Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 92689 |
|---|---|
| ensemblid | ENSG00000197712.12 |
| hgncid | 25087 |
| symbol | FAM114A1 |
| name | family with sequence similarity 114 member A1 |
| refseq_nuc | NM_138389.4 |
| refseq_prot | NP_612398.2 |
| ensembl_nuc | ENST00000358869.5 |
| ensembl_prot | ENSP00000351740.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 38867806 |
| end | 38945739 |
| strand | + |
| ver | v1.2 |
| region | chr4:38867806-38945739 |
| region5000 | chr4:38862806-38950739 |
| regionname0 | FAM114A1_chr4_38867806_38945739 |
| regionname5000 | FAM114A1_chr4_38862806_38950739 |
| 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 | 563 | 268 | 49 | 48 | 130 | 7 | 32 | 97 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002 | 0/0 | 563 | 54 | 27 | 9 | 13 | 2 | 3 | 10 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0003 | 0/0 | 563 | 9 | 3 | 2 | 2 | 0 | 2 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0004 | 0/0 | 563 | 9 | 0 | 6 | 1 | 1 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0005 | 0/0 | 563 | 8 | 5 | 0 | 0 | 0 | 3 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0006 | 0/0 | 563 | 5 | 0 | 4 | 1 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0007 | 0/0 | 563 | 4 | 0 | 0 | 2 | 0 | 2 | 2 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0008 | 0/0 | 563 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0009 | 0/0 | 563 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0010 | 0/0 | 563 | 2 | 0 | 1 | 1 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0011 | 0/0 | 563 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0012 | 0/0 | 563 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0013 | 0/0 | 563 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0014 | 0/0 | 563 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0015 | 0/0 | 563 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0016 | 0/0 | 563 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0017 | 0/0 | 563 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0018 | 0/0 | 563 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1692 | 142 | 31 | 25 | 60 | 4 | 21 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0002 | 1/0 | 1692 | 68 | 4 | 21 | 32 | 2 | 8 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0003 | 0/0 | 1692 | 32 | 17 | 4 | 10 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0004 | 0/0 | 1692 | 26 | 8 | 0 | 18 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0005 | 0/0 | 1692 | 10 | 1 | 0 | 8 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0006 | 0/0 | 1692 | 7 | 1 | 3 | 0 | 1 | 2 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0007 | 0/0 | 1692 | 6 | 0 | 4 | 0 | 1 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0008 | 0/0 | 1692 | 6 | 0 | 0 | 6 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0009 | 0/0 | 1692 | 6 | 1 | 1 | 1 | 1 | 2 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0010 | 0/0 | 1692 | 4 | 0 | 4 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0011 | 0/0 | 1692 | 4 | 2 | 1 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0012 | 0/0 | 1692 | 3 | 1 | 0 | 0 | 0 | 2 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0013 | 0/0 | 1692 | 3 | 0 | 0 | 3 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0014 | 0/0 | 1692 | 3 | 3 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0015 | 0/0 | 1692 | 3 | 3 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0016 | 0/0 | 1692 | 2 | 1 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0017 | 0/0 | 1692 | 2 | 0 | 1 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0018 | 0/0 | 1692 | 2 | 0 | 2 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0019 | 0/0 | 1692 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0020 | 0/0 | 1692 | 2 | 1 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0021 | 0/0 | 1692 | 2 | 0 | 0 | 1 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0022 | 0/0 | 1692 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0023 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0024 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0025 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0026 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0027 | 0/0 | 1692 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0028 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0029 | 0/0 | 1692 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0030 | 0/0 | 1692 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0031 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0032 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0033 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0034 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0035 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0036 | 0/0 | 1692 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0037 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0038 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0039 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0040 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0041 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0042 | 0/0 | 1692 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0043 | 0/0 | 1692 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0044 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0045 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0046 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0047 | 0/0 | 1692 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0048 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0049 | 0/0 | 1692 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0050 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0051 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0052 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0053 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0054 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0055 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0056 | 0/0 | 1692 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| c0057 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| 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 | 2369 | 86 | 12 | 26 | 34 | 2 | 10 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0002 | 0/0 | 2373 | 83 | 15 | 13 | 39 | 1 | 15 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0003 | 0/0 | 2368 | 32 | 5 | 8 | 13 | 1 | 5 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0004 | 0/0 | 2368 | 25 | 3 | 3 | 12 | 3 | 4 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0005 | 0/0 | 2373 | 24 | 23 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0006 | 0/0 | 2368 | 21 | 0 | 4 | 17 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0007 | 0/0 | 2369 | 15 | 3 | 1 | 10 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0008 | 0/0 | 2368 | 9 | 0 | 0 | 9 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0009 | 0/0 | 2367 | 7 | 0 | 4 | 0 | 0 | 3 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0010 | 0/0 | 2368 | 7 | 6 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0011 | 0/0 | 2367 | 6 | 4 | 1 | 0 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0012 | 0/0 | 2374 | 6 | 3 | 1 | 1 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0013 | 0/0 | 2370 | 4 | 0 | 0 | 2 | 1 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0014 | 0/0 | 2373 | 4 | 4 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0015 | 0/0 | 2367 | 3 | 0 | 2 | 0 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0016 | 0/0 | 2369 | 3 | 1 | 1 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0017 | 0/0 | 2369 | 3 | 0 | 0 | 3 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0018 | 0/0 | 2368 | 2 | 0 | 0 | 2 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0019 | 0/0 | 2369 | 2 | 0 | 0 | 2 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0020 | 0/0 | 2368 | 2 | 0 | 0 | 2 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0021 | 0/0 | 2369 | 2 | 0 | 1 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0022 | 0/0 | 2373 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0023 | 0/0 | 2373 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0024 | 0/0 | 2374 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0025 | 0/0 | 2368 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0026 | 0/0 | 2368 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0027 | 0/0 | 2368 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0028 | 0/0 | 2369 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0029 | 0/0 | 2369 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0030 | 0/0 | 2369 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0031 | 0/0 | 2373 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0032 | 0/0 | 2373 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0033 | 0/0 | 2373 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0034 | 0/0 | 2369 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0035 | 0/0 | 2369 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0036 | 0/0 | 2373 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0037 | 0/0 | 2373 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0038 | 0/0 | 2373 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0039 | 0/0 | 2373 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0040 | 0/0 | 2374 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0041 | 0/0 | 2369 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0042 | 0/0 | 2373 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0043 | 0/0 | 2369 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| t0044 | 0/0 | 2374 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| 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 | 4 | 0 | 0 | 4 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0100 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0204 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0350 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1692 | 142 | 31 | 25 | 60 | 4 | 21 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0002 | 1/0 | 1692 | 68 | 4 | 21 | 32 | 2 | 8 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0004 | 0/0 | 1692 | 26 | 8 | 0 | 18 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0005 | 0/0 | 1692 | 10 | 1 | 0 | 8 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0008 | 0/0 | 1692 | 6 | 0 | 0 | 6 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0009 | 0/0 | 1692 | 6 | 1 | 1 | 1 | 1 | 2 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0013 | 0/0 | 1692 | 3 | 0 | 0 | 3 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0023 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0037 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0038 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0039 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0043 | 0/0 | 1692 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0044 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0046 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0003 | 0/0 | 1692 | 32 | 17 | 4 | 10 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0006 | 0/0 | 1692 | 7 | 1 | 3 | 0 | 1 | 2 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0016 | 0/0 | 1692 | 2 | 1 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0022 | 0/0 | 1692 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0025 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0026 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0027 | 0/0 | 1692 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0028 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0029 | 0/0 | 1692 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0032 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0034 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0053 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0054 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0056 | 0/0 | 1692 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0057 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0003c0011 | 0/0 | 1692 | 4 | 2 | 1 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0003c0020 | 0/0 | 1692 | 2 | 1 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0003c0036 | 0/0 | 1692 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0003c0041 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0003c0042 | 0/0 | 1692 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0004c0007 | 0/0 | 1692 | 6 | 0 | 4 | 0 | 1 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0004c0018 | 0/0 | 1692 | 2 | 0 | 2 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0004c0024 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0005c0012 | 0/0 | 1692 | 3 | 1 | 0 | 0 | 0 | 2 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0005c0015 | 0/0 | 1692 | 3 | 3 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0005c0030 | 0/0 | 1692 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0005c0055 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0006c0010 | 0/0 | 1692 | 4 | 0 | 4 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0006c0035 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0007c0021 | 0/0 | 1692 | 2 | 0 | 0 | 1 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0007c0048 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0007c0049 | 0/0 | 1692 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0008c0014 | 0/0 | 1692 | 3 | 3 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0009c0019 | 0/0 | 1692 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0010c0017 | 0/0 | 1692 | 2 | 0 | 1 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0011c0050 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0012c0051 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0013c0040 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0014c0045 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0015c0047 | 0/0 | 1692 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0016c0033 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0017c0031 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0018c0052 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4060 | 18 | 3 | 5 | 6 | 0 | 3 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0001t0002 | 0/0 | 4064 | 55 | 6 | 11 | 25 | 1 | 12 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0001t0004 | 0/0 | 4059 | 14 | 2 | 3 | 4 | 2 | 3 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0001t0005 | 0/0 | 4064 | 8 | 8 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0001t0006 | 0/0 | 4059 | 8 | 0 | 0 | 8 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0001t0007 | 0/0 | 4060 | 6 | 3 | 0 | 3 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0001t0008 | 0/0 | 4059 | 5 | 0 | 0 | 5 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0001t0009 | 0/0 | 4058 | 2 | 0 | 1 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0001t0010 | 0/0 | 4059 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0001t0011 | 0/0 | 4058 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0001t0012 | 0/0 | 4065 | 4 | 1 | 1 | 1 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0001t0013 | 0/0 | 4061 | 2 | 0 | 0 | 1 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0001t0014 | 0/0 | 4064 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0001t0015 | 0/0 | 4058 | 2 | 0 | 2 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0001t0016 | 0/0 | 4060 | 2 | 1 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0001t0017 | 0/0 | 4060 | 2 | 0 | 0 | 2 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0001t0021 | 0/0 | 4060 | 2 | 0 | 1 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0001t0026 | 0/0 | 4059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0001t0027 | 0/0 | 4059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0001t0031 | 0/0 | 4064 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0001t0035 | 0/0 | 4060 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0001t0038 | 0/0 | 4064 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0001t0041 | 0/0 | 4060 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0001t0042 | 0/0 | 4064 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0002t0001 | 1/0 | 4060 | 44 | 2 | 14 | 21 | 2 | 4 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0002t0002 | 0/0 | 4064 | 7 | 0 | 1 | 4 | 0 | 2 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0002t0006 | 0/0 | 4059 | 4 | 0 | 4 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0002t0007 | 0/0 | 4060 | 4 | 0 | 0 | 3 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0002t0008 | 0/0 | 4059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0002t0011 | 0/0 | 4058 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0002t0013 | 0/0 | 4061 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0002t0014 | 0/0 | 4064 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0002t0019 | 0/0 | 4060 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0002t0020 | 0/0 | 4059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0002t0028 | 0/0 | 4060 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0002t0037 | 0/0 | 4064 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0002t0040 | 0/0 | 4065 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0004t0001 | 0/0 | 4060 | 2 | 1 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0004t0002 | 0/0 | 4064 | 9 | 2 | 0 | 7 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0004t0004 | 0/0 | 4059 | 4 | 0 | 0 | 4 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0004t0006 | 0/0 | 4059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0004t0007 | 0/0 | 4060 | 2 | 0 | 0 | 2 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0004t0008 | 0/0 | 4059 | 2 | 0 | 0 | 2 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0004t0011 | 0/0 | 4058 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0004t0022 | 0/0 | 4064 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0004t0029 | 0/0 | 4060 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0004t0039 | 0/0 | 4064 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0005t0003 | 0/0 | 4059 | 10 | 1 | 0 | 8 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0008t0006 | 0/0 | 4059 | 6 | 0 | 0 | 6 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0009t0003 | 0/0 | 4059 | 5 | 1 | 1 | 1 | 1 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0009t0010 | 0/0 | 4059 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0013t0001 | 0/0 | 4060 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0013t0002 | 0/0 | 4064 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0013t0006 | 0/0 | 4059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0023t0002 | 0/0 | 4064 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0037t0003 | 0/0 | 4059 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0038t0005 | 0/0 | 4064 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0039t0024 | 0/0 | 4065 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0043t0001 | 0/0 | 4060 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0044t0024 | 0/0 | 4065 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0001c0046t0002 | 0/0 | 4064 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0003t0001 | 0/0 | 4060 | 6 | 1 | 2 | 3 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0003t0002 | 0/0 | 4064 | 5 | 4 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0003t0004 | 0/0 | 4059 | 4 | 1 | 0 | 2 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0003t0005 | 0/0 | 4064 | 7 | 7 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0003t0006 | 0/0 | 4059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0003t0007 | 0/0 | 4060 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0003t0010 | 0/0 | 4059 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0003t0012 | 0/0 | 4065 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0003t0016 | 0/0 | 4060 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0003t0017 | 0/0 | 4060 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0003t0018 | 0/0 | 4059 | 2 | 0 | 0 | 2 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0003t0032 | 0/0 | 4064 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0006t0001 | 0/0 | 4060 | 5 | 0 | 3 | 0 | 0 | 2 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0006t0010 | 0/0 | 4059 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0006t0011 | 0/0 | 4058 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0016t0001 | 0/0 | 4060 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0016t0007 | 0/0 | 4060 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0022t0005 | 0/0 | 4064 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0022t0010 | 0/0 | 4059 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0025t0003 | 0/0 | 4059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0026t0005 | 0/0 | 4064 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0027t0003 | 0/0 | 4059 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0028t0030 | 0/0 | 4060 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0029t0043 | 0/0 | 4060 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0032t0044 | 0/0 | 4065 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0034t0020 | 0/0 | 4059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0053t0001 | 0/0 | 4060 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0054t0036 | 0/0 | 4064 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0056t0005 | 0/0 | 4064 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0002c0057t0005 | 0/0 | 4064 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0003c0011t0001 | 0/0 | 4060 | 2 | 0 | 1 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0003c0011t0002 | 0/0 | 4064 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0003c0011t0014 | 0/0 | 4064 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0003c0020t0003 | 0/0 | 4059 | 2 | 1 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0003c0036t0004 | 0/0 | 4059 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0003c0041t0003 | 0/0 | 4059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0003c0042t0003 | 0/0 | 4059 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0004c0007t0009 | 0/0 | 4058 | 4 | 0 | 3 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0004c0007t0015 | 0/0 | 4058 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0004c0007t0025 | 0/0 | 4059 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0004c0018t0003 | 0/0 | 4059 | 2 | 0 | 2 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0004c0024t0001 | 0/0 | 4060 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0005c0012t0001 | 0/0 | 4060 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0005c0012t0033 | 0/0 | 4064 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0005c0012t0034 | 0/0 | 4060 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0005c0015t0002 | 0/0 | 4064 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0005c0015t0005 | 0/0 | 4064 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0005c0030t0003 | 0/0 | 4059 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0005c0055t0012 | 0/0 | 4065 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0006c0010t0003 | 0/0 | 4059 | 3 | 0 | 3 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0006c0010t0007 | 0/0 | 4060 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0006c0035t0003 | 0/0 | 4059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0007c0021t0004 | 0/0 | 4059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0007c0021t0013 | 0/0 | 4061 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0007c0048t0008 | 0/0 | 4059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0007c0049t0002 | 0/0 | 4064 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0008c0014t0001 | 0/0 | 4060 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0008c0014t0005 | 0/0 | 4064 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0008c0014t0023 | 0/0 | 4064 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0009c0019t0001 | 0/0 | 4060 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0010c0017t0003 | 0/0 | 4059 | 2 | 0 | 1 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0011c0050t0003 | 0/0 | 4059 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0012c0051t0005 | 0/0 | 4064 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0013c0040t0023 | 0/0 | 4064 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0014c0045t0004 | 0/0 | 4059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0015c0047t0009 | 0/0 | 4058 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0016c0033t0011 | 0/0 | 4058 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0017c0031t0019 | 0/0 | 4060 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| a0018c0052t0005 | 0/0 | 4064 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | copy fasta | chr4 | 38862806 | 38950739 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0001g0100 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0004g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0004g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0005g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0005g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0005g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0005g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0005g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0006g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0006g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0006g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0006g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0006g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0006g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0006g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0006g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0007g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0007g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0007g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0007g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0007g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0007g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0008g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0008g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0008g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0008g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0008g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0009g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0009g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0010g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0010g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0011g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0012g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0012g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0012g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0012g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0013g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0013g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0014g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0014g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0015g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0015g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0016g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0016g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0017g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0017g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0021g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0021g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0026g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0027g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0031g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0035g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0038g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0041g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0001t0042g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0204 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0006g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0006g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0006g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0006g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0007g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0007g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0007g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0007g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0008g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0011g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0013g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0014g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0019g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0020g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0028g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0037g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0002t0040g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0004t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0004t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0004t0002g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0004t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0004t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0004t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0004t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0004t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0004t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0004t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0004t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0004t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0004t0006g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0004t0007g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0004t0007g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0004t0008g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0004t0008g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0004t0011g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0004t0011g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0004t0022g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0004t0029g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0004t0039g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0005t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0005t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0005t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0005t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0005t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0005t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0005t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0005t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0005t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0005t0003g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0008t0006g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0008t0006g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0008t0006g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0008t0006g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0008t0006g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0008t0006g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0009t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0009t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0009t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0009t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0009t0003g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0009t0010g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0013t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0013t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0013t0006g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0023t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0037t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0038t0005g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0039t0024g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0043t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0044t0024g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0001c0046t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0003t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0003t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0003t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0003t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0003t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0003t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0003t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0003t0002g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0003t0004g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0003t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0003t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0003t0004g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0003t0005g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0003t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0003t0005g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0003t0005g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0003t0005g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0003t0005g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0003t0005g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0003t0006g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0003t0007g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0003t0010g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0003t0010g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0003t0012g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0003t0016g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0003t0017g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0003t0018g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0003t0018g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0003t0032g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0006t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0006t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0006t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0006t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0006t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0006t0010g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0006t0011g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0016t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0016t0007g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0022t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0022t0010g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0025t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0026t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0027t0003g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0028t0030g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0029t0043g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0032t0044g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0034t0020g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0053t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0054t0036g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0056t0005g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0002c0057t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0003c0011t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0003c0011t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0003c0011t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0003c0011t0014g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0003c0020t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0003c0020t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0003c0036t0004g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0003c0041t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0003c0042t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0004c0007t0009g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0004c0007t0009g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0004c0007t0009g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0004c0007t0009g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0004c0007t0015g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0004c0007t0025g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0004c0018t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0004c0018t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0004c0024t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0005c0012t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0005c0012t0033g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0005c0012t0034g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0005c0015t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0005c0015t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0005c0015t0005g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0005c0030t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0005c0055t0012g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0006c0010t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0006c0010t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0006c0010t0003g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0006c0010t0007g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0006c0035t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0007c0021t0004g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0007c0021t0013g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0007c0048t0008g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0007c0049t0002g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0008c0014t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0008c0014t0005g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0008c0014t0023g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0009c0019t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0009c0019t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0010c0017t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0010c0017t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0011c0050t0003g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0012c0051t0005g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0013c0040t0023g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0014c0045t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0015c0047t0009g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0016c0033t0011g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0017c0031t0019g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| a0018c0052t0005g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0206 | EUR | GBR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0049 | EUR | GBR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG00140 | hp1 | a0001 | c0001 | t0013 | g0237 | EUR | GBR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG00140 | hp2 | a0002 | c0003 | t0004 | g0024 | EUR | GBR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0350 | EUR | FIN | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG00323 | hp2 | a0004 | c0007 | t0015 | g0033 | EUR | FIN | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | CHS | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG00408 | hp2 | a0001 | c0002 | t0002 | g0141 | EAS | CHS | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG00438 | hp2 | a0001 | c0013 | t0001 | g0290 | EAS | CHS | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG00544 | hp1 | a0001 | c0008 | t0006 | g0051 | EAS | CHS | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG00544 | hp2 | a0002 | c0003 | t0006 | g0037 | EAS | CHS | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | CHS | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG00558 | hp2 | a0001 | c0008 | t0006 | g0053 | EAS | CHS | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG00597 | hp1 | a0001 | c0004 | t0007 | g0136 | EAS | CHS | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG00597 | hp2 | a0001 | c0008 | t0006 | g0059 | EAS | CHS | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | CHS | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG00609 | hp2 | a0001 | c0002 | t0020 | g0236 | EAS | CHS | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG00621 | hp1 | a0002 | c0016 | t0007 | g0124 | EAS | CHS | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG00621 | hp2 | a0001 | c0008 | t0006 | g0052 | EAS | CHS | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG00639 | hp1 | a0002 | c0003 | t0016 | g0035 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0217 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG00642 | hp2 | a0001 | c0002 | t0006 | g0327 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG00673 | hp1 | a0001 | c0001 | t0006 | g0304 | EAS | CHS | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | CHS | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0182 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG00735 | hp2 | a0001 | c0009 | t0003 | g0092 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG00741 | hp1 | a0001 | c0002 | t0028 | g0351 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG00741 | hp2 | a0004 | c0007 | t0009 | g0034 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01069 | hp1 | a0004 | c0018 | t0003 | g0022 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0268 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01070 | hp2 | a0004 | c0007 | t0025 | g0036 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01071 | hp2 | a0004 | c0018 | t0003 | g0026 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01074 | hp1 | a0001 | c0002 | t0006 | g0329 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01074 | hp2 | a0001 | c0001 | t0015 | g0215 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0196 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0203 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01099 | hp1 | a0002 | c0006 | t0001 | g0021 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0087 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01106 | hp2 | a0003 | c0020 | t0003 | g0101 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01109 | hp1 | a0001 | c0001 | t0009 | g0154 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01109 | hp2 | a0002 | c0056 | t0005 | g0252 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01167 | hp2 | a0001 | c0043 | t0001 | g0006 