Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 149297 |
|---|---|
| ensemblid | ENSG00000188859.7 |
| hgncid | 13495 |
| symbol | FAM78B |
| name | family with sequence similarity 78 member B |
| refseq_nuc | NM_001017961.5 |
| refseq_prot | NP_001017961.1 |
| ensembl_nuc | ENST00000354422.4 |
| ensembl_prot | ENSP00000346404.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 166069299 |
| end | 166167001 |
| strand | - |
| ver | v1.2 |
| region | chr1:166069299-166167001 |
| region5000 | chr1:166064299-166172001 |
| regionname0 | FAM78B_chr1_166069299_166167001 |
| regionname5000 | FAM78B_chr1_166064299_166172001 |
| 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 | 261 | 318 | 82 | 68 | 130 | 8 | 28 | 92 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 786 | 241 | 70 | 45 | 97 | 7 | 20 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| c0002 | 0/0 | 786 | 77 | 12 | 23 | 33 | 1 | 8 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| 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 | 1/0 | 1696 | 137 | 35 | 20 | 68 | 2 | 11 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| t0002 | 0/1 | 1696 | 61 | 9 | 18 | 24 | 2 | 7 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| t0003 | 0/0 | 1696 | 49 | 1 | 14 | 26 | 1 | 7 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| t0004 | 0/0 | 1696 | 17 | 16 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| t0005 | 0/0 | 1696 | 16 | 0 | 9 | 7 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| t0006 | 0/0 | 1696 | 8 | 0 | 4 | 0 | 3 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| t0007 | 0/0 | 1696 | 5 | 5 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| t0008 | 0/0 | 1696 | 3 | 3 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| t0009 | 0/0 | 1696 | 3 | 3 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| t0010 | 0/0 | 1696 | 3 | 2 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| t0011 | 0/0 | 1696 | 2 | 2 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| t0012 | 0/0 | 1696 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| t0013 | 0/0 | 1696 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| t0014 | 0/0 | 1696 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| t0015 | 0/0 | 1696 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| t0016 | 0/0 | 1696 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| t0017 | 0/0 | 1696 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| t0018 | 0/0 | 1696 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| t0019 | 0/0 | 1696 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| t0020 | 0/0 | 1696 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| t0021 | 0/0 | 1696 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| t0022 | 0/0 | 1696 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| t0023 | 0/0 | 1696 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| t0024 | 0/0 | 1696 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| t0025 | 0/0 | 1696 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0051 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0293 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 786 | 241 | 70 | 45 | 97 | 7 | 20 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| a0001c0002 | 0/0 | 786 | 77 | 12 | 23 | 33 | 1 | 8 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2481 | 130 | 28 | 20 | 68 | 2 | 11 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| a0001c0001t0002 | 0/1 | 2481 | 61 | 9 | 18 | 24 | 2 | 7 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| a0001c0001t0003 | 0/0 | 2481 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| a0001c0001t0004 | 0/0 | 2481 | 17 | 16 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| a0001c0001t0006 | 0/0 | 2481 | 8 | 0 | 4 | 0 | 3 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| a0001c0001t0007 | 0/0 | 2481 | 5 | 5 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| a0001c0001t0008 | 0/0 | 2481 | 3 | 3 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| a0001c0001t0009 | 0/0 | 2481 | 3 | 3 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| a0001c0001t0011 | 0/0 | 2481 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| a0001c0001t0012 | 0/0 | 2481 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| a0001c0001t0013 | 0/0 | 2481 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| a0001c0001t0014 | 0/0 | 2481 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| a0001c0001t0016 | 0/0 | 2481 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| a0001c0001t0017 | 0/0 | 2481 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| a0001c0001t0018 | 0/0 | 2481 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| a0001c0001t0019 | 0/0 | 2481 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| a0001c0001t0020 | 0/0 | 2481 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| a0001c0001t0021 | 0/0 | 2481 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| a0001c0001t0023 | 0/0 | 2481 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| a0001c0001t0024 | 0/0 | 2481 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| a0001c0001t0025 | 0/0 | 2481 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| a0001c0002t0001 | 0/0 | 2481 | 7 | 7 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| a0001c0002t0003 | 0/0 | 2481 | 48 | 0 | 14 | 26 | 1 | 7 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| a0001c0002t0005 | 0/0 | 2481 | 16 | 0 | 9 | 7 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| a0001c0002t0010 | 0/0 | 2481 | 3 | 2 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| a0001c0002t0011 | 0/0 | 2481 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| a0001c0002t0015 | 0/0 | 2481 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| a0001c0002t0022 | 0/0 | 2481 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | copy fasta | chr1 | 166064299 | 166172001 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0051 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0293 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0004g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0004g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0006g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0006g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0006g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0006g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0006g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0006g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0006g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0006g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0007g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0007g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0007g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0007g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0007g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0008g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0008g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0008g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0009g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0009g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0009g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0011g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0012g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0013g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0014g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0016g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0017g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0018g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0019g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0020g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0021g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0023g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0024g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0001t0025g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0005g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0005g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0005g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0005g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0005g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0005g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0005g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0005g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0005g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0005g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0005g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0005g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0005g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0005g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0005g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0005g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0010g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0010g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0010g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0011g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0015g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| a0001c0002t0022g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0003 | g0206 | EUR | GBR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00140 | hp2 | a0001 | c0001 | t0006 | g0103 | EUR | GBR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00323 | hp1 | a0001 | c0001 | t0006 | g0180 | EUR | FIN | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0152 | EUR | FIN | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00438 | hp1 | a0001 | c0002 | t0003 | g0122 | EAS | CHS | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00438 | hp2 | a0001 | c0002 | t0003 | g0288 | EAS | CHS | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00544 | hp1 | a0001 | c0002 | t0005 | g0306 | EAS | CHS | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00597 | hp1 | a0001 | c0001 | t0012 | g0003 | EAS | CHS | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | CHS | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00642 | hp2 | a0001 | c0002 | t0003 | g0119 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | CHS | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00735 | hp2 | a0001 | c0001 | t0006 | g0100 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00738 | hp1 | a0001 | c0002 | t0003 | g0208 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0080 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00741 | hp1 | a0001 | c0002 | t0003 | g0197 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG00741 | hp2 | a0001 | c0002 | t0003 | g0088 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0250 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0215 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01070 | hp2 | a0001 | c0001 | t0006 | g0145 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0214 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01074 | hp1 | a0001 | c0002 | t0003 | g0196 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01081 | hp2 | a0001 | c0002 | t0003 | g0209 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01099 | hp1 | a0001 | c0002 | t0003 | g0199 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01106 | hp2 | a0001 | c0002 | t0003 | g0198 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01168 | hp1 | a0001 | c0002 | t0003 | g0095 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01168 | hp2 | a0001 | c0002 | t0003 | g0279 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01169 | hp2 | a0001 | c0002 | t0003 | g0137 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0228 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01192 | hp1 | a0001 | c0002 | t0005 | g0302 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01243 | hp2 | a0001 | c0001 | t0025 | g0316 | AMR | PUR | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01255 | hp1 | a0001 | c0002 | t0003 | g0086 | AMR | CLM | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0267 | AMR | CLM | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0266 | AMR | CLM | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01261 | hp1 | a0001 | c0002 | t0005 | g0301 | AMR | CLM | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | CLM | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01358 | hp1 | a0001 | c0001 | t0006 | g0294 | AMR | CLM | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0263 | AMR | CLM | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | CLM | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01361 | hp2 | a0001 | c0002 | t0005 | g0299 | AMR | CLM | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01433 | hp2 | a0001 | c0002 | t0003 | g0063 | AMR | CLM | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01515 | hp1 | a0001 | c0001 | t0006 | g0147 | EUR | IBS | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0295 | EUR | IBS | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0029 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01934 | hp1 | a0001 | c0002 | t0005 | g0303 | AMR | PEL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01943 | hp2 | a0001 | c0002 | t0005 | g0308 | AMR | PEL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0265 | AMR | PEL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01952 | hp2 | a0001 | c0002 | t0005 | g0304 | AMR | PEL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01981 | hp1 | a0001 | c0002 | t0005 | g0307 | AMR | PEL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02004 | hp1 | a0001 | c0002 | t0003 | g0132 | AMR | PEL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02004 | hp2 | a0001 | c0001 | t0006 | g0148 | AMR | PEL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | KHV | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | KHV | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | KHV | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02055 | hp2 | a0001 | c0002 | t0015 | g0030 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | KHV | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | KHV | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | KHV | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02083 | hp2 | a0001 | c0002 | t0003 | g0085 | EAS | KHV | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02129 | hp2 | a0001 | c0002 | t0003 | g0084 | EAS | KHV | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0195 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02148 | hp1 | a0001 | c0002 | t0005 | g0300 | AMR | PEL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0242 | AMR | PEL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CDX | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | CDX | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CDX | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02165 | hp2 | a0001 | c0002 | t0003 | g0093 | EAS | CDX | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02258 | hp2 | a0001 | c0002 | t0011 | g0010 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0170 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02293 | hp1 | a0001 | c0002 | t0005 | g0305 | AMR | PEL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02300 | hp1 | a0001 | c0001 | t0019 | g0238 | AMR | PEL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | PEL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02451 | hp1 | a0001 | c0001 | t0009 | g0036 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02523 | hp1 | a0001 | c0002 | t0005 | g0309 | EAS | KHV | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | KHV | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02572 | hp2 | a0001 | c0001 | t0017 | g0141 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0179 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0055 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02723 | hp2 | a0001 | c0001 | t0007 | g0032 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02735 | hp1 | a0001 | c0002 | t0003 | g0204 | SAS | PJL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0229 | SAS | PJL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0292 | SAS | PJL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0193 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02896 | hp1 | a0001 | c0001 | t0007 | g0026 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0023 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02897 | hp2 | a0001 | c0001 | t0007 | g0028 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02922 | hp1 | a0001 | c0001 | t0009 | g0296 | AFR | ESN | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02965 | hp1 | a0001 | c0001 | t0014 | g0031 | AFR | ESN | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | ESN | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0048 | AFR | ESN | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02970 | hp2 | a0001 | c0002 | t0010 | g0161 | AFR | ESN | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | ESN | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03017 | hp1 | a0001 | c0002 | t0003 | g0074 | SAS | PJL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03017 | hp2 | a0001 | c0001 | t0006 | g0144 | SAS | PJL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | MSL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03130 | hp1 | a0001 | c0001 | t0018 | g0052 | AFR | ESN | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03130 | hp2 | a0001 | c0001 | t0009 | g0297 | AFR | ESN | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0025 | AFR | ESN | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0046 | AFR | ESN | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0213 | AFR | MSL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03225 | hp2 | a0001 | c0001 | t0011 | g0016 | AFR | MSL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03239 | hp1 | a0001 | c0002 | t0003 | g0201 | SAS | PJL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | MSL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0146 | AFR | MSL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | MSL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0257 | SAS | PJL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0056 | AFR | ESN | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0019 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03579 | hp1 | a0001 | c0001 | t0008 | g0006 | AFR | MSL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03579 | hp2 | a0001 | c0001 | t0013 | g0033 | AFR | MSL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03669 | hp1 | a0001 | c0002 | t0003 | g0239 | SAS | PJL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03669 | hp2 | a0001 | c0002 | t0003 | g0205 | SAS | PJL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0236 | SAS | STU | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03688 | hp2 | a0001 | c0002 | t0003 | g0034 | SAS | STU | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03704 | hp2 | a0001 | c0002 | t0003 | g0175 | SAS | PJL | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03834 | hp1 | a0001 | c0002 | t0010 | g0202 | SAS | BEB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0274 | SAS | BEB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0275 | SAS | BEB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | BEB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | STU | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | STU | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | STU | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG04228 | hp2 | a0001 | c0001 | t0021 | g0200 | SAS | STU | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18522 | hp1 | a0001 | c0002 | t0010 | g0160 | AFR | YRI | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18522 | hp2 | a0001 | c0001 | t0008 | g0004 | AFR | YRI | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18747 | hp1 | a0001 | c0002 | t0003 | g0185 | EAS | CHB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18906 | hp1 | a0001 | c0001 | t0007 | g0027 | AFR | YRI | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | YRI | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18942 | hp2 | a0001 | c0002 | t0005 | g0312 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18949 | hp1 | a0001 | c0002 | t0003 | g0133 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18952 | hp2 | a0001 | c0002 | t0003 | g0089 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18954 | hp1 | a0001 | c0001 | t0024 | g0315 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18954 | hp2 | a0001 | c0002 | t0003 | g0262 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18962 | hp2 | a0001 | c0002 | t0003 | g0090 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18963 | hp1 | a0001 | c0002 | t0005 | g0310 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18967 | hp1 | a0001 | c0002 | t0003 | g0083 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18977 | hp1 | a0001 | c0002 | t0005 | g0311 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18979 | hp1 | a0001 | c0002 | t0003 | g0087 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18986 | hp1 | a0001 | c0002 | t0003 | g0155 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18987 | hp2 | a0001 | c0001 | t0016 | g0071 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18990 | hp1 | a0001 | c0002 | t0003 | g0120 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19000 | hp1 | a0001 | c0001 | t0020 | g0126 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19002 | hp1 | a0001 | c0002 | t0003 | g0261 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19003 | hp1 | a0001 | c0002 | t0003 | g0283 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19003 | hp2 | a0001 | c0002 | t0003 | g0094 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19006 | hp2 | a0001 | c0002 | t0003 | g0284 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19007 | hp1 | a0001 | c0002 | t0005 | g0314 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19010 | hp2 | a0001 | c0002 | t0003 | g0285 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0173 | AFR | LWK | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | LWK | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19060 | hp1 | a0001 | c0002 | t0003 | g0230 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19063 | hp2 | a0001 | c0002 | t0003 | g0291 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19065 | hp2 | a0001 | c0002 | t0003 | g0187 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19072 | hp2 | a0001 | c0001 | t0023 | g0298 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19074 | hp2 | a0001 | c0002 | t0005 | g0313 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19079 | hp1 | a0001 | c0002 | t0003 | g0249 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19086 | hp2 | a0001 | c0002 | t0003 | g0290 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19089 | hp2 | a0001 | c0002 | t0003 | g0121 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19091 | hp1 | a0001 | c0002 | t0003 | g0289 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19240 | hp1 | a0001 | c0001 | t0008 | g0005 | AFR | YRI | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0024 | AFR | YRI | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0216 | EUR | TSI | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0104 | EUR | TSI | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0207 | SAS | GIH | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | GIH | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0021 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02559 | hp1 | a0001 | c0002 | t0022 | g0099 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0047 | AFR | USA | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | USA | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0293 | REF | REF | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0051 | REF | REF | FAM78B_chr1_166064299_166172001 | FAM78B | chr1 | 166064299 | 166172001 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:166070661
|
C | G | 1 | a0001c0002 | 77 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
synonymous_variant | LOW | c.366G>C | p.Val122Val | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 2/2 | 1119/2481 | 366/786 | 122/261 | chr1 | 166070661 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:166069362
|
A | G | 1 | a0001c0001t0023 | 1 | NA19072.hp2 | 3_prime_UTR_variant | MODIFIER | c.*879T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 2/2 | 879 | chr1 | 166069362 | |||||
| chr1:166069558
|
G | C | 1 | a0001c0001t0006 | 8 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*683C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 2/2 | 683 | chr1 | 166069558 | |||||
| chr1:166069562
|
G | A | 1 | a0001c0001t0018 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*679C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 2/2 | 679 | chr1 | 166069562 | |||||
| chr1:166069605
|
T | C | 5 | a0001c0001t0003a0001c0002t0003a0001c0002t0005others(2): Show | 69 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*636A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 2/2 | 636 | chr1 | 166069605 | |||||
| chr1:166069623
|
C | T | 1 | a0001c0001t0020 | 1 | NA19000.hp1 | 3_prime_UTR_variant | MODIFIER | c.*618G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 2/2 | 618 | chr1 | 166069623 | |||||
| chr1:166069685
|
T | C | 2 | a0001c0002t0010a0001c0002t0015 | 4 | HG02055.hp2 HG02970.hp2 HG03834.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*556A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 2/2 | 556 | chr1 | 166069685 | |||||
| chr1:166069730
|
A | G | 7 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(4): Show | 78 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*511T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 2/2 | 511 | chr1 | 166069730 | |||||
| chr1:166069784
|
C | T | 1 | a0001c0001t0019 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*457G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 2/2 | 457 | chr1 | 166069784 | |||||
| chr1:166069961
|
G | A | 1 | a0001c0001t0009 | 3 | HG02451.hp1 HG02922.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*280C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 2/2 | 280 | chr1 | 166069961 | |||||
| chr1:166070011
|
C | G | 4 | a0001c0001t0004a0001c0001t0013a0001c0001t0017others(1): Show | 20 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*230G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 2/2 | 230 | chr1 | 166070011 | |||||
| chr1:166070045
|
A | G | 1 | a0001c0001t0016 | 1 | NA18987.hp2 | 3_prime_UTR_variant | MODIFIER | c.*196T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 2/2 | 196 | chr1 | 166070045 | |||||
| chr1:166070048
|
G | C | 1 | a0001c0001t0021 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*193C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 2/2 | 193 | chr1 | 166070048 | |||||
| chr1:166070064
|
A | C | 1 | a0001c0001t0009 | 3 | HG02451.hp1 HG02922.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*177T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 2/2 | 177 | chr1 | 166070064 | |||||
| chr1:166070194
|
C | A | 1 | a0001c0002t0022 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*47G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 2/2 | 47 | chr1 | 166070194 | |||||
| chr1:166166495
|
G | A | 2 | a0001c0001t0023a0001c0002t0005 | 17 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(14): Show |
5_prime_UTR_variant | MODIFIER | c.-247C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/2 | 247 | chr1 | 166166495 | |||||
| chr1:166166794
|
G | T | 4 | a0001c0001t0007a0001c0001t0013a0001c0001t0014others(1): Show | 8 | HG01891.hp1 HG02055.hp2 HG02723.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-546C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/2 | 546 | chr1 | 166166794 | |||||
| chr1:166166803
|
G | A | 1 | a0001c0001t0024 | 1 | NA18954.hp1 | 5_prime_UTR_variant | MODIFIER | c.-555C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/2 | 555 | chr1 | 166166803 | |||||
| chr1:166166854
|
C | T | 3 | a0001c0001t0004a0001c0001t0011a0001c0002t0011 | 19 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(16): Show |
5_prime_UTR_variant | MODIFIER | c.-606G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/2 | 606 | chr1 | 166166854 | |||||
| chr1:166166866
|
G | C | 1 | a0001c0001t0025 | 1 | HG01243.hp2 | 5_prime_UTR_variant | MODIFIER | c.-618C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/2 | 618 | chr1 | 166166866 | |||||
| chr1:166166880
|
A | C | 1 | a0001c0001t0008 | 3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
5_prime_UTR_variant | MODIFIER | c.-632T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/2 | 632 | chr1 | 166166880 | |||||
| chr1:166166957
|
A | G | 1 | a0001c0001t0012 | 1 | HG00597.hp1 | 5_prime_UTR_variant | MODIFIER | c.-709T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/2 | 709 | chr1 | 166166957 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:166070807
|
G | T | 1 | a0001c0001t0002g0128 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.264-44C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166070807 | ||||||
| chr1:166070825
|
A | T | 1 | a0001c0001t0023g0298 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.264-62T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166070825 | ||||||
| chr1:166070907
|
G | C | 5 | a0001c0001t0002g0002a0001c0001t0002g0066a0001c0001t0002g0080others(2): Show | 6 | HG00639.hp2 HG00738.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.264-144C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166070907 | ||||||
| chr1:166071045
|
C | T | 61 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0058others(58): Show | 61 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.264-282G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166071045 | ||||||
| chr1:166071122
|
G | A | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.264-359C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166071122 | ||||||
| chr1:166071318
|
G | T | 61 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0054others(58): Show | 62 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.264-555C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166071318 | ||||||
| chr1:166071411
|
C | T | 26 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0004g0009others(23): Show | 26 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.264-648G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166071411 | ||||||
| chr1:166071415
|
G | A | 1 | a0001c0002t0003g0291 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.264-652C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166071415 | ||||||
| chr1:166071529
|
G | A | 3 | a0001c0001t0002g0214a0001c0001t0002g0215a0001c0001t0002g0216 | 3 | HG01070.hp1 HG01071.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.264-766C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166071529 | ||||||
| chr1:166071556
|
C | A | 1 | a0001c0001t0024g0315 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.264-793G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166071556 | ||||||
| chr1:166071557
|
C | T | 1 | a0001c0002t0003g0196 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.264-794G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166071557 | ||||||
| chr1:166071579
|
A | G | 2 | a0001c0001t0002g0146a0001c0001t0002g0162 | 2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.264-816T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166071579 | ||||||
| chr1:166071880
|
T | C | 1 | a0001c0001t0001g0282 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.264-1117A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166071880 | ||||||
| chr1:166071932
|
G | A | 88 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0054others(85): Show | 89 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.264-1169C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166071932 | ||||||
| chr1:166071936
|
G | A | 1 | a0001c0001t0023g0298 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.264-1173C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166071936 | ||||||
| chr1:166072227
|
A | G | 1 | a0001c0002t0003g0230 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.264-1464T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166072227 | ||||||
| chr1:166072231
|
A | G | 30 | a0001c0001t0002g0002a0001c0001t0002g0038a0001c0001t0002g0053others(27): Show | 31 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.264-1468T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166072231 | ||||||
| chr1:166072310
|
G | A | 28 | a0001c0001t0002g0002a0001c0001t0002g0038a0001c0001t0002g0053others(25): Show | 29 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.264-1547C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166072310 | ||||||
| chr1:166072316
|
G | A | 9 | a0001c0001t0002g0053a0001c0001t0002g0081a0001c0001t0002g0171others(6): Show | 9 | HG01081.hp1 HG01891.hp1 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.264-1553C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166072316 | ||||||
| chr1:166072410
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.264-1647C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166072410 | ||||||
| chr1:166072494
|
G | A | 6 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(3): Show | 6 | HG02615.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.264-1731C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166072494 | ||||||
| chr1:166072547
|
G | T | 2 | a0001c0001t0001g0244a0001c0001t0001g0253 | 2 | HG00597.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.264-1784C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166072547 | ||||||
| chr1:166072550
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.264-1787G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166072550 | ||||||
| chr1:166072580
|
T | C | 3 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006 | 3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-1817A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166072580 | ||||||
| chr1:166072825
|
G | C | 1 | a0001c0001t0023g0298 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.264-2062C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166072825 | ||||||
| chr1:166072943
|
G | C | 1 | a0001c0002t0022g0099 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.264-2180C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166072943 | ||||||
| chr1:166073110
|
G | T | 26 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0004g0009others(23): Show | 26 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.264-2347C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166073110 | ||||||
| chr1:166073168
|
T | A | 28 | a0001c0001t0002g0002a0001c0001t0002g0038a0001c0001t0002g0053others(25): Show | 29 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.264-2405A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166073168 | ||||||
| chr1:166073421
|
C | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0054others(113): Show | 118 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.264-2658G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166073421 | ||||||
| chr1:166073497
|
CCTCT | C | 27 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0004g0009others(24): Show | 27 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.264-2738_264-2735d others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166073497 | ||||||
| chr1:166073518
|
C | T | 2 | a0001c0001t0001g0182a0001c0001t0001g0217 | 2 | HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.264-2755G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166073518 | ||||||
| chr1:166073530
|
T | C | 10 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(7): Show | 10 | HG02615.hp2 HG02818.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.264-2767A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166073530 | ||||||
| chr1:166073532
|
CTCTCTTT | C | 9 | a0001c0001t0001g0037a0001c0001t0001g0040a0001c0001t0001g0041others(6): Show | 9 | HG02615.hp2 HG02818.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.264-2776_264-2770d others(9): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166073532 | ||||||
| chr1:166073536
|
C | CT | 66 | a0001c0001t0003g0195a0001c0002t0003g0034a0001c0002t0003g0063others(63): Show | 66 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.264-2774dupA | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166073536 | ||||||
| chr1:166073536
|
C | T | 1 | a0001c0001t0023g0298 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.264-2773G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166073536 | ||||||
| chr1:166073536
|
CTTTT | C | 26 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0004g0009others(23): Show | 26 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.264-2777_264-2774d others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166073536 | ||||||
| chr1:166073537
|
T | TC | 12 | a0001c0001t0002g0002a0001c0001t0002g0066a0001c0001t0002g0080others(9): Show | 13 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.264-2775_264-2774i others(3): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166073537 | ||||||
| chr1:166073538
|
T | C | 16 | a0001c0001t0002g0038a0001c0001t0002g0053a0001c0001t0002g0081others(13): Show | 16 | HG01081.hp1 HG01891.hp1 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.264-2775A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166073538 | ||||||
| chr1:166073551
|
T | C | 2 | a0001c0001t0001g0211a0001c0001t0001g0278 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.264-2788A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166073551 | ||||||
| chr1:166073700
|
T | C | 1 | a0001c0001t0001g0061 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.264-2937A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166073700 | ||||||
| chr1:166073776
|
G | A | 1 | a0001c0001t0023g0298 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.264-3013C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166073776 | ||||||
| chr1:166073973
|
C | T | 1 | a0001c0001t0002g0225 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.264-3210G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166073973 | ||||||
| chr1:166074155
|
C | T | 1 | a0001c0002t0001g0179 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.264-3392G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166074155 | ||||||
| chr1:166074221
|
G | C | 61 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0054others(58): Show | 62 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.264-3458C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166074221 | ||||||
| chr1:166074442
|
T | C | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG02559.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.264-3679A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166074442 | ||||||
| chr1:166074547
|
A | C | 23 | a0001c0001t0001g0049a0001c0001t0001g0073a0001c0001t0001g0096others(20): Show | 23 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(20): Show |
intron_variant | MODIFIER | c.264-3784T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166074547 | ||||||
| chr1:166074616
|
A | G | 1 | a0001c0001t0001g0245 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.264-3853T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166074616 | ||||||
| chr1:166074702
|
T | C | 1 | a0001c0001t0023g0298 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.264-3939A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166074702 | ||||||
| chr1:166074724
|
C | T | 2 | a0001c0002t0001g0046a0001c0002t0001g0213 | 2 | HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.264-3961G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166074724 | ||||||
| chr1:166074818
|
T | A | 1 | a0001c0001t0002g0101 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.264-4055A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166074818 | ||||||
| chr1:166074820
|
