Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 51466 |
|---|---|
| ensemblid | ENSG00000196405.13 |
| hgncid | 20234 |
| symbol | EVL |
| name | Enah/Vasp-like |
| refseq_nuc | NM_016337.3 |
| refseq_prot | NP_057421.1 |
| ensembl_nuc | ENST00000392920.8 |
| ensembl_prot | ENSP00000376652.3 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 100065422 |
| end | 100144236 |
| strand | + |
| ver | v1.2 |
| region | chr14:100065422-100144236 |
| region5000 | chr14:100060422-100149236 |
| regionname0 | EVL_chr14_100065422_100144236 |
| regionname5000 | EVL_chr14_100060422_100149236 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 418 | 340 | 82 | 70 | 146 | 6 | 34 | 112 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| a0002 | 0/0 | 418 | 14 | 14 | 0 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1257 | 294 | 45 | 66 | 143 | 6 | 32 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| c0002 | 0/0 | 1257 | 36 | 29 | 3 | 2 | 0 | 2 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| c0003 | 0/0 | 1257 | 10 | 10 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| c0004 | 0/0 | 1257 | 5 | 5 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| c0005 | 0/0 | 1257 | 4 | 4 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| c0006 | 0/0 | 1257 | 3 | 3 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| c0007 | 0/0 | 1257 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| c0008 | 0/0 | 1257 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| 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 | 1/1 | 578 | 325 | 76 | 65 | 142 | 6 | 34 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| t0002 | 0/0 | 578 | 18 | 18 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| t0003 | 0/0 | 578 | 3 | 0 | 3 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| t0004 | 0/0 | 578 | 2 | 2 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| t0005 | 0/0 | 578 | 2 | 0 | 0 | 2 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| t0006 | 0/0 | 578 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| t0007 | 0/0 | 578 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| t0008 | 0/0 | 578 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| t0009 | 0/0 | 578 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0004 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0005 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0161 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0296 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1257 | 294 | 45 | 66 | 143 | 6 | 32 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| a0001c0002 | 0/0 | 1257 | 36 | 29 | 3 | 2 | 0 | 2 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| a0001c0004 | 0/0 | 1257 | 5 | 5 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| a0001c0006 | 0/0 | 1257 | 3 | 3 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| a0001c0007 | 0/0 | 1257 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| a0001c0008 | 0/0 | 1257 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| a0002c0003 | 0/0 | 1257 | 10 | 10 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| a0002c0005 | 0/0 | 1257 | 4 | 4 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1834 | 280 | 40 | 61 | 139 | 6 | 32 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| a0001c0001t0002 | 0/0 | 1834 | 4 | 4 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| a0001c0001t0003 | 0/0 | 1834 | 3 | 0 | 3 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| a0001c0001t0004 | 0/0 | 1834 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| a0001c0001t0005 | 0/0 | 1834 | 2 | 0 | 0 | 2 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| a0001c0001t0006 | 0/0 | 1834 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| a0001c0001t0007 | 0/0 | 1834 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| a0001c0001t0008 | 0/0 | 1834 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| a0001c0001t0009 | 0/0 | 1834 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| a0001c0002t0001 | 0/0 | 1834 | 25 | 18 | 3 | 2 | 0 | 2 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| a0001c0002t0002 | 0/0 | 1834 | 10 | 10 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| a0001c0002t0004 | 0/0 | 1834 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| a0001c0004t0001 | 0/0 | 1834 | 5 | 5 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| a0001c0006t0001 | 0/0 | 1834 | 3 | 3 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| a0001c0007t0001 | 0/0 | 1834 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| a0001c0008t0001 | 0/0 | 1834 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| a0002c0003t0001 | 0/0 | 1834 | 10 | 10 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| a0002c0005t0002 | 0/0 | 1834 | 4 | 4 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | copy fasta | chr14 | 100060422 | 100149236 |
| 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 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0161 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0296 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0002g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0005g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0005g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0006g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0007g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0008g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0001t0009g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0002t0001g0005 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0002t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0002t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0002t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0002t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0002t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0002t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0002t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0002t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0002t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0002t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0002t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0002t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0002t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0002t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0002t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0002t0002g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0002t0002g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0002t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0004t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0004t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0004t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0004t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0004t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0006t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0006t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0006t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0007t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0001c0008t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0002c0003t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0002c0003t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0002c0003t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0002c0003t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0002c0003t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0002c0003t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0002c0003t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0002c0003t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0002c0003t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0002c0003t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0002c0005t0002g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0002c0005t0002g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0002c0005t0002g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| a0002c0005t0002g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0153 | EUR | GBR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0322 | EUR | GBR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0106 | EUR | GBR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0266 | EUR | GBR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | CHS | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG00609 | hp2 | a0001 | c0001 | t0009 | g0228 | EAS | CHS | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0330 | AMR | PUR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0131 | AMR | PUR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0116 | AMR | PUR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0032 | AMR | PUR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | CLM | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0200 | AMR | CLM | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | CLM | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0302 | EUR | IBS | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0183 | EUR | IBS | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01884 | hp1 | a0002 | c0005 | t0002 | g0343 | AFR | ACB | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01884 | hp2 | a0001 | c0002 | t0004 | g0209 | AFR | ACB | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01943 | hp2 | a0001 | c0001 | t0006 | g0318 | AMR | PEL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0033 | AMR | PEL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | PEL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02004 | hp2 | a0001 | c0008 | t0001 | g0227 | AMR | PEL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02055 | hp1 | a0002 | c0003 | t0001 | g0028 | AFR | ACB | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | KHV | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02071 | hp1 | a0001 | c0001 | t0005 | g0258 | EAS | KHV | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | KHV | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | KHV | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | KHV | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | KHV | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | KHV | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02145 | hp2 | a0001 | c0004 | t0001 | g0040 | AFR | ACB | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CDX | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02165 | hp2 | a0001 | c0001 | t0008 | g0012 | EAS | CDX | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0335 | AFR | ACB | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0207 | AFR | ACB | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0287 | AFR | ACB | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0339 | AFR | ACB | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0282 | AFR | ACB | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0334 | AFR | ACB | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0210 | AFR | GWD | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02572 | hp2 | a0002 | c0003 | t0001 | g0043 | AFR | GWD | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02615 | hp1 | a0002 | c0003 | t0001 | g0029 | AFR | GWD | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0289 | AFR | GWD | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0213 | AFR | GWD | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0277 | AFR | GWD | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0206 | AFR | GWD | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02809 | hp2 | a0001 | c0006 | t0001 | g0202 | AFR | GWD | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02818 | hp1 | a0001 | c0004 | t0001 | g0221 | AFR | GWD | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0201 | AFR | GWD | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02886 | hp1 | a0001 | c0004 | t0001 | g0222 | AFR | GWD | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02895 | hp1 | a0002 | c0005 | t0002 | g0341 | AFR | GWD | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02896 | hp1 | a0002 | c0005 | t0002 | g0340 | AFR | GWD | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02896 | hp2 | a0001 | c0006 | t0001 | g0203 | AFR | GWD | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02897 | hp1 | a0002 | c0005 | t0002 | g0342 | AFR | GWD | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02897 | hp2 | a0001 | c0006 | t0001 | g0204 | AFR | GWD | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | ESN | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02965 | hp1 | a0002 | c0003 | t0001 | g0051 | AFR | ESN | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0216 | AFR | ESN | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02970 | hp1 | a0001 | c0002 | t0002 | g0333 | AFR | ESN | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ESN | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | MSL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0278 | AFR | MSL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03130 | hp1 | a0001 | c0004 | t0001 | g0219 | AFR | ESN | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03130 | hp2 | a0002 | c0003 | t0001 | g0049 | AFR | ESN | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0211 | AFR | ESN | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03139 | hp2 | a0002 | c0003 | t0001 | g0048 | AFR | ESN | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03209 | hp1 | a0001 | c0002 | t0002 | g0336 | AFR | MSL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0288 | AFR | MSL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03225 | hp1 | a0002 | c0003 | t0001 | g0047 | AFR | MSL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0332 | AFR | MSL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0212 | AFR | MSL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | MSL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | MSL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | MSL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | ESN | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0286 | AFR | GWD | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0331 | AFR | GWD | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0285 | AFR | MSL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0290 | AFR | MSL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0034 | SAS | BEB | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0295 | SAS | BEB | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | BEB | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | STU | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | STU | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0035 | SAS | BEB | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | STU | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | STU | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18522 | hp1 | a0001 | c0004 | t0001 | g0220 | AFR | YRI | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | CHB | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | CHB | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | YRI | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0283 | AFR | YRI | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18982 | hp2 | a0001 | c0001 | t0005 | g0248 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18999 | hp1 | a0001 | c0007 | t0001 | g0314 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0281 | AFR | LWK | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | LWK | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19043 | hp1 | a0002 | c0003 | t0001 | g0045 | AFR | LWK | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | LWK | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | YRI | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | YRI | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA20129 | hp1 | a0002 | c0003 | t0001 | g0050 | AFR | ASW | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | ASW | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | GIH | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01123 | hp1 | a0001 | c0001 | t0007 | g0107 | AMR | CLM | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0279 | AFR | ACB | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0214 | AFR | ACB | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02486 | hp2 | a0002 | c0003 | t0001 | g0044 | AFR | ACB | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | MSL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0284 | AFR | MSL | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0236 | AFR | USA | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | USA | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0215 | AFR | USA | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | USA | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA21309 | hp1 | a0001 | c0002 | t0002 | g0208 | AFR | LWK | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0217 | AFR | LWK | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0161 | REF | REF | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0296 | REF | REF | EVL_chr14_100060422_100149236 | EVL | chr14 | 100060422 | 100149236 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:100135929
|
C | G | 1 | a0002 | 14 | HG01884.hp1 HG02055.hp1 HG02486.hp2 others(11): Show |
missense_variant | MODERATE | c.925C>G | p.Pro309Ala | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 9/14 | 1004/1834 | 925/1257 | 309/418 | chr14 | 100135929 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:100097531
|
G | A | 2 | a0001c0004a0002c0005 | 9 | HG01884.hp1 HG02145.hp2 HG02818.hp1 others(6): Show |
synonymous_variant | LOW | c.231G>A | p.Thr77Thr | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/14 | 310/1834 | 231/1257 | 77/418 | chr14 | 100097531 | ||
| chr14:100097606
|
G | A | 2 | a0001c0002a0001c0006 | 39 | HG01346.hp1 HG01358.hp2 HG01884.hp2 others(36): Show |
synonymous_variant | LOW | c.306G>A | p.Thr102Thr | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/14 | 385/1834 | 306/1257 | 102/418 | chr14 | 100097606 | ||
| chr14:100128700
|
A | G | 1 | a0001c0008 | 1 | HG02004.hp2 | synonymous_variant | LOW | c.669A>G | p.Ser223Ser | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 6/14 | 748/1834 | 669/1257 | 223/418 | chr14 | 100128700 | ||
| chr14:100129571
|
C | T | 1 | a0001c0006 | 3 | HG02809.hp2 HG02896.hp2 HG02897.hp2 |
synonymous_variant | LOW | c.726C>T | p.Asp242Asp | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 7/14 | 805/1834 | 726/1257 | 242/418 | chr14 | 100129571 | ||
| chr14:100141777
|
G | A | 1 | a0001c0007 | 1 | NA18999.hp1 | synonymous_variant | LOW | c.1203G>A | p.Lys401Lys | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 13/14 | 1282/1834 | 1203/1257 | 401/418 | chr14 | 100141777 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:100143769
|
G | A | 1 | a0001c0001t0006 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*31G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 14/14 | 31 | chr14 | 100143769 | |||||
| chr14:100143770
|
C | G | 1 | a0001c0001t0006 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*32C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 14/14 | 32 | chr14 | 100143770 | |||||
| chr14:100143776
|
C | T | 1 | a0001c0001t0009 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*38C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 14/14 | 38 | chr14 | 100143776 | |||||
| chr14:100143790
|
A | G | 3 | a0001c0001t0002a0001c0002t0002a0002c0005t0002 | 18 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*52A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 14/14 | 52 | chr14 | 100143790 | |||||
| chr14:100144092
|
G | A | 1 | a0001c0001t0003 | 3 | HG01167.hp1 HG01169.hp1 HG01175.hp1 |
3_prime_UTR_variant | MODIFIER | c.*354G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 14/14 | 354 | chr14 | 100144092 | |||||
| chr14:100144101
|
C | T | 1 | a0001c0001t0005 | 2 | HG02071.hp1 NA18982.hp2 |
3_prime_UTR_variant | MODIFIER | c.*363C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 14/14 | 363 | chr14 | 100144101 | |||||
| chr14:100144185
|
C | T | 1 | a0001c0001t0008 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*447C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 14/14 | 447 | chr14 | 100144185 | |||||
| chr14:100144187
|
T | C | 2 | a0001c0001t0004a0001c0002t0004 | 2 | HG01884.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*449T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 14/14 | 449 | chr14 | 100144187 | |||||
| chr14:100144194
|
C | T | 1 | a0001c0001t0007 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*456C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 14/14 | 456 | chr14 | 100144194 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:100065721
|
G | C | 8 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(5): Show | 8 | HG02165.hp2 NA18979.hp2 NA18998.hp1 others(5): Show |
intron_variant | MODIFIER | c.11+210G>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100065721 | ||||||
| chr14:100065963
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.11+452G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100065963 | ||||||
| chr14:100066051
|
C | T | 4 | a0002c0005t0002g0340a0002c0005t0002g0341a0002c0005t0002g0342others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.11+540C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100066051 | ||||||
| chr14:100066135
|
T | C | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(217): Show | 225 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.11+624T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100066135 | ||||||
| chr14:100066198
|
A | G | 5 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0229others(2): Show | 5 | HG00609.hp2 HG01243.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.11+687A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100066198 | ||||||
| chr14:100066302
|
G | A | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(217): Show | 225 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.11+791G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100066302 | ||||||
| chr14:100066343
|
C | T | 1 | a0001c0001t0001g0224 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.11+832C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100066343 | ||||||
| chr14:100066399
|
T | C | 1 | a0001c0001t0001g0230 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.11+888T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100066399 | ||||||
| chr14:100066428
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.11+917G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100066428 | ||||||
| chr14:100066439
|
C | T | 1 | a0001c0001t0001g0339 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.11+928C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100066439 | ||||||
| chr14:100066453
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.11+942C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100066453 | ||||||
| chr14:100066472
|
A | G | 211 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(208): Show | 216 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.11+961A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100066472 | ||||||
| chr14:100066573
|
T | C | 2 | a0002c0003t0001g0028a0002c0003t0001g0029 | 2 | HG02055.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.11+1062T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100066573 | ||||||
| chr14:100066576
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.11+1065T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100066576 | ||||||
| chr14:100066709
|
T | A | 1 | a0001c0001t0001g0231 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.11+1198T>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100066709 | ||||||
| chr14:100066745
|
T | C | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0003g0032 | 3 | HG00735.hp1 HG00741.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.11+1234T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100066745 | ||||||
| chr14:100066792
|
C | T | 2 | a0001c0001t0001g0337a0001c0001t0001g0338 | 2 | NA19005.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.11+1281C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100066792 | ||||||
| chr14:100066793
|
G | A | 3 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035 | 3 | HG01952.hp1 HG03831.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.11+1282G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100066793 | ||||||
| chr14:100066865
|
C | T | 216 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(213): Show | 221 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(218): Show |
intron_variant | MODIFIER | c.11+1354C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100066865 | ||||||
| chr14:100066894
|
C | G | 4 | a0001c0004t0001g0219a0001c0004t0001g0220a0001c0004t0001g0221others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.11+1383C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100066894 | ||||||
| chr14:100066997
|
C | T | 216 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(213): Show | 221 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(218): Show |
intron_variant | MODIFIER | c.11+1486C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100066997 | ||||||
| chr14:100067013
|
G | A | 5 | a0001c0004t0001g0040a0001c0004t0001g0219a0001c0004t0001g0220others(2): Show | 5 | HG02145.hp2 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.11+1502G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100067013 | ||||||
| chr14:100067065
|
G | A | 216 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(213): Show | 221 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(218): Show |
intron_variant | MODIFIER | c.11+1554G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100067065 | ||||||
| chr14:100067085
|
G | A | 1 | a0001c0001t0001g0041 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.11+1574G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100067085 | ||||||
| chr14:100067162
|
A | C | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0003g0032 | 3 | HG00735.hp1 HG00741.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.11+1651A>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100067162 | ||||||
| chr14:100067195
|
G | A | 1 | a0001c0001t0001g0042 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.11+1684G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100067195 | ||||||
| chr14:100067268
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.11+1757A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100067268 | ||||||
| chr14:100067419
|
G | A | 262 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(259): Show | 270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.11+1908G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100067419 | ||||||
| chr14:100067448
|
G | A | 216 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(213): Show | 221 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(218): Show |
intron_variant | MODIFIER | c.11+1937G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100067448 | ||||||
| chr14:100067478
|
T | C | 11 | a0001c0001t0001g0046a0002c0003t0001g0028a0002c0003t0001g0029others(8): Show | 11 | HG01099.hp1 HG02055.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.11+1967T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100067478 | ||||||
| chr14:100067791
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.11+2280G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100067791 | ||||||
| chr14:100067808
|
G | A | 1 | a0001c0001t0001g0276 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.11+2297G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100067808 | ||||||
| chr14:100068005
|
C | T | 1 | a0001c0001t0001g0017 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.11+2494C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100068005 | ||||||
| chr14:100068093
|
A | T | 4 | a0001c0002t0002g0333a0001c0002t0002g0334a0001c0002t0002g0335others(1): Show | 4 | HG02257.hp2 HG02451.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.11+2582A>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100068093 | ||||||
| chr14:100068194
|
A | G | 24 | a0001c0001t0001g0009a0001c0001t0001g0262a0001c0001t0001g0263others(21): Show | 25 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.11+2683A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100068194 | ||||||