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0235 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01175 | hp2 | a0001 | c0001 | t0015 | g0240 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01192 | hp2 | a0004 | c0007 | t0009 | g0027 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01243 | hp1 | a0002 | c0029 | t0043 | g0115 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0214 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0198 | AMR | CLM | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01255 | hp2 | a0002 | c0006 | t0001 | g0353 | AMR | CLM | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0183 | AMR | CLM | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01256 | hp2 | a0004 | c0007 | t0009 | g0032 | AMR | CLM | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01257 | hp1 | a0001 | c0002 | t0011 | g0147 | AMR | CLM | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01257 | hp2 | a0002 | c0003 | t0001 | g0127 | AMR | CLM | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0253 | AMR | CLM | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0137 | AMR | CLM | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0090 | AMR | CLM | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0202 | AMR | CLM | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01361 | hp2 | a0001 | c0001 | t0021 | g0068 | AMR | CLM | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01433 | hp1 | a0006 | c0010 | t0003 | g0174 | AMR | CLM | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | CLM | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0169 | AMR | CLM | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0091 | AMR | CLM | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01516 | hp1 | a0001 | c0009 | t0003 | g0070 | EUR | IBS | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0200 | EUR | IBS | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0231 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01884 | hp2 | a0003 | c0011 | t0014 | g0269 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01891 | hp1 | a0001 | c0044 | t0024 | g0226 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01891 | hp2 | a0002 | c0003 | t0005 | g0364 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0263 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01943 | hp2 | a0003 | c0011 | t0001 | g0302 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0151 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01975 | hp2 | a0010 | c0017 | t0003 | g0125 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01978 | hp1 | a0002 | c0003 | t0002 | g0130 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01978 | hp2 | a0001 | c0002 | t0006 | g0188 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0197 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01993 | hp2 | a0006 | c0010 | t0007 | g0177 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02004 | hp1 | a0006 | c0010 | t0003 | g0144 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0313 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | KHV | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02027 | hp2 | a0004 | c0024 | t0001 | g0116 | EAS | KHV | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | KHV | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02040 | hp2 | a0003 | c0041 | t0003 | g0162 | EAS | KHV | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0189 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0181 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02074 | hp1 | a0001 | c0001 | t0007 | g0230 | EAS | KHV | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0086 | EAS | KHV | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | KHV | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | KHV | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0336 | EAS | KHV | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02132 | hp1 | a0001 | c0005 | t0003 | g0283 | EAS | KHV | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | KHV | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02135 | hp2 | a0001 | c0001 | t0038 | g0298 | EAS | KHV | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02145 | hp1 | a0002 | c0057 | t0005 | g0251 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02145 | hp2 | a0002 | c0032 | t0044 | g0352 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02148 | hp1 | a0001 | c0001 | t0012 | g0334 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02148 | hp2 | a0002 | c0006 | t0001 | g0121 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02165 | hp1 | a0001 | c0005 | t0003 | g0216 | EAS | CDX | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02165 | hp2 | a0002 | c0003 | t0007 | g0117 | EAS | CDX | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02257 | hp1 | a0013 | c0040 | t0023 | g0234 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02257 | hp2 | a0001 | c0001 | t0007 | g0227 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02258 | hp1 | a0003 | c0020 | t0003 | g0046 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0301 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02273 | hp1 | a0002 | c0003 | t0001 | g0126 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02273 | hp2 | a0001 | c0002 | t0006 | g0176 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02280 | hp1 | a0002 | c0003 | t0005 | g0339 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02280 | hp2 | a0002 | c0003 | t0004 | g0342 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0201 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02300 | hp2 | a0006 | c0010 | t0003 | g0317 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0276 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02451 | hp2 | a0002 | c0003 | t0002 | g0043 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | KHV | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02523 | hp2 | a0001 | c0001 | t0013 | g0225 | EAS | KHV | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02602 | hp1 | a0001 | c0001 | t0009 | g0153 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02602 | hp2 | a0001 | c0005 | t0003 | g0323 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02615 | hp1 | a0002 | c0003 | t0005 | g0355 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0277 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02622 | hp1 | a0005 | c0012 | t0033 | g0341 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02622 | hp2 | a0008 | c0014 | t0001 | g0012 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02630 | hp1 | a0001 | c0004 | t0002 | g0286 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0193 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02647 | hp1 | a0005 | c0015 | t0002 | g0244 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02647 | hp2 | a0001 | c0004 | t0029 | g0015 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02698 | hp1 | a0005 | c0030 | t0003 | g0113 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0318 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02717 | hp1 | a0002 | c0053 | t0001 | g0245 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02717 | hp2 | a0001 | c0001 | t0035 | g0311 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02723 | hp1 | a0002 | c0003 | t0002 | g0045 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0079 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0222 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02738 | hp1 | a0001 | c0001 | t0012 | g0333 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02738 | hp2 | a0003 | c0042 | t0003 | g0170 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02809 | hp1 | a0002 | c0003 | t0010 | g0362 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02809 | hp2 | a0012 | c0051 | t0005 | g0344 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02818 | hp1 | a0002 | c0003 | t0032 | g0357 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02818 | hp2 | a0002 | c0054 | t0036 | g0243 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02886 | hp1 | a0001 | c0001 | t0014 | g0295 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02886 | hp2 | a0002 | c0003 | t0001 | g0359 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02896 | hp1 | a0001 | c0037 | t0003 | g0007 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02896 | hp2 | a0001 | c0004 | t0022 | g0003 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02897 | hp1 | a0005 | c0015 | t0002 | g0250 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02897 | hp2 | a0001 | c0004 | t0022 | g0003 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02922 | hp1 | a0005 | c0055 | t0012 | g0356 | AFR | ESN | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02922 | hp2 | a0001 | c0039 | t0024 | g0261 | AFR | ESN | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02965 | hp1 | a0001 | c0001 | t0012 | g0172 | AFR | ESN | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02965 | hp2 | a0002 | c0003 | t0005 | g0343 | AFR | ESN | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02970 | hp2 | a0001 | c0001 | t0010 | g0299 | AFR | ESN | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0211 | AFR | ESN | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02976 | hp2 | a0005 | c0015 | t0005 | g0246 | AFR | ESN | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0314 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0065 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03041 | hp1 | a0008 | c0014 | t0005 | g0310 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03041 | hp2 | a0002 | c0003 | t0005 | g0042 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03098 | hp1 | a0001 | c0001 | t0007 | g0256 | AFR | MSL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03098 | hp2 | a0002 | c0003 | t0012 | g0112 | AFR | MSL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03130 | hp1 | a0001 | c0001 | t0011 | g0010 | AFR | ESN | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03130 | hp2 | a0002 | c0003 | t0005 | g0360 | AFR | ESN | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03139 | hp1 | a0009 | c0019 | t0001 | g0282 | AFR | ESN | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03139 | hp2 | a0001 | c0001 | t0042 | g0210 | AFR | ESN | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0209 | AFR | ESN | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03195 | hp2 | a0002 | c0026 | t0005 | g0039 | AFR | ESN | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | MSL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | MSL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03225 | hp1 | a0001 | c0004 | t0001 | g0260 | AFR | MSL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03225 | hp2 | a0003 | c0011 | t0002 | g0312 | AFR | MSL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03239 | hp1 | a0001 | c0002 | t0037 | g0199 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0308 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03453 | hp1 | a0002 | c0003 | t0002 | g0358 | AFR | MSL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0014 | AFR | MSL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03486 | hp1 | a0001 | c0004 | t0002 | g0004 | AFR | MSL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03486 | hp2 | a0002 | c0022 | t0005 | g0249 | AFR | MSL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0167 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03490 | hp2 | a0002 | c0006 | t0001 | g0020 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0272 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03491 | hp2 | a0004 | c0007 | t0009 | g0025 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0271 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0232 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03516 | hp1 | a0001 | c0001 | t0014 | g0194 | AFR | ESN | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0297 | AFR | ESN | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03579 | hp2 | a0011 | c0050 | t0003 | g0345 | AFR | MSL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0069 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03654 | hp2 | a0003 | c0036 | t0004 | g0009 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03688 | hp1 | a0002 | c0006 | t0001 | g0038 | SAS | STU | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0192 | SAS | STU | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03704 | hp1 | a0007 | c0049 | t0002 | g0348 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0224 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03831 | hp1 | a0001 | c0002 | t0007 | g0171 | SAS | BEB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0233 | SAS | BEB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03834 | hp1 | a0007 | c0021 | t0013 | g0340 | SAS | BEB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03834 | hp2 | a0002 | c0027 | t0003 | g0031 | SAS | BEB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0180 | SAS | BEB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03927 | hp2 | a0005 | c0012 | t0001 | g0029 | SAS | BEB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0257 | SAS | STU | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG04115 | hp2 | a0015 | c0047 | t0009 | g0155 | SAS | STU | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0139 | SAS | BEB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0330 | SAS | BEB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG04199 | hp1 | a0001 | c0009 | t0010 | g0332 | SAS | STU | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG04199 | hp2 | a0005 | c0012 | t0034 | g0023 | SAS | STU | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0221 | SAS | STU | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | STU | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | STU | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG04228 | hp2 | a0001 | c0001 | t0016 | g0322 | SAS | STU | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18522 | hp1 | a0002 | c0022 | t0010 | g0248 | AFR | YRI | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18522 | hp2 | a0001 | c0038 | t0005 | g0011 | AFR | YRI | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18612 | hp1 | a0001 | c0001 | t0008 | g0055 | EAS | CHB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | CHB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18906 | hp1 | a0002 | c0003 | t0005 | g0044 | AFR | YRI | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18906 | hp2 | a0001 | c0005 | t0003 | g0274 | AFR | YRI | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18940 | hp1 | a0001 | c0002 | t0008 | g0074 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0190 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18941 | hp1 | a0001 | c0046 | t0002 | g0096 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18941 | hp2 | a0001 | c0001 | t0017 | g0138 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18942 | hp2 | a0001 | c0004 | t0006 | g0258 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18945 | hp2 | a0001 | c0001 | t0006 | g0148 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18950 | hp1 | a0001 | c0004 | t0008 | g0098 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18950 | hp2 | a0007 | c0021 | t0004 | g0347 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0279 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18951 | hp2 | a0001 | c0005 | t0003 | g0159 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18952 | hp1 | a0001 | c0004 | t0002 | g0349 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18953 | hp1 | a0001 | c0004 | t0002 | g0058 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18953 | hp2 | a0017 | c0031 | t0019 | g0030 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18954 | hp1 | a0001 | c0001 | t0006 | g0056 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0262 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18956 | hp1 | a0007 | c0048 | t0008 | g0346 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18956 | hp2 | a0001 | c0004 | t0007 | g0331 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18959 | hp1 | a0001 | c0001 | t0004 | g0266 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18960 | hp1 | a0001 | c0004 | t0004 | g0073 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0307 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18962 | hp2 | a0001 | c0002 | t0007 | g0366 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18963 | hp1 | a0001 | c0013 | t0006 | g0173 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0324 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0018 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18970 | hp1 | a0001 | c0009 | t0003 | g0160 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18970 | hp2 | a0001 | c0004 | t0002 | g0001 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18971 | hp2 | a0001 | c0002 | t0007 | g0303 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0319 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18974 | hp1 | a0001 | c0001 | t0008 | g0110 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18974 | hp2 | a0001 | c0001 | t0012 | g0184 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18978 | hp1 | a0002 | c0003 | t0004 | g0129 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18978 | hp2 | a0014 | c0045 | t0004 | g0185 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18979 | hp1 | a0002 | c0003 | t0001 | g0131 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18979 | hp2 | a0001 | c0008 | t0006 | g0089 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18980 | hp1 | a0001 | c0004 | t0002 | g0001 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0267 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18981 | hp1 | a0001 | c0001 | t0006 | g0078 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0293 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18983 | hp2 | a0001 | c0001 | t0007 | g0273 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18987 | hp2 | a0001 | c0004 | t0001 | g0072 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18988 | hp1 | a0001 | c0001 | t0027 | g0054 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18988 | hp2 | a0010 | c0017 | t0003 | g0134 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18992 | hp1 | a0001 | c0001 | t0006 | g0057 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18992 | hp2 | a0001 | c0001 | t0008 | g0218 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18993 | hp1 | a0001 | c0004 | t0004 | g0107 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18993 | hp2 | a0001 | c0004 | t0039 | g0309 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18999 | hp1 | a0002 | c0003 | t0018 | g0119 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19000 | hp2 | a0001 | c0002 | t0013 | g0164 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19002 | hp1 | a0002 | c0003 | t0001 | g0122 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19002 | hp2 | a0001 | c0004 | t0004 | g0105 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19004 | hp1 | a0001 | c0013 | t0002 | g0085 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19004 | hp2 | a0002 | c0003 | t0001 | g0120 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19005 | hp1 | a0001 | c0001 | t0008 | g0239 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19007 | hp1 | a0001 | c0005 | t0003 | g0093 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19007 | hp2 | a0002 | c0025 | t0003 | g0123 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19009 | hp2 | a0001 | c0001 | t0007 | g0166 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19030 | hp1 | a0001 | c0009 | t0003 | g0335 | AFR | LWK | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19030 | hp2 | a0001 | c0004 | t0011 | g0255 | AFR | LWK | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19043 | hp1 | a0001 | c0001 | t0007 | g0320 | AFR | LWK | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19043 | hp2 | a0001 | c0004 | t0011 | g0145 | AFR | LWK | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19054 | hp2 | a0001 | c0001 | t0008 | g0109 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19057 | hp1 | a0001 | c0004 | t0002 | g0064 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19060 | hp1 | a0001 | c0008 | t0006 | g0111 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19060 | hp2 | a0002 | c0034 | t0020 | g0133 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19062 | hp1 | a0001 | c0001 | t0026 | g0316 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19062 | hp2 | a0001 | c0002 | t0007 | g0365 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19063 | hp1 | a0001 | c0004 | t0002 | g0001 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19066 | hp1 | a0002 | c0003 | t0018 | g0128 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19066 | hp2 | a0001 | c0005 | t0003 | g0285 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19068 | hp2 | a0002 | c0003 | t0004 | g0118 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19070 | hp2 | a0001 | c0001 | t0031 | g0289 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19078 | hp1 | a0001 | c0002 | t0001 | g0265 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19078 | hp2 | a0001 | c0023 | t0002 | g0104 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19079 | hp1 | a0001 | c0004 | t0004 | g0076 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19079 | hp2 | a0001 | c0001 | t0006 | g0294 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19083 | hp1 | a0001 | c0005 | t0003 | g0077 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19084 | hp1 | a0003 | c0011 | t0001 | g0084 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19085 | hp1 | a0001 | c0002 | t0019 | g0288 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19085 | hp2 | a0001 | c0004 | t0008 | g0048 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19086 | hp1 | a0001 | c0001 | t0021 | g0220 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19086 | hp2 | a0001 | c0001 | t0006 | g0061 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19088 | hp1 | a0002 | c0003 | t0017 | g0132 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19088 | hp2 | a0006 | c0035 | t0003 | g0207 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19090 | hp1 | a0001 | c0001 | t0017 | g0300 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19090 | hp2 | a0001 | c0001 | t0006 | g0149 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19091 | hp1 | a0001 | c0004 | t0002 | g0001 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19091 | hp2 | a0001 | c0005 | t0003 | g0140 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19240 | hp1 | a0001 | c0001 | t0010 | g0259 | AFR | YRI | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA19240 | hp2 | a0009 | c0019 | t0001 | g0321 | AFR | YRI | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0292 | AFR | ASW | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0142 | AFR | ASW | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0254 | EUR | TSI | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA20805 | hp2 | a0002 | c0006 | t0011 | g0028 | EUR | TSI | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0186 | SAS | GIH | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA20905 | hp2 | a0001 | c0009 | t0003 | g0270 | SAS | GIH | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0103 | AMR | CLM | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG01123 | hp2 | a0001 | c0001 | t0041 | g0328 | AMR | CLM | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02109 | hp1 | a0002 | c0006 | t0010 | g0337 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02109 | hp2 | a0016 | c0033 | t0011 | g0354 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02486 | hp1 | a0002 | c0028 | t0030 | g0363 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02559 | hp1 | a0001 | c0002 | t0040 | g0306 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG02559 | hp2 | a0018 | c0052 | t0005 | g0247 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03471 | hp1 | a0002 | c0016 | t0001 | g0361 | AFR | MSL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG03471 | hp2 | a0002 | c0003 | t0010 | g0338 | AFR | MSL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG06807 | hp1 | a0001 | c0002 | t0014 | g0156 | AFR | USA | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | USA | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18955 | hp1 | a0001 | c0005 | t0003 | g0158 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0326 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA20300 | hp1 | a0008 | c0014 | t0023 | g0305 | AFR | USA | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA20300 | hp2 | a0002 | c0003 | t0002 | g0114 | AFR | USA | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0281 | AFR | LWK | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| NA21309 | hp2 | a0001 | c0001 | t0016 | g0205 | AFR | LWK | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0100 | REF | REF | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0204 | REF | REF | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:38878197
|
C | T | 3 | a0007a0011a0012 | 6 | HG02809.hp2 HG03579.hp2 HG03704.hp1 others(3): Show |
missense_variant | MODERATE | c.119C>T | p.Ser40Leu | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/15 | 305/4060 | 119/1692 | 40/563 | chr4 | 38878197 | ||
| chr4:38878328
|
G | A | 7 | a0002a0004a0005others(4): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
missense_variant | MODERATE | c.250G>A | p.Gly84Arg | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/15 | 436/4060 | 250/1692 | 84/563 | chr4 | 38878328 | ||
| chr4:38878425
|
T | C | 7 | a0002a0004a0005others(4): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
missense_variant&splice_region_variant | MODERATE | c.347T>C | p.Leu116Pro | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/15 | 533/4060 | 347/1692 | 116/563 | chr4 | 38878425 | ||
| chr4:38891810
|
C | T | 1 | a0016 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.416C>T | p.Ser139Leu | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/15 | 602/4060 | 416/1692 | 139/563 | chr4 | 38891810 | ||
| chr4:38905522
|
G | T | 1 | a0015 | 1 | HG04115.hp2 | missense_variant&splice_region_variant | MODERATE | c.437G>T | p.Gly146Val | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 5/15 | 623/4060 | 437/1692 | 146/563 | chr4 | 38905522 | ||
| chr4:38905784
|
G | A | 1 | a0018 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.580G>A | p.Ala194Thr | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/15 | 766/4060 | 580/1692 | 194/563 | chr4 | 38905784 | ||
| chr4:38908695
|
C | T | 1 | a0017 | 1 | NA18953.hp2 | missense_variant | MODERATE | c.761C>T | p.Thr254Met | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/15 | 947/4060 | 761/1692 | 254/563 | chr4 | 38908695 | ||
| chr4:38922788
|
T | C | 1 | a0013 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.964T>C | p.Ser322Pro | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/15 | 1150/4060 | 964/1692 | 322/563 | chr4 | 38922788 | ||
| chr4:38929271
|
C | T | 1 | a0014 | 1 | NA18978.hp2 | missense_variant | MODERATE | c.1099C>T | p.Arg367Cys | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/15 | 1285/4060 | 1099/1692 | 367/563 | chr4 | 38929271 | ||
| chr4:38929272
|
G | A | 2 | a0006a0010 | 7 | HG01433.hp1 HG01975.hp2 HG01993.hp2 others(4): Show |
missense_variant | MODERATE | c.1100G>A | p.Arg367His | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/15 | 1286/4060 | 1100/1692 | 367/563 | chr4 | 38929272 | ||
| chr4:38931493
|
G | A | 1 | a0009 | 2 | HG03139.hp1 NA19240.hp2 |
missense_variant | MODERATE | c.1204G>A | p.Val402Met | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 11/15 | 1390/4060 | 1204/1692 | 402/563 | chr4 | 38931493 | ||
| chr4:38932238
|
G | A | 5 | a0003a0004a0006others(2): Show | 26 | HG00323.hp2 HG00741.hp2 HG01069.hp1 others(23): Show |
missense_variant | MODERATE | c.1327G>A | p.Val443Ile | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/15 | 1513/4060 | 1327/1692 | 443/563 | chr4 | 38932238 | ||
| chr4:38932248
|
C | T | 3 | a0005a0008a0012 | 12 | HG02622.hp1 HG02622.hp2 HG02647.hp1 others(9): Show |
missense_variant | MODERATE | c.1337C>T | p.Ser446Leu | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/15 | 1523/4060 | 1337/1692 | 446/563 | chr4 | 38932248 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:38878099
|
C | T | 8 | a0002c0022a0002c0053a0002c0054others(5): Show | 11 | HG01109.hp2 HG02145.hp1 HG02559.hp2 others(8): Show |
synonymous_variant | LOW | c.21C>T | p.Asp7Asp | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/15 | 207/4060 | 21/1692 | 7/563 | chr4 | 38878099 | ||
| chr4:38878315
|
G | A | 1 | a0001c0023 | 1 | NA19078.hp2 | synonymous_variant | LOW | c.237G>A | p.Glu79Glu | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/15 | 423/4060 | 237/1692 | 79/563 | chr4 | 38878315 | ||
| chr4:38891769
|
A | G | 1 | a0002c0034 | 1 | NA19060.hp2 | synonymous_variant | LOW | c.375A>G | p.Gly125Gly | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/15 | 561/4060 | 375/1692 | 125/563 | chr4 | 38891769 | ||
| chr4:38905535
|
G | A | 5 | a0002c0022a0002c0053a0002c0054others(2): Show | 8 | HG02559.hp2 HG02647.hp1 HG02717.hp1 others(5): Show |
synonymous_variant | LOW | c.450G>A | p.Thr150Thr | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 5/15 | 636/4060 | 450/1692 | 150/563 | chr4 | 38905535 | ||
| chr4:38905601
|
A | G | 2 | a0002c0032a0002c0057 | 2 | HG02145.hp1 HG02145.hp2 |
synonymous_variant | LOW | c.516A>G | p.Gly172Gly | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 5/15 | 702/4060 | 516/1692 | 172/563 | chr4 | 38905601 | ||
| chr4:38914989
|
G | A | 2 | a0001c0008a0001c0023 | 7 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(4): Show |
synonymous_variant | LOW | c.861G>A | p.Ala287Ala | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/15 | 1047/4060 | 861/1692 | 287/563 | chr4 | 38914989 | ||
| chr4:38915010
|
T | C | 17 | a0001c0004a0001c0013a0001c0037others(14): Show | 48 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(45): Show |
synonymous_variant | LOW | c.882T>C | p.Asp294Asp | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/15 | 1068/4060 | 882/1692 | 294/563 | chr4 | 38915010 | ||
| chr4:38915064
|
C | T | 1 | a0001c0046 | 1 | NA18941.hp1 | synonymous_variant | LOW | c.936C>T | p.Ser312Ser | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/15 | 1122/4060 | 936/1692 | 312/563 | chr4 | 38915064 | ||
| chr4:38929300
|
A | G | 4 | a0003c0020a0004c0007a0004c0018others(1): Show | 11 | HG00323.hp2 HG00741.hp2 HG01069.hp1 others(8): Show |
synonymous_variant | LOW | c.1128A>G | p.Leu376Leu | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/15 | 1314/4060 | 1128/1692 | 376/563 | chr4 | 38929300 | ||
| chr4:38932279
|
G | T | 8 | a0001c0038a0001c0039a0001c0043others(5): Show | 8 | HG01167.hp2 HG01243.hp1 HG01891.hp1 others(5): Show |
synonymous_variant | LOW | c.1368G>T | p.Ala456Ala | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/15 | 1554/4060 | 1368/1692 | 456/563 | chr4 | 38932279 | ||
| chr4:38935751
|
T | C | 45 | a0001c0001a0001c0004a0001c0008others(42): Show | 276 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(273): Show |
synonymous_variant | LOW | c.1497T>C | p.Ser499Ser | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/15 | 1683/4060 | 1497/1692 | 499/563 | chr4 | 38935751 | ||
| chr4:38943548
|
A | G | 15 | a0001c0005a0001c0009a0001c0037others(12): Show | 35 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(32): Show |
synonymous_variant | LOW | c.1683A>G | p.Ala561Ala | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1869/4060 | 1683/1692 | 561/563 | chr4 | 38943548 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:38943596
|
C | T | 13 | a0001c0001t0005a0001c0038t0005a0002c0003t0005others(10): Show | 26 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*39C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 39 | chr4 | 38943596 | |||||
| chr4:38943655
|
T | C | 1 | a0002c0003t0018 | 2 | NA18999.hp1 NA19066.hp1 |
3_prime_UTR_variant | MODIFIER | c.*98T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 98 | chr4 | 38943655 | |||||
| chr4:38943658
|
A | G | 1 | a0001c0001t0042 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*101A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 101 | chr4 | 38943658 | |||||
| chr4:38943842
|
G | C | 77 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(74): Show | 165 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(162): Show |
3_prime_UTR_variant | MODIFIER | c.*285G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 285 | chr4 | 38943842 | |||||
| chr4:38943883
|
A | C | 1 | a0001c0001t0041 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*326A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 326 | chr4 | 38943883 | |||||
| chr4:38943949
|
T | C | 1 | a0005c0012t0033 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*392T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 392 | chr4 | 38943949 | |||||
| chr4:38944001
|
G | A | 1 | a0001c0001t0042 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*444G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 444 | chr4 | 38944001 | |||||
| chr4:38944068
|
C | CT | 6 | a0001c0001t0013a0001c0002t0013a0001c0002t0028others(3): Show | 7 | HG00140.hp1 HG00741.hp1 HG02486.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*530dupT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 531 | INFO_REALIGN_3_PRIME | chr4 | 38944068 | ||||
| chr4:38944068
|
C | CTTTT | 35 | a0001c0001t0002a0001c0001t0005a0001c0001t0014others(32): Show | 123 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*527_*530dupTTTT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 531 | INFO_REALIGN_3_PRIME | chr4 | 38944068 | ||||
| chr4:38944068
|
C | CTTTTT | 7 | a0001c0001t0012a0001c0002t0040a0001c0039t0024others(4): Show | 10 | HG01891.hp1 HG02145.hp2 HG02148.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*526_*530dupTTTTT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 531 | INFO_REALIGN_3_PRIME | chr4 | 38944068 | ||||
| chr4:38944154
|
C | T | 1 | a0001c0001t0042 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*597C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 597 | chr4 | 38944154 | |||||
| chr4:38944213
|
T | C | 46 | a0001c0001t0002a0001c0001t0005a0001c0001t0012others(43): Show | 138 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*656T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 656 | chr4 | 38944213 | |||||
| chr4:38944225
|
C | T | 1 | a0001c0004t0039 | 1 | NA18993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*668C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 668 | chr4 | 38944225 | |||||
| chr4:38944317
|
G | A | 2 | a0001c0001t0016a0002c0003t0016 | 3 | HG00639.hp1 HG04228.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*760G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 760 | chr4 | 38944317 | |||||
| chr4:38944350
|
T | G | 2 | a0001c0002t0019a0017c0031t0019 | 2 | NA18953.hp2 NA19085.hp1 |
3_prime_UTR_variant | MODIFIER | c.*793T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 793 | chr4 | 38944350 | |||||
| chr4:38944359
|
C | T | 54 | a0001c0001t0004a0001c0001t0006a0001c0001t0008others(51): Show | 120 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*802C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 802 | chr4 | 38944359 | |||||
| chr4:38944366
|
G | A | 2 | a0001c0001t0042a0001c0004t0022 | 3 | HG02896.hp2 HG02897.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*809G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 809 | chr4 | 38944366 | |||||
| chr4:38944398
|
T | C | 45 | a0001c0001t0002a0001c0001t0005a0001c0001t0012others(42): Show | 137 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*841T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 841 | chr4 | 38944398 | |||||
| chr4:38944410
|
T | C | 1 | a0005c0012t0034 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*853T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 853 | chr4 | 38944410 | |||||
| chr4:38944432
|
G | A | 24 | a0001c0001t0005a0001c0001t0014a0001c0001t0042others(21): Show | 39 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*875G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 875 | chr4 | 38944432 | |||||
| chr4:38944520
|
C | T | 1 | a0002c0054t0036 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*963C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 963 | chr4 | 38944520 | |||||
| chr4:38944533
|
G | A | 44 | a0001c0001t0002a0001c0001t0005a0001c0001t0012others(41): Show | 136 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*976G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 976 | chr4 | 38944533 | |||||
| chr4:38944536
|
G | A | 2 | a0001c0001t0017a0002c0003t0017 | 3 | NA18941.hp2 NA19088.hp1 NA19090.hp1 |
3_prime_UTR_variant | MODIFIER | c.*979G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 979 | chr4 | 38944536 | |||||
| chr4:38944647
|
G | A | 54 | a0001c0001t0004a0001c0001t0006a0001c0001t0008others(51): Show | 120 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*1090G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1090 | chr4 | 38944647 | |||||
| chr4:38944651
|
C | T | 1 | a0001c0001t0027 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1094C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1094 | chr4 | 38944651 | |||||
| chr4:38944654
|
G | A | 7 | a0001c0001t0006a0001c0001t0027a0001c0002t0006others(4): Show | 22 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1097G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1097 | chr4 | 38944654 | |||||
| chr4:38944709
|
G | A | 2 | a0008c0014t0023a0013c0040t0023 | 2 | HG02257.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1152G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1152 | chr4 | 38944709 | |||||
| chr4:38944803
|
C | T | 1 | a0001c0001t0038 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1246C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1246 | chr4 | 38944803 | |||||
| chr4:38944804
|
G | A | 11 | a0001c0001t0006a0001c0001t0008a0001c0001t0027others(8): Show | 31 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1247G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1247 | chr4 | 38944804 | |||||
| chr4:38944827
|
C | T | 15 | a0001c0005t0003a0001c0009t0003a0001c0037t0003others(12): Show | 33 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1270C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1270 | chr4 | 38944827 | |||||
| chr4:38944844
|
GA | G | 54 | a0001c0001t0004a0001c0001t0006a0001c0001t0008others(51): Show | 120 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*1293delA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1293 | INFO_REALIGN_3_PRIME | chr4 | 38944844 | ||||
| chr4:38944860
|
A | G | 54 | a0001c0001t0004a0001c0001t0006a0001c0001t0008others(51): Show | 120 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*1303A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1303 | chr4 | 38944860 | |||||
| chr4:38944865
|
A | G | 45 | a0001c0001t0002a0001c0001t0005a0001c0001t0012others(42): Show | 137 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*1308A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1308 | chr4 | 38944865 | |||||
| chr4:38945070
|
A | T | 2 | a0001c0002t0020a0002c0034t0020 | 2 | HG00609.hp2 NA19060.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1513A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1513 | chr4 | 38945070 | |||||
| chr4:38945107
|
G | A | 1 | a0001c0001t0042 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1550G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1550 | chr4 | 38945107 | |||||
| chr4:38945116
|
G | A | 2 | a0001c0001t0042a0005c0012t0034 | 2 | HG03139.hp2 HG04199.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1559G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1559 | chr4 | 38945116 | |||||
| chr4:38945137
|
G | A | 4 | a0001c0001t0009a0004c0007t0009a0004c0007t0025others(1): Show | 8 | HG00741.hp2 HG01070.hp2 HG01109.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1580G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1580 | chr4 | 38945137 | |||||
| chr4:38945156
|
T | C | 1 | a0001c0001t0042 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1599T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1599 | chr4 | 38945156 | |||||
| chr4:38945173
|
C | T | 16 | a0001c0001t0026a0001c0005t0003a0001c0009t0003others(13): Show | 34 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1616C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1616 | chr4 | 38945173 | |||||
| chr4:38945175
|
G | C | 2 | a0001c0001t0015a0004c0007t0015 | 3 | HG00323.hp2 HG01074.hp2 HG01175.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1618G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1618 | chr4 | 38945175 | |||||
| chr4:38945203
|
C | T | 54 | a0001c0001t0004a0001c0001t0006a0001c0001t0008others(51): Show | 120 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*1646C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1646 | chr4 | 38945203 | |||||
| chr4:38945243
|
C | T | 1 | a0001c0001t0042 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1686C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1686 | chr4 | 38945243 | |||||
| chr4:38945267
|
G | C | 1 | a0001c0002t0037 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1710G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1710 | chr4 | 38945267 | |||||
| chr4:38945327
|
GC | G | 10 | a0001c0001t0009a0001c0001t0011a0001c0001t0015others(7): Show | 16 | HG00323.hp2 HG00741.hp2 HG01074.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1772delC | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1772 | INFO_REALIGN_3_PRIME | chr4 | 38945327 | ||||
| chr4:38945393
|
G | A | 10 | a0001c0001t0004a0001c0002t0020a0001c0002t0028others(7): Show | 30 | HG00140.hp2 HG00609.hp2 HG00741.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1836G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1836 | chr4 | 38945393 | |||||
| chr4:38945615
|
A | G | 2 | a0001c0039t0024a0001c0044t0024 | 2 | HG01891.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2058A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 2058 | chr4 | 38945615 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:38867901
|