A | G | 64 | a0001c0002t0003g0034a0001c0002t0003g0063a0001c0002t0003g0074others(61): Show | 64 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.264-4057T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166074820 | ||||||
| chr1:166074853
|
T | C | 61 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0054others(58): Show | 62 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.264-4090A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166074853 | ||||||
| chr1:166074867
|
C | A | 26 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0004g0009others(23): Show | 26 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.264-4104G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166074867 | ||||||
| chr1:166075012
|
T | C | 1 | a0001c0001t0002g0080 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.264-4249A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166075012 | ||||||
| chr1:166075092
|
C | G | 1 | a0001c0001t0024g0315 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.264-4329G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166075092 | ||||||
| chr1:166075158
|
T | C | 29 | a0001c0001t0002g0002a0001c0001t0002g0038a0001c0001t0002g0053others(26): Show | 30 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.264-4395A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166075158 | ||||||
| chr1:166075331
|
T | A | 62 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0054others(59): Show | 63 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.264-4568A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166075331 | ||||||
| chr1:166075423
|
T | TTG | 3 | a0001c0001t0001g0271a0001c0001t0001g0273a0001c0001t0001g0286 | 3 | HG00423.hp1 HG00673.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.264-4662_264-4661d others(4): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166075423 | ||||||
| chr1:166075441
|
T | C | 1 | a0001c0001t0009g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.264-4678A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166075441 | ||||||
| chr1:166075492
|
C | T | 61 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0054others(58): Show | 62 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.264-4729G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166075492 | ||||||
| chr1:166075494
|
C | T | 71 | a0001c0002t0001g0046a0001c0002t0001g0213a0001c0002t0003g0034others(68): Show | 71 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.264-4731G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166075494 | ||||||
| chr1:166075564
|
T | G | 1 | a0001c0001t0001g0130 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.264-4801A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166075564 | ||||||
| chr1:166076010
|
A | G | 150 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(147): Show | 151 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.264-5247T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076010 | ||||||
| chr1:166076014
|
C | CCACTCTT others(95): Show |
1 | a0001c0001t0001g0150 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-5252_264-5251i others(104): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076014 | ||||||
| chr1:166076028
|
C | G | 26 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0004g0009others(23): Show | 26 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.264-5265G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076028 | ||||||
| chr1:166076030
|
G | A | 71 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(68): Show | 71 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.264-5267C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076030 | ||||||
| chr1:166076166
|
C | T | 1 | a0001c0002t0003g0201 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.264-5403G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076166 | ||||||
| chr1:166076185
|
A | T | 1 | a0001c0001t0001g0150 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-5422T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076185 | ||||||
| chr1:166076187
|
G | A | 239 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(236): Show | 241 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.264-5424C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076187 | ||||||
| chr1:166076379
|
G | A | 61 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0058others(58): Show | 61 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.264-5616C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076379 | ||||||
| chr1:166076441
|
T | A | 3 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0136 | 3 | HG02040.hp1 NA18942.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.264-5678A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076441 | ||||||
| chr1:166076462
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.264-5699C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076462 | ||||||
| chr1:166076481
|
C | A | 26 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0004g0009others(23): Show | 26 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.264-5718G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076481 | ||||||
| chr1:166076519
|
T | A | 1 | a0001c0001t0001g0150 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-5756A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076519 | ||||||
| chr1:166076544
|
T | C | 61 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0054others(58): Show | 62 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.264-5781A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076544 | ||||||
| chr1:166076653
|
A | G | 1 | a0001c0001t0004g0023 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.264-5890T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076653 | ||||||
| chr1:166076656
|
T | C | 1 | a0001c0001t0002g0193 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.264-5893A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076656 | ||||||
| chr1:166076666
|
A | T | 1 | a0001c0001t0001g0150 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-5903T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076666 | ||||||
| chr1:166076720
|
A | T | 1 | a0001c0001t0001g0150 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-5957T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076720 | ||||||
| chr1:166076723
|
T | G | 1 | a0001c0001t0001g0150 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-5960A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076723 | ||||||
| chr1:166076724
|
G | T | 1 | a0001c0001t0001g0150 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-5961C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076724 | ||||||
| chr1:166076745
|
T | C | 3 | a0001c0001t0002g0053a0001c0001t0002g0171a0001c0001t0002g0173 | 3 | HG01081.hp1 HG02258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.264-5982A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076745 | ||||||
| chr1:166076758
|
A | G | 1 | a0001c0001t0023g0298 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.264-5995T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076758 | ||||||
| chr1:166076802
|
C | T | 3 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0158 | 3 | NA18947.hp2 NA19063.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.264-6039G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076802 | ||||||
| chr1:166076948
|
C | A | 71 | a0001c0002t0001g0046a0001c0002t0001g0213a0001c0002t0003g0034others(68): Show | 71 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.264-6185G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076948 | ||||||
| chr1:166076956
|
T | A | 1 | a0001c0001t0001g0150 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-6193A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166076956 | ||||||
| chr1:166077031
|
T | C | 1 | a0001c0001t0002g0241 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.264-6268A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077031 | ||||||
| chr1:166077157
|
A | T | 1 | a0001c0002t0001g0056 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.264-6394T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077157 | ||||||
| chr1:166077173
|
A | T | 1 | a0001c0001t0001g0150 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-6410T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077173 | ||||||
| chr1:166077211
|
T | A | 1 | a0001c0001t0001g0150 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-6448A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077211 | ||||||
| chr1:166077273
|
G | A | 1 | a0001c0001t0001g0150 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-6510C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077273 | ||||||
| chr1:166077451
|
A | C | 29 | a0001c0001t0002g0002a0001c0001t0002g0038a0001c0001t0002g0053others(26): Show | 30 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.264-6688T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077451 | ||||||
| chr1:166077558
|
T | A | 1 | a0001c0001t0001g0150 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-6795A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077558 | ||||||
| chr1:166077587
|
A | AAATACAT others(29): Show |
1 | a0001c0001t0001g0244 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.264-6860_264-6825d others(38): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077587 | ||||||
| chr1:166077587
|
AAATACAT others(29): Show |
A | 1 | a0001c0001t0001g0287 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.264-6860_264-6825d others(38): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077587 | ||||||
| chr1:166077629
|
A | T | 1 | a0001c0001t0001g0150 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-6866T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077629 | ||||||
| chr1:166077657
|
TAATA | T | 61 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0058others(58): Show | 61 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.264-6898_264-6895d others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077657 | ||||||
| chr1:166077661
|
A | ACATATAA others(23): Show |
26 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0004g0009others(23): Show | 26 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.264-6899_264-6898i others(32): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077661 | ||||||
| chr1:166077672
|
A | G | 29 | a0001c0001t0002g0002a0001c0001t0002g0038a0001c0001t0002g0053others(26): Show | 30 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.264-6909T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077672 | ||||||
| chr1:166077688
|
TA | T | 14 | a0001c0001t0004g0008a0001c0001t0004g0011a0001c0001t0004g0012others(11): Show | 14 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.264-6926delT | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077688 | ||||||
| chr1:166077696
|
A | AATAAATA others(27): Show |
1 | a0001c0001t0023g0298 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.264-6934_264-6933i others(36): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077696 | ||||||
| chr1:166077699
|
TAATA | T | 12 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(9): Show | 12 | HG02615.hp2 HG02818.hp1 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.264-6940_264-6937d others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077699 | ||||||
| chr1:166077701
|
A | T | 1 | a0001c0001t0023g0298 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.264-6938T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077701 | ||||||
| chr1:166077702
|
T | A | 1 | a0001c0001t0023g0298 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.264-6939A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077702 | ||||||
| chr1:166077703
|
A | T | 1 | a0001c0001t0023g0298 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.264-6940T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077703 | ||||||
| chr1:166077731
|
A | T | 1 | a0001c0001t0001g0150 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-6968T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077731 | ||||||
| chr1:166077733
|
T | A | 1 | a0001c0001t0001g0150 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-6970A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077733 | ||||||
| chr1:166077735
|
TAATA | T | 29 | a0001c0001t0002g0002a0001c0001t0002g0038a0001c0001t0002g0053others(26): Show | 30 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.264-6976_264-6973d others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077735 | ||||||
| chr1:166077740
|
A | T | 1 | a0001c0001t0001g0150 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-6977T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077740 | ||||||
| chr1:166077742
|
T | C | 1 | a0001c0001t0001g0150 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-6979A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077742 | ||||||
| chr1:166077744
|
C | A | 1 | a0001c0001t0001g0150 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-6981G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077744 | ||||||
| chr1:166077745
|
A | T | 1 | a0001c0001t0001g0150 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-6982T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077745 | ||||||
| chr1:166077746
|
T | A | 1 | a0001c0001t0001g0150 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-6983A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077746 | ||||||
| chr1:166077760
|
T | A | 1 | a0001c0001t0001g0150 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-6997A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077760 | ||||||
| chr1:166077819
|
TATATAA | T | 6 | a0001c0002t0003g0074a0001c0002t0003g0093a0001c0002t0003g0230others(3): Show | 6 | HG02055.hp2 HG02165.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.264-7062_264-7057d others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077819 | ||||||
| chr1:166077821
|
TATAA | T | 66 | a0001c0001t0002g0207a0001c0002t0001g0046a0001c0002t0001g0213others(63): Show | 66 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.264-7062_264-7059d others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077821 | ||||||
| chr1:166077836
|
T | A | 1 | a0001c0001t0001g0110 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.264-7073A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077836 | ||||||
| chr1:166077836
|
T | C | 1 | a0001c0001t0009g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.264-7073A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077836 | ||||||
| chr1:166077837
|
TTATATAT others(118): Show |
T | 59 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0054others(56): Show | 60 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.264-7199_264-7075d others(2): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077837 | ||||||
| chr1:166077837
|
TTATATAT others(120): Show |
T | 2 | a0001c0001t0002g0038a0001c0001t0002g0193 | 2 | HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.264-7201_264-7075d others(2): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077837 | ||||||
| chr1:166077844
|
TATAATAA others(122): Show |
T | 1 | a0001c0001t0020g0126 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.264-7210_264-7082d others(2): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077844 | ||||||
| chr1:166077849
|
TAATATAT others(117): Show |
T | 148 | a0001c0001t0001g0163a0001c0001t0001g0251a0001c0001t0002g0002others(145): Show | 149 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.264-7210_264-7087d others(2): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077849 | ||||||
| chr1:166077850
|
AAT | A | 10 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(7): Show | 10 | HG02615.hp2 HG02818.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.264-7089_264-7088d others(4): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077850 | ||||||
| chr1:166077853
|
A | T | 1 | a0001c0001t0001g0150 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-7090T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077853 | ||||||
| chr1:166077865
|
TATATATA others(54): Show |
T | 6 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0055others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.264-7163_264-7103d others(63): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077865 | ||||||
| chr1:166077874
|
TTATATAT others(6): Show |
T | 53 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0058others(50): Show | 53 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.264-7124_264-7112d others(15): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077874 | ||||||
| chr1:166077874
|
TTATATAT others(78): Show |
T | 3 | a0001c0001t0002g0292a0001c0001t0002g0293a0001c0001t0002g0295 | 3 | HG01515.hp2 HG02738.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.264-7196_264-7112d others(87): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077874 | ||||||
| chr1:166077874
|
TTATATAT others(92): Show |
T | 29 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(26): Show | 29 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.264-7210_264-7112d others(101): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077874 | ||||||
| chr1:166077875
|
T | A | 9 | a0001c0001t0001g0096a0001c0001t0001g0150a0001c0001t0001g0152others(6): Show | 9 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(6): Show |
intron_variant | MODIFIER | c.264-7112A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077875 | ||||||
| chr1:166077881
|
TATAATAA others(7): Show |
T | 1 | a0001c0001t0001g0150 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-7132_264-7119d others(16): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077881 | ||||||
| chr1:166077887
|
A | T | 7 | a0001c0001t0001g0152a0001c0001t0001g0210a0001c0001t0001g0220others(4): Show | 7 | HG00323.hp2 HG00423.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.264-7124T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077887 | ||||||
| chr1:166077888
|
A | T | 7 | a0001c0001t0001g0152a0001c0001t0001g0210a0001c0001t0001g0220others(4): Show | 7 | HG00323.hp2 HG00423.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.264-7125T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077888 | ||||||
| chr1:166077889
|
A | T | 1 | a0001c0001t0001g0096 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.264-7126T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077889 | ||||||
| chr1:166077890
|
T | TATATA | 7 | a0001c0001t0001g0152a0001c0001t0001g0210a0001c0001t0001g0220others(4): Show | 7 | HG00323.hp2 HG00423.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.264-7132_264-7128d others(7): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077890 | ||||||
| chr1:166077908
|
ATAATT | A | 50 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0058others(47): Show | 50 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.264-7150_264-7146d others(7): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077908 | ||||||
| chr1:166077908
|
ATAATTAT | A | 3 | a0001c0001t0001g0150a0001c0001t0001g0252a0001c0001t0001g0271 | 3 | NA18941.hp2 NA18990.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.264-7152_264-7146d others(9): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077908 | ||||||
| chr1:166077913
|
T | A | 8 | a0001c0001t0001g0152a0001c0001t0001g0210a0001c0001t0001g0220others(5): Show | 8 | HG00323.hp2 HG00423.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.264-7150A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077913 | ||||||
| chr1:166077913
|
TATATATA others(3): Show |
T | 1 | a0001c0001t0001g0096 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.264-7160_264-7151d others(12): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077913 | ||||||
| chr1:166077921
|
T | A | 50 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0058others(47): Show | 50 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.264-7158A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077921 | ||||||
| chr1:166077922
|
A | T | 50 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0058others(47): Show | 50 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.264-7159T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077922 | ||||||
| chr1:166077923
|
A | ATT | 7 | a0001c0001t0001g0152a0001c0001t0001g0210a0001c0001t0001g0220others(4): Show | 7 | HG00323.hp2 HG00423.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.264-7161_264-7160i others(4): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077923 | ||||||
| chr1:166077923
|
A | ATTTATAT others(13): Show |
1 | a0001c0001t0001g0222 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.264-7161_264-7160i others(22): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077923 | ||||||
| chr1:166077923
|
A | T | 50 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0058others(47): Show | 50 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.264-7160T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077923 | ||||||
| chr1:166077925
|
A | T | 3 | a0001c0001t0001g0150a0001c0001t0001g0252a0001c0001t0001g0271 | 3 | NA18941.hp2 NA18990.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.264-7162T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077925 | ||||||
| chr1:166077926
|
A | T | 62 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0058others(59): Show | 62 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.264-7163T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077926 | ||||||
| chr1:166077935
|
T | TAATATAT others(31): Show |
1 | a0001c0001t0001g0045 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.264-7210_264-7173d others(40): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077935 | ||||||
| chr1:166077948
|
TTATATAT others(7): Show |
T | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.264-7199_264-7186d others(16): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077948 | ||||||
| chr1:166077955
|
TATAATTA others(8): Show |
T | 1 | a0001c0001t0001g0150 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-7207_264-7193d others(17): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077955 | ||||||
| chr1:166077960
|
TTATATAT others(6): Show |
T | 56 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0058others(53): Show | 56 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.264-7210_264-7198d others(15): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077960 | ||||||
| chr1:166077961
|
T | A | 1 | a0001c0001t0001g0222 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.264-7198A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077961 | ||||||
| chr1:166077961
|
TATATATA others(6): Show |
T | 8 | a0001c0001t0001g0152a0001c0001t0018g0052a0001c0002t0001g0047others(5): Show | 8 | HG00323.hp2 HG02258.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.264-7211_264-7199d others(15): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077961 | ||||||
| chr1:166077970
|
A | AATTTATA others(3): Show |
1 | a0001c0001t0001g0222 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.264-7208_264-7207i others(12): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077970 | ||||||
| chr1:166077972
|
TA | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0054others(63): Show | 67 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.264-7210delT | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077972 | ||||||
| chr1:166077976
|
T | G | 1 | a0001c0001t0002g0232 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.264-7213A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077976 | ||||||
| chr1:166077988
|
A | T | 1 | a0001c0001t0001g0150 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-7225T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077988 | ||||||
| chr1:166077989
|
T | A | 1 | a0001c0001t0001g0150 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-7226A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077989 | ||||||
| chr1:166077990
|
A | T | 1 | a0001c0001t0001g0150 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-7227T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077990 | ||||||
| chr1:166077996
|
A | T | 78 | a0001c0001t0002g0171a0001c0001t0002g0173a0001c0001t0002g0207others(75): Show | 78 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.264-7233T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166077996 | ||||||
| chr1:166078009
|
A | G | 1 | a0001c0001t0023g0298 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.264-7246T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166078009 | ||||||
| chr1:166078024
|
A | T | 11 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(8): Show | 11 | HG02451.hp1 HG02615.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.264-7261T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166078024 | ||||||
| chr1:166078096
|
A | G | 60 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0058others(57): Show | 60 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.264-7333T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166078096 | ||||||
| chr1:166078145
|
C | T | 1 | a0001c0001t0009g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.264-7382G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166078145 | ||||||
| chr1:166078147
|
T | C | 1 | a0001c0001t0009g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.264-7384A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166078147 | ||||||
| chr1:166078167
|
G | T | 3 | a0001c0002t0010g0160a0001c0002t0010g0161a0001c0002t0015g0030 | 3 | HG02055.hp2 HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.264-7404C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166078167 | ||||||
| chr1:166078272
|
G | A | 29 | a0001c0001t0002g0002a0001c0001t0002g0038a0001c0001t0002g0053others(26): Show | 30 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.264-7509C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166078272 | ||||||
| chr1:166078441
|
A | G | 49 | a0001c0001t0001g0163a0001c0001t0002g0064a0001c0001t0002g0118others(46): Show | 49 | HG00609.hp1 HG00642.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.264-7678T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166078441 | ||||||
| chr1:166078553
|
G | A | 61 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0054others(58): Show | 62 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.264-7790C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166078553 | ||||||
| chr1:166078559
|
C | A | 61 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0058others(58): Show | 61 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.264-7796G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166078559 | ||||||
| chr1:166078603
|
G | A | 1 | a0001c0001t0001g0150 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-7840C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166078603 | ||||||
| chr1:166078604
|
A | C | 1 | a0001c0001t0001g0150 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-7841T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166078604 | ||||||
| chr1:166078607
|
C | G | 1 | a0001c0001t0001g0150 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-7844G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166078607 | ||||||
| chr1:166078797
|
G | T | 1 | a0001c0001t0001g0150 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-8034C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166078797 | ||||||
| chr1:166078816
|
A | G | 166 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0054others(163): Show | 168 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.264-8053T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166078816 | ||||||
| chr1:166078927
|
G | GT | 64 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0058others(61): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.264-8165dupA | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166078927 | ||||||
| chr1:166078927
|
GT | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0054others(134): Show | 138 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.264-8165delA | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166078927 | ||||||
| chr1:166078927
|
GTT | G | 28 | a0001c0001t0002g0002a0001c0001t0002g0038a0001c0001t0002g0053others(25): Show | 29 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.264-8166_264-8165d others(4): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166078927 | ||||||
| chr1:166078956
|
G | C | 61 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0054others(58): Show | 62 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.264-8193C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166078956 | ||||||
| chr1:166079044
|
G | C | 1 | a0001c0001t0001g0150 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-8281C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166079044 | ||||||
| chr1:166079086
|
C | T | 1 | a0001c0001t0002g0162 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.264-8323G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166079086 | ||||||
| chr1:166079140
|
C | T | 61 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0058others(58): Show | 61 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.264-8377G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166079140 | ||||||
| chr1:166079167
|
C | T | 1 | a0001c0001t0008g0004 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.264-8404G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166079167 | ||||||
| chr1:166079351
|
T | C | 29 | a0001c0001t0002g0002a0001c0001t0002g0038a0001c0001t0002g0053others(26): Show | 30 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.264-8588A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166079351 | ||||||
| chr1:166079507
|
G | A | 310 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(307): Show | 312 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(309): Show |
intron_variant | MODIFIER | c.264-8744C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166079507 | ||||||
| chr1:166079534
|
G | C | 2 | a0001c0001t0001g0001a0001c0001t0001g0057 | 3 | HG00639.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.264-8771C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166079534 | ||||||
| chr1:166079579
|
T | G | 1 | a0001c0002t0001g0048 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.264-8816A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166079579 | ||||||
| chr1:166079742
|
T | C | 61 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0058others(58): Show | 61 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.264-8979A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166079742 | ||||||
| chr1:166079788
|
T | C | 1 | a0001c0001t0002g0240 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.264-9025A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166079788 | ||||||
| chr1:166079807
|
C | T | 12 | a0001c0001t0001g0220a0001c0001t0001g0222a0001c0001t0001g0231others(9): Show | 12 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.264-9044G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166079807 | ||||||
| chr1:166079923
|
T | C | 1 | a0001c0001t0001g0150 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-9160A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166079923 | ||||||
| chr1:166080033
|
T | C | 116 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0058others(113): Show | 117 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.264-9270A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166080033 | ||||||
| chr1:166080089
|
G | A | 9 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(6): Show | 9 | HG02615.hp2 HG02818.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.264-9326C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166080089 | ||||||
| chr1:166080164
|
T | C | 1 | a0001c0002t0005g0310 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.264-9401A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166080164 | ||||||
| chr1:166080303
|
T | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0040a0001c0001t0001g0049others(148): Show | 153 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.264-9540A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166080303 | ||||||
| chr1:166080340
|
CCCA | C | 46 | a0001c0001t0001g0152a0001c0001t0001g0163a0001c0001t0001g0248others(43): Show | 46 | HG00323.hp2 HG00609.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.264-9580_264-9578d others(5): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166080340 | ||||||
| chr1:166080520
|
C | T | 1 | a0001c0002t0022g0099 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.264-9757G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166080520 | ||||||
| chr1:166080585
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.264-9822C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166080585 | ||||||
| chr1:166081140
|
C | T | 2 | a0001c0001t0001g0247a0001c0001t0001g0268 | 2 | HG00621.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.264-10377G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166081140 | ||||||
| chr1:166081149
|
A | T | 1 | a0001c0002t0022g0099 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.264-10386T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166081149 | ||||||
| chr1:166081308
|
G | A | 3 | a0001c0001t0001g0069a0001c0001t0009g0296a0001c0001t0009g0297 | 3 | HG02922.hp1 HG03130.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.264-10545C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166081308 | ||||||
| chr1:166081314
|
G | A | 1 | a0001c0001t0023g0298 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.264-10551C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166081314 | ||||||
| chr1:166081319
|
G | T | 1 | a0001c0001t0001g0150 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-10556C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166081319 | ||||||
| chr1:166081320
|
T | G | 1 | a0001c0001t0001g0150 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-10557A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166081320 | ||||||
| chr1:166081372
|
G | A | 1 | a0001c0001t0002g0250 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.264-10609C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166081372 | ||||||
| chr1:166081680
|
G | A | 307 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(304): Show | 309 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(306): Show |
intron_variant | MODIFIER | c.264-10917C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166081680 | ||||||
| chr1:166081834
|
A | G | 19 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0011others(16): Show | 19 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.264-11071T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166081834 | ||||||
| chr1:166082084
|
C | T | 3 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006 | 3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-11321G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166082084 | ||||||
| chr1:166082157
|
C | T | 3 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006 | 3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-11394G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166082157 | ||||||
| chr1:166082163
|
G | A | 315 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(312): Show | 317 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.264-11400C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166082163 | ||||||
| chr1:166082225
|
C | G | 1 | a0001c0001t0021g0200 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.264-11462G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166082225 | ||||||
| chr1:166082264
|
A | T | 1 | a0001c0001t0021g0200 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.264-11501T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166082264 | ||||||
| chr1:166082350
|
G | T | 120 | a0001c0001t0001g0054a0001c0001t0001g0082a0001c0001t0001g0152others(117): Show | 120 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.264-11587C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166082350 | ||||||
| chr1:166082482
|
T | C | 1 | a0001c0001t0002g0172 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.264-11719A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166082482 | ||||||
| chr1:166082534
|
G | C | 1 | a0001c0002t0003g0205 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.264-11771C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166082534 | ||||||
| chr1:166082559
|
A | G | 3 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006 | 3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-11796T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166082559 | ||||||
| chr1:166082842
|
G | A | 3 | a0001c0001t0004g0007a0001c0001t0009g0296a0001c0001t0009g0297 | 3 | HG01243.hp1 HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.264-12079C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166082842 | ||||||
| chr1:166082865
|
A | ACGAGTGT others(1): Show |
6 | a0001c0001t0001g0182a0001c0001t0008g0004a0001c0001t0008g0005others(3): Show | 6 | HG00544.hp1 HG03516.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.264-12110_264-1210 others(12): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166082865 | ||||||
| chr1:166083082
|
G | T | 18 | a0001c0001t0004g0009a0001c0001t0004g0011a0001c0001t0004g0012others(15): Show | 18 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.264-12319C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166083082 | ||||||
| chr1:166083096
|
G | T | 3 | a0001c0001t0009g0036a0001c0001t0009g0296a0001c0001t0009g0297 | 3 | HG02451.hp1 HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.264-12333C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166083096 | ||||||
| chr1:166083221
|
G | A | 2 | a0001c0001t0001g0050a0001c0001t0001g0067 | 2 | HG01099.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.264-12458C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166083221 | ||||||
| chr1:166083289
|
G | C | 67 | a0001c0001t0001g0054a0001c0001t0001g0082a0001c0001t0001g0157others(64): Show | 67 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.264-12526C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166083289 | ||||||
| chr1:166083433
|
T | C | 1 | a0001c0001t0018g0052 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.264-12670A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166083433 | ||||||
| chr1:166083493
|
A | G | 1 | a0001c0001t0001g0068 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.264-12730T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166083493 | ||||||
| chr1:166083540
|
G | T | 11 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0191others(8): Show | 11 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.264-12777C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166083540 | ||||||
| chr1:166083558
|
G | A | 84 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0050others(81): Show | 85 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.264-12795C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166083558 | ||||||
| chr1:166083642
|
C | T | 3 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006 | 3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-12879G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166083642 | ||||||
| chr1:166083799
|
CT | C | 8 | a0001c0001t0001g0098a0001c0001t0001g0109a0001c0001t0001g0110others(5): Show | 8 | HG02109.hp2 HG02647.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.264-13037delA | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166083799 | ||||||
| chr1:166083799
|
CTT | C | 133 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0049others(130): Show | 135 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.264-13038_264-1303 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166083799 | ||||||
| chr1:166083799
|
CTTT | C | 19 | a0001c0001t0001g0061a0001c0001t0001g0070a0001c0001t0001g0188others(16): Show | 19 | HG01069.hp2 HG01070.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.264-13039_264-1303 others(7): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166083799 | ||||||
| chr1:166083799
|
CTTTT | C | 145 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(142): Show | 145 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.264-13040_264-1303 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166083799 | ||||||
| chr1:166083981
|