| chr14:100068312
|
G | A | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0052others(4): Show | 7 | HG00735.hp1 HG00741.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.11+2801G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100068312 | ||||||
| chr14:100068382
|
T | C | 1 | a0001c0001t0001g0231 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.11+2871T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100068382 | ||||||
| chr14:100068504
|
A | G | 1 | a0001c0001t0001g0339 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.11+2993A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100068504 | ||||||
| chr14:100068621
|
T | C | 166 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 170 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.11+3110T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100068621 | ||||||
| chr14:100068681
|
A | G | 1 | a0001c0001t0001g0018 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.11+3170A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100068681 | ||||||
| chr14:100068725
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.11+3214G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100068725 | ||||||
| chr14:100068749
|
G | A | 1 | a0001c0001t0001g0056 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.11+3238G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100068749 | ||||||
| chr14:100068816
|
G | A | 9 | a0001c0004t0001g0040a0001c0004t0001g0219a0001c0004t0001g0220others(6): Show | 9 | HG01884.hp1 HG02145.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.11+3305G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100068816 | ||||||
| chr14:100068891
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.11+3380T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100068891 | ||||||
| chr14:100068897
|
T | C | 39 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0046others(36): Show | 40 | HG00735.hp1 HG00741.hp2 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.11+3386T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100068897 | ||||||
| chr14:100068932
|
A | C | 3 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261 | 3 | HG00597.hp2 NA18993.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.11+3421A>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100068932 | ||||||
| chr14:100069010
|
G | A | 217 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(214): Show | 222 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.11+3499G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100069010 | ||||||
| chr14:100069113
|
C | T | 166 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 170 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.11+3602C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100069113 | ||||||
| chr14:100069323
|
C | G | 46 | a0001c0001t0001g0006a0001c0001t0001g0232a0001c0001t0001g0233others(43): Show | 49 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.11+3812C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100069323 | ||||||
| chr14:100069580
|
G | A | 7 | a0001c0002t0001g0005a0001c0002t0001g0200a0001c0002t0001g0201others(4): Show | 8 | HG01346.hp1 HG01358.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.11+4069G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100069580 | ||||||
| chr14:100069591
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.11+4080G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100069591 | ||||||
| chr14:100069677
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.11+4166A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100069677 | ||||||
| chr14:100069728
|
C | T | 28 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0052others(25): Show | 29 | HG00735.hp1 HG00741.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.11+4217C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100069728 | ||||||
| chr14:100069764
|
G | A | 167 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(164): Show | 171 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.11+4253G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100069764 | ||||||
| chr14:100069855
|
C | T | 10 | a0001c0001t0001g0058a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG02132.hp2 HG02135.hp1 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.11+4344C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100069855 | ||||||
| chr14:100069907
|
A | G | 7 | a0001c0002t0001g0210a0001c0002t0001g0211a0001c0002t0001g0212others(4): Show | 7 | HG02109.hp2 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.11+4396A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100069907 | ||||||
| chr14:100069916
|
G | T | 5 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(2): Show | 5 | HG01109.hp1 HG01928.hp2 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.11+4405G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100069916 | ||||||
| chr14:100069949
|
G | A | 1 | a0001c0001t0001g0010 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.11+4438G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100069949 | ||||||
| chr14:100069953
|
A | G | 46 | a0001c0001t0001g0006a0001c0001t0001g0232a0001c0001t0001g0233others(43): Show | 49 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.11+4442A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100069953 | ||||||
| chr14:100070062
|
T | TA | 17 | a0001c0001t0001g0223a0001c0001t0001g0233a0001c0001t0001g0234others(14): Show | 20 | HG01346.hp1 HG01358.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.11+4568dupA | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 100070062 | |||||
| chr14:100070062
|
T | TAA | 11 | a0001c0001t0001g0046a0001c0001t0001g0059a0002c0003t0001g0028others(8): Show | 11 | HG01099.hp1 HG02055.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.11+4567_11+4568dup others(2): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 100070062 | |||||
| chr14:100070062
|
TA | T | 17 | a0001c0001t0001g0016a0001c0001t0001g0180a0001c0001t0001g0181others(14): Show | 17 | HG00099.hp2 HG01168.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.11+4568delA | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 100070062 | |||||
| chr14:100070071
|
A | T | 1 | a0001c0001t0001g0185 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.11+4560A>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100070071 | ||||||
| chr14:100070076
|
A | G | 9 | a0001c0004t0001g0040a0001c0004t0001g0219a0001c0004t0001g0220others(6): Show | 9 | HG01884.hp1 HG02145.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.11+4565A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100070076 | ||||||
| chr14:100070099
|
T | A | 28 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0052others(25): Show | 29 | HG00735.hp1 HG00741.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.11+4588T>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100070099 | ||||||
| chr14:100070222
|
C | T | 177 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 181 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.11+4711C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100070222 | ||||||
| chr14:100070225
|
A | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 181 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.11+4714A>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100070225 | ||||||
| chr14:100070230
|
T | C | 6 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235others(3): Show | 8 | HG02055.hp2 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.11+4719T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100070230 | ||||||
| chr14:100070602
|
G | A | 2 | a0001c0002t0001g0005a0001c0002t0001g0200 | 3 | HG01346.hp1 HG01358.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.11+5091G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100070602 | ||||||
| chr14:100070759
|
T | C | 28 | a0001c0001t0001g0009a0001c0001t0001g0280a0001c0001t0001g0322others(25): Show | 29 | HG00099.hp2 HG00639.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.11+5248T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100070759 | ||||||
| chr14:100071091
|
C | G | 4 | a0002c0005t0002g0340a0002c0005t0002g0341a0002c0005t0002g0342others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.11+5580C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100071091 | ||||||
| chr14:100071106
|
G | T | 1 | a0001c0001t0001g0179 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.11+5595G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100071106 | ||||||
| chr14:100071196
|
T | C | 3 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035 | 3 | HG01952.hp1 HG03831.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.11+5685T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100071196 | ||||||
| chr14:100071297
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.11+5786C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100071297 | ||||||
| chr14:100071354
|
T | C | 4 | a0002c0005t0002g0340a0002c0005t0002g0341a0002c0005t0002g0342others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.11+5843T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100071354 | ||||||
| chr14:100071403
|
A | G | 3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177 | 3 | HG02630.hp1 HG02717.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.11+5892A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100071403 | ||||||
| chr14:100071511
|
T | C | 11 | a0001c0001t0001g0046a0002c0003t0001g0028a0002c0003t0001g0029others(8): Show | 11 | HG01099.hp1 HG02055.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.11+6000T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100071511 | ||||||
| chr14:100071678
|
G | A | 45 | a0001c0001t0001g0006a0001c0001t0001g0232a0001c0001t0001g0233others(42): Show | 48 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.11+6167G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100071678 | ||||||
| chr14:100071787
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.11+6276G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100071787 | ||||||
| chr14:100071879
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.11+6368A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100071879 | ||||||
| chr14:100071880
|
G | A | 294 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(291): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.11+6369G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100071880 | ||||||
| chr14:100071968
|
T | G | 10 | a0001c0001t0001g0009a0001c0001t0001g0325a0001c0001t0001g0326others(7): Show | 11 | HG00639.hp2 HG01109.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.11+6457T>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100071968 | ||||||
| chr14:100072155
|
C | T | 1 | a0001c0001t0001g0321 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.11+6644C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100072155 | ||||||
| chr14:100072317
|
C | T | 4 | a0002c0005t0002g0340a0002c0005t0002g0341a0002c0005t0002g0342others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.11+6806C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100072317 | ||||||
| chr14:100072338
|
A | G | 4 | a0002c0005t0002g0340a0002c0005t0002g0341a0002c0005t0002g0342others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.11+6827A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100072338 | ||||||
| chr14:100072412
|
T | A | 1 | a0001c0001t0001g0223 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.11+6901T>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100072412 | ||||||
| chr14:100072465
|
T | C | 291 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(288): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.11+6954T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100072465 | ||||||
| chr14:100072764
|
A | G | 48 | a0001c0001t0001g0046a0001c0002t0001g0005a0001c0002t0001g0033others(45): Show | 49 | HG01099.hp1 HG01346.hp1 HG01358.hp2 others(46): Show |
intron_variant | MODIFIER | c.11+7253A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100072764 | ||||||
| chr14:100072887
|
C | T | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.11+7376C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100072887 | ||||||
| chr14:100072904
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.11+7393A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100072904 | ||||||
| chr14:100072933
|
G | A | 2 | a0001c0002t0001g0206a0001c0002t0004g0209 | 2 | HG01884.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.11+7422G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100072933 | ||||||
| chr14:100073011
|
A | G | 1 | a0001c0001t0001g0171 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.11+7500A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100073011 | ||||||
| chr14:100073096
|
A | C | 291 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(288): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.11+7585A>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100073096 | ||||||
| chr14:100073215
|
G | C | 1 | a0001c0001t0001g0223 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.11+7704G>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100073215 | ||||||
| chr14:100073242
|
A | G | 55 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0052others(52): Show | 56 | HG00735.hp1 HG00741.hp2 HG01175.hp1 others(53): Show |
intron_variant | MODIFIER | c.11+7731A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100073242 | ||||||
| chr14:100073320
|
C | CT | 32 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0046others(29): Show | 34 | HG00597.hp1 HG01069.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.11+7825dupT | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 100073320 | |||||
| chr14:100073335
|
T | G | 2 | a0001c0001t0001g0280a0001c0001t0001g0322 | 2 | HG00099.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.11+7824T>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100073335 | ||||||
| chr14:100073336
|
T | G | 19 | a0001c0001t0001g0009a0001c0001t0001g0172a0001c0001t0001g0173others(16): Show | 20 | HG00099.hp2 HG00639.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.11+7825T>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100073336 | ||||||
| chr14:100073390
|
C | T | 10 | a0001c0002t0001g0210a0001c0002t0001g0211a0001c0002t0001g0212others(7): Show | 10 | HG02109.hp2 HG02280.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.11+7879C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100073390 | ||||||
| chr14:100073418
|
C | T | 8 | a0001c0001t0001g0008a0001c0001t0001g0315a0001c0001t0001g0316others(5): Show | 9 | HG01943.hp2 NA18942.hp2 NA18946.hp2 others(6): Show |
intron_variant | MODIFIER | c.11+7907C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100073418 | ||||||
| chr14:100073549
|
G | A | 4 | a0002c0005t0002g0340a0002c0005t0002g0341a0002c0005t0002g0342others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.11+8038G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100073549 | ||||||
| chr14:100073559
|
G | C | 1 | a0001c0002t0002g0281 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.11+8048G>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100073559 | ||||||
| chr14:100073700
|
C | G | 1 | a0001c0001t0005g0258 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.11+8189C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100073700 | ||||||
| chr14:100073700
|
C | T | 1 | a0001c0001t0001g0155 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.11+8189C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100073700 | ||||||
| chr14:100074002
|
C | CGGGGGCG others(2): Show |
53 | a0001c0001t0001g0006a0001c0001t0001g0232a0001c0001t0001g0233others(50): Show | 56 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.11+8500_11+8508dup others(9): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 100074002 | |||||
| chr14:100074002
|
C | CGGGGGCG others(3): Show |
1 | a0001c0001t0001g0274 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.11+8496_11+8505dup others(10): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 100074002 | |||||
| chr14:100074019
|
G | T | 1 | a0001c0002t0001g0217 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.11+8508G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100074019 | ||||||
| chr14:100074166
|
G | A | 1 | a0001c0002t0001g0217 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.11+8655G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100074166 | ||||||
| chr14:100074231
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.11+8720C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100074231 | ||||||
| chr14:100074336
|
A | T | 1 | a0001c0001t0001g0332 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.11+8825A>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100074336 | ||||||
| chr14:100074339
|
T | G | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG00738.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.11+8828T>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100074339 | ||||||
| chr14:100074405
|
T | C | 1 | a0001c0001t0001g0262 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.11+8894T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100074405 | ||||||
| chr14:100074559
|
G | A | 12 | a0001c0001t0001g0046a0001c0001t0001g0223a0002c0003t0001g0028others(9): Show | 12 | HG01099.hp1 HG02055.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.11+9048G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100074559 | ||||||
| chr14:100074687
|
G | T | 1 | a0001c0001t0001g0231 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.11+9176G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100074687 | ||||||
| chr14:100074703
|
C | T | 1 | a0001c0001t0001g0154 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.11+9192C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100074703 | ||||||
| chr14:100074726
|
C | A | 3 | a0001c0001t0001g0230a0001c0001t0001g0292a0001c0001t0001g0323 | 3 | HG02040.hp2 NA18950.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.11+9215C>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100074726 | ||||||
| chr14:100074762
|
G | A | 1 | a0002c0003t0001g0043 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.11+9251G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100074762 | ||||||
| chr14:100075011
|
C | T | 2 | a0001c0002t0001g0206a0001c0002t0004g0209 | 2 | HG01884.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.11+9500C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100075011 | ||||||
| chr14:100075029
|
T | C | 2 | a0001c0002t0002g0207a0001c0002t0002g0208 | 2 | HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.11+9518T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100075029 | ||||||
| chr14:100075095
|
G | C | 1 | a0001c0002t0001g0033 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.11+9584G>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100075095 | ||||||
| chr14:100075349
|
C | G | 1 | a0001c0001t0001g0170 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.12-9338C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100075349 | ||||||
| chr14:100075350
|
G | A | 4 | a0002c0005t0002g0340a0002c0005t0002g0341a0002c0005t0002g0342others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.12-9337G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100075350 | ||||||
| chr14:100075724
|
C | T | 168 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(165): Show | 172 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.12-8963C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100075724 | ||||||
| chr14:100075783
|
T | C | 5 | a0001c0004t0001g0040a0001c0004t0001g0219a0001c0004t0001g0220others(2): Show | 5 | HG02145.hp2 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.12-8904T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100075783 | ||||||
| chr14:100075784
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.12-8903G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100075784 | ||||||
| chr14:100075811
|
A | T | 1 | a0001c0002t0001g0217 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.12-8876A>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100075811 | ||||||
| chr14:100075865
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.12-8822G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100075865 | ||||||
| chr14:100075883
|
C | G | 1 | a0001c0001t0001g0153 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.12-8804C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100075883 | ||||||
| chr14:100075888
|
T | C | 1 | a0001c0001t0001g0231 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.12-8799T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100075888 | ||||||
| chr14:100075956
|
G | A | 8 | a0001c0001t0001g0008a0001c0001t0001g0315a0001c0001t0001g0316others(5): Show | 9 | HG01943.hp2 NA18942.hp2 NA18946.hp2 others(6): Show |
intron_variant | MODIFIER | c.12-8731G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100075956 | ||||||
| chr14:100076041
|
G | T | 1 | a0001c0001t0003g0032 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.12-8646G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100076041 | ||||||
| chr14:100076077
|
C | T | 8 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(5): Show | 8 | HG00438.hp2 HG00597.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.12-8610C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100076077 | ||||||
| chr14:100076158
|
G | C | 1 | a0001c0001t0001g0238 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.12-8529G>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100076158 | ||||||
| chr14:100076328
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.12-8359A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100076328 | ||||||
| chr14:100076428
|
C | A | 1 | a0001c0001t0001g0275 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.12-8259C>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100076428 | ||||||
| chr14:100076560
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.12-8127G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100076560 | ||||||
| chr14:100076601
|
A | T | 1 | a0001c0001t0001g0174 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.12-8086A>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100076601 | ||||||
| chr14:100076622
|
A | G | 1 | a0001c0001t0001g0261 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.12-8065A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100076622 | ||||||
| chr14:100076773
|
A | G | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0052others(4): Show | 7 | HG00735.hp1 HG00741.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.12-7914A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100076773 | ||||||
| chr14:100077015
|
C | T | 2 | a0001c0001t0001g0319a0001c0001t0001g0321 | 2 | NA18942.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.12-7672C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100077015 | ||||||
| chr14:100077050
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.12-7637G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100077050 | ||||||
| chr14:100077163
|
G | A | 5 | a0001c0004t0001g0040a0001c0004t0001g0219a0001c0004t0001g0220others(2): Show | 5 | HG02145.hp2 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.12-7524G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100077163 | ||||||
| chr14:100077184
|
G | A | 5 | a0001c0004t0001g0040a0001c0004t0001g0219a0001c0004t0001g0220others(2): Show | 5 | HG02145.hp2 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.12-7503G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100077184 | ||||||
| chr14:100077550
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.12-7137G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100077550 | ||||||
| chr14:100077596
|
G | A | 10 | a0001c0001t0001g0006a0001c0001t0001g0239a0001c0001t0001g0240others(7): Show | 11 | HG02486.hp2 NA18747.hp1 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.12-7091G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100077596 | ||||||
| chr14:100077670
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.12-7017G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100077670 | ||||||
| chr14:100077710
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.12-6977G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100077710 | ||||||
| chr14:100077812
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.12-6875G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100077812 | ||||||
| chr14:100077828
|
A | G | 10 | a0001c0001t0001g0009a0001c0001t0001g0325a0001c0001t0001g0326others(7): Show | 11 | HG00639.hp2 HG01109.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.12-6859A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100077828 | ||||||
| chr14:100077934
|
G | A | 37 | a0001c0002t0001g0005a0001c0002t0001g0033a0001c0002t0001g0034others(34): Show | 38 | HG01346.hp1 HG01358.hp2 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.12-6753G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100077934 | ||||||
| chr14:100077939
|
A | AT | 55 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0046others(52): Show | 56 | HG00735.hp1 HG00741.hp2 HG01099.hp1 others(53): Show |
intron_variant | MODIFIER | c.12-6739dupT | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 100077939 | |||||
| chr14:100078025
|
T | C | 299 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(296): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.12-6662T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100078025 | ||||||
| chr14:100078063
|
T | C | 248 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(245): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.12-6624T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100078063 | ||||||
| chr14:100078137
|
G | A | 5 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(2): Show | 5 | HG01109.hp1 HG01928.hp2 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.12-6550G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100078137 | ||||||
| chr14:100078284
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.12-6403C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100078284 | ||||||
| chr14:100078299
|
A | T | 1 | a0001c0001t0001g0231 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.12-6388A>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100078299 | ||||||
| chr14:100078310
|
G | T | 2 | a0001c0002t0001g0005a0001c0002t0001g0200 | 3 | HG01346.hp1 HG01358.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.12-6377G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100078310 | ||||||
| chr14:100078415
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.12-6272A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100078415 | ||||||
| chr14:100078458
|
C | T | 1 | a0001c0002t0001g0200 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.12-6229C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100078458 | ||||||
| chr14:100078459
|
G | A | 1 | a0001c0001t0001g0068 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.12-6228G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100078459 | ||||||
| chr14:100078463
|
A | G | 74 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(71): Show | 75 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.12-6224A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100078463 | ||||||
| chr14:100078510
|
T | A | 1 | a0001c0001t0001g0274 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.12-6177T>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100078510 | ||||||
| chr14:100078536
|
G | C | 1 | a0001c0001t0001g0069 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.12-6151G>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100078536 | ||||||
| chr14:100078572
|
A | T | 5 | a0001c0004t0001g0040a0001c0004t0001g0219a0001c0004t0001g0220others(2): Show | 5 | HG02145.hp2 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.12-6115A>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100078572 | ||||||
| chr14:100078581
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.12-6106G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100078581 | ||||||
| chr14:100078705
|
T | C | 296 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(293): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.12-5982T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100078705 | ||||||
| chr14:100078793
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.12-5894G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100078793 | ||||||
