | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(154): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.376+11A>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 6/9 | chr5 | 139455312 | ||||||
| chr5:139455316
|
G | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(154): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
splice_region_variant&intron_variant | LOW | c.376+7C>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 6/9 | chr5 | 139455316 | ||||||
| chr5:139455650
|
T | G | 1 | a0001c0001t0001g0058 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.263-214A>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 5/9 | chr5 | 139455650 | ||||||
| chr5:139455766
|
C | G | 1 | a0001c0001t0001g0094 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.263-330G>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 5/9 | chr5 | 139455766 | ||||||
| chr5:139455814
|
T | TA | 65 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(62): Show | 161 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.263-379dupT | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 5/9 | chr5 | 139455814 | ||||||
| chr5:139455814
|
T | TAA | 15 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0040others(12): Show | 28 | HG01106.hp1 HG01106.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.263-380_263-379dup others(2): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 5/9 | chr5 | 139455814 | ||||||
| chr5:139455814
|
T | TAAAA | 14 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0024others(11): Show | 20 | HG02129.hp1 HG02723.hp2 HG02809.hp1 others(17): Show |
intron_variant | MODIFIER | c.263-382_263-379dup others(4): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 5/9 | chr5 | 139455814 | ||||||
| chr5:139455814
|
T | TAAAAA | 6 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0054others(3): Show | 8 | HG01243.hp2 HG02145.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.263-383_263-379dup others(5): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 5/9 | chr5 | 139455814 | ||||||
| chr5:139455814
|
TAAAAAAA others(7): Show |
T | 1 | a0001c0001t0001g0144 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.263-392_263-379del others(14): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 5/9 | chr5 | 139455814 | ||||||
| chr5:139455883
|
G | A | 2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.263-447C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 5/9 | chr5 | 139455883 | ||||||
| chr5:139456117
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.262+357C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 5/9 | chr5 | 139456117 | ||||||
| chr5:139456187
|
C | CA | 2 | a0001c0001t0001g0035a0001c0001t0001g0108 | 3 | NA18965.hp1 NA19004.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.262+286dupT | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 5/9 | chr5 | 139456187 | ||||||
| chr5:139456204
|
A | G | 3 | a0001c0001t0001g0029a0001c0001t0001g0092a0001c0001t0001g0093 | 4 | HG00673.hp1 HG02129.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.262+270T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 5/9 | chr5 | 139456204 | ||||||
| chr5:139456211
|
C | T | 5 | a0001c0001t0001g0009a0001c0001t0001g0044a0001c0001t0001g0065others(2): Show | 8 | HG02109.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.262+263G>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 5/9 | chr5 | 139456211 | ||||||
| chr5:139456267
|
A | G | 1 | a0001c0001t0001g0006 | 5 | HG01123.hp1 HG01168.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.262+207T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 5/9 | chr5 | 139456267 | ||||||
| chr5:139456273
|
A | C | 3 | a0001c0001t0001g0133a0001c0001t0001g0138a0001c0001t0001g0142 | 3 | HG01891.hp1 HG02818.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.262+201T>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 5/9 | chr5 | 139456273 | ||||||
| chr5:139456327
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.262+147A>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 5/9 | chr5 | 139456327 | ||||||
| chr5:139456440
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.262+34C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 5/9 | chr5 | 139456440 | ||||||
| chr5:139456464
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.262+10G>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 5/9 | chr5 | 139456464 | ||||||
| chr5:139457068
|
G | T | 3 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072 | 3 | HG00280.hp2 HG01123.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.217+477C>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 4/9 | chr5 | 139457068 | ||||||
| chr5:139457282
|
C | T | 1 | a0001c0001t0001g0091 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.217+263G>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 4/9 | chr5 | 139457282 | ||||||
| chr5:139457294
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.217+251C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 4/9 | chr5 | 139457294 | ||||||
| chr5:139457384
|
C | A | 1 | a0001c0001t0001g0061 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.217+161G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 4/9 | chr5 | 139457384 | ||||||
| chr5:139457485
|
C | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0115 | 5 | HG02895.hp1 HG02897.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.217+60G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 4/9 | chr5 | 139457485 | ||||||
| chr5:139458045
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.106+94G>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 2/9 | chr5 | 139458045 | ||||||
| chr5:139458317
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.62-134A>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458317 | ||||||
| chr5:139458320
|
G | GT | 3 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0063 | 7 | HG02145.hp1 HG02622.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.62-138dupA | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458320 | ||||||
| chr5:139458324
|