C | T | 315 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(312): Show | 317 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.264-13218G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166083981 | ||||||
| chr1:166084119
|
C | T | 1 | a0001c0001t0001g0115 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.264-13356G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084119 | ||||||
| chr1:166084205
|
C | CCA | 56 | a0001c0001t0001g0082a0001c0001t0001g0097a0001c0001t0001g0117others(53): Show | 56 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.264-13444_264-1344 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084205 | ||||||
| chr1:166084205
|
C | CCACA | 85 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0050others(82): Show | 87 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.264-13446_264-1344 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084205 | ||||||
| chr1:166084205
|
C | CCACACA | 11 | a0001c0001t0001g0057a0001c0001t0001g0072a0001c0001t0001g0079others(8): Show | 11 | HG00597.hp2 HG00639.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.264-13448_264-1344 others(10): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084205 | ||||||
| chr1:166084205
|
C | CCACACAC others(1): Show |
15 | a0001c0001t0001g0054a0001c0001t0001g0151a0001c0001t0001g0152others(12): Show | 15 | HG00323.hp2 HG00597.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.264-13450_264-1344 others(12): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084205 | ||||||
| chr1:166084205
|
C | CCACACAC others(3): Show |
4 | a0001c0001t0025g0316a0001c0002t0003g0083a0001c0002t0003g0133others(1): Show | 4 | HG01243.hp2 NA18949.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-13452_264-1344 others(14): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084205 | ||||||
| chr1:166084205
|
C | CCACACAC others(7): Show |
3 | a0001c0001t0002g0193a0001c0001t0008g0004a0001c0001t0008g0005 | 3 | HG02895.hp2 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-13456_264-1344 others(18): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084205 | ||||||
| chr1:166084205
|
C | CCACACAC others(11): Show |
1 | a0001c0001t0014g0031 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.264-13460_264-1344 others(22): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084205 | ||||||
| chr1:166084205
|
C | CCACACAC others(17): Show |
1 | a0001c0001t0001g0042 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.264-13466_264-1344 others(28): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084205 | ||||||
| chr1:166084205
|
CCA | C | 9 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(6): Show | 9 | HG01081.hp1 HG02155.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.264-13444_264-1344 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084205 | ||||||
| chr1:166084224
|
C | CACACACA others(15): Show |
3 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0055 | 3 | HG02723.hp1 HG02970.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.264-13462_264-1346 others(26): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084224 | ||||||
| chr1:166084226
|
C | CACACACA others(13): Show |
1 | a0001c0002t0011g0010 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.264-13464_264-1346 others(24): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084226 | ||||||
| chr1:166084228
|
C | CACACACA others(11): Show |
1 | a0001c0002t0001g0046 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.264-13466_264-1346 others(22): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084228 | ||||||
| chr1:166084228
|
C | CACAT | 3 | a0001c0002t0003g0087a0001c0002t0003g0089a0001c0002t0003g0120 | 3 | NA18952.hp2 NA18979.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.264-13466_264-1346 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084228 | ||||||
| chr1:166084231
|
ACACACAC others(5): Show |
A | 2 | a0001c0001t0001g0248a0001c0001t0002g0228 | 2 | HG01106.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.264-13480_264-1346 others(16): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084231 | ||||||
| chr1:166084235
|
ACACTCTC others(3): Show |
A | 4 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0191others(1): Show | 4 | HG02145.hp1 HG02257.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-13482_264-1347 others(14): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084235 | ||||||
| chr1:166084237
|
A | ACACACAC others(19): Show |
1 | a0001c0001t0001g0037 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.264-13475_264-1347 others(30): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | ||||||
| chr1:166084237
|
A | ACACACAC others(17): Show |
1 | a0001c0001t0001g0040 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.264-13475_264-1347 others(28): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | ||||||
| chr1:166084237
|
A | ACACACAC others(15): Show |
1 | a0001c0001t0001g0039 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.264-13475_264-1347 others(26): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | ||||||
| chr1:166084237
|
A | ACACACAC others(13): Show |
1 | a0001c0001t0001g0041 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.264-13475_264-1347 others(24): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | ||||||
| chr1:166084237
|
A | ACACACAC others(11): Show |
2 | a0001c0001t0008g0006a0001c0002t0001g0213 | 2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.264-13475_264-1347 others(22): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | ||||||
| chr1:166084237
|
A | ACACACAC others(9): Show |
1 | a0001c0001t0001g0176 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.264-13475_264-1347 others(20): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | ||||||
| chr1:166084237
|
A | ACACACAC others(7): Show |
1 | a0001c0001t0002g0038 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.264-13475_264-1347 others(18): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | ||||||
| chr1:166084237
|
A | ACACACAC others(3): Show |
1 | a0001c0001t0001g0096 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.264-13475_264-1347 others(14): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | ||||||
| chr1:166084237
|
A | ACACACAC others(5): Show |
1 | a0001c0001t0002g0172 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.264-13475_264-1347 others(16): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | ||||||
| chr1:166084237
|
A | ACACACAC others(1): Show |
7 | a0001c0001t0001g0049a0001c0001t0001g0102a0001c0001t0001g0105others(4): Show | 7 | HG00735.hp1 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.264-13475_264-1347 others(12): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | ||||||
| chr1:166084237
|
A | ACACACAC others(3): Show |
3 | a0001c0001t0001g0106a0001c0001t0001g0150a0001c0001t0001g0282 | 3 | HG02129.hp1 HG04204.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.264-13475_264-1347 others(14): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | ||||||
| chr1:166084237
|
A | ACACACAC others(5): Show |
1 | a0001c0001t0001g0287 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.264-13475_264-1347 others(16): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | ||||||
| chr1:166084237
|
A | ACACACAC others(7): Show |
3 | a0001c0001t0001g0190a0001c0001t0021g0200a0001c0002t0005g0302 | 3 | HG01192.hp1 HG04204.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.264-13475_264-1347 others(18): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | ||||||
| chr1:166084237
|
A | ACACACAC others(9): Show |
1 | a0001c0002t0003g0208 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.264-13475_264-1347 others(20): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | ||||||
| chr1:166084237
|
A | ACACACAC others(11): Show |
3 | a0001c0002t0003g0198a0001c0002t0003g0199a0001c0002t0003g0209 | 3 | HG01081.hp2 HG01099.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.264-13475_264-1347 others(22): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | ||||||
| chr1:166084237
|
A | ACACACT | 4 | a0001c0001t0001g0098a0001c0001t0001g0138a0001c0002t0003g0085others(1): Show | 4 | HG02083.hp2 HG02735.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-13475_264-1347 others(10): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | ||||||
| chr1:166084237
|
A | ACACACTC others(1): Show |
3 | a0001c0002t0003g0034a0001c0002t0003g0283a0001c0002t0005g0304 | 3 | HG01952.hp2 HG03688.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.264-13475_264-1347 others(12): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | ||||||
| chr1:166084237
|
A | ACACACTC others(5): Show |
25 | a0001c0001t0001g0212a0001c0001t0001g0286a0001c0001t0002g0207others(22): Show | 25 | HG00140.hp1 HG00438.hp2 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.264-13475_264-1347 others(16): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | ||||||
| chr1:166084237
|
A | ACACACTC others(7): Show |
5 | a0001c0001t0002g0295a0001c0002t0003g0279a0001c0002t0005g0311others(2): Show | 5 | HG01168.hp2 HG01515.hp2 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.264-13475_264-1347 others(18): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | ||||||
| chr1:166084237
|
A | ACACACTC others(9): Show |
1 | a0001c0001t0002g0292 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.264-13475_264-1347 others(20): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | ||||||
| chr1:166084237
|
A | ACACT | 8 | a0001c0001t0001g0073a0001c0001t0001g0092a0001c0001t0001g0104others(5): Show | 8 | HG00558.hp2 HG02922.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.264-13475_264-1347 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | ||||||
| chr1:166084237
|
A | ACACTCTC others(5): Show |
1 | a0001c0001t0002g0293 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.264-13475_264-1347 others(16): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | ||||||
| chr1:166084237
|
A | ACACTCTC others(7): Show |
1 | a0001c0002t0005g0309 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.264-13475_264-1347 others(18): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | ||||||
| chr1:166084237
|
A | T | 4 | a0001c0001t0001g0174a0001c0002t0003g0087a0001c0002t0003g0089others(1): Show | 4 | HG03041.hp2 NA18952.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-13474T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | ||||||
| chr1:166084237
|
ACT | A | 9 | a0001c0001t0002g0214a0001c0001t0002g0215a0001c0001t0002g0229others(6): Show | 9 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.264-13476_264-1347 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | ||||||
| chr1:166084237
|
ACTCT | A | 5 | a0001c0001t0001g0159a0001c0001t0001g0253a0001c0001t0013g0033others(2): Show | 5 | HG00544.hp1 HG02886.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.264-13478_264-1347 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | ||||||
| chr1:166084237
|
ACTCTCT | A | 4 | a0001c0001t0007g0026a0001c0001t0007g0027a0001c0001t0007g0028others(1): Show | 4 | HG02723.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-13480_264-1347 others(10): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084237 | ||||||
| chr1:166084239
|
T | A | 98 | a0001c0001t0001g0054a0001c0001t0001g0065a0001c0001t0001g0082others(95): Show | 98 | HG00140.hp2 HG00423.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.264-13476A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084239 | ||||||
| chr1:166084241
|
T | A | 80 | a0001c0001t0001g0054a0001c0001t0001g0082a0001c0001t0001g0124others(77): Show | 80 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.264-13478A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084241 | ||||||
| chr1:166084243
|
T | A | 69 | a0001c0001t0001g0054a0001c0001t0001g0082a0001c0001t0001g0159others(66): Show | 69 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.264-13480A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084243 | ||||||
| chr1:166084245
|
T | A | 10 | a0001c0001t0001g0159a0001c0001t0002g0214a0001c0001t0002g0215others(7): Show | 10 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.264-13482A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084245 | ||||||
| chr1:166084247
|
T | A | 2 | a0001c0001t0002g0214a0001c0001t0002g0215 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.264-13484A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084247 | ||||||
| chr1:166084256
|
CTCTCTCT others(3): Show |
C | 1 | a0001c0001t0001g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.264-13503_264-1349 others(14): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084256 | ||||||
| chr1:166084266
|
T | C | 1 | a0001c0002t0001g0046 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.264-13503A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084266 | ||||||
| chr1:166084268
|
C | T | 1 | a0001c0002t0001g0046 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.264-13505G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084268 | ||||||
| chr1:166084278
|
C | G | 1 | a0001c0001t0001g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.264-13515G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084278 | ||||||
| chr1:166084676
|
C | G | 1 | a0001c0001t0001g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.264-13913G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084676 | ||||||
| chr1:166084793
|
C | T | 1 | a0001c0001t0002g0080 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.264-14030G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084793 | ||||||
| chr1:166084884
|
G | A | 5 | a0001c0002t0001g0046a0001c0002t0001g0047a0001c0002t0001g0048others(2): Show | 5 | HG02258.hp2 HG02723.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.264-14121C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084884 | ||||||
| chr1:166084907
|
A | G | 2 | a0001c0001t0023g0298a0001c0002t0005g0306 | 2 | HG00544.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.264-14144T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084907 | ||||||
| chr1:166084938
|
G | A | 2 | a0001c0001t0001g0248a0001c0001t0002g0228 | 2 | HG01106.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.264-14175C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084938 | ||||||
| chr1:166084945
|
C | A | 1 | a0001c0001t0002g0246 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.264-14182G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084945 | ||||||
| chr1:166084951
|
G | T | 1 | a0001c0001t0002g0064 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.264-14188C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084951 | ||||||
| chr1:166084978
|
T | G | 71 | a0001c0001t0001g0054a0001c0001t0001g0082a0001c0001t0001g0194others(68): Show | 71 | HG00423.hp1 HG00609.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.264-14215A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166084978 | ||||||
| chr1:166085230
|
C | T | 2 | a0001c0002t0010g0160a0001c0002t0010g0161 | 2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.264-14467G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166085230 | ||||||
| chr1:166085409
|
A | C | 220 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(217): Show | 222 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.264-14646T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166085409 | ||||||
| chr1:166085478
|
A | C | 1 | a0001c0001t0004g0007 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.264-14715T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166085478 | ||||||
| chr1:166085531
|
G | A | 309 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(306): Show | 311 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.264-14768C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166085531 | ||||||
| chr1:166085661
|
A | C | 7 | a0001c0001t0002g0207a0001c0002t0003g0198a0001c0002t0003g0199others(4): Show | 7 | HG00140.hp1 HG01081.hp2 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.264-14898T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166085661 | ||||||
| chr1:166085857
|
T | C | 1 | a0001c0002t0003g0198 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.264-15094A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166085857 | ||||||
| chr1:166086073
|
C | CT | 17 | a0001c0001t0001g0096a0001c0001t0001g0106a0001c0001t0001g0115others(14): Show | 17 | HG00558.hp1 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-15311dupA | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166086073 | ||||||
| chr1:166086073
|
CT | C | 6 | a0001c0001t0001g0159a0001c0001t0001g0166a0001c0001t0001g0168others(3): Show | 6 | HG01515.hp2 HG02280.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.264-15311delA | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166086073 | ||||||
| chr1:166086082
|
T | C | 1 | a0001c0001t0002g0246 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.264-15319A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166086082 | ||||||
| chr1:166086096
|
A | G | 2 | a0001c0001t0023g0298a0001c0002t0005g0306 | 2 | HG00544.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.264-15333T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166086096 | ||||||
| chr1:166086156
|
G | A | 1 | a0001c0001t0002g0216 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.264-15393C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166086156 | ||||||
| chr1:166086261
|
C | T | 1 | a0001c0002t0003g0090 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.264-15498G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166086261 | ||||||
| chr1:166086273
|
T | G | 1 | a0001c0001t0001g0189 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.264-15510A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166086273 | ||||||
| chr1:166086285
|
C | T | 1 | a0001c0002t0003g0034 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.264-15522G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166086285 | ||||||
| chr1:166086336
|
CAAAG | C | 5 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0135others(2): Show | 5 | HG01257.hp1 HG01943.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.264-15577_264-1557 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166086336 | ||||||
| chr1:166086472
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.264-15709C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166086472 | ||||||
| chr1:166086504
|
G | T | 17 | a0001c0001t0023g0298a0001c0002t0003g0086a0001c0002t0005g0299others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-15741C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166086504 | ||||||
| chr1:166086771
|
A | G | 1 | a0001c0001t0014g0031 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.264-16008T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166086771 | ||||||
| chr1:166086838
|
C | T | 2 | a0001c0002t0001g0056a0001c0002t0001g0179 | 2 | HG02615.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.264-16075G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166086838 | ||||||
| chr1:166086879
|
G | A | 1 | a0001c0001t0013g0033 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.264-16116C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166086879 | ||||||
| chr1:166087063
|
C | T | 1 | a0001c0001t0006g0103 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.264-16300G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166087063 | ||||||
| chr1:166087071
|
AT | A | 16 | a0001c0001t0023g0298a0001c0002t0005g0299a0001c0002t0005g0300others(13): Show | 16 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.264-16309delA | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166087071 | ||||||
| chr1:166087210
|
C | T | 17 | a0001c0001t0023g0298a0001c0002t0003g0086a0001c0002t0005g0299others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-16447G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166087210 | ||||||
| chr1:166087342
|
C | T | 5 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0191others(2): Show | 5 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.264-16579G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166087342 | ||||||
| chr1:166087576
|
G | GT | 17 | a0001c0001t0023g0298a0001c0002t0003g0086a0001c0002t0005g0299others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-16814dupA | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166087576 | ||||||
| chr1:166087657
|
T | C | 17 | a0001c0001t0023g0298a0001c0002t0003g0086a0001c0002t0005g0299others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-16894A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166087657 | ||||||
| chr1:166087917
|
T | C | 1 | a0001c0001t0002g0265 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.264-17154A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166087917 | ||||||
| chr1:166088128
|
C | T | 1 | a0001c0001t0004g0024 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.264-17365G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166088128 | ||||||
| chr1:166088137
|
G | T | 2 | a0001c0001t0001g0248a0001c0001t0002g0228 | 2 | HG01106.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.264-17374C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166088137 | ||||||
| chr1:166088261
|
C | T | 1 | a0001c0001t0002g0193 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.264-17498G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166088261 | ||||||
| chr1:166088327
|
T | C | 33 | a0001c0001t0001g0190a0001c0001t0001g0203a0001c0001t0001g0210others(30): Show | 33 | HG00140.hp1 HG00438.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.264-17564A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166088327 | ||||||
| chr1:166088633
|
C | T | 74 | a0001c0001t0001g0054a0001c0001t0001g0157a0001c0001t0001g0194others(71): Show | 74 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.264-17870G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166088633 | ||||||
| chr1:166088680
|
C | T | 1 | a0001c0001t0002g0250 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.264-17917G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166088680 | ||||||
| chr1:166088779
|
C | G | 17 | a0001c0001t0023g0298a0001c0002t0003g0086a0001c0002t0005g0299others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-18016G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166088779 | ||||||
| chr1:166088872
|
A | T | 1 | a0001c0002t0003g0230 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.264-18109T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166088872 | ||||||
| chr1:166089175
|
C | A | 1 | a0001c0001t0008g0005 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.264-18412G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166089175 | ||||||
| chr1:166089340
|
C | T | 4 | a0001c0001t0001g0076a0001c0001t0001g0142a0001c0002t0003g0095others(1): Show | 4 | HG01168.hp1 HG01169.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-18577G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166089340 | ||||||
| chr1:166089412
|
C | T | 1 | a0001c0001t0014g0031 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.264-18649G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166089412 | ||||||
| chr1:166089520
|
G | C | 3 | a0001c0002t0003g0198a0001c0002t0003g0199a0001c0002t0003g0209 | 3 | HG01081.hp2 HG01099.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.264-18757C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166089520 | ||||||
| chr1:166089615
|
AG | A | 17 | a0001c0001t0023g0298a0001c0002t0003g0086a0001c0002t0005g0299others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-18853delC | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166089615 | ||||||
| chr1:166089861
|
G | A | 4 | a0001c0002t0001g0046a0001c0002t0001g0047a0001c0002t0001g0048others(1): Show | 4 | HG02723.hp1 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-19098C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166089861 | ||||||
| chr1:166089917
|
G | A | 6 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(3): Show | 6 | HG02615.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.264-19154C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166089917 | ||||||
| chr1:166090275
|
G | A | 17 | a0001c0001t0023g0298a0001c0002t0003g0086a0001c0002t0005g0299others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-19512C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166090275 | ||||||
| chr1:166090288
|
A | AACAT | 17 | a0001c0001t0023g0298a0001c0002t0003g0086a0001c0002t0005g0299others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-19529_264-1952 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166090288 | ||||||
| chr1:166090569
|
CA | C | 12 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0191others(9): Show | 12 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.264-19807delT | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166090569 | ||||||
| chr1:166090788
|
C | A | 1 | a0001c0001t0001g0078 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.264-20025G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166090788 | ||||||
| chr1:166091256
|
G | C | 1 | a0001c0002t0003g0290 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.264-20493C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166091256 | ||||||
| chr1:166091312
|
T | A | 315 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(312): Show | 317 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.264-20549A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166091312 | ||||||
| chr1:166091317
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.264-20554A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166091317 | ||||||
| chr1:166091392
|
G | A | 309 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(306): Show | 311 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.264-20629C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166091392 | ||||||
| chr1:166091417
|
C | T | 315 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(312): Show | 317 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.264-20654G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166091417 | ||||||
| chr1:166091675
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.264-20912G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166091675 | ||||||
| chr1:166091717
|
G | A | 17 | a0001c0001t0023g0298a0001c0002t0003g0086a0001c0002t0005g0299others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-20954C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166091717 | ||||||
| chr1:166091841
|
A | G | 17 | a0001c0001t0023g0298a0001c0002t0003g0086a0001c0002t0005g0299others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-21078T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166091841 | ||||||
| chr1:166092032
|
A | ATTT | 65 | a0001c0001t0001g0054a0001c0001t0001g0157a0001c0001t0001g0194others(62): Show | 65 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.264-21272_264-2127 others(7): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166092032 | ||||||
| chr1:166092032
|
AT | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(205): Show | 210 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.264-21270delA | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166092032 | ||||||
| chr1:166092032
|
ATT | A | 23 | a0001c0001t0002g0038a0001c0001t0002g0193a0001c0001t0006g0148others(20): Show | 23 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.264-21271_264-2127 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166092032 | ||||||
| chr1:166092218
|
A | G | 4 | a0001c0001t0004g0007a0001c0001t0009g0036a0001c0001t0009g0296others(1): Show | 4 | HG01243.hp1 HG02451.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-21455T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166092218 | ||||||
| chr1:166092757
|
T | C | 2 | a0001c0001t0001g0129a0001c0001t0001g0154 | 2 | HG02071.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.264-21994A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166092757 | ||||||
| chr1:166092952
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.264-22189G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166092952 | ||||||
| chr1:166092963
|
C | T | 1 | a0001c0002t0001g0213 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.264-22200G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166092963 | ||||||
| chr1:166093025
|
A | G | 19 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0011others(16): Show | 19 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.264-22262T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166093025 | ||||||
| chr1:166093060
|
A | T | 308 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(305): Show | 310 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.264-22297T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166093060 | ||||||
| chr1:166093061
|
A | T | 1 | a0001c0002t0003g0284 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.264-22298T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166093061 | ||||||
| chr1:166093355
|
A | G | 2 | a0001c0001t0001g0143a0001c0001t0002g0101 | 2 | HG01175.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.264-22592T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166093355 | ||||||
| chr1:166093588
|
A | G | 4 | a0001c0001t0004g0007a0001c0001t0009g0036a0001c0001t0009g0296others(1): Show | 4 | HG01243.hp1 HG02451.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-22825T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166093588 | ||||||
| chr1:166093598
|
G | A | 13 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0191others(10): Show | 13 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.264-22835C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166093598 | ||||||
| chr1:166093750
|
CT | C | 12 | a0001c0001t0001g0070a0001c0001t0001g0077a0001c0001t0001g0078others(9): Show | 12 | HG01168.hp2 HG01257.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.264-22988delA | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166093750 | ||||||
| chr1:166093840
|
T | C | 1 | a0001c0002t0003g0122 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.264-23077A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166093840 | ||||||
| chr1:166094003
|
C | CTG | 26 | a0001c0001t0001g0190a0001c0001t0001g0192a0001c0001t0001g0210others(23): Show | 26 | HG00438.hp2 HG00673.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.264-23242_264-2324 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094003 | ||||||
| chr1:166094003
|
C | CTGTG | 14 | a0001c0001t0001g0203a0001c0001t0001g0211a0001c0001t0001g0212others(11): Show | 14 | HG00140.hp1 HG00741.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.264-23244_264-2324 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094003 | ||||||
| chr1:166094003
|
C | CTGTGTG | 14 | a0001c0001t0001g0176a0001c0001t0004g0009a0001c0001t0004g0012others(11): Show | 14 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.264-23246_264-2324 others(10): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094003 | ||||||
| chr1:166094003
|
C | CTGTGTGT others(3): Show |
5 | a0001c0001t0002g0236a0001c0001t0002g0237a0001c0001t0002g0257others(2): Show | 5 | HG02055.hp2 HG02083.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.264-23250_264-2324 others(14): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094003 | ||||||
| chr1:166094003
|
C | CTGTGTGT others(5): Show |
5 | a0001c0001t0001g0191a0001c0001t0001g0235a0001c0001t0002g0038others(2): Show | 5 | HG01255.hp2 HG02280.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.264-23252_264-2324 others(16): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094003 | ||||||
| chr1:166094003
|
C | CTGTGTGT others(7): Show |
6 | a0001c0001t0001g0188a0001c0001t0001g0194a0001c0001t0001g0245others(3): Show | 6 | HG00423.hp1 HG00673.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.264-23254_264-2324 others(18): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094003 | ||||||
| chr1:166094003
|
C | CTGTGTGT others(9): Show |
6 | a0001c0001t0001g0189a0001c0001t0001g0227a0001c0001t0002g0226others(3): Show | 6 | HG02257.hp1 HG03209.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.264-23256_264-2324 others(20): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094003 | ||||||
| chr1:166094003
|
C | CTGTGTGT others(11): Show |
10 | a0001c0001t0001g0224a0001c0001t0001g0231a0001c0001t0001g0252others(7): Show | 10 | HG01175.hp1 HG02015.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.264-23258_264-2324 others(22): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094003 | ||||||
| chr1:166094003
|
C | CTGTGTGT others(13): Show |
7 | a0001c0001t0001g0280a0001c0001t0002g0254a0001c0001t0002g0259others(4): Show | 7 | HG00609.hp1 HG02040.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.264-23260_264-2324 others(24): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094003 | ||||||
| chr1:166094003
|
C | CTGTGTGT others(15): Show |
13 | a0001c0001t0001g0054a0001c0001t0001g0222a0001c0001t0001g0243others(10): Show | 13 | HG00597.hp2 HG00621.hp2 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.264-23262_264-2324 others(26): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094003 | ||||||
| chr1:166094003
|
C | CTGTGTGT others(17): Show |
7 | a0001c0001t0001g0248a0001c0001t0002g0223a0001c0001t0002g0246others(4): Show | 7 | HG01106.hp1 HG02451.hp2 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.264-23264_264-2324 others(28): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094003 | ||||||
| chr1:166094003
|
C | CTGTGTGT others(19): Show |
10 | a0001c0001t0001g0157a0001c0001t0001g0268a0001c0001t0001g0269others(7): Show | 10 | HG00558.hp2 HG01071.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.264-23266_264-2324 others(30): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094003 | ||||||
| chr1:166094003
|
C | CTGTGTGT others(21): Show |
4 | a0001c0001t0001g0220a0001c0001t0002g0232a0001c0001t0002g0250others(1): Show | 4 | HG01069.hp1 HG01952.hp1 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-23268_264-2324 others(32): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094003 | ||||||
| chr1:166094003
|
C | CTGTGTGT others(23): Show |
4 | a0001c0001t0001g0234a0001c0001t0002g0216a0001c0001t0002g0218others(1): Show | 4 | HG01358.hp2 NA19083.hp1 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-23270_264-2324 others(34): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094003 | ||||||
| chr1:166094003
|
C | CTGTGTGT others(25): Show |
1 | a0001c0001t0008g0005 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.264-23272_264-2324 others(36): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094003 | ||||||
| chr1:166094003
|
C | CTGTGTGT others(27): Show |
1 | a0001c0001t0002g0221 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.264-23274_264-2324 others(38): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094003 | ||||||
| chr1:166094003
|
CTG | C | 25 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0123others(22): Show | 25 | HG00140.hp2 HG01070.hp2 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.264-23242_264-2324 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094003 | ||||||
| chr1:166094003
|
CTGTGTGT others(3): Show |
C | 1 | a0001c0002t0005g0305 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.264-23250_264-2324 others(14): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094003 | ||||||
| chr1:166094003
|
CTGTGTGT others(9): Show |
C | 4 | a0001c0002t0001g0046a0001c0002t0001g0047a0001c0002t0001g0048others(1): Show | 4 | HG02723.hp1 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-23256_264-2324 others(20): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094003 | ||||||
| chr1:166094035
|
G | C | 128 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0049others(125): Show | 130 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.264-23272C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094035 | ||||||
| chr1:166094035
|
G | GTC | 13 | a0001c0001t0001g0060a0001c0001t0001g0116a0001c0001t0001g0136others(10): Show | 13 | HG00323.hp2 HG00642.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.264-23273_264-2327 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094035 | ||||||
| chr1:166094047
|
G | GTGTGTGT others(10): Show |
1 | a0001c0001t0002g0275 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.264-23285_264-2328 others(21): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094047 | ||||||
| chr1:166094047
|
G | GTGTGTGT others(14): Show |
1 | a0001c0001t0002g0241 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.264-23285_264-2328 others(25): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094047 | ||||||
| chr1:166094047
|
G | GTGTGTGT others(18): Show |
1 | a0001c0001t0002g0215 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.264-23285_264-2328 others(29): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094047 | ||||||
| chr1:166094052
|
T | A | 1 | a0001c0002t0003g0185 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.264-23289A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094052 | ||||||
| chr1:166094397
|
C | T | 3 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0062 | 4 | HG00639.hp1 HG01261.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-23634G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094397 | ||||||
| chr1:166094417
|
T | C | 2 | a0001c0001t0001g0114a0001c0001t0016g0071 | 2 | NA18971.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.264-23654A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094417 | ||||||
| chr1:166094419
|
T | A | 1 | a0001c0001t0001g0091 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.264-23656A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094419 | ||||||
| chr1:166094606
|
G | T | 4 | a0001c0001t0004g0007a0001c0001t0009g0036a0001c0001t0009g0296others(1): Show | 4 | HG01243.hp1 HG02451.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-23843C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094606 | ||||||
| chr1:166094607
|
A | G | 21 | a0001c0001t0002g0038a0001c0001t0004g0008a0001c0001t0004g0009others(18): Show | 21 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.264-23844T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094607 | ||||||
| chr1:166094620
|
G | C | 1 | a0001c0002t0001g0046 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.264-23857C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094620 | ||||||
| chr1:166094750
|
C | G | 7 | a0001c0001t0001g0287a0001c0002t0003g0283a0001c0002t0003g0284others(4): Show | 7 | HG00438.hp2 NA18960.hp1 NA19003.hp1 others(4): Show |
intron_variant | MODIFIER | c.264-23987G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094750 | ||||||
| chr1:166094778
|
C | T | 4 | a0001c0002t0001g0046a0001c0002t0001g0047a0001c0002t0001g0048others(1): Show | 4 | HG02723.hp1 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-24015G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166094778 | ||||||
| chr1:166095016
|
G | C | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0011others(15): Show | 18 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.264-24253C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166095016 | ||||||
| chr1:166095199
|
C | T | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.264-24436G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166095199 | ||||||
| chr1:166095252
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.264-24489C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166095252 | ||||||
| chr1:166095765
|
G | A | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-25002C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166095765 | ||||||
| chr1:166095824
|
C | T | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-25061G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166095824 | ||||||
| chr1:166095830
|
G | A | 17 | a0001c0001t0023g0298a0001c0002t0003g0086a0001c0002t0005g0299others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-25067C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166095830 | ||||||
| chr1:166095908
|
C | A | 76 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(73): Show | 76 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.264-25145G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166095908 | ||||||
| chr1:166096116
|