| chr14:100078824
|
A | T | 1 | a0001c0002t0001g0217 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.12-5863A>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100078824 | ||||||
| chr14:100078836
|
T | C | 3 | a0001c0001t0001g0294a0001c0001t0001g0337a0001c0001t0001g0338 | 3 | NA19005.hp1 NA19012.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.12-5851T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100078836 | ||||||
| chr14:100078860
|
A | C | 113 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0031others(110): Show | 117 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.12-5827A>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100078860 | ||||||
| chr14:100079030
|
A | G | 4 | a0001c0004t0001g0219a0001c0004t0001g0220a0001c0004t0001g0221others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.12-5657A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100079030 | ||||||
| chr14:100079083
|
G | A | 11 | a0001c0001t0001g0046a0002c0003t0001g0028a0002c0003t0001g0029others(8): Show | 11 | HG01099.hp1 HG02055.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.12-5604G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100079083 | ||||||
| chr14:100079204
|
G | A | 1 | a0001c0007t0001g0314 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.12-5483G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100079204 | ||||||
| chr14:100079221
|
G | A | 57 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0046others(54): Show | 58 | HG00735.hp1 HG00741.hp2 HG01099.hp1 others(55): Show |
intron_variant | MODIFIER | c.12-5466G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100079221 | ||||||
| chr14:100079392
|
A | G | 12 | a0001c0001t0001g0009a0001c0001t0001g0280a0001c0001t0001g0322others(9): Show | 13 | HG00099.hp2 HG00639.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.12-5295A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100079392 | ||||||
| chr14:100079401
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.12-5286A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100079401 | ||||||
| chr14:100079478
|
C | T | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0275 | 3 | HG02258.hp1 HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.12-5209C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100079478 | ||||||
| chr14:100079503
|
A | T | 3 | a0002c0003t0001g0048a0002c0003t0001g0049a0002c0003t0001g0050 | 3 | HG03130.hp2 HG03139.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.12-5184A>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100079503 | ||||||
| chr14:100079549
|
G | A | 2 | a0002c0003t0001g0028a0002c0003t0001g0029 | 2 | HG02055.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.12-5138G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100079549 | ||||||
| chr14:100080000
|
G | C | 20 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235others(17): Show | 22 | HG00140.hp2 HG00733.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.12-4687G>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100080000 | ||||||
| chr14:100080052
|
A | T | 17 | a0001c0001t0001g0042a0001c0001t0001g0058a0001c0001t0001g0140others(14): Show | 17 | HG02027.hp1 HG02056.hp2 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.12-4635A>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100080052 | ||||||
| chr14:100080074
|
T | A | 2 | a0001c0002t0002g0207a0001c0002t0002g0208 | 2 | HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.12-4613T>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100080074 | ||||||
| chr14:100080118
|
A | G | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0052others(4): Show | 7 | HG00735.hp1 HG00741.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.12-4569A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100080118 | ||||||
| chr14:100080140
|
G | A | 9 | a0001c0004t0001g0040a0001c0004t0001g0219a0001c0004t0001g0220others(6): Show | 9 | HG01884.hp1 HG02145.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.12-4547G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100080140 | ||||||
| chr14:100080222
|
A | G | 1 | a0001c0001t0001g0223 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.12-4465A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100080222 | ||||||
| chr14:100080448
|
G | A | 1 | a0001c0001t0001g0247 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.12-4239G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100080448 | ||||||
| chr14:100080531
|
A | G | 11 | a0001c0001t0001g0046a0002c0003t0001g0028a0002c0003t0001g0029others(8): Show | 11 | HG01099.hp1 HG02055.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.12-4156A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100080531 | ||||||
| chr14:100080718
|
G | A | 3 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035 | 3 | HG01952.hp1 HG03831.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.12-3969G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100080718 | ||||||
| chr14:100080723
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | NA18979.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.12-3964G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100080723 | ||||||
| chr14:100080741
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.12-3946C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100080741 | ||||||
| chr14:100080765
|
C | T | 1 | a0001c0001t0001g0257 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.12-3922C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100080765 | ||||||
| chr14:100080959
|
A | C | 4 | a0001c0004t0001g0219a0001c0004t0001g0220a0001c0004t0001g0221others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.12-3728A>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100080959 | ||||||
| chr14:100081000
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.12-3687G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100081000 | ||||||
| chr14:100081002
|
G | A | 166 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 170 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.12-3685G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100081002 | ||||||
| chr14:100081212
|
C | T | 1 | a0001c0001t0001g0260 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.12-3475C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100081212 | ||||||
| chr14:100081300
|
C | T | 3 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113 | 3 | HG01256.hp2 HG01258.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.12-3387C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100081300 | ||||||
| chr14:100081440
|
T | C | 1 | a0001c0001t0001g0295 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.12-3247T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100081440 | ||||||
| chr14:100081464
|
G | A | 166 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 170 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.12-3223G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100081464 | ||||||
| chr14:100081497
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.12-3190A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100081497 | ||||||
| chr14:100081513
|
C | CA | 56 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0013others(53): Show | 60 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.12-3156dupA | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 100081513 | |||||
| chr14:100081513
|
CA | C | 173 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(170): Show | 177 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.12-3156delA | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 100081513 | |||||
| chr14:100081513
|
CAA | C | 53 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0046others(50): Show | 54 | HG00673.hp2 HG00735.hp1 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.12-3157_12-3156del others(2): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 100081513 | |||||
| chr14:100081535
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.12-3152A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100081535 | ||||||
| chr14:100081536
|
C | T | 166 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 170 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.12-3151C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100081536 | ||||||
| chr14:100081554
|
A | C | 1 | a0001c0002t0001g0217 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.12-3133A>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100081554 | ||||||
| chr14:100081672
|
C | T | 5 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(2): Show | 5 | HG01952.hp1 HG02258.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.12-3015C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100081672 | ||||||
| chr14:100081690
|
C | T | 48 | a0001c0001t0001g0046a0001c0002t0001g0005a0001c0002t0001g0033others(45): Show | 49 | HG01099.hp1 HG01346.hp1 HG01358.hp2 others(46): Show |
intron_variant | MODIFIER | c.12-2997C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100081690 | ||||||
| chr14:100081795
|
G | A | 25 | a0001c0002t0001g0005a0001c0002t0001g0200a0001c0002t0001g0201others(22): Show | 26 | HG01346.hp1 HG01358.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.12-2892G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100081795 | ||||||
| chr14:100081826
|
G | A | 5 | a0001c0004t0001g0040a0001c0004t0001g0219a0001c0004t0001g0220others(2): Show | 5 | HG02145.hp2 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.12-2861G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100081826 | ||||||
| chr14:100082064
|
C | T | 1 | a0001c0001t0001g0293 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.12-2623C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100082064 | ||||||
| chr14:100082152
|
G | A | 4 | a0001c0002t0001g0284a0001c0002t0002g0282a0001c0002t0002g0283others(1): Show | 4 | HG02451.hp1 HG03471.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.12-2535G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100082152 | ||||||
| chr14:100082182
|
CGCATCCC others(4): Show |
C | 4 | a0002c0005t0002g0340a0002c0005t0002g0341a0002c0005t0002g0342others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.12-2503_12-2493del others(11): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 100082182 | |||||
| chr14:100082228
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.12-2459C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100082228 | ||||||
| chr14:100082427
|
TC | T | 3 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055 | 3 | NA18982.hp1 NA18993.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.12-2258delC | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 100082427 | |||||
| chr14:100082440
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.12-2247C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100082440 | ||||||
| chr14:100082820
|
T | C | 1 | a0001c0001t0001g0325 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.12-1867T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100082820 | ||||||
| chr14:100082821
|
A | T | 12 | a0001c0001t0001g0009a0001c0001t0001g0280a0001c0001t0001g0322others(9): Show | 13 | HG00099.hp2 HG00639.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.12-1866A>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100082821 | ||||||
| chr14:100082921
|
G | A | 5 | a0001c0004t0001g0040a0001c0004t0001g0219a0001c0004t0001g0220others(2): Show | 5 | HG02145.hp2 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.12-1766G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100082921 | ||||||
| chr14:100082951
|
C | G | 46 | a0001c0001t0001g0006a0001c0001t0001g0232a0001c0001t0001g0233others(43): Show | 49 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.12-1736C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100082951 | ||||||
| chr14:100082986
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.12-1701C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100082986 | ||||||
| chr14:100083071
|
T | C | 7 | a0001c0002t0001g0210a0001c0002t0001g0211a0001c0002t0001g0212others(4): Show | 7 | HG02109.hp2 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.12-1616T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100083071 | ||||||
| chr14:100083090
|
C | T | 2 | a0001c0002t0001g0206a0001c0002t0004g0209 | 2 | HG01884.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.12-1597C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100083090 | ||||||
| chr14:100083241
|
G | A | 5 | a0001c0004t0001g0040a0001c0004t0001g0219a0001c0004t0001g0220others(2): Show | 5 | HG02145.hp2 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.12-1446G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100083241 | ||||||
| chr14:100083421
|
G | A | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0052others(4): Show | 7 | HG00735.hp1 HG00741.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.12-1266G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100083421 | ||||||
| chr14:100083472
|
A | G | 6 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235others(3): Show | 8 | HG02055.hp2 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.12-1215A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100083472 | ||||||
| chr14:100083534
|
A | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0170 | 2 | HG03492.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.12-1153A>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100083534 | ||||||
| chr14:100083552
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.12-1135C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100083552 | ||||||
| chr14:100083664
|
A | G | 1 | a0002c0003t0001g0044 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.12-1023A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100083664 | ||||||
| chr14:100083905
|
C | T | 3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177 | 3 | HG02630.hp1 HG02717.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.12-782C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100083905 | ||||||
| chr14:100083916
|
T | A | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0015others(1): Show | 4 | NA18998.hp1 NA19054.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.12-771T>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100083916 | ||||||
| chr14:100083996
|
G | T | 1 | a0001c0001t0001g0018 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.12-691G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100083996 | ||||||
| chr14:100084038
|
T | TTC | 5 | a0001c0004t0001g0040a0001c0004t0001g0219a0001c0004t0001g0220others(2): Show | 5 | HG02145.hp2 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.12-635_12-634dupCT | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 100084038 | |||||
| chr14:100084052
|
C | CT | 58 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0052others(55): Show | 60 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.12-618dupT | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 100084052 | |||||
| chr14:100084052
|
C | CTT | 41 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0003g0032others(38): Show | 42 | HG00735.hp1 HG00741.hp2 HG01175.hp1 others(39): Show |
intron_variant | MODIFIER | c.12-619_12-618dupTT | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 100084052 | |||||
| chr14:100084052
|
C | CTTT | 8 | a0001c0001t0001g0046a0001c0002t0001g0215a0002c0003t0001g0043others(5): Show | 8 | HG01099.hp1 HG02572.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.12-620_12-618dupTT others(1): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 100084052 | |||||
| chr14:100084052
|
CT | C | 11 | a0001c0001t0001g0011a0001c0001t0001g0036a0001c0001t0001g0074others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG03041.hp2 others(8): Show |
intron_variant | MODIFIER | c.12-618delT | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 100084052 | |||||
| chr14:100084053
|
T | TC | 4 | a0002c0005t0002g0340a0002c0005t0002g0341a0002c0005t0002g0342others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.12-634_12-633insC | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100084053 | ||||||
| chr14:100084069
|
T | C | 2 | a0001c0001t0001g0059a0001c0001t0001g0114 | 2 | HG02698.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.12-618T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100084069 | ||||||
| chr14:100084226
|
G | A | 66 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0046others(63): Show | 67 | HG00735.hp1 HG00741.hp2 HG01099.hp1 others(64): Show |
intron_variant | MODIFIER | c.12-461G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100084226 | ||||||
| chr14:100084243
|
G | A | 1 | a0001c0004t0001g0219 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.12-444G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100084243 | ||||||
| chr14:100084297
|
A | C | 9 | a0001c0004t0001g0040a0001c0004t0001g0219a0001c0004t0001g0220others(6): Show | 9 | HG01884.hp1 HG02145.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.12-390A>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100084297 | ||||||
| chr14:100084430
|
C | A | 19 | a0001c0002t0001g0005a0001c0002t0001g0200a0001c0002t0001g0205others(16): Show | 20 | HG01346.hp1 HG01358.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.12-257C>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100084430 | ||||||
| chr14:100084432
|
C | T | 37 | a0001c0002t0001g0005a0001c0002t0001g0033a0001c0002t0001g0034others(34): Show | 38 | HG01346.hp1 HG01358.hp2 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.12-255C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100084432 | ||||||
| chr14:100084504
|
C | T | 1 | a0001c0001t0001g0182 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.12-183C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100084504 | ||||||
| chr14:100084586
|
T | A | 1 | a0001c0001t0001g0249 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.12-101T>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100084586 | ||||||
| chr14:100084592
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.12-95T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100084592 | ||||||
| chr14:100084630
|
A | G | 1 | a0001c0001t0007g0107 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.12-57A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100084630 | ||||||
| chr14:100084640
|
C | G | 1 | a0001c0001t0001g0075 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.12-47C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 1/13 | chr14 | 100084640 | ||||||
| chr14:100085053
|
A | G | 5 | a0001c0004t0001g0040a0001c0004t0001g0219a0001c0004t0001g0220others(2): Show | 5 | HG02145.hp2 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.180+198A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100085053 | ||||||
| chr14:100085064
|
A | G | 51 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(48): Show | 53 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(50): Show |
intron_variant | MODIFIER | c.180+209A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100085064 | ||||||
| chr14:100085075
|
A | G | 6 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235others(3): Show | 8 | HG02055.hp2 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.180+220A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100085075 | ||||||
| chr14:100085359
|
A | G | 1 | a0001c0001t0001g0313 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.180+504A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100085359 | ||||||
| chr14:100085398
|
A | C | 27 | a0001c0001t0001g0006a0001c0001t0001g0232a0001c0001t0001g0238others(24): Show | 28 | HG00423.hp2 HG00597.hp2 HG01993.hp1 others(25): Show |
intron_variant | MODIFIER | c.180+543A>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100085398 | ||||||
| chr14:100085771
|
C | T | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0052others(4): Show | 7 | HG00735.hp1 HG00741.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.180+916C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100085771 | ||||||
| chr14:100085907
|
T | C | 7 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(4): Show | 7 | HG01952.hp1 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.180+1052T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100085907 | ||||||
| chr14:100085921
|
T | A | 175 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(172): Show | 183 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.180+1066T>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100085921 | ||||||
| chr14:100085924
|
A | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0068a0001c0001t0001g0076 | 4 | HG02615.hp2 NA18522.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.180+1069A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100085924 | ||||||
| chr14:100085931
|
G | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0068a0001c0001t0001g0076 | 4 | HG02615.hp2 NA18522.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.180+1076G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100085931 | ||||||
| chr14:100085943
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.180+1088C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100085943 | ||||||
| chr14:100085957
|
C | T | 1 | a0001c0004t0001g0040 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.180+1102C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100085957 | ||||||
| chr14:100085972
|
A | C | 112 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0031others(109): Show | 116 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.180+1117A>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100085972 | ||||||
| chr14:100085986
|
G | A | 1 | a0001c0002t0001g0210 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.180+1131G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100085986 | ||||||
| chr14:100086294
|
C | T | 1 | a0001c0001t0001g0312 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.180+1439C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100086294 | ||||||
| chr14:100086545
|
G | A | 1 | a0001c0001t0001g0297 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.180+1690G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100086545 | ||||||
| chr14:100086559
|
A | G | 1 | a0001c0002t0001g0034 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.180+1704A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100086559 | ||||||
| chr14:100086681
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.180+1826G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100086681 | ||||||
| chr14:100086936
|
C | T | 5 | a0001c0001t0001g0297a0001c0001t0001g0309a0001c0001t0001g0310others(2): Show | 5 | HG02056.hp1 HG02071.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.180+2081C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100086936 | ||||||
| chr14:100086993
|
G | C | 4 | a0001c0001t0001g0226a0001c0001t0001g0229a0001c0001t0009g0228others(1): Show | 4 | HG00609.hp2 HG01978.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.180+2138G>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100086993 | ||||||
| chr14:100087014
|
A | G | 1 | a0001c0001t0001g0271 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.180+2159A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100087014 | ||||||
| chr14:100087032
|
G | A | 172 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(169): Show | 179 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.180+2177G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100087032 | ||||||
| chr14:100087052
|
G | A | 10 | a0001c0001t0001g0009a0001c0001t0001g0325a0001c0001t0001g0326others(7): Show | 11 | HG00639.hp2 HG01109.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.180+2197G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100087052 | ||||||
| chr14:100087066
|
T | C | 6 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0265others(3): Show | 6 | HG00140.hp2 HG02145.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.180+2211T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100087066 | ||||||
| chr14:100087312
|
G | C | 2 | a0002c0003t0001g0028a0002c0003t0001g0029 | 2 | HG02055.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.180+2457G>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100087312 | ||||||
| chr14:100087352
|
G | T | 4 | a0002c0005t0002g0340a0002c0005t0002g0341a0002c0005t0002g0342others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.180+2497G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100087352 | ||||||
| chr14:100087421
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.180+2566C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100087421 | ||||||
| chr14:100087513
|
G | A | 7 | a0001c0002t0001g0210a0001c0002t0001g0211a0001c0002t0001g0212others(4): Show | 7 | HG02109.hp2 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.180+2658G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100087513 | ||||||
| chr14:100087544
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.180+2689G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100087544 | ||||||
| chr14:100087547
|
G | A | 1 | a0001c0001t0001g0326 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.180+2692G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100087547 | ||||||
| chr14:100087569
|
G | A | 8 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0146others(5): Show | 8 | HG00735.hp1 HG00741.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.180+2714G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100087569 | ||||||
| chr14:100087585
|
G | C | 5 | a0001c0002t0001g0277a0001c0002t0001g0278a0001c0002t0001g0279others(2): Show | 5 | HG02109.hp1 HG02723.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.180+2730G>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100087585 | ||||||
| chr14:100087600
|
C | T | 7 | a0001c0001t0001g0238a0001c0001t0001g0247a0001c0001t0001g0251others(4): Show | 7 | HG01993.hp1 NA18955.hp2 NA18968.hp1 others(4): Show |
intron_variant | MODIFIER | c.180+2745C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100087600 | ||||||
| chr14:100087765
|
C | CCTGCTCT others(3): Show |
46 | a0001c0001t0001g0006a0001c0001t0001g0232a0001c0001t0001g0233others(43): Show | 49 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.180+2930_180+2939d others(12): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 100087765 | |||||
| chr14:100087820
|
T | G | 1 | a0001c0001t0001g0069 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.180+2965T>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100087820 | ||||||
| chr14:100087947
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.180+3092A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100087947 | ||||||
| chr14:100088025
|
A | G | 47 | a0001c0001t0001g0006a0001c0001t0001g0223a0001c0001t0001g0232others(44): Show | 50 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.180+3170A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100088025 | ||||||
| chr14:100088045
|
A | G | 4 | a0002c0005t0002g0340a0002c0005t0002g0341a0002c0005t0002g0342others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.180+3190A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100088045 | ||||||
| chr14:100088589
|
A | G | 176 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(173): Show | 183 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.180+3734A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100088589 | ||||||
| chr14:100088598
|
C | T | 5 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(2): Show | 5 | HG01952.hp1 HG02258.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.180+3743C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100088598 | ||||||
| chr14:100088981
|
A | G | 4 | a0001c0004t0001g0219a0001c0004t0001g0220a0001c0004t0001g0221others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.180+4126A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100088981 | ||||||
| chr14:100089047
|
T | A | 11 | a0001c0001t0001g0046a0002c0003t0001g0028a0002c0003t0001g0029others(8): Show | 11 | HG01099.hp1 HG02055.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.180+4192T>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100089047 | ||||||
| chr14:100089118
|
T | C | 5 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(2): Show | 5 | HG01109.hp1 HG01928.hp2 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.180+4263T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100089118 | ||||||
| chr14:100089195
|