T | G | 1 | a0001c0001t0001g0059 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.62-141A>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458324 | ||||||
| chr5:139458325
|
G | GT | 22 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0024others(19): Show | 28 | HG00733.hp2 HG01243.hp2 HG02056.hp1 others(25): Show |
intron_variant | MODIFIER | c.62-143dupA | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458325 | ||||||
| chr5:139458325
|
G | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0063others(2): Show | 9 | HG01109.hp2 HG02145.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.62-142C>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458325 | ||||||
| chr5:139458330
|
T | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0041 | 4 | HG00558.hp2 HG02027.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-147A>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458330 | ||||||
| chr5:139458472
|
T | G | 1 | a0001c0001t0001g0110 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.62-289A>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458472 | ||||||
| chr5:139458484
|
G | A | 2 | a0001c0001t0001g0132a0001c0001t0001g0137 | 2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.62-301C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458484 | ||||||
| chr5:139458489
|
C | T | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.62-306G>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458489 | ||||||
| chr5:139458500
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.62-329_62-318dupTT others(10): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | ||||||
| chr5:139458500
|
C | CAAAAAAA others(6): Show |
5 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(2): Show | 5 | HG01069.hp1 HG02523.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.62-330_62-318dupTT others(11): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | ||||||
| chr5:139458500
|
C | CAAAAAAA others(7): Show |
5 | a0001c0001t0001g0021a0001c0001t0001g0138a0001c0001t0001g0139others(2): Show | 7 | HG01071.hp2 HG01358.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.62-331_62-318dupTT others(12): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | ||||||
| chr5:139458500
|
C | CAAAAAAA others(8): Show |
2 | a0001c0001t0001g0141a0002c0002t0001g0140 | 2 | HG02280.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.62-332_62-318dupTT others(13): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | ||||||
| chr5:139458500
|
C | CAAAAAAA others(9): Show |
1 | a0001c0001t0001g0142 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.62-333_62-318dupTT others(14): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | ||||||
| chr5:139458500
|
C | CAAAAAAA others(13): Show |
1 | a0001c0001t0001g0154 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.62-337_62-318dupTT others(18): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | ||||||
| chr5:139458500
|
C | CAACAAAA others(6): Show |
2 | a0001c0001t0001g0036a0001c0001t0001g0130 | 3 | HG01993.hp1 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.62-318_62-317insTT others(11): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | ||||||
| chr5:139458500
|
C | CAACAAAA others(7): Show |
1 | a0001c0001t0001g0131 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.62-318_62-317insTT others(12): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | ||||||
| chr5:139458500
|
C | CAACAACA others(7): Show |
1 | a0001c0001t0001g0128 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.62-318_62-317insTT others(12): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | ||||||
| chr5:139458500
|
C | CAACAACA others(8): Show |
1 | a0001c0001t0001g0066 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.62-318_62-317insTT others(13): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | ||||||
| chr5:139458500
|
C | CAACAACA others(11): Show |
1 | a0001c0001t0001g0129 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.62-318_62-317insTT others(16): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | ||||||
| chr5:139458500
|
CA | C | 11 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0046others(8): Show | 27 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.62-318delT | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | ||||||
| chr5:139458500
|
CAA | C | 7 | a0001c0001t0001g0016a0001c0001t0001g0034a0001c0001t0001g0035others(4): Show | 11 | HG02129.hp1 HG03688.hp1 NA18944.hp2 others(8): Show |
intron_variant | MODIFIER | c.62-319_62-318delTT | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | ||||||
| chr5:139458500
|
CAAA | C | 10 | a0001c0001t0001g0023a0001c0001t0001g0037a0001c0001t0001g0055others(7): Show | 12 | HG01884.hp2 HG02965.hp2 HG03579.hp2 others(9): Show |
intron_variant | MODIFIER | c.62-320_62-318delTT others(1): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | ||||||
| chr5:139458500
|
CAAAAAAA | C | 8 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0025others(5): Show | 15 | HG02109.hp1 HG02145.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.62-324_62-318delTT others(5): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | ||||||
| chr5:139458500
|
CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0001g0009a0001c0001t0001g0114a0001c0001t0001g0115 | 6 | HG02895.hp1 HG02897.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.62-328_62-318delTT others(9): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | ||||||
| chr5:139458500
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | NA18522.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.62-329_62-318delTT others(10): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | ||||||
| chr5:139458500
|
CAAAAAAA others(6): Show |
C | 5 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0052others(2): Show | 7 | HG02965.hp1 NA18612.hp1 NA19030.hp1 others(4): Show |
intron_variant | MODIFIER | c.62-330_62-318delTT others(11): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | ||||||
| chr5:139458500
|
CAAAAAAA others(7): Show |