A | G | 1 | a0001c0001t0001g0112 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.264-25353T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166096116 | ||||||
| chr1:166096164
|
C | T | 4 | a0001c0001t0001g0092a0001c0001t0001g0117a0001c0001t0001g0129others(1): Show | 4 | HG02071.hp2 NA18747.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-25401G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166096164 | ||||||
| chr1:166096201
|
T | A | 4 | a0001c0002t0001g0046a0001c0002t0001g0047a0001c0002t0001g0048others(1): Show | 4 | HG02723.hp1 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-25438A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166096201 | ||||||
| chr1:166096330
|
T | C | 3 | a0001c0001t0009g0036a0001c0001t0009g0296a0001c0001t0009g0297 | 3 | HG02451.hp1 HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.264-25567A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166096330 | ||||||
| chr1:166096448
|
C | T | 1 | a0001c0001t0004g0008 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.264-25685G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166096448 | ||||||
| chr1:166096493
|
T | TTTG | 17 | a0001c0001t0023g0298a0001c0002t0003g0086a0001c0002t0005g0299others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-25733_264-2573 others(7): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166096493 | ||||||
| chr1:166096529
|
A | G | 1 | a0001c0001t0002g0153 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.264-25766T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166096529 | ||||||
| chr1:166096589
|
A | G | 312 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(309): Show | 314 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.264-25826T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166096589 | ||||||
| chr1:166096677
|
G | T | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0011others(15): Show | 18 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.264-25914C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166096677 | ||||||
| chr1:166096685
|
C | G | 1 | a0001c0001t0001g0177 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.264-25922G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166096685 | ||||||
| chr1:166096852
|
G | A | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-26089C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166096852 | ||||||
| chr1:166096869
|
C | G | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-26106G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166096869 | ||||||
| chr1:166096871
|
G | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0049others(135): Show | 140 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.264-26108C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166096871 | ||||||
| chr1:166096929
|
G | A | 4 | a0001c0001t0004g0007a0001c0001t0009g0036a0001c0001t0009g0296others(1): Show | 4 | HG01243.hp1 HG02451.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-26166C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166096929 | ||||||
| chr1:166097138
|
C | T | 17 | a0001c0001t0023g0298a0001c0002t0003g0086a0001c0002t0005g0299others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-26375G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166097138 | ||||||
| chr1:166097258
|
T | C | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-26495A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166097258 | ||||||
| chr1:166097434
|
C | T | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-26671G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166097434 | ||||||
| chr1:166097444
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.264-26681C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166097444 | ||||||
| chr1:166097557
|
GACCA | G | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-26798_264-2679 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166097557 | ||||||
| chr1:166097579
|
C | T | 1 | a0001c0001t0002g0064 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.264-26816G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166097579 | ||||||
| chr1:166097580
|
G | A | 5 | a0001c0001t0001g0097a0001c0001t0001g0165a0001c0001t0001g0166others(2): Show | 5 | HG00423.hp2 NA18970.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.264-26817C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166097580 | ||||||
| chr1:166098001
|
C | T | 2 | a0001c0001t0001g0174a0001c0001t0002g0172 | 2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.264-27238G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166098001 | ||||||
| chr1:166098091
|
G | A | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-27328C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166098091 | ||||||
| chr1:166098255
|
T | G | 2 | a0001c0001t0004g0023a0001c0002t0011g0010 | 2 | HG02258.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.264-27492A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166098255 | ||||||
| chr1:166098338
|
C | T | 1 | a0001c0001t0002g0146 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.264-27575G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166098338 | ||||||
| chr1:166098341
|
C | T | 1 | a0001c0002t0001g0179 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.264-27578G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166098341 | ||||||
| chr1:166098383
|
G | A | 1 | a0001c0001t0001g0253 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.264-27620C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166098383 | ||||||
| chr1:166098569
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.264-27806A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166098569 | ||||||
| chr1:166098621
|
C | T | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-27858G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166098621 | ||||||
| chr1:166098769
|
C | T | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-28006G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166098769 | ||||||
| chr1:166098900
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.264-28137A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166098900 | ||||||
| chr1:166098915
|
G | A | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-28152C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166098915 | ||||||
| chr1:166098916
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.264-28153T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166098916 | ||||||
| chr1:166098959
|
T | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0049others(136): Show | 141 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.264-28196A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166098959 | ||||||
| chr1:166098986
|
C | T | 17 | a0001c0001t0023g0298a0001c0002t0003g0086a0001c0002t0005g0299others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-28223G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166098986 | ||||||
| chr1:166099054
|
G | A | 1 | a0001c0001t0018g0052 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.264-28291C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166099054 | ||||||
| chr1:166099079
|
G | T | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-28316C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166099079 | ||||||
| chr1:166099469
|
G | A | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-28706C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166099469 | ||||||
| chr1:166099476
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.264-28713G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166099476 | ||||||
| chr1:166099499
|
CAACT | C | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0044others(1): Show | 4 | HG02559.hp2 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-28740_264-2873 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166099499 | ||||||
| chr1:166099537
|
A | C | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-28774T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166099537 | ||||||
| chr1:166099597
|
G | A | 21 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0135others(18): Show | 22 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.264-28834C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166099597 | ||||||
| chr1:166099610
|
A | G | 1 | a0001c0001t0025g0316 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.264-28847T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166099610 | ||||||
| chr1:166099645
|
A | T | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-28882T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166099645 | ||||||
| chr1:166099650
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.264-28887A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166099650 | ||||||
| chr1:166099668
|
AACAG | A | 17 | a0001c0001t0023g0298a0001c0002t0003g0086a0001c0002t0005g0299others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-28909_264-2890 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166099668 | ||||||
| chr1:166099787
|
T | C | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-29024A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166099787 | ||||||
| chr1:166099860
|
C | T | 4 | a0001c0002t0001g0046a0001c0002t0001g0047a0001c0002t0001g0048others(1): Show | 4 | HG02723.hp1 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-29097G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166099860 | ||||||
| chr1:166100156
|
T | A | 1 | a0001c0001t0001g0177 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.264-29393A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166100156 | ||||||
| chr1:166100262
|
G | T | 312 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(309): Show | 314 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.264-29499C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166100262 | ||||||
| chr1:166100309
|
C | T | 94 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(91): Show | 94 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.264-29546G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166100309 | ||||||
| chr1:166100405
|
C | G | 1 | a0001c0001t0001g0129 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.264-29642G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166100405 | ||||||
| chr1:166100413
|
T | C | 76 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(73): Show | 76 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.264-29650A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166100413 | ||||||
| chr1:166100443
|
C | A | 3 | a0001c0001t0001g0220a0001c0001t0001g0222a0001c0001t0001g0234 | 3 | NA18987.hp1 NA18991.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.264-29680G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166100443 | ||||||
| chr1:166100522
|
C | T | 1 | a0001c0002t0001g0046 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.264-29759G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166100522 | ||||||
| chr1:166100524
|
G | A | 312 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(309): Show | 314 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.264-29761C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166100524 | ||||||
| chr1:166100547
|
C | A | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-29784G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166100547 | ||||||
| chr1:166100552
|
G | T | 3 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0062 | 4 | HG00639.hp1 HG01261.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-29789C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166100552 | ||||||
| chr1:166100674
|
C | A | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-29911G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166100674 | ||||||
| chr1:166100718
|
C | A | 1 | a0001c0002t0001g0056 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.264-29955G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166100718 | ||||||
| chr1:166100719
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.264-29956G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166100719 | ||||||
| chr1:166101036
|
A | G | 6 | a0001c0001t0001g0115a0001c0002t0003g0087a0001c0002t0003g0089others(3): Show | 6 | HG00438.hp1 NA18952.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.264-30273T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166101036 | ||||||
| chr1:166101059
|
G | A | 3 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0055 | 3 | HG02723.hp1 HG02970.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.264-30296C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166101059 | ||||||
| chr1:166101133
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.264-30370G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166101133 | ||||||
| chr1:166101282
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.264-30519G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166101282 | ||||||
| chr1:166101462
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.264-30699T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166101462 | ||||||
| chr1:166101502
|
G | C | 3 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006 | 3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-30739C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166101502 | ||||||
| chr1:166101527
|
A | C | 4 | a0001c0002t0001g0046a0001c0002t0001g0047a0001c0002t0001g0048others(1): Show | 4 | HG02723.hp1 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-30764T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166101527 | ||||||
| chr1:166101642
|
A | T | 1 | a0001c0001t0002g0225 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.264-30879T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166101642 | ||||||
| chr1:166101731
|
G | C | 1 | a0001c0001t0001g0174 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.264-30968C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166101731 | ||||||
| chr1:166101796
|
TC | T | 6 | a0001c0002t0003g0083a0001c0002t0003g0084a0001c0002t0003g0085others(3): Show | 6 | HG00642.hp2 HG00741.hp2 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.264-31034delG | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166101796 | ||||||
| chr1:166101877
|
C | T | 4 | a0001c0002t0001g0046a0001c0002t0001g0047a0001c0002t0001g0048others(1): Show | 4 | HG02723.hp1 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-31114G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166101877 | ||||||
| chr1:166101880
|
G | T | 1 | a0001c0001t0012g0003 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.264-31117C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166101880 | ||||||
| chr1:166101906
|
G | A | 17 | a0001c0001t0023g0298a0001c0002t0003g0086a0001c0002t0005g0299others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-31143C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166101906 | ||||||
| chr1:166101931
|
A | C | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.264-31168T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166101931 | ||||||
| chr1:166101993
|
A | G | 1 | a0001c0002t0003g0175 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.264-31230T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166101993 | ||||||
| chr1:166102013
|
G | A | 4 | a0001c0002t0001g0046a0001c0002t0001g0047a0001c0002t0001g0048others(1): Show | 4 | HG02723.hp1 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-31250C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102013 | ||||||
| chr1:166102032
|
A | G | 4 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(1): Show | 4 | NA18970.hp2 NA18977.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-31269T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102032 | ||||||
| chr1:166102237
|
A | C | 315 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(312): Show | 317 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.264-31474T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102237 | ||||||
| chr1:166102273
|
G | A | 2 | a0001c0001t0002g0236a0001c0001t0002g0257 | 2 | HG03492.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.264-31510C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102273 | ||||||
| chr1:166102335
|
C | A | 1 | a0001c0001t0002g0193 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.264-31572G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102335 | ||||||
| chr1:166102366
|
G | A | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-31603C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102366 | ||||||
| chr1:166102366
|
G | T | 1 | a0001c0001t0008g0004 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.264-31603C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102366 | ||||||
| chr1:166102374
|
A | T | 1 | a0001c0001t0008g0004 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.264-31611T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102374 | ||||||
| chr1:166102375
|
A | G | 1 | a0001c0001t0008g0004 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.264-31612T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102375 | ||||||
| chr1:166102393
|
A | G | 1 | a0001c0001t0008g0004 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.264-31630T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102393 | ||||||
| chr1:166102422
|
A | T | 1 | a0001c0001t0008g0004 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.264-31659T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102422 | ||||||
| chr1:166102432
|
G | A | 1 | a0001c0001t0008g0004 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.264-31669C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102432 | ||||||
| chr1:166102463
|
G | A | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-31700C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102463 | ||||||
| chr1:166102463
|
G | T | 1 | a0001c0001t0008g0004 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.264-31700C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102463 | ||||||
| chr1:166102469
|
T | C | 1 | a0001c0001t0008g0004 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.264-31706A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102469 | ||||||
| chr1:166102470
|
C | A | 1 | a0001c0001t0008g0004 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.264-31707G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102470 | ||||||
| chr1:166102473
|
T | C | 1 | a0001c0001t0008g0004 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.264-31710A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102473 | ||||||
| chr1:166102481
|
A | C | 1 | a0001c0001t0008g0004 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.264-31718T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102481 | ||||||
| chr1:166102493
|
A | C | 1 | a0001c0001t0001g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.264-31730T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102493 | ||||||
| chr1:166102663
|
C | A | 76 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(73): Show | 76 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.264-31900G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102663 | ||||||
| chr1:166102673
|
A | G | 1 | a0001c0001t0009g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.264-31910T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102673 | ||||||
| chr1:166102756
|
A | T | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-31993T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102756 | ||||||
| chr1:166102757
|
C | T | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-31994G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102757 | ||||||
| chr1:166102799
|
T | C | 17 | a0001c0001t0023g0298a0001c0002t0003g0086a0001c0002t0005g0299others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-32036A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102799 | ||||||
| chr1:166102823
|
T | C | 5 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0191others(2): Show | 5 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.264-32060A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102823 | ||||||
| chr1:166102852
|
G | A | 5 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0191others(2): Show | 5 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.264-32089C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102852 | ||||||
| chr1:166102853
|
C | T | 5 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0191others(2): Show | 5 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.264-32090G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102853 | ||||||
| chr1:166102854
|
A | G | 5 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0191others(2): Show | 5 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.264-32091T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102854 | ||||||
| chr1:166102918
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.264-32155G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166102918 | ||||||
| chr1:166103118
|
G | A | 2 | a0001c0001t0023g0298a0001c0002t0005g0306 | 2 | HG00544.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.264-32355C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166103118 | ||||||
| chr1:166103153
|
C | A | 1 | a0001c0002t0003g0175 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.264-32390G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166103153 | ||||||
| chr1:166103171
|
A | G | 3 | a0001c0001t0001g0174a0001c0001t0002g0172a0001c0002t0022g0099 | 3 | HG02280.hp1 HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.264-32408T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166103171 | ||||||
| chr1:166103256
|
G | T | 2 | a0001c0001t0007g0032a0001c0001t0014g0031 | 2 | HG02723.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.264-32493C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166103256 | ||||||
| chr1:166103350
|
G | A | 3 | a0001c0001t0001g0174a0001c0001t0002g0172a0001c0002t0022g0099 | 3 | HG02280.hp1 HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.264-32587C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166103350 | ||||||
| chr1:166103450
|
C | T | 3 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006 | 3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-32687G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166103450 | ||||||
| chr1:166103481
|
G | A | 4 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(1): Show | 4 | HG00735.hp1 HG01192.hp2 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-32718C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166103481 | ||||||
| chr1:166103656
|
G | A | 2 | a0001c0001t0001g0176a0001c0002t0001g0213 | 2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.264-32893C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166103656 | ||||||
| chr1:166103679
|
G | A | 312 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(309): Show | 314 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.264-32916C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166103679 | ||||||
| chr1:166103719
|
C | T | 68 | a0001c0001t0001g0054a0001c0001t0001g0157a0001c0001t0001g0194others(65): Show | 68 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.264-32956G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166103719 | ||||||
| chr1:166103745
|
T | C | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-32982A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166103745 | ||||||
| chr1:166103772
|
C | A | 1 | a0001c0001t0001g0116 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.264-33009G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166103772 | ||||||
| chr1:166103772
|
C | G | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-33009G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166103772 | ||||||
| chr1:166103789
|
T | C | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-33026A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166103789 | ||||||
| chr1:166103922
|
A | G | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-33159T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166103922 | ||||||
| chr1:166103970
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.264-33207G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166103970 | ||||||
| chr1:166103972
|
G | A | 1 | a0001c0001t0001g0058 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.264-33209C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166103972 | ||||||
| chr1:166103989
|
C | G | 3 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006 | 3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-33226G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166103989 | ||||||
| chr1:166104127
|
G | C | 1 | a0001c0001t0002g0237 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.264-33364C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166104127 | ||||||
| chr1:166104137
|
T | C | 1 | a0001c0002t0003g0090 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.264-33374A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166104137 | ||||||
| chr1:166104287
|
C | T | 8 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(5): Show | 8 | HG02559.hp2 HG02615.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.264-33524G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166104287 | ||||||
| chr1:166104288
|
T | G | 8 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(5): Show | 8 | HG02559.hp2 HG02615.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.264-33525A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166104288 | ||||||
| chr1:166104319
|
G | C | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-33556C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166104319 | ||||||
| chr1:166104322
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.264-33559G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166104322 | ||||||
| chr1:166104379
|
T | A | 96 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(93): Show | 96 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.264-33616A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166104379 | ||||||
| chr1:166104498
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.264-33735A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166104498 | ||||||
| chr1:166104575
|
GC | G | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-33813delG | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166104575 | ||||||
| chr1:166104657
|
G | T | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-33894C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166104657 | ||||||
| chr1:166104673
|
C | A | 13 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(10): Show | 13 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.264-33910G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166104673 | ||||||
| chr1:166104733
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.264-33970A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166104733 | ||||||
| chr1:166104735
|
C | T | 10 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0135others(7): Show | 11 | HG00639.hp2 HG00738.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.264-33972G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166104735 | ||||||
| chr1:166104792
|
T | C | 3 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0055 | 3 | HG02723.hp1 HG02970.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.264-34029A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166104792 | ||||||
| chr1:166104897
|
G | A | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-34134C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166104897 | ||||||
| chr1:166104910
|
A | C | 3 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006 | 3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-34147T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166104910 | ||||||
| chr1:166105086
|
C | G | 5 | a0001c0001t0001g0203a0001c0001t0004g0007a0001c0001t0009g0036others(2): Show | 5 | HG01243.hp1 HG02451.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.264-34323G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166105086 | ||||||
| chr1:166105096
|
C | A | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-34333G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166105096 | ||||||
| chr1:166105101
|
G | A | 13 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(10): Show | 13 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.264-34338C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166105101 | ||||||
| chr1:166105111
|
T | C | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-34348A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166105111 | ||||||
| chr1:166105282
|
C | G | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-34519G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166105282 | ||||||
| chr1:166105400
|
C | T | 68 | a0001c0001t0001g0054a0001c0001t0001g0157a0001c0001t0001g0194others(65): Show | 68 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.264-34637G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166105400 | ||||||
| chr1:166105405
|
A | G | 17 | a0001c0001t0023g0298a0001c0002t0003g0086a0001c0002t0005g0299others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-34642T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166105405 | ||||||
| chr1:166105486
|
A | G | 17 | a0001c0001t0023g0298a0001c0002t0003g0086a0001c0002t0005g0299others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-34723T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166105486 | ||||||
| chr1:166105499
|
A | C | 17 | a0001c0001t0023g0298a0001c0002t0003g0086a0001c0002t0005g0299others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-34736T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166105499 | ||||||
| chr1:166105541
|
C | T | 20 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0011others(17): Show | 20 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.264-34778G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166105541 | ||||||
| chr1:166105682
|
T | C | 7 | a0001c0001t0002g0240a0001c0001t0002g0241a0001c0001t0002g0242others(4): Show | 7 | HG00642.hp1 HG01257.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.264-34919A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166105682 | ||||||
| chr1:166105751
|
G | C | 1 | a0001c0002t0022g0099 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.264-34988C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166105751 | ||||||
| chr1:166105906
|
C | T | 96 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(93): Show | 96 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.264-35143G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166105906 | ||||||
| chr1:166105986
|
C | G | 3 | a0001c0001t0001g0117a0001c0001t0001g0168a0001c0001t0001g0169 | 3 | HG02922.hp2 HG03195.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.264-35223G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166105986 | ||||||
| chr1:166106054
|
T | A | 1 | a0001c0001t0001g0070 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.264-35291A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166106054 | ||||||
| chr1:166106101
|
C | G | 4 | a0001c0001t0001g0091a0001c0001t0001g0113a0001c0001t0001g0116others(1): Show | 4 | HG02155.hp2 HG02165.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-35338G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166106101 | ||||||
| chr1:166106123
|
G | A | 2 | a0001c0001t0001g0248a0001c0001t0002g0228 | 2 | HG01106.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.264-35360C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166106123 | ||||||
| chr1:166106148
|
T | C | 3 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006 | 3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-35385A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166106148 | ||||||
| chr1:166106155
|
G | A | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-35392C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166106155 | ||||||
| chr1:166106194
|
C | T | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-35431G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166106194 | ||||||
| chr1:166106203
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.264-35440A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166106203 | ||||||
| chr1:166106349
|
T | TA | 75 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(72): Show | 75 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.264-35587dupT | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166106349 | ||||||
| chr1:166106409
|
A | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0049others(137): Show | 142 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.264-35646T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166106409 | ||||||
| chr1:166106446
|
A | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0049others(136): Show | 141 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.264-35683T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166106446 | ||||||
| chr1:166106514
|
T | C | 3 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006 | 3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-35751A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166106514 | ||||||
| chr1:166106549
|
A | G | 3 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0055 | 3 | HG02723.hp1 HG02970.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.264-35786T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166106549 | ||||||
| chr1:166106646
|
C | T | 1 | a0001c0002t0001g0046 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.264-35883G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166106646 | ||||||
| chr1:166106806
|
T | C | 1 | a0001c0001t0001g0150 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.264-36043A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166106806 | ||||||
| chr1:166106843
|
G | C | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-36080C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166106843 | ||||||
| chr1:166106858
|
A | T | 1 | a0001c0001t0002g0038 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.264-36095T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166106858 | ||||||
| chr1:166107162
|
G | T | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-36399C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166107162 | ||||||
| chr1:166107330
|
C | T | 11 | a0001c0001t0001g0235a0001c0001t0002g0229a0001c0001t0002g0240others(8): Show | 11 | HG00642.hp1 HG01257.hp2 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.264-36567G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166107330 | ||||||
| chr1:166107341
|
T | C | 1 | a0001c0001t0006g0180 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.264-36578A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166107341 | ||||||
| chr1:166107356
|
A | G | 13 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(10): Show | 13 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.264-36593T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166107356 | ||||||
| chr1:166107595
|
G | C | 1 | a0001c0001t0002g0193 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.264-36832C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166107595 | ||||||
| chr1:166107631
|
A | T | 17 | a0001c0001t0023g0298a0001c0002t0003g0086a0001c0002t0005g0299others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-36868T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166107631 | ||||||
| chr1:166107653
|
T | C | 1 | a0001c0002t0005g0313 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.264-36890A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166107653 | ||||||
| chr1:166107682
|
A | G | 17 | a0001c0001t0001g0049a0001c0001t0001g0096a0001c0001t0001g0102others(14): Show | 17 | HG00323.hp2 HG00558.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-36919T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166107682 | ||||||
| chr1:166108015
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.264-37252G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166108015 | ||||||
| chr1:166108316
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.264-37553C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166108316 | ||||||
| chr1:166108334
|
C | G | 4 | a0001c0001t0004g0007a0001c0001t0009g0036a0001c0001t0009g0296others(1): Show | 4 | HG01243.hp1 HG02451.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-37571G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166108334 | ||||||
| chr1:166108351
|
T | C | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-37588A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166108351 | ||||||
| chr1:166108360
|
A | G | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-37597T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166108360 | ||||||
| chr1:166108383
|
C | G | 2 | a0001c0001t0001g0243a0001c0001t0001g0244 | 2 | HG00597.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.264-37620G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166108383 | ||||||
| chr1:166108674
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.264-37911G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166108674 | ||||||
| chr1:166109044
|
A | G | 8 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(5): Show | 8 | HG02559.hp2 HG02615.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.264-38281T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109044 | ||||||
| chr1:166109176
|
A | G | 3 | a0001c0001t0004g0008a0001c0001t0004g0024a0001c0001t0004g0025 | 3 | HG02451.hp2 HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.264-38413T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109176 | ||||||
| chr1:166109482
|
T | C | 1 | a0001c0002t0003g0089 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.264-38719A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109482 | ||||||
| chr1:166109516
|
G | A | 2 | a0001c0001t0001g0098a0001c0001t0001g0138 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.264-38753C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109516 | ||||||
| chr1:166109566
|
G | A | 68 | a0001c0001t0001g0054a0001c0001t0001g0157a0001c0001t0001g0194others(65): Show | 68 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.264-38803C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109566 | ||||||
| chr1:166109655
|
A | G | 1 | a0001c0001t0002g0162 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.264-38892T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109655 | ||||||
| chr1:166109806
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.264-39043C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109806 | ||||||
| chr1:166109806
|
GTATATAT others(83): Show |
G | 17 | a0001c0001t0023g0298a0001c0002t0003g0086a0001c0002t0005g0299others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-39133_264-3904 others(94): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109806 | ||||||
| chr1:166109812
|
A | ATG | 3 | a0001c0001t0001g0190a0001c0001t0002g0162a0001c0001t0004g0020 | 3 | HG03453.hp2 HG04204.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.264-39051_264-3905 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109812 | ||||||
| chr1:166109814
|
G | GTA | 13 | a0001c0001t0001g0077a0001c0001t0001g0109a0001c0001t0001g0139others(10): Show | 13 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.264-39053_264-3905 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109814 | ||||||
| chr1:166109814
|
G | GTATA | 5 | a0001c0001t0001g0110a0001c0001t0021g0200a0001c0002t0003g0208others(2): Show | 5 | HG00738.hp1 HG02647.hp2 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.264-39055_264-3905 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109814 | ||||||
| chr1:166109814
|
GTATATAT others(29): Show |
G | 3 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0055 | 3 | HG02723.hp1 HG02970.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.264-39087_264-3905 others(40): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109814 | ||||||
| chr1:166109814
|
GTATATAT others(51): Show |
G | 3 | a0001c0001t0001g0039a0001c0001t0002g0236a0001c0001t0002g0257 | 3 | HG03492.hp1 HG03540.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.264-39109_264-3905 others(62): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109814 | ||||||