C | A | 12 | a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0005g0005others(9): Show | 12 | HG01167.hp2 HG02486.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.-158+67C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 1/14 | chr4 | 38867901 | ||||||
| chr4:38867926
|
C | A | 4 | a0001c0001t0001g0019a0001c0001t0002g0016a0001c0001t0002g0017others(1): Show | 4 | HG02080.hp1 HG02135.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.-158+92C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 1/14 | chr4 | 38867926 | ||||||
| chr4:38867941
|
G | A | 19 | a0002c0003t0004g0024a0002c0003t0006g0037a0002c0003t0016g0035others(16): Show | 19 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.-158+107G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 1/14 | chr4 | 38867941 | ||||||
| chr4:38868144
|
TGCGTGAA others(35): Show |
T | 1 | a0002c0026t0005g0039 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-157-253_-157-212d others(44): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 1/14 | chr4 | 38868144 | ||||||
| chr4:38868288
|
G | A | 2 | a0001c0001t0001g0041a0001c0001t0002g0040 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-157-110G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 1/14 | chr4 | 38868288 | ||||||
| chr4:38868667
|
C | T | 2 | a0001c0002t0007g0365a0001c0002t0007g0366 | 2 | NA18962.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.-9+121C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38868667 | ||||||
| chr4:38868764
|
G | A | 5 | a0002c0003t0002g0043a0002c0003t0002g0045a0002c0003t0005g0042others(2): Show | 5 | HG02451.hp2 HG02723.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+218G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38868764 | ||||||
| chr4:38868850
|
C | T | 31 | a0002c0003t0001g0359a0002c0003t0002g0358a0002c0003t0004g0024others(28): Show | 31 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.-9+304C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38868850 | ||||||
| chr4:38868991
|
G | A | 1 | a0002c0006t0001g0020 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-9+445G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38868991 | ||||||
| chr4:38869209
|
G | A | 1 | a0003c0020t0003g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-9+663G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38869209 | ||||||
| chr4:38869241
|
A | G | 1 | a0002c0032t0044g0352 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-9+695A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38869241 | ||||||
| chr4:38869352
|
A | G | 1 | a0001c0002t0028g0351 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-9+806A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38869352 | ||||||
| chr4:38869420
|
A | T | 1 | a0002c0026t0005g0039 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-9+874A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38869420 | ||||||
| chr4:38869596
|
C | T | 1 | a0001c0002t0001g0350 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-9+1050C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38869596 | ||||||
| chr4:38869695
|
C | T | 1 | a0001c0004t0002g0349 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-9+1149C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38869695 | ||||||
| chr4:38869713
|
G | GT | 5 | a0007c0021t0004g0347a0007c0048t0008g0346a0007c0049t0002g0348others(2): Show | 5 | HG02809.hp2 HG03579.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+1172dupT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 38869713 | |||||
| chr4:38869719
|
G | T | 11 | a0002c0003t0004g0342a0002c0003t0005g0339a0002c0003t0005g0343others(8): Show | 11 | HG02280.hp1 HG02280.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-9+1173G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38869719 | ||||||
| chr4:38869725
|
T | G | 1 | a0001c0001t0002g0047 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-9+1179T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38869725 | ||||||
| chr4:38869764
|
T | C | 72 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0099others(69): Show | 77 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.-9+1218T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38869764 | ||||||
| chr4:38869798
|
A | T | 1 | a0002c0006t0010g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-9+1252A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38869798 | ||||||
| chr4:38869805
|
T | A | 5 | a0002c0003t0002g0114a0002c0003t0012g0112a0002c0029t0043g0115others(2): Show | 5 | HG01243.hp1 HG02027.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+1259T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38869805 | ||||||
| chr4:38869806
|
T | A | 62 | a0001c0002t0007g0365a0001c0002t0007g0366a0002c0003t0001g0120others(59): Show | 62 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.-9+1260T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38869806 | ||||||
| chr4:38869901
|
C | T | 1 | a0003c0020t0003g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-9+1355C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38869901 | ||||||
| chr4:38869904
|
T | C | 2 | a0002c0003t0005g0339a0002c0003t0010g0338 | 2 | HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-9+1358T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38869904 | ||||||
| chr4:38870015
|
C | A | 1 | a0002c0003t0007g0117 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-9+1469C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38870015 | ||||||
| chr4:38870047
|
G | A | 36 | a0002c0003t0001g0359a0002c0003t0002g0114a0002c0003t0002g0358others(33): Show | 36 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.-9+1501G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38870047 | ||||||
| chr4:38870086
|
A | T | 2 | a0002c0003t0005g0364a0002c0028t0030g0363 | 2 | HG01891.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-9+1540A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38870086 | ||||||
| chr4:38870162
|
C | T | 87 | a0001c0001t0001g0041a0001c0001t0001g0264a0001c0001t0001g0275others(84): Show | 88 | HG00438.hp2 HG00642.hp2 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.-9+1616C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38870162 | ||||||
| chr4:38870276
|
C | T | 23 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(20): Show | 23 | HG00621.hp1 HG01257.hp2 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.-9+1730C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38870276 | ||||||
| chr4:38870498
|
C | G | 2 | a0001c0001t0004g0253a0001c0001t0004g0254 | 2 | HG01261.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-9+1952C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38870498 | ||||||
| chr4:38870514
|
G | A | 2 | a0001c0001t0007g0256a0001c0004t0011g0255 | 2 | HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-9+1968G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38870514 | ||||||
| chr4:38870546
|
G | A | 2 | a0001c0001t0004g0257a0002c0026t0005g0039 | 2 | HG03195.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-9+2000G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38870546 | ||||||
| chr4:38870562
|
C | T | 1 | a0001c0001t0002g0336 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-9+2016C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38870562 | ||||||
| chr4:38870592
|
C | T | 53 | a0002c0003t0001g0359a0002c0003t0002g0114a0002c0003t0002g0358others(50): Show | 53 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.-9+2046C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38870592 | ||||||
| chr4:38870648
|
T | G | 1 | a0001c0004t0006g0258 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-9+2102T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38870648 | ||||||
| chr4:38870744
|
A | G | 36 | a0002c0003t0001g0359a0002c0003t0002g0114a0002c0003t0002g0358others(33): Show | 36 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.-9+2198A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38870744 | ||||||
| chr4:38870758
|
C | T | 1 | a0001c0002t0001g0242 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-9+2212C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38870758 | ||||||
| chr4:38870926
|
G | A | 2 | a0001c0001t0010g0259a0001c0004t0001g0260 | 2 | HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-9+2380G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38870926 | ||||||
| chr4:38870971
|
G | A | 47 | a0002c0003t0001g0359a0002c0003t0002g0114a0002c0003t0002g0358others(44): Show | 47 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.-9+2425G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38870971 | ||||||
| chr4:38870991
|
A | C | 5 | a0002c0003t0004g0342a0002c0003t0005g0339a0002c0003t0005g0343others(2): Show | 5 | HG02280.hp1 HG02280.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+2445A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38870991 | ||||||
| chr4:38871086
|
C | CT | 12 | a0001c0001t0002g0238a0001c0001t0002g0241a0001c0001t0005g0231others(9): Show | 12 | HG00140.hp1 HG00609.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.-9+2561dupT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 38871086 | |||||
| chr4:38871086
|
CT | C | 50 | a0001c0001t0001g0019a0001c0001t0002g0106a0001c0001t0002g0325others(47): Show | 50 | HG00408.hp1 HG00597.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.-9+2561delT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 38871086 | |||||
| chr4:38871086
|
CTT | C | 191 | a0001c0001t0001g0041a0001c0001t0001g0050a0001c0001t0001g0099others(188): Show | 197 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.-9+2560_-9+2561del others(2): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 38871086 | |||||
| chr4:38871086
|
CTTT | C | 10 | a0001c0001t0004g0262a0001c0039t0024g0261a0002c0003t0004g0342others(7): Show | 10 | HG01255.hp2 HG02109.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-9+2559_-9+2561del others(3): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 38871086 | |||||
| chr4:38871092
|
T | C | 1 | a0001c0004t0008g0048 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-9+2546T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38871092 | ||||||
| chr4:38871168
|
T | C | 23 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(20): Show | 23 | HG00621.hp1 HG01257.hp2 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.-9+2622T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38871168 | ||||||
| chr4:38871194
|
A | G | 2 | a0001c0001t0007g0256a0001c0004t0011g0255 | 2 | HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-9+2648A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38871194 | ||||||
| chr4:38871535
|
A | G | 1 | a0001c0001t0012g0334 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-9+2989A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38871535 | ||||||
| chr4:38871604
|
G | A | 1 | a0002c0028t0030g0363 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-9+3058G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38871604 | ||||||
| chr4:38871711
|
C | T | 68 | a0001c0001t0001g0050a0001c0001t0001g0099a0001c0001t0001g0100others(65): Show | 73 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.-9+3165C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38871711 | ||||||
| chr4:38871870
|
G | A | 5 | a0002c0003t0002g0114a0002c0003t0012g0112a0002c0029t0043g0115others(2): Show | 5 | HG01243.hp1 HG02027.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+3324G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38871870 | ||||||
| chr4:38871878
|
G | T | 1 | a0002c0006t0001g0038 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-9+3332G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38871878 | ||||||
| chr4:38872096
|
T | C | 14 | a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0004g0253others(11): Show | 14 | HG01167.hp2 HG01261.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-9+3550T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38872096 | ||||||
| chr4:38872175
|
T | A | 67 | a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0004g0253others(64): Show | 67 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.-9+3629T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38872175 | ||||||
| chr4:38872190
|
T | C | 87 | a0001c0001t0001g0041a0001c0001t0001g0264a0001c0001t0001g0275others(84): Show | 88 | HG00438.hp2 HG00642.hp2 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.-9+3644T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38872190 | ||||||
| chr4:38872272
|
C | G | 1 | a0002c0003t0005g0343 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-9+3726C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38872272 | ||||||
| chr4:38872377
|
T | C | 67 | a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0004g0253others(64): Show | 67 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.-9+3831T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38872377 | ||||||
| chr4:38872558
|
G | A | 1 | a0001c0001t0002g0263 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-9+4012G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38872558 | ||||||
| chr4:38872677
|
T | C | 1 | a0002c0006t0010g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-9+4131T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38872677 | ||||||
| chr4:38872683
|
A | G | 3 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0241 | 3 | HG00558.hp1 HG00673.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.-9+4137A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38872683 | ||||||
| chr4:38872746
|
T | C | 1 | a0001c0001t0002g0049 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-9+4200T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38872746 | ||||||
| chr4:38872866
|
T | A | 30 | a0002c0003t0001g0359a0002c0003t0002g0358a0002c0003t0004g0024others(27): Show | 30 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.-9+4320T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38872866 | ||||||
| chr4:38873005
|
A | G | 1 | a0010c0017t0003g0134 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-9+4459A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38873005 | ||||||
| chr4:38873014
|
T | A | 1 | a0002c0003t0018g0119 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-9+4468T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38873014 | ||||||
| chr4:38873016
|
A | G | 53 | a0002c0003t0001g0359a0002c0003t0002g0114a0002c0003t0002g0358others(50): Show | 53 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.-9+4470A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38873016 | ||||||
| chr4:38873024
|
C | T | 53 | a0002c0003t0001g0359a0002c0003t0002g0114a0002c0003t0002g0358others(50): Show | 53 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.-9+4478C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38873024 | ||||||
| chr4:38873181
|
A | G | 67 | a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0004g0253others(64): Show | 67 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.-9+4635A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38873181 | ||||||
| chr4:38873275
|
A | G | 1 | a0001c0001t0012g0333 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-9+4729A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38873275 | ||||||
| chr4:38873307
|
T | C | 1 | a0001c0001t0001g0264 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-9+4761T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38873307 | ||||||
| chr4:38873344
|
C | T | 23 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(20): Show | 23 | HG00621.hp1 HG01257.hp2 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.-8-4727C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38873344 | ||||||
| chr4:38873440
|
C | A | 1 | a0002c0003t0012g0112 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-8-4631C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38873440 | ||||||
| chr4:38873471
|
T | C | 1 | a0003c0020t0003g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-8-4600T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38873471 | ||||||
| chr4:38873518
|
A | G | 90 | a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0004g0253others(87): Show | 90 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.-8-4553A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38873518 | ||||||
| chr4:38873646
|
G | C | 1 | a0001c0002t0001g0137 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-8-4425G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38873646 | ||||||
| chr4:38873694
|
T | C | 76 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-4377T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38873694 | ||||||
| chr4:38873772
|
G | T | 24 | a0002c0003t0001g0359a0002c0003t0002g0358a0002c0003t0004g0024others(21): Show | 24 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.-8-4299G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38873772 | ||||||
| chr4:38873912
|
C | T | 1 | a0003c0020t0003g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-8-4159C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38873912 | ||||||
| chr4:38874075
|
T | G | 76 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-3996T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874075 | ||||||
| chr4:38874076
|
G | A | 11 | a0002c0022t0005g0249a0002c0022t0010g0248a0002c0053t0001g0245others(8): Show | 11 | HG01109.hp2 HG02145.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8-3995G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874076 | ||||||
| chr4:38874092
|
G | T | 2 | a0001c0001t0016g0322a0001c0005t0003g0323 | 2 | HG02602.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-8-3979G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874092 | ||||||
| chr4:38874116
|
C | T | 53 | a0002c0003t0001g0359a0002c0003t0002g0114a0002c0003t0002g0358others(50): Show | 53 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.-8-3955C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874116 | ||||||
| chr4:38874176
|
A | G | 76 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-3895A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874176 | ||||||
| chr4:38874247
|
A | G | 76 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-3824A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874247 | ||||||
| chr4:38874276
|
G | A | 1 | a0012c0051t0005g0344 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-8-3795G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874276 | ||||||
| chr4:38874288
|
T | C | 6 | a0002c0003t0004g0342a0002c0003t0005g0339a0002c0003t0005g0343others(3): Show | 6 | HG02145.hp2 HG02280.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-3783T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874288 | ||||||
| chr4:38874290
|
A | T | 1 | a0009c0019t0001g0321 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-8-3781A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874290 | ||||||
| chr4:38874329
|
G | A | 6 | a0002c0003t0004g0342a0002c0003t0005g0339a0002c0003t0005g0343others(3): Show | 6 | HG02145.hp2 HG02280.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-3742G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874329 | ||||||
| chr4:38874438
|
A | G | 1 | a0004c0024t0001g0116 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-8-3633A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874438 | ||||||
| chr4:38874514
|
T | C | 1 | a0001c0002t0001g0265 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-8-3557T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874514 | ||||||
| chr4:38874612
|
A | G | 76 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-3459A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874612 | ||||||
| chr4:38874646
|
C | A | 47 | a0002c0003t0001g0359a0002c0003t0002g0114a0002c0003t0002g0358others(44): Show | 47 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.-8-3425C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874646 | ||||||
| chr4:38874715
|
G | T | 1 | a0001c0001t0007g0227 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-8-3356G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874715 | ||||||
| chr4:38874745
|
C | T | 1 | a0002c0032t0044g0352 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-8-3326C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874745 | ||||||
| chr4:38874746
|
G | T | 1 | a0001c0002t0001g0103 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-8-3325G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874746 | ||||||
| chr4:38874769
|
T | G | 76 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-3302T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874769 | ||||||
| chr4:38874771
|
T | C | 46 | a0002c0003t0001g0359a0002c0003t0002g0114a0002c0003t0002g0358others(43): Show | 46 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.-8-3300T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874771 | ||||||
| chr4:38874839
|
T | C | 3 | a0002c0003t0004g0342a0002c0003t0005g0343a0005c0012t0033g0341 | 3 | HG02280.hp2 HG02622.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-8-3232T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874839 | ||||||
| chr4:38874988
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-8-3083T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874988 | ||||||
| chr4:38875186
|
A | C | 14 | a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0004g0253others(11): Show | 14 | HG01167.hp2 HG01261.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8-2885A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38875186 | ||||||
| chr4:38875188
|
TA | T | 76 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-2882delA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38875188 | ||||||
| chr4:38875202
|
T | G | 46 | a0002c0003t0001g0359a0002c0003t0002g0114a0002c0003t0002g0358others(43): Show | 46 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.-8-2869T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38875202 | ||||||
| chr4:38875205
|
A | G | 14 | a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0004g0253others(11): Show | 14 | HG01167.hp2 HG01261.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8-2866A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38875205 | ||||||
| chr4:38875218
|
T | C | 4 | a0001c0001t0017g0138a0001c0002t0002g0139a0001c0002t0002g0141others(1): Show | 4 | HG00408.hp2 HG04184.hp1 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-2853T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38875218 | ||||||
| chr4:38875319
|
T | C | 1 | a0001c0001t0004g0257 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-8-2752T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38875319 | ||||||
| chr4:38875376
|
G | A | 4 | a0001c0001t0001g0019a0001c0001t0002g0016a0001c0001t0002g0017others(1): Show | 4 | HG02080.hp1 HG02135.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-2695G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38875376 | ||||||
| chr4:38875432
|
A | G | 5 | a0002c0003t0004g0342a0002c0003t0005g0339a0002c0003t0005g0343others(2): Show | 5 | HG02280.hp1 HG02280.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-2639A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38875432 | ||||||
| chr4:38875463
|
C | T | 1 | a0001c0044t0024g0226 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-8-2608C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38875463 | ||||||
| chr4:38875464
|
G | C | 76 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-2607G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38875464 | ||||||
| chr4:38875635
|
C | T | 76 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-2436C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38875635 | ||||||
| chr4:38875651
|
G | T | 1 | a0001c0001t0002g0102 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-8-2420G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38875651 | ||||||
| chr4:38875724
|
C | T | 1 | a0001c0009t0010g0332 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-8-2347C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38875724 | ||||||
| chr4:38875836
|
T | C | 53 | a0002c0003t0001g0359a0002c0003t0002g0114a0002c0003t0002g0358others(50): Show | 53 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.-8-2235T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38875836 | ||||||
| chr4:38875850
|
A | G | 1 | a0003c0020t0003g0101 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-8-2221A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38875850 | ||||||
| chr4:38875874
|
G | A | 6 | a0002c0003t0002g0114a0002c0003t0012g0112a0002c0006t0010g0337others(3): Show | 6 | HG01243.hp1 HG02027.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8-2197G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38875874 | ||||||
| chr4:38875881
|
C | G | 1 | a0001c0001t0013g0225 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-8-2190C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38875881 | ||||||
| chr4:38876061
|
G | A | 76 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-2010G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876061 | ||||||
| chr4:38876099
|
T | C | 76 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-1972T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876099 | ||||||
| chr4:38876103
|
A | G | 76 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-1968A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876103 | ||||||
| chr4:38876122
|
AT | A | 169 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0099others(166): Show | 174 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.-8-1941delT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 38876122 | |||||
| chr4:38876156
|
CT | C | 23 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(20): Show | 23 | HG00621.hp1 HG01257.hp2 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.-8-1913delT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 38876156 | |||||
| chr4:38876159
|
ATTCTTTT | A | 43 | a0001c0001t0001g0041a0001c0001t0001g0296a0001c0001t0001g0314others(40): Show | 43 | HG00673.hp1 HG01943.hp1 HG01943.hp2 others(40): Show |
intron_variant | MODIFIER | c.-8-1902_-8-1896del others(7): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 38876159 | |||||
| chr4:38876166
|
TTTC | T | 26 | a0002c0003t0001g0120a0002c0003t0001g0359a0002c0003t0002g0358others(23): Show | 26 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.-8-1902_-8-1900del others(3): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 38876166 | |||||
| chr4:38876167
|
TTC | T | 34 | a0002c0003t0001g0122a0002c0003t0001g0126a0002c0003t0001g0127others(31): Show | 34 | HG00621.hp1 HG01109.hp2 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.-8-1902_-8-1901del others(2): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 38876167 | |||||
| chr4:38876168
|
TC | T | 7 | a0002c0003t0002g0114a0002c0003t0002g0130a0002c0003t0004g0118others(4): Show | 7 | HG01243.hp1 HG01978.hp1 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-1902delC | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876168 | ||||||
| chr4:38876169
|
C | CT | 22 | a0001c0001t0001g0019a0001c0001t0001g0099a0001c0001t0001g0100others(19): Show | 22 | HG00438.hp1 HG00642.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.-8-1882dupT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 38876169 | |||||
| chr4:38876169
|
C | T | 7 | a0002c0003t0004g0342a0002c0003t0005g0339a0002c0003t0005g0343others(4): Show | 7 | HG02145.hp2 HG02280.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-1902C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876169 | ||||||
| chr4:38876169
|
CT | C | 24 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0001t0002g0146others(21): Show | 24 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.-8-1882delT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 38876169 | |||||
| chr4:38876173
|
T | C | 3 | a0001c0001t0005g0005a0001c0004t0002g0004a0001c0043t0001g0006 | 3 | HG01167.hp2 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-8-1898T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876173 | ||||||
| chr4:38876195
|
G | A | 76 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-1876G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876195 | ||||||
| chr4:38876208
|
C | T | 10 | a0001c0001t0002g0013a0001c0001t0005g0005a0001c0001t0005g0014others(7): Show | 10 | HG01167.hp2 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8-1863C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876208 | ||||||
| chr4:38876257
|
C | T | 4 | a0002c0003t0001g0359a0002c0003t0005g0360a0002c0003t0010g0362others(1): Show | 4 | HG02809.hp1 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-1814C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876257 | ||||||
| chr4:38876450
|
T | C | 76 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-1621T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876450 | ||||||
| chr4:38876451
|
G | A | 76 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-1620G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876451 | ||||||
| chr4:38876459
|
T | C | 76 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-1612T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876459 | ||||||
| chr4:38876460
|
T | C | 84 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(81): Show | 84 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.-8-1611T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876460 | ||||||
| chr4:38876461
|
G | A | 76 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-1610G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876461 | ||||||
| chr4:38876462
|
C | T | 76 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-1609C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876462 | ||||||
| chr4:38876463
|
A | G | 76 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-1608A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876463 | ||||||
| chr4:38876466
|
C | A | 76 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-1605C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876466 | ||||||
| chr4:38876467
|
T | G | 76 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-1604T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876467 | ||||||
| chr4:38876473
|
C | A | 76 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-1598C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876473 | ||||||
| chr4:38876531
|
T | C | 2 | a0001c0001t0006g0148a0001c0001t0006g0149 | 2 | NA18945.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.-8-1540T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876531 | ||||||
| chr4:38876573
|
T | C | 169 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0099others(166): Show | 174 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.-8-1498T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876573 | ||||||
| chr4:38876591
|
C | T | 1 | a0001c0001t0005g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-8-1480C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876591 | ||||||
| chr4:38876598
|
A | C | 1 | a0001c0002t0028g0351 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-8-1473A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876598 | ||||||
| chr4:38876671
|
G | A | 1 | a0001c0037t0003g0007 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-8-1400G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876671 | ||||||
| chr4:38876766
|
A | G | 76 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-1305A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876766 | ||||||
| chr4:38876859
|
T | C | 76 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-1212T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876859 | ||||||
| chr4:38876873
|
G | A | 23 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(20): Show | 23 | HG00621.hp1 HG01257.hp2 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.-8-1198G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876873 | ||||||
| chr4:38877076
|
C | T | 23 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(20): Show | 23 | HG00621.hp1 HG01257.hp2 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.-8-995C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38877076 | ||||||
| chr4:38877101
|
G | A | 1 | a0002c0003t0005g0042 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-8-970G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38877101 | ||||||
| chr4:38877132
|
C | A | 10 | a0001c0001t0002g0013a0001c0001t0005g0005a0001c0001t0005g0014others(7): Show | 10 | HG01167.hp2 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8-939C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38877132 | ||||||
| chr4:38877189
|
A | G | 1 | a0001c0001t0002g0013 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-8-882A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38877189 | ||||||
| chr4:38877263
|
G | A | 76 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-808G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38877263 | ||||||
| chr4:38877362
|
A | C | 47 | a0002c0003t0001g0359a0002c0003t0002g0114a0002c0003t0002g0358others(44): Show | 47 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.-8-709A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38877362 | ||||||
| chr4:38877382
|
A | C | 4 | a0001c0001t0001g0019a0001c0001t0002g0016a0001c0001t0002g0017others(1): Show | 4 | HG02080.hp1 HG02135.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-689A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38877382 | ||||||
| chr4:38877457
|
A | T | 1 | a0002c0006t0010g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-8-614A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38877457 | ||||||
| chr4:38877487
|
A | G | 4 | a0007c0021t0004g0347a0007c0021t0013g0340a0007c0048t0008g0346others(1): Show | 4 | HG03704.hp1 HG03834.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-584A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38877487 | ||||||
| chr4:38877531
|
G | A | 1 | a0001c0009t0010g0332 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-8-540G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38877531 | ||||||
| chr4:38877665
|
TA | T | 47 | a0002c0003t0001g0359a0002c0003t0002g0114a0002c0003t0002g0358others(44): Show | 47 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.-8-398delA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 38877665 | |||||
| chr4:38877691
|
G | A | 76 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-380G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38877691 | ||||||
| chr4:38877763
|
G | A | 2 | a0007c0021t0004g0347a0007c0048t0008g0346 | 2 | NA18950.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.-8-308G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38877763 | ||||||
| chr4:38877827
|
C | G | 76 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-244C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38877827 | ||||||
| chr4:38877878
|
C | T | 6 | a0007c0021t0004g0347a0007c0021t0013g0340a0007c0048t0008g0346others(3): Show | 6 | HG02809.hp2 HG03579.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8-193C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38877878 | ||||||
| chr4:38877879
|
G | A | 76 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-192G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38877879 | ||||||
| chr4:38877896
|
G | A | 2 | a0002c0003t0005g0339a0002c0003t0010g0338 | 2 | HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-8-175G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38877896 | ||||||
| chr4:38877919
|
A | G | 76 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-152A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38877919 | ||||||
| chr4:38877960
|
G | A | 76 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-111G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38877960 | ||||||
| chr4:38877964
|
C | CA | 132 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(129): Show | 137 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.-8-92dupA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 38877964 | |||||
| chr4:38877964
|
C | CAA | 12 | a0001c0001t0002g0016a0001c0004t0001g0072a0002c0003t0004g0342others(9): Show | 12 | HG01069.hp1 HG01255.hp2 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.-8-93_-8-92dupAA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 38877964 | |||||
| chr4:38877964
|
C | CAAA | 60 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(57): Show | 60 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.-8-94_-8-92dupAAA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 38877964 | |||||
| chr4:38877964
|
C | CAAAA | 6 | a0002c0003t0001g0359a0002c0003t0005g0360a0002c0003t0010g0338others(3): Show | 6 | HG02145.hp2 HG02148.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-95_-8-92dupAAAA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 38877964 | |||||
| chr4:38877978
|
AAG | A | 6 | a0007c0021t0004g0347a0007c0021t0013g0340a0007c0048t0008g0346others(3): Show | 6 | HG02809.hp2 HG03579.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8-92_-8-91delAG | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38877978 | ||||||
| chr4:38878034
|
C | T | 76 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-37C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38878034 | ||||||
| chr4:38878468
|
C | T | 1 | a0001c0004t0008g0098 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.348+42C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38878468 | ||||||
| chr4:38878507
|
G | A | 1 | a0001c0039t0024g0261 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.348+81G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38878507 | ||||||
| chr4:38878515
|
A | T | 76 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.348+89A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38878515 | ||||||
| chr4:38878546
|
C | T | 76 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.348+120C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38878546 | ||||||
| chr4:38878560
|
A | ATGTGT | 76 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.348+135_348+139dup others(5): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38878560 | |||||
| chr4:38878692
|
C | A | 169 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0099others(166): Show | 174 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.348+266C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38878692 | ||||||
| chr4:38878763
|
A | G | 76 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.348+337A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38878763 | ||||||
| chr4:38878879
|
C | A | 1 | a0001c0001t0002g0065 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.348+453C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38878879 | ||||||
| chr4:38878957
|
G | C | 2 | a0001c0004t0001g0072a0001c0004t0004g0073 | 2 | NA18960.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.348+531G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38878957 | ||||||
| chr4:38878977
|
C | T | 1 | a0002c0006t0010g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.348+551C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38878977 | ||||||
| chr4:38879172
|
T | G | 76 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.348+746T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38879172 | ||||||
| chr4:38879274
|
C | A | 6 | a0007c0021t0004g0347a0007c0021t0013g0340a0007c0048t0008g0346others(3): Show | 6 | HG02809.hp2 HG03579.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.348+848C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38879274 | ||||||
| chr4:38879365
|
C | T | 1 | a0002c0003t0007g0117 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.348+939C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38879365 | ||||||
| chr4:38879541
|
A | T | 76 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.348+1115A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38879541 | ||||||
| chr4:38879561
|
C | T | 1 | a0002c0003t0002g0358 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.348+1135C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38879561 | ||||||
| chr4:38879567
|
G | A | 76 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.348+1141G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38879567 | ||||||
| chr4:38879590
|
G | A | 4 | a0001c0001t0001g0019a0001c0001t0002g0016a0001c0001t0002g0017others(1): Show | 4 | HG02080.hp1 HG02135.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+1164G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38879590 | ||||||
| chr4:38879607
|
G | T | 1 | a0001c0004t0007g0331 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.348+1181G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38879607 | ||||||
| chr4:38879608
|
C | T | 1 | a0001c0004t0007g0331 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.348+1182C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38879608 | ||||||
| chr4:38879623
|
C | T | 82 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(79): Show | 82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+1197C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38879623 | ||||||
| chr4:38879644
|
A | AGCCC | 82 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(79): Show | 82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+1220_348+1221i others(6): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38879644 | |||||
| chr4:38879723
|
TA | T | 82 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(79): Show | 82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+1299delA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38879723 | |||||
| chr4:38879742
|
T | G | 82 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(79): Show | 82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+1316T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38879742 | ||||||
| chr4:38879758
|
G | C | 4 | a0007c0021t0004g0347a0007c0021t0013g0340a0007c0048t0008g0346others(1): Show | 4 | HG03704.hp1 HG03834.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.348+1332G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38879758 | ||||||
| chr4:38879793
|
T | C | 68 | a0001c0001t0001g0050a0001c0001t0001g0099a0001c0001t0001g0100others(65): Show | 73 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.348+1367T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38879793 | ||||||
| chr4:38879801
|
G | A | 82 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(79): Show | 82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+1375G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38879801 | ||||||