T | C | 1 | a0001c0002t0001g0034 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.180+4340T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100089195 | ||||||
| chr14:100089288
|
AT | A | 3 | a0001c0002t0001g0287a0001c0002t0001g0288a0001c0002t0001g0289 | 3 | HG02280.hp1 HG02622.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.180+4437delT | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 100089288 | |||||
| chr14:100089473
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.180+4618G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100089473 | ||||||
| chr14:100089810
|
G | A | 3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177 | 3 | HG02630.hp1 HG02717.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.180+4955G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100089810 | ||||||
| chr14:100089920
|
G | A | 9 | a0001c0004t0001g0040a0001c0004t0001g0219a0001c0004t0001g0220others(6): Show | 9 | HG01884.hp1 HG02145.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.180+5065G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100089920 | ||||||
| chr14:100090011
|
A | G | 46 | a0001c0001t0001g0006a0001c0001t0001g0232a0001c0001t0001g0233others(43): Show | 49 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.180+5156A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100090011 | ||||||
| chr14:100090077
|
A | G | 11 | a0001c0001t0001g0046a0002c0003t0001g0028a0002c0003t0001g0029others(8): Show | 11 | HG01099.hp1 HG02055.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.180+5222A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100090077 | ||||||
| chr14:100090148
|
G | A | 4 | a0001c0002t0002g0333a0001c0002t0002g0334a0001c0002t0002g0335others(1): Show | 4 | HG02257.hp2 HG02451.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.180+5293G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100090148 | ||||||
| chr14:100090296
|
G | A | 4 | a0002c0005t0002g0340a0002c0005t0002g0341a0002c0005t0002g0342others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.180+5441G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100090296 | ||||||
| chr14:100090321
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.180+5466C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100090321 | ||||||
| chr14:100090322
|
C | T | 4 | a0001c0004t0001g0219a0001c0004t0001g0220a0001c0004t0001g0221others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.180+5467C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100090322 | ||||||
| chr14:100090323
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0076 | 3 | HG02615.hp2 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.180+5468G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100090323 | ||||||
| chr14:100090337
|
C | G | 9 | a0001c0004t0001g0040a0001c0004t0001g0219a0001c0004t0001g0220others(6): Show | 9 | HG01884.hp1 HG02145.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.180+5482C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100090337 | ||||||
| chr14:100090406
|
C | T | 5 | a0001c0004t0001g0040a0001c0004t0001g0219a0001c0004t0001g0220others(2): Show | 5 | HG02145.hp2 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.180+5551C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100090406 | ||||||
| chr14:100090592
|
A | G | 6 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235others(3): Show | 8 | HG02055.hp2 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.180+5737A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100090592 | ||||||
| chr14:100090604
|
T | G | 1 | a0001c0001t0001g0118 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.180+5749T>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100090604 | ||||||
| chr14:100090632
|
C | A | 12 | a0001c0001t0001g0009a0001c0001t0001g0280a0001c0001t0001g0322others(9): Show | 13 | HG00099.hp2 HG00639.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.180+5777C>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100090632 | ||||||
| chr14:100090754
|
T | C | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0052others(4): Show | 7 | HG00735.hp1 HG00741.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.180+5899T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100090754 | ||||||
| chr14:100090756
|
C | T | 113 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0031others(110): Show | 117 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.180+5901C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100090756 | ||||||
| chr14:100090928
|
A | G | 40 | a0001c0001t0001g0006a0001c0001t0001g0232a0001c0001t0001g0238others(37): Show | 41 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.180+6073A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100090928 | ||||||
| chr14:100091115
|
T | G | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0052others(4): Show | 7 | HG00735.hp1 HG00741.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.180+6260T>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100091115 | ||||||
| chr14:100091353
|
C | T | 1 | a0001c0002t0001g0217 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.181-6128C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100091353 | ||||||
| chr14:100091394
|
C | CTCTG | 113 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0031others(110): Show | 117 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.181-6085_181-6082d others(6): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 100091394 | |||||
| chr14:100091422
|
T | C | 46 | a0001c0001t0001g0006a0001c0001t0001g0232a0001c0001t0001g0233others(43): Show | 49 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.181-6059T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100091422 | ||||||
| chr14:100091454
|
G | A | 13 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(10): Show | 13 | HG01952.hp1 HG02109.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.181-6027G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100091454 | ||||||
| chr14:100091467
|
A | G | 113 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0031others(110): Show | 117 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.181-6014A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100091467 | ||||||
| chr14:100091584
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.181-5897C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100091584 | ||||||
| chr14:100091605
|
G | A | 51 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(48): Show | 53 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(50): Show |
intron_variant | MODIFIER | c.181-5876G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100091605 | ||||||
| chr14:100091620
|
A | G | 176 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(173): Show | 183 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.181-5861A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100091620 | ||||||
| chr14:100091660
|
C | A | 1 | a0001c0001t0001g0077 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.181-5821C>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100091660 | ||||||
| chr14:100091773
|
A | G | 7 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(4): Show | 7 | HG01952.hp1 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.181-5708A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100091773 | ||||||
| chr14:100091779
|
A | T | 1 | a0001c0001t0001g0039 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.181-5702A>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100091779 | ||||||
| chr14:100091912
|
C | G | 6 | a0001c0001t0001g0293a0001c0001t0001g0305a0001c0001t0001g0306others(3): Show | 6 | HG01192.hp2 HG02004.hp1 NA19000.hp2 others(3): Show |
intron_variant | MODIFIER | c.181-5569C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100091912 | ||||||
| chr14:100092007
|
G | A | 3 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035 | 3 | HG01952.hp1 HG03831.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.181-5474G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100092007 | ||||||
| chr14:100092102
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.181-5379G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100092102 | ||||||
| chr14:100092104
|
A | G | 6 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235others(3): Show | 8 | HG02055.hp2 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.181-5377A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100092104 | ||||||
| chr14:100092135
|
G | T | 1 | a0001c0001t0001g0152 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.181-5346G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100092135 | ||||||
| chr14:100092149
|
G | C | 19 | a0001c0002t0001g0005a0001c0002t0001g0200a0001c0002t0001g0205others(16): Show | 20 | HG01346.hp1 HG01358.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.181-5332G>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100092149 | ||||||
| chr14:100092209
|
T | A | 2 | a0001c0001t0001g0298a0001c0001t0001g0299 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.181-5272T>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100092209 | ||||||
| chr14:100092222
|
A | G | 51 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(48): Show | 53 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(50): Show |
intron_variant | MODIFIER | c.181-5259A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100092222 | ||||||
| chr14:100092319
|
T | G | 113 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0031others(110): Show | 117 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.181-5162T>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100092319 | ||||||
| chr14:100092333
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.181-5148T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100092333 | ||||||
| chr14:100092337
|
C | T | 47 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(44): Show | 49 | HG01168.hp2 HG01169.hp2 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.181-5144C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100092337 | ||||||
| chr14:100092340
|
A | G | 1 | a0001c0001t0001g0223 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.181-5141A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100092340 | ||||||
| chr14:100092387
|
TCAG | T | 7 | a0001c0002t0001g0287a0001c0002t0001g0288a0001c0002t0001g0289others(4): Show | 7 | HG02257.hp2 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.181-5090_181-5088d others(5): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 100092387 | |||||
| chr14:100092649
|
C | T | 1 | a0001c0001t0001g0249 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.181-4832C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100092649 | ||||||
| chr14:100092650
|
G | T | 2 | a0001c0002t0001g0206a0001c0002t0004g0209 | 2 | HG01884.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.181-4831G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100092650 | ||||||
| chr14:100092706
|
G | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0105 | 2 | HG02027.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.181-4775G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100092706 | ||||||
| chr14:100092718
|
G | T | 1 | a0001c0001t0001g0199 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.181-4763G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100092718 | ||||||
| chr14:100092923
|
A | G | 1 | a0001c0001t0001g0267 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.181-4558A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100092923 | ||||||
| chr14:100093144
|
A | G | 7 | a0001c0002t0001g0210a0001c0002t0001g0211a0001c0002t0001g0212others(4): Show | 7 | HG02109.hp2 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.181-4337A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100093144 | ||||||
| chr14:100093182
|
T | G | 46 | a0001c0001t0001g0006a0001c0001t0001g0232a0001c0001t0001g0233others(43): Show | 49 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.181-4299T>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100093182 | ||||||
| chr14:100093280
|
T | G | 1 | a0001c0001t0001g0157 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.181-4201T>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100093280 | ||||||
| chr14:100093435
|
G | A | 2 | a0001c0002t0001g0206a0001c0002t0004g0209 | 2 | HG01884.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.181-4046G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100093435 | ||||||
| chr14:100093647
|
C | T | 1 | a0001c0002t0001g0206 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.181-3834C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100093647 | ||||||
| chr14:100093816
|
C | G | 5 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(2): Show | 5 | HG01952.hp1 HG02258.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.181-3665C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100093816 | ||||||
| chr14:100093953
|
T | C | 7 | a0001c0002t0001g0210a0001c0002t0001g0211a0001c0002t0001g0212others(4): Show | 7 | HG02109.hp2 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.181-3528T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100093953 | ||||||
| chr14:100094045
|
G | A | 8 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0052others(5): Show | 8 | HG00735.hp1 HG00741.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.181-3436G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100094045 | ||||||
| chr14:100094071
|
T | A | 1 | a0001c0001t0001g0223 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.181-3410T>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100094071 | ||||||
| chr14:100094141
|
A | AGTC | 23 | a0001c0002t0001g0005a0001c0002t0001g0200a0001c0002t0001g0201others(20): Show | 24 | HG01346.hp1 HG01358.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.181-3339_181-3337d others(5): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 100094141 | |||||
| chr14:100094162
|
A | G | 10 | a0001c0001t0001g0331a0001c0004t0001g0040a0001c0004t0001g0219others(7): Show | 10 | HG01884.hp1 HG02145.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.181-3319A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100094162 | ||||||
| chr14:100094293
|
C | T | 4 | a0001c0002t0001g0201a0001c0006t0001g0202a0001c0006t0001g0203others(1): Show | 4 | HG02809.hp2 HG02818.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.181-3188C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100094293 | ||||||
| chr14:100094326
|
C | T | 47 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(44): Show | 49 | HG01168.hp2 HG01169.hp2 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.181-3155C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100094326 | ||||||
| chr14:100094358
|
C | A | 2 | a0001c0001t0001g0298a0001c0001t0001g0299 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.181-3123C>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100094358 | ||||||
| chr14:100094358
|
C | G | 1 | a0001c0001t0001g0138 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.181-3123C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100094358 | ||||||
| chr14:100094540
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.181-2941G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100094540 | ||||||
| chr14:100094580
|
T | TA | 6 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0111others(3): Show | 6 | HG01256.hp2 HG01258.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.181-2888dupA | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 100094580 | |||||
| chr14:100094598
|
A | G | 75 | a0001c0001t0001g0006a0001c0001t0001g0046a0001c0001t0001g0232others(72): Show | 77 | HG00423.hp2 HG00597.hp2 HG01099.hp1 others(74): Show |
intron_variant | MODIFIER | c.181-2883A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100094598 | ||||||
| chr14:100094614
|
T | C | 20 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235others(17): Show | 22 | HG00140.hp2 HG00733.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.181-2867T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100094614 | ||||||
| chr14:100094702
|
C | T | 1 | a0001c0002t0001g0205 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.181-2779C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100094702 | ||||||
| chr14:100094780
|
G | A | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0003g0032 | 3 | HG00735.hp1 HG00741.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.181-2701G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100094780 | ||||||
| chr14:100094868
|
C | T | 3 | a0001c0001t0001g0027a0001c0001t0001g0291a0001c0001t0002g0290 | 3 | HG03098.hp1 HG03579.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.181-2613C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100094868 | ||||||
| chr14:100094898
|
G | T | 1 | a0001c0001t0001g0137 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.181-2583G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100094898 | ||||||
| chr14:100094933
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.181-2548C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100094933 | ||||||
| chr14:100094976
|
G | A | 1 | a0001c0001t0001g0171 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.181-2505G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100094976 | ||||||
| chr14:100095039
|
T | TA | 4 | a0001c0004t0001g0219a0001c0004t0001g0220a0001c0004t0001g0221others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.181-2435dupA | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 100095039 | |||||
| chr14:100095069
|
G | C | 126 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(123): Show | 130 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(127): Show |
intron_variant | MODIFIER | c.181-2412G>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100095069 | ||||||
| chr14:100095107
|
C | T | 43 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0052others(40): Show | 44 | HG00735.hp1 HG00741.hp2 HG01175.hp1 others(41): Show |
intron_variant | MODIFIER | c.181-2374C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100095107 | ||||||
| chr14:100095248
|
AT | A | 3 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039 | 3 | HG02129.hp2 NA18985.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.181-2228delT | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 100095248 | |||||
| chr14:100095250
|
T | A | 3 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039 | 3 | HG02129.hp2 NA18985.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.181-2231T>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100095250 | ||||||
| chr14:100095613
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.181-1868G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100095613 | ||||||
| chr14:100095662
|
G | C | 1 | a0001c0001t0001g0294 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.181-1819G>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100095662 | ||||||
| chr14:100095662
|
G | T | 1 | a0001c0001t0001g0261 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.181-1819G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100095662 | ||||||
| chr14:100095721
|
T | TTTG | 23 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0052others(20): Show | 25 | HG00735.hp1 HG00741.hp2 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.181-1739_181-1737d others(5): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 100095721 | |||||
| chr14:100095816
|
C | T | 19 | a0001c0002t0001g0005a0001c0002t0001g0200a0001c0002t0001g0205others(16): Show | 20 | HG01346.hp1 HG01358.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.181-1665C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100095816 | ||||||
| chr14:100095838
|
G | A | 46 | a0001c0001t0001g0006a0001c0001t0001g0239a0001c0001t0001g0240others(43): Show | 48 | HG01346.hp1 HG01358.hp2 HG01884.hp2 others(45): Show |
intron_variant | MODIFIER | c.181-1643G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100095838 | ||||||
| chr14:100095886
|
C | G | 49 | a0001c0001t0001g0046a0001c0002t0001g0005a0001c0002t0001g0033others(46): Show | 50 | HG01099.hp1 HG01346.hp1 HG01358.hp2 others(47): Show |
intron_variant | MODIFIER | c.181-1595C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100095886 | ||||||
| chr14:100095971
|
G | A | 5 | a0001c0004t0001g0040a0001c0004t0001g0219a0001c0004t0001g0220others(2): Show | 5 | HG02145.hp2 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.181-1510G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100095971 | ||||||
| chr14:100095979
|
T | G | 1 | a0001c0001t0001g0231 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.181-1502T>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100095979 | ||||||
| chr14:100096104
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.181-1377G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100096104 | ||||||
| chr14:100096163
|
T | C | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.181-1318T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100096163 | ||||||
| chr14:100096322
|
A | C | 2 | a0001c0002t0001g0206a0001c0002t0004g0209 | 2 | HG01884.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.181-1159A>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100096322 | ||||||
| chr14:100096422
|
A | C | 12 | a0001c0001t0001g0009a0001c0001t0001g0280a0001c0001t0001g0322others(9): Show | 13 | HG00099.hp2 HG00639.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.181-1059A>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100096422 | ||||||
| chr14:100096477
|
A | G | 2 | a0001c0001t0001g0297a0001c0001t0001g0311 | 2 | HG02056.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.181-1004A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100096477 | ||||||
| chr14:100096562
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.181-919G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100096562 | ||||||
| chr14:100096804
|
C | G | 4 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(1): Show | 4 | HG01109.hp2 HG02280.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.181-677C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100096804 | ||||||
| chr14:100096922
|
T | G | 1 | a0001c0004t0001g0040 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.181-559T>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100096922 | ||||||
| chr14:100097134
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.181-347T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100097134 | ||||||
| chr14:100097203
|
AAACCAGA others(7): Show |
A | 2 | a0001c0001t0001g0026a0001c0001t0001g0104 | 2 | NA19009.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.181-273_181-260del others(14): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 100097203 | |||||
| chr14:100097224
|
C | A | 1 | a0001c0006t0001g0202 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.181-257C>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100097224 | ||||||
| chr14:100097270
|
A | G | 59 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(56): Show | 62 | HG00099.hp2 HG00639.hp2 HG01109.hp2 others(59): Show |
intron_variant | MODIFIER | c.181-211A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100097270 | ||||||
| chr14:100097332
|
G | A | 326 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(323): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.181-149G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100097332 | ||||||
| chr14:100097344
|
T | C | 1 | a0001c0001t0001g0120 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.181-137T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100097344 | ||||||
| chr14:100097345
|
TG | T | 47 | a0001c0001t0001g0006a0001c0001t0001g0223a0001c0001t0001g0232others(44): Show | 50 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.181-135delG | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100097345 | ||||||
| chr14:100097425
|
C | T | 59 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(56): Show | 62 | HG00099.hp2 HG00639.hp2 HG01109.hp2 others(59): Show |
intron_variant | MODIFIER | c.181-56C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 2/13 | chr14 | 100097425 | ||||||
| chr14:100097683
|
G | A | 4 | a0002c0005t0002g0340a0002c0005t0002g0341a0002c0005t0002g0342others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.358+25G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100097683 | ||||||
| chr14:100097737
|
G | T | 1 | a0001c0001t0001g0052 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.358+79G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100097737 | ||||||
| chr14:100097807
|
T | C | 113 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0031others(110): Show | 117 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.358+149T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100097807 | ||||||
| chr14:100097839
|
G | A | 1 | a0001c0001t0001g0193 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.358+181G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100097839 | ||||||
| chr14:100098050
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.358+392T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100098050 | ||||||
| chr14:100098149
|
C | G | 75 | a0001c0001t0001g0006a0001c0001t0001g0046a0001c0001t0001g0232others(72): Show | 77 | HG00423.hp2 HG00597.hp2 HG01099.hp1 others(74): Show |
intron_variant | MODIFIER | c.358+491C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100098149 | ||||||
| chr14:100098277
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.358+619C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100098277 | ||||||
| chr14:100098339
|
G | A | 38 | a0001c0002t0001g0005a0001c0002t0001g0033a0001c0002t0001g0034others(35): Show | 39 | HG01346.hp1 HG01358.hp2 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.358+681G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100098339 | ||||||
| chr14:100098393
|
G | C | 2 | a0001c0001t0001g0291a0001c0001t0002g0290 | 2 | HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.358+735G>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100098393 | ||||||
| chr14:100098488
|
A | G | 2 | a0001c0002t0001g0005a0001c0002t0001g0200 | 3 | HG01346.hp1 HG01358.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.358+830A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100098488 | ||||||
| chr14:100098881
|
GA | G | 4 | a0001c0002t0002g0333a0001c0002t0002g0334a0001c0002t0002g0335others(1): Show | 4 | HG02257.hp2 HG02451.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.358+1225delA | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr14 | 100098881 | |||||
| chr14:100099179
|
C | CA | 58 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0030others(55): Show | 59 | HG00099.hp2 HG00438.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.358+1541dupA | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr14 | 100099179 | |||||
| chr14:100099180
|
A | C | 2 | a0001c0002t0002g0207a0001c0002t0002g0208 | 2 | HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.358+1522A>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100099180 | ||||||
| chr14:100099254
|
T | C | 172 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(169): Show | 179 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.358+1596T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100099254 | ||||||
| chr14:100099263
|
C | G | 1 | a0001c0001t0001g0103 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.358+1605C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100099263 | ||||||
| chr14:100099281
|
G | A | 11 | a0001c0001t0001g0046a0002c0003t0001g0028a0002c0003t0001g0029others(8): Show | 11 | HG01099.hp1 HG02055.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.358+1623G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100099281 | ||||||
| chr14:100099286
|
C | T | 1 | a0001c0002t0001g0216 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.358+1628C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100099286 | ||||||
| chr14:100099685
|
G | A | 29 | a0001c0001t0001g0006a0001c0001t0001g0223a0001c0001t0001g0232others(26): Show | 30 | HG00423.hp2 HG00597.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.358+2027G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100099685 | ||||||
| chr14:100099700
|
G | A | 14 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235others(11): Show | 16 | HG00733.hp2 HG02055.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.358+2042G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100099700 | ||||||
| chr14:100099727
|