| chr1:166109814
|
GTATATAT others(81): Show |
G | 2 | a0001c0001t0002g0229a0001c0002t0003g0239 | 2 | HG02735.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.264-39139_264-3905 others(92): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109814 | ||||||
| chr1:166109816
|
A | G | 30 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0191others(27): Show | 30 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.264-39053T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109816 | ||||||
| chr1:166109816
|
ATATATAT others(59): Show |
A | 1 | a0001c0001t0002g0258 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.264-39119_264-3905 others(70): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109816 | ||||||
| chr1:166109818
|
A | G | 1 | a0001c0001t0009g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.264-39055T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109818 | ||||||
| chr1:166109818
|
ATATATAT others(43): Show |
A | 1 | a0001c0001t0001g0217 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.264-39105_264-3905 others(54): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109818 | ||||||
| chr1:166109820
|
ATATATAT others(35): Show |
A | 1 | a0001c0001t0001g0227 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.264-39099_264-3905 others(46): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109820 | ||||||
| chr1:166109822
|
ATATATAT others(11): Show |
A | 1 | a0001c0002t0001g0046 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.264-39077_264-3906 others(22): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109822 | ||||||
| chr1:166109822
|
ATATATAT others(37): Show |
A | 6 | a0001c0001t0001g0252a0001c0001t0001g0268a0001c0001t0002g0242others(3): Show | 6 | HG00609.hp1 HG01069.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.264-39103_264-3906 others(48): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109822 | ||||||
| chr1:166109824
|
A | ATATATAT others(105): Show |
1 | a0001c0001t0001g0070 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.264-39062_264-3906 others(116): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109824 | ||||||
| chr1:166109824
|
A | G | 62 | a0001c0001t0001g0037a0001c0001t0001g0040a0001c0001t0001g0041others(59): Show | 62 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.264-39061T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109824 | ||||||
| chr1:166109826
|
ATATATGT others(49): Show |
A | 2 | a0001c0001t0001g0037a0001c0001t0002g0038 | 2 | HG02976.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.264-39119_264-3906 others(60): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109826 | ||||||
| chr1:166109828
|
ATATG | A | 4 | a0001c0001t0001g0073a0001c0001t0001g0142a0001c0001t0007g0026others(1): Show | 4 | HG02622.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-39069_264-3906 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109828 | ||||||
| chr1:166109828
|
ATATGTAT others(5): Show |
A | 3 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006 | 3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-39077_264-3906 others(16): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109828 | ||||||
| chr1:166109828
|
ATATGTAT others(33): Show |
A | 5 | a0001c0001t0001g0235a0001c0001t0001g0248a0001c0001t0001g0269others(2): Show | 5 | HG01106.hp1 HG01255.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.264-39105_264-3906 others(44): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109828 | ||||||
| chr1:166109828
|
ATATGTAT others(47): Show |
A | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0044others(1): Show | 4 | HG02559.hp2 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-39119_264-3906 others(58): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109828 | ||||||
| chr1:166109830
|
ATG | A | 5 | a0001c0001t0001g0112a0001c0001t0002g0080a0001c0001t0006g0103others(2): Show | 5 | HG00140.hp2 HG00738.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.264-39069_264-3906 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109830 | ||||||
| chr1:166109830
|
ATGTATAT others(31): Show |
A | 13 | a0001c0001t0001g0194a0001c0001t0001g0224a0001c0001t0001g0277others(10): Show | 13 | HG00673.hp2 HG01257.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.264-39105_264-3906 others(42): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109830 | ||||||
| chr1:166109830
|
ATGTATAT others(53): Show |
A | 3 | a0001c0001t0001g0040a0001c0001t0001g0243a0001c0001t0001g0244 | 3 | HG00597.hp2 HG02615.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.264-39127_264-3906 others(64): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109830 | ||||||
| chr1:166109831
|
T | C | 35 | a0001c0001t0001g0054a0001c0001t0001g0157a0001c0001t0001g0220others(32): Show | 35 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.264-39068A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109831 | ||||||
| chr1:166109832
|
G | A | 237 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0049others(234): Show | 239 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(236): Show |
intron_variant | MODIFIER | c.264-39069C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109832 | ||||||
| chr1:166109837
|
T | C | 1 | a0001c0001t0001g0156 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.264-39074A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109837 | ||||||
| chr1:166109838
|
A | ATATG | 13 | a0001c0001t0001g0210a0001c0001t0001g0286a0001c0001t0001g0287others(10): Show | 13 | HG00140.hp1 HG00673.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.264-39076_264-3907 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109838 | ||||||
| chr1:166109840
|
G | A | 233 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0049others(230): Show | 235 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.264-39077C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109840 | ||||||
| chr1:166109841
|
T | C | 3 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006 | 3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-39078A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109841 | ||||||
| chr1:166109842
|
A | G | 2 | a0001c0001t0001g0212a0001c0001t0004g0020 | 2 | HG02074.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.264-39079T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109842 | ||||||
| chr1:166109843
|
T | C | 4 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006others(1): Show | 4 | HG01433.hp2 HG03579.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-39080A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109843 | ||||||
| chr1:166109844
|
A | G | 2 | a0001c0001t0001g0163a0001c0002t0001g0056 | 2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.264-39081T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109844 | ||||||
| chr1:166109846
|
A | ATGTATG | 4 | a0001c0001t0004g0008a0001c0001t0004g0019a0001c0001t0004g0024others(1): Show | 4 | HG02451.hp2 HG03139.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-39084_264-3908 others(10): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109846 | ||||||
| chr1:166109846
|
A | G | 16 | a0001c0001t0004g0009a0001c0001t0004g0011a0001c0001t0004g0012others(13): Show | 16 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.264-39083T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109846 | ||||||
| chr1:166109848
|
A | G | 3 | a0001c0001t0001g0163a0001c0001t0001g0182a0001c0002t0001g0056 | 3 | HG03209.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.264-39085T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109848 | ||||||
| chr1:166109850
|
A | G | 27 | a0001c0001t0001g0123a0001c0001t0001g0163a0001c0001t0001g0188others(24): Show | 27 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.264-39087T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109850 | ||||||
| chr1:166109852
|
A | ATGTG | 18 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0004g0009others(15): Show | 18 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.264-39090_264-3908 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109852 | ||||||
| chr1:166109852
|
A | G | 11 | a0001c0001t0001g0072a0001c0001t0001g0182a0001c0001t0001g0191others(8): Show | 11 | HG01167.hp2 HG02145.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.264-39089T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109852 | ||||||
| chr1:166109854
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0117 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.264-39092_264-3909 others(28): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109854 | ||||||
| chr1:166109854
|
A | ATATATAT others(5): Show |
2 | a0001c0001t0001g0129a0001c0001t0001g0154 | 2 | HG02071.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.264-39092_264-3909 others(16): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109854 | ||||||
| chr1:166109854
|
A | ATATATAT others(39): Show |
1 | a0001c0001t0001g0091 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.264-39092_264-3909 others(50): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109854 | ||||||
| chr1:166109854
|
A | ATG | 10 | a0001c0001t0001g0059a0001c0001t0001g0075a0001c0001t0001g0076others(7): Show | 10 | HG00609.hp2 HG00741.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.264-39092_264-3909 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109854 | ||||||
| chr1:166109854
|
A | ATGTATG | 5 | a0001c0001t0001g0111a0001c0001t0001g0159a0001c0001t0002g0146others(2): Show | 5 | HG01358.hp1 HG02572.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.264-39092_264-3909 others(10): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109854 | ||||||
| chr1:166109854
|
A | G | 16 | a0001c0001t0001g0062a0001c0001t0001g0065a0001c0001t0001g0072others(13): Show | 16 | HG00544.hp2 HG01074.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.264-39091T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109854 | ||||||
| chr1:166109854
|
ATATATAT others(21): Show |
A | 5 | a0001c0001t0001g0222a0001c0001t0001g0271a0001c0001t0001g0276others(2): Show | 5 | NA18941.hp2 NA18954.hp2 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.264-39119_264-3909 others(32): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109854 | ||||||
| chr1:166109854
|
ATATATAT others(29): Show |
A | 10 | a0001c0001t0001g0220a0001c0001t0001g0231a0001c0001t0001g0234others(7): Show | 10 | HG00621.hp2 HG01952.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.264-39127_264-3909 others(40): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109854 | ||||||
| chr1:166109856
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0130 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.264-39094_264-3909 others(18): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109856 | ||||||
| chr1:166109856
|
A | ATATATAT others(3): Show |
7 | a0001c0001t0001g0097a0001c0001t0001g0131a0001c0001t0001g0165others(4): Show | 7 | HG00423.hp2 HG02155.hp2 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.264-39094_264-3909 others(14): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109856 | ||||||
| chr1:166109856
|
A | ATATGTAT others(3): Show |
9 | a0001c0001t0001g0096a0001c0001t0001g0143a0001c0001t0002g0173others(6): Show | 9 | HG00558.hp1 HG00735.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.264-39094_264-3909 others(14): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109856 | ||||||
| chr1:166109856
|
A | ATATGTG | 20 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0116others(17): Show | 20 | HG00597.hp1 HG00621.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.264-39094_264-3909 others(10): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109856 | ||||||
| chr1:166109856
|
A | ATGTATGT others(1): Show |
10 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0001g0098others(7): Show | 10 | HG00735.hp1 HG02258.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.264-39094_264-3909 others(12): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109856 | ||||||
| chr1:166109856
|
A | ATGTG | 17 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0057others(14): Show | 18 | HG00639.hp1 HG00642.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.264-39094_264-3909 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109856 | ||||||
| chr1:166109856
|
A | G | 29 | a0001c0001t0001g0059a0001c0001t0001g0062a0001c0001t0001g0065others(26): Show | 29 | HG00544.hp2 HG00609.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.264-39093T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109856 | ||||||
| chr1:166109856
|
ATATATGT others(19): Show |
A | 4 | a0001c0001t0001g0054a0001c0001t0001g0273a0001c0001t0002g0241others(1): Show | 4 | HG00423.hp1 HG00642.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-39119_264-3909 others(30): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109856 | ||||||
| chr1:166109856
|
ATATATGT others(27): Show |
A | 8 | a0001c0001t0001g0253a0001c0001t0002g0219a0001c0001t0002g0226others(5): Show | 8 | HG01175.hp1 HG02055.hp2 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.264-39127_264-3909 others(38): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109856 | ||||||
| chr1:166109858
|
A | G | 4 | a0001c0001t0001g0070a0001c0001t0001g0079a0001c0001t0004g0007others(1): Show | 4 | HG01070.hp2 HG01243.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-39095T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109858 | ||||||
| chr1:166109858
|
ATATGTAT others(25): Show |
A | 3 | a0001c0001t0001g0157a0001c0002t0003g0133a0001c0002t0003g0261 | 3 | HG00558.hp2 NA18949.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.264-39127_264-3909 others(36): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109858 | ||||||
| chr1:166109860
|
A | G | 4 | a0001c0001t0001g0174a0001c0001t0001g0176a0001c0001t0002g0172others(1): Show | 4 | HG01243.hp1 HG02280.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-39097T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109860 | ||||||
| chr1:166109860
|
ATGTATGT others(15): Show |
A | 1 | a0001c0001t0002g0221 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.264-39119_264-3909 others(26): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109860 | ||||||
| chr1:166109860
|
ATGTATGT others(23): Show |
A | 4 | a0001c0001t0002g0214a0001c0001t0002g0215a0001c0001t0002g0240others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-39127_264-3909 others(34): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109860 | ||||||
| chr1:166109862
|
G | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0049others(133): Show | 137 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.264-39099C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109862 | ||||||
| chr1:166109862
|
G | GTGTATAT others(1): Show |
4 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0156others(1): Show | 4 | HG01433.hp2 NA18971.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-39100_264-3909 others(12): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109862 | ||||||
| chr1:166109864
|
A | G | 2 | a0001c0001t0001g0073a0001c0001t0001g0079 | 2 | HG01346.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.264-39101T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109864 | ||||||
| chr1:166109866
|
G | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0049others(104): Show | 108 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.264-39103C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109866 | ||||||
| chr1:166109866
|
G | GTGTATAT others(5): Show |
12 | a0001c0001t0001g0108a0001c0001t0001g0251a0001c0001t0002g0101others(9): Show | 12 | HG00323.hp1 HG00438.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.264-39115_264-3910 others(16): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109866 | ||||||
| chr1:166109868
|
G | A | 35 | a0001c0001t0001g0061a0001c0001t0001g0070a0001c0001t0001g0073others(32): Show | 35 | HG01192.hp2 HG01243.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.264-39105C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109868 | ||||||
| chr1:166109869
|
T | C | 13 | a0001c0001t0001g0194a0001c0001t0001g0224a0001c0001t0001g0277others(10): Show | 13 | HG00673.hp2 HG01257.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.264-39106A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109869 | ||||||
| chr1:166109870
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0104 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.264-39108_264-3910 others(14): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109870 | ||||||
| chr1:166109870
|
A | G | 3 | a0001c0001t0001g0116a0001c0001t0001g0125a0001c0001t0001g0167 | 3 | HG02165.hp1 NA18942.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.264-39107T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109870 | ||||||
| chr1:166109871
|
T | C | 5 | a0001c0001t0001g0235a0001c0001t0001g0248a0001c0001t0001g0269others(2): Show | 5 | HG01106.hp1 HG01255.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.264-39108A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109871 | ||||||
| chr1:166109873
|
T | C | 1 | a0001c0001t0001g0227 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.264-39110A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109873 | ||||||
| chr1:166109874
|
A | ATATATGT others(13): Show |
3 | a0001c0001t0003g0195a0001c0001t0006g0103a0001c0001t0006g0144 | 3 | HG00140.hp2 HG02145.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.264-39112_264-3911 others(24): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109874 | ||||||
| chr1:166109874
|
A | G | 2 | a0001c0001t0001g0217a0001c0001t0004g0007 | 2 | HG01243.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.264-39111T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109874 | ||||||
| chr1:166109875
|
T | C | 6 | a0001c0001t0001g0252a0001c0001t0001g0268a0001c0001t0002g0242others(3): Show | 6 | HG00609.hp1 HG01069.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.264-39112A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109875 | ||||||
| chr1:166109876
|
A | ATATG | 14 | a0001c0001t0001g0050a0001c0001t0001g0077a0001c0001t0001g0078others(11): Show | 15 | HG00639.hp2 HG00738.hp2 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.264-39114_264-3911 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109876 | ||||||
| chr1:166109876
|
A | G | 3 | a0001c0001t0001g0073a0001c0001t0001g0079a0001c0001t0004g0007 | 3 | HG01243.hp1 HG01346.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.264-39113T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109876 | ||||||
| chr1:166109878
|
A | ATGTATAT others(17): Show |
2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG00323.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.264-39116_264-3911 others(28): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109878 | ||||||
| chr1:166109878
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.264-39115T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109878 | ||||||
| chr1:166109880
|
ATG | A | 6 | a0001c0001t0001g0268a0001c0001t0002g0260a0001c0001t0002g0274others(3): Show | 6 | HG00609.hp1 HG02451.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.264-39119_264-3911 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109880 | ||||||
| chr1:166109881
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.264-39118A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109881 | ||||||
| chr1:166109882
|
G | A | 43 | a0001c0001t0001g0050a0001c0001t0001g0070a0001c0001t0001g0073others(40): Show | 44 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.264-39119C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109882 | ||||||
| chr1:166109882
|
G | GTATATAT others(25): Show |
1 | a0001c0002t0003g0197 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.264-39120_264-3911 others(36): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109882 | ||||||
| chr1:166109882
|
G | GTATATAT others(17): Show |
1 | a0001c0002t0003g0279 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.264-39120_264-3911 others(28): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109882 | ||||||
| chr1:166109882
|
G | GTATATAT others(19): Show |
1 | a0001c0001t0021g0200 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.264-39120_264-3911 others(30): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109882 | ||||||
| chr1:166109882
|
G | GTATATAT others(23): Show |
3 | a0001c0001t0001g0286a0001c0002t0003g0034a0001c0002t0003g0288 | 3 | HG00438.hp2 HG00673.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.264-39120_264-3911 others(34): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109882 | ||||||
| chr1:166109882
|
G | GTATATAT others(25): Show |
5 | a0001c0001t0001g0203a0001c0002t0003g0204a0001c0002t0003g0283others(2): Show | 5 | HG02735.hp1 NA19003.hp1 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.264-39120_264-3911 others(36): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109882 | ||||||
| chr1:166109882
|
G | GTATATAT others(27): Show |
4 | a0001c0002t0003g0196a0001c0002t0003g0284a0001c0002t0003g0285others(1): Show | 4 | HG01074.hp1 HG02523.hp1 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-39120_264-3911 others(38): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109882 | ||||||
| chr1:166109882
|
G | GTATATAT others(29): Show |
2 | a0001c0001t0001g0282a0001c0002t0003g0290 | 2 | HG02129.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.264-39120_264-3911 others(40): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109882 | ||||||
| chr1:166109882
|
G | GTATATAT others(31): Show |
1 | a0001c0001t0001g0287 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.264-39120_264-3911 others(42): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109882 | ||||||
| chr1:166109882
|
G | GTATATAT others(27): Show |
2 | a0001c0001t0002g0207a0001c0002t0003g0206 | 2 | HG00140.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.264-39120_264-3911 others(38): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109882 | ||||||
| chr1:166109882
|
G | GTATATAT others(29): Show |
3 | a0001c0001t0001g0210a0001c0002t0003g0201a0001c0002t0010g0202 | 3 | HG03239.hp1 HG03490.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.264-39120_264-3911 others(40): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109882 | ||||||
| chr1:166109882
|
G | GTATATAT others(31): Show |
2 | a0001c0002t0003g0198a0001c0002t0003g0209 | 2 | HG01081.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.264-39120_264-3911 others(42): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109882 | ||||||
| chr1:166109882
|
G | GTATATAT others(33): Show |
1 | a0001c0002t0003g0199 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.264-39120_264-3911 others(44): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109882 | ||||||
| chr1:166109882
|
G | GTATATAT others(25): Show |
1 | a0001c0002t0003g0208 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.264-39120_264-3911 others(36): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109882 | ||||||
| chr1:166109882
|
G | GTATATAT others(21): Show |
1 | a0001c0002t0003g0205 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.264-39120_264-3911 others(32): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109882 | ||||||
| chr1:166109882
|
G | GTATATAT others(23): Show |
2 | a0001c0001t0001g0211a0001c0001t0001g0278 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.264-39120_264-3911 others(34): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109882 | ||||||
| chr1:166109882
|
G | GTATATAT others(25): Show |
1 | a0001c0001t0001g0212 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.264-39120_264-3911 others(36): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109882 | ||||||
| chr1:166109882
|
G | GTGTATAT others(1): Show |
8 | a0001c0001t0001g0190a0001c0001t0002g0170a0001c0001t0007g0026others(5): Show | 8 | HG01891.hp1 HG02280.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.264-39120_264-3911 others(12): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109882 | ||||||
| chr1:166109882
|
GTATATAT others(9): Show |
G | 3 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006 | 3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-39135_264-3912 others(20): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109882 | ||||||
| chr1:166109885
|
T | C | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0044others(1): Show | 4 | HG02559.hp2 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-39122A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109885 | ||||||
| chr1:166109886
|
A | ATATG | 8 | a0001c0001t0001g0049a0001c0001t0001g0104a0001c0001t0001g0106others(5): Show | 8 | HG01243.hp2 HG01358.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.264-39127_264-3912 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109886 | ||||||
| chr1:166109886
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.264-39123T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109886 | ||||||
| chr1:166109887
|
T | C | 2 | a0001c0001t0001g0037a0001c0001t0002g0038 | 2 | HG02976.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.264-39124A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109887 | ||||||
| chr1:166109889
|
T | C | 3 | a0001c0001t0001g0039a0001c0001t0002g0236a0001c0001t0002g0257 | 3 | HG03492.hp1 HG03540.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.264-39126A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109889 | ||||||
| chr1:166109890
|
G | A | 85 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0041others(82): Show | 85 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.264-39127C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109890 | ||||||
| chr1:166109890
|
G | GTA | 18 | a0001c0001t0001g0092a0001c0001t0001g0098a0001c0001t0001g0116others(15): Show | 18 | HG00544.hp2 HG00621.hp1 HG02165.hp1 others(15): Show |
intron_variant | MODIFIER | c.264-39129_264-3912 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109890 | ||||||
| chr1:166109890
|
G | GTATA | 5 | a0001c0001t0001g0127a0001c0001t0001g0143a0001c0001t0006g0145others(2): Show | 5 | HG00323.hp1 HG00609.hp2 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.264-39131_264-3912 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109890 | ||||||
| chr1:166109890
|
G | GTATATA | 3 | a0001c0001t0002g0118a0001c0001t0006g0100a0001c0001t0006g0148 | 3 | HG00735.hp2 HG02004.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.264-39133_264-3912 others(10): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109890 | ||||||
| chr1:166109890
|
G | GTATATAT others(3): Show |
2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | NA18971.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.264-39137_264-3912 others(14): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109890 | ||||||
| chr1:166109890
|
G | GTATGTA | 5 | a0001c0001t0001g0096a0001c0001t0001g0102a0001c0001t0001g0108others(2): Show | 5 | HG00558.hp1 HG00735.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.264-39128_264-3912 others(10): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109890 | ||||||
| chr1:166109890
|
GTA | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0057others(51): Show | 55 | HG00423.hp2 HG00597.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.264-39129_264-3912 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109890 | ||||||
| chr1:166109890
|
GTATA | G | 28 | a0001c0001t0001g0043a0001c0001t0001g0188a0001c0001t0001g0189others(25): Show | 28 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.264-39131_264-3912 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109890 | ||||||
| chr1:166109890
|
GTATATA | G | 3 | a0001c0001t0002g0053a0001c0001t0007g0027a0001c0001t0018g0052 | 3 | HG01081.hp1 HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.264-39133_264-3912 others(10): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109890 | ||||||
| chr1:166109891
|
T | C | 3 | a0001c0001t0001g0040a0001c0001t0001g0243a0001c0001t0001g0244 | 3 | HG00597.hp2 HG02615.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.264-39128A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109891 | ||||||
| chr1:166109892
|
A | ATATATAT others(27): Show |
1 | a0001c0001t0001g0113 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.264-39130_264-3912 others(38): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109892 | ||||||
| chr1:166109892
|
A | ATATATG | 14 | a0001c0001t0001g0050a0001c0001t0001g0070a0001c0001t0001g0077others(11): Show | 15 | HG00639.hp2 HG00738.hp2 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.264-39130_264-3912 others(10): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109892 | ||||||
| chr1:166109892
|
A | ATATGTAT others(5): Show |
2 | a0001c0001t0001g0125a0001c0001t0001g0167 | 2 | NA18942.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.264-39130_264-3912 others(16): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109892 | ||||||
| chr1:166109892
|
A | G | 2 | a0001c0001t0002g0146a0001c0001t0002g0162 | 2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.264-39129T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109892 | ||||||
| chr1:166109894
|
A | ATATG | 4 | a0001c0001t0001g0079a0001c0001t0001g0176a0001c0001t0002g0066others(1): Show | 4 | HG01346.hp1 HG01346.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-39132_264-3913 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109894 | ||||||
| chr1:166109894
|
A | G | 3 | a0001c0001t0004g0007a0001c0001t0004g0023a0001c0002t0011g0010 | 3 | HG01243.hp1 HG02258.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.264-39131T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109894 | ||||||
| chr1:166109896
|
A | ATG | 7 | a0001c0001t0001g0190a0001c0001t0007g0026a0001c0001t0007g0028others(4): Show | 7 | HG01891.hp1 HG02723.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.264-39134_264-3913 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109896 | ||||||
| chr1:166109896
|
A | G | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0011others(15): Show | 18 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.264-39133T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109896 | ||||||
| chr1:166109897
|
T | C | 2 | a0001c0001t0001g0282a0001c0001t0002g0258 | 2 | HG02129.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.264-39134A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109897 | ||||||
| chr1:166109898
|
A | G | 23 | a0001c0001t0001g0073a0001c0001t0001g0176a0001c0001t0004g0022others(20): Show | 23 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.264-39135T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109898 | ||||||
| chr1:166109902
|
A | G | 6 | a0001c0001t0001g0182a0001c0002t0001g0046a0001c0002t0001g0047others(3): Show | 6 | HG01433.hp2 HG02723.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.264-39139T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109902 | ||||||
| chr1:166109904
|
A | G | 5 | a0001c0001t0001g0135a0001c0002t0003g0095a0001c0002t0003g0120others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.264-39141T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109904 | ||||||
| chr1:166109910
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.264-39147T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109910 | ||||||
| chr1:166109912
|
A | G | 1 | a0001c0002t0003g0185 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.264-39149T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109912 | ||||||
| chr1:166109919
|
T | A | 2 | a0001c0001t0001g0131a0001c0001t0001g0158 | 2 | NA19063.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.264-39156A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166109919 | ||||||
| chr1:166110124
|
T | C | 3 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006 | 3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-39361A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166110124 | ||||||
| chr1:166110142
|
A | T | 1 | a0001c0001t0002g0274 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.264-39379T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166110142 | ||||||
| chr1:166110268
|
A | G | 1 | a0001c0001t0001g0057 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.264-39505T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166110268 | ||||||
| chr1:166110294
|
G | A | 3 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006 | 3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-39531C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166110294 | ||||||
| chr1:166110303
|
C | T | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-39540G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166110303 | ||||||
| chr1:166110424
|
G | C | 1 | a0001c0001t0001g0041 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.264-39661C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166110424 | ||||||
| chr1:166110869
|
A | G | 4 | a0001c0001t0004g0007a0001c0001t0009g0036a0001c0001t0009g0296others(1): Show | 4 | HG01243.hp1 HG02451.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-40106T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166110869 | ||||||
| chr1:166110921
|
C | T | 3 | a0001c0002t0003g0198a0001c0002t0003g0199a0001c0002t0003g0209 | 3 | HG01081.hp2 HG01099.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.264-40158G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166110921 | ||||||
| chr1:166110937
|
T | C | 4 | a0001c0002t0001g0046a0001c0002t0001g0047a0001c0002t0001g0048others(1): Show | 4 | HG02723.hp1 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-40174A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166110937 | ||||||
| chr1:166111188
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.264-40425A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166111188 | ||||||
| chr1:166111225
|
C | T | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-40462G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166111225 | ||||||
| chr1:166111468
|
A | G | 7 | a0001c0001t0007g0026a0001c0001t0007g0027a0001c0001t0007g0028others(4): Show | 7 | HG01891.hp1 HG02723.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.264-40705T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166111468 | ||||||
| chr1:166111475
|
T | C | 1 | a0001c0001t0002g0128 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.264-40712A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166111475 | ||||||
| chr1:166111502
|
C | T | 1 | a0001c0001t0008g0004 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.264-40739G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166111502 | ||||||
| chr1:166111503
|
G | A | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-40740C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166111503 | ||||||
| chr1:166111598
|
G | A | 13 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(10): Show | 13 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.264-40835C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166111598 | ||||||
| chr1:166111674
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.264-40911A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166111674 | ||||||
| chr1:166111709
|
T | C | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-40946A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166111709 | ||||||
| chr1:166112096
|
C | T | 8 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(5): Show | 8 | HG02559.hp2 HG02615.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.264-41333G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166112096 | ||||||
| chr1:166112137
|
A | G | 17 | a0001c0001t0023g0298a0001c0002t0003g0086a0001c0002t0005g0299others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-41374T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166112137 | ||||||
| chr1:166112332
|
T | A | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-41569A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166112332 | ||||||
| chr1:166112491
|
G | C | 3 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006 | 3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-41728C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166112491 | ||||||
| chr1:166112505
|
C | A | 1 | a0001c0001t0002g0221 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.264-41742G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166112505 | ||||||
| chr1:166112588
|
C | T | 1 | a0001c0002t0005g0309 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.264-41825G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166112588 | ||||||
| chr1:166112610
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.264-41847G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166112610 | ||||||
| chr1:166112617
|
A | C | 3 | a0001c0001t0001g0159a0001c0001t0002g0171a0001c0001t0002g0173 | 3 | HG02258.hp1 HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.264-41854T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166112617 | ||||||
| chr1:166112696
|
A | G | 6 | a0001c0001t0002g0241a0001c0001t0002g0242a0001c0001t0002g0263others(3): Show | 6 | HG00642.hp1 HG01257.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.264-41933T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166112696 | ||||||
| chr1:166112825
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.264-42062A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166112825 | ||||||
| chr1:166112876
|
G | A | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-42113C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166112876 | ||||||
| chr1:166112913
|
G | A | 1 | a0001c0002t0003g0230 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.264-42150C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166112913 | ||||||
| chr1:166113115
|
C | T | 76 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(73): Show | 76 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.264-42352G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166113115 | ||||||
| chr1:166113170
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.264-42407G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166113170 | ||||||
| chr1:166113443
|
C | T | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0011others(15): Show | 18 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.264-42680G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166113443 | ||||||
| chr1:166113582
|
T | C | 4 | a0001c0002t0001g0046a0001c0002t0001g0047a0001c0002t0001g0048others(1): Show | 4 | HG02723.hp1 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-42819A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166113582 | ||||||
| chr1:166113658
|
C | G | 76 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(73): Show | 76 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.264-42895G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166113658 | ||||||
| chr1:166113720
|
G | A | 8 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(5): Show | 8 | HG02559.hp2 HG02615.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.264-42957C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166113720 | ||||||
| chr1:166113921
|
A | G | 4 | a0001c0002t0001g0046a0001c0002t0001g0047a0001c0002t0001g0048others(1): Show | 4 | HG02723.hp1 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-43158T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166113921 | ||||||
| chr1:166113995
|
G | A | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-43232C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166113995 | ||||||
| chr1:166114090
|
C | T | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-43327G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166114090 | ||||||
| chr1:166114251
|
T | G | 165 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0049others(162): Show | 167 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.264-43488A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166114251 | ||||||
| chr1:166114274
|
A | G | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.264-43511T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166114274 | ||||||
| chr1:166114348
|
T | C | 1 | a0001c0001t0001g0058 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.264-43585A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166114348 | ||||||