| chr4:38879884
|
T | C | 82 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(79): Show | 82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+1458T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38879884 | ||||||
| chr4:38879904
|
C | T | 1 | a0002c0032t0044g0352 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.348+1478C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38879904 | ||||||
| chr4:38879921
|
T | G | 3 | a0001c0001t0009g0153a0001c0001t0009g0154a0015c0047t0009g0155 | 3 | HG01109.hp1 HG02602.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.348+1495T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38879921 | ||||||
| chr4:38880074
|
TAAATA | T | 10 | a0002c0003t0001g0359a0002c0006t0001g0353a0002c0006t0011g0028others(7): Show | 10 | HG01255.hp2 HG02698.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.348+1674_348+1678d others(7): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880074 | |||||
| chr4:38880074
|
TAAATAAA others(3): Show |
T | 80 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0099others(77): Show | 85 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.348+1669_348+1678d others(12): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880074 | |||||
| chr4:38880085
|
A | AAATAGAG others(3): Show |
2 | a0004c0007t0025g0036a0018c0052t0005g0247 | 2 | HG01070.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.348+1663_348+1664i others(12): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880085 | |||||
| chr4:38880085
|
A | AAATAGAG others(13): Show |
3 | a0002c0003t0012g0112a0002c0003t0032g0357a0005c0055t0012g0356 | 3 | HG02818.hp1 HG02922.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.348+1663_348+1664i others(22): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880085 | |||||
| chr4:38880085
|
AAATAAAA others(18): Show |
A | 1 | a0002c0028t0030g0363 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.348+1664_348+1688d others(27): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880085 | |||||
| chr4:38880087
|
A | ATAGAG | 13 | a0002c0003t0005g0360a0002c0003t0016g0035a0002c0006t0001g0021others(10): Show | 13 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.348+1663_348+1664i others(7): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880087 | |||||
| chr4:38880087
|
A | ATAGAGTA others(8): Show |
5 | a0002c0003t0006g0037a0002c0003t0010g0362a0002c0006t0010g0337others(2): Show | 5 | HG00544.hp2 HG01109.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.348+1663_348+1664i others(17): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880087 | |||||
| chr4:38880087
|
ATAAAATA others(13): Show |
A | 2 | a0002c0003t0004g0024a0002c0003t0005g0364 | 2 | HG00140.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.348+1664_348+1683d others(22): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880087 | |||||
| chr4:38880090
|
A | G | 32 | a0002c0003t0002g0114a0002c0003t0005g0355a0002c0003t0005g0360others(29): Show | 32 | HG00323.hp2 HG00544.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.348+1664A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880090 | ||||||
| chr4:38880092
|
A | G | 12 | a0002c0003t0002g0114a0002c0003t0005g0355a0002c0022t0005g0249others(9): Show | 12 | HG01070.hp2 HG01243.hp1 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.348+1666A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880092 | ||||||
| chr4:38880095
|
A | AAATAGAG others(13): Show |
4 | a0002c0003t0001g0127a0002c0003t0002g0130a0002c0003t0007g0117others(1): Show | 4 | HG01257.hp2 HG01978.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.348+1673_348+1674i others(22): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880095 | |||||
| chr4:38880095
|
A | AAATAGAG others(18): Show |
1 | a0002c0003t0004g0118 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.348+1673_348+1674i others(27): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880095 | |||||
| chr4:38880095
|
A | AAATAGAG others(23): Show |
1 | a0002c0003t0005g0339 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.348+1673_348+1674i others(32): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880095 | |||||
| chr4:38880095
|
A | AAATAGAG others(33): Show |
3 | a0002c0003t0004g0129a0002c0003t0018g0119a0002c0003t0018g0128 | 3 | NA18978.hp1 NA18999.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.348+1673_348+1674i others(42): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880095 | |||||
| chr4:38880095
|
A | AAATAGAG others(58): Show |
3 | a0002c0003t0002g0043a0002c0003t0005g0042a0002c0003t0005g0044 | 3 | HG02451.hp2 HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.348+1673_348+1674i others(67): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880095 | |||||
| chr4:38880095
|
A | AAATAGAG others(68): Show |
1 | a0002c0026t0005g0039 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.348+1673_348+1674i others(77): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880095 | |||||
| chr4:38880095
|
A | AAATAGAG others(68): Show |
1 | a0002c0003t0002g0045 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.348+1673_348+1674i others(77): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880095 | |||||
| chr4:38880095
|
A | G | 35 | a0002c0003t0001g0359a0002c0003t0002g0114a0002c0003t0005g0355others(32): Show | 35 | HG00323.hp2 HG00544.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.348+1669A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880095 | ||||||
| chr4:38880097
|
A | ATAGAG | 6 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0131others(3): Show | 6 | HG00621.hp1 HG02148.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.348+1673_348+1674i others(7): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880097 | |||||
| chr4:38880097
|
A | ATAGAGTA others(8): Show |
5 | a0002c0003t0001g0126a0002c0003t0017g0132a0002c0034t0020g0133others(2): Show | 5 | HG01975.hp2 HG02273.hp1 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.348+1673_348+1674i others(17): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880097 | |||||
| chr4:38880097
|
A | ATAGAGTA others(3): Show |
1 | a0002c0022t0010g0248 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.348+1673_348+1674i others(12): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880097 | |||||
| chr4:38880097
|
A | G | 17 | a0002c0003t0001g0359a0002c0003t0005g0360a0002c0003t0016g0035others(14): Show | 17 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.348+1671A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880097 | ||||||
| chr4:38880097
|
ATAAAATA others(3): Show |
A | 4 | a0002c0003t0004g0342a0002c0003t0005g0343a0002c0032t0044g0352others(1): Show | 4 | HG02145.hp2 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+1674_348+1683d others(12): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880097 | |||||
| chr4:38880100
|
A | G | 69 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(66): Show | 69 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.348+1674A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880100 | ||||||
| chr4:38880102
|
A | G | 19 | a0002c0003t0002g0114a0002c0003t0002g0358a0002c0003t0005g0042others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.348+1676A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880102 | ||||||
| chr4:38880107
|
G | A | 57 | a0002c0003t0001g0126a0002c0003t0001g0127a0002c0003t0002g0045others(54): Show | 57 | HG00323.hp2 HG00544.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.348+1681G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880107 | ||||||
| chr4:38880107
|
G | GTAGAA | 29 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0223others(26): Show | 29 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.348+1747_348+1751d others(7): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880107 | |||||
| chr4:38880107
|
G | GTAGAATA others(3): Show |
17 | a0001c0001t0001g0314a0001c0001t0002g0287a0001c0001t0002g0313others(14): Show | 17 | HG00438.hp2 HG00642.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.348+1742_348+1751d others(12): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880107 | |||||
| chr4:38880107
|
G | GTAGAATA others(8): Show |
3 | a0001c0001t0026g0316a0001c0002t0001g0217a0001c0005t0003g0216 | 3 | HG00639.hp2 HG02165.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.348+1737_348+1751d others(17): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880107 | |||||
| chr4:38880107
|
G | GTAGAATA others(13): Show |
3 | a0001c0001t0002g0291a0001c0001t0004g0318a0006c0010t0003g0317 | 3 | HG02083.hp1 HG02300.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.348+1732_348+1751d others(22): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880107 | |||||
| chr4:38880107
|
G | GTAGAATA others(53): Show |
1 | a0001c0001t0008g0218 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.348+1692_348+1751d others(62): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880107 | |||||
| chr4:38880107
|
G | GTAGAATA others(18): Show |
1 | a0007c0049t0002g0348 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.348+1690_348+1691i others(27): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880107 | |||||
| chr4:38880107
|
G | GTAGAATA others(23): Show |
2 | a0007c0021t0013g0340a0012c0051t0005g0344 | 2 | HG02809.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.348+1690_348+1691i others(32): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880107 | |||||
| chr4:38880107
|
G | GTAGAATA others(28): Show |
1 | a0007c0048t0008g0346 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.348+1690_348+1691i others(37): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880107 | |||||
| chr4:38880107
|
G | GTAGAATA others(113): Show |
1 | a0007c0021t0004g0347 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.348+1690_348+1691i others(122): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880107 | |||||
| chr4:38880107
|
GTAGAA | G | 37 | a0001c0001t0001g0175a0001c0001t0001g0275a0001c0001t0001g0296others(34): Show | 38 | HG00673.hp2 HG00735.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.348+1747_348+1751d others(7): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880107 | |||||
| chr4:38880107
|
GTAGAATA others(3): Show |
G | 17 | a0001c0001t0001g0165a0001c0001t0002g0168a0001c0001t0004g0268others(14): Show | 17 | HG00597.hp1 HG01069.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.348+1742_348+1751d others(12): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880107 | |||||
| chr4:38880107
|
GTAGAATA others(8): Show |
G | 14 | a0001c0001t0001g0163a0001c0001t0002g0292a0001c0001t0004g0262others(11): Show | 14 | HG00741.hp1 HG02040.hp2 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.348+1737_348+1751d others(17): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880107 | |||||
| chr4:38880107
|
GTAGAATA others(13): Show |
G | 4 | a0001c0001t0005g0014a0001c0001t0005g0231a0001c0001t0007g0227others(1): Show | 4 | HG01884.hp1 HG02257.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.348+1732_348+1751d others(22): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880107 | |||||
| chr4:38880107
|
GTAGAATA others(18): Show |
G | 8 | a0001c0001t0005g0005a0001c0001t0007g0230a0001c0002t0014g0156others(5): Show | 8 | HG01167.hp2 HG02074.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.348+1727_348+1751d others(27): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880107 | |||||
| chr4:38880107
|
GTAGAATA others(23): Show |
G | 6 | a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0004g0253others(3): Show | 6 | HG01261.hp1 HG02486.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.348+1722_348+1751d others(32): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880107 | |||||
| chr4:38880107
|
GTAGAATA others(38): Show |
G | 71 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0099others(68): Show | 76 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.348+1707_348+1751d others(47): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880107 | |||||
| chr4:38880111
|
AATAGAAT others(37): Show |
A | 1 | a0001c0004t0001g0072 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.348+1687_348+1730d others(46): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880111 | |||||
| chr4:38880112
|
A | G | 14 | a0002c0003t0002g0358a0002c0003t0004g0024a0002c0003t0004g0342others(11): Show | 14 | HG00140.hp2 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.348+1686A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880112 | ||||||
| chr4:38880117
|
A | G | 1 | a0002c0028t0030g0363 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.348+1691A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880117 | ||||||
| chr4:38880122
|
A | G | 2 | a0002c0003t0004g0024a0002c0003t0005g0364 | 2 | HG00140.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.348+1696A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880122 | ||||||
| chr4:38880127
|
A | G | 1 | a0002c0028t0030g0363 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.348+1701A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880127 | ||||||
| chr4:38880156
|
A | C | 1 | a0001c0004t0001g0072 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.348+1730A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880156 | ||||||
| chr4:38880177
|
A | ATAGAATA others(16): Show |
2 | a0001c0002t0001g0152a0001c0002t0001g0319 | 2 | NA18973.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.348+1751_348+1752i others(25): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880177 | ||||||
| chr4:38880200
|
G | C | 82 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(79): Show | 82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+1774G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880200 | ||||||
| chr4:38880267
|
G | C | 342 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(339): Show | 348 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(345): Show |
intron_variant | MODIFIER | c.348+1841G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880267 | ||||||
| chr4:38880274
|
T | G | 2 | a0002c0003t0004g0342a0005c0012t0033g0341 | 2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.348+1848T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880274 | ||||||
| chr4:38880278
|
C | T | 1 | a0001c0002t0002g0141 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.348+1852C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880278 | ||||||
| chr4:38880290
|
A | G | 1 | a0002c0032t0044g0352 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.348+1864A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880290 | ||||||
| chr4:38880319
|
A | G | 82 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(79): Show | 82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+1893A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880319 | ||||||
| chr4:38880352
|
T | G | 7 | a0001c0002t0001g0135a0001c0002t0001g0157a0001c0002t0001g0161others(4): Show | 7 | NA18951.hp2 NA18955.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.348+1926T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880352 | ||||||
| chr4:38880408
|
C | T | 82 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(79): Show | 82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+1982C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880408 | ||||||
| chr4:38880611
|
T | A | 1 | a0001c0005t0003g0285 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.348+2185T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880611 | ||||||
| chr4:38880685
|
A | G | 82 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(79): Show | 82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+2259A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880685 | ||||||
| chr4:38880713
|
T | G | 1 | a0003c0020t0003g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.348+2287T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880713 | ||||||
| chr4:38880716
|
G | A | 24 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(21): Show | 24 | HG00621.hp1 HG01257.hp2 HG01975.hp2 others(21): Show |
intron_variant | MODIFIER | c.348+2290G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880716 | ||||||
| chr4:38880847
|
T | C | 1 | a0001c0002t0008g0074 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.348+2421T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880847 | ||||||
| chr4:38880886
|
T | C | 1 | a0003c0020t0003g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.348+2460T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880886 | ||||||
| chr4:38880913
|
G | A | 1 | a0002c0057t0005g0251 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.348+2487G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880913 | ||||||
| chr4:38880951
|
G | A | 7 | a0001c0002t0001g0135a0001c0002t0001g0157a0001c0002t0001g0161others(4): Show | 7 | NA18951.hp2 NA18955.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.348+2525G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880951 | ||||||
| chr4:38880978
|
A | G | 16 | a0002c0003t0002g0114a0002c0003t0012g0112a0002c0022t0005g0249others(13): Show | 16 | HG01109.hp2 HG01243.hp1 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.348+2552A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880978 | ||||||
| chr4:38881138
|
T | C | 12 | a0001c0001t0002g0271a0001c0001t0002g0272a0001c0001t0004g0253others(9): Show | 13 | HG01069.hp2 HG01261.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.348+2712T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38881138 | ||||||
| chr4:38881201
|
C | CA | 61 | a0001c0001t0002g0008a0001c0001t0002g0150a0001c0001t0005g0005others(58): Show | 61 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.348+2789dupA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38881201 | |||||
| chr4:38881201
|
C | CAA | 37 | a0001c0001t0002g0013a0001c0001t0011g0010a0001c0002t0014g0156others(34): Show | 37 | HG00621.hp1 HG01257.hp2 HG01975.hp2 others(34): Show |
intron_variant | MODIFIER | c.348+2788_348+2789d others(4): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38881201 | |||||
| chr4:38881352
|
C | G | 1 | a0002c0006t0010g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.348+2926C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38881352 | ||||||
| chr4:38881458
|
C | T | 82 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(79): Show | 82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+3032C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38881458 | ||||||
| chr4:38881624
|
A | G | 18 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(15): Show | 18 | HG00621.hp1 HG01257.hp2 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.348+3198A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38881624 | ||||||
| chr4:38881630
|
C | T | 24 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(21): Show | 24 | HG00621.hp1 HG01257.hp2 HG01975.hp2 others(21): Show |
intron_variant | MODIFIER | c.348+3204C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38881630 | ||||||
| chr4:38881684
|
G | C | 82 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(79): Show | 82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+3258G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38881684 | ||||||
| chr4:38881773
|
T | C | 82 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(79): Show | 82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+3347T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38881773 | ||||||
| chr4:38881846
|
A | T | 1 | a0001c0001t0002g0063 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.348+3420A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38881846 | ||||||
| chr4:38881880
|
A | G | 1 | a0001c0004t0007g0136 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.348+3454A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38881880 | ||||||
| chr4:38882041
|
G | A | 2 | a0002c0003t0005g0364a0002c0028t0030g0363 | 2 | HG01891.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.348+3615G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882041 | ||||||
| chr4:38882070
|
T | C | 5 | a0001c0001t0001g0296a0001c0001t0010g0299a0001c0001t0014g0295others(2): Show | 5 | HG02723.hp2 HG02886.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.348+3644T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882070 | ||||||
| chr4:38882108
|
C | T | 13 | a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0005g0005others(10): Show | 13 | HG01167.hp2 HG02486.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.348+3682C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882108 | ||||||
| chr4:38882166
|
G | C | 1 | a0002c0006t0001g0020 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.348+3740G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882166 | ||||||
| chr4:38882168
|
C | T | 47 | a0002c0003t0001g0359a0002c0003t0002g0114a0002c0003t0002g0358others(44): Show | 47 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.348+3742C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882168 | ||||||
| chr4:38882173
|
G | A | 5 | a0002c0003t0017g0132a0007c0021t0004g0347a0007c0021t0013g0340others(2): Show | 5 | HG03704.hp1 HG03834.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.348+3747G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882173 | ||||||
| chr4:38882174
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.348+3748C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882174 | ||||||
| chr4:38882178
|
G | C | 1 | a0001c0001t0002g0278 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.348+3752G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882178 | ||||||
| chr4:38882180
|
T | C | 82 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(79): Show | 82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+3754T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882180 | ||||||
| chr4:38882185
|
G | A | 1 | a0002c0003t0005g0042 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.348+3759G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882185 | ||||||
| chr4:38882269
|
A | G | 82 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(79): Show | 82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+3843A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882269 | ||||||
| chr4:38882278
|
G | C | 64 | a0002c0003t0001g0359a0002c0003t0002g0043a0002c0003t0002g0045others(61): Show | 64 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.348+3852G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882278 | ||||||
| chr4:38882282
|
G | A | 19 | a0001c0008t0006g0051a0002c0003t0001g0120a0002c0003t0001g0122others(16): Show | 19 | HG00544.hp1 HG00621.hp1 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.348+3856G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882282 | ||||||
| chr4:38882318
|
C | CA | 153 | a0001c0001t0001g0050a0001c0001t0001g0100a0001c0001t0001g0165others(150): Show | 158 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.348+3915dupA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38882318 | |||||
| chr4:38882318
|
C | CAA | 25 | a0001c0001t0001g0019a0001c0001t0001g0099a0001c0001t0002g0008others(22): Show | 25 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.348+3914_348+3915d others(4): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38882318 | |||||
| chr4:38882318
|
CA | C | 7 | a0001c0001t0001g0284a0001c0001t0002g0013a0001c0001t0002g0271others(4): Show | 7 | HG01074.hp1 HG01123.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.348+3915delA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38882318 | |||||
| chr4:38882318
|
CAAAAAAA others(3): Show |
C | 2 | a0002c0003t0005g0339a0002c0003t0010g0338 | 2 | HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.348+3906_348+3915d others(12): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38882318 | |||||
| chr4:38882414
|
G | T | 4 | a0001c0001t0001g0019a0001c0001t0002g0016a0001c0001t0002g0017others(1): Show | 4 | HG02080.hp1 HG02135.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+3988G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882414 | ||||||
| chr4:38882428
|
G | A | 8 | a0001c0001t0002g0287a0001c0001t0002g0291a0001c0001t0002g0336others(5): Show | 8 | HG02027.hp1 HG02083.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.348+4002G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882428 | ||||||
| chr4:38882432
|
C | A | 6 | a0007c0021t0004g0347a0007c0021t0013g0340a0007c0048t0008g0346others(3): Show | 6 | HG02809.hp2 HG03579.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.348+4006C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882432 | ||||||
| chr4:38882445
|
T | C | 1 | a0003c0020t0003g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.348+4019T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882445 | ||||||
| chr4:38882614
|
A | T | 1 | a0005c0030t0003g0113 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.348+4188A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882614 | ||||||
| chr4:38882670
|
A | G | 10 | a0001c0001t0002g0008a0001c0001t0005g0005a0001c0001t0005g0014others(7): Show | 10 | HG01167.hp2 HG02486.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.348+4244A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882670 | ||||||
| chr4:38882679
|
C | T | 1 | a0001c0002t0001g0196 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.348+4253C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882679 | ||||||
| chr4:38882752
|
TG | T | 162 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0099others(159): Show | 165 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.348+4328delG | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38882752 | |||||
| chr4:38882798
|
A | G | 82 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(79): Show | 82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+4372A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882798 | ||||||
| chr4:38882893
|
A | G | 46 | a0002c0003t0001g0359a0002c0003t0002g0114a0002c0003t0002g0358others(43): Show | 46 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.348+4467A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882893 | ||||||
| chr4:38883005
|
CT | C | 82 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(79): Show | 82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+4582delT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38883005 | |||||
| chr4:38883041
|
G | C | 1 | a0001c0009t0003g0335 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.348+4615G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38883041 | ||||||
| chr4:38883267
|
C | T | 2 | a0001c0002t0006g0327a0001c0002t0006g0329 | 2 | HG00642.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.348+4841C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38883267 | ||||||
| chr4:38883298
|
C | T | 2 | a0001c0001t0007g0256a0001c0004t0011g0255 | 2 | HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.348+4872C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38883298 | ||||||
| chr4:38883338
|
G | T | 1 | a0002c0006t0010g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.348+4912G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38883338 | ||||||
| chr4:38883410
|
G | A | 2 | a0001c0001t0006g0148a0001c0001t0006g0149 | 2 | NA18945.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.348+4984G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38883410 | ||||||
| chr4:38883416
|
C | G | 16 | a0002c0003t0002g0114a0002c0003t0012g0112a0002c0022t0005g0249others(13): Show | 16 | HG01109.hp2 HG01243.hp1 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.348+4990C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38883416 | ||||||
| chr4:38883423
|
T | TAAAAGAC others(293): Show |
1 | a0002c0006t0010g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.348+5012_348+5013i others(302): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38883423 | |||||
| chr4:38883635
|
G | A | 82 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(79): Show | 82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+5209G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38883635 | ||||||
| chr4:38883774
|
T | C | 1 | a0003c0020t0003g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.348+5348T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38883774 | ||||||
| chr4:38883814
|
G | A | 1 | a0001c0001t0002g0067 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.348+5388G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38883814 | ||||||
| chr4:38883844
|
C | T | 1 | a0001c0004t0008g0098 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.348+5418C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38883844 | ||||||
| chr4:38883890
|
G | A | 1 | a0003c0011t0014g0269 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.348+5464G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38883890 | ||||||
| chr4:38884180
|
G | A | 1 | a0017c0031t0019g0030 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.348+5754G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38884180 | ||||||
| chr4:38884180
|
G | T | 1 | a0002c0006t0010g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.348+5754G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38884180 | ||||||
| chr4:38884224
|
A | G | 5 | a0002c0003t0002g0043a0002c0003t0002g0045a0002c0003t0005g0042others(2): Show | 5 | HG02451.hp2 HG02723.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.348+5798A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38884224 | ||||||
| chr4:38884269
|
G | A | 1 | a0002c0034t0020g0133 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.348+5843G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38884269 | ||||||
| chr4:38884341
|
C | T | 1 | a0001c0001t0012g0184 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.348+5915C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38884341 | ||||||
| chr4:38884378
|
G | A | 2 | a0001c0001t0002g0065a0001c0001t0002g0102 | 2 | HG01981.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.348+5952G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38884378 | ||||||
| chr4:38884399
|
G | A | 11 | a0002c0003t0002g0043a0002c0003t0002g0045a0002c0003t0004g0342others(8): Show | 11 | HG02145.hp2 HG02280.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.348+5973G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38884399 | ||||||
| chr4:38884522
|
A | G | 82 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(79): Show | 82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+6096A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38884522 | ||||||
| chr4:38884659
|
G | A | 1 | a0007c0021t0004g0347 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.348+6233G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38884659 | ||||||
| chr4:38884672
|
G | A | 82 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(79): Show | 82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+6246G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38884672 | ||||||
| chr4:38884772
|
G | C | 82 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(79): Show | 82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+6346G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38884772 | ||||||
| chr4:38884773
|
G | T | 82 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(79): Show | 82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+6347G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38884773 | ||||||
| chr4:38884799
|
G | A | 69 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0099others(66): Show | 72 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.348+6373G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38884799 | ||||||
| chr4:38884829
|
C | T | 10 | a0001c0001t0002g0008a0001c0001t0005g0005a0001c0001t0005g0014others(7): Show | 10 | HG01167.hp2 HG02486.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.348+6403C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38884829 | ||||||
| chr4:38885031
|
G | A | 1 | a0001c0001t0002g0049 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.348+6605G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38885031 | ||||||
| chr4:38885044
|
G | A | 82 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(79): Show | 82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+6618G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38885044 | ||||||
| chr4:38885116
|
C | T | 82 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(79): Show | 82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.349-6627C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38885116 | ||||||
| chr4:38885161
|
G | A | 82 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(79): Show | 82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.349-6582G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38885161 | ||||||
| chr4:38885607
|
A | G | 6 | a0001c0001t0002g0315a0001c0001t0002g0325a0001c0002t0001g0279others(3): Show | 6 | HG02132.hp1 NA18951.hp1 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.349-6136A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38885607 | ||||||
| chr4:38885681
|
G | T | 18 | a0002c0003t0001g0120a0002c0003t0001g0122a0002c0003t0001g0126others(15): Show | 18 | HG00621.hp1 HG01257.hp2 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.349-6062G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38885681 | ||||||
| chr4:38885730
|
C | T | 165 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0099others(162): Show | 168 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.349-6013C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38885730 | ||||||
| chr4:38885919
|
T | C | 6 | a0001c0001t0005g0297a0001c0001t0005g0301a0001c0001t0007g0320others(3): Show | 6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-5824T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38885919 | ||||||
| chr4:38886172
|
CT | C | 24 | a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0005g0014others(21): Show | 24 | HG01257.hp1 HG02145.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.349-5554delT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38886172 | |||||
| chr4:38886273
|
G | A | 1 | a0003c0020t0003g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.349-5470G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38886273 | ||||||
| chr4:38886296
|
C | T | 1 | a0001c0004t0008g0048 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.349-5447C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38886296 | ||||||
| chr4:38886312
|
C | T | 85 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0099others(82): Show | 88 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.349-5431C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38886312 | ||||||
| chr4:38886316
|
A | G | 1 | a0002c0006t0010g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.349-5427A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38886316 | ||||||
| chr4:38886373
|
T | G | 85 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0099others(82): Show | 88 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.349-5370T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38886373 | ||||||
| chr4:38886421
|
T | G | 1 | a0001c0001t0002g0241 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.349-5322T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38886421 | ||||||
| chr4:38886547
|
G | T | 1 | a0002c0003t0005g0042 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.349-5196G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38886547 | ||||||
| chr4:38886550
|
C | G | 1 | a0001c0001t0001g0165 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.349-5193C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38886550 | ||||||
| chr4:38886922
|
C | T | 47 | a0002c0003t0001g0359a0002c0003t0002g0114a0002c0003t0002g0358others(44): Show | 47 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.349-4821C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38886922 | ||||||
| chr4:38886927
|
C | CA | 16 | a0001c0001t0001g0099a0001c0001t0002g0013a0001c0001t0002g0075others(13): Show | 16 | HG00438.hp1 HG01257.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.349-4798dupA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38886927 | |||||
| chr4:38886927
|
CA | C | 14 | a0001c0002t0001g0242a0001c0002t0002g0018a0002c0003t0002g0043others(11): Show | 14 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.349-4798delA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38886927 | |||||
| chr4:38886989
|
C | T | 168 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0099others(165): Show | 171 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.349-4754C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38886989 | ||||||
| chr4:38887080
|
A | T | 1 | a0001c0001t0005g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.349-4663A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38887080 | ||||||
| chr4:38887121
|
G | A | 1 | a0001c0001t0002g0080 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.349-4622G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38887121 | ||||||
| chr4:38887175
|
T | C | 1 | a0001c0001t0002g0287 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.349-4568T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38887175 | ||||||
| chr4:38887195
|
A | G | 2 | a0001c0001t0001g0041a0001c0001t0002g0040 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.349-4548A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38887195 | ||||||
| chr4:38887220
|
C | T | 11 | a0002c0003t0002g0043a0002c0003t0002g0045a0002c0003t0004g0342others(8): Show | 11 | HG02145.hp2 HG02280.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.349-4523C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38887220 | ||||||
| chr4:38887272
|
C | T | 5 | a0002c0003t0002g0114a0002c0003t0012g0112a0002c0029t0043g0115others(2): Show | 5 | HG01243.hp1 HG02027.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.349-4471C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38887272 | ||||||
| chr4:38887776
|
G | A | 1 | a0003c0020t0003g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.349-3967G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38887776 | ||||||
| chr4:38887953
|
T | C | 1 | a0001c0001t0007g0273 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.349-3790T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38887953 | ||||||
| chr4:38888014
|
A | G | 1 | a0001c0001t0004g0268 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.349-3729A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38888014 | ||||||
| chr4:38888020
|
A | G | 4 | a0007c0021t0004g0347a0007c0021t0013g0340a0007c0048t0008g0346others(1): Show | 4 | HG03704.hp1 HG03834.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.349-3723A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38888020 | ||||||
| chr4:38888105
|
A | T | 1 | a0001c0004t0001g0072 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.349-3638A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38888105 | ||||||
| chr4:38888190
|
A | G | 85 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0099others(82): Show | 88 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.349-3553A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38888190 | ||||||
| chr4:38888651
|
T | C | 1 | a0001c0001t0001g0264 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.349-3092T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38888651 | ||||||
| chr4:38888717
|
T | C | 1 | a0001c0001t0002g0278 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.349-3026T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38888717 | ||||||
| chr4:38888723
|
A | G | 11 | a0002c0003t0002g0043a0002c0003t0002g0045a0002c0003t0004g0342others(8): Show | 11 | HG02145.hp2 HG02280.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.349-3020A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38888723 | ||||||
| chr4:38888841
|
G | C | 3 | a0001c0001t0035g0311a0001c0002t0040g0306a0003c0011t0002g0312 | 3 | HG02559.hp1 HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.349-2902G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38888841 | ||||||
| chr4:38888849
|
A | G | 1 | a0001c0002t0001g0206 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.349-2894A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38888849 | ||||||
| chr4:38888930
|
AT | A | 6 | a0007c0021t0004g0347a0007c0021t0013g0340a0007c0048t0008g0346others(3): Show | 6 | HG02809.hp2 HG03579.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-2807delT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38888930 | |||||
| chr4:38888951
|
T | C | 2 | a0001c0001t0010g0259a0001c0004t0001g0260 | 2 | HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.349-2792T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38888951 | ||||||
| chr4:38889170
|
C | T | 1 | a0003c0020t0003g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.349-2573C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38889170 | ||||||
| chr4:38889328
|
G | A | 1 | a0001c0013t0006g0173 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.349-2415G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38889328 | ||||||
| chr4:38889335
|
G | T | 1 | a0002c0003t0005g0042 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.349-2408G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38889335 | ||||||
| chr4:38889406
|
A | G | 11 | a0002c0022t0005g0249a0002c0022t0010g0248a0002c0053t0001g0245others(8): Show | 11 | HG01109.hp2 HG02145.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.349-2337A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38889406 | ||||||
| chr4:38889528
|
A | G | 1 | a0001c0001t0001g0275 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.349-2215A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38889528 | ||||||
| chr4:38889552
|
C | T | 75 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0099others(72): Show | 78 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.349-2191C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38889552 | ||||||
| chr4:38889558
|
G | A | 1 | a0005c0055t0012g0356 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.349-2185G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38889558 | ||||||
| chr4:38889813
|
G | A | 43 | a0002c0003t0001g0359a0002c0003t0002g0358a0002c0003t0004g0024others(40): Show | 43 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.349-1930G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38889813 | ||||||
| chr4:38889885
|
G | A | 1 | a0002c0006t0010g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.349-1858G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38889885 | ||||||