CT | C | 6 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0117others(3): Show | 6 | HG00735.hp1 HG00741.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.358+2085delT | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr14 | 100099727 | |||||
| chr14:100099743
|
T | A | 150 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(147): Show | 156 | HG00423.hp2 HG00597.hp2 HG00639.hp1 others(153): Show |
intron_variant | MODIFIER | c.358+2085T>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100099743 | ||||||
| chr14:100099743
|
T | TA | 21 | a0001c0001t0001g0009a0001c0001t0001g0223a0001c0001t0001g0263others(18): Show | 22 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.358+2087dupA | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr14 | 100099743 | |||||
| chr14:100099744
|
A | C | 52 | a0001c0001t0001g0006a0001c0001t0001g0046a0001c0001t0001g0231others(49): Show | 53 | HG00423.hp2 HG00597.hp2 HG01099.hp1 others(50): Show |
intron_variant | MODIFIER | c.358+2086A>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100099744 | ||||||
| chr14:100099744
|
A | G | 2 | a0001c0001t0001g0165a0001c0001t0001g0170 | 2 | HG03492.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.358+2086A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100099744 | ||||||
| chr14:100099780
|
G | A | 16 | a0001c0001t0001g0046a0001c0001t0001g0156a0001c0002t0001g0277others(13): Show | 16 | HG01099.hp1 HG01175.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.358+2122G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100099780 | ||||||
| chr14:100099786
|
G | C | 1 | a0001c0001t0001g0231 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.358+2128G>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100099786 | ||||||
| chr14:100099853
|
G | A | 163 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(160): Show | 170 | HG00099.hp2 HG00423.hp2 HG00597.hp2 others(167): Show |
intron_variant | MODIFIER | c.358+2195G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100099853 | ||||||
| chr14:100099869
|
G | A | 5 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(2): Show | 5 | HG01952.hp1 HG02258.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.358+2211G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100099869 | ||||||
| chr14:100100003
|
C | CA | 81 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0019others(78): Show | 81 | HG00099.hp2 HG00597.hp2 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.358+2363dupA | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr14 | 100100003 | |||||
| chr14:100100003
|
C | CAA | 9 | a0001c0001t0001g0081a0001c0002t0002g0207a0001c0002t0004g0209others(6): Show | 9 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.358+2362_358+2363d others(4): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr14 | 100100003 | |||||
| chr14:100100003
|
CA | C | 18 | a0001c0001t0001g0231a0001c0001t0001g0233a0001c0001t0001g0234others(15): Show | 20 | HG00140.hp2 HG00733.hp2 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.358+2363delA | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr14 | 100100003 | |||||
| chr14:100100019
|
A | C | 1 | a0002c0005t0002g0343 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.358+2361A>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100100019 | ||||||
| chr14:100100190
|
C | T | 16 | a0001c0001t0001g0009a0001c0001t0001g0280a0001c0001t0001g0322others(13): Show | 17 | HG00099.hp2 HG00639.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.358+2532C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100100190 | ||||||
| chr14:100100543
|
C | A | 12 | a0001c0001t0001g0009a0001c0001t0001g0280a0001c0001t0001g0322others(9): Show | 13 | HG00099.hp2 HG00639.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.358+2885C>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100100543 | ||||||
| chr14:100100559
|
G | A | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0052others(4): Show | 7 | HG00735.hp1 HG00741.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.358+2901G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100100559 | ||||||
| chr14:100100618
|
C | G | 1 | a0001c0001t0001g0120 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.358+2960C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100100618 | ||||||
| chr14:100100778
|
C | T | 4 | a0002c0005t0002g0340a0002c0005t0002g0341a0002c0005t0002g0342others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.358+3120C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100100778 | ||||||
| chr14:100100784
|
C | CA | 33 | a0001c0001t0001g0018a0001c0001t0001g0027a0001c0001t0001g0031others(30): Show | 33 | HG00438.hp2 HG00735.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.358+3151dupA | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr14 | 100100784 | |||||
| chr14:100100784
|
CA | C | 80 | a0001c0001t0001g0006a0001c0001t0001g0046a0001c0001t0001g0117others(77): Show | 82 | HG00423.hp2 HG00597.hp2 HG01099.hp1 others(79): Show |
intron_variant | MODIFIER | c.358+3151delA | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr14 | 100100784 | |||||
| chr14:100100865
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.358+3207G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100100865 | ||||||
| chr14:100101126
|
G | A | 47 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(44): Show | 49 | HG01168.hp2 HG01169.hp2 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.358+3468G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100101126 | ||||||
| chr14:100101258
|
G | C | 1 | a0001c0001t0001g0138 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.358+3600G>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100101258 | ||||||
| chr14:100101274
|
C | G | 9 | a0001c0004t0001g0040a0001c0004t0001g0219a0001c0004t0001g0220others(6): Show | 9 | HG01884.hp1 HG02145.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.358+3616C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100101274 | ||||||
| chr14:100101443
|
G | A | 10 | a0001c0001t0001g0058a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG02132.hp2 HG02135.hp1 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.358+3785G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100101443 | ||||||
| chr14:100101546
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.358+3888G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100101546 | ||||||
| chr14:100101701
|
T | C | 1 | a0001c0001t0001g0181 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.358+4043T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100101701 | ||||||
| chr14:100101713
|
A | C | 10 | a0001c0001t0001g0231a0001c0004t0001g0040a0001c0004t0001g0219others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.358+4055A>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100101713 | ||||||
| chr14:100101756
|
C | G | 4 | a0001c0002t0001g0201a0001c0006t0001g0202a0001c0006t0001g0203others(1): Show | 4 | HG02809.hp2 HG02818.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.358+4098C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100101756 | ||||||
| chr14:100102000
|
G | T | 2 | a0001c0002t0001g0033a0001c0002t0001g0035 | 2 | HG01952.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.358+4342G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100102000 | ||||||
| chr14:100102132
|
C | T | 1 | a0001c0001t0001g0038 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.358+4474C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100102132 | ||||||
| chr14:100102238
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.358+4580C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100102238 | ||||||
| chr14:100102429
|
G | T | 4 | a0001c0002t0001g0206a0001c0002t0002g0207a0001c0002t0002g0208others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.358+4771G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100102429 | ||||||
| chr14:100102474
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.358+4816C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100102474 | ||||||
| chr14:100102573
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.358+4915G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100102573 | ||||||
| chr14:100102868
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.358+5210C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100102868 | ||||||
| chr14:100102873
|
G | A | 5 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(2): Show | 5 | NA18959.hp2 NA18982.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.358+5215G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100102873 | ||||||
| chr14:100102946
|
A | G | 2 | a0001c0001t0001g0102a0001c0001t0001g0127 | 2 | HG00733.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.358+5288A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100102946 | ||||||
| chr14:100103027
|
G | A | 1 | a0001c0001t0001g0015 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.358+5369G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100103027 | ||||||
| chr14:100103050
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.358+5392C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100103050 | ||||||
| chr14:100103056
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.358+5398C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100103056 | ||||||
| chr14:100103100
|
C | CA | 7 | a0001c0001t0001g0018a0001c0001t0001g0061a0001c0001t0001g0062others(4): Show | 7 | HG00673.hp1 HG00738.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.358+5459dupA | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr14 | 100103100 | |||||
| chr14:100103100
|
CA | C | 157 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(154): Show | 163 | HG00099.hp2 HG00423.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.358+5459delA | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr14 | 100103100 | |||||
| chr14:100103100
|
CAA | C | 7 | a0001c0001t0001g0046a0002c0003t0001g0043a0002c0003t0001g0045others(4): Show | 7 | HG01099.hp1 HG02572.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.358+5458_358+5459d others(4): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr14 | 100103100 | |||||
| chr14:100103187
|
A | AT | 95 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0041others(92): Show | 100 | HG00099.hp2 HG00423.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.358+5529_358+5530i others(3): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100103187 | ||||||
| chr14:100103187
|
A | ATT | 8 | a0001c0002t0001g0217a0002c0003t0001g0029a0002c0003t0001g0044others(5): Show | 8 | HG02486.hp2 HG02615.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.358+5529_358+5530i others(4): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100103187 | ||||||
| chr14:100103187
|
AG | A | 5 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0223others(2): Show | 5 | HG00733.hp2 HG00735.hp1 HG00741.hp2 others(2): Show |
intron_variant | MODIFIER | c.358+5530delG | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100103187 | ||||||
| chr14:100103188
|
G | GT | 55 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(52): Show | 57 | HG00673.hp1 HG01168.hp2 HG01169.hp2 others(54): Show |
intron_variant | MODIFIER | c.358+5545dupT | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr14 | 100103188 | |||||
| chr14:100103188
|
G | T | 126 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0041others(123): Show | 131 | HG00099.hp2 HG00423.hp2 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.358+5530G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100103188 | ||||||
| chr14:100103367
|
T | C | 5 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235others(2): Show | 7 | HG02055.hp2 HG02647.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.358+5709T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100103367 | ||||||
| chr14:100103470
|
T | C | 336 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(333): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.358+5812T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100103470 | ||||||
| chr14:100103610
|
G | A | 25 | a0001c0001t0001g0009a0001c0001t0001g0117a0001c0001t0001g0175others(22): Show | 26 | HG00639.hp2 HG00733.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.358+5952G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100103610 | ||||||
| chr14:100103615
|
C | T | 4 | a0002c0005t0002g0340a0002c0005t0002g0341a0002c0005t0002g0342others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.358+5957C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100103615 | ||||||
| chr14:100103625
|
C | G | 1 | a0001c0001t0001g0229 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.358+5967C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100103625 | ||||||
| chr14:100103699
|
A | G | 29 | a0001c0001t0001g0223a0001c0001t0001g0270a0001c0001t0001g0273others(26): Show | 30 | HG01346.hp1 HG01358.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.358+6041A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100103699 | ||||||
| chr14:100104047
|
G | A | 14 | a0001c0001t0001g0009a0001c0001t0001g0326a0001c0001t0001g0327others(11): Show | 15 | HG00639.hp2 HG01109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.358+6389G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100104047 | ||||||
| chr14:100104732
|
T | A | 1 | a0001c0001t0008g0012 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.358+7074T>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100104732 | ||||||
| chr14:100104826
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.358+7168G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100104826 | ||||||
| chr14:100104854
|
A | T | 63 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(60): Show | 65 | HG00438.hp1 HG01167.hp2 HG01168.hp2 others(62): Show |
intron_variant | MODIFIER | c.358+7196A>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100104854 | ||||||
| chr14:100104871
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.358+7213G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100104871 | ||||||
| chr14:100104902
|
CT | C | 80 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(77): Show | 82 | HG00438.hp1 HG00735.hp1 HG01069.hp1 others(79): Show |
intron_variant | MODIFIER | c.358+7270delT | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr14 | 100104902 | |||||
| chr14:100104902
|
CTT | C | 163 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(160): Show | 168 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.358+7269_358+7270d others(4): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr14 | 100104902 | |||||
| chr14:100104902
|
CTTT | C | 33 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0042others(30): Show | 35 | HG01361.hp1 HG02055.hp1 HG02055.hp2 others(32): Show |
intron_variant | MODIFIER | c.358+7268_358+7270d others(5): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr14 | 100104902 | |||||
| chr14:100104902
|
CTTTT | C | 9 | a0001c0001t0001g0046a0001c0001t0001g0231a0001c0001t0001g0322others(6): Show | 9 | HG00099.hp2 HG01099.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.358+7267_358+7270d others(6): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr14 | 100104902 | |||||
| chr14:100104905
|
T | C | 1 | a0001c0001t0001g0015 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.358+7247T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100104905 | ||||||
| chr14:100105065
|
G | T | 5 | a0001c0001t0001g0280a0001c0001t0001g0322a0001c0002t0001g0033others(2): Show | 5 | HG00099.hp2 HG01361.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.358+7407G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100105065 | ||||||
| chr14:100105097
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.358+7439A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100105097 | ||||||
| chr14:100105111
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.358+7453G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100105111 | ||||||
| chr14:100105129
|
A | G | 69 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0031others(66): Show | 73 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.358+7471A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100105129 | ||||||
| chr14:100105261
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.358+7603G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100105261 | ||||||
| chr14:100105396
|
C | T | 1 | a0002c0003t0001g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.358+7738C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100105396 | ||||||
| chr14:100105425
|
T | C | 215 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(212): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.358+7767T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100105425 | ||||||
| chr14:100105508
|
A | G | 66 | a0001c0001t0001g0006a0001c0001t0001g0046a0001c0001t0001g0118others(63): Show | 70 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.358+7850A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100105508 | ||||||
| chr14:100105517
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.358+7859G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100105517 | ||||||
| chr14:100105531
|
C | T | 14 | a0001c0001t0001g0223a0001c0001t0004g0236a0001c0002t0001g0206others(11): Show | 14 | HG01884.hp2 HG02055.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.358+7873C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100105531 | ||||||
| chr14:100105544
|
A | G | 23 | a0001c0001t0001g0009a0001c0001t0001g0262a0001c0001t0001g0263others(20): Show | 24 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.358+7886A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100105544 | ||||||
| chr14:100105858
|
A | T | 2 | a0001c0006t0001g0203a0001c0006t0001g0204 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.358+8200A>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100105858 | ||||||
| chr14:100105936
|
A | G | 10 | a0002c0003t0001g0028a0002c0003t0001g0029a0002c0003t0001g0043others(7): Show | 10 | HG02055.hp1 HG02486.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.358+8278A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100105936 | ||||||
| chr14:100106073
|
C | T | 22 | a0001c0001t0001g0009a0001c0001t0001g0262a0001c0001t0001g0263others(19): Show | 23 | HG00639.hp2 HG00733.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.358+8415C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100106073 | ||||||
| chr14:100106171
|
G | T | 8 | a0001c0001t0001g0001a0001c0001t0001g0097a0001c0001t0001g0156others(5): Show | 10 | HG01069.hp2 HG01074.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.358+8513G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100106171 | ||||||
| chr14:100106437
|
C | T | 1 | a0001c0001t0001g0301 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.358+8779C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100106437 | ||||||
| chr14:100106498
|
C | T | 2 | a0001c0001t0001g0232a0001c0001t0001g0255 | 2 | HG00423.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.358+8840C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100106498 | ||||||
| chr14:100106548
|
A | G | 10 | a0002c0003t0001g0028a0002c0003t0001g0029a0002c0003t0001g0043others(7): Show | 10 | HG02055.hp1 HG02486.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.358+8890A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100106548 | ||||||
| chr14:100106617
|
G | T | 215 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(212): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.358+8959G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100106617 | ||||||
| chr14:100106701
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.358+9043C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100106701 | ||||||
| chr14:100106973
|
G | C | 2 | a0001c0001t0001g0018a0001c0001t0001g0105 | 2 | HG02027.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.358+9315G>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100106973 | ||||||
| chr14:100106991
|
C | T | 64 | a0001c0001t0001g0006a0001c0001t0001g0046a0001c0001t0001g0118others(61): Show | 68 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.358+9333C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100106991 | ||||||
| chr14:100106998
|
C | T | 3 | a0001c0002t0002g0282a0001c0002t0002g0283a0001c0002t0002g0285 | 3 | HG02451.hp1 HG03579.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.358+9340C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100106998 | ||||||
| chr14:100107157
|
C | G | 1 | a0001c0001t0001g0246 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.358+9499C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100107157 | ||||||
| chr14:100107217
|
G | A | 4 | a0001c0002t0001g0277a0001c0002t0001g0278a0001c0002t0001g0279others(1): Show | 4 | HG02109.hp1 HG02723.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.358+9559G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100107217 | ||||||
| chr14:100107480
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.358+9822C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100107480 | ||||||
| chr14:100107713
|
G | C | 1 | a0001c0001t0001g0247 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.358+10055G>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100107713 | ||||||
| chr14:100107839
|
G | A | 4 | a0001c0002t0001g0201a0001c0006t0001g0202a0001c0006t0001g0203others(1): Show | 4 | HG02809.hp2 HG02818.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.358+10181G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100107839 | ||||||
| chr14:100107855
|
G | A | 1 | a0001c0001t0001g0120 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.358+10197G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100107855 | ||||||
| chr14:100107951
|
C | G | 4 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0237others(1): Show | 6 | HG02055.hp2 HG02723.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.358+10293C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100107951 | ||||||
| chr14:100108179
|
G | A | 5 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0154others(2): Show | 5 | HG02083.hp1 NA18959.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.358+10521G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100108179 | ||||||
| chr14:100108274
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.358+10616C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100108274 | ||||||
| chr14:100108286
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.358+10628G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100108286 | ||||||
| chr14:100108391
|
A | G | 1 | a0001c0002t0001g0213 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.358+10733A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100108391 | ||||||
| chr14:100108456
|
C | T | 1 | a0001c0002t0001g0284 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.358+10798C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100108456 | ||||||
| chr14:100108480
|
G | T | 1 | a0001c0002t0002g0207 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.358+10822G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100108480 | ||||||
| chr14:100108741
|
G | T | 4 | a0001c0004t0001g0219a0001c0004t0001g0220a0001c0004t0001g0221others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.358+11083G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100108741 | ||||||
| chr14:100109049
|
G | A | 1 | a0001c0002t0001g0200 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.358+11391G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100109049 | ||||||
| chr14:100109191
|
T | C | 1 | a0001c0001t0001g0156 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.358+11533T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100109191 | ||||||
| chr14:100109271
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.358+11613G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100109271 | ||||||
| chr14:100109394
|
C | T | 3 | a0002c0003t0001g0048a0002c0003t0001g0049a0002c0003t0001g0050 | 3 | HG03130.hp2 HG03139.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.358+11736C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100109394 | ||||||
| chr14:100109800
|
G | A | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0052others(4): Show | 7 | HG00735.hp1 HG00741.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.358+12142G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100109800 | ||||||
| chr14:100109810
|
T | A | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0052others(4): Show | 7 | HG00735.hp1 HG00741.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.358+12152T>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100109810 | ||||||
| chr14:100109923
|
C | T | 1 | a0001c0002t0001g0034 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.358+12265C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100109923 | ||||||
| chr14:100110038
|
A | G | 3 | a0001c0001t0001g0294a0001c0001t0001g0337a0001c0001t0001g0338 | 3 | NA19005.hp1 NA19012.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.358+12380A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100110038 | ||||||
| chr14:100110180
|
C | G | 1 | a0001c0001t0001g0151 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.358+12522C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100110180 | ||||||
| chr14:100110325
|
G | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0170 | 2 | HG03492.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.358+12667G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100110325 | ||||||
| chr14:100110475
|
G | A | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0052others(4): Show | 7 | HG00735.hp1 HG00741.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.358+12817G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100110475 | ||||||
| chr14:100110517
|
GC | G | 4 | a0001c0002t0001g0277a0001c0002t0001g0278a0001c0002t0001g0279others(1): Show | 4 | HG02109.hp1 HG02723.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.358+12862delC | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr14 | 100110517 | |||||
| chr14:100110658
|
T | C | 328 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(325): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.359-12881T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100110658 | ||||||
| chr14:100110841
|
G | A | 8 | a0001c0001t0001g0003a0001c0001t0001g0057a0001c0001t0001g0068others(5): Show | 9 | HG01884.hp2 HG02615.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.359-12698G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100110841 | ||||||
| chr14:100110986
|
G | C | 8 | a0001c0001t0001g0003a0001c0001t0001g0057a0001c0001t0001g0068others(5): Show | 9 | HG01884.hp2 HG02615.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.359-12553G>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100110986 | ||||||
| chr14:100111113
|
C | G | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0052others(4): Show | 7 | HG00735.hp1 HG00741.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.359-12426C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100111113 | ||||||
| chr14:100111147
|
C | CT | 3 | a0001c0001t0001g0118a0001c0001t0001g0303a0001c0001t0009g0228 | 3 | HG00609.hp1 HG00609.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.359-12392_359-1239 others(5): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100111147 | ||||||
| chr14:100111148
|
A | AT | 116 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0018others(113): Show | 119 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.359-12366dupT | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr14 | 100111148 | |||||
| chr14:100111148
|
A | ATT | 21 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0062others(18): Show | 21 | HG01099.hp2 HG01192.hp1 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.359-12367_359-1236 others(6): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr14 | 100111148 | |||||
| chr14:100111148
|
A | C | 3 | a0001c0001t0001g0118a0001c0001t0001g0303a0001c0001t0009g0228 | 3 | HG00609.hp1 HG00609.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.359-12391A>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100111148 | ||||||
| chr14:100111148
|
A | T | 24 | a0001c0001t0001g0006a0001c0001t0001g0225a0001c0001t0001g0229others(21): Show | 25 | HG00423.hp2 HG00597.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.359-12391A>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100111148 | ||||||
| chr14:100111148
|