| chr1:166114539
|
A | G | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | NA18998.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.264-43776T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166114539 | ||||||
| chr1:166114541
|
G | A | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | NA18998.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.264-43778C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166114541 | ||||||
| chr1:166114735
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.264-43972G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166114735 | ||||||
| chr1:166114790
|
A | C | 4 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(1): Show | 4 | HG02615.hp2 HG02976.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-44027T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166114790 | ||||||
| chr1:166114800
|
G | A | 3 | a0001c0001t0001g0043a0001c0001t0002g0053a0001c0001t0018g0052 | 3 | HG01081.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.264-44037C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166114800 | ||||||
| chr1:166114862
|
A | C | 1 | a0001c0001t0023g0298 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.264-44099T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166114862 | ||||||
| chr1:166115059
|
A | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0049others(137): Show | 142 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.264-44296T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115059 | ||||||
| chr1:166115334
|
G | T | 1 | a0001c0002t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.264-44571C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115334 | ||||||
| chr1:166115342
|
G | C | 1 | a0001c0002t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.264-44579C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115342 | ||||||
| chr1:166115343
|
G | T | 1 | a0001c0002t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.264-44580C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115343 | ||||||
| chr1:166115347
|
G | A | 1 | a0001c0002t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.264-44584C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115347 | ||||||
| chr1:166115351
|
G | T | 1 | a0001c0002t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.264-44588C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115351 | ||||||
| chr1:166115353
|
A | T | 1 | a0001c0002t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.264-44590T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115353 | ||||||
| chr1:166115354
|
T | C | 1 | a0001c0002t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.264-44591A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115354 | ||||||
| chr1:166115355
|
G | C | 1 | a0001c0002t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.264-44592C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115355 | ||||||
| chr1:166115356
|
G | T | 1 | a0001c0002t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.264-44593C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115356 | ||||||
| chr1:166115358
|
T | TCCCCTCC others(7): Show |
1 | a0001c0002t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.264-44596_264-4459 others(18): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115358 | ||||||
| chr1:166115359
|
A | T | 1 | a0001c0002t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.264-44596T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115359 | ||||||
| chr1:166115362
|
T | A | 1 | a0001c0002t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.264-44599A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115362 | ||||||
| chr1:166115363
|
G | T | 1 | a0001c0002t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.264-44600C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115363 | ||||||
| chr1:166115365
|
A | T | 1 | a0001c0002t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.264-44602T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115365 | ||||||
| chr1:166115366
|
G | A | 1 | a0001c0002t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.264-44603C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115366 | ||||||
| chr1:166115369
|
A | T | 1 | a0001c0002t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.264-44606T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115369 | ||||||
| chr1:166115471
|
G | A | 76 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(73): Show | 76 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.264-44708C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115471 | ||||||
| chr1:166115580
|
T | C | 3 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006 | 3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264-44817A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115580 | ||||||
| chr1:166115633
|
G | A | 1 | a0001c0001t0006g0180 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.264-44870C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115633 | ||||||
| chr1:166115700
|
G | A | 2 | a0001c0001t0002g0214a0001c0001t0002g0215 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.264-44937C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115700 | ||||||
| chr1:166115710
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.264-44947G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115710 | ||||||
| chr1:166115736
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.264-44973G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115736 | ||||||
| chr1:166115873
|
G | C | 1 | a0001c0001t0002g0258 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.264-45110C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115873 | ||||||
| chr1:166115896
|
T | C | 68 | a0001c0001t0001g0054a0001c0001t0001g0157a0001c0001t0001g0194others(65): Show | 68 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.264-45133A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115896 | ||||||
| chr1:166115915
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.264-45152C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115915 | ||||||
| chr1:166115953
|
T | C | 20 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0011others(17): Show | 20 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.264-45190A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166115953 | ||||||
| chr1:166116021
|
T | C | 32 | a0001c0001t0001g0203a0001c0001t0001g0210a0001c0001t0001g0211others(29): Show | 32 | HG00140.hp1 HG00438.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.264-45258A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166116021 | ||||||
| chr1:166116185
|
G | A | 2 | a0001c0001t0001g0129a0001c0001t0001g0154 | 2 | HG02071.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.264-45422C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166116185 | ||||||
| chr1:166116227
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.264-45464A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166116227 | ||||||
| chr1:166116236
|
T | C | 13 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(10): Show | 13 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.264-45473A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166116236 | ||||||
| chr1:166116390
|
A | G | 312 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(309): Show | 314 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.264-45627T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166116390 | ||||||
| chr1:166116430
|
T | G | 1 | a0001c0002t0001g0213 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.264-45667A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166116430 | ||||||
| chr1:166116504
|
G | A | 17 | a0001c0001t0023g0298a0001c0002t0003g0086a0001c0002t0005g0299others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-45741C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166116504 | ||||||
| chr1:166116565
|
C | T | 76 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(73): Show | 76 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.264-45802G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166116565 | ||||||
| chr1:166116915
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.264-46152G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166116915 | ||||||
| chr1:166116934
|
G | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0049others(136): Show | 141 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.264-46171C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166116934 | ||||||
| chr1:166117734
|
T | C | 1 | a0001c0002t0003g0034 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.264-46971A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166117734 | ||||||
| chr1:166117753
|
T | G | 1 | a0001c0001t0001g0092 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.264-46990A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166117753 | ||||||
| chr1:166117861
|
C | G | 4 | a0001c0001t0001g0058a0001c0001t0001g0109a0001c0001t0001g0110others(1): Show | 4 | HG02109.hp2 HG02647.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-47098G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166117861 | ||||||
| chr1:166117964
|
G | A | 13 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(10): Show | 13 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.264-47201C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166117964 | ||||||
| chr1:166118143
|
C | T | 3 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0055 | 3 | HG02723.hp1 HG02970.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.264-47380G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166118143 | ||||||
| chr1:166118341
|
T | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0049others(195): Show | 200 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.264-47578A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166118341 | ||||||
| chr1:166118365
|
T | C | 1 | a0001c0001t0001g0069 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.264-47602A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166118365 | ||||||
| chr1:166118384
|
T | C | 76 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(73): Show | 76 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.263+47602A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166118384 | ||||||
| chr1:166118456
|
T | C | 17 | a0001c0001t0023g0298a0001c0002t0003g0086a0001c0002t0005g0299others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+47530A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166118456 | ||||||
| chr1:166118533
|
A | G | 17 | a0001c0001t0023g0298a0001c0002t0003g0086a0001c0002t0005g0299others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+47453T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166118533 | ||||||
| chr1:166118617
|
A | G | 312 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(309): Show | 314 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.263+47369T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166118617 | ||||||
| chr1:166118673
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.263+47313A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166118673 | ||||||
| chr1:166118717
|
C | T | 1 | a0001c0002t0001g0179 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.263+47269G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166118717 | ||||||
| chr1:166118748
|
A | G | 13 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(10): Show | 13 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.263+47238T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166118748 | ||||||
| chr1:166118910
|
C | G | 1 | a0001c0001t0001g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.263+47076G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166118910 | ||||||
| chr1:166118910
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.263+47076G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166118910 | ||||||
| chr1:166118985
|
G | A | 17 | a0001c0001t0023g0298a0001c0002t0003g0086a0001c0002t0005g0299others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+47001C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166118985 | ||||||
| chr1:166119130
|
G | T | 1 | a0001c0001t0001g0096 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.263+46856C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166119130 | ||||||
| chr1:166119167
|
C | T | 1 | a0001c0001t0004g0007 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.263+46819G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166119167 | ||||||
| chr1:166119168
|
A | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0049others(137): Show | 142 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.263+46818T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166119168 | ||||||
| chr1:166119190
|
A | G | 4 | a0001c0002t0001g0046a0001c0002t0001g0047a0001c0002t0001g0048others(1): Show | 4 | HG02723.hp1 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.263+46796T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166119190 | ||||||
| chr1:166119616
|
G | A | 13 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(10): Show | 13 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.263+46370C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166119616 | ||||||
| chr1:166119774
|
C | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0049others(136): Show | 141 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.263+46212G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166119774 | ||||||
| chr1:166119886
|
G | A | 17 | a0001c0001t0023g0298a0001c0002t0003g0086a0001c0002t0005g0299others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+46100C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166119886 | ||||||
| chr1:166120083
|
T | C | 1 | a0001c0001t0002g0274 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.263+45903A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166120083 | ||||||
| chr1:166120416
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.263+45570C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166120416 | ||||||
| chr1:166120486
|
T | C | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.263+45500A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166120486 | ||||||
| chr1:166120491
|
T | C | 68 | a0001c0001t0001g0054a0001c0001t0001g0157a0001c0001t0001g0194others(65): Show | 68 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.263+45495A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166120491 | ||||||
| chr1:166120569
|
C | T | 1 | a0001c0001t0009g0296 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.263+45417G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166120569 | ||||||
| chr1:166120586
|
G | C | 312 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(309): Show | 314 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.263+45400C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166120586 | ||||||
| chr1:166120645
|
C | T | 3 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0186 | 3 | HG00544.hp2 HG00621.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.263+45341G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166120645 | ||||||
| chr1:166120738
|
G | A | 93 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.263+45248C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166120738 | ||||||
| chr1:166120748
|
AAGAGCAG others(3): Show |
A | 76 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(73): Show | 76 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.263+45228_263+4523 others(14): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166120748 | ||||||
| chr1:166120898
|
C | A | 3 | a0001c0001t0004g0007a0001c0001t0009g0296a0001c0001t0009g0297 | 3 | HG01243.hp1 HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.263+45088G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166120898 | ||||||
| chr1:166120902
|
C | T | 303 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(300): Show | 305 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.263+45084G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166120902 | ||||||
| chr1:166121284
|
T | C | 2 | a0001c0001t0001g0176a0001c0002t0001g0213 | 2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.263+44702A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166121284 | ||||||
| chr1:166121318
|
T | C | 1 | a0001c0002t0003g0205 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.263+44668A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166121318 | ||||||
| chr1:166121329
|
C | T | 21 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0004g0009others(18): Show | 21 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.263+44657G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166121329 | ||||||
| chr1:166121332
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.263+44654C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166121332 | ||||||
| chr1:166121532
|
T | C | 1 | a0001c0001t0001g0134 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.263+44454A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166121532 | ||||||
| chr1:166121589
|
C | A | 6 | a0001c0001t0001g0115a0001c0002t0003g0087a0001c0002t0003g0089others(3): Show | 6 | HG00438.hp1 NA18952.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.263+44397G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166121589 | ||||||
| chr1:166121749
|
G | A | 3 | a0001c0001t0004g0007a0001c0001t0009g0296a0001c0001t0009g0297 | 3 | HG01243.hp1 HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.263+44237C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166121749 | ||||||
| chr1:166121758
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.263+44228A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166121758 | ||||||
| chr1:166121806
|
C | T | 17 | a0001c0001t0023g0298a0001c0002t0003g0086a0001c0002t0005g0299others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+44180G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166121806 | ||||||
| chr1:166121807
|
G | A | 1 | a0001c0001t0009g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.263+44179C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166121807 | ||||||
| chr1:166121966
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.263+44020G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166121966 | ||||||
| chr1:166121997
|
T | C | 1 | a0001c0001t0002g0193 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.263+43989A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166121997 | ||||||
| chr1:166122033
|
C | G | 1 | a0001c0001t0006g0103 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.263+43953G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166122033 | ||||||
| chr1:166122312
|
A | G | 303 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(300): Show | 305 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.263+43674T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166122312 | ||||||
| chr1:166122529
|
C | T | 303 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(300): Show | 305 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.263+43457G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166122529 | ||||||
| chr1:166122759
|
G | A | 5 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(2): Show | 5 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.263+43227C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166122759 | ||||||
| chr1:166122967
|
C | T | 3 | a0001c0002t0003g0088a0001c0002t0003g0119a0001c0002t0003g0132 | 3 | HG00642.hp2 HG00741.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.263+43019G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166122967 | ||||||
| chr1:166123080
|
C | T | 11 | a0001c0001t0001g0054a0001c0001t0001g0217a0001c0001t0001g0243others(8): Show | 11 | HG00597.hp2 HG01106.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.263+42906G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166123080 | ||||||
| chr1:166123188
|
C | T | 21 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0004g0009others(18): Show | 21 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.263+42798G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166123188 | ||||||
| chr1:166123233
|
C | G | 1 | a0001c0001t0009g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.263+42753G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166123233 | ||||||
| chr1:166123233
|
C | T | 1 | a0001c0001t0001g0123 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.263+42753G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166123233 | ||||||
| chr1:166123338
|
C | T | 1 | a0001c0002t0005g0307 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.263+42648G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166123338 | ||||||
| chr1:166123436
|
G | A | 4 | a0001c0002t0001g0046a0001c0002t0001g0047a0001c0002t0001g0048others(1): Show | 4 | HG02723.hp1 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.263+42550C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166123436 | ||||||
| chr1:166123467
|
C | A | 23 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0004g0009others(20): Show | 23 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.263+42519G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166123467 | ||||||
| chr1:166123504
|
T | G | 1 | a0001c0001t0002g0226 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.263+42482A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166123504 | ||||||
| chr1:166123516
|
A | G | 1 | a0001c0001t0007g0032 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.263+42470T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166123516 | ||||||
| chr1:166123802
|
G | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0049others(194): Show | 199 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.263+42184C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166123802 | ||||||
| chr1:166123836
|
C | G | 75 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(72): Show | 75 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.263+42150G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166123836 | ||||||
| chr1:166124042
|
A | C | 75 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(72): Show | 75 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.263+41944T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166124042 | ||||||
| chr1:166124080
|
C | T | 1 | a0001c0001t0024g0315 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.263+41906G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166124080 | ||||||
| chr1:166124131
|
C | A | 4 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006others(1): Show | 4 | HG02451.hp1 HG03579.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.263+41855G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166124131 | ||||||
| chr1:166124181
|
C | G | 2 | a0001c0001t0009g0296a0001c0001t0009g0297 | 2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.263+41805G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166124181 | ||||||
| chr1:166124347
|
T | C | 312 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(309): Show | 314 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.263+41639A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166124347 | ||||||
| chr1:166124392
|
G | A | 8 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(5): Show | 8 | HG02559.hp2 HG02615.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.263+41594C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166124392 | ||||||
| chr1:166124488
|
G | C | 1 | a0001c0001t0019g0238 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.263+41498C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166124488 | ||||||
| chr1:166124693
|
C | T | 1 | a0001c0001t0019g0238 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.263+41293G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166124693 | ||||||
| chr1:166124828
|
T | C | 2 | a0001c0001t0001g0091a0001c0001t0001g0113 | 2 | NA18952.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.263+41158A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166124828 | ||||||
| chr1:166124943
|
AC | A | 5 | a0001c0001t0001g0079a0001c0001t0002g0002a0001c0001t0002g0080others(2): Show | 6 | HG00639.hp2 HG00738.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.263+41042delG | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166124943 | ||||||
| chr1:166125076
|
C | T | 140 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0049others(137): Show | 142 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.263+40910G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166125076 | ||||||
| chr1:166125230
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.263+40756G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166125230 | ||||||
| chr1:166125267
|
T | G | 2 | a0001c0001t0001g0211a0001c0001t0001g0278 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.263+40719A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166125267 | ||||||
| chr1:166125268
|
A | G | 2 | a0001c0001t0001g0211a0001c0001t0001g0278 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.263+40718T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166125268 | ||||||
| chr1:166125326
|
T | C | 211 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0049others(208): Show | 213 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.263+40660A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166125326 | ||||||
| chr1:166125362
|
A | G | 211 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0049others(208): Show | 213 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.263+40624T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166125362 | ||||||
| chr1:166125645
|
T | C | 4 | a0001c0002t0001g0046a0001c0002t0001g0047a0001c0002t0001g0048others(1): Show | 4 | HG02723.hp1 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.263+40341A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166125645 | ||||||
| chr1:166125700
|
C | T | 1 | a0001c0002t0001g0046 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.263+40286G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166125700 | ||||||
| chr1:166125755
|
C | T | 211 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0049others(208): Show | 213 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.263+40231G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166125755 | ||||||
| chr1:166125832
|
A | AT | 34 | a0001c0001t0001g0070a0001c0001t0001g0098a0001c0001t0001g0134others(31): Show | 34 | HG01169.hp2 HG01243.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.263+40153dupA | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166125832 | ||||||
| chr1:166125832
|
A | ATT | 169 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0049others(166): Show | 171 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.263+40152_263+4015 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166125832 | ||||||
| chr1:166125832
|
A | ATTT | 13 | a0001c0001t0001g0078a0001c0001t0001g0115a0001c0001t0001g0168others(10): Show | 13 | HG00438.hp1 HG01993.hp2 HG02129.hp2 others(10): Show |
intron_variant | MODIFIER | c.263+40151_263+4015 others(7): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166125832 | ||||||
| chr1:166125858
|
C | T | 2 | a0001c0002t0001g0056a0001c0002t0001g0179 | 2 | HG02615.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.263+40128G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166125858 | ||||||
| chr1:166125893
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.263+40093C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166125893 | ||||||
| chr1:166125901
|
A | G | 315 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(312): Show | 317 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.263+40085T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166125901 | ||||||
| chr1:166125994
|
G | A | 7 | a0001c0001t0006g0100a0001c0001t0006g0103a0001c0001t0006g0144others(4): Show | 7 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.263+39992C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166125994 | ||||||
| chr1:166126381
|
T | C | 312 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(309): Show | 314 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.263+39605A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166126381 | ||||||
| chr1:166126427
|
T | C | 14 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(11): Show | 14 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.263+39559A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166126427 | ||||||
| chr1:166126542
|
T | A | 2 | a0001c0001t0002g0219a0001c0001t0002g0226 | 2 | NA19011.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.263+39444A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166126542 | ||||||
| chr1:166126728
|
G | A | 72 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(69): Show | 72 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.263+39258C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166126728 | ||||||
| chr1:166126834
|
G | A | 1 | a0001c0001t0002g0275 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.263+39152C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166126834 | ||||||
| chr1:166126983
|
A | G | 2 | a0001c0001t0002g0171a0001c0001t0002g0173 | 2 | HG02258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.263+39003T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166126983 | ||||||
| chr1:166127005
|
C | T | 286 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(283): Show | 288 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.263+38981G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166127005 | ||||||
| chr1:166127045
|
G | C | 1 | a0001c0002t0003g0175 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.263+38941C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166127045 | ||||||
| chr1:166127111
|
A | T | 1 | a0001c0001t0001g0253 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.263+38875T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166127111 | ||||||
| chr1:166127155
|
G | C | 1 | a0001c0001t0001g0176 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.263+38831C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166127155 | ||||||
| chr1:166127181
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.263+38805A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166127181 | ||||||
| chr1:166127302
|
T | G | 2 | a0001c0001t0001g0134a0001c0002t0003g0074 | 2 | HG02015.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.263+38684A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166127302 | ||||||
| chr1:166127328
|
C | T | 74 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(71): Show | 74 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.263+38658G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166127328 | ||||||
| chr1:166127379
|
T | C | 1 | a0001c0001t0002g0053 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.263+38607A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166127379 | ||||||
| chr1:166127392
|
T | A | 1 | a0001c0001t0002g0193 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.263+38594A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166127392 | ||||||
| chr1:166127589
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.263+38397T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166127589 | ||||||
| chr1:166127625
|
T | C | 1 | a0001c0002t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.263+38361A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166127625 | ||||||
| chr1:166127762
|
G | A | 1 | a0001c0001t0001g0150 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.263+38224C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166127762 | ||||||
| chr1:166127783
|
C | T | 1 | a0001c0001t0024g0315 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.263+38203G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166127783 | ||||||
| chr1:166128207
|
T | TA | 17 | a0001c0001t0023g0298a0001c0002t0003g0086a0001c0002t0005g0299others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+37778_263+3777 others(5): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166128207 | ||||||
| chr1:166128214
|
T | C | 18 | a0001c0001t0023g0298a0001c0002t0001g0213a0001c0002t0003g0086others(15): Show | 18 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.263+37772A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166128214 | ||||||
| chr1:166128214
|
T | TATTC | 290 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(287): Show | 292 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.263+37768_263+3777 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166128214 | ||||||
| chr1:166128427
|
C | G | 17 | a0001c0001t0023g0298a0001c0002t0003g0086a0001c0002t0005g0299others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+37559G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166128427 | ||||||
| chr1:166128521
|
C | T | 73 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(70): Show | 73 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.263+37465G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166128521 | ||||||
| chr1:166128577
|
T | C | 1 | a0001c0001t0002g0118 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.263+37409A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166128577 | ||||||
| chr1:166128688
|
C | T | 2 | a0001c0002t0001g0056a0001c0002t0001g0179 | 2 | HG02615.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.263+37298G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166128688 | ||||||
| chr1:166128716
|
T | C | 1 | a0001c0001t0001g0269 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.263+37270A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166128716 | ||||||
| chr1:166128847
|
G | A | 3 | a0001c0001t0004g0007a0001c0001t0009g0296a0001c0001t0009g0297 | 3 | HG01243.hp1 HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.263+37139C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166128847 | ||||||
| chr1:166128942
|
A | G | 6 | a0001c0002t0003g0083a0001c0002t0003g0084a0001c0002t0003g0085others(3): Show | 6 | HG00642.hp2 HG00741.hp2 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.263+37044T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166128942 | ||||||
| chr1:166129158
|
G | A | 4 | a0001c0002t0001g0046a0001c0002t0001g0047a0001c0002t0001g0048others(1): Show | 4 | HG02723.hp1 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.263+36828C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166129158 | ||||||
| chr1:166129328
|
T | C | 14 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(11): Show | 14 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.263+36658A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166129328 | ||||||
| chr1:166129344
|
C | G | 315 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(312): Show | 317 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.263+36642G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166129344 | ||||||
| chr1:166129438
|
A | G | 214 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0049others(211): Show | 216 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.263+36548T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166129438 | ||||||
| chr1:166129530
|
T | C | 2 | a0001c0001t0001g0098a0001c0001t0001g0138 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.263+36456A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166129530 | ||||||
| chr1:166129551
|
C | A | 17 | a0001c0001t0023g0298a0001c0002t0003g0086a0001c0002t0005g0299others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+36435G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166129551 | ||||||
| chr1:166129724
|
T | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0049others(197): Show | 202 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.263+36262A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166129724 | ||||||
| chr1:166129973
|
A | G | 3 | a0001c0001t0001g0134a0001c0002t0003g0074a0001c0002t0003g0093 | 3 | HG02015.hp1 HG02165.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.263+36013T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166129973 | ||||||
| chr1:166129980
|
T | C | 32 | a0001c0001t0001g0203a0001c0001t0001g0210a0001c0001t0001g0211others(29): Show | 32 | HG00140.hp1 HG00438.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.263+36006A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166129980 | ||||||
| chr1:166130057
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.263+35929T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166130057 | ||||||
| chr1:166130079
|
G | C | 214 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0049others(211): Show | 216 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.263+35907C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166130079 | ||||||
| chr1:166130188
|
TC | T | 14 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(11): Show | 14 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.263+35797delG | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166130188 | ||||||
| chr1:166130353
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.263+35633T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166130353 | ||||||
| chr1:166130405
|
A | G | 315 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(312): Show | 317 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.263+35581T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166130405 | ||||||
| chr1:166130684
|
T | C | 75 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(72): Show | 75 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.263+35302A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166130684 | ||||||
| chr1:166130684
|
T | G | 1 | a0001c0001t0001g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.263+35302A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166130684 | ||||||
| chr1:166130753
|
A | G | 21 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0050others(18): Show | 22 | HG00639.hp1 HG01099.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.263+35233T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166130753 | ||||||
| chr1:166130981
|
C | CT | 40 | a0001c0001t0001g0041a0001c0001t0001g0050a0001c0001t0001g0065others(37): Show | 40 | HG00738.hp1 HG01175.hp2 HG01358.hp2 others(37): Show |
intron_variant | MODIFIER | c.263+35004dupA | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166130981 | ||||||
| chr1:166130981
|
CT | C | 13 | a0001c0001t0001g0037a0001c0001t0001g0072a0001c0001t0001g0078others(10): Show | 13 | HG01069.hp1 HG01167.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.263+35004delA | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166130981 | ||||||
| chr1:166130981
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.263+34992_263+3500 others(17): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166130981 | ||||||
| chr1:166131011
|
A | G | 289 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(286): Show | 291 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.263+34975T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166131011 | ||||||
| chr1:166131014
|
G | C | 1 | a0001c0001t0001g0115 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.263+34972C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166131014 | ||||||
| chr1:166131166
|
A | G | 1 | a0001c0002t0003g0291 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.263+34820T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166131166 | ||||||
| chr1:166131193
|
T | A | 2 | a0001c0002t0001g0056a0001c0002t0001g0179 | 2 | HG02615.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.263+34793A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166131193 | ||||||
| chr1:166131239
|
G | A | 4 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006others(1): Show | 4 | HG02451.hp1 HG03579.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.263+34747C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166131239 | ||||||
| chr1:166131487
|
G | A | 1 | a0001c0001t0002g0193 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.263+34499C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166131487 | ||||||
| chr1:166131707