| chr4:38890064
|
T | C | 1 | a0002c0006t0010g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.349-1679T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38890064 | ||||||
| chr4:38890116
|
A | G | 108 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0099others(105): Show | 112 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.349-1627A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38890116 | ||||||
| chr4:38890180
|
G | T | 1 | a0001c0001t0010g0259 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.349-1563G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38890180 | ||||||
| chr4:38890273
|
C | T | 14 | a0002c0003t0004g0024a0002c0003t0016g0035a0002c0006t0001g0021others(11): Show | 14 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.349-1470C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38890273 | ||||||
| chr4:38890319
|
C | T | 3 | a0002c0003t0004g0342a0002c0003t0005g0343a0005c0012t0033g0341 | 3 | HG02280.hp2 HG02622.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.349-1424C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38890319 | ||||||
| chr4:38890320
|
G | A | 11 | a0002c0022t0005g0249a0002c0022t0010g0248a0002c0053t0001g0245others(8): Show | 11 | HG01109.hp2 HG02145.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.349-1423G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38890320 | ||||||
| chr4:38890327
|
C | T | 17 | a0001c0001t0002g0271a0001c0001t0002g0272a0001c0001t0004g0253others(14): Show | 18 | HG01069.hp2 HG01261.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.349-1416C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38890327 | ||||||
| chr4:38890380
|
T | C | 144 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0099others(141): Show | 148 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.349-1363T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38890380 | ||||||
| chr4:38890381
|
G | A | 15 | a0001c0001t0002g0271a0001c0001t0002g0272a0001c0001t0004g0268others(12): Show | 16 | HG01069.hp2 HG01884.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.349-1362G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38890381 | ||||||
| chr4:38890397
|
G | A | 3 | a0001c0001t0004g0253a0001c0001t0007g0256a0001c0004t0011g0255 | 3 | HG01261.hp1 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.349-1346G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38890397 | ||||||
| chr4:38890401
|
C | CA | 29 | a0001c0001t0002g0013a0001c0001t0002g0271a0001c0001t0002g0272others(26): Show | 30 | HG00140.hp2 HG01069.hp2 HG01261.hp1 others(27): Show |
intron_variant | MODIFIER | c.349-1331dupA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38890401 | |||||
| chr4:38890401
|
C | CAA | 100 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0099others(97): Show | 103 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.349-1332_349-1331d others(4): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38890401 | |||||
| chr4:38890401
|
CA | C | 11 | a0002c0022t0005g0249a0002c0022t0010g0248a0002c0053t0001g0245others(8): Show | 11 | HG01109.hp2 HG02145.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.349-1331delA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38890401 | |||||
| chr4:38890413
|
C | A | 75 | a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0002g0271others(72): Show | 76 | HG00621.hp1 HG01069.hp2 HG01167.hp2 others(73): Show |
intron_variant | MODIFIER | c.349-1330C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38890413 | ||||||
| chr4:38890589
|
G | T | 5 | a0002c0003t0002g0114a0002c0003t0012g0112a0002c0029t0043g0115others(2): Show | 5 | HG01243.hp1 HG02027.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.349-1154G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38890589 | ||||||
| chr4:38890600
|
C | T | 75 | a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0002g0271others(72): Show | 76 | HG00621.hp1 HG01069.hp2 HG01167.hp2 others(73): Show |
intron_variant | MODIFIER | c.349-1143C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38890600 | ||||||
| chr4:38890703
|
G | T | 1 | a0001c0001t0002g0222 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.349-1040G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38890703 | ||||||
| chr4:38891023
|
G | C | 1 | a0001c0001t0017g0138 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.349-720G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38891023 | ||||||
| chr4:38891028
|
T | C | 69 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0099others(66): Show | 72 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.349-715T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38891028 | ||||||
| chr4:38891119
|
C | T | 2 | a0001c0002t0001g0180a0001c0002t0001g0233 | 2 | HG03831.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.349-624C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38891119 | ||||||
| chr4:38891180
|
G | A | 1 | a0001c0001t0027g0054 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.349-563G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38891180 | ||||||
| chr4:38891189
|
G | C | 6 | a0001c0001t0002g0013a0001c0001t0007g0256a0001c0001t0011g0010others(3): Show | 6 | HG02109.hp1 HG02896.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-554G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38891189 | ||||||
| chr4:38891274
|
C | T | 1 | a0002c0006t0010g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.349-469C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38891274 | ||||||
| chr4:38891285
|
T | C | 6 | a0007c0021t0004g0347a0007c0021t0013g0340a0007c0048t0008g0346others(3): Show | 6 | HG02809.hp2 HG03579.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-458T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38891285 | ||||||
| chr4:38891309
|
A | G | 6 | a0007c0021t0004g0347a0007c0021t0013g0340a0007c0048t0008g0346others(3): Show | 6 | HG02809.hp2 HG03579.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-434A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38891309 | ||||||
| chr4:38891357
|
T | TA | 155 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0099others(152): Show | 159 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.349-384dupA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38891357 | |||||
| chr4:38891412
|
C | G | 1 | a0013c0040t0023g0234 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.349-331C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38891412 | ||||||
| chr4:38891465
|
A | G | 3 | a0002c0003t0004g0342a0002c0003t0005g0343a0005c0012t0033g0341 | 3 | HG02280.hp2 HG02622.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.349-278A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38891465 | ||||||
| chr4:38891472
|
G | C | 1 | a0002c0006t0010g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.349-271G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38891472 | ||||||
| chr4:38891622
|
C | T | 1 | a0001c0001t0004g0277 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.349-121C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38891622 | ||||||
| chr4:38891674
|
A | T | 12 | a0001c0001t0002g0013a0001c0001t0007g0256a0001c0001t0011g0010others(9): Show | 12 | HG02258.hp1 HG02809.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.349-69A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38891674 | ||||||
| chr4:38891850
|
T | C | 1 | a0002c0006t0001g0020 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.436+20T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38891850 | ||||||
| chr4:38892115
|
G | A | 27 | a0001c0001t0002g0008a0001c0001t0002g0271a0001c0001t0002g0272others(24): Show | 28 | HG01069.hp2 HG01167.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.436+285G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38892115 | ||||||
| chr4:38892221
|
C | A | 41 | a0001c0001t0002g0013a0001c0001t0004g0257a0001c0001t0007g0256others(38): Show | 41 | HG00621.hp1 HG01243.hp1 HG01257.hp2 others(38): Show |
intron_variant | MODIFIER | c.436+391C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38892221 | ||||||
| chr4:38892222
|
G | T | 92 | a0001c0001t0001g0050a0001c0001t0001g0099a0001c0001t0001g0100others(89): Show | 96 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.436+392G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38892222 | ||||||
| chr4:38892387
|
T | C | 2 | a0002c0006t0010g0337a0003c0020t0003g0046 | 2 | HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.436+557T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38892387 | ||||||
| chr4:38892552
|
A | G | 27 | a0001c0001t0002g0008a0001c0001t0002g0271a0001c0001t0002g0272others(24): Show | 28 | HG01069.hp2 HG01167.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.436+722A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38892552 | ||||||
| chr4:38892577
|
T | C | 1 | a0003c0020t0003g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.436+747T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38892577 | ||||||
| chr4:38892605
|
G | A | 10 | a0001c0001t0001g0175a0001c0001t0001g0187a0001c0001t0002g0186others(7): Show | 10 | HG01346.hp2 HG01433.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.436+775G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38892605 | ||||||
| chr4:38892759
|
A | G | 144 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0099others(141): Show | 148 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.436+929A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38892759 | ||||||
| chr4:38892857
|
C | T | 1 | a0001c0037t0003g0007 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.436+1027C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38892857 | ||||||
| chr4:38892958
|
C | T | 4 | a0001c0001t0001g0019a0001c0001t0002g0016a0001c0001t0002g0017others(1): Show | 4 | HG02080.hp1 HG02135.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.436+1128C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38892958 | ||||||
| chr4:38893067
|
A | G | 4 | a0001c0001t0002g0008a0001c0001t0004g0253a0001c0001t0004g0254others(1): Show | 4 | HG01261.hp1 HG02486.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+1237A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38893067 | ||||||
| chr4:38893206
|
A | G | 1 | a0001c0001t0006g0149 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.436+1376A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38893206 | ||||||
| chr4:38893284
|
G | T | 3 | a0001c0001t0002g0013a0001c0001t0011g0010a0001c0037t0003g0007 | 3 | HG02896.hp1 HG02970.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.436+1454G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38893284 | ||||||
| chr4:38893408
|
T | G | 25 | a0001c0001t0002g0008a0001c0001t0002g0271a0001c0001t0002g0272others(22): Show | 26 | HG01069.hp2 HG01167.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.436+1578T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38893408 | ||||||
| chr4:38893550
|
G | A | 1 | a0001c0001t0002g0067 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.436+1720G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38893550 | ||||||
| chr4:38893887
|
G | A | 1 | a0003c0020t0003g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.436+2057G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38893887 | ||||||
| chr4:38894119
|
C | T | 5 | a0001c0001t0001g0019a0001c0001t0002g0016a0001c0001t0002g0017others(2): Show | 5 | HG02080.hp1 HG02135.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.436+2289C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38894119 | ||||||
| chr4:38894162
|
C | CA | 23 | a0001c0001t0002g0047a0001c0001t0002g0189a0001c0001t0002g0313others(20): Show | 23 | HG00609.hp2 HG01109.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.436+2358dupA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38894162 | |||||
| chr4:38894162
|
CAAAAAA | C | 76 | a0001c0001t0001g0050a0001c0001t0001g0099a0001c0001t0001g0100others(73): Show | 79 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.436+2353_436+2358d others(8): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38894162 | |||||
| chr4:38894162
|
CAAAAAAA | C | 87 | a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0002g0271others(84): Show | 88 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.436+2352_436+2358d others(9): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38894162 | |||||
| chr4:38894347
|
A | T | 5 | a0001c0001t0012g0172a0002c0003t0002g0114a0002c0029t0043g0115others(2): Show | 5 | HG01243.hp1 HG02965.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.436+2517A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38894347 | ||||||
| chr4:38894508
|
C | A | 4 | a0001c0001t0002g0013a0001c0001t0011g0010a0001c0037t0003g0007others(1): Show | 4 | HG02109.hp1 HG02896.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.436+2678C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38894508 | ||||||
| chr4:38894531
|
A | G | 7 | a0001c0001t0002g0287a0001c0001t0002g0291a0001c0001t0002g0336others(4): Show | 7 | HG02027.hp1 HG02083.hp1 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.436+2701A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38894531 | ||||||
| chr4:38894642
|
A | G | 1 | a0002c0003t0006g0037 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.436+2812A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38894642 | ||||||
| chr4:38894648
|
G | A | 5 | a0002c0003t0002g0043a0002c0003t0002g0045a0002c0003t0005g0042others(2): Show | 5 | HG02451.hp2 HG02723.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.436+2818G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38894648 | ||||||
| chr4:38894653
|
G | T | 2 | a0002c0003t0001g0359a0002c0003t0005g0360 | 2 | HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.436+2823G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38894653 | ||||||
| chr4:38894661
|
G | A | 1 | a0001c0001t0002g0292 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.436+2831G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38894661 | ||||||
| chr4:38894775
|
C | T | 10 | a0002c0003t0002g0043a0002c0003t0002g0045a0002c0003t0004g0342others(7): Show | 10 | HG02280.hp1 HG02280.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.436+2945C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38894775 | ||||||
| chr4:38894862
|
G | A | 36 | a0001c0001t0002g0271a0001c0001t0002g0272a0001c0001t0004g0257others(33): Show | 37 | HG00621.hp1 HG01069.hp2 HG01257.hp2 others(34): Show |
intron_variant | MODIFIER | c.436+3032G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38894862 | ||||||
| chr4:38895205
|
G | A | 1 | a0002c0003t0005g0360 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.436+3375G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38895205 | ||||||
| chr4:38895345
|
C | T | 1 | a0002c0029t0043g0115 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.436+3515C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38895345 | ||||||
| chr4:38895386
|
G | A | 3 | a0002c0003t0004g0342a0002c0003t0005g0343a0005c0012t0033g0341 | 3 | HG02280.hp2 HG02622.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.436+3556G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38895386 | ||||||
| chr4:38895410
|
C | T | 25 | a0001c0001t0004g0257a0002c0003t0001g0120a0002c0003t0001g0122others(22): Show | 25 | HG00621.hp1 HG01255.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.436+3580C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38895410 | ||||||
| chr4:38895442
|
A | G | 8 | a0001c0001t0001g0175a0001c0001t0001g0187a0001c0001t0002g0186others(5): Show | 8 | HG01346.hp2 HG01433.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.436+3612A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38895442 | ||||||
| chr4:38895505
|
C | T | 1 | a0001c0002t0007g0171 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.436+3675C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38895505 | ||||||
| chr4:38895633
|
G | A | 162 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(159): Show | 166 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.436+3803G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38895633 | ||||||
| chr4:38895669
|
A | G | 42 | a0001c0001t0001g0041a0001c0001t0002g0040a0001c0001t0002g0271others(39): Show | 43 | HG00621.hp1 HG01069.hp2 HG01255.hp2 others(40): Show |
intron_variant | MODIFIER | c.436+3839A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38895669 | ||||||
| chr4:38895686
|
G | A | 1 | a0012c0051t0005g0344 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.436+3856G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38895686 | ||||||
| chr4:38895690
|
C | T | 9 | a0002c0003t0002g0043a0002c0003t0002g0045a0002c0003t0005g0042others(6): Show | 9 | HG02280.hp1 HG02451.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.436+3860C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38895690 | ||||||
| chr4:38895691
|
G | A | 1 | a0001c0001t0021g0068 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.436+3861G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38895691 | ||||||
| chr4:38895774
|
G | A | 42 | a0001c0001t0001g0041a0001c0001t0002g0040a0001c0001t0002g0271others(39): Show | 43 | HG00621.hp1 HG01069.hp2 HG01255.hp2 others(40): Show |
intron_variant | MODIFIER | c.436+3944G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38895774 | ||||||
| chr4:38895779
|
T | G | 1 | a0001c0004t0002g0349 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.436+3949T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38895779 | ||||||
| chr4:38895781
|
C | A | 2 | a0001c0001t0007g0256a0001c0004t0011g0255 | 2 | HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.436+3951C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38895781 | ||||||
| chr4:38895850
|
T | C | 1 | a0001c0005t0003g0285 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.436+4020T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38895850 | ||||||
| chr4:38896133
|
A | G | 17 | a0001c0001t0001g0041a0001c0001t0002g0040a0001c0001t0002g0271others(14): Show | 18 | HG01069.hp2 HG01884.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.436+4303A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38896133 | ||||||
| chr4:38896557
|
A | G | 1 | a0001c0001t0002g0102 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.436+4727A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38896557 | ||||||
| chr4:38896585
|
G | A | 1 | a0002c0003t0005g0364 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.436+4755G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38896585 | ||||||
| chr4:38896626
|
GT | G | 164 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(161): Show | 168 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.436+4798delT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38896626 | |||||
| chr4:38896848
|
G | C | 170 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(167): Show | 174 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.436+5018G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38896848 | ||||||
| chr4:38897113
|
T | C | 5 | a0002c0003t0005g0355a0002c0003t0032g0357a0002c0006t0001g0353others(2): Show | 5 | HG01255.hp2 HG02109.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.436+5283T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38897113 | ||||||
| chr4:38897348
|
C | A | 1 | a0001c0001t0001g0163 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.436+5518C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38897348 | ||||||
| chr4:38897389
|
T | C | 1 | a0001c0039t0024g0261 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.436+5559T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38897389 | ||||||
| chr4:38897487
|
C | T | 25 | a0001c0001t0004g0257a0002c0003t0001g0120a0002c0003t0001g0122others(22): Show | 25 | HG00621.hp1 HG01255.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.436+5657C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38897487 | ||||||
| chr4:38897682
|
A | G | 6 | a0001c0001t0002g0095a0001c0001t0008g0109a0001c0001t0008g0110others(3): Show | 6 | HG02080.hp2 NA18940.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.436+5852A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38897682 | ||||||
| chr4:38897718
|
CA | C | 10 | a0002c0003t0002g0043a0002c0003t0002g0045a0002c0003t0004g0342others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.436+5890delA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38897718 | |||||
| chr4:38897777
|
TA | T | 12 | a0002c0003t0016g0035a0002c0006t0001g0021a0002c0006t0011g0028others(9): Show | 12 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.436+5959delA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38897777 | |||||
| chr4:38897848
|
C | T | 5 | a0001c0002t0001g0094a0007c0021t0004g0347a0007c0021t0013g0340others(2): Show | 5 | HG02132.hp2 HG03704.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.436+6018C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38897848 | ||||||
| chr4:38897853
|
G | A | 45 | a0001c0001t0001g0041a0001c0001t0002g0008a0001c0001t0002g0040others(42): Show | 45 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.436+6023G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38897853 | ||||||
| chr4:38897938
|
T | C | 45 | a0001c0001t0001g0041a0001c0001t0002g0008a0001c0001t0002g0040others(42): Show | 45 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.436+6108T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38897938 | ||||||
| chr4:38897945
|
C | CA | 35 | a0001c0001t0001g0099a0001c0001t0002g0075a0001c0001t0002g0080others(32): Show | 38 | HG00438.hp1 HG00609.hp1 HG02080.hp2 others(35): Show |
intron_variant | MODIFIER | c.436+6128dupA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38897945 | |||||
| chr4:38898027
|
C | T | 12 | a0001c0001t0007g0256a0001c0004t0011g0255a0002c0003t0002g0043others(9): Show | 12 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.436+6197C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38898027 | ||||||
| chr4:38898086
|
A | G | 12 | a0001c0001t0007g0256a0001c0004t0011g0255a0002c0003t0002g0043others(9): Show | 12 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.436+6256A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38898086 | ||||||
| chr4:38898099
|
G | A | 12 | a0001c0001t0007g0256a0001c0004t0011g0255a0002c0003t0002g0043others(9): Show | 12 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.436+6269G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38898099 | ||||||
| chr4:38898126
|
A | G | 2 | a0002c0032t0044g0352a0002c0057t0005g0251 | 2 | HG02145.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.436+6296A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38898126 | ||||||
| chr4:38898232
|
A | C | 1 | a0001c0001t0001g0195 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.436+6402A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38898232 | ||||||
| chr4:38898243
|
G | C | 1 | a0001c0001t0002g0292 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.436+6413G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38898243 | ||||||
| chr4:38898257
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.436+6427C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38898257 | ||||||
| chr4:38898258
|
G | A | 7 | a0001c0002t0001g0094a0007c0021t0004g0347a0007c0021t0013g0340others(4): Show | 7 | HG02132.hp2 HG02809.hp2 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.436+6428G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38898258 | ||||||
| chr4:38898313
|
C | T | 2 | a0001c0002t0001g0152a0001c0002t0001g0319 | 2 | NA18973.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.436+6483C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38898313 | ||||||
| chr4:38898379
|
C | T | 1 | a0008c0014t0023g0305 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.436+6549C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38898379 | ||||||
| chr4:38898436
|
C | G | 111 | a0001c0001t0001g0041a0001c0001t0001g0050a0001c0001t0001g0099others(108): Show | 114 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.436+6606C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38898436 | ||||||
| chr4:38898469
|
G | A | 2 | a0001c0001t0007g0256a0001c0004t0011g0255 | 2 | HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.436+6639G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38898469 | ||||||
| chr4:38898512
|
A | C | 124 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(121): Show | 127 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.436+6682A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38898512 | ||||||
| chr4:38898764
|
C | A | 20 | a0001c0001t0004g0257a0002c0003t0001g0120a0002c0003t0001g0122others(17): Show | 20 | HG00621.hp1 HG01257.hp2 HG01975.hp2 others(17): Show |
intron_variant | MODIFIER | c.437-6758C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38898764 | ||||||
| chr4:38898776
|
A | G | 346 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(343): Show | 352 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(349): Show |
intron_variant | MODIFIER | c.437-6746A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38898776 | ||||||
| chr4:38898843
|
A | G | 1 | a0001c0001t0009g0154 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.437-6679A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38898843 | ||||||
| chr4:38898910
|
A | T | 12 | a0001c0001t0007g0256a0001c0004t0011g0255a0002c0003t0002g0043others(9): Show | 12 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.437-6612A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38898910 | ||||||
| chr4:38898946
|
A | ATG | 12 | a0001c0001t0007g0256a0001c0004t0011g0255a0002c0003t0002g0043others(9): Show | 12 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.437-6574_437-6573d others(4): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38898946 | |||||
| chr4:38898968
|
TATATATG others(11): Show |
T | 70 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0099others(67): Show | 73 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.437-6535_437-6518d others(20): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38898968 | |||||
| chr4:38898973
|
A | ATGTTATA others(14): Show |
12 | a0001c0001t0007g0256a0001c0004t0011g0255a0002c0003t0002g0043others(9): Show | 12 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.437-6530_437-6529i others(23): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38898973 | |||||
| chr4:38899001
|
T | C | 4 | a0001c0001t0017g0138a0001c0002t0002g0139a0001c0002t0002g0141others(1): Show | 4 | HG00408.hp2 HG04184.hp1 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.437-6521T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38899001 | ||||||
| chr4:38899038
|
T | TAGAC | 22 | a0001c0001t0002g0271a0001c0001t0002g0272a0001c0001t0004g0268others(19): Show | 23 | HG01069.hp2 HG01884.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.437-6483_437-6482i others(6): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38899038 | |||||
| chr4:38899040
|
T | G | 22 | a0001c0001t0002g0271a0001c0001t0002g0272a0001c0001t0004g0268others(19): Show | 23 | HG01069.hp2 HG01884.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.437-6482T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38899040 | ||||||
| chr4:38899040
|
T | TATAGACA others(1): Show |
23 | a0002c0003t0004g0024a0002c0003t0006g0037a0002c0003t0016g0035others(20): Show | 23 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.437-6481_437-6480i others(10): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38899040 | |||||
| chr4:38899042
|
G | GACAGAT | 138 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(135): Show | 141 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.437-6478_437-6473d others(8): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38899042 | |||||
| chr4:38899042
|
G | T | 45 | a0001c0001t0002g0271a0001c0001t0002g0272a0001c0001t0004g0268others(42): Show | 46 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.437-6480G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38899042 | ||||||
| chr4:38899085
|
T | C | 2 | a0001c0001t0002g0063a0001c0001t0004g0086 | 2 | HG02074.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.437-6437T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38899085 | ||||||
| chr4:38899242
|
G | A | 1 | a0001c0009t0003g0270 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.437-6280G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38899242 | ||||||
| chr4:38899254
|
C | T | 3 | a0001c0001t0007g0256a0001c0004t0011g0255a0002c0003t0002g0358 | 3 | HG03098.hp1 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.437-6268C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38899254 | ||||||
| chr4:38899255
|
G | A | 1 | a0004c0007t0009g0025 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.437-6267G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38899255 | ||||||
| chr4:38899274
|
C | T | 1 | a0001c0001t0002g0016 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.437-6248C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38899274 | ||||||
| chr4:38899381
|
A | G | 12 | a0001c0001t0007g0256a0001c0004t0011g0255a0002c0003t0002g0043others(9): Show | 12 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.437-6141A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38899381 | ||||||
| chr4:38899454
|
G | A | 1 | a0001c0001t0009g0154 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.437-6068G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38899454 | ||||||
| chr4:38899651
|
C | T | 12 | a0001c0001t0007g0256a0001c0004t0011g0255a0002c0003t0002g0043others(9): Show | 12 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.437-5871C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38899651 | ||||||
| chr4:38899855
|
T | G | 1 | a0001c0001t0002g0292 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.437-5667T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38899855 | ||||||
| chr4:38899908
|
T | A | 175 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(172): Show | 179 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.437-5614T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38899908 | ||||||
| chr4:38899954
|
A | G | 12 | a0001c0001t0002g0271a0001c0001t0002g0272a0001c0001t0004g0268others(9): Show | 13 | HG01069.hp2 HG01884.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.437-5568A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38899954 | ||||||
| chr4:38900011
|
C | T | 8 | a0002c0003t0002g0043a0002c0003t0002g0045a0002c0003t0004g0342others(5): Show | 8 | HG02280.hp2 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.437-5511C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38900011 | ||||||
| chr4:38900148
|
A | C | 183 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(180): Show | 187 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.437-5374A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38900148 | ||||||
| chr4:38900225
|
T | A | 14 | a0001c0001t0007g0256a0001c0002t0002g0307a0001c0002t0028g0351others(11): Show | 14 | HG00741.hp1 HG02145.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.437-5297T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38900225 | ||||||
| chr4:38900225
|
T | TA | 8 | a0001c0001t0021g0220a0001c0001t0035g0311a0001c0002t0001g0152others(5): Show | 8 | HG00597.hp1 HG01243.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.437-5285dupA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38900225 | |||||
| chr4:38900225
|
TA | T | 172 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(169): Show | 176 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.437-5285delA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38900225 | |||||
| chr4:38900234
|
A | C | 12 | a0001c0001t0007g0256a0001c0004t0011g0255a0002c0003t0002g0043others(9): Show | 12 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.437-5288A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38900234 | ||||||
| chr4:38900264
|
G | A | 6 | a0001c0001t0012g0334a0001c0001t0041g0328a0001c0002t0001g0324others(3): Show | 6 | HG00642.hp2 HG01074.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.437-5258G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38900264 | ||||||
| chr4:38900334
|
A | G | 12 | a0001c0001t0007g0256a0001c0004t0011g0255a0002c0003t0002g0043others(9): Show | 12 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.437-5188A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38900334 | ||||||
| chr4:38900512
|
C | T | 183 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(180): Show | 187 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.437-5010C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38900512 | ||||||
| chr4:38900810
|
T | C | 12 | a0001c0001t0007g0256a0001c0004t0011g0255a0002c0003t0002g0043others(9): Show | 12 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.437-4712T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38900810 | ||||||
| chr4:38900851
|
G | A | 10 | a0002c0003t0002g0043a0002c0003t0002g0045a0002c0003t0004g0342others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-4671G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38900851 | ||||||
| chr4:38900947
|
C | CA | 8 | a0002c0022t0005g0249a0002c0022t0010g0248a0002c0053t0001g0245others(5): Show | 8 | HG02559.hp2 HG02647.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.437-4565dupA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38900947 | |||||
| chr4:38900947
|
CA | C | 146 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(143): Show | 150 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.437-4565delA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38900947 | |||||
| chr4:38900991
|
A | G | 10 | a0002c0003t0002g0043a0002c0003t0002g0045a0002c0003t0004g0342others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-4531A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38900991 | ||||||
| chr4:38901092
|
C | T | 3 | a0001c0001t0002g0008a0001c0002t0014g0156a0008c0014t0001g0012 | 3 | HG02486.hp2 HG02622.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.437-4430C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38901092 | ||||||
| chr4:38901204
|
A | T | 1 | a0001c0008t0006g0053 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.437-4318A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38901204 | ||||||
| chr4:38901287
|
GT | G | 10 | a0002c0003t0002g0043a0002c0003t0002g0045a0002c0003t0004g0342others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-4225delT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38901287 | |||||
| chr4:38901321
|
TGTC | T | 171 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(168): Show | 175 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.437-4197_437-4195d others(5): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38901321 | |||||
| chr4:38901440
|
G | A | 10 | a0002c0003t0002g0043a0002c0003t0002g0045a0002c0003t0004g0342others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-4082G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38901440 | ||||||
| chr4:38901477
|
A | G | 1 | a0001c0001t0002g0063 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.437-4045A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38901477 | ||||||
| chr4:38901530
|
G | A | 2 | a0001c0001t0007g0256a0001c0004t0011g0255 | 2 | HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.437-3992G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38901530 | ||||||
| chr4:38901572
|
A | G | 10 | a0002c0003t0002g0043a0002c0003t0002g0045a0002c0003t0004g0342others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-3950A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38901572 | ||||||
| chr4:38901594
|
T | G | 10 | a0002c0003t0002g0043a0002c0003t0002g0045a0002c0003t0004g0342others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-3928T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38901594 | ||||||
| chr4:38901705
|
G | A | 8 | a0002c0003t0002g0043a0002c0003t0002g0045a0002c0003t0004g0342others(5): Show | 8 | HG02280.hp2 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.437-3817G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38901705 | ||||||
| chr4:38901715
|
G | A | 10 | a0002c0003t0002g0043a0002c0003t0002g0045a0002c0003t0004g0342others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-3807G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38901715 | ||||||
| chr4:38901716
|
A | G | 1 | a0001c0009t0003g0270 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.437-3806A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38901716 | ||||||
| chr4:38901748
|
G | A | 2 | a0001c0001t0009g0153a0001c0001t0009g0154 | 2 | HG01109.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.437-3774G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38901748 | ||||||
| chr4:38901791
|
G | A | 8 | a0002c0022t0005g0249a0002c0022t0010g0248a0002c0053t0001g0245others(5): Show | 8 | HG02559.hp2 HG02647.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.437-3731G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38901791 | ||||||
| chr4:38901989
|
C | T | 10 | a0002c0003t0002g0043a0002c0003t0002g0045a0002c0003t0004g0342others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-3533C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38901989 | ||||||
| chr4:38902027
|
G | A | 10 | a0002c0003t0002g0043a0002c0003t0002g0045a0002c0003t0004g0342others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-3495G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38902027 | ||||||
| chr4:38902126
|
T | C | 1 | a0001c0001t0002g0209 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.437-3396T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38902126 | ||||||
| chr4:38902154
|
C | T | 2 | a0001c0001t0007g0256a0001c0004t0011g0255 | 2 | HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.437-3368C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38902154 | ||||||
| chr4:38902220
|
T | C | 1 | a0001c0001t0002g0087 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.437-3302T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38902220 | ||||||
| chr4:38902330
|
G | A | 10 | a0002c0003t0002g0043a0002c0003t0002g0045a0002c0003t0004g0342others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-3192G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38902330 | ||||||
| chr4:38902370
|
C | T | 3 | a0001c0001t0007g0256a0001c0004t0002g0064a0001c0004t0011g0255 | 3 | HG03098.hp1 NA19030.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.437-3152C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38902370 | ||||||
| chr4:38902371
|
G | A | 10 | a0002c0003t0002g0043a0002c0003t0002g0045a0002c0003t0004g0342others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-3151G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38902371 | ||||||
| chr4:38902414
|
C | T | 14 | a0001c0001t0002g0271a0001c0001t0002g0272a0001c0001t0004g0268others(11): Show | 15 | HG01069.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.437-3108C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38902414 | ||||||
| chr4:38902560
|
A | G | 10 | a0002c0003t0002g0043a0002c0003t0002g0045a0002c0003t0004g0342others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-2962A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38902560 | ||||||
| chr4:38902601
|
G | C | 8 | a0002c0003t0002g0043a0002c0003t0002g0045a0002c0003t0004g0342others(5): Show | 8 | HG02280.hp2 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.437-2921G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38902601 | ||||||
| chr4:38902669
|
C | T | 1 | a0001c0001t0004g0262 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.437-2853C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38902669 | ||||||
| chr4:38902688
|
G | A | 10 | a0002c0003t0002g0043a0002c0003t0002g0045a0002c0003t0004g0342others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-2834G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38902688 | ||||||
| chr4:38902714
|
A | T | 8 | a0002c0022t0005g0249a0002c0022t0010g0248a0002c0053t0001g0245others(5): Show | 8 | HG02559.hp2 HG02647.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.437-2808A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38902714 | ||||||
| chr4:38902760
|
G | C | 10 | a0002c0003t0002g0043a0002c0003t0002g0045a0002c0003t0004g0342others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-2762G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38902760 | ||||||
| chr4:38902899
|
T | G | 2 | a0002c0003t0005g0339a0002c0003t0010g0338 | 2 | HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.437-2623T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38902899 | ||||||
| chr4:38902960
|
T | C | 184 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(181): Show | 188 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.437-2562T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38902960 | ||||||
| chr4:38903043
|
C | G | 10 | a0002c0003t0002g0043a0002c0003t0002g0045a0002c0003t0004g0342others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-2479C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38903043 | ||||||
| chr4:38903112
|
T | G | 10 | a0002c0003t0002g0043a0002c0003t0002g0045a0002c0003t0004g0342others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-2410T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38903112 | ||||||
| chr4:38903158
|
T | C | 1 | a0003c0020t0003g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.437-2364T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38903158 | ||||||
| chr4:38903185
|
G | A | 3 | a0001c0001t0006g0056a0001c0001t0006g0057a0001c0004t0002g0058 | 3 | NA18953.hp1 NA18954.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.437-2337G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38903185 | ||||||
| chr4:38903205
|
T | A | 1 | a0008c0014t0023g0305 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.437-2317T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38903205 | ||||||
| chr4:38903279
|
G | A | 1 | a0002c0003t0002g0045 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.437-2243G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38903279 | ||||||
| chr4:38903511
|
C | T | 10 | a0002c0003t0002g0043a0002c0003t0002g0045a0002c0003t0004g0342others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-2011C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38903511 | ||||||
| chr4:38903573
|
A | T | 173 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(170): Show | 177 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.437-1949A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38903573 | ||||||