AT | A | 16 | a0001c0001t0001g0046a0001c0001t0001g0064a0001c0001t0001g0233others(13): Show | 18 | HG00673.hp1 HG01099.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.359-12366delT | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr14 | 100111148 | |||||
| chr14:100111148
|
ATT | A | 21 | a0001c0001t0001g0013a0001c0001t0001g0057a0001c0001t0001g0068others(18): Show | 21 | HG01261.hp2 HG02055.hp1 HG02129.hp1 others(18): Show |
intron_variant | MODIFIER | c.359-12367_359-1236 others(6): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr14 | 100111148 | |||||
| chr14:100111148
|
ATTT | A | 58 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(55): Show | 61 | HG01168.hp2 HG01169.hp2 HG01192.hp2 others(58): Show |
intron_variant | MODIFIER | c.359-12368_359-1236 others(7): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr14 | 100111148 | |||||
| chr14:100111148
|
ATTTT | A | 6 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0052others(3): Show | 6 | HG00735.hp1 HG00741.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.359-12369_359-1236 others(8): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr14 | 100111148 | |||||
| chr14:100111149
|
T | A | 3 | a0001c0001t0001g0118a0001c0001t0001g0303a0001c0001t0009g0228 | 3 | HG00609.hp1 HG00609.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.359-12390T>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100111149 | ||||||
| chr14:100111149
|
T | C | 24 | a0001c0001t0001g0006a0001c0001t0001g0225a0001c0001t0001g0229others(21): Show | 25 | HG00423.hp2 HG00597.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.359-12390T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100111149 | ||||||
| chr14:100111150
|
T | A | 24 | a0001c0001t0001g0006a0001c0001t0001g0225a0001c0001t0001g0229others(21): Show | 25 | HG00423.hp2 HG00597.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.359-12389T>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100111150 | ||||||
| chr14:100111150
|
T | C | 1 | a0001c0001t0001g0316 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.359-12389T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100111150 | ||||||
| chr14:100111151
|
T | A | 1 | a0001c0001t0001g0316 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.359-12388T>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100111151 | ||||||
| chr14:100111204
|
C | T | 274 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(271): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.359-12335C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100111204 | ||||||
| chr14:100111402
|
C | T | 8 | a0001c0002t0002g0281a0001c0002t0002g0282a0001c0002t0002g0283others(5): Show | 8 | HG02257.hp2 HG02451.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.359-12137C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100111402 | ||||||
| chr14:100111478
|
G | T | 4 | a0002c0005t0002g0340a0002c0005t0002g0341a0002c0005t0002g0342others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.359-12061G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100111478 | ||||||
| chr14:100111553
|
T | C | 322 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(319): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.359-11986T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100111553 | ||||||
| chr14:100111880
|
A | G | 71 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(68): Show | 73 | HG00099.hp2 HG01167.hp2 HG01168.hp2 others(70): Show |
intron_variant | MODIFIER | c.359-11659A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100111880 | ||||||
| chr14:100112003
|
C | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0180 | 2 | HG01168.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.359-11536C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100112003 | ||||||
| chr14:100112117
|
C | G | 4 | a0001c0004t0001g0219a0001c0004t0001g0220a0001c0004t0001g0221others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.359-11422C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100112117 | ||||||
| chr14:100112131
|
C | T | 4 | a0001c0001t0001g0101a0001c0001t0001g0121a0001c0001t0003g0116others(1): Show | 4 | HG01081.hp1 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.359-11408C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100112131 | ||||||
| chr14:100112135
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.359-11404C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100112135 | ||||||
| chr14:100112387
|
C | T | 1 | a0001c0004t0001g0040 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.359-11152C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100112387 | ||||||
| chr14:100112613
|
C | G | 3 | a0001c0002t0001g0213a0001c0002t0002g0207a0001c0002t0002g0208 | 3 | HG02258.hp2 HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.359-10926C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100112613 | ||||||
| chr14:100112676
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.359-10863C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100112676 | ||||||
| chr14:100113049
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.359-10490G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100113049 | ||||||
| chr14:100113123
|
A | G | 1 | a0001c0001t0001g0274 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.359-10416A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100113123 | ||||||
| chr14:100113396
|
C | T | 7 | a0001c0001t0001g0003a0001c0001t0001g0057a0001c0001t0001g0068others(4): Show | 8 | HG01884.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.359-10143C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100113396 | ||||||
| chr14:100113559
|
G | A | 8 | a0001c0002t0002g0281a0001c0002t0002g0282a0001c0002t0002g0283others(5): Show | 8 | HG02257.hp2 HG02451.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.359-9980G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100113559 | ||||||
| chr14:100113581
|
G | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0315a0001c0001t0001g0317 | 4 | NA18946.hp2 NA18977.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.359-9958G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100113581 | ||||||
| chr14:100113785
|
A | G | 1 | a0001c0001t0001g0233 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.359-9754A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100113785 | ||||||
| chr14:100113846
|
C | T | 6 | a0002c0003t0001g0043a0002c0003t0001g0045a0002c0003t0001g0047others(3): Show | 6 | HG02572.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.359-9693C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100113846 | ||||||
| chr14:100114109
|
G | C | 1 | a0001c0001t0001g0137 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.359-9430G>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100114109 | ||||||
| chr14:100114159
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.359-9380C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100114159 | ||||||
| chr14:100114161
|
A | G | 1 | a0001c0001t0001g0016 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.359-9378A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100114161 | ||||||
| chr14:100114170
|
C | CG | 186 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(183): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.359-9362dupG | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr14 | 100114170 | |||||
| chr14:100114204
|
C | T | 1 | a0001c0001t0001g0322 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.359-9335C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100114204 | ||||||
| chr14:100114265
|
C | T | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0052others(4): Show | 7 | HG00735.hp1 HG00741.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.359-9274C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100114265 | ||||||
| chr14:100114631
|
G | A | 4 | a0002c0005t0002g0340a0002c0005t0002g0341a0002c0005t0002g0342others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.359-8908G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100114631 | ||||||
| chr14:100114731
|
A | G | 184 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(181): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.359-8808A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100114731 | ||||||
| chr14:100114800
|
G | C | 117 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0020others(114): Show | 119 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.359-8739G>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100114800 | ||||||
| chr14:100114851
|
A | G | 3 | a0001c0001t0004g0236a0001c0002t0001g0206a0001c0002t0004g0209 | 3 | HG01884.hp2 HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.359-8688A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100114851 | ||||||
| chr14:100115045
|
C | CA | 38 | a0001c0001t0001g0009a0001c0001t0001g0092a0001c0001t0001g0223others(35): Show | 39 | HG00639.hp2 HG00733.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.359-8483dupA | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr14 | 100115045 | |||||
| chr14:100115045
|
CA | C | 198 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(195): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.359-8483delA | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr14 | 100115045 | |||||
| chr14:100115180
|
CAGAA | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0057a0001c0001t0001g0068others(4): Show | 8 | HG01884.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.359-8354_359-8351d others(6): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr14 | 100115180 | |||||
| chr14:100115181
|
A | G | 7 | a0001c0001t0001g0046a0001c0002t0001g0210a0001c0002t0001g0211others(4): Show | 7 | HG01099.hp1 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.359-8358A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100115181 | ||||||
| chr14:100115263
|
CCTGGAAG others(7): Show |
C | 1 | a0001c0001t0001g0272 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.359-8271_359-8258d others(16): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr14 | 100115263 | |||||
| chr14:100115299
|
T | C | 283 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(280): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.359-8240T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100115299 | ||||||
| chr14:100115406
|
G | C | 184 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(181): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.359-8133G>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100115406 | ||||||
| chr14:100115453
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.359-8086T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100115453 | ||||||
| chr14:100115472
|
G | A | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0003g0032 | 3 | HG00735.hp1 HG00741.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.359-8067G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100115472 | ||||||
| chr14:100115990
|
G | A | 14 | a0001c0001t0001g0046a0001c0001t0001g0233a0001c0001t0001g0234others(11): Show | 16 | HG01099.hp1 HG02055.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.359-7549G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100115990 | ||||||
| chr14:100116002
|
C | T | 1 | a0001c0001t0001g0224 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.359-7537C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100116002 | ||||||
| chr14:100116003
|
G | A | 1 | a0001c0002t0001g0200 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.359-7536G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100116003 | ||||||
| chr14:100116110
|
G | A | 4 | a0002c0005t0002g0340a0002c0005t0002g0341a0002c0005t0002g0342others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.359-7429G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100116110 | ||||||
| chr14:100116404
|
G | A | 1 | a0001c0001t0001g0328 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.359-7135G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100116404 | ||||||
| chr14:100116476
|
T | A | 1 | a0001c0001t0001g0014 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.359-7063T>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100116476 | ||||||
| chr14:100116564
|
G | C | 1 | a0001c0001t0001g0179 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.359-6975G>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100116564 | ||||||
| chr14:100116587
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.359-6952G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100116587 | ||||||
| chr14:100116668
|
C | T | 1 | a0001c0001t0005g0248 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.359-6871C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100116668 | ||||||
| chr14:100116781
|
C | T | 18 | a0001c0001t0001g0003a0001c0001t0001g0057a0001c0001t0001g0068others(15): Show | 19 | HG01884.hp2 HG02055.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.359-6758C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100116781 | ||||||
| chr14:100116784
|
G | A | 2 | a0001c0001t0001g0108a0001c0001t0007g0107 | 2 | HG01123.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.359-6755G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100116784 | ||||||
| chr14:100116809
|
T | A | 1 | a0001c0001t0001g0271 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.359-6730T>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100116809 | ||||||
| chr14:100116864
|
G | T | 1 | a0001c0001t0001g0025 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.359-6675G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100116864 | ||||||
| chr14:100116993
|
G | A | 283 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(280): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.359-6546G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100116993 | ||||||
| chr14:100117012
|
A | G | 283 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(280): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.359-6527A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100117012 | ||||||
| chr14:100117154
|
G | C | 121 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0020others(118): Show | 123 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.359-6385G>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100117154 | ||||||
| chr14:100117255
|
C | G | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.359-6284C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100117255 | ||||||
| chr14:100117356
|
G | A | 1 | a0001c0002t0001g0217 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.359-6183G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100117356 | ||||||
| chr14:100117612
|
G | A | 283 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(280): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.359-5927G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100117612 | ||||||
| chr14:100117779
|
A | T | 1 | a0001c0001t0001g0014 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.359-5760A>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100117779 | ||||||
| chr14:100118085
|
C | T | 1 | a0001c0002t0001g0211 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.359-5454C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100118085 | ||||||
| chr14:100118193
|
G | A | 58 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(55): Show | 60 | HG01168.hp2 HG01169.hp2 HG01192.hp2 others(57): Show |
intron_variant | MODIFIER | c.359-5346G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100118193 | ||||||
| chr14:100118206
|
C | T | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0052others(4): Show | 7 | HG00735.hp1 HG00741.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.359-5333C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100118206 | ||||||
| chr14:100118277
|
G | A | 1 | a0001c0001t0001g0041 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.359-5262G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100118277 | ||||||
| chr14:100118439
|
T | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0057a0001c0001t0001g0068others(4): Show | 8 | HG01884.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.359-5100T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100118439 | ||||||
| chr14:100118468
|
C | A | 1 | a0001c0001t0001g0086 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.359-5071C>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100118468 | ||||||
| chr14:100118576
|
C | G | 1 | a0001c0001t0001g0014 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.359-4963C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100118576 | ||||||
| chr14:100118877
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.359-4662G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100118877 | ||||||
| chr14:100118901
|
A | T | 28 | a0001c0001t0001g0006a0001c0001t0001g0118a0001c0001t0001g0225others(25): Show | 29 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.359-4638A>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100118901 | ||||||
| chr14:100119132
|
G | T | 1 | a0001c0001t0001g0250 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.359-4407G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100119132 | ||||||
| chr14:100119243
|
T | A | 1 | a0001c0004t0001g0040 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.359-4296T>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100119243 | ||||||
| chr14:100119418
|
C | T | 37 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0030others(34): Show | 39 | HG00639.hp2 HG00733.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.359-4121C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100119418 | ||||||
| chr14:100119477
|
C | T | 57 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(54): Show | 59 | HG01168.hp2 HG01169.hp2 HG01192.hp2 others(56): Show |
intron_variant | MODIFIER | c.359-4062C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100119477 | ||||||
| chr14:100119596
|
C | T | 1 | a0001c0001t0001g0161 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.359-3943C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100119596 | ||||||
| chr14:100119747
|
C | T | 1 | a0001c0001t0001g0128 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.359-3792C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100119747 | ||||||
| chr14:100119812
|
TAGGCAGA others(4): Show |
T | 1 | a0001c0001t0001g0231 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.359-3719_359-3709d others(13): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr14 | 100119812 | |||||
| chr14:100119897
|
A | G | 1 | a0001c0001t0001g0250 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.359-3642A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100119897 | ||||||
| chr14:100120076
|
T | C | 11 | a0001c0001t0001g0223a0002c0003t0001g0028a0002c0003t0001g0029others(8): Show | 11 | HG02055.hp1 HG02486.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.359-3463T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100120076 | ||||||
| chr14:100120304
|
C | A | 1 | a0001c0001t0001g0128 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.359-3235C>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100120304 | ||||||
| chr14:100120370
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.359-3169G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100120370 | ||||||
| chr14:100120420
|
A | G | 282 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(279): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.359-3119A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100120420 | ||||||
| chr14:100120599
|
C | T | 1 | a0002c0003t0001g0047 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.359-2940C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100120599 | ||||||
| chr14:100120916
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.359-2623G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100120916 | ||||||
| chr14:100121042
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.359-2497G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100121042 | ||||||
| chr14:100121091
|
G | A | 60 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(57): Show | 63 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.359-2448G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100121091 | ||||||
| chr14:100121113
|
C | T | 11 | a0001c0001t0001g0223a0002c0003t0001g0028a0002c0003t0001g0029others(8): Show | 11 | HG02055.hp1 HG02486.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.359-2426C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100121113 | ||||||
| chr14:100121278
|
C | T | 1 | a0001c0002t0001g0200 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.359-2261C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100121278 | ||||||
| chr14:100121469
|
G | C | 1 | a0002c0003t0001g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.359-2070G>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100121469 | ||||||
| chr14:100121476
|
C | A | 57 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(54): Show | 59 | HG01168.hp2 HG01169.hp2 HG01192.hp2 others(56): Show |
intron_variant | MODIFIER | c.359-2063C>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100121476 | ||||||
| chr14:100121486
|
G | C | 4 | a0001c0004t0001g0219a0001c0004t0001g0220a0001c0004t0001g0221others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.359-2053G>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100121486 | ||||||
| chr14:100121524
|
G | A | 12 | a0001c0001t0001g0046a0001c0001t0001g0233a0001c0001t0001g0234others(9): Show | 14 | HG01099.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.359-2015G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100121524 | ||||||
| chr14:100121602
|
G | A | 29 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0057others(26): Show | 31 | HG00639.hp2 HG00733.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.359-1937G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100121602 | ||||||
| chr14:100121692
|
C | T | 4 | a0001c0004t0001g0219a0001c0004t0001g0220a0001c0004t0001g0221others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.359-1847C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100121692 | ||||||
| chr14:100121738
|
C | G | 1 | a0001c0001t0001g0118 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.359-1801C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100121738 | ||||||
| chr14:100121881
|
C | G | 1 | a0001c0001t0001g0152 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.359-1658C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100121881 | ||||||
| chr14:100121942
|
T | C | 246 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.359-1597T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100121942 | ||||||
| chr14:100122086
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.359-1453C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100122086 | ||||||
| chr14:100122148
|
G | A | 29 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0057others(26): Show | 31 | HG00639.hp2 HG00733.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.359-1391G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100122148 | ||||||
| chr14:100122164
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.359-1375A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100122164 | ||||||
| chr14:100122341
|
C | T | 4 | a0002c0005t0002g0340a0002c0005t0002g0341a0002c0005t0002g0342others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.359-1198C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100122341 | ||||||
| chr14:100122488
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.359-1051G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100122488 | ||||||
| chr14:100122722
|
G | C | 1 | a0001c0001t0001g0321 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.359-817G>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100122722 | ||||||
| chr14:100122889
|
G | T | 1 | a0001c0001t0001g0078 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.359-650G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100122889 | ||||||
| chr14:100122903
|
G | T | 1 | a0001c0001t0001g0082 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.359-636G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100122903 | ||||||
| chr14:100122959
|
C | T | 1 | a0001c0001t0001g0275 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.359-580C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100122959 | ||||||
| chr14:100123159
|
T | A | 5 | a0001c0002t0002g0281a0001c0002t0002g0333a0001c0002t0002g0334others(2): Show | 5 | HG02257.hp2 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.359-380T>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100123159 | ||||||
| chr14:100123228
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.359-311C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100123228 | ||||||
| chr14:100123233
|
C | T | 3 | a0002c0005t0002g0340a0002c0005t0002g0341a0002c0005t0002g0342 | 3 | HG02895.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.359-306C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 3/13 | chr14 | 100123233 | ||||||
| chr14:100123782
|
G | A | 1 | a0001c0001t0001g0042 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.422+180G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | chr14 | 100123782 | ||||||
| chr14:100123937
|
A | T | 1 | a0001c0001t0001g0085 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.422+335A>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | chr14 | 100123937 | ||||||
| chr14:100124001
|
A | G | 1 | a0001c0002t0001g0034 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.422+399A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | chr14 | 100124001 | ||||||
| chr14:100124108
|
C | T | 5 | a0001c0001t0001g0250a0001c0002t0001g0201a0001c0006t0001g0202others(2): Show | 5 | HG02809.hp2 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.422+506C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | chr14 | 100124108 | ||||||
| chr14:100124459
|
C | G | 1 | a0001c0001t0001g0223 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.422+857C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | chr14 | 100124459 | ||||||
| chr14:100124537
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.422+935C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | chr14 | 100124537 | ||||||
| chr14:100124575
|
G | T | 14 | a0001c0004t0001g0219a0001c0004t0001g0220a0001c0004t0001g0221others(11): Show | 14 | HG02055.hp1 HG02486.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.422+973G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | chr14 | 100124575 | ||||||
| chr14:100124780
|
C | T | 1 | a0001c0002t0001g0213 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.422+1178C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | chr14 | 100124780 | ||||||
| chr14:100124959
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.422+1357C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | chr14 | 100124959 | ||||||
| chr14:100124987
|
C | T | 2 | a0001c0002t0002g0207a0001c0002t0002g0208 | 2 | HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.422+1385C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | chr14 | 100124987 | ||||||
| chr14:100124995
|
C | T | 27 | a0001c0001t0001g0006a0001c0001t0001g0118a0001c0001t0001g0229others(24): Show | 28 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.422+1393C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | chr14 | 100124995 | ||||||
| chr14:100125004
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.422+1402G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | chr14 | 100125004 | ||||||
| chr14:100125047
|
GAC | G | 92 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(89): Show | 97 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.422+1460_422+1461d others(4): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 100125047 | |||||
| chr14:100125117
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.422+1515C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | chr14 | 100125117 | ||||||
| chr14:100125122
|
C | CCA | 116 | a0001c0001t0001g0007a0001c0001t0001g0019a0001c0001t0001g0020others(113): Show | 117 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.422+1548_422+1549d others(4): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 100125122 | |||||
| chr14:100125122
|
C | CCACA | 117 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0010others(114): Show | 122 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.422+1546_422+1549d others(6): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 100125122 | |||||