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.263+34279C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166131707 | ||||||
| chr1:166132156
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.263+33830A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166132156 | ||||||
| chr1:166132296
|
C | CCTAA | 84 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0050others(81): Show | 85 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.263+33686_263+3368 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166132296 | ||||||
| chr1:166132365
|
G | A | 64 | a0001c0001t0001g0194a0001c0001t0001g0217a0001c0001t0001g0220others(61): Show | 64 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.263+33621C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166132365 | ||||||
| chr1:166132779
|
C | A | 1 | a0001c0001t0017g0141 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.263+33207G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166132779 | ||||||
| chr1:166133123
|
T | A | 1 | a0001c0001t0001g0092 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.263+32863A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166133123 | ||||||
| chr1:166133190
|
C | A | 4 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0158others(1): Show | 4 | HG00597.hp1 NA18947.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.263+32796G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166133190 | ||||||
| chr1:166133529
|
CTG | C | 72 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(69): Show | 72 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.263+32455_263+3245 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166133529 | ||||||
| chr1:166133601
|
T | TA | 33 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0135others(30): Show | 33 | HG00544.hp1 HG01070.hp2 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.263+32384dupT | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166133601 | ||||||
| chr1:166133601
|
T | TAA | 202 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0049others(199): Show | 204 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.263+32383_263+3238 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166133601 | ||||||
| chr1:166133664
|
A | C | 1 | a0001c0001t0002g0281 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.263+32322T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166133664 | ||||||
| chr1:166133762
|
T | C | 3 | a0001c0001t0001g0043a0001c0001t0002g0053a0001c0001t0018g0052 | 3 | HG01081.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.263+32224A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166133762 | ||||||
| chr1:166134022
|
C | G | 1 | a0001c0001t0002g0292 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.263+31964G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166134022 | ||||||
| chr1:166134040
|
C | T | 1 | a0001c0001t0001g0287 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.263+31946G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166134040 | ||||||
| chr1:166134273
|
G | T | 16 | a0001c0001t0023g0298a0001c0002t0005g0299a0001c0002t0005g0300others(13): Show | 16 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.263+31713C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166134273 | ||||||
| chr1:166134435
|
T | C | 279 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0049others(276): Show | 281 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.263+31551A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166134435 | ||||||
| chr1:166134454
|
C | T | 1 | a0001c0001t0006g0144 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.263+31532G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166134454 | ||||||
| chr1:166134458
|
A | G | 2 | a0001c0001t0001g0098a0001c0001t0001g0138 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.263+31528T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166134458 | ||||||
| chr1:166134516
|
G | GTAATAA | 15 | a0001c0001t0023g0298a0001c0002t0005g0299a0001c0002t0005g0300others(12): Show | 15 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.263+31464_263+3146 others(10): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166134516 | ||||||
| chr1:166134519
|
A | G | 2 | a0001c0001t0002g0221a0001c0001t0002g0275 | 2 | HG03927.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.263+31467T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166134519 | ||||||
| chr1:166134540
|
A | ATAG | 3 | a0001c0001t0001g0106a0001c0001t0001g0152a0001c0001t0001g0181 | 3 | HG00323.hp2 HG03704.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.263+31445_263+3144 others(7): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166134540 | ||||||
| chr1:166134540
|
A | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0049others(193): Show | 198 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.263+31446T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166134540 | ||||||
| chr1:166134733
|
C | T | 1 | a0001c0001t0018g0052 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.263+31253G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166134733 | ||||||
| chr1:166135183
|
A | C | 1 | a0001c0001t0001g0163 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.263+30803T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166135183 | ||||||
| chr1:166135186
|
C | T | 16 | a0001c0001t0023g0298a0001c0002t0005g0299a0001c0002t0005g0300others(13): Show | 16 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.263+30800G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166135186 | ||||||
| chr1:166135200
|
C | T | 78 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(75): Show | 78 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.263+30786G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166135200 | ||||||
| chr1:166135428
|
T | C | 32 | a0001c0001t0001g0203a0001c0001t0001g0210a0001c0001t0001g0211others(29): Show | 32 | HG00140.hp1 HG00438.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.263+30558A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166135428 | ||||||
| chr1:166135489
|
C | A | 1 | a0001c0001t0002g0193 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.263+30497G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166135489 | ||||||
| chr1:166135531
|
G | C | 1 | a0001c0001t0001g0248 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.263+30455C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166135531 | ||||||
| chr1:166135625
|
T | A | 3 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006 | 3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.263+30361A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166135625 | ||||||
| chr1:166136060
|
A | G | 32 | a0001c0001t0001g0203a0001c0001t0001g0210a0001c0001t0001g0211others(29): Show | 32 | HG00140.hp1 HG00438.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.263+29926T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166136060 | ||||||
| chr1:166136077
|
C | A | 2 | a0001c0001t0001g0176a0001c0002t0001g0213 | 2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.263+29909G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166136077 | ||||||
| chr1:166136151
|
T | C | 16 | a0001c0001t0023g0298a0001c0002t0005g0299a0001c0002t0005g0300others(13): Show | 16 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.263+29835A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166136151 | ||||||
| chr1:166136221
|
T | C | 4 | a0001c0002t0001g0046a0001c0002t0001g0047a0001c0002t0001g0048others(1): Show | 4 | HG02723.hp1 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.263+29765A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166136221 | ||||||
| chr1:166136244
|
A | C | 32 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(29): Show | 32 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.263+29742T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166136244 | ||||||
| chr1:166136363
|
G | T | 1 | a0001c0002t0010g0160 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.263+29623C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166136363 | ||||||
| chr1:166136373
|
G | C | 1 | a0001c0002t0001g0046 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.263+29613C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166136373 | ||||||
| chr1:166136376
|
G | A | 8 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(5): Show | 8 | HG02559.hp2 HG02615.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.263+29610C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166136376 | ||||||
| chr1:166136387
|
G | A | 1 | a0001c0001t0002g0237 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.263+29599C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166136387 | ||||||
| chr1:166136419
|
A | G | 312 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(309): Show | 314 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.263+29567T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166136419 | ||||||
| chr1:166136465
|
C | G | 1 | a0001c0001t0001g0217 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.263+29521G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166136465 | ||||||
| chr1:166136491
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.263+29495A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166136491 | ||||||
| chr1:166136652
|
A | C | 1 | a0001c0001t0001g0116 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.263+29334T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166136652 | ||||||
| chr1:166136678
|
C | T | 279 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0049others(276): Show | 281 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.263+29308G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166136678 | ||||||
| chr1:166136729
|
T | G | 1 | a0001c0001t0017g0141 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.263+29257A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166136729 | ||||||
| chr1:166136898
|
T | C | 2 | a0001c0002t0003g0095a0001c0002t0003g0137 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.263+29088A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166136898 | ||||||
| chr1:166136934
|
G | A | 2 | a0001c0001t0002g0171a0001c0001t0002g0173 | 2 | HG02258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.263+29052C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166136934 | ||||||
| chr1:166137002
|
A | T | 1 | a0001c0002t0003g0279 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.263+28984T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166137002 | ||||||
| chr1:166137059
|
T | C | 1 | a0001c0001t0009g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.263+28927A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166137059 | ||||||
| chr1:166137302
|
T | C | 2 | a0001c0002t0001g0056a0001c0002t0001g0179 | 2 | HG02615.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.263+28684A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166137302 | ||||||
| chr1:166137500
|
C | CT | 6 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0004g0009others(3): Show | 6 | HG00597.hp2 HG02257.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.263+28485dupA | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166137500 | ||||||
| chr1:166137500
|
CT | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0049others(194): Show | 199 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.263+28485delA | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166137500 | ||||||
| chr1:166137654
|
G | A | 7 | a0001c0001t0001g0287a0001c0002t0003g0283a0001c0002t0003g0284others(4): Show | 7 | HG00438.hp2 NA18960.hp1 NA19003.hp1 others(4): Show |
intron_variant | MODIFIER | c.263+28332C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166137654 | ||||||
| chr1:166137923
|
G | C | 1 | a0001c0001t0001g0163 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.263+28063C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166137923 | ||||||
| chr1:166138027
|
A | G | 16 | a0001c0001t0023g0298a0001c0002t0005g0299a0001c0002t0005g0300others(13): Show | 16 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.263+27959T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166138027 | ||||||
| chr1:166138054
|
C | G | 4 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006others(1): Show | 4 | HG02451.hp1 HG03579.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.263+27932G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166138054 | ||||||
| chr1:166138130
|
G | C | 16 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(13): Show | 16 | HG02451.hp1 HG02559.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.263+27856C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166138130 | ||||||
| chr1:166138133
|
G | A | 1 | a0001c0002t0003g0187 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.263+27853C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166138133 | ||||||
| chr1:166138333
|
C | T | 1 | a0001c0001t0002g0162 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.263+27653G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166138333 | ||||||
| chr1:166138388
|
C | A | 64 | a0001c0001t0001g0194a0001c0001t0001g0217a0001c0001t0001g0220others(61): Show | 64 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.263+27598G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166138388 | ||||||
| chr1:166138474
|
C | A | 1 | a0001c0001t0002g0237 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.263+27512G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166138474 | ||||||
| chr1:166138544
|
T | C | 1 | a0001c0001t0001g0140 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.263+27442A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166138544 | ||||||
| chr1:166138546
|
A | G | 295 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0049others(292): Show | 297 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.263+27440T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166138546 | ||||||
| chr1:166138741
|
T | C | 64 | a0001c0001t0001g0194a0001c0001t0001g0217a0001c0001t0001g0220others(61): Show | 64 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.263+27245A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166138741 | ||||||
| chr1:166138850
|
G | A | 31 | a0001c0001t0001g0203a0001c0001t0001g0210a0001c0001t0001g0211others(28): Show | 31 | HG00140.hp1 HG00438.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.263+27136C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166138850 | ||||||
| chr1:166138875
|
G | T | 2 | a0001c0001t0009g0296a0001c0001t0009g0297 | 2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.263+27111C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166138875 | ||||||
| chr1:166138905
|
T | C | 5 | a0001c0001t0001g0079a0001c0001t0002g0002a0001c0001t0002g0080others(2): Show | 6 | HG00639.hp2 HG00738.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.263+27081A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166138905 | ||||||
| chr1:166138974
|
T | C | 4 | a0001c0001t0001g0058a0001c0001t0001g0109a0001c0001t0001g0110others(1): Show | 4 | HG02109.hp2 HG02647.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.263+27012A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166138974 | ||||||
| chr1:166139077
|
A | G | 4 | a0001c0002t0001g0046a0001c0002t0001g0047a0001c0002t0001g0048others(1): Show | 4 | HG02723.hp1 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.263+26909T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166139077 | ||||||
| chr1:166139099
|
A | T | 4 | a0001c0002t0001g0046a0001c0002t0001g0047a0001c0002t0001g0048others(1): Show | 4 | HG02723.hp1 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.263+26887T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166139099 | ||||||
| chr1:166139288
|
C | A | 295 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0049others(292): Show | 297 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.263+26698G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166139288 | ||||||
| chr1:166139428
|
A | T | 2 | a0001c0001t0009g0296a0001c0001t0009g0297 | 2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.263+26558T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166139428 | ||||||
| chr1:166139489
|
T | C | 1 | a0001c0002t0003g0132 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.263+26497A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166139489 | ||||||
| chr1:166139629
|
C | G | 279 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0049others(276): Show | 281 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.263+26357G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166139629 | ||||||
| chr1:166139650
|
T | C | 295 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0049others(292): Show | 297 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.263+26336A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166139650 | ||||||
| chr1:166139878
|
C | G | 1 | a0001c0001t0001g0287 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.263+26108G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166139878 | ||||||
| chr1:166139889
|
T | G | 279 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0049others(276): Show | 281 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.263+26097A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166139889 | ||||||
| chr1:166139920
|
C | A | 1 | a0001c0001t0001g0154 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.263+26066G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166139920 | ||||||
| chr1:166139937
|
C | G | 2 | a0001c0001t0009g0296a0001c0001t0009g0297 | 2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.263+26049G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166139937 | ||||||
| chr1:166140139
|
G | A | 3 | a0001c0001t0001g0280a0001c0001t0002g0259a0001c0001t0002g0260 | 3 | HG00609.hp1 HG02040.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.263+25847C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166140139 | ||||||
| chr1:166140158
|
C | T | 4 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006others(1): Show | 4 | HG02451.hp1 HG03579.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.263+25828G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166140158 | ||||||
| chr1:166140396
|
T | G | 1 | a0001c0001t0004g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.263+25590A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166140396 | ||||||
| chr1:166140471
|
C | T | 2 | a0001c0001t0002g0229a0001c0002t0003g0239 | 2 | HG02735.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.263+25515G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166140471 | ||||||
| chr1:166140474
|
T | C | 8 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(5): Show | 8 | HG02559.hp2 HG02615.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.263+25512A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166140474 | ||||||
| chr1:166140631
|
G | A | 3 | a0001c0001t0004g0008a0001c0001t0004g0024a0001c0001t0004g0025 | 3 | HG02451.hp2 HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.263+25355C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166140631 | ||||||
| chr1:166140647
|
T | C | 2 | a0001c0001t0009g0296a0001c0001t0009g0297 | 2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.263+25339A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166140647 | ||||||
| chr1:166140726
|
C | T | 277 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0049others(274): Show | 279 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.263+25260G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166140726 | ||||||
| chr1:166140756
|
G | T | 258 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0049others(255): Show | 260 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.263+25230C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166140756 | ||||||
| chr1:166140944
|
T | C | 229 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0049others(226): Show | 231 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.263+25042A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166140944 | ||||||
| chr1:166141258
|
T | C | 15 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(12): Show | 15 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.263+24728A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166141258 | ||||||
| chr1:166141285
|
A | G | 1 | a0001c0001t0001g0154 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.263+24701T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166141285 | ||||||
| chr1:166141349
|
T | C | 3 | a0001c0002t0001g0046a0001c0002t0001g0047a0001c0002t0001g0048 | 3 | HG02970.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.263+24637A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166141349 | ||||||
| chr1:166141370
|
C | T | 1 | a0001c0001t0024g0315 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.263+24616G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166141370 | ||||||
| chr1:166141456
|
T | C | 229 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0049others(226): Show | 231 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.263+24530A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166141456 | ||||||
| chr1:166141675
|
T | C | 9 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(6): Show | 9 | HG02451.hp1 HG02559.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.263+24311A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166141675 | ||||||
| chr1:166141685
|
T | C | 141 | a0001c0001t0001g0001a0001c0001t0001g0049a0001c0001t0001g0050others(138): Show | 143 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.263+24301A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166141685 | ||||||
| chr1:166141784
|
A | T | 3 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006 | 3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.263+24202T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166141784 | ||||||
| chr1:166141845
|
T | C | 1 | a0001c0001t0009g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.263+24141A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166141845 | ||||||
| chr1:166142049
|
C | A | 1 | a0001c0002t0003g0034 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.263+23937G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166142049 | ||||||
| chr1:166142209
|
G | A | 1 | a0001c0001t0004g0007 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.263+23777C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166142209 | ||||||
| chr1:166142212
|
T | C | 3 | a0001c0002t0001g0046a0001c0002t0001g0047a0001c0002t0001g0048 | 3 | HG02970.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.263+23774A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166142212 | ||||||
| chr1:166142320
|
C | T | 1 | a0001c0001t0002g0228 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.263+23666G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166142320 | ||||||
| chr1:166142346
|
C | T | 1 | a0001c0001t0002g0267 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.263+23640G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166142346 | ||||||
| chr1:166142394
|
G | A | 3 | a0001c0001t0017g0141a0001c0002t0010g0160a0001c0002t0010g0161 | 3 | HG02572.hp2 HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.263+23592C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166142394 | ||||||
| chr1:166142527
|
G | A | 1 | a0001c0001t0001g0073 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.263+23459C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166142527 | ||||||
| chr1:166142595
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.263+23391C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166142595 | ||||||
| chr1:166142668
|
C | T | 1 | a0001c0001t0002g0228 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.263+23318G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166142668 | ||||||
| chr1:166142679
|
C | A | 1 | a0001c0002t0003g0187 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.263+23307G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166142679 | ||||||
| chr1:166142888
|
A | G | 2 | a0001c0001t0009g0296a0001c0001t0009g0297 | 2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.263+23098T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166142888 | ||||||
| chr1:166142985
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.263+23001T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166142985 | ||||||
| chr1:166143166
|
A | T | 1 | a0001c0002t0022g0099 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.263+22820T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166143166 | ||||||
| chr1:166143219
|
T | C | 4 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(1): Show | 4 | HG02615.hp2 HG02976.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.263+22767A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166143219 | ||||||
| chr1:166143280
|
G | A | 2 | a0001c0001t0002g0293a0001c0002t0003g0205 | 2 | HG03669.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.263+22706C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166143280 | ||||||
| chr1:166143347
|
G | A | 1 | a0001c0001t0019g0238 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.263+22639C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166143347 | ||||||
| chr1:166143369
|
T | C | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.263+22617A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166143369 | ||||||
| chr1:166143506
|
C | T | 2 | a0001c0001t0001g0276a0001c0001t0002g0162 | 2 | HG03453.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.263+22480G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166143506 | ||||||
| chr1:166143509
|
G | A | 3 | a0001c0001t0002g0214a0001c0001t0002g0215a0001c0001t0002g0216 | 3 | HG01070.hp1 HG01071.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.263+22477C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166143509 | ||||||
| chr1:166143593
|
T | C | 1 | a0001c0001t0018g0052 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.263+22393A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166143593 | ||||||
| chr1:166143662
|
T | G | 287 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(284): Show | 289 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.263+22324A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166143662 | ||||||
| chr1:166143668
|
T | C | 286 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(283): Show | 288 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.263+22318A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166143668 | ||||||
| chr1:166143712
|
C | G | 1 | a0001c0001t0002g0267 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.263+22274G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166143712 | ||||||
| chr1:166143719
|
G | T | 1 | a0001c0001t0002g0267 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.263+22267C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166143719 | ||||||
| chr1:166143829
|
T | C | 32 | a0001c0001t0001g0203a0001c0001t0001g0210a0001c0001t0001g0211others(29): Show | 32 | HG00140.hp1 HG00438.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.263+22157A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166143829 | ||||||
| chr1:166144118
|
G | A | 267 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(264): Show | 269 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.263+21868C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166144118 | ||||||
| chr1:166144168
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.263+21818A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166144168 | ||||||
| chr1:166144314
|
GC | G | 16 | a0001c0001t0023g0298a0001c0002t0005g0299a0001c0002t0005g0300others(13): Show | 16 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.263+21671delG | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166144314 | ||||||
| chr1:166144618
|
G | C | 1 | a0001c0001t0001g0176 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.263+21368C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166144618 | ||||||
| chr1:166144621
|
C | T | 1 | a0001c0001t0001g0115 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.263+21365G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166144621 | ||||||
| chr1:166144724
|
C | G | 1 | a0001c0001t0001g0210 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.263+21262G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166144724 | ||||||
| chr1:166144791
|
AAAG | A | 3 | a0001c0001t0002g0214a0001c0001t0002g0215a0001c0001t0002g0216 | 3 | HG01070.hp1 HG01071.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.263+21192_263+2119 others(7): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166144791 | ||||||
| chr1:166144944
|
T | C | 1 | a0001c0002t0003g0034 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.263+21042A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166144944 | ||||||
| chr1:166145107
|
T | A | 5 | a0001c0001t0001g0049a0001c0001t0001g0096a0001c0001t0001g0107others(2): Show | 5 | HG00558.hp1 NA18949.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.263+20879A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166145107 | ||||||
| chr1:166145196
|
A | G | 17 | a0001c0001t0023g0298a0001c0002t0005g0299a0001c0002t0005g0300others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+20790T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166145196 | ||||||
| chr1:166145375
|
C | T | 255 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(252): Show | 257 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(254): Show |
intron_variant | MODIFIER | c.263+20611G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166145375 | ||||||
| chr1:166145402
|
G | A | 17 | a0001c0001t0023g0298a0001c0002t0005g0299a0001c0002t0005g0300others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+20584C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166145402 | ||||||
| chr1:166145603
|
A | C | 1 | a0001c0001t0001g0109 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.263+20383T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166145603 | ||||||
| chr1:166145723
|
C | T | 31 | a0001c0001t0001g0203a0001c0001t0001g0210a0001c0001t0001g0211others(28): Show | 31 | HG00140.hp1 HG00438.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.263+20263G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166145723 | ||||||
| chr1:166145777
|
T | G | 3 | a0001c0002t0001g0046a0001c0002t0001g0047a0001c0002t0001g0048 | 3 | HG02970.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.263+20209A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166145777 | ||||||
| chr1:166145785
|
T | C | 3 | a0001c0001t0001g0043a0001c0001t0002g0053a0001c0001t0018g0052 | 3 | HG01081.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.263+20201A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166145785 | ||||||
| chr1:166145980
|
T | C | 2 | a0001c0002t0001g0047a0001c0002t0001g0048 | 2 | HG02970.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.263+20006A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166145980 | ||||||
| chr1:166146152
|
T | C | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0011others(15): Show | 18 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.263+19834A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166146152 | ||||||
| chr1:166146224
|
T | A | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0011others(15): Show | 18 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.263+19762A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166146224 | ||||||
| chr1:166146259
|
A | G | 3 | a0001c0002t0001g0055a0001c0002t0001g0056a0001c0002t0001g0179 | 3 | HG02615.hp1 HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.263+19727T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166146259 | ||||||
| chr1:166146281
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.263+19705G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166146281 | ||||||
| chr1:166146324
|
T | C | 31 | a0001c0001t0001g0203a0001c0001t0001g0210a0001c0001t0001g0211others(28): Show | 31 | HG00140.hp1 HG00438.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.263+19662A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166146324 | ||||||
| chr1:166146531
|
C | G | 1 | a0001c0001t0002g0064 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.263+19455G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166146531 | ||||||
| chr1:166146623
|
A | G | 286 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(283): Show | 288 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.263+19363T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166146623 | ||||||
| chr1:166146749
|
T | A | 100 | a0001c0001t0001g0035a0001c0001t0001g0054a0001c0001t0001g0194others(97): Show | 100 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.263+19237A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166146749 | ||||||
| chr1:166146803
|
T | C | 3 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006 | 3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.263+19183A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166146803 | ||||||
| chr1:166147035
|
G | C | 1 | a0001c0001t0002g0246 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.263+18951C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166147035 | ||||||
| chr1:166147036
|
G | T | 17 | a0001c0001t0023g0298a0001c0002t0005g0299a0001c0002t0005g0300others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+18950C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166147036 | ||||||
| chr1:166147060
|
T | A | 17 | a0001c0001t0023g0298a0001c0002t0005g0299a0001c0002t0005g0300others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+18926A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166147060 | ||||||
| chr1:166147250
|
T | C | 1 | a0001c0002t0022g0099 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.263+18736A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166147250 | ||||||
| chr1:166147396
|
G | C | 2 | a0001c0001t0001g0143a0001c0001t0002g0101 | 2 | HG01175.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.263+18590C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166147396 | ||||||
| chr1:166147412
|
T | TG | 8 | a0001c0001t0001g0054a0001c0001t0001g0243a0001c0001t0001g0244others(5): Show | 8 | HG00597.hp2 HG01255.hp2 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.263+18573dupC | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166147412 | ||||||
| chr1:166147637
|
A | AT | 13 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006others(10): Show | 13 | HG00544.hp1 HG02523.hp1 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.263+18348dupA | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166147637 | ||||||
| chr1:166147637
|
A | ATT | 12 | a0001c0001t0001g0182a0001c0002t0005g0299a0001c0002t0005g0300others(9): Show | 12 | HG01192.hp1 HG01261.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.263+18347_263+1834 others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166147637 | ||||||
| chr1:166147693
|
G | A | 100 | a0001c0001t0001g0035a0001c0001t0001g0054a0001c0001t0001g0194others(97): Show | 100 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.263+18293C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166147693 | ||||||
| chr1:166147743
|
C | T | 264 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(261): Show | 266 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.263+18243G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166147743 | ||||||
| chr1:166147937
|
A | G | 1 | a0001c0001t0004g0007 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.263+18049T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166147937 | ||||||
| chr1:166147954
|
T | C | 3 | a0001c0001t0001g0043a0001c0001t0002g0053a0001c0001t0018g0052 | 3 | HG01081.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.263+18032A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166147954 | ||||||
| chr1:166148080
|
G | A | 290 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(287): Show | 292 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.263+17906C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166148080 | ||||||
| chr1:166148081
|
T | C | 1 | a0001c0001t0018g0052 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.263+17905A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166148081 | ||||||
| chr1:166148270
|
T | C | 2 | a0001c0002t0003g0284a0001c0002t0003g0285 | 2 | NA19006.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.263+17716A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166148270 | ||||||
| chr1:166148299
|
G | A | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG00323.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.263+17687C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166148299 | ||||||
| chr1:166148332
|
G | C | 1 | a0001c0002t0003g0239 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.263+17654C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166148332 | ||||||
| chr1:166148344
|
T | C | 286 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(283): Show | 288 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.263+17642A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166148344 | ||||||
| chr1:166148377
|
T | C | 2 | a0001c0001t0009g0296a0001c0001t0009g0297 | 2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.263+17609A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166148377 | ||||||
| chr1:166148546
|
C | T | 2 | a0001c0002t0001g0047a0001c0002t0001g0048 | 2 | HG02970.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.263+17440G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166148546 | ||||||
| chr1:166148631
|
C | T | 91 | a0001c0001t0001g0035a0001c0001t0001g0194a0001c0001t0001g0203others(88): Show | 91 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.263+17355G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166148631 | ||||||
| chr1:166148644
|
T | C | 7 | a0001c0001t0002g0240a0001c0001t0002g0241a0001c0001t0002g0242others(4): Show | 7 | HG00642.hp1 HG01257.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.263+17342A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166148644 | ||||||
| chr1:166148673
|
C | T | 9 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(6): Show | 9 | HG02451.hp1 HG02559.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.263+17313G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166148673 | ||||||
| chr1:166148786
|
C | T | 6 | a0001c0001t0001g0076a0001c0001t0001g0142a0001c0001t0001g0143others(3): Show | 6 | HG01168.hp1 HG01169.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.263+17200G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166148786 | ||||||
| chr1:166148824
|
C | G | 286 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(283): Show | 288 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.263+17162G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166148824 | ||||||
| chr1:166148875
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.263+17111T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166148875 | ||||||
| chr1:166149011
|
A | G | 1 | a0001c0001t0001g0114 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.263+16975T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166149011 | ||||||
| chr1:166149153
|
T | C | 3 | a0001c0002t0001g0055a0001c0002t0001g0056a0001c0002t0001g0179 | 3 | HG02615.hp1 HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.263+16833A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166149153 | ||||||
| chr1:166149245
|
TAAAC | T | 144 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0039others(141): Show | 144 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.263+16737_263+1674 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166149245 | ||||||
| chr1:166149245
|
TAAACAAA others(1): Show |
T | 7 | a0001c0001t0007g0026a0001c0001t0007g0027a0001c0001t0007g0028others(4): Show | 7 | HG00544.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.263+16733_263+1674 others(12): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166149245 | ||||||
| chr1:166149245
|
TAAACAAA others(5): Show |