| chr4:38903664
|
C | G | 4 | a0001c0001t0001g0019a0001c0001t0002g0016a0001c0001t0002g0017others(1): Show | 4 | HG02080.hp1 HG02135.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.437-1858C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38903664 | ||||||
| chr4:38903723
|
C | T | 1 | a0001c0001t0002g0168 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.437-1799C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38903723 | ||||||
| chr4:38903842
|
A | G | 175 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(172): Show | 179 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.437-1680A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38903842 | ||||||
| chr4:38903863
|
T | C | 3 | a0001c0001t0002g0013a0001c0001t0011g0010a0001c0037t0003g0007 | 3 | HG02896.hp1 HG02970.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.437-1659T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38903863 | ||||||
| chr4:38903873
|
C | G | 1 | a0001c0023t0002g0104 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.437-1649C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38903873 | ||||||
| chr4:38903917
|
A | G | 1 | a0001c0023t0002g0104 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.437-1605A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38903917 | ||||||
| chr4:38903931
|
A | T | 10 | a0002c0003t0002g0043a0002c0003t0002g0045a0002c0003t0004g0342others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-1591A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38903931 | ||||||
| chr4:38903966
|
T | C | 1 | a0001c0001t0008g0055 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.437-1556T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38903966 | ||||||
| chr4:38904105
|
G | A | 11 | a0001c0001t0002g0271a0001c0001t0002g0272a0001c0001t0004g0268others(8): Show | 12 | HG01069.hp2 HG01884.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.437-1417G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38904105 | ||||||
| chr4:38904110
|
T | G | 70 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0099others(67): Show | 73 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.437-1412T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38904110 | ||||||
| chr4:38904144
|
C | T | 8 | a0002c0003t0002g0043a0002c0003t0002g0045a0002c0003t0004g0342others(5): Show | 8 | HG02280.hp2 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.437-1378C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38904144 | ||||||
| chr4:38904152
|
C | T | 10 | a0002c0003t0002g0043a0002c0003t0002g0045a0002c0003t0004g0342others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-1370C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38904152 | ||||||
| chr4:38904164
|
G | A | 1 | a0001c0001t0008g0218 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.437-1358G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38904164 | ||||||
| chr4:38904173
|
C | T | 3 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0223 | 3 | HG00642.hp1 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.437-1349C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38904173 | ||||||
| chr4:38904298
|
A | G | 10 | a0002c0003t0002g0043a0002c0003t0002g0045a0002c0003t0004g0342others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-1224A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38904298 | ||||||
| chr4:38904323
|
G | T | 2 | a0002c0056t0005g0252a0005c0055t0012g0356 | 2 | HG01109.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.437-1199G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38904323 | ||||||
| chr4:38904370
|
T | C | 10 | a0002c0003t0002g0043a0002c0003t0002g0045a0002c0003t0004g0342others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-1152T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38904370 | ||||||
| chr4:38904389
|
G | A | 1 | a0002c0016t0001g0361 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.437-1133G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38904389 | ||||||
| chr4:38904416
|
C | T | 1 | a0002c0003t0032g0357 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.437-1106C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38904416 | ||||||
| chr4:38904417
|
C | A | 10 | a0002c0003t0002g0043a0002c0003t0002g0045a0002c0003t0004g0342others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-1105C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38904417 | ||||||
| chr4:38904467
|
C | T | 4 | a0001c0001t0006g0078a0001c0001t0006g0294a0001c0001t0006g0304others(1): Show | 4 | HG00673.hp1 NA18981.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.437-1055C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38904467 | ||||||
| chr4:38904599
|
G | A | 1 | a0001c0001t0038g0298 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.437-923G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38904599 | ||||||
| chr4:38904673
|
A | G | 7 | a0001c0002t0001g0094a0007c0021t0004g0347a0007c0021t0013g0340others(4): Show | 7 | HG02132.hp2 HG02809.hp2 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.437-849A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38904673 | ||||||
| chr4:38904935
|
T | G | 4 | a0002c0003t0001g0359a0002c0003t0005g0360a0002c0003t0010g0362others(1): Show | 4 | HG02809.hp1 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.437-587T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38904935 | ||||||
| chr4:38904960
|
G | A | 10 | a0002c0003t0002g0043a0002c0003t0002g0045a0002c0003t0004g0342others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-562G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38904960 | ||||||
| chr4:38905096
|
A | G | 130 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(127): Show | 133 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.437-426A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38905096 | ||||||
| chr4:38905125
|
G | A | 2 | a0002c0003t0005g0339a0002c0003t0010g0338 | 2 | HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.437-397G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38905125 | ||||||
| chr4:38905218
|
G | A | 1 | a0001c0001t0042g0210 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.437-304G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38905218 | ||||||
| chr4:38905255
|
C | T | 7 | a0001c0001t0002g0146a0001c0001t0002g0238a0001c0001t0006g0148others(4): Show | 7 | HG01106.hp1 NA18945.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.437-267C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38905255 | ||||||
| chr4:38905256
|
G | A | 1 | a0002c0003t0002g0358 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.437-266G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38905256 | ||||||
| chr4:38905330
|
C | T | 65 | a0001c0001t0001g0050a0001c0001t0001g0099a0001c0001t0001g0100others(62): Show | 68 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.437-192C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38905330 | ||||||
| chr4:38905400
|
T | A | 19 | a0002c0003t0002g0043a0002c0003t0002g0045a0002c0003t0004g0342others(16): Show | 19 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.437-122T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38905400 | ||||||
| chr4:38905400
|
T | TA | 8 | a0001c0001t0035g0311a0001c0002t0040g0306a0002c0003t0005g0355others(5): Show | 8 | HG01255.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.437-107dupA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38905400 | |||||
| chr4:38905400
|
TA | T | 7 | a0001c0001t0001g0213a0001c0001t0002g0062a0001c0001t0017g0138others(4): Show | 7 | HG00323.hp1 HG01070.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.437-107delA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38905400 | |||||
| chr4:38905401
|
A | T | 44 | a0001c0001t0001g0041a0001c0001t0002g0008a0001c0001t0002g0040others(41): Show | 44 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.437-121A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38905401 | ||||||
| chr4:38905402
|
A | T | 3 | a0001c0001t0001g0041a0001c0043t0001g0006a0002c0027t0003g0031 | 3 | HG01167.hp2 HG03579.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.437-120A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38905402 | ||||||
| chr4:38905412
|
A | G | 10 | a0002c0003t0002g0043a0002c0003t0002g0045a0002c0003t0004g0342others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-110A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38905412 | ||||||
| chr4:38905457
|
T | C | 10 | a0002c0003t0002g0043a0002c0003t0002g0045a0002c0003t0004g0342others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-65T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38905457 | ||||||
| chr4:38905476
|
C | T | 1 | a0001c0001t0009g0153 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.437-46C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38905476 | ||||||
| chr4:38905721
|
G | A | 2 | a0002c0032t0044g0352a0002c0057t0005g0251 | 2 | HG02145.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.551-34G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 5/14 | chr4 | 38905721 | ||||||
| chr4:38905986
|
G | T | 8 | a0001c0001t0012g0172a0002c0003t0006g0037a0002c0006t0001g0020others(5): Show | 8 | HG00544.hp2 HG01243.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.657+125G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38905986 | ||||||
| chr4:38906020
|
C | T | 1 | a0002c0006t0001g0038 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.657+159C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38906020 | ||||||
| chr4:38906269
|
G | A | 2 | a0002c0032t0044g0352a0002c0057t0005g0251 | 2 | HG02145.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.657+408G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38906269 | ||||||
| chr4:38906336
|
C | G | 1 | a0002c0003t0005g0364 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.657+475C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38906336 | ||||||
| chr4:38906338
|
T | TC | 4 | a0001c0001t0001g0041a0001c0004t0011g0255a0001c0038t0005g0011others(1): Show | 4 | HG03471.hp2 HG03579.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.657+480dupC | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr4 | 38906338 | |||||
| chr4:38906367
|
C | T | 76 | a0001c0001t0001g0165a0001c0001t0001g0264a0001c0001t0001g0284others(73): Show | 79 | HG00408.hp2 HG00597.hp1 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.657+506C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38906367 | ||||||
| chr4:38906390
|
TC | T | 48 | a0001c0001t0002g0047a0001c0001t0002g0063a0001c0001t0002g0292others(45): Show | 50 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.657+534delC | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr4 | 38906390 | |||||
| chr4:38906417
|
G | A | 134 | a0001c0001t0001g0100a0001c0001t0002g0047a0001c0001t0002g0063others(131): Show | 136 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.657+556G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38906417 | ||||||
| chr4:38906465
|
G | T | 2 | a0001c0001t0002g0017a0001c0002t0002g0018 | 2 | NA18966.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.657+604G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38906465 | ||||||
| chr4:38906484
|
A | G | 1 | a0001c0002t0001g0103 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.657+623A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38906484 | ||||||
| chr4:38906544
|
G | GT | 4 | a0001c0004t0002g0349a0001c0004t0007g0331a0005c0012t0001g0029others(1): Show | 4 | HG02698.hp1 HG03927.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.657+690dupT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr4 | 38906544 | |||||
| chr4:38906604
|
G | A | 4 | a0001c0043t0001g0006a0002c0003t0002g0043a0002c0003t0002g0045others(1): Show | 4 | HG01167.hp2 HG02451.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.657+743G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38906604 | ||||||
| chr4:38906787
|
G | A | 2 | a0002c0003t0018g0119a0002c0003t0018g0128 | 2 | NA18999.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.657+926G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38906787 | ||||||
| chr4:38906969
|
T | A | 9 | a0001c0001t0002g0221a0001c0001t0002g0222a0001c0001t0002g0224others(6): Show | 9 | HG01081.hp2 HG02145.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.657+1108T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38906969 | ||||||
| chr4:38906995
|
G | C | 143 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0099others(140): Show | 143 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.657+1134G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38906995 | ||||||
| chr4:38907016
|
T | G | 5 | a0001c0001t0009g0154a0001c0004t0002g0349a0001c0004t0007g0331others(2): Show | 5 | HG01109.hp1 HG02698.hp1 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.657+1155T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38907016 | ||||||
| chr4:38907022
|
G | A | 196 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(193): Show | 199 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.657+1161G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38907022 | ||||||
| chr4:38907577
|
G | A | 1 | a0001c0002t0001g0217 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.658-1015G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38907577 | ||||||
| chr4:38907655
|
A | G | 11 | a0002c0006t0011g0028a0003c0020t0003g0101a0004c0007t0009g0025others(8): Show | 11 | HG00323.hp2 HG00741.hp2 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.658-937A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38907655 | ||||||
| chr4:38907706
|
A | G | 7 | a0001c0001t0005g0193a0001c0002t0014g0156a0008c0014t0001g0012others(4): Show | 7 | HG02559.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.658-886A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38907706 | ||||||
| chr4:38907833
|
A | T | 7 | a0001c0001t0005g0193a0001c0002t0014g0156a0008c0014t0001g0012others(4): Show | 7 | HG02559.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.658-759A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38907833 | ||||||
| chr4:38907853
|
A | G | 4 | a0001c0004t0002g0349a0001c0004t0007g0331a0005c0012t0001g0029others(1): Show | 4 | HG02698.hp1 HG03927.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.658-739A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38907853 | ||||||
| chr4:38908297
|
C | G | 9 | a0001c0001t0001g0195a0001c0001t0001g0296a0001c0001t0002g0189others(6): Show | 9 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.658-295C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38908297 | ||||||
| chr4:38908413
|
A | G | 1 | a0018c0052t0005g0247 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.658-179A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38908413 | ||||||
| chr4:38908741
|
G | T | 48 | a0001c0001t0001g0165a0001c0001t0002g0040a0001c0001t0002g0271others(45): Show | 52 | HG00735.hp2 HG01069.hp2 HG01516.hp1 others(49): Show |
intron_variant | MODIFIER | c.792+15G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38908741 | ||||||
| chr4:38908872
|
C | T | 17 | a0001c0001t0001g0195a0001c0001t0001g0296a0001c0001t0002g0189others(14): Show | 17 | HG02055.hp1 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.792+146C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38908872 | ||||||
| chr4:38908925
|
C | T | 48 | a0001c0001t0001g0165a0001c0001t0002g0040a0001c0001t0002g0271others(45): Show | 52 | HG00735.hp2 HG01069.hp2 HG01516.hp1 others(49): Show |
intron_variant | MODIFIER | c.792+199C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38908925 | ||||||
| chr4:38908938
|
A | G | 1 | a0001c0001t0005g0193 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.792+212A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38908938 | ||||||
| chr4:38908948
|
G | A | 1 | a0018c0052t0005g0247 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.792+222G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38908948 | ||||||
| chr4:38909109
|
A | G | 123 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0099others(120): Show | 123 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.792+383A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38909109 | ||||||
| chr4:38909170
|
C | T | 165 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(162): Show | 165 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.792+444C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38909170 | ||||||
| chr4:38909332
|
T | C | 6 | a0001c0001t0005g0193a0001c0002t0014g0156a0008c0014t0001g0012others(3): Show | 6 | HG02622.hp2 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.792+606T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38909332 | ||||||
| chr4:38909452
|
A | G | 1 | a0001c0001t0002g0146 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.792+726A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38909452 | ||||||
| chr4:38909547
|
A | T | 219 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(216): Show | 223 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.792+821A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38909547 | ||||||
| chr4:38909550
|
CTT | C | 61 | a0001c0001t0001g0041a0001c0001t0001g0195a0001c0001t0001g0296others(58): Show | 61 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.792+825_792+826del others(2): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38909550 | ||||||
| chr4:38909584
|
A | G | 60 | a0001c0001t0001g0165a0001c0001t0002g0040a0001c0001t0002g0049others(57): Show | 64 | HG00099.hp2 HG00735.hp2 HG01069.hp2 others(61): Show |
intron_variant | MODIFIER | c.792+858A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38909584 | ||||||
| chr4:38909694
|
A | G | 58 | a0001c0001t0001g0165a0001c0001t0002g0040a0001c0001t0002g0049others(55): Show | 62 | HG00099.hp2 HG00735.hp2 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.792+968A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38909694 | ||||||
| chr4:38909724
|
C | T | 61 | a0001c0001t0001g0041a0001c0001t0001g0195a0001c0001t0001g0296others(58): Show | 61 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.792+998C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38909724 | ||||||
| chr4:38909974
|
G | A | 50 | a0001c0001t0001g0165a0001c0001t0002g0040a0001c0001t0002g0049others(47): Show | 54 | HG00099.hp2 HG01255.hp1 HG01255.hp2 others(51): Show |
intron_variant | MODIFIER | c.792+1248G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38909974 | ||||||
| chr4:38910095
|
C | T | 1 | a0001c0001t0002g0013 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.792+1369C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38910095 | ||||||
| chr4:38910116
|
G | A | 2 | a0005c0012t0001g0029a0005c0030t0003g0113 | 2 | HG02698.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.792+1390G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38910116 | ||||||
| chr4:38910142
|
G | A | 50 | a0001c0001t0001g0165a0001c0001t0002g0040a0001c0001t0002g0049others(47): Show | 54 | HG00099.hp2 HG01255.hp1 HG01255.hp2 others(51): Show |
intron_variant | MODIFIER | c.792+1416G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38910142 | ||||||
| chr4:38910168
|
G | A | 13 | a0001c0001t0001g0165a0001c0004t0001g0072a0001c0004t0002g0001others(10): Show | 16 | HG04228.hp1 NA18942.hp2 NA18950.hp1 others(13): Show |
intron_variant | MODIFIER | c.792+1442G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38910168 | ||||||
| chr4:38910220
|
T | C | 219 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(216): Show | 223 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.792+1494T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38910220 | ||||||
| chr4:38910261
|
G | A | 1 | a0001c0008t0006g0089 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.792+1535G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38910261 | ||||||
| chr4:38910587
|
G | C | 219 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(216): Show | 223 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.792+1861G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38910587 | ||||||
| chr4:38910602
|
T | G | 1 | a0005c0030t0003g0113 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.792+1876T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38910602 | ||||||
| chr4:38910749
|
C | T | 1 | a0001c0001t0006g0061 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.792+2023C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38910749 | ||||||
| chr4:38910863
|
A | G | 94 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0099others(91): Show | 94 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.792+2137A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38910863 | ||||||
| chr4:38911000
|
G | A | 219 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(216): Show | 223 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.792+2274G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38911000 | ||||||
| chr4:38911023
|
G | A | 1 | a0001c0001t0001g0275 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.792+2297G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38911023 | ||||||
| chr4:38911195
|
C | T | 213 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(210): Show | 217 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(214): Show |
intron_variant | MODIFIER | c.792+2469C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38911195 | ||||||
| chr4:38911259
|
C | T | 3 | a0001c0001t0042g0210a0002c0003t0002g0043a0002c0003t0010g0338 | 3 | HG02451.hp2 HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.792+2533C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38911259 | ||||||
| chr4:38911263
|
A | C | 219 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(216): Show | 223 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.792+2537A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38911263 | ||||||
| chr4:38911337
|
G | A | 3 | a0001c0001t0042g0210a0002c0003t0002g0043a0002c0003t0010g0338 | 3 | HG02451.hp2 HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.792+2611G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38911337 | ||||||
| chr4:38911377
|
A | G | 219 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(216): Show | 223 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.792+2651A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38911377 | ||||||
| chr4:38911503
|
T | G | 1 | a0018c0052t0005g0247 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.792+2777T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38911503 | ||||||
| chr4:38911750
|
G | A | 12 | a0001c0001t0002g0008a0001c0001t0011g0010a0001c0001t0035g0311others(9): Show | 12 | HG01109.hp2 HG01167.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.792+3024G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38911750 | ||||||
| chr4:38911786
|
T | TTATCCTA | 12 | a0001c0001t0017g0138a0001c0004t0002g0064a0001c0004t0002g0349others(9): Show | 12 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(9): Show |
intron_variant | MODIFIER | c.792+3061_792+3067d others(9): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr4 | 38911786 | |||||
| chr4:38911804
|
G | A | 1 | a0001c0001t0002g0081 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.792+3078G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38911804 | ||||||
| chr4:38911806
|
A | G | 1 | a0007c0021t0004g0347 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.792+3080A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38911806 | ||||||
| chr4:38911833
|
TTTTTTTT others(4): Show |
T | 1 | a0001c0046t0002g0096 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.793-3078_793-3068d others(13): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr4 | 38911833 | |||||
| chr4:38911834
|
TTTTTTTT others(3): Show |
T | 1 | a0001c0001t0002g0168 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.793-3070_793-3061d others(12): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr4 | 38911834 | |||||
| chr4:38911844
|
C | CT | 45 | a0001c0001t0001g0175a0001c0001t0001g0264a0001c0001t0002g0040others(42): Show | 45 | HG00558.hp2 HG00609.hp2 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.793-3068dupT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr4 | 38911844 | |||||
| chr4:38911844
|
C | T | 1 | a0002c0003t0004g0129 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.793-3077C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38911844 | ||||||
| chr4:38911850
|
TTTTCTTT others(4): Show |
T | 111 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0099others(108): Show | 111 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.793-3067_793-3057d others(13): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr4 | 38911850 | |||||
| chr4:38911851
|
T | C | 10 | a0001c0001t0002g0049a0001c0001t0002g0091a0001c0001t0002g0308others(7): Show | 10 | HG00099.hp2 HG01255.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.793-3070T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38911851 | ||||||
| chr4:38911861
|
C | CT | 18 | a0001c0001t0002g0013a0001c0001t0007g0227a0001c0001t0013g0237others(15): Show | 18 | HG00140.hp1 HG01361.hp1 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.793-3043dupT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr4 | 38911861 | |||||
| chr4:38911861
|
CT | C | 53 | a0001c0001t0001g0041a0001c0001t0002g0008a0001c0001t0002g0049others(50): Show | 53 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.793-3043delT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr4 | 38911861 | |||||
| chr4:38911861
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0002t0001g0169 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.793-3053_793-3043d others(13): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr4 | 38911861 | |||||
| chr4:38911862
|
T | C | 111 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0099others(108): Show | 111 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.793-3059T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38911862 | ||||||
| chr4:38912007
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.793-2914T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38912007 | ||||||
| chr4:38912165
|
G | A | 1 | a0015c0047t0009g0155 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.793-2756G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38912165 | ||||||
| chr4:38912280
|
T | C | 17 | a0001c0001t0001g0195a0001c0001t0001g0296a0001c0001t0002g0189others(14): Show | 17 | HG02055.hp1 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.793-2641T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38912280 | ||||||
| chr4:38912330
|
G | C | 221 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(218): Show | 225 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(222): Show |
intron_variant | MODIFIER | c.793-2591G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38912330 | ||||||
| chr4:38912369
|
C | T | 1 | a0002c0057t0005g0251 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.793-2552C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38912369 | ||||||
| chr4:38912450
|
T | G | 1 | a0001c0001t0002g0013 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.793-2471T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38912450 | ||||||
| chr4:38912485
|
A | T | 1 | a0001c0001t0002g0091 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.793-2436A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38912485 | ||||||
| chr4:38912500
|
T | C | 8 | a0001c0001t0004g0281a0001c0001t0007g0256a0001c0002t0040g0306others(5): Show | 8 | HG01891.hp1 HG02280.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.793-2421T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38912500 | ||||||
| chr4:38912612
|
G | C | 1 | a0001c0001t0007g0227 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.793-2309G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38912612 | ||||||
| chr4:38912674
|
G | A | 6 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0223others(3): Show | 6 | HG00140.hp1 HG00642.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.793-2247G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38912674 | ||||||
| chr4:38912677
|
T | C | 6 | a0001c0001t0005g0193a0001c0002t0014g0156a0008c0014t0001g0012others(3): Show | 6 | HG02622.hp2 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.793-2244T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38912677 | ||||||
| chr4:38912724
|
C | A | 4 | a0001c0001t0002g0008a0001c0001t0011g0010a0001c0009t0003g0335others(1): Show | 4 | HG02486.hp2 HG02559.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.793-2197C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38912724 | ||||||
| chr4:38912767
|
C | T | 2 | a0002c0053t0001g0245a0002c0054t0036g0243 | 2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.793-2154C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38912767 | ||||||
| chr4:38912819
|
G | C | 13 | a0001c0001t0017g0138a0001c0004t0002g0064a0001c0004t0002g0349others(10): Show | 13 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.793-2102G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38912819 | ||||||
| chr4:38913000
|
C | T | 1 | a0008c0014t0023g0305 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.793-1921C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38913000 | ||||||
| chr4:38913160
|
TA | T | 19 | a0001c0001t0002g0271a0001c0001t0002g0272a0001c0001t0004g0268others(16): Show | 19 | HG00323.hp2 HG00735.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.793-1758delA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr4 | 38913160 | |||||
| chr4:38913234
|
G | C | 1 | a0002c0003t0002g0358 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.793-1687G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38913234 | ||||||
| chr4:38913680
|
G | A | 8 | a0001c0001t0002g0049a0001c0001t0002g0091a0001c0001t0002g0308others(5): Show | 8 | HG00099.hp2 HG01255.hp1 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.793-1241G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38913680 | ||||||
| chr4:38913699
|
T | C | 51 | a0001c0001t0002g0080a0001c0001t0002g0292a0001c0001t0005g0301others(48): Show | 55 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.793-1222T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38913699 | ||||||
| chr4:38913866
|
G | A | 3 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0223 | 3 | HG00642.hp1 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.793-1055G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38913866 | ||||||
| chr4:38914055
|
G | A | 1 | a0001c0001t0002g0095 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.793-866G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38914055 | ||||||
| chr4:38914065
|
A | G | 1 | a0008c0014t0023g0305 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.793-856A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38914065 | ||||||
| chr4:38914244
|
A | G | 2 | a0002c0053t0001g0245a0002c0054t0036g0243 | 2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.793-677A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38914244 | ||||||
| chr4:38914424
|
G | A | 1 | a0002c0054t0036g0243 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.793-497G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38914424 | ||||||
| chr4:38914514
|
C | A | 47 | a0001c0001t0002g0080a0001c0001t0002g0292a0001c0001t0005g0301others(44): Show | 51 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.793-407C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38914514 | ||||||
| chr4:38914844
|
A | C | 343 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(340): Show | 349 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(346): Show |
intron_variant | MODIFIER | c.793-77A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38914844 | ||||||
| chr4:38915293
|
T | G | 219 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(216): Show | 223 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.945+220T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38915293 | ||||||
| chr4:38915323
|
C | T | 3 | a0001c0001t0010g0259a0001c0005t0003g0274a0002c0028t0030g0363 | 3 | HG02486.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.945+250C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38915323 | ||||||
| chr4:38915445
|
A | G | 3 | a0001c0001t0005g0231a0002c0003t0002g0045a0002c0003t0005g0364 | 3 | HG01884.hp1 HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.945+372A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38915445 | ||||||
| chr4:38915606
|
C | T | 1 | a0018c0052t0005g0247 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.945+533C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38915606 | ||||||
| chr4:38915712
|
T | C | 3 | a0001c0001t0010g0259a0001c0005t0003g0274a0002c0028t0030g0363 | 3 | HG02486.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.945+639T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38915712 | ||||||
| chr4:38915717
|
A | AT | 49 | a0001c0001t0001g0041a0001c0001t0001g0195a0001c0001t0001g0296others(46): Show | 49 | HG01109.hp2 HG01167.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.945+651dupT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38915717 | |||||
| chr4:38915744
|
G | GGT | 51 | a0001c0001t0002g0221a0001c0001t0002g0313a0001c0001t0004g0060others(48): Show | 51 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.945+720_945+721dup others(2): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38915744 | |||||
| chr4:38915744
|
G | GGTGT | 8 | a0001c0001t0005g0297a0001c0002t0001g0090a0001c0002t0001g0235others(5): Show | 8 | HG00597.hp2 HG01175.hp1 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.945+718_945+721dup others(4): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38915744 | |||||
| chr4:38915744
|
GGT | G | 51 | a0001c0001t0001g0099a0001c0001t0001g0284a0001c0001t0001g0314others(48): Show | 51 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.945+720_945+721del others(2): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38915744 | |||||
| chr4:38915744
|
GGTGT | G | 39 | a0001c0001t0001g0195a0001c0001t0001g0212a0001c0001t0001g0213others(36): Show | 39 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.945+718_945+721del others(4): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38915744 | |||||
| chr4:38915744
|
GGTGTGT | G | 29 | a0001c0001t0002g0013a0001c0001t0002g0040a0001c0001t0002g0065others(26): Show | 29 | HG00408.hp1 HG01891.hp1 HG01981.hp1 others(26): Show |
intron_variant | MODIFIER | c.945+716_945+721del others(6): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38915744 | |||||
| chr4:38915744
|
GGTGTGTG others(1): Show |
G | 52 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0165others(49): Show | 52 | HG00609.hp1 HG00673.hp2 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.945+714_945+721del others(8): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38915744 | |||||
| chr4:38915744
|
GGTGTGTG others(3): Show |
G | 4 | a0001c0001t0002g0069a0001c0001t0002g0229a0002c0006t0001g0353others(1): Show | 4 | HG00558.hp1 HG01255.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.945+712_945+721del others(10): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38915744 | |||||
| chr4:38915744
|
GGTGTGTG others(5): Show |
G | 21 | a0001c0001t0001g0163a0001c0001t0001g0175a0001c0001t0002g0088others(18): Show | 21 | HG00408.hp2 HG00544.hp2 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.945+710_945+721del others(12): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38915744 | |||||
| chr4:38915744
|
GGTGTGTG others(11): Show |
G | 2 | a0001c0001t0042g0210a0002c0003t0002g0043 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.945+704_945+721del others(18): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38915744 | |||||
| chr4:38915744
|
GGTGTGTG others(15): Show |
G | 1 | a0001c0008t0006g0111 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.945+700_945+721del others(22): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38915744 | |||||
| chr4:38915771
|
G | GTC | 43 | a0001c0004t0001g0072a0001c0004t0001g0260a0001c0004t0002g0001others(40): Show | 47 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.945+699_945+700ins others(2): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38915771 | |||||
| chr4:38915783
|
GTGTGTGT others(5): Show |
G | 1 | a0001c0001t0002g0082 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.945+712_945+723del others(12): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38915783 | |||||
| chr4:38915787
|
GTGTGTGT | G | 4 | a0001c0001t0002g0071a0001c0001t0002g0168a0001c0001t0002g0228others(1): Show | 4 | HG01192.hp1 HG02523.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.945+716_945+722del others(7): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38915787 | |||||
| chr4:38915793
|
GT | G | 4 | a0001c0001t0001g0187a0001c0001t0002g0315a0001c0002t0001g0279others(1): Show | 4 | HG00642.hp2 HG01346.hp2 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.945+723delT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38915793 | |||||
| chr4:38915805
|
AGCACTTA others(93): Show |
A | 3 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0223 | 3 | HG00642.hp1 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.945+734_945+833del others(100): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38915805 | |||||
| chr4:38915862
|
T | C | 1 | a0001c0001t0042g0210 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.945+789T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38915862 | ||||||
| chr4:38916073
|
C | T | 37 | a0001c0001t0002g0049a0001c0001t0002g0091a0001c0001t0002g0271others(34): Show | 37 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.945+1000C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38916073 | ||||||
| chr4:38916082
|
G | C | 43 | a0001c0004t0001g0072a0001c0004t0001g0260a0001c0004t0002g0001others(40): Show | 47 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.945+1009G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38916082 | ||||||
| chr4:38916209
|
A | G | 87 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0099others(84): Show | 87 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.945+1136A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38916209 | ||||||
| chr4:38916253
|
C | T | 43 | a0001c0004t0001g0072a0001c0004t0001g0260a0001c0004t0002g0001others(40): Show | 47 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.945+1180C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38916253 | ||||||
| chr4:38916362
|
A | G | 43 | a0001c0004t0001g0072a0001c0004t0001g0260a0001c0004t0002g0001others(40): Show | 47 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.945+1289A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38916362 | ||||||
| chr4:38916472
|
T | A | 19 | a0001c0001t0001g0195a0001c0001t0001g0296a0001c0001t0002g0189others(16): Show | 19 | HG02055.hp1 HG02145.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.945+1399T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38916472 | ||||||
| chr4:38916551
|
C | T | 128 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0099others(125): Show | 132 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.945+1478C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38916551 | ||||||
| chr4:38916563
|
G | A | 1 | a0001c0005t0003g0323 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.945+1490G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38916563 | ||||||
| chr4:38916608
|
A | G | 1 | a0006c0035t0003g0207 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.945+1535A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38916608 | ||||||
| chr4:38916658
|
G | A | 43 | a0001c0004t0001g0072a0001c0004t0001g0260a0001c0004t0002g0001others(40): Show | 47 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.945+1585G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38916658 | ||||||
| chr4:38916829
|
G | T | 43 | a0001c0004t0001g0072a0001c0004t0001g0260a0001c0004t0002g0001others(40): Show | 47 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.945+1756G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38916829 | ||||||
| chr4:38916897
|
A | G | 49 | a0001c0001t0001g0041a0001c0001t0001g0195a0001c0001t0001g0296others(46): Show | 49 | HG01109.hp2 HG01167.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.945+1824A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38916897 | ||||||
| chr4:38916968
|
G | A | 11 | a0001c0001t0002g0271a0001c0001t0002g0272a0001c0001t0004g0268others(8): Show | 11 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.945+1895G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38916968 | ||||||
| chr4:38916991
|
C | A | 43 | a0001c0004t0001g0072a0001c0004t0001g0260a0001c0004t0002g0001others(40): Show | 47 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.945+1918C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38916991 | ||||||
| chr4:38917069
|
C | T | 85 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0099others(82): Show | 85 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.945+1996C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38917069 | ||||||
| chr4:38917120
|
A | G | 3 | a0001c0001t0002g0047a0003c0011t0001g0302a0006c0010t0003g0174 | 3 | HG01433.hp1 HG01943.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.945+2047A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38917120 | ||||||
| chr4:38917149
|
C | CAAAT | 38 | a0001c0001t0001g0041a0001c0001t0002g0091a0001c0001t0002g0271others(35): Show | 38 | HG01069.hp2 HG01255.hp1 HG01346.hp1 others(35): Show |
intron_variant | MODIFIER | c.945+2112_945+2115d others(6): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38917149 | |||||
| chr4:38917149
|
C | CAAATAAA others(1): Show |
37 | a0001c0001t0001g0195a0001c0001t0001g0212a0001c0001t0001g0213others(34): Show | 37 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.945+2108_945+2115d others(10): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38917149 | |||||
| chr4:38917149
|
C | CAAATAAA others(5): Show |
82 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0099others(79): Show | 82 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.945+2104_945+2115d others(14): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38917149 | |||||
| chr4:38917149
|
C | CAAATAAA others(9): Show |
13 | a0001c0001t0001g0163a0001c0001t0001g0175a0001c0001t0002g0016others(10): Show | 13 | HG01099.hp2 HG01123.hp2 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.945+2100_945+2115d others(18): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38917149 | |||||