| chr14:100125122
|
C | CCACACA | 27 | a0001c0001t0001g0006a0001c0001t0001g0064a0001c0001t0001g0078others(24): Show | 28 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.422+1544_422+1549d others(8): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 100125122 | |||||
| chr14:100125122
|
C | CCACACAC others(5): Show |
1 | a0001c0002t0001g0213 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.422+1538_422+1549d others(14): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 100125122 | |||||
| chr14:100125122
|
CCA | C | 10 | a0001c0001t0001g0046a0001c0001t0004g0236a0001c0002t0001g0206others(7): Show | 10 | HG01099.hp1 HG01884.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.422+1548_422+1549d others(4): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 100125122 | |||||
| chr14:100125122
|
CCACA | C | 8 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(5): Show | 8 | HG02055.hp1 HG02486.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.422+1546_422+1549d others(6): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 100125122 | |||||
| chr14:100125122
|
CCACACA | C | 9 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0003g0032others(6): Show | 9 | HG00735.hp1 HG00741.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.422+1544_422+1549d others(8): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 100125122 | |||||
| chr14:100125122
|
CCACACAC others(3): Show |
C | 1 | a0001c0001t0001g0256 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.422+1540_422+1549d others(12): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 100125122 | |||||
| chr14:100125150
|
A | ACACACAC others(7): Show |
1 | a0001c0001t0001g0332 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.422+1549_422+1550i others(16): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 100125150 | |||||
| chr14:100125150
|
A | ACACACAC others(5): Show |
10 | a0001c0001t0001g0009a0001c0001t0001g0275a0001c0001t0001g0325others(7): Show | 11 | HG00639.hp2 HG01109.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.422+1549_422+1550i others(14): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 100125150 | |||||
| chr14:100125150
|
A | ACACACAC others(3): Show |
12 | a0001c0001t0001g0057a0001c0001t0001g0068a0001c0001t0001g0263others(9): Show | 12 | HG00733.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.422+1549_422+1550i others(12): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 100125150 | |||||
| chr14:100125150
|
A | ACACACC | 2 | a0001c0001t0001g0003a0001c0001t0001g0076 | 3 | HG02615.hp2 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.422+1549_422+1550i others(8): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 100125150 | |||||
| chr14:100125150
|
A | C | 3 | a0001c0001t0004g0236a0001c0002t0001g0206a0001c0002t0004g0209 | 3 | HG01884.hp2 HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.422+1548A>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | chr14 | 100125150 | ||||||
| chr14:100125169
|
T | TAC | 16 | a0001c0001t0001g0046a0001c0001t0001g0234a0001c0001t0001g0237others(13): Show | 16 | HG01099.hp1 HG01192.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.423-1513_423-1512d others(4): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 100125169 | |||||
| chr14:100125169
|
T | TACAC | 31 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0057others(28): Show | 35 | HG00639.hp2 HG01109.hp2 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.423-1515_423-1512d others(6): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 100125169 | |||||
| chr14:100125169
|
T | TACACAC | 3 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0271 | 3 | HG00733.hp2 HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.423-1517_423-1512d others(8): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 100125169 | |||||
| chr14:100125169
|
T | TACACACA others(1): Show |
5 | a0002c0003t0001g0045a0002c0003t0001g0047a0002c0003t0001g0048others(2): Show | 5 | HG03130.hp2 HG03139.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.423-1519_423-1512d others(10): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 100125169 | |||||
| chr14:100125169
|
T | TACACACA others(3): Show |
3 | a0002c0003t0001g0028a0002c0003t0001g0029a0002c0003t0001g0043 | 3 | HG02055.hp1 HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.423-1521_423-1512d others(12): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 100125169 | |||||
| chr14:100125169
|
T | TACACACA others(5): Show |
2 | a0002c0003t0001g0044a0002c0003t0001g0051 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.423-1523_423-1512d others(14): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 100125169 | |||||
| chr14:100125169
|
TAC | T | 172 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(169): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.423-1513_423-1512d others(4): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 100125169 | |||||
| chr14:100125169
|
TACAC | T | 31 | a0001c0001t0001g0006a0001c0001t0001g0026a0001c0001t0001g0064others(28): Show | 32 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.423-1515_423-1512d others(6): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 100125169 | |||||
| chr14:100125221
|
C | A | 282 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(279): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.423-1486C>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | chr14 | 100125221 | ||||||
| chr14:100125223
|
G | T | 2 | a0001c0001t0001g0111a0001c0001t0001g0113 | 2 | HG01256.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.423-1484G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | chr14 | 100125223 | ||||||
| chr14:100125223
|
GACAC | G | 14 | a0001c0001t0001g0009a0001c0001t0001g0262a0001c0001t0001g0272others(11): Show | 15 | HG00639.hp2 HG01109.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.423-1475_423-1472d others(6): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 100125223 | |||||
| chr14:100125253
|
T | TAC | 23 | a0001c0001t0001g0092a0001c0001t0001g0098a0001c0001t0001g0148others(20): Show | 23 | HG01123.hp1 HG01261.hp2 HG02056.hp1 others(20): Show |
intron_variant | MODIFIER | c.423-1415_423-1414d others(4): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 100125253 | |||||
| chr14:100125253
|
T | TACAC | 5 | a0001c0001t0001g0057a0001c0001t0001g0068a0002c0003t0001g0043others(2): Show | 5 | HG02572.hp2 HG02895.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.423-1417_423-1414d others(6): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 100125253 | |||||
| chr14:100125253
|
T | TACACAC | 3 | a0001c0001t0001g0076a0001c0001t0004g0236a0001c0002t0004g0209 | 3 | HG01884.hp2 HG06807.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.423-1419_423-1414d others(8): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 100125253 | |||||
| chr14:100125253
|
TAC | T | 101 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(98): Show | 103 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.423-1415_423-1414d others(4): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 100125253 | |||||
| chr14:100125253
|
TACAC | T | 46 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(43): Show | 47 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.423-1417_423-1414d others(6): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 100125253 | |||||
| chr14:100125253
|
TACACAC | T | 41 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0091others(38): Show | 44 | HG00639.hp2 HG01109.hp2 HG02027.hp2 others(41): Show |
intron_variant | MODIFIER | c.423-1419_423-1414d others(8): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 100125253 | |||||
| chr14:100125253
|
TACACACA others(1): Show |
T | 8 | a0001c0001t0001g0046a0001c0001t0001g0052a0001c0001t0001g0053others(5): Show | 8 | HG01099.hp1 HG02630.hp2 HG04204.hp2 others(5): Show |
intron_variant | MODIFIER | c.423-1421_423-1414d others(10): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 100125253 | |||||
| chr14:100125253
|
TACACACA others(3): Show |
T | 3 | a0001c0002t0001g0210a0001c0002t0001g0212a0001c0002t0001g0216 | 3 | HG02572.hp1 HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.423-1423_423-1414d others(12): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 100125253 | |||||
| chr14:100125253
|
TACACACA others(5): Show |
T | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0003g0032 | 3 | HG00735.hp1 HG00741.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.423-1425_423-1414d others(14): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 100125253 | |||||
| chr14:100125297
|
A | G | 282 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(279): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.423-1410A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | chr14 | 100125297 | ||||||
| chr14:100125363
|
C | T | 2 | a0001c0001t0001g0293a0001c0001t0001g0308 | 2 | HG01192.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.423-1344C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | chr14 | 100125363 | ||||||
| chr14:100125397
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.423-1310G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | chr14 | 100125397 | ||||||
| chr14:100125558
|
A | AT | 28 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0118others(25): Show | 29 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.423-1134dupT | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 100125558 | |||||
| chr14:100125599
|
G | A | 27 | a0001c0001t0001g0006a0001c0001t0001g0118a0001c0001t0001g0229others(24): Show | 28 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.423-1108G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | chr14 | 100125599 | ||||||
| chr14:100125718
|
G | C | 3 | a0001c0002t0001g0213a0001c0002t0002g0207a0001c0002t0002g0208 | 3 | HG02258.hp2 HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.423-989G>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | chr14 | 100125718 | ||||||
| chr14:100125801
|
G | A | 12 | a0001c0001t0001g0046a0001c0001t0001g0233a0001c0001t0001g0234others(9): Show | 14 | HG01099.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.423-906G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | chr14 | 100125801 | ||||||
| chr14:100125845
|
C | T | 179 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(176): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.423-862C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | chr14 | 100125845 | ||||||
| chr14:100126014
|
G | A | 4 | a0001c0001t0001g0280a0001c0001t0001g0322a0001c0002t0001g0033others(1): Show | 4 | HG00099.hp2 HG01361.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.423-693G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | chr14 | 100126014 | ||||||
| chr14:100126063
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.423-644C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | chr14 | 100126063 | ||||||
| chr14:100126067
|
C | G | 1 | a0001c0001t0001g0249 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.423-640C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | chr14 | 100126067 | ||||||
| chr14:100126182
|
C | T | 2 | a0001c0002t0002g0207a0001c0002t0002g0208 | 2 | HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.423-525C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | chr14 | 100126182 | ||||||
| chr14:100126240
|
G | A | 1 | a0001c0002t0001g0213 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.423-467G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | chr14 | 100126240 | ||||||
| chr14:100126622
|
G | A | 112 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0020others(109): Show | 114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.423-85G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | chr14 | 100126622 | ||||||
| chr14:100126666
|
G | C | 2 | a0001c0001t0001g0152a0001c0001t0001g0169 | 2 | HG00438.hp2 HG00597.hp1 |
intron_variant | MODIFIER | c.423-41G>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | chr14 | 100126666 | ||||||
| chr14:100126694
|
G | C | 1 | a0001c0001t0001g0250 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.423-13G>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 4/13 | chr14 | 100126694 | ||||||
| chr14:100126876
|
A | G | 27 | a0001c0001t0001g0006a0001c0001t0001g0118a0001c0001t0001g0229others(24): Show | 28 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.487+105A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 5/13 | chr14 | 100126876 | ||||||
| chr14:100126965
|
C | T | 4 | a0002c0003t0001g0028a0002c0003t0001g0029a0002c0003t0001g0044others(1): Show | 4 | HG02055.hp1 HG02486.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.487+194C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 5/13 | chr14 | 100126965 | ||||||
| chr14:100127098
|
G | A | 1 | a0001c0001t0001g0302 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.487+327G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 5/13 | chr14 | 100127098 | ||||||
| chr14:100127175
|
C | A | 1 | a0001c0001t0001g0136 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.487+404C>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 5/13 | chr14 | 100127175 | ||||||
| chr14:100127246
|
T | G | 9 | a0001c0001t0001g0006a0001c0001t0001g0239a0001c0001t0001g0240others(6): Show | 10 | NA18747.hp1 NA18949.hp2 NA18951.hp1 others(7): Show |
intron_variant | MODIFIER | c.487+475T>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 5/13 | chr14 | 100127246 | ||||||
| chr14:100127510
|
C | T | 1 | a0001c0001t0001g0078 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.487+739C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 5/13 | chr14 | 100127510 | ||||||
| chr14:100127720
|
C | T | 10 | a0002c0003t0001g0028a0002c0003t0001g0029a0002c0003t0001g0043others(7): Show | 10 | HG02055.hp1 HG02486.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.488-799C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 5/13 | chr14 | 100127720 | ||||||
| chr14:100127865
|
G | A | 36 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0030others(33): Show | 38 | HG00639.hp2 HG00733.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.488-654G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 5/13 | chr14 | 100127865 | ||||||
| chr14:100127991
|
G | A | 1 | a0001c0001t0001g0271 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.488-528G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 5/13 | chr14 | 100127991 | ||||||
| chr14:100128028
|
C | T | 4 | a0001c0001t0001g0280a0001c0001t0001g0322a0001c0002t0001g0033others(1): Show | 4 | HG00099.hp2 HG01361.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.488-491C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 5/13 | chr14 | 100128028 | ||||||
| chr14:100128037
|
G | A | 57 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0030others(54): Show | 59 | HG00639.hp2 HG00733.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.488-482G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 5/13 | chr14 | 100128037 | ||||||
| chr14:100128307
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.488-212G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 5/13 | chr14 | 100128307 | ||||||
| chr14:100128340
|
G | T | 1 | a0001c0001t0001g0020 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.488-179G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 5/13 | chr14 | 100128340 | ||||||
| chr14:100128361
|
C | T | 29 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0057others(26): Show | 31 | HG00639.hp2 HG00733.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.488-158C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 5/13 | chr14 | 100128361 | ||||||
| chr14:100128364
|
G | A | 3 | a0001c0001t0001g0031a0001c0001t0001g0172a0001c0001t0001g0173 | 3 | HG00735.hp1 HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.488-155G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 5/13 | chr14 | 100128364 | ||||||
| chr14:100128402
|
C | G | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0052others(4): Show | 7 | HG00735.hp1 HG00741.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.488-117C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 5/13 | chr14 | 100128402 | ||||||
| chr14:100128493
|
G | C | 4 | a0001c0004t0001g0219a0001c0004t0001g0220a0001c0004t0001g0221others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.488-26G>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 5/13 | chr14 | 100128493 | ||||||
| chr14:100128784
|
G | A | 1 | a0001c0001t0002g0290 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.717+36G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 6/13 | chr14 | 100128784 | ||||||
| chr14:100128941
|
T | A | 282 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(279): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.717+193T>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 6/13 | chr14 | 100128941 | ||||||
| chr14:100129014
|
C | T | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0052others(4): Show | 7 | HG00735.hp1 HG00741.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.717+266C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 6/13 | chr14 | 100129014 | ||||||
| chr14:100129184
|
A | G | 219 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(216): Show | 226 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.718-379A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 6/13 | chr14 | 100129184 | ||||||
| chr14:100129316
|
C | G | 29 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0057others(26): Show | 31 | HG00639.hp2 HG00733.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.718-247C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 6/13 | chr14 | 100129316 | ||||||
| chr14:100129335
|
G | C | 29 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0057others(26): Show | 31 | HG00639.hp2 HG00733.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.718-228G>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 6/13 | chr14 | 100129335 | ||||||
| chr14:100129346
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.718-217G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 6/13 | chr14 | 100129346 | ||||||
| chr14:100129543
|
G | A | 28 | a0001c0001t0001g0006a0001c0001t0001g0118a0001c0001t0001g0229others(25): Show | 29 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.718-20G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 6/13 | chr14 | 100129543 | ||||||
| chr14:100129726
|
A | G | 28 | a0001c0001t0001g0006a0001c0001t0001g0118a0001c0001t0001g0229others(25): Show | 29 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.839+42A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 7/13 | chr14 | 100129726 | ||||||
| chr14:100129737
|
C | T | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0052others(4): Show | 7 | HG00735.hp1 HG00741.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.839+53C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 7/13 | chr14 | 100129737 | ||||||
| chr14:100129905
|
G | A | 1 | a0001c0002t0001g0213 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.839+221G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 7/13 | chr14 | 100129905 | ||||||
| chr14:100129906
|
C | G | 1 | a0001c0001t0001g0232 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.839+222C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 7/13 | chr14 | 100129906 | ||||||
| chr14:100129984
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.839+300A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 7/13 | chr14 | 100129984 | ||||||
| chr14:100130025
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.839+341G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 7/13 | chr14 | 100130025 | ||||||
| chr14:100130088
|
G | C | 4 | a0001c0004t0001g0219a0001c0004t0001g0220a0001c0004t0001g0221others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.839+404G>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 7/13 | chr14 | 100130088 | ||||||
| chr14:100130217
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.839+533G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 7/13 | chr14 | 100130217 | ||||||
| chr14:100130245
|
C | A | 4 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0127others(1): Show | 4 | HG00733.hp1 HG01952.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.839+561C>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 7/13 | chr14 | 100130245 | ||||||
| chr14:100130307
|
C | T | 2 | a0001c0006t0001g0203a0001c0006t0001g0204 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.839+623C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 7/13 | chr14 | 100130307 | ||||||
| chr14:100130308
|
G | A | 1 | a0001c0001t0001g0197 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.839+624G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 7/13 | chr14 | 100130308 | ||||||
| chr14:100130495
|
G | C | 4 | a0002c0005t0002g0340a0002c0005t0002g0341a0002c0005t0002g0342others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.839+811G>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 7/13 | chr14 | 100130495 | ||||||
| chr14:100130518
|
A | G | 13 | a0001c0001t0001g0046a0001c0001t0001g0233a0001c0001t0001g0234others(10): Show | 15 | HG01099.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.839+834A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 7/13 | chr14 | 100130518 | ||||||
| chr14:100130652
|
T | C | 1 | a0001c0001t0001g0031 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.839+968T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 7/13 | chr14 | 100130652 | ||||||
| chr14:100130661
|
T | C | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0052others(4): Show | 7 | HG00735.hp1 HG00741.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.839+977T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 7/13 | chr14 | 100130661 | ||||||
| chr14:100130747
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.839+1063C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 7/13 | chr14 | 100130747 | ||||||
| chr14:100130787
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.839+1103G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 7/13 | chr14 | 100130787 | ||||||
| chr14:100130861
|
C | T | 29 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0057others(26): Show | 31 | HG00639.hp2 HG00733.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.839+1177C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 7/13 | chr14 | 100130861 | ||||||
| chr14:100130896
|
T | G | 4 | a0001c0001t0001g0280a0001c0001t0001g0322a0001c0002t0001g0033others(1): Show | 4 | HG00099.hp2 HG01361.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.839+1212T>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 7/13 | chr14 | 100130896 | ||||||
| chr14:100131077
|
A | G | 1 | a0001c0001t0001g0010 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.839+1393A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 7/13 | chr14 | 100131077 | ||||||
| chr14:100131132
|
G | A | 2 | a0001c0001t0001g0235a0001c0001t0001g0276 | 2 | HG02647.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.839+1448G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 7/13 | chr14 | 100131132 | ||||||
| chr14:100131333
|
C | A | 1 | a0001c0004t0001g0040 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.840-1386C>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 7/13 | chr14 | 100131333 | ||||||
| chr14:100131341
|
G | A | 83 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(80): Show | 88 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.840-1378G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 7/13 | chr14 | 100131341 | ||||||
| chr14:100131474
|
G | A | 29 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0057others(26): Show | 31 | HG00639.hp2 HG00733.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.840-1245G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 7/13 | chr14 | 100131474 | ||||||
| chr14:100131764
|
A | T | 1 | a0001c0001t0001g0237 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.840-955A>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 7/13 | chr14 | 100131764 | ||||||
| chr14:100131971
|
C | T | 4 | a0001c0004t0001g0219a0001c0004t0001g0220a0001c0004t0001g0221others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.840-748C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 7/13 | chr14 | 100131971 | ||||||
| chr14:100132080
|
G | A | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0052others(4): Show | 7 | HG00735.hp1 HG00741.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.840-639G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 7/13 | chr14 | 100132080 | ||||||
| chr14:100132226
|
C | T | 6 | a0001c0001t0001g0297a0001c0001t0001g0300a0001c0001t0001g0309others(3): Show | 6 | HG02056.hp1 HG02071.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.840-493C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 7/13 | chr14 | 100132226 | ||||||
| chr14:100132248
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.840-471G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 7/13 | chr14 | 100132248 | ||||||
| chr14:100132354
|
A | G | 281 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(278): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.840-365A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 7/13 | chr14 | 100132354 | ||||||
| chr14:100132403
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.840-316C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 7/13 | chr14 | 100132403 | ||||||
| chr14:100132410
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.840-309G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 7/13 | chr14 | 100132410 | ||||||
| chr14:100132580
|
C | T | 4 | a0001c0001t0001g0235a0001c0001t0001g0276a0001c0001t0001g0291others(1): Show | 4 | HG02647.hp1 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.840-139C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 7/13 | chr14 | 100132580 | ||||||
| chr14:100132713
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG02886.hp2 | splice_region_variant&intron_variant | LOW | c.840-6G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 7/13 | chr14 | 100132713 | ||||||
| chr14:100132827
|
G | A | 156 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(153): Show | 160 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.900+48G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 8/13 | chr14 | 100132827 | ||||||
| chr14:100132857
|
C | G | 4 | a0002c0003t0001g0028a0002c0003t0001g0029a0002c0003t0001g0044others(1): Show | 4 | HG02055.hp1 HG02486.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.900+78C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 8/13 | chr14 | 100132857 | ||||||
| chr14:100132875
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.900+96C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 8/13 | chr14 | 100132875 | ||||||
| chr14:100132995
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.900+216C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 8/13 | chr14 | 100132995 | ||||||
| chr14:100133005
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.900+226C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 8/13 | chr14 | 100133005 | ||||||
| chr14:100133100
|
G | T | 282 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(279): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.900+321G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 8/13 | chr14 | 100133100 | ||||||
| chr14:100133182
|
T | C | 121 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0020others(118): Show | 123 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.900+403T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 8/13 | chr14 | 100133182 | ||||||
| chr14:100133202
|
C | A | 1 | a0001c0001t0001g0010 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.900+423C>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 8/13 | chr14 | 100133202 | ||||||
| chr14:100133703
|
C | T | 5 | a0001c0002t0002g0281a0001c0002t0002g0333a0001c0002t0002g0334others(2): Show | 5 | HG02257.hp2 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.900+924C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 8/13 | chr14 | 100133703 | ||||||
| chr14:100133823
|
G | GCTACT | 59 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(56): Show | 61 | HG00438.hp1 HG01167.hp2 HG01168.hp2 others(58): Show |
intron_variant | MODIFIER | c.900+1046_900+1050d others(7): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr14 | 100133823 | |||||