C | 40 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(37): Show | 124 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.62-331_62-318delTT others(12): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | ||||||
| chr5:139458500
|
CAAAAAAA others(8): Show |
C | 42 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(39): Show | 126 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.62-332_62-318delTT others(13): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458500 | ||||||
| chr5:139458640
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.62-457T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458640 | ||||||
| chr5:139458771
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.62-588C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458771 | ||||||
| chr5:139458845
|
C | CA | 8 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0037others(5): Show | 13 | HG01884.hp2 HG02145.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.62-663dupT | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458845 | ||||||
| chr5:139458861
|
G | A | 1 | a0001c0001t0001g0038 | 2 | HG00741.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.62-678C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139458861 | ||||||
| chr5:139459102
|
AAACTAGT others(20): Show |
A | 1 | a0001c0001t0001g0146 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.62-946_62-920delCT others(25): Show |
ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139459102 | ||||||
| chr5:139459227
|
A | G | 1 | a0001c0001t0001g0017 | 3 | HG00597.hp1 HG02027.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.62-1044T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139459227 | ||||||
| chr5:139459380
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.62-1197G>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139459380 | ||||||
| chr5:139459452
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.62-1269T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139459452 | ||||||
| chr5:139459744
|
C | G | 1 | a0001c0001t0001g0066 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.62-1561G>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139459744 | ||||||
| chr5:139459769
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.62-1586C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139459769 | ||||||
| chr5:139459871
|
A | C | 1 | a0001c0001t0001g0065 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.62-1688T>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139459871 | ||||||
| chr5:139460110
|
C | A | 1 | a0001c0001t0001g0148 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.62-1927G>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139460110 | ||||||
| chr5:139460133
|
G | GT | 24 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0016others(21): Show | 35 | HG01243.hp2 HG02109.hp1 HG02129.hp1 others(32): Show |
intron_variant | MODIFIER | c.62-1951dupA | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139460133 | ||||||
| chr5:139460384
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.62-2201G>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139460384 | ||||||
| chr5:139460802
|
G | C | 2 | a0001c0001t0001g0039a0001c0001t0001g0149 | 3 | HG01081.hp1 HG01934.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.61+1808C>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139460802 | ||||||
| chr5:139461077
|
G | T | 1 | a0001c0001t0001g0046 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.61+1533C>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139461077 | ||||||
| chr5:139461244
|
G | A | 1 | a0001c0001t0001g0014 | 4 | HG00099.hp1 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+1366C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139461244 | ||||||
| chr5:139461560
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.61+1050C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139461560 | ||||||
| chr5:139461718
|
C | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0045 | 3 | HG03490.hp2 HG03492.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.61+892G>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139461718 | ||||||
| chr5:139461763
|
C | G | 1 | a0001c0001t0001g0044 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.61+847G>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139461763 | ||||||
| chr5:139461821
|
A | T | 1 | a0001c0001t0001g0043 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.61+789T>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139461821 | ||||||
| chr5:139461865
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.61+745A>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139461865 | ||||||
| chr5:139461879
|
T | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0040a0001c0001t0001g0151others(3): Show | 11 | HG01074.hp2 HG01081.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.61+731A>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139461879 | ||||||
| chr5:139461953
|
A | G | 1 | a0001c0001t0001g0009 | 4 | HG02895.hp1 HG02897.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+657T>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139461953 | ||||||
| chr5:139462071
|
C | G | 1 | a0001c0001t0001g0042 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.61+539G>C | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139462071 | ||||||
| chr5:139462234
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.61+376C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139462234 | ||||||
| chr5:139462265
|
T | C | 1 | a0001c0001t0001g0156 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.61+345A>G | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139462265 | ||||||
| chr5:139462420
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.61+190C>T | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139462420 | ||||||
| chr5:139462593
|
C | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0041 | 4 | HG00558.hp2 HG02027.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+17G>A | ECSCR | ENSG00000249751.4 | transcript | ENST00000618155.3 | protein_coding | 1/9 | chr5 | 139462593 |