| chr4:38917149
|
C | CAAATAAA others(13): Show |
1 | a0001c0001t0035g0311 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.945+2096_945+2115d others(22): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38917149 | |||||
| chr4:38917149
|
CAAAT | C | 3 | a0001c0001t0005g0014a0002c0003t0005g0044a0003c0011t0014g0269 | 3 | HG01884.hp2 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.945+2112_945+2115d others(6): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38917149 | |||||
| chr4:38917149
|
CAAATAAA others(5): Show |
C | 1 | a0001c0001t0002g0263 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.945+2104_945+2115d others(14): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38917149 | |||||
| chr4:38917149
|
CAAATAAA others(9): Show |
C | 43 | a0001c0004t0001g0072a0001c0004t0001g0260a0001c0004t0002g0001others(40): Show | 47 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.945+2100_945+2115d others(18): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38917149 | |||||
| chr4:38917185
|
T | TAAATAAA others(5): Show |
1 | a0005c0012t0034g0023 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.945+2115_945+2116i others(14): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38917185 | |||||
| chr4:38917185
|
T | TAAATAAA others(9): Show |
1 | a0001c0001t0011g0010 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.945+2115_945+2116i others(18): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38917185 | |||||
| chr4:38917185
|
T | TAAATAAA others(9): Show |
1 | a0001c0001t0002g0008 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.945+2115_945+2116i others(18): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38917185 | |||||
| chr4:38917185
|
T | TAAATAAA others(13): Show |
1 | a0001c0009t0003g0335 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.945+2115_945+2116i others(22): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38917185 | |||||
| chr4:38917218
|
A | T | 11 | a0002c0006t0011g0028a0003c0020t0003g0101a0004c0007t0009g0025others(8): Show | 11 | HG00323.hp2 HG00741.hp2 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.945+2145A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38917218 | ||||||
| chr4:38917235
|
G | A | 6 | a0001c0001t0005g0193a0001c0002t0014g0156a0008c0014t0001g0012others(3): Show | 6 | HG02622.hp2 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.945+2162G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38917235 | ||||||
| chr4:38917337
|
C | CA | 43 | a0001c0004t0001g0072a0001c0004t0001g0260a0001c0004t0002g0001others(40): Show | 47 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.945+2275dupA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38917337 | |||||
| chr4:38917499
|
T | C | 220 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(217): Show | 224 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.945+2426T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38917499 | ||||||
| chr4:38917545
|
A | C | 7 | a0001c0001t0001g0187a0001c0001t0001g0284a0001c0002t0001g0142others(4): Show | 7 | HG00642.hp2 HG01074.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.945+2472A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38917545 | ||||||
| chr4:38917600
|
T | TTTG | 43 | a0001c0004t0001g0072a0001c0004t0001g0260a0001c0004t0002g0001others(40): Show | 47 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.945+2533_945+2535d others(5): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38917600 | |||||
| chr4:38917748
|
C | T | 10 | a0001c0001t0001g0041a0001c0001t0004g0281a0001c0001t0007g0256others(7): Show | 10 | HG01884.hp2 HG01891.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.945+2675C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38917748 | ||||||
| chr4:38917795
|
A | C | 43 | a0001c0004t0001g0072a0001c0004t0001g0260a0001c0004t0002g0001others(40): Show | 47 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.945+2722A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38917795 | ||||||
| chr4:38917943
|
G | A | 90 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0099others(87): Show | 90 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.945+2870G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38917943 | ||||||
| chr4:38917944
|
C | T | 39 | a0001c0001t0002g0049a0001c0001t0002g0091a0001c0001t0002g0271others(36): Show | 39 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.945+2871C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38917944 | ||||||
| chr4:38917949
|
A | G | 220 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(217): Show | 224 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.945+2876A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38917949 | ||||||
| chr4:38918014
|
C | T | 90 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0099others(87): Show | 90 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.945+2941C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38918014 | ||||||
| chr4:38918093
|
G | A | 1 | a0001c0001t0010g0299 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.945+3020G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38918093 | ||||||
| chr4:38918220
|
G | A | 2 | a0001c0001t0002g0278a0001c0001t0007g0230 | 2 | HG02074.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.945+3147G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38918220 | ||||||
| chr4:38918376
|
G | A | 41 | a0001c0004t0001g0072a0001c0004t0001g0260a0001c0004t0002g0001others(38): Show | 45 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.945+3303G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38918376 | ||||||
| chr4:38918707
|
C | G | 4 | a0001c0001t0002g0013a0001c0001t0007g0227a0002c0003t0005g0355others(1): Show | 4 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.945+3634C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38918707 | ||||||
| chr4:38918788
|
G | A | 41 | a0001c0004t0001g0072a0001c0004t0001g0260a0001c0004t0002g0001others(38): Show | 45 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.945+3715G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38918788 | ||||||
| chr4:38918820
|
G | A | 1 | a0002c0003t0010g0338 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.945+3747G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38918820 | ||||||
| chr4:38918862
|
G | A | 2 | a0001c0001t0042g0210a0002c0003t0002g0043 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.945+3789G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38918862 | ||||||
| chr4:38918917
|
C | T | 7 | a0001c0001t0002g0049a0001c0001t0002g0091a0001c0001t0002g0308others(4): Show | 7 | HG00099.hp2 HG01255.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.945+3844C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38918917 | ||||||
| chr4:38918970
|
A | T | 48 | a0001c0001t0002g0049a0001c0001t0002g0091a0001c0001t0002g0308others(45): Show | 52 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.946-3800A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38918970 | ||||||
| chr4:38919048
|
G | C | 1 | a0002c0003t0004g0024 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.946-3722G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38919048 | ||||||
| chr4:38919084
|
C | T | 14 | a0001c0001t0002g0088a0001c0001t0002g0150a0001c0001t0002g0178others(11): Show | 14 | HG00408.hp2 HG00544.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.946-3686C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38919084 | ||||||
| chr4:38919421
|
C | T | 58 | a0001c0001t0001g0195a0001c0001t0001g0296a0001c0001t0002g0095others(55): Show | 61 | HG00597.hp1 HG00621.hp1 HG02027.hp2 others(58): Show |
intron_variant | MODIFIER | c.946-3349C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38919421 | ||||||
| chr4:38919670
|
T | A | 1 | a0002c0003t0005g0355 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.946-3100T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38919670 | ||||||
| chr4:38919909
|
A | G | 2 | a0001c0001t0007g0273a0017c0031t0019g0030 | 2 | NA18953.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.946-2861A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38919909 | ||||||
| chr4:38919933
|
G | T | 5 | a0001c0002t0001g0135a0001c0002t0001g0161a0001c0002t0001g0219others(2): Show | 5 | NA18951.hp1 NA18955.hp2 NA19057.hp2 others(2): Show |
intron_variant | MODIFIER | c.946-2837G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38919933 | ||||||
| chr4:38919938
|
C | T | 1 | a0001c0001t0002g0308 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.946-2832C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38919938 | ||||||
| chr4:38920436
|
A | T | 3 | a0002c0003t0001g0359a0002c0053t0001g0245a0002c0054t0036g0243 | 3 | HG02717.hp1 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.946-2334A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38920436 | ||||||
| chr4:38920512
|
A | G | 9 | a0001c0001t0014g0295a0001c0001t0035g0311a0001c0004t0011g0145others(6): Show | 9 | HG01109.hp2 HG02109.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.946-2258A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38920512 | ||||||
| chr4:38920701
|
T | C | 3 | a0002c0003t0001g0359a0002c0053t0001g0245a0002c0054t0036g0243 | 3 | HG02717.hp1 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.946-2069T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38920701 | ||||||
| chr4:38920711
|
T | G | 78 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0099others(75): Show | 78 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.946-2059T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38920711 | ||||||
| chr4:38920737
|
T | C | 93 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0099others(90): Show | 94 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.946-2033T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38920737 | ||||||
| chr4:38920946
|
T | C | 211 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(208): Show | 215 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(212): Show |
intron_variant | MODIFIER | c.946-1824T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38920946 | ||||||
| chr4:38920973
|
A | T | 210 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(207): Show | 214 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.946-1797A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38920973 | ||||||
| chr4:38921012
|
C | A | 12 | a0001c0001t0005g0014a0001c0001t0014g0295a0001c0001t0035g0311others(9): Show | 12 | HG01109.hp2 HG02109.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.946-1758C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38921012 | ||||||
| chr4:38921036
|
G | C | 12 | a0001c0001t0005g0014a0001c0001t0014g0295a0001c0001t0035g0311others(9): Show | 12 | HG01109.hp2 HG02109.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.946-1734G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38921036 | ||||||
| chr4:38921116
|
T | C | 23 | a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0002g0209others(20): Show | 23 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.946-1654T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38921116 | ||||||
| chr4:38921171
|
T | C | 16 | a0001c0001t0001g0041a0001c0001t0005g0231a0001c0001t0007g0256others(13): Show | 16 | HG01255.hp2 HG01884.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.946-1599T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38921171 | ||||||
| chr4:38921338
|
GCCTCAAA others(132): Show |
G | 2 | a0001c0001t0014g0295a0001c0009t0003g0335 | 2 | HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.946-1410_946-1272d others(2): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38921338 | |||||
| chr4:38921358
|
A | G | 1 | a0001c0001t0005g0276 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.946-1412A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38921358 | ||||||
| chr4:38921597
|
T | G | 1 | a0002c0003t0010g0362 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.946-1173T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38921597 | ||||||
| chr4:38921621
|
A | G | 1 | a0001c0002t0020g0236 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.946-1149A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38921621 | ||||||
| chr4:38921740
|
A | C | 2 | a0002c0028t0030g0363a0011c0050t0003g0345 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.946-1030A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38921740 | ||||||
| chr4:38921782
|
G | A | 1 | a0002c0003t0002g0358 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.946-988G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38921782 | ||||||
| chr4:38921822
|
T | C | 1 | a0001c0001t0042g0210 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.946-948T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38921822 | ||||||
| chr4:38921891
|
G | GA | 203 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0099others(200): Show | 208 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.946-878dupA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38921891 | |||||
| chr4:38921973
|
C | T | 6 | a0002c0003t0002g0043a0002c0003t0005g0343a0002c0006t0001g0353others(3): Show | 6 | HG01109.hp2 HG01255.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.946-797C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38921973 | ||||||
| chr4:38922000
|
G | A | 1 | a0005c0030t0003g0113 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.946-770G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38922000 | ||||||
| chr4:38922005
|
G | A | 2 | a0001c0001t0005g0014a0002c0003t0005g0044 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.946-765G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38922005 | ||||||
| chr4:38922210
|
G | A | 15 | a0001c0001t0001g0050a0001c0001t0004g0318a0001c0001t0005g0297others(12): Show | 15 | HG01891.hp1 HG01943.hp2 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.946-560G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38922210 | ||||||
| chr4:38922306
|
C | T | 10 | a0002c0006t0011g0028a0003c0020t0003g0101a0004c0007t0009g0025others(7): Show | 10 | HG00323.hp2 HG00741.hp2 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.946-464C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38922306 | ||||||
| chr4:38922400
|
A | G | 49 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(46): Show | 49 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.946-370A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38922400 | ||||||
| chr4:38922484
|
C | T | 1 | a0001c0001t0042g0210 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.946-286C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38922484 | ||||||
| chr4:38922490
|
T | C | 1 | a0002c0003t0010g0362 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.946-280T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38922490 | ||||||
| chr4:38922501
|
C | T | 6 | a0001c0002t0002g0139a0001c0002t0002g0141a0001c0013t0002g0085others(3): Show | 6 | HG00408.hp2 HG00544.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.946-269C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38922501 | ||||||
| chr4:38922502
|
T | C | 1 | a0001c0001t0014g0295 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.946-268T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38922502 | ||||||
| chr4:38922609
|
A | C | 38 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(35): Show | 38 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.946-161A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38922609 | ||||||
| chr4:38922614
|
G | T | 1 | a0001c0001t0006g0149 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.946-156G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38922614 | ||||||
| chr4:38922619
|
A | G | 3 | a0001c0039t0024g0261a0001c0044t0024g0226a0002c0026t0005g0039 | 3 | HG01891.hp1 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.946-151A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38922619 | ||||||
| chr4:38922641
|
A | G | 2 | a0001c0001t0005g0014a0002c0003t0005g0044 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.946-129A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38922641 | ||||||
| chr4:38922654
|
C | T | 30 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(27): Show | 30 | HG00323.hp2 HG00597.hp1 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.946-116C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38922654 | ||||||
| chr4:38922709
|
G | A | 38 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(35): Show | 38 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.946-61G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38922709 | ||||||
| chr4:38922737
|
A | G | 35 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(32): Show | 35 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.946-33A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38922737 | ||||||
| chr4:38922990
|
G | C | 2 | a0001c0001t0005g0014a0002c0003t0005g0044 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1069+97G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38922990 | ||||||
| chr4:38923035
|
G | C | 1 | a0001c0001t0002g0013 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1069+142G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923035 | ||||||
| chr4:38923142
|
G | A | 37 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(34): Show | 37 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.1069+249G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923142 | ||||||
| chr4:38923149
|
T | C | 35 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(32): Show | 35 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.1069+256T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923149 | ||||||
| chr4:38923156
|
A | G | 35 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(32): Show | 35 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.1069+263A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923156 | ||||||
| chr4:38923198
|
C | T | 2 | a0003c0020t0003g0046a0011c0050t0003g0345 | 2 | HG02258.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1069+305C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923198 | ||||||
| chr4:38923224
|
C | CT | 169 | a0001c0001t0001g0041a0001c0001t0001g0050a0001c0001t0001g0099others(166): Show | 175 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.1069+349dupT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr4 | 38923224 | |||||
| chr4:38923224
|
C | CTT | 10 | a0001c0001t0001g0019a0001c0001t0002g0080a0001c0001t0002g0168others(7): Show | 10 | HG02055.hp1 HG02135.hp1 HG03453.hp2 others(7): Show |
intron_variant | MODIFIER | c.1069+348_1069+349d others(4): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr4 | 38923224 | |||||
| chr4:38923224
|
C | CTTT | 18 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(15): Show | 18 | HG00597.hp1 HG00621.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.1069+347_1069+349d others(5): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr4 | 38923224 | |||||
| chr4:38923224
|
C | CTTTT | 11 | a0001c0002t0001g0196a0001c0002t0040g0306a0002c0006t0011g0028others(8): Show | 11 | HG00323.hp2 HG00741.hp2 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.1069+346_1069+349d others(6): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr4 | 38923224 | |||||
| chr4:38923250
|
A | C | 35 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(32): Show | 35 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.1069+357A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923250 | ||||||
| chr4:38923255
|
C | T | 1 | a0004c0007t0009g0025 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1069+362C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923255 | ||||||
| chr4:38923380
|
G | A | 3 | a0001c0001t0002g0013a0001c0004t0022g0003a0003c0011t0014g0269 | 4 | HG01884.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1069+487G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923380 | ||||||
| chr4:38923463
|
T | C | 35 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(32): Show | 35 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.1069+570T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923463 | ||||||
| chr4:38923472
|
C | T | 2 | a0001c0001t0005g0014a0002c0003t0005g0044 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1069+579C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923472 | ||||||
| chr4:38923508
|
G | A | 36 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(33): Show | 36 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.1069+615G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923508 | ||||||
| chr4:38923516
|
T | C | 43 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(40): Show | 43 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.1069+623T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923516 | ||||||
| chr4:38923596
|
T | C | 1 | a0003c0042t0003g0170 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1069+703T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923596 | ||||||
| chr4:38923596
|
T | G | 35 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(32): Show | 35 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.1069+703T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923596 | ||||||
| chr4:38923689
|
A | C | 1 | a0002c0032t0044g0352 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1069+796A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923689 | ||||||
| chr4:38923708
|
T | G | 37 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(34): Show | 37 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.1069+815T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923708 | ||||||
| chr4:38923738
|
C | A | 2 | a0001c0001t0005g0014a0002c0003t0005g0044 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1069+845C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923738 | ||||||
| chr4:38923745
|
C | T | 2 | a0001c0001t0005g0014a0002c0003t0005g0044 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1069+852C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923745 | ||||||
| chr4:38923746
|
A | G | 37 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(34): Show | 37 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.1069+853A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923746 | ||||||
| chr4:38923750
|
G | A | 2 | a0001c0001t0005g0014a0002c0003t0005g0044 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1069+857G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923750 | ||||||
| chr4:38923799
|
C | G | 2 | a0001c0001t0005g0014a0002c0003t0005g0044 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1069+906C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923799 | ||||||
| chr4:38923801
|
T | C | 37 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(34): Show | 37 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.1069+908T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923801 | ||||||
| chr4:38923804
|
A | G | 29 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(26): Show | 29 | HG00323.hp2 HG00597.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.1069+911A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923804 | ||||||
| chr4:38923811
|
T | G | 35 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(32): Show | 35 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.1069+918T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923811 | ||||||
| chr4:38923882
|
A | G | 2 | a0003c0020t0003g0046a0011c0050t0003g0345 | 2 | HG02258.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1069+989A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923882 | ||||||
| chr4:38924048
|
A | G | 35 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(32): Show | 35 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.1069+1155A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924048 | ||||||
| chr4:38924097
|
T | C | 6 | a0001c0002t0002g0139a0001c0002t0002g0141a0001c0013t0002g0085others(3): Show | 6 | HG00408.hp2 HG00544.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1069+1204T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924097 | ||||||
| chr4:38924101
|
G | A | 36 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(33): Show | 36 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.1069+1208G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924101 | ||||||
| chr4:38924162
|
GAT | G | 35 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(32): Show | 35 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.1069+1278_1069+127 others(6): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr4 | 38924162 | |||||
| chr4:38924181
|
A | G | 3 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0223 | 3 | HG00642.hp1 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1069+1288A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924181 | ||||||
| chr4:38924203
|
T | A | 35 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(32): Show | 35 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.1069+1310T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924203 | ||||||
| chr4:38924212
|
A | G | 35 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(32): Show | 35 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.1069+1319A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924212 | ||||||
| chr4:38924226
|
A | G | 37 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(34): Show | 37 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.1069+1333A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924226 | ||||||
| chr4:38924290
|
G | T | 37 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(34): Show | 37 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.1069+1397G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924290 | ||||||
| chr4:38924292
|
A | G | 37 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(34): Show | 37 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.1069+1399A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924292 | ||||||
| chr4:38924297
|
A | G | 37 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(34): Show | 37 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.1069+1404A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924297 | ||||||
| chr4:38924316
|
G | T | 2 | a0001c0001t0005g0014a0002c0003t0005g0044 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1069+1423G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924316 | ||||||
| chr4:38924352
|
C | T | 29 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(26): Show | 29 | HG00323.hp2 HG00597.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.1069+1459C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924352 | ||||||
| chr4:38924367
|
G | C | 1 | a0001c0002t0001g0103 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1069+1474G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924367 | ||||||
| chr4:38924387
|
G | A | 3 | a0001c0001t0002g0013a0001c0001t0042g0210a0003c0011t0014g0269 | 3 | HG01884.hp2 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1069+1494G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924387 | ||||||
| chr4:38924627
|
A | G | 1 | a0001c0001t0012g0334 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1069+1734A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924627 | ||||||
| chr4:38924642
|
C | G | 2 | a0001c0002t0001g0180a0001c0002t0001g0233 | 2 | HG03831.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1069+1749C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924642 | ||||||
| chr4:38924651
|
G | T | 34 | a0001c0001t0002g0013a0001c0001t0005g0297a0001c0001t0042g0210others(31): Show | 34 | HG01433.hp1 HG01884.hp2 HG01943.hp2 others(31): Show |
intron_variant | MODIFIER | c.1069+1758G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924651 | ||||||
| chr4:38924675
|
G | A | 1 | a0007c0021t0004g0347 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1069+1782G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924675 | ||||||
| chr4:38924694
|
G | A | 31 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(28): Show | 31 | HG00323.hp2 HG00597.hp1 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.1069+1801G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924694 | ||||||
| chr4:38924855
|
C | A | 29 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(26): Show | 29 | HG00323.hp2 HG00597.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.1069+1962C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924855 | ||||||
| chr4:38925061
|
T | C | 1 | a0001c0001t0017g0300 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1069+2168T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38925061 | ||||||
| chr4:38925079
|
C | T | 2 | a0001c0001t0011g0010a0002c0003t0010g0362 | 2 | HG02809.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1069+2186C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38925079 | ||||||
| chr4:38925239
|
C | T | 10 | a0002c0006t0011g0028a0003c0020t0003g0101a0004c0007t0009g0025others(7): Show | 10 | HG00323.hp2 HG00741.hp2 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.1069+2346C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38925239 | ||||||
| chr4:38925364
|
G | T | 1 | a0001c0002t0002g0141 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1069+2471G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38925364 | ||||||
| chr4:38925392
|
A | C | 6 | a0001c0002t0002g0139a0001c0002t0002g0141a0001c0013t0002g0085others(3): Show | 6 | HG00408.hp2 HG00544.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1069+2499A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38925392 | ||||||
| chr4:38925393
|
T | C | 2 | a0001c0001t0011g0010a0002c0003t0010g0362 | 2 | HG02809.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1069+2500T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38925393 | ||||||
| chr4:38925411
|
G | T | 1 | a0002c0003t0005g0042 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1069+2518G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38925411 | ||||||
| chr4:38925531
|
C | G | 5 | a0001c0002t0040g0306a0001c0004t0011g0145a0001c0038t0005g0011others(2): Show | 5 | HG02257.hp1 HG02559.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1069+2638C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38925531 | ||||||
| chr4:38925609
|
A | G | 243 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(240): Show | 248 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(245): Show |
intron_variant | MODIFIER | c.1069+2716A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38925609 | ||||||
| chr4:38925760
|
C | T | 1 | a0001c0009t0003g0070 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1069+2867C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38925760 | ||||||
| chr4:38925775
|
T | C | 238 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(235): Show | 242 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.1069+2882T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38925775 | ||||||
| chr4:38925870
|
A | AT | 117 | a0001c0001t0001g0100a0001c0001t0001g0195a0001c0001t0001g0264others(114): Show | 120 | HG00140.hp2 HG00408.hp1 HG00609.hp2 others(117): Show |
intron_variant | MODIFIER | c.1069+2987dupT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr4 | 38925870 | |||||
| chr4:38925870
|
AT | A | 29 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(26): Show | 29 | HG00323.hp2 HG00597.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.1069+2987delT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr4 | 38925870 | |||||
| chr4:38926057
|
T | C | 3 | a0005c0012t0001g0029a0005c0012t0034g0023a0005c0030t0003g0113 | 3 | HG02698.hp1 HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1069+3164T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38926057 | ||||||
| chr4:38926273
|
G | A | 1 | a0001c0001t0012g0184 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1070-2969G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38926273 | ||||||
| chr4:38926340
|
G | A | 29 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(26): Show | 29 | HG00323.hp2 HG00597.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.1070-2902G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38926340 | ||||||
| chr4:38926360
|
C | A | 1 | a0001c0001t0001g0264 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1070-2882C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38926360 | ||||||
| chr4:38926422
|
A | G | 1 | a0001c0001t0011g0010 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1070-2820A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38926422 | ||||||
| chr4:38926430
|
C | G | 2 | a0001c0001t0005g0211a0002c0057t0005g0251 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1070-2812C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38926430 | ||||||
| chr4:38926457
|
C | CT | 7 | a0001c0001t0002g0150a0001c0001t0026g0316a0001c0004t0004g0107others(4): Show | 7 | HG01099.hp1 HG02738.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.1070-2771dupT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr4 | 38926457 | |||||
| chr4:38926458
|
T | C | 2 | a0001c0002t0001g0219a0003c0011t0014g0269 | 2 | HG01884.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1070-2784T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38926458 | ||||||
| chr4:38926477
|
T | TA | 3 | a0001c0001t0005g0231a0002c0003t0005g0364a0018c0052t0005g0247 | 3 | HG01884.hp1 HG01891.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1070-2764dupA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr4 | 38926477 | |||||
| chr4:38926563
|
C | T | 2 | a0003c0020t0003g0046a0011c0050t0003g0345 | 2 | HG02258.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1070-2679C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38926563 | ||||||
| chr4:38926658
|
G | A | 29 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(26): Show | 29 | HG00323.hp2 HG00597.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.1070-2584G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38926658 | ||||||
| chr4:38926705
|
G | A | 8 | a0001c0001t0004g0281a0001c0001t0010g0259a0001c0001t0010g0299others(5): Show | 8 | HG02280.hp1 HG02818.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1070-2537G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38926705 | ||||||
| chr4:38926735
|
C | T | 1 | a0001c0004t0007g0136 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1070-2507C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38926735 | ||||||
| chr4:38926752
|
G | A | 1 | a0001c0001t0002g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1070-2490G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38926752 | ||||||
| chr4:38926929
|
CCTTAGAG others(2): Show |
C | 29 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(26): Show | 29 | HG00323.hp2 HG00597.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.1070-2308_1070-230 others(13): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr4 | 38926929 | |||||
| chr4:38926944
|
C | G | 1 | a0001c0013t0006g0173 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1070-2298C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38926944 | ||||||
| chr4:38927020
|
A | G | 233 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(230): Show | 236 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.1070-2222A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927020 | ||||||
| chr4:38927047
|
G | A | 1 | a0001c0002t0020g0236 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1070-2195G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927047 | ||||||
| chr4:38927049
|
T | G | 34 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(31): Show | 34 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.1070-2193T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927049 | ||||||
| chr4:38927054
|
T | C | 34 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(31): Show | 34 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.1070-2188T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927054 | ||||||
| chr4:38927111
|
A | G | 34 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(31): Show | 34 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.1070-2131A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927111 | ||||||
| chr4:38927133
|
C | A | 2 | a0001c0002t0002g0139a0001c0002t0002g0141 | 2 | HG00408.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1070-2109C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927133 | ||||||
| chr4:38927189
|
T | A | 34 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(31): Show | 34 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.1070-2053T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927189 | ||||||
| chr4:38927354
|
T | G | 65 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(62): Show | 66 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.1070-1888T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927354 | ||||||
| chr4:38927457
|
G | A | 4 | a0001c0038t0005g0011a0001c0043t0001g0006a0002c0029t0043g0115others(1): Show | 4 | HG01167.hp2 HG01243.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1070-1785G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927457 | ||||||
| chr4:38927464
|
G | T | 3 | a0005c0012t0001g0029a0005c0012t0034g0023a0005c0030t0003g0113 | 3 | HG02698.hp1 HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1070-1778G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927464 | ||||||
| chr4:38927480
|
C | T | 4 | a0001c0001t0002g0238a0001c0001t0002g0241a0001c0001t0002g0280others(1): Show | 4 | HG00673.hp2 HG01106.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.1070-1762C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927480 | ||||||
| chr4:38927696
|
T | C | 1 | a0002c0006t0001g0020 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1070-1546T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927696 | ||||||
| chr4:38927718
|
C | G | 3 | a0001c0039t0024g0261a0001c0044t0024g0226a0002c0026t0005g0039 | 3 | HG01891.hp1 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1070-1524C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927718 | ||||||
| chr4:38927811
|
G | C | 2 | a0001c0001t0012g0172a0003c0011t0014g0269 | 2 | HG01884.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1070-1431G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927811 | ||||||
| chr4:38927826
|
G | A | 6 | a0001c0038t0005g0011a0001c0043t0001g0006a0002c0003t0032g0357others(3): Show | 6 | HG01167.hp2 HG01243.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1070-1416G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927826 | ||||||
| chr4:38927828
|
C | T | 149 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(146): Show | 152 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.1070-1414C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927828 | ||||||
| chr4:38927833
|
G | A | 149 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(146): Show | 152 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.1070-1409G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927833 | ||||||
| chr4:38927880
|
C | T | 1 | a0003c0011t0014g0269 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1070-1362C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927880 | ||||||
| chr4:38927943
|
A | G | 6 | a0001c0002t0002g0139a0001c0002t0002g0141a0001c0013t0002g0085others(3): Show | 6 | HG00408.hp2 HG00544.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1070-1299A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927943 | ||||||
| chr4:38927951
|
G | T | 14 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(11): Show | 14 | HG00597.hp1 HG00621.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.1070-1291G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927951 | ||||||
| chr4:38927969
|
A | G | 14 | a0001c0001t0002g0067a0001c0001t0002g0271a0001c0001t0002g0272others(11): Show | 14 | HG00597.hp1 HG00621.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.1070-1273A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927969 | ||||||
| chr4:38927971
|
C | T | 1 | a0001c0001t0042g0210 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1070-1271C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927971 | ||||||
| chr4:38927981
|
C | G | 8 | a0005c0012t0033g0341a0005c0015t0002g0244a0005c0015t0002g0250others(5): Show | 8 | HG02622.hp1 HG02622.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1070-1261C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927981 | ||||||
| chr4:38928093
|
C | T | 29 | a0001c0038t0005g0011a0001c0043t0001g0006a0002c0003t0032g0357others(26): Show | 29 | HG00323.hp2 HG00741.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.1070-1149C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38928093 | ||||||
| chr4:38928138
|
C | T | 1 | a0001c0002t0001g0179 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1070-1104C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38928138 | ||||||
| chr4:38928151
|
CT | C | 50 | a0001c0001t0002g0013a0001c0001t0012g0172a0001c0001t0042g0210others(47): Show | 50 | HG00323.hp2 HG00741.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.1070-1090delT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38928151 | ||||||
| chr4:38928163
|
G | A | 2 | a0001c0001t0005g0014a0002c0003t0005g0044 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1070-1079G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38928163 | ||||||
| chr4:38928196
|
C | G | 1 | a0001c0001t0002g0097 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1070-1046C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38928196 | ||||||
| chr4:38928636
|
C | G | 9 | a0003c0011t0002g0312a0005c0012t0033g0341a0005c0015t0002g0244others(6): Show | 9 | HG02622.hp1 HG02622.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1070-606C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38928636 | ||||||
| chr4:38928681
|
G | C | 4 | a0001c0001t0007g0166a0001c0001t0007g0273a0001c0004t0007g0331others(1): Show | 4 | NA18953.hp2 NA18956.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.1070-561G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38928681 | ||||||
| chr4:38928812
|
G | A | 31 | a0001c0001t0002g0013a0001c0001t0012g0172a0001c0013t0006g0173others(28): Show | 31 | HG00323.hp2 HG00741.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.1070-430G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38928812 | ||||||
| chr4:38928848
|