| chr14:100133880
|
T | G | 1 | a0001c0001t0001g0322 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.900+1101T>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 8/13 | chr14 | 100133880 | ||||||
| chr14:100133949
|
AAAC | A | 14 | a0001c0004t0001g0219a0001c0004t0001g0220a0001c0004t0001g0221others(11): Show | 14 | HG02055.hp1 HG02486.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.900+1182_900+1184d others(5): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr14 | 100133949 | |||||
| chr14:100133981
|
C | T | 1 | a0001c0001t0001g0310 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.900+1202C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 8/13 | chr14 | 100133981 | ||||||
| chr14:100134020
|
C | G | 59 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(56): Show | 61 | HG00438.hp1 HG01167.hp2 HG01168.hp2 others(58): Show |
intron_variant | MODIFIER | c.900+1241C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 8/13 | chr14 | 100134020 | ||||||
| chr14:100134042
|
C | T | 4 | a0001c0001t0001g0235a0001c0001t0001g0276a0001c0001t0001g0291others(1): Show | 4 | HG02647.hp1 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.900+1263C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 8/13 | chr14 | 100134042 | ||||||
| chr14:100134059
|
C | T | 1 | a0001c0001t0003g0032 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.900+1280C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 8/13 | chr14 | 100134059 | ||||||
| chr14:100134219
|
A | T | 1 | a0001c0001t0001g0229 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.900+1440A>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 8/13 | chr14 | 100134219 | ||||||
| chr14:100134319
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.900+1540C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 8/13 | chr14 | 100134319 | ||||||
| chr14:100134465
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.901-1440C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 8/13 | chr14 | 100134465 | ||||||
| chr14:100134466
|
A | G | 218 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(215): Show | 225 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.901-1439A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 8/13 | chr14 | 100134466 | ||||||
| chr14:100134917
|
C | G | 5 | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0001g0093others(2): Show | 5 | NA18944.hp1 NA18949.hp1 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.901-988C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 8/13 | chr14 | 100134917 | ||||||
| chr14:100135031
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.901-874G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 8/13 | chr14 | 100135031 | ||||||
| chr14:100135040
|
G | A | 1 | a0001c0002t0004g0209 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.901-865G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 8/13 | chr14 | 100135040 | ||||||
| chr14:100135057
|
G | A | 1 | a0001c0004t0001g0040 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.901-848G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 8/13 | chr14 | 100135057 | ||||||
| chr14:100135097
|
TGAG | T | 4 | a0001c0001t0001g0235a0001c0001t0001g0276a0001c0001t0001g0291others(1): Show | 4 | HG02647.hp1 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.901-803_901-801del others(3): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr14 | 100135097 | |||||
| chr14:100135107
|
T | G | 59 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(56): Show | 61 | HG00438.hp1 HG01167.hp2 HG01168.hp2 others(58): Show |
intron_variant | MODIFIER | c.901-798T>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 8/13 | chr14 | 100135107 | ||||||
| chr14:100135155
|
C | T | 1 | a0001c0001t0001g0280 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.901-750C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 8/13 | chr14 | 100135155 | ||||||
| chr14:100135218
|
G | A | 4 | a0001c0001t0001g0235a0001c0001t0001g0276a0001c0001t0001g0291others(1): Show | 4 | HG02647.hp1 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.901-687G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 8/13 | chr14 | 100135218 | ||||||
| chr14:100135285
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.901-620C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 8/13 | chr14 | 100135285 | ||||||
| chr14:100135478
|
C | T | 2 | a0001c0001t0005g0248a0001c0001t0005g0258 | 2 | HG02071.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.901-427C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 8/13 | chr14 | 100135478 | ||||||
| chr14:100135801
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.901-104C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 8/13 | chr14 | 100135801 | ||||||
| chr14:100135806
|
G | A | 7 | a0001c0001t0001g0046a0001c0002t0001g0210a0001c0002t0001g0211others(4): Show | 7 | HG01099.hp1 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.901-99G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 8/13 | chr14 | 100135806 | ||||||
| chr14:100135807
|
G | A | 7 | a0001c0001t0001g0046a0001c0002t0001g0210a0001c0002t0001g0211others(4): Show | 7 | HG01099.hp1 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.901-98G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 8/13 | chr14 | 100135807 | ||||||
| chr14:100136000
|
G | C | 1 | a0001c0001t0001g0137 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.964+32G>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 9/13 | chr14 | 100136000 | ||||||
| chr14:100136100
|
C | G | 1 | a0001c0001t0001g0302 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.964+132C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 9/13 | chr14 | 100136100 | ||||||
| chr14:100136107
|
T | C | 7 | a0001c0001t0001g0046a0001c0002t0001g0210a0001c0002t0001g0211others(4): Show | 7 | HG01099.hp1 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.964+139T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 9/13 | chr14 | 100136107 | ||||||
| chr14:100136113
|
TCCCCCAG others(6): Show |
T | 117 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0020others(114): Show | 119 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.964+150_964+162del others(13): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 100136113 | |||||
| chr14:100136114
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.964+146C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 9/13 | chr14 | 100136114 | ||||||
| chr14:100136119
|
A | C | 1 | a0001c0001t0001g0057 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.964+151A>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 9/13 | chr14 | 100136119 | ||||||
| chr14:100136374
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.964+406G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 9/13 | chr14 | 100136374 | ||||||
| chr14:100136462
|
A | G | 5 | a0001c0001t0001g0250a0001c0002t0001g0201a0001c0006t0001g0202others(2): Show | 5 | HG02809.hp2 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.964+494A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 9/13 | chr14 | 100136462 | ||||||
| chr14:100136469
|
G | A | 4 | a0002c0003t0001g0028a0002c0003t0001g0029a0002c0003t0001g0044others(1): Show | 4 | HG02055.hp1 HG02486.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+501G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 9/13 | chr14 | 100136469 | ||||||
| chr14:100136495
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.964+527C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 9/13 | chr14 | 100136495 | ||||||
| chr14:100136586
|
C | T | 4 | a0001c0001t0001g0235a0001c0001t0001g0276a0001c0001t0001g0291others(1): Show | 4 | HG02647.hp1 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+618C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 9/13 | chr14 | 100136586 | ||||||
| chr14:100136587
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.964+619G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 9/13 | chr14 | 100136587 | ||||||
| chr14:100136650
|
G | A | 7 | a0001c0001t0001g0046a0001c0002t0001g0210a0001c0002t0001g0211others(4): Show | 7 | HG01099.hp1 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.964+682G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 9/13 | chr14 | 100136650 | ||||||
| chr14:100136682
|
C | T | 3 | a0001c0001t0001g0121a0001c0001t0003g0116a0001c0001t0003g0131 | 3 | HG01081.hp1 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.964+714C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 9/13 | chr14 | 100136682 | ||||||
| chr14:100136854
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.965-724A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 9/13 | chr14 | 100136854 | ||||||
| chr14:100136879
|
T | G | 4 | a0001c0001t0001g0280a0001c0001t0001g0322a0001c0002t0001g0033others(1): Show | 4 | HG00099.hp2 HG01361.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-699T>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 9/13 | chr14 | 100136879 | ||||||
| chr14:100137007
|
G | A | 4 | a0002c0005t0002g0340a0002c0005t0002g0341a0002c0005t0002g0342others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-571G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 9/13 | chr14 | 100137007 | ||||||
| chr14:100137019
|
C | G | 29 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0057others(26): Show | 31 | HG00639.hp2 HG00733.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.965-559C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 9/13 | chr14 | 100137019 | ||||||
| chr14:100137021
|
AC | A | 281 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(278): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.965-552delC | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 100137021 | |||||
| chr14:100137037
|
G | T | 1 | a0001c0001t0001g0120 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.965-541G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 9/13 | chr14 | 100137037 | ||||||
| chr14:100137062
|
C | A | 281 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(278): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.965-516C>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 9/13 | chr14 | 100137062 | ||||||
| chr14:100137181
|
C | A | 4 | a0001c0004t0001g0219a0001c0004t0001g0220a0001c0004t0001g0221others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-397C>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 9/13 | chr14 | 100137181 | ||||||
| chr14:100137215
|
C | T | 12 | a0001c0001t0001g0046a0001c0001t0001g0233a0001c0001t0001g0234others(9): Show | 14 | HG01099.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.965-363C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 9/13 | chr14 | 100137215 | ||||||
| chr14:100137398
|
A | T | 58 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0031others(55): Show | 61 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.965-180A>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 9/13 | chr14 | 100137398 | ||||||
| chr14:100137425
|
C | G | 1 | a0001c0001t0001g0275 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.965-153C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 9/13 | chr14 | 100137425 | ||||||
| chr14:100137664
|
C | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0244 | 3 | NA18957.hp1 NA18962.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1031+20C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 10/13 | chr14 | 100137664 | ||||||
| chr14:100137997
|
A | G | 46 | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0001g0041others(43): Show | 46 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.1094+195A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | chr14 | 100137997 | ||||||
| chr14:100138022
|
G | T | 1 | a0001c0001t0005g0258 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1094+220G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | chr14 | 100138022 | ||||||
| chr14:100138044
|
AG | A | 112 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(109): Show | 114 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.1094+250delG | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 100138044 | |||||
| chr14:100138051
|
G | T | 1 | a0001c0001t0001g0301 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1094+249G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | chr14 | 100138051 | ||||||
| chr14:100138065
|
C | G | 4 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(1): Show | 4 | NA18959.hp2 NA18982.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1094+263C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | chr14 | 100138065 | ||||||
| chr14:100138238
|
A | G | 1 | a0001c0001t0001g0041 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1094+436A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | chr14 | 100138238 | ||||||
| chr14:100138307
|
C | T | 6 | a0001c0001t0001g0095a0001c0001t0001g0180a0001c0004t0001g0219others(3): Show | 6 | HG01168.hp1 HG01978.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1094+505C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | chr14 | 100138307 | ||||||
| chr14:100138319
|
A | G | 5 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(2): Show | 5 | HG02080.hp2 HG02132.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.1094+517A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | chr14 | 100138319 | ||||||
| chr14:100138373
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1094+571A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | chr14 | 100138373 | ||||||
| chr14:100138485
|
C | T | 99 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(96): Show | 101 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(98): Show |
intron_variant | MODIFIER | c.1094+683C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | chr14 | 100138485 | ||||||
| chr14:100138530
|
C | G | 3 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055 | 3 | NA18982.hp1 NA18993.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1094+728C>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | chr14 | 100138530 | ||||||
| chr14:100138639
|
G | A | 46 | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0001g0041others(43): Show | 46 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.1094+837G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | chr14 | 100138639 | ||||||
| chr14:100139006
|
T | C | 1 | a0001c0004t0001g0040 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1094+1204T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | chr14 | 100139006 | ||||||
| chr14:100139047
|
C | T | 1 | a0001c0004t0001g0219 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1094+1245C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | chr14 | 100139047 | ||||||
| chr14:100139128
|
C | T | 53 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(50): Show | 55 | HG01168.hp2 HG01169.hp2 HG01192.hp2 others(52): Show |
intron_variant | MODIFIER | c.1094+1326C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | chr14 | 100139128 | ||||||
| chr14:100139193
|
T | A | 1 | a0001c0001t0001g0118 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1094+1391T>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | chr14 | 100139193 | ||||||
| chr14:100139244
|
G | T | 3 | a0001c0002t0001g0213a0001c0002t0002g0207a0001c0002t0002g0208 | 3 | HG02258.hp2 HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1094+1442G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | chr14 | 100139244 | ||||||
| chr14:100139284
|
G | A | 1 | a0001c0001t0001g0161 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1094+1482G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | chr14 | 100139284 | ||||||
| chr14:100139484
|
A | G | 3 | a0001c0002t0001g0213a0001c0002t0002g0207a0001c0002t0002g0208 | 3 | HG02258.hp2 HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1094+1682A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | chr14 | 100139484 | ||||||
| chr14:100139497
|
C | T | 4 | a0002c0005t0002g0340a0002c0005t0002g0341a0002c0005t0002g0342others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1095-1683C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | chr14 | 100139497 | ||||||
| chr14:100139634
|
G | A | 1 | a0001c0002t0004g0209 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1095-1546G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | chr14 | 100139634 | ||||||
| chr14:100139763
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1095-1417G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | chr14 | 100139763 | ||||||
| chr14:100139859
|
G | A | 7 | a0001c0001t0001g0003a0001c0001t0001g0057a0001c0001t0001g0068others(4): Show | 8 | HG01884.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1095-1321G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | chr14 | 100139859 | ||||||
| chr14:100139913
|
C | T | 1 | a0001c0001t0001g0078 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1095-1267C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | chr14 | 100139913 | ||||||
| chr14:100139983
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1095-1197G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | chr14 | 100139983 | ||||||
| chr14:100140142
|
T | G | 24 | a0001c0001t0001g0011a0001c0001t0001g0042a0001c0001t0001g0058others(21): Show | 24 | HG00438.hp1 HG02027.hp1 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.1095-1038T>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | chr14 | 100140142 | ||||||
| chr14:100140147
|
AG | A | 53 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(50): Show | 55 | HG01168.hp2 HG01169.hp2 HG01192.hp2 others(52): Show |
intron_variant | MODIFIER | c.1095-1031delG | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 100140147 | |||||
| chr14:100140341
|
G | T | 299 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(296): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.1095-839G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | chr14 | 100140341 | ||||||
| chr14:100140415
|
A | G | 11 | a0001c0001t0001g0223a0002c0003t0001g0028a0002c0003t0001g0029others(8): Show | 11 | HG02055.hp1 HG02486.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1095-765A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | chr14 | 100140415 | ||||||
| chr14:100140445
|
TGCTGAAA others(12): Show |
T | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0052others(4): Show | 7 | HG00735.hp1 HG00741.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1095-717_1095-699d others(21): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 100140445 | |||||
| chr14:100140524
|
G | A | 1 | a0001c0001t0001g0161 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1095-656G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | chr14 | 100140524 | ||||||
| chr14:100140526
|
G | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0170 | 2 | HG03492.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.1095-654G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | chr14 | 100140526 | ||||||
| chr14:100140578
|
T | C | 1 | a0001c0001t0001g0252 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1095-602T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | chr14 | 100140578 | ||||||
| chr14:100140629
|
C | T | 4 | a0001c0004t0001g0219a0001c0004t0001g0220a0001c0004t0001g0221others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1095-551C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | chr14 | 100140629 | ||||||
| chr14:100140684
|
C | T | 2 | a0001c0002t0002g0207a0001c0002t0002g0208 | 2 | HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1095-496C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | chr14 | 100140684 | ||||||
| chr14:100140698
|
G | A | 39 | a0001c0001t0001g0006a0001c0001t0001g0046a0001c0001t0001g0118others(36): Show | 42 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.1095-482G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | chr14 | 100140698 | ||||||
| chr14:100140728
|
G | A | 2 | a0001c0001t0001g0110a0001c0001t0001g0223 | 2 | HG00673.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1095-452G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | chr14 | 100140728 | ||||||
| chr14:100140788
|
CA | C | 25 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0052others(22): Show | 25 | HG00735.hp1 HG00741.hp2 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.1095-390delA | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 100140788 | |||||
| chr14:100141023
|
T | C | 132 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0019others(129): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.1095-157T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | chr14 | 100141023 | ||||||
| chr14:100141032
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1095-148G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | chr14 | 100141032 | ||||||
| chr14:100141138
|
C | CCTGT | 3 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055 | 3 | NA18982.hp1 NA18993.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1095-39_1095-36dup others(4): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 100141138 | |||||
| chr14:100141258
|
C | T | 53 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(50): Show | 55 | HG01168.hp2 HG01169.hp2 HG01192.hp2 others(52): Show |
intron_variant | MODIFIER | c.1161+12C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 12/13 | chr14 | 100141258 | ||||||
| chr14:100141525
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1162-211C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 12/13 | chr14 | 100141525 | ||||||
| chr14:100141526
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1162-210G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 12/13 | chr14 | 100141526 | ||||||
| chr14:100141551
|
G | A | 1 | a0001c0001t0001g0149 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1162-185G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 12/13 | chr14 | 100141551 | ||||||
| chr14:100141581
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1162-155C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 12/13 | chr14 | 100141581 | ||||||
| chr14:100141586
|
C | T | 1 | a0001c0002t0002g0207 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1162-150C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 12/13 | chr14 | 100141586 | ||||||
| chr14:100141611
|
A | T | 1 | a0001c0001t0001g0169 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1162-125A>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 12/13 | chr14 | 100141611 | ||||||
| chr14:100141691
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1162-45G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 12/13 | chr14 | 100141691 | ||||||
| chr14:100141728
|
C | T | 1 | a0001c0001t0001g0301 | 1 | HG02080.hp1 | splice_region_variant&intron_variant | LOW | c.1162-8C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 12/13 | chr14 | 100141728 | ||||||
| chr14:100141836
|
C | T | 10 | a0002c0003t0001g0028a0002c0003t0001g0029a0002c0003t0001g0043others(7): Show | 10 | HG02055.hp1 HG02486.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1219+43C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 13/13 | chr14 | 100141836 | ||||||
| chr14:100141850
|
C | T | 2 | a0001c0002t0002g0207a0001c0002t0002g0208 | 2 | HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1219+57C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 13/13 | chr14 | 100141850 | ||||||
| chr14:100141937
|
T | C | 122 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0019others(119): Show | 124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.1219+144T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 13/13 | chr14 | 100141937 | ||||||
| chr14:100142244
|
AAGGTCTA others(21): Show |
A | 4 | a0001c0001t0001g0235a0001c0001t0001g0276a0001c0001t0001g0291others(1): Show | 4 | HG02647.hp1 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1219+454_1219+481d others(30): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr14 | 100142244 | |||||
| chr14:100142315
|
A | G | 229 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(226): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.1219+522A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 13/13 | chr14 | 100142315 | ||||||
| chr14:100142403
|
C | T | 2 | a0001c0002t0002g0207a0001c0002t0002g0208 | 2 | HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1219+610C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 13/13 | chr14 | 100142403 | ||||||
| chr14:100142462
|
G | T | 29 | a0001c0001t0001g0009a0001c0001t0001g0235a0001c0001t0001g0262others(26): Show | 30 | HG00099.hp2 HG00639.hp2 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.1219+669G>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 13/13 | chr14 | 100142462 | ||||||
| chr14:100142605
|
T | C | 27 | a0001c0001t0001g0006a0001c0001t0001g0118a0001c0001t0001g0229others(24): Show | 28 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.1219+812T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 13/13 | chr14 | 100142605 | ||||||
| chr14:100142644
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1219+851A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 13/13 | chr14 | 100142644 | ||||||
| chr14:100142785
|
T | C | 5 | a0001c0001t0001g0280a0001c0001t0001g0322a0001c0002t0001g0033others(2): Show | 5 | HG00099.hp2 HG01361.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1220-916T>C | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 13/13 | chr14 | 100142785 | ||||||
| chr14:100142935
|
C | T | 3 | a0001c0001t0001g0256a0001c0001t0005g0248a0001c0001t0005g0258 | 3 | HG02071.hp1 NA18982.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1220-766C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 13/13 | chr14 | 100142935 | ||||||
| chr14:100142939
|
G | GGTA | 13 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0052others(10): Show | 13 | HG00735.hp1 HG00741.hp2 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.1220-760_1220-758d others(5): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr14 | 100142939 | |||||
| chr14:100143028
|
G | A | 12 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0052others(9): Show | 12 | HG00735.hp1 HG00741.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1220-673G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 13/13 | chr14 | 100143028 | ||||||
| chr14:100143148
|
C | T | 6 | a0002c0003t0001g0043a0002c0003t0001g0045a0002c0003t0001g0047others(3): Show | 6 | HG02572.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1220-553C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 13/13 | chr14 | 100143148 | ||||||
| chr14:100143317
|
G | A | 4 | a0001c0002t0002g0285a0002c0003t0001g0028a0002c0003t0001g0044others(1): Show | 4 | HG02055.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1220-384G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 13/13 | chr14 | 100143317 | ||||||
| chr14:100143403
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1220-298G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 13/13 | chr14 | 100143403 | ||||||
| chr14:100143551
|
A | G | 130 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(127): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.1220-150A>G | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 13/13 | chr14 | 100143551 | ||||||
| chr14:100143620
|
C | T | 8 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(5): Show | 8 | HG01175.hp1 HG01884.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.1220-81C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 13/13 | chr14 | 100143620 | ||||||
| chr14:100143635
|
G | A | 3 | a0001c0001t0001g0057a0001c0001t0001g0068a0001c0002t0004g0209 | 3 | HG01884.hp2 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1220-66G>A | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 13/13 | chr14 | 100143635 | ||||||
| chr14:100143650
|
C | T | 1 | a0001c0001t0001g0042 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1220-51C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 13/13 | chr14 | 100143650 | ||||||
| chr14:100143651
|
GGGCTGCA others(8): Show |
G | 29 | a0001c0001t0001g0057a0001c0001t0001g0063a0001c0001t0001g0068others(26): Show | 30 | HG01346.hp1 HG01358.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.1220-41_1220-27del others(15): Show |
EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr14 | 100143651 | |||||
| chr14:100143684
|
C | T | 1 | a0001c0004t0001g0040 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1220-17C>T | EVL | ENSG00000196405.13 | transcript | ENST00000392920.8 | protein_coding | 13/13 | chr14 | 100143684 |