A | G | 212 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(209): Show | 215 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.1070-394A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38928848 | ||||||
| chr4:38929058
|
G | A | 15 | a0001c0013t0006g0173a0002c0025t0003g0123a0003c0011t0001g0084others(12): Show | 15 | HG01433.hp1 HG01943.hp2 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.1070-184G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38929058 | ||||||
| chr4:38929065
|
C | T | 7 | a0001c0001t0007g0227a0001c0001t0007g0256a0001c0001t0007g0320others(4): Show | 7 | HG02257.hp2 HG02717.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1070-177C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38929065 | ||||||
| chr4:38929098
|
T | C | 9 | a0003c0011t0002g0312a0005c0012t0033g0341a0005c0015t0002g0244others(6): Show | 9 | HG02622.hp1 HG02622.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1070-144T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38929098 | ||||||
| chr4:38929115
|
G | T | 1 | a0001c0001t0002g0238 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1070-127G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38929115 | ||||||
| chr4:38929171
|
T | C | 1 | a0001c0001t0002g0013 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1070-71T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38929171 | ||||||
| chr4:38929222
|
C | A | 2 | a0001c0001t0005g0014a0002c0003t0005g0044 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1070-20C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38929222 | ||||||
| chr4:38929342
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1161+9T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38929342 | ||||||
| chr4:38929364
|
T | TA | 5 | a0001c0001t0042g0210a0005c0012t0001g0029a0005c0012t0034g0023others(2): Show | 5 | HG02698.hp1 HG02976.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1161+40dupA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr4 | 38929364 | |||||
| chr4:38929364
|
T | TAA | 166 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(163): Show | 169 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.1161+39_1161+40dup others(2): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr4 | 38929364 | |||||
| chr4:38929374
|
C | A | 172 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(169): Show | 175 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.1161+41C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38929374 | ||||||
| chr4:38929476
|
A | C | 167 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.1161+143A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38929476 | ||||||
| chr4:38929639
|
C | T | 167 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.1161+306C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38929639 | ||||||
| chr4:38929784
|
A | T | 167 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.1161+451A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38929784 | ||||||
| chr4:38929808
|
T | C | 1 | a0001c0001t0001g0100 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1161+475T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38929808 | ||||||
| chr4:38929956
|
G | A | 2 | a0003c0020t0003g0046a0011c0050t0003g0345 | 2 | HG02258.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1161+623G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38929956 | ||||||
| chr4:38929977
|
T | A | 11 | a0001c0002t0001g0002a0001c0002t0001g0135a0001c0002t0001g0157others(8): Show | 13 | NA18945.hp1 NA18951.hp1 NA18952.hp2 others(10): Show |
intron_variant | MODIFIER | c.1161+644T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38929977 | ||||||
| chr4:38930025
|
T | C | 10 | a0001c0009t0003g0335a0005c0012t0033g0341a0005c0015t0002g0244others(7): Show | 10 | HG02622.hp1 HG02622.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1161+692T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38930025 | ||||||
| chr4:38930475
|
T | C | 174 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(171): Show | 177 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.1162-976T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38930475 | ||||||
| chr4:38930544
|
C | A | 26 | a0002c0025t0003g0123a0003c0011t0001g0084a0003c0011t0001g0302others(23): Show | 26 | HG00323.hp2 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.1162-907C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38930544 | ||||||
| chr4:38930581
|
G | T | 1 | a0001c0046t0002g0096 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1162-870G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38930581 | ||||||
| chr4:38930904
|
G | A | 1 | a0001c0001t0042g0210 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1162-547G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38930904 | ||||||
| chr4:38930990
|
G | A | 3 | a0005c0012t0001g0029a0005c0012t0034g0023a0005c0030t0003g0113 | 3 | HG02698.hp1 HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1162-461G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38930990 | ||||||
| chr4:38931061
|
A | T | 1 | a0001c0001t0002g0221 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1162-390A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38931061 | ||||||
| chr4:38931087
|
T | A | 1 | a0001c0001t0007g0230 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1162-364T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38931087 | ||||||
| chr4:38931094
|
A | G | 1 | a0002c0006t0010g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1162-357A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38931094 | ||||||
| chr4:38931138
|
C | T | 3 | a0005c0012t0001g0029a0005c0012t0034g0023a0005c0030t0003g0113 | 3 | HG02698.hp1 HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1162-313C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38931138 | ||||||
| chr4:38931208
|
T | C | 3 | a0001c0039t0024g0261a0001c0044t0024g0226a0002c0026t0005g0039 | 3 | HG01891.hp1 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1162-243T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38931208 | ||||||
| chr4:38931217
|
T | C | 3 | a0005c0012t0001g0029a0005c0012t0034g0023a0005c0030t0003g0113 | 3 | HG02698.hp1 HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1162-234T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38931217 | ||||||
| chr4:38931301
|
C | A | 283 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(280): Show | 287 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(284): Show |
intron_variant | MODIFIER | c.1162-150C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38931301 | ||||||
| chr4:38931322
|
G | A | 2 | a0001c0001t0004g0200a0001c0002t0001g0169 | 2 | HG01496.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1162-129G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38931322 | ||||||
| chr4:38931400
|
A | C | 1 | a0018c0052t0005g0247 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1162-51A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38931400 | ||||||
| chr4:38931414
|
C | T | 1 | a0002c0003t0002g0045 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1162-37C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38931414 | ||||||
| chr4:38931415
|
G | T | 2 | a0001c0001t0005g0014a0002c0003t0005g0044 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1162-36G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38931415 | ||||||
| chr4:38931443
|
C | T | 1 | a0008c0014t0023g0305 | 1 | NA20300.hp1 | splice_region_variant&intron_variant | LOW | c.1162-8C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38931443 | ||||||
| chr4:38931824
|
G | A | 1 | a0006c0035t0003g0207 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1323+212G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 11/14 | chr4 | 38931824 | ||||||
| chr4:38931970
|
A | G | 147 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(144): Show | 150 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.1324-265A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 11/14 | chr4 | 38931970 | ||||||
| chr4:38931989
|
C | G | 1 | a0001c0001t0042g0210 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1324-246C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 11/14 | chr4 | 38931989 | ||||||
| chr4:38932069
|
A | C | 144 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(141): Show | 147 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.1324-166A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 11/14 | chr4 | 38932069 | ||||||
| chr4:38932105
|
A | G | 144 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(141): Show | 147 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.1324-130A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 11/14 | chr4 | 38932105 | ||||||
| chr4:38932135
|
G | C | 9 | a0005c0012t0033g0341a0005c0015t0002g0244a0005c0015t0002g0250others(6): Show | 9 | HG02622.hp1 HG02622.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1324-100G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 11/14 | chr4 | 38932135 | ||||||
| chr4:38932182
|
T | C | 1 | a0001c0001t0012g0172 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1324-53T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 11/14 | chr4 | 38932182 | ||||||
| chr4:38932379
|
G | A | 12 | a0005c0012t0001g0029a0005c0012t0033g0341a0005c0012t0034g0023others(9): Show | 12 | HG02622.hp1 HG02622.hp2 HG02647.hp1 others(9): Show |
splice_region_variant&intron_variant | LOW | c.1463+5G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38932379 | ||||||
| chr4:38932447
|
C | T | 1 | a0007c0049t0002g0348 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1463+73C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38932447 | ||||||
| chr4:38932628
|
T | C | 166 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(163): Show | 169 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.1463+254T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38932628 | ||||||
| chr4:38932697
|
A | G | 3 | a0005c0012t0001g0029a0005c0012t0034g0023a0005c0030t0003g0113 | 3 | HG02698.hp1 HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1463+323A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38932697 | ||||||
| chr4:38932841
|
A | T | 9 | a0005c0012t0033g0341a0005c0015t0002g0244a0005c0015t0002g0250others(6): Show | 9 | HG02622.hp1 HG02622.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1463+467A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38932841 | ||||||
| chr4:38932857
|
A | AT | 151 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(148): Show | 155 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.1463+498dupT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr4 | 38932857 | |||||
| chr4:38932857
|
A | ATTT | 6 | a0005c0015t0002g0244a0005c0015t0002g0250a0005c0015t0005g0246others(3): Show | 6 | HG02647.hp1 HG02809.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1463+496_1463+498d others(5): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr4 | 38932857 | |||||
| chr4:38932968
|
C | T | 2 | a0001c0001t0012g0172a0002c0003t0010g0362 | 2 | HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1463+594C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38932968 | ||||||
| chr4:38933001
|
G | A | 2 | a0001c0001t0002g0336a0002c0006t0001g0021 | 2 | HG01099.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1463+627G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38933001 | ||||||
| chr4:38933176
|
T | A | 2 | a0001c0001t0005g0014a0002c0003t0005g0044 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1463+802T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38933176 | ||||||
| chr4:38933443
|
C | T | 1 | a0001c0002t0001g0094 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1463+1069C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38933443 | ||||||
| chr4:38933522
|
T | A | 1 | a0003c0036t0004g0009 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1463+1148T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38933522 | ||||||
| chr4:38933546
|
T | C | 1 | a0001c0001t0002g0315 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1463+1172T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38933546 | ||||||
| chr4:38933842
|
T | C | 4 | a0001c0001t0005g0231a0002c0003t0005g0364a0013c0040t0023g0234others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1463+1468T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38933842 | ||||||
| chr4:38933922
|
G | A | 1 | a0003c0011t0002g0312 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1463+1548G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38933922 | ||||||
| chr4:38934015
|
G | A | 1 | a0001c0001t0015g0240 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1463+1641G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38934015 | ||||||
| chr4:38934138
|
C | G | 68 | a0001c0001t0002g0013a0001c0001t0002g0040a0001c0001t0002g0292others(65): Show | 68 | HG00323.hp2 HG00741.hp2 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.1464-1580C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38934138 | ||||||
| chr4:38934245
|
A | G | 1 | a0001c0001t0004g0281 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1464-1473A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38934245 | ||||||
| chr4:38934262
|
C | T | 1 | a0005c0015t0005g0246 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1464-1456C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38934262 | ||||||
| chr4:38934333
|
A | G | 19 | a0001c0001t0001g0100a0001c0001t0001g0296a0001c0001t0002g0189others(16): Show | 19 | HG01109.hp2 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1464-1385A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38934333 | ||||||
| chr4:38934337
|
A | G | 9 | a0001c0001t0007g0166a0001c0001t0007g0273a0001c0002t0001g0094others(6): Show | 9 | HG00597.hp1 HG00621.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.1464-1381A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38934337 | ||||||
| chr4:38934458
|
A | G | 2 | a0001c0001t0002g0008a0002c0003t0002g0114 | 2 | HG02486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1464-1260A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38934458 | ||||||
| chr4:38934527
|
T | C | 1 | a0001c0001t0002g0280 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1464-1191T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38934527 | ||||||
| chr4:38934588
|
A | C | 1 | a0002c0054t0036g0243 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1464-1130A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38934588 | ||||||
| chr4:38934806
|
C | T | 2 | a0001c0001t0007g0230a0002c0003t0007g0117 | 2 | HG02074.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1464-912C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38934806 | ||||||
| chr4:38934918
|
CT | C | 21 | a0001c0001t0001g0100a0001c0001t0005g0014a0001c0001t0006g0061others(18): Show | 21 | HG00323.hp1 HG02109.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.1464-787delT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr4 | 38934918 | |||||
| chr4:38934919
|
T | C | 3 | a0001c0002t0040g0306a0001c0005t0003g0274a0002c0028t0030g0363 | 3 | HG02486.hp1 HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1464-799T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38934919 | ||||||
| chr4:38935152
|
G | A | 1 | a0001c0008t0006g0111 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1464-566G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38935152 | ||||||
| chr4:38935212
|
G | A | 199 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(196): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.1464-506G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38935212 | ||||||
| chr4:38935236
|
C | T | 1 | a0001c0023t0002g0104 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1464-482C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38935236 | ||||||
| chr4:38935393
|
G | C | 5 | a0001c0001t0005g0014a0002c0003t0005g0044a0005c0012t0001g0029others(2): Show | 5 | HG02698.hp1 HG03453.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.1464-325G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38935393 | ||||||
| chr4:38935396
|
A | G | 5 | a0001c0001t0005g0014a0002c0003t0005g0044a0005c0012t0001g0029others(2): Show | 5 | HG02698.hp1 HG03453.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.1464-322A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38935396 | ||||||
| chr4:38935398
|
A | G | 5 | a0001c0001t0005g0014a0002c0003t0005g0044a0005c0012t0001g0029others(2): Show | 5 | HG02698.hp1 HG03453.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.1464-320A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38935398 | ||||||
| chr4:38935434
|
A | G | 39 | a0001c0001t0001g0264a0001c0001t0004g0277a0001c0001t0005g0005others(36): Show | 39 | HG00735.hp2 HG00741.hp2 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.1464-284A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38935434 | ||||||
| chr4:38935462
|
A | G | 1 | a0001c0001t0035g0311 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1464-256A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38935462 | ||||||
| chr4:38935580
|
A | T | 10 | a0001c0001t0002g0013a0001c0001t0002g0040a0001c0001t0002g0292others(7): Show | 10 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1464-138A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38935580 | ||||||
| chr4:38935600
|
C | T | 1 | a0001c0001t0035g0311 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1464-118C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38935600 | ||||||
| chr4:38935655
|
G | A | 2 | a0001c0001t0005g0014a0002c0003t0005g0044 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1464-63G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38935655 | ||||||
| chr4:38936088
|
TG | T | 3 | a0001c0001t0014g0295a0001c0009t0003g0335a0001c0037t0003g0007 | 3 | HG02886.hp1 HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1536+299delG | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936088 | ||||||
| chr4:38936098
|
G | GT | 10 | a0001c0001t0005g0005a0001c0001t0005g0193a0001c0001t0005g0211others(7): Show | 10 | HG01109.hp2 HG02258.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1536+320dupT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 38936098 | |||||
| chr4:38936098
|
G | T | 6 | a0001c0001t0005g0014a0001c0001t0042g0210a0002c0003t0005g0044others(3): Show | 6 | HG02698.hp1 HG03139.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1536+308G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936098 | ||||||
| chr4:38936100
|
T | G | 6 | a0001c0001t0005g0014a0001c0001t0042g0210a0002c0003t0005g0044others(3): Show | 6 | HG02698.hp1 HG03139.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1536+310T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936100 | ||||||
| chr4:38936102
|
T | TG | 18 | a0001c0001t0001g0100a0001c0001t0002g0189a0001c0001t0002g0209others(15): Show | 18 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1536+312_1536+313i others(3): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936102 | ||||||
| chr4:38936143
|
G | A | 2 | a0001c0001t0035g0311a0003c0011t0014g0269 | 2 | HG01884.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1536+353G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936143 | ||||||
| chr4:38936153
|
C | T | 11 | a0001c0001t0005g0005a0001c0001t0005g0193a0001c0001t0005g0211others(8): Show | 11 | HG00735.hp2 HG01109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1536+363C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936153 | ||||||
| chr4:38936155
|
C | G | 23 | a0001c0001t0001g0264a0001c0001t0009g0153a0001c0004t0001g0072others(20): Show | 23 | HG00735.hp2 HG00741.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.1536+365C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936155 | ||||||
| chr4:38936178
|
T | C | 6 | a0001c0001t0005g0014a0001c0001t0042g0210a0002c0003t0005g0044others(3): Show | 6 | HG02698.hp1 HG03139.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1536+388T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936178 | ||||||
| chr4:38936197
|
G | A | 198 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(195): Show | 202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.1536+407G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936197 | ||||||
| chr4:38936259
|
AT | A | 4 | a0001c0001t0042g0210a0005c0012t0001g0029a0005c0012t0034g0023others(1): Show | 4 | HG02698.hp1 HG03139.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.1536+477delT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 38936259 | |||||
| chr4:38936315
|
C | T | 3 | a0005c0012t0001g0029a0005c0012t0034g0023a0005c0030t0003g0113 | 3 | HG02698.hp1 HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1536+525C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936315 | ||||||
| chr4:38936316
|
G | A | 1 | a0001c0001t0008g0218 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1536+526G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936316 | ||||||
| chr4:38936329
|
C | T | 1 | a0001c0004t0029g0015 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1536+539C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936329 | ||||||
| chr4:38936354
|
A | G | 3 | a0005c0012t0001g0029a0005c0012t0034g0023a0005c0030t0003g0113 | 3 | HG02698.hp1 HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1536+564A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936354 | ||||||
| chr4:38936374
|
G | A | 3 | a0001c0001t0002g0189a0001c0001t0002g0209a0002c0003t0012g0112 | 3 | HG02055.hp1 HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1536+584G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936374 | ||||||
| chr4:38936548
|
A | AT | 17 | a0001c0001t0001g0284a0001c0001t0002g0189a0001c0001t0002g0191others(14): Show | 17 | HG00408.hp2 HG00438.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.1536+780dupT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 38936548 | |||||
| chr4:38936548
|
AT | A | 39 | a0001c0001t0001g0100a0001c0001t0002g0222a0001c0001t0004g0183others(36): Show | 39 | HG01109.hp2 HG01256.hp1 HG01993.hp2 others(36): Show |
intron_variant | MODIFIER | c.1536+780delT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 38936548 | |||||
| chr4:38936577
|
G | C | 2 | a0001c0001t0004g0183a0004c0007t0009g0027 | 2 | HG01192.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.1536+787G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936577 | ||||||
| chr4:38936656
|
G | A | 1 | a0001c0001t0035g0311 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1536+866G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936656 | ||||||
| chr4:38936701
|
C | T | 16 | a0001c0001t0004g0277a0001c0001t0005g0005a0001c0001t0005g0193others(13): Show | 16 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1536+911C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936701 | ||||||
| chr4:38936702
|
G | A | 7 | a0001c0001t0007g0227a0001c0001t0007g0256a0001c0001t0007g0320others(4): Show | 7 | HG01255.hp2 HG02257.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1536+912G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936702 | ||||||
| chr4:38936720
|
C | G | 3 | a0005c0012t0001g0029a0005c0012t0034g0023a0005c0030t0003g0113 | 3 | HG02698.hp1 HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1536+930C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936720 | ||||||
| chr4:38936741
|
C | T | 22 | a0001c0001t0001g0264a0001c0001t0009g0153a0001c0004t0001g0072others(19): Show | 22 | HG00735.hp2 HG00741.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.1536+951C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936741 | ||||||
| chr4:38936776
|
C | A | 1 | a0001c0004t0002g0058 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1536+986C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936776 | ||||||
| chr4:38936868
|
G | C | 1 | a0001c0001t0005g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1536+1078G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936868 | ||||||
| chr4:38936937
|
A | T | 262 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(259): Show | 266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.1536+1147A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936937 | ||||||
| chr4:38937262
|
G | C | 1 | a0002c0003t0001g0359 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1536+1472G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38937262 | ||||||
| chr4:38937495
|
G | A | 39 | a0001c0001t0001g0050a0001c0001t0001g0165a0001c0001t0001g0314others(36): Show | 39 | HG00544.hp2 HG00639.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.1536+1705G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38937495 | ||||||
| chr4:38937534
|
A | G | 104 | a0001c0001t0001g0041a0001c0001t0001g0099a0001c0001t0001g0163others(101): Show | 107 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.1536+1744A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38937534 | ||||||
| chr4:38937602
|
C | T | 2 | a0001c0001t0005g0014a0002c0003t0005g0044 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1536+1812C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38937602 | ||||||
| chr4:38937636
|
T | C | 25 | a0001c0001t0001g0100a0001c0001t0002g0189a0001c0001t0002g0209others(22): Show | 25 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.1536+1846T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38937636 | ||||||
| chr4:38937702
|
C | T | 1 | a0003c0011t0014g0269 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1536+1912C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38937702 | ||||||
| chr4:38937797
|
C | T | 1 | a0003c0011t0014g0269 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1536+2007C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38937797 | ||||||
| chr4:38937808
|
C | T | 1 | a0001c0013t0001g0290 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1536+2018C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38937808 | ||||||
| chr4:38937882
|
G | A | 3 | a0005c0012t0001g0029a0005c0012t0034g0023a0005c0030t0003g0113 | 3 | HG02698.hp1 HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1536+2092G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38937882 | ||||||
| chr4:38937895
|
C | T | 1 | a0001c0001t0031g0289 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1536+2105C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38937895 | ||||||
| chr4:38937933
|
C | T | 75 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0212others(72): Show | 76 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.1536+2143C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38937933 | ||||||
| chr4:38938213
|
T | A | 64 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0212others(61): Show | 65 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.1536+2423T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38938213 | ||||||
| chr4:38938267
|
A | G | 1 | a0001c0001t0001g0100 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1536+2477A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38938267 | ||||||
| chr4:38938495
|
A | T | 3 | a0005c0012t0001g0029a0005c0012t0034g0023a0005c0030t0003g0113 | 3 | HG02698.hp1 HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1537-2473A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38938495 | ||||||
| chr4:38938516
|
G | A | 1 | a0001c0001t0042g0210 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1537-2452G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38938516 | ||||||
| chr4:38938595
|
C | T | 1 | a0001c0001t0002g0069 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1537-2373C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38938595 | ||||||
| chr4:38938628
|
C | T | 1 | a0005c0015t0005g0246 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1537-2340C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38938628 | ||||||
| chr4:38939009
|
A | G | 122 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(119): Show | 123 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.1537-1959A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38939009 | ||||||
| chr4:38939193
|
T | C | 150 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(147): Show | 151 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.1537-1775T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38939193 | ||||||
| chr4:38939212
|
A | G | 46 | a0001c0001t0001g0050a0001c0001t0001g0100a0001c0001t0001g0165others(43): Show | 46 | HG00544.hp2 HG00639.hp1 HG01167.hp2 others(43): Show |
intron_variant | MODIFIER | c.1537-1756A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38939212 | ||||||
| chr4:38939524
|
G | A | 1 | a0016c0033t0011g0354 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1537-1444G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38939524 | ||||||
| chr4:38939836
|
C | T | 6 | a0001c0001t0010g0259a0001c0001t0010g0299a0001c0004t0029g0015others(3): Show | 6 | HG02280.hp1 HG02647.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1537-1132C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38939836 | ||||||
| chr4:38939844
|
T | C | 46 | a0001c0001t0001g0050a0001c0001t0001g0100a0001c0001t0001g0165others(43): Show | 46 | HG00544.hp2 HG00639.hp1 HG01167.hp2 others(43): Show |
intron_variant | MODIFIER | c.1537-1124T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38939844 | ||||||
| chr4:38939886
|
C | CT | 130 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(127): Show | 131 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.1537-1064dupT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 38939886 | |||||
| chr4:38939886
|
CTTT | C | 23 | a0001c0001t0001g0264a0001c0001t0009g0153a0001c0004t0001g0072others(20): Show | 23 | HG00735.hp2 HG00741.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.1537-1066_1537-106 others(7): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 38939886 | |||||
| chr4:38939962
|
C | A | 6 | a0001c0001t0004g0277a0001c0001t0005g0014a0001c0038t0005g0011others(3): Show | 6 | HG02145.hp2 HG02280.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1537-1006C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38939962 | ||||||
| chr4:38940047
|
C | G | 1 | a0001c0001t0002g0308 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1537-921C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38940047 | ||||||
| chr4:38940053
|
T | G | 1 | a0005c0012t0033g0341 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1537-915T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38940053 | ||||||
| chr4:38940074
|
G | A | 64 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0212others(61): Show | 65 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.1537-894G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38940074 | ||||||
| chr4:38940087
|
C | T | 3 | a0001c0001t0002g0228a0001c0046t0002g0096a0003c0011t0002g0312 | 3 | HG02523.hp1 HG03225.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.1537-881C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38940087 | ||||||
| chr4:38940382
|
GA | G | 257 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0050others(254): Show | 258 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.1537-577delA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 38940382 | |||||
| chr4:38940383
|
A | G | 1 | a0001c0004t0002g0001 | 4 | NA18970.hp2 NA18980.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.1537-585A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38940383 | ||||||
| chr4:38940394
|
G | A | 77 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0212others(74): Show | 78 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.1537-574G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38940394 | ||||||
| chr4:38940598
|
C | T | 1 | a0002c0006t0010g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1537-370C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38940598 | ||||||
| chr4:38940668
|
C | T | 3 | a0001c0001t0004g0266a0002c0003t0004g0118a0002c0003t0004g0129 | 3 | NA18959.hp1 NA18978.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1537-300C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38940668 | ||||||
| chr4:38940669
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1537-299G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38940669 | ||||||
| chr4:38940680
|
C | A | 1 | a0001c0004t0029g0015 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1537-288C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38940680 | ||||||
| chr4:38940781
|
C | T | 1 | a0001c0001t0004g0262 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1537-187C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38940781 | ||||||
| chr4:38941076
|
C | CT | 244 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0099others(241): Show | 248 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.1590+69dupT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr4 | 38941076 | |||||
| chr4:38941076
|
C | CTT | 16 | a0001c0001t0001g0175a0001c0001t0001g0187a0001c0001t0001g0284others(13): Show | 16 | HG01123.hp2 HG01257.hp2 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.1590+68_1590+69dup others(2): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr4 | 38941076 | |||||
| chr4:38941168
|
C | T | 1 | a0001c0001t0035g0311 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1590+147C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38941168 | ||||||
| chr4:38941227
|
T | C | 7 | a0006c0010t0003g0144a0006c0010t0003g0174a0006c0010t0003g0317others(4): Show | 7 | HG01433.hp1 HG01975.hp2 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.1590+206T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38941227 | ||||||
| chr4:38941443
|
A | G | 3 | a0005c0012t0001g0029a0005c0012t0034g0023a0005c0030t0003g0113 | 3 | HG02698.hp1 HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1590+422A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38941443 | ||||||
| chr4:38941469
|
C | T | 2 | a0001c0001t0005g0014a0002c0003t0005g0044 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1590+448C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38941469 | ||||||
| chr4:38941523
|
C | T | 2 | a0001c0002t0007g0365a0001c0002t0007g0366 | 2 | NA18962.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1590+502C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38941523 | ||||||
| chr4:38941561
|
T | C | 1 | a0001c0002t0006g0188 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1590+540T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38941561 | ||||||
| chr4:38941657
|
A | T | 4 | a0001c0002t0001g0002a0001c0002t0001g0157a0001c0002t0001g0208others(1): Show | 6 | NA18945.hp1 NA18952.hp2 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.1590+636A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38941657 | ||||||
| chr4:38941739
|
C | T | 1 | a0002c0003t0004g0129 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1590+718C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38941739 | ||||||
| chr4:38941778
|
A | G | 2 | a0001c0001t0014g0194a0001c0004t0001g0260 | 2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1590+757A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38941778 | ||||||
| chr4:38941835
|
A | G | 2 | a0001c0001t0002g0228a0001c0046t0002g0096 | 2 | HG02523.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.1590+814A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38941835 | ||||||
| chr4:38941878
|
A | G | 1 | a0007c0049t0002g0348 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1590+857A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38941878 | ||||||
| chr4:38941924
|
C | A | 10 | a0001c0001t0002g0189a0001c0001t0002g0209a0001c0001t0009g0153others(7): Show | 10 | HG00741.hp2 HG01070.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.1590+903C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38941924 | ||||||
| chr4:38941941
|
A | T | 1 | a0001c0001t0002g0063 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1590+920A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38941941 | ||||||
| chr4:38942010
|
A | G | 154 | a0001c0001t0001g0175a0001c0001t0001g0187a0001c0001t0001g0284others(151): Show | 157 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.1590+989A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38942010 | ||||||
| chr4:38942077
|
A | C | 1 | a0002c0003t0010g0362 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1590+1056A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38942077 | ||||||
| chr4:38942113
|
C | T | 1 | a0001c0001t0005g0297 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1590+1092C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38942113 | ||||||
| chr4:38942187
|
T | C | 60 | a0001c0001t0001g0050a0001c0001t0004g0266a0001c0001t0006g0056others(57): Show | 62 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.1590+1166T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38942187 | ||||||
| chr4:38942213
|
T | A | 31 | a0001c0001t0001g0019a0001c0001t0001g0275a0001c0001t0004g0060others(28): Show | 31 | HG00140.hp2 HG00609.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.1590+1192T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38942213 | ||||||
| chr4:38942426
|
G | GAA | 6 | a0001c0001t0008g0109a0001c0001t0008g0110a0001c0001t0008g0218others(3): Show | 6 | NA18956.hp1 NA18974.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.1591-1027_1591-102 others(6): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr4 | 38942426 | |||||
| chr4:38942447
|
C | T | 1 | a0001c0001t0002g0224 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1591-1009C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38942447 | ||||||
| chr4:38942480
|
C | T | 124 | a0001c0001t0001g0019a0001c0001t0001g0275a0001c0001t0004g0060others(121): Show | 124 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.1591-976C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38942480 | ||||||
| chr4:38942562
|
T | C | 1 | a0001c0001t0004g0268 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1591-894T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38942562 | ||||||
| chr4:38942589
|
C | G | 1 | a0003c0041t0003g0162 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1591-867C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38942589 | ||||||
| chr4:38942597
|
T | G | 2 | a0001c0004t0002g0286a0002c0003t0002g0045 | 2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1591-859T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38942597 | ||||||
| chr4:38942704
|
C | G | 11 | a0001c0001t0002g0013a0001c0001t0002g0040a0001c0001t0002g0292others(8): Show | 11 | HG02257.hp1 HG02451.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.1591-752C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38942704 | ||||||
| chr4:38942729
|
A | G | 2 | a0001c0001t0014g0194a0001c0002t0014g0156 | 2 | HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1591-727A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38942729 | ||||||
| chr4:38942817
|
G | A | 2 | a0002c0003t0010g0362a0002c0006t0010g0337 | 2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1591-639G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38942817 | ||||||
| chr4:38942865
|
C | G | 3 | a0001c0002t0001g0167a0001c0002t0001g0232a0001c0002t0019g0288 | 3 | HG03490.hp1 HG03492.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1591-591C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38942865 | ||||||
| chr4:38942872
|
TACCCTGG others(17): Show |
T | 94 | a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0002g0016others(91): Show | 97 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.1591-581_1591-558d others(26): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr4 | 38942872 | |||||
| chr4:38942961
|
G | A | 2 | a0001c0039t0024g0261a0001c0044t0024g0226 | 2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1591-495G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38942961 | ||||||
| chr4:38942970
|
A | G | 257 | a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0002g0016others(254): Show | 261 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(258): Show |
intron_variant | MODIFIER | c.1591-486A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38942970 | ||||||
| chr4:38943019
|
C | T | 35 | a0001c0001t0005g0005a0001c0001t0005g0014a0001c0001t0005g0193others(32): Show | 35 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.1591-437C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38943019 | ||||||
| chr4:38943070
|
G | C | 1 | a0001c0001t0007g0320 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1591-386G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38943070 | ||||||
| chr4:38943125
|
G | A | 8 | a0001c0001t0004g0200a0001c0001t0004g0253a0001c0001t0004g0254others(5): Show | 8 | HG00140.hp2 HG00741.hp1 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.1591-331G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38943125 | ||||||
| chr4:38943142
|
A | G | 3 | a0001c0002t0001g0167a0001c0002t0001g0232a0001c0002t0019g0288 | 3 | HG03490.hp1 HG03492.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1591-314A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38943142 | ||||||
| chr4:38943171
|
G | A | 2 | a0002c0003t0010g0362a0002c0006t0010g0337 | 2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1591-285G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38943171 | ||||||
| chr4:38943191
|
C | CA | 104 | a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0002g0016others(101): Show | 107 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.1591-244dupA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr4 | 38943191 | |||||
| chr4:38943191
|
C | CAA | 10 | a0001c0001t0002g0017a0001c0001t0002g0071a0001c0001t0002g0168others(7): Show | 10 | HG01106.hp1 HG01192.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.1591-245_1591-244d others(4): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr4 | 38943191 | |||||
| chr4:38943191
|
CA | C | 46 | a0001c0001t0004g0060a0001c0001t0004g0086a0001c0001t0004g0192others(43): Show | 46 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.1591-244delA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr4 | 38943191 | |||||
| chr4:38943254
|
C | G | 1 | a0001c0001t0005g0276 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1591-202C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38943254 | ||||||
| chr4:38943355
|
A | AT | 259 | a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0002g0016others(256): Show | 263 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.1591-100dupT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr4 | 38943355 |