T | 138 | a0001c0001t0001g0001a0001c0001t0001g0049a0001c0001t0001g0050others(135): Show | 140 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.263+16729_263+1674 others(16): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166149245 | ||||||
| chr1:166149262
|
AAACAAAC others(4): Show |
A | 1 | a0001c0002t0003g0133 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.263+16713_263+1672 others(15): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166149262 | ||||||
| chr1:166149316
|
T | C | 312 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(309): Show | 314 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.263+16670A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166149316 | ||||||
| chr1:166149410
|
A | G | 115 | a0001c0001t0001g0035a0001c0001t0001g0054a0001c0001t0001g0188others(112): Show | 115 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.263+16576T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166149410 | ||||||
| chr1:166149646
|
T | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0050a0001c0001t0001g0057others(75): Show | 79 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.263+16340A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166149646 | ||||||
| chr1:166149659
|
C | T | 99 | a0001c0001t0001g0035a0001c0001t0001g0194a0001c0001t0001g0203others(96): Show | 99 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.263+16327G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166149659 | ||||||
| chr1:166150010
|
T | C | 3 | a0001c0002t0001g0046a0001c0002t0001g0047a0001c0002t0001g0048 | 3 | HG02970.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.263+15976A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166150010 | ||||||
| chr1:166150014
|
G | C | 3 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006 | 3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.263+15972C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166150014 | ||||||
| chr1:166150045
|
C | G | 265 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(262): Show | 267 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.263+15941G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166150045 | ||||||
| chr1:166150107
|
G | A | 1 | a0001c0002t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.263+15879C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166150107 | ||||||
| chr1:166150107
|
G | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0050a0001c0001t0001g0057others(75): Show | 79 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.263+15879C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166150107 | ||||||
| chr1:166150137
|
T | G | 17 | a0001c0001t0023g0298a0001c0002t0005g0299a0001c0002t0005g0300others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+15849A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166150137 | ||||||
| chr1:166150177
|
G | A | 78 | a0001c0001t0001g0001a0001c0001t0001g0050a0001c0001t0001g0057others(75): Show | 79 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.263+15809C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166150177 | ||||||
| chr1:166150201
|
G | A | 1 | a0001c0001t0001g0220 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.263+15785C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166150201 | ||||||
| chr1:166150202
|
A | AC | 286 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(283): Show | 288 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.263+15783dupG | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166150202 | ||||||
| chr1:166150202
|
A | C | 1 | a0001c0001t0001g0220 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.263+15784T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166150202 | ||||||
| chr1:166150222
|
G | C | 3 | a0001c0002t0001g0046a0001c0002t0001g0047a0001c0002t0001g0048 | 3 | HG02970.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.263+15764C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166150222 | ||||||
| chr1:166150717
|
G | C | 1 | a0001c0001t0001g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.263+15269C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166150717 | ||||||
| chr1:166150794
|
T | C | 2 | a0001c0001t0009g0296a0001c0001t0009g0297 | 2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.263+15192A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166150794 | ||||||
| chr1:166150884
|
A | C | 1 | a0001c0001t0002g0170 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.263+15102T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166150884 | ||||||
| chr1:166151090
|
G | A | 3 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006 | 3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.263+14896C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166151090 | ||||||
| chr1:166151228
|
C | T | 2 | a0001c0001t0001g0098a0001c0001t0001g0138 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.263+14758G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166151228 | ||||||
| chr1:166151274
|
G | T | 3 | a0001c0002t0001g0055a0001c0002t0001g0056a0001c0002t0001g0179 | 3 | HG02615.hp1 HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.263+14712C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166151274 | ||||||
| chr1:166151284
|
T | C | 1 | a0001c0002t0005g0313 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.263+14702A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166151284 | ||||||
| chr1:166151390
|
T | C | 3 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006 | 3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.263+14596A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166151390 | ||||||
| chr1:166151414
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.263+14572C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166151414 | ||||||
| chr1:166151477
|
C | T | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | NA18998.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.263+14509G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166151477 | ||||||
| chr1:166151738
|
G | A | 1 | a0001c0001t0002g0038 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.263+14248C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166151738 | ||||||
| chr1:166151857
|
A | T | 290 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(287): Show | 292 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.263+14129T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166151857 | ||||||
| chr1:166151934
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.263+14052C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166151934 | ||||||
| chr1:166151959
|
C | T | 1 | a0001c0001t0002g0081 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.263+14027G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166151959 | ||||||
| chr1:166151981
|
C | G | 1 | a0001c0001t0006g0100 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.263+14005G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166151981 | ||||||
| chr1:166151993
|
G | C | 1 | a0001c0001t0002g0162 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.263+13993C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166151993 | ||||||
| chr1:166152081
|
G | C | 262 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(259): Show | 264 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.263+13905C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152081 | ||||||
| chr1:166152166
|
T | A | 15 | a0001c0001t0001g0049a0001c0001t0001g0096a0001c0001t0001g0104others(12): Show | 15 | HG00323.hp2 HG00558.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.263+13820A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152166 | ||||||
| chr1:166152340
|
G | A | 3 | a0001c0001t0001g0134a0001c0002t0003g0074a0001c0002t0003g0093 | 3 | HG02015.hp1 HG02165.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.263+13646C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152340 | ||||||
| chr1:166152358
|
G | T | 3 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006 | 3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.263+13628C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152358 | ||||||
| chr1:166152377
|
G | T | 2 | a0001c0001t0009g0296a0001c0001t0009g0297 | 2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.263+13609C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152377 | ||||||
| chr1:166152522
|
A | G | 1 | a0001c0001t0001g0251 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.263+13464T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152522 | ||||||
| chr1:166152529
|
C | T | 99 | a0001c0001t0001g0035a0001c0001t0001g0194a0001c0001t0001g0203others(96): Show | 99 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.263+13457G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152529 | ||||||
| chr1:166152577
|
G | C | 3 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006 | 3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.263+13409C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152577 | ||||||
| chr1:166152596
|
C | T | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.263+13390G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152596 | ||||||
| chr1:166152654
|
G | GGATT | 11 | a0001c0001t0001g0042a0001c0001t0001g0163a0001c0001t0004g0015others(8): Show | 11 | HG02109.hp1 HG02615.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.263+13328_263+1333 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152654 | ||||||
| chr1:166152654
|
G | GGATTGAT others(5): Show |
1 | a0001c0001t0002g0038 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.263+13331_263+1333 others(16): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152654 | ||||||
| chr1:166152655
|
G | GATTGATT others(5): Show |
3 | a0001c0001t0001g0037a0001c0001t0004g0019a0001c0002t0011g0010 | 3 | HG02258.hp2 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.263+13330_263+1333 others(16): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152655 | ||||||
| chr1:166152655
|
G | GATTGATT others(1): Show |
5 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0044others(2): Show | 5 | HG02257.hp2 HG02559.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.263+13330_263+1333 others(12): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152655 | ||||||
| chr1:166152655
|
G | GATTGATT others(5): Show |
2 | a0001c0001t0001g0039a0001c0001t0001g0040 | 2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.263+13330_263+1333 others(16): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152655 | ||||||
| chr1:166152655
|
G | GATTT | 38 | a0001c0001t0001g0050a0001c0001t0001g0082a0001c0001t0001g0098others(35): Show | 38 | HG00544.hp1 HG01069.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.263+13327_263+1333 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152655 | ||||||
| chr1:166152655
|
G | GATTTATT others(1): Show |
3 | a0001c0001t0001g0061a0001c0001t0004g0012a0001c0001t0004g0018 | 3 | HG02965.hp2 HG03098.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.263+13323_263+1333 others(12): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152655 | ||||||
| chr1:166152655
|
G | GATTTATT others(5): Show |
1 | a0001c0001t0004g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.263+13319_263+1333 others(16): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152655 | ||||||
| chr1:166152655
|
GATTT | G | 25 | a0001c0001t0001g0049a0001c0001t0001g0169a0001c0001t0001g0188others(22): Show | 25 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.263+13327_263+1333 others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152655 | ||||||
| chr1:166152655
|
GATTTATT others(5): Show |
G | 8 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0268others(5): Show | 8 | HG00597.hp1 HG00621.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.263+13319_263+1333 others(16): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152655 | ||||||
| chr1:166152655
|
GATTTATT others(17): Show |
G | 1 | a0001c0001t0008g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.263+13307_263+1333 others(28): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152655 | ||||||
| chr1:166152659
|
T | G | 12 | a0001c0001t0001g0054a0001c0001t0001g0075a0001c0001t0001g0134others(9): Show | 12 | HG00597.hp2 HG01081.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.263+13327A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152659 | ||||||
| chr1:166152663
|
T | G | 1 | a0001c0001t0001g0075 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.263+13323A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152663 | ||||||
| chr1:166152665
|
T | G | 1 | a0001c0001t0002g0275 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.263+13321A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152665 | ||||||
| chr1:166152695
|
T | G | 1 | a0001c0001t0001g0058 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.263+13291A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152695 | ||||||
| chr1:166152695
|
T | TATTGATT others(1): Show |
3 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111 | 3 | HG02109.hp2 HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.263+13290_263+1329 others(12): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152695 | ||||||
| chr1:166152731
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.263+13255C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152731 | ||||||
| chr1:166152732
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.263+13254G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166152732 | ||||||
| chr1:166153010
|
A | G | 10 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(7): Show | 10 | HG02451.hp1 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.263+12976T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166153010 | ||||||
| chr1:166153142
|
G | C | 2 | a0001c0001t0002g0053a0001c0001t0018g0052 | 2 | HG01081.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.263+12844C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166153142 | ||||||
| chr1:166153179
|
T | C | 6 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006others(3): Show | 6 | HG02970.hp1 HG03195.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.263+12807A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166153179 | ||||||
| chr1:166153385
|
C | A | 1 | a0001c0001t0001g0269 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.263+12601G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166153385 | ||||||
| chr1:166153386
|
C | T | 3 | a0001c0002t0001g0055a0001c0002t0001g0056a0001c0002t0001g0179 | 3 | HG02615.hp1 HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.263+12600G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166153386 | ||||||
| chr1:166153395
|
T | C | 10 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(7): Show | 10 | HG02451.hp1 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.263+12591A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166153395 | ||||||
| chr1:166153539
|
G | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0050a0001c0001t0001g0057others(75): Show | 79 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.263+12447C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166153539 | ||||||
| chr1:166153559
|
T | G | 17 | a0001c0001t0023g0298a0001c0002t0005g0299a0001c0002t0005g0300others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+12427A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166153559 | ||||||
| chr1:166153565
|
T | C | 17 | a0001c0001t0023g0298a0001c0002t0005g0299a0001c0002t0005g0300others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+12421A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166153565 | ||||||
| chr1:166153703
|
C | T | 17 | a0001c0001t0023g0298a0001c0002t0005g0299a0001c0002t0005g0300others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+12283G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166153703 | ||||||
| chr1:166153777
|
G | C | 25 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006others(22): Show | 25 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.263+12209C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166153777 | ||||||
| chr1:166153877
|
G | C | 17 | a0001c0001t0023g0298a0001c0002t0005g0299a0001c0002t0005g0300others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+12109C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166153877 | ||||||
| chr1:166153887
|
T | C | 3 | a0001c0001t0004g0008a0001c0001t0004g0024a0001c0001t0004g0025 | 3 | HG02451.hp2 HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.263+12099A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166153887 | ||||||
| chr1:166154295
|
G | A | 10 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(7): Show | 10 | HG02451.hp1 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.263+11691C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166154295 | ||||||
| chr1:166154351
|
C | T | 2 | a0001c0001t0009g0296a0001c0001t0009g0297 | 2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.263+11635G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166154351 | ||||||
| chr1:166154500
|
G | C | 1 | a0001c0001t0002g0270 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.263+11486C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166154500 | ||||||
| chr1:166154589
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.263+11397T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166154589 | ||||||
| chr1:166154605
|
C | T | 17 | a0001c0001t0023g0298a0001c0002t0005g0299a0001c0002t0005g0300others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+11381G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166154605 | ||||||
| chr1:166154871
|
C | T | 1 | a0001c0001t0006g0294 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.263+11115G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166154871 | ||||||
| chr1:166154873
|
C | T | 3 | a0001c0002t0001g0046a0001c0002t0001g0047a0001c0002t0001g0048 | 3 | HG02970.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.263+11113G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166154873 | ||||||
| chr1:166154897
|
A | G | 313 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(310): Show | 315 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.263+11089T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166154897 | ||||||
| chr1:166154908
|
T | C | 1 | a0001c0002t0003g0249 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.263+11078A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166154908 | ||||||
| chr1:166155030
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.263+10956G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166155030 | ||||||
| chr1:166155037
|
G | A | 6 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006others(3): Show | 6 | HG02970.hp1 HG03195.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.263+10949C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166155037 | ||||||
| chr1:166155119
|
A | G | 23 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006others(20): Show | 23 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.263+10867T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166155119 | ||||||
| chr1:166155190
|
A | C | 3 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006 | 3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.263+10796T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166155190 | ||||||
| chr1:166155217
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.263+10769G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166155217 | ||||||
| chr1:166155323
|
C | A | 1 | a0001c0001t0001g0135 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.263+10663G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166155323 | ||||||
| chr1:166155362
|
G | A | 291 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(288): Show | 293 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.263+10624C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166155362 | ||||||
| chr1:166155448
|
C | A | 1 | a0001c0001t0001g0043 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.263+10538G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166155448 | ||||||
| chr1:166155499
|
C | T | 23 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006others(20): Show | 23 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.263+10487G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166155499 | ||||||
| chr1:166155549
|
T | G | 1 | a0001c0001t0001g0136 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.263+10437A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166155549 | ||||||
| chr1:166155687
|
C | A | 1 | a0001c0001t0001g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.263+10299G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166155687 | ||||||
| chr1:166155765
|
A | G | 10 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(7): Show | 10 | HG02451.hp1 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.263+10221T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166155765 | ||||||
| chr1:166155926
|
T | C | 3 | a0001c0002t0001g0055a0001c0002t0001g0056a0001c0002t0001g0179 | 3 | HG02615.hp1 HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.263+10060A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166155926 | ||||||
| chr1:166156002
|
G | A | 291 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(288): Show | 293 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.263+9984C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166156002 | ||||||
| chr1:166156014
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.263+9972T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166156014 | ||||||
| chr1:166156155
|
C | A | 3 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006 | 3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.263+9831G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166156155 | ||||||
| chr1:166156186
|
T | C | 114 | a0001c0001t0001g0035a0001c0001t0001g0188a0001c0001t0001g0189others(111): Show | 114 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.263+9800A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166156186 | ||||||
| chr1:166156222
|
C | T | 1 | a0001c0001t0012g0003 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.263+9764G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166156222 | ||||||
| chr1:166156273
|
G | A | 2 | a0001c0001t0001g0286a0001c0002t0003g0291 | 2 | HG00673.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.263+9713C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166156273 | ||||||
| chr1:166156356
|
T | G | 23 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006others(20): Show | 23 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.263+9630A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166156356 | ||||||
| chr1:166156365
|
G | C | 3 | a0001c0002t0001g0046a0001c0002t0001g0047a0001c0002t0001g0048 | 3 | HG02970.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.263+9621C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166156365 | ||||||
| chr1:166156370
|
G | A | 2 | a0001c0001t0001g0174a0001c0001t0002g0172 | 2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.263+9616C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166156370 | ||||||
| chr1:166156446
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.263+9540A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166156446 | ||||||
| chr1:166156560
|
T | A | 1 | a0001c0001t0001g0188 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.263+9426A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166156560 | ||||||
| chr1:166156561
|
A | T | 1 | a0001c0001t0001g0188 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.263+9425T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166156561 | ||||||
| chr1:166156608
|
G | A | 17 | a0001c0001t0023g0298a0001c0002t0005g0299a0001c0002t0005g0300others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+9378C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166156608 | ||||||
| chr1:166156745
|
T | C | 3 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006 | 3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.263+9241A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166156745 | ||||||
| chr1:166156749
|
A | C | 2 | a0001c0002t0003g0095a0001c0002t0003g0137 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.263+9237T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166156749 | ||||||
| chr1:166156793
|
T | C | 3 | a0001c0001t0001g0159a0001c0001t0001g0176a0001c0002t0001g0213 | 3 | HG02818.hp1 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.263+9193A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166156793 | ||||||
| chr1:166156882
|
A | G | 291 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(288): Show | 293 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.263+9104T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166156882 | ||||||
| chr1:166156982
|
AGAG | A | 3 | a0001c0002t0001g0046a0001c0002t0001g0047a0001c0002t0001g0048 | 3 | HG02970.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.263+9001_263+9003d others(5): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166156982 | ||||||
| chr1:166157027
|
GGGC | G | 45 | a0001c0001t0001g0057a0001c0001t0001g0076a0001c0001t0001g0077others(42): Show | 45 | HG00621.hp1 HG00639.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.263+8956_263+8958d others(5): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157027 | ||||||
| chr1:166157030
|
C | T | 2 | a0001c0001t0008g0005a0001c0001t0008g0006 | 2 | HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.263+8956G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157030 | ||||||
| chr1:166157030
|
CGGCGGA | C | 26 | a0001c0001t0001g0044a0001c0001t0001g0163a0001c0001t0001g0165others(23): Show | 26 | HG00423.hp1 HG01891.hp1 HG02723.hp2 others(23): Show |
intron_variant | MODIFIER | c.263+8950_263+8955d others(8): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157030 | ||||||
| chr1:166157031
|
GGC | G | 26 | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0050others(23): Show | 27 | HG00544.hp1 HG00544.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.263+8953_263+8954d others(4): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157031 | ||||||
| chr1:166157031
|
GGCGGA | G | 77 | a0001c0001t0001g0035a0001c0001t0001g0039a0001c0001t0001g0040others(74): Show | 78 | HG00323.hp2 HG00438.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.263+8950_263+8954d others(7): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157031 | ||||||
| chr1:166157032
|
GC | G | 8 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0002t0005g0300others(5): Show | 8 | HG01192.hp1 HG01261.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.263+8953delG | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157032 | ||||||
| chr1:166157032
|
GCGGA | G | 94 | a0001c0001t0001g0054a0001c0001t0001g0058a0001c0001t0001g0096others(91): Show | 94 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.263+8950_263+8953d others(6): Show |
FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157032 | ||||||
| chr1:166157033
|
C | G | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0002t0005g0299 | 3 | HG01361.hp2 NA18998.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.263+8953G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157033 | ||||||
| chr1:166157035
|
G | C | 1 | a0001c0002t0005g0299 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.263+8951C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157035 | ||||||
| chr1:166157035
|
GA | G | 10 | a0001c0001t0004g0007a0001c0001t0004g0011a0001c0001t0004g0012others(7): Show | 10 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.263+8950delT | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157035 | ||||||
| chr1:166157036
|
A | C | 6 | a0001c0002t0005g0300a0001c0002t0005g0301a0001c0002t0005g0302others(3): Show | 6 | HG01192.hp1 HG01261.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.263+8950T>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157036 | ||||||
| chr1:166157036
|
A | G | 78 | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0050others(75): Show | 79 | HG00544.hp1 HG00544.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.263+8950T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157036 | ||||||
| chr1:166157036
|
A | T | 1 | a0001c0001t0008g0004 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.263+8950T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157036 | ||||||
| chr1:166157037
|
G | C | 4 | a0001c0002t0005g0306a0001c0002t0005g0307a0001c0002t0005g0308others(1): Show | 4 | HG00544.hp1 HG01943.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.263+8949C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157037 | ||||||
| chr1:166157038
|
G | C | 6 | a0001c0001t0023g0298a0001c0002t0005g0310a0001c0002t0005g0311others(3): Show | 6 | NA18942.hp2 NA18963.hp1 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.263+8948C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157038 | ||||||
| chr1:166157042
|
G | C | 1 | a0001c0001t0001g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.263+8944C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157042 | ||||||
| chr1:166157099
|
T | G | 1 | a0001c0001t0001g0276 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.263+8887A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157099 | ||||||
| chr1:166157186
|
C | G | 3 | a0001c0002t0001g0046a0001c0002t0001g0047a0001c0002t0001g0048 | 3 | HG02970.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.263+8800G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157186 | ||||||
| chr1:166157295
|
C | G | 3 | a0001c0001t0002g0214a0001c0001t0002g0215a0001c0001t0002g0216 | 3 | HG01070.hp1 HG01071.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.263+8691G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157295 | ||||||
| chr1:166157335
|
G | C | 23 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006others(20): Show | 23 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.263+8651C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157335 | ||||||
| chr1:166157545
|
G | T | 1 | a0001c0001t0004g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.263+8441C>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157545 | ||||||
| chr1:166157710
|
C | T | 3 | a0001c0001t0004g0008a0001c0001t0004g0024a0001c0001t0004g0025 | 3 | HG02451.hp2 HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.263+8276G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157710 | ||||||
| chr1:166157730
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.263+8256A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157730 | ||||||
| chr1:166157760
|
T | C | 1 | a0001c0001t0001g0277 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.263+8226A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157760 | ||||||
| chr1:166157891
|
G | A | 2 | a0001c0001t0009g0296a0001c0001t0009g0297 | 2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.263+8095C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166157891 | ||||||
| chr1:166158132
|
C | G | 3 | a0001c0002t0001g0046a0001c0002t0001g0047a0001c0002t0001g0048 | 3 | HG02970.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.263+7854G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166158132 | ||||||
| chr1:166158217
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.263+7769G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166158217 | ||||||
| chr1:166158262
|
C | T | 3 | a0001c0002t0001g0055a0001c0002t0001g0056a0001c0002t0001g0179 | 3 | HG02615.hp1 HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.263+7724G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166158262 | ||||||
| chr1:166158550
|
G | A | 4 | a0001c0001t0001g0174a0001c0001t0002g0171a0001c0001t0002g0172others(1): Show | 4 | HG02258.hp1 HG02280.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.263+7436C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166158550 | ||||||
| chr1:166158607
|
C | T | 2 | a0001c0001t0009g0296a0001c0001t0009g0297 | 2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.263+7379G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166158607 | ||||||
| chr1:166158691
|
C | T | 1 | a0001c0001t0023g0298 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.263+7295G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166158691 | ||||||
| chr1:166158792
|
C | T | 272 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(269): Show | 274 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.263+7194G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166158792 | ||||||
| chr1:166158823
|
C | G | 272 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(269): Show | 274 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.263+7163G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166158823 | ||||||
| chr1:166159118
|
C | G | 289 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(286): Show | 291 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.263+6868G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166159118 | ||||||
| chr1:166159141
|
T | G | 1 | a0001c0001t0001g0212 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.263+6845A>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166159141 | ||||||
| chr1:166159152
|
T | C | 266 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(263): Show | 268 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.263+6834A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166159152 | ||||||
| chr1:166159169
|
A | G | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0011others(15): Show | 18 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.263+6817T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166159169 | ||||||
| chr1:166159339
|
C | T | 1 | a0001c0001t0009g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.263+6647G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166159339 | ||||||
| chr1:166159385
|
C | T | 31 | a0001c0001t0001g0203a0001c0001t0001g0210a0001c0001t0001g0211others(28): Show | 31 | HG00140.hp1 HG00438.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.263+6601G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166159385 | ||||||
| chr1:166159410
|
C | T | 2 | a0001c0001t0009g0296a0001c0001t0009g0297 | 2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.263+6576G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166159410 | ||||||
| chr1:166159723
|
A | T | 137 | a0001c0001t0001g0035a0001c0001t0001g0054a0001c0001t0001g0188others(134): Show | 137 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.263+6263T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166159723 | ||||||
| chr1:166159752
|
C | G | 4 | a0001c0001t0007g0026a0001c0001t0007g0027a0001c0001t0007g0028others(1): Show | 4 | HG01891.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.263+6234G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166159752 | ||||||
| chr1:166159847
|
T | C | 1 | a0001c0002t0003g0175 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.263+6139A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166159847 | ||||||
| chr1:166159915
|
G | A | 17 | a0001c0001t0023g0298a0001c0002t0005g0299a0001c0002t0005g0300others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+6071C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166159915 | ||||||
| chr1:166159959
|
C | G | 1 | a0001c0001t0001g0057 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.263+6027G>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166159959 | ||||||
| chr1:166160169
|
C | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0049a0001c0001t0001g0050others(136): Show | 141 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.263+5817G>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166160169 | ||||||
| chr1:166160263
|
T | C | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0011others(15): Show | 18 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.263+5723A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166160263 | ||||||
| chr1:166160429
|
G | A | 1 | a0001c0001t0012g0003 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.263+5557C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166160429 | ||||||
| chr1:166160719
|
G | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0049a0001c0001t0001g0050others(136): Show | 141 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.263+5267C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166160719 | ||||||
| chr1:166160756
|
T | C | 8 | a0001c0001t0007g0026a0001c0001t0007g0027a0001c0001t0007g0028others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.263+5230A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166160756 | ||||||
| chr1:166160900
|
G | A | 3 | a0001c0002t0001g0046a0001c0002t0001g0047a0001c0002t0001g0048 | 3 | HG02970.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.263+5086C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166160900 | ||||||
| chr1:166160981
|
G | A | 140 | a0001c0001t0001g0001a0001c0001t0001g0049a0001c0001t0001g0050others(137): Show | 142 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.263+5005C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166160981 | ||||||
| chr1:166161156
|
T | A | 1 | a0001c0001t0001g0176 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.263+4830A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166161156 | ||||||
| chr1:166161157
|
CT | C | 18 | a0001c0001t0001g0278a0001c0001t0023g0298a0001c0002t0005g0299others(15): Show | 18 | HG00544.hp1 HG01169.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.263+4828delA | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166161157 | ||||||
| chr1:166161233
|
A | G | 36 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(33): Show | 36 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(33): Show |
intron_variant | MODIFIER | c.263+4753T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166161233 | ||||||
| chr1:166161891
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.263+4095C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166161891 | ||||||
| chr1:166161904
|
C | T | 17 | a0001c0001t0023g0298a0001c0002t0005g0299a0001c0002t0005g0300others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+4082G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166161904 | ||||||
| chr1:166162010
|
C | T | 1 | a0001c0001t0004g0007 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.263+3976G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166162010 | ||||||
| chr1:166162174
|
C | T | 100 | a0001c0001t0001g0035a0001c0001t0001g0194a0001c0001t0001g0203others(97): Show | 100 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.263+3812G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166162174 | ||||||
| chr1:166162208
|
G | A | 313 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(310): Show | 315 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.263+3778C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166162208 | ||||||
| chr1:166162248
|
G | C | 2 | a0001c0001t0004g0024a0001c0001t0004g0025 | 2 | HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.263+3738C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166162248 | ||||||
| chr1:166162436
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.263+3550C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166162436 | ||||||
| chr1:166162442
|
G | A | 1 | a0001c0002t0003g0034 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.263+3544C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166162442 | ||||||
| chr1:166162855
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.263+3131G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166162855 | ||||||
| chr1:166162956
|
G | C | 1 | a0001c0002t0001g0179 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.263+3030C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166162956 | ||||||
| chr1:166162979
|
C | T | 1 | a0001c0001t0003g0195 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.263+3007G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166162979 | ||||||
| chr1:166163082
|
T | A | 17 | a0001c0001t0023g0298a0001c0002t0005g0299a0001c0002t0005g0300others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+2904A>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166163082 | ||||||
| chr1:166163126
|
G | A | 1 | a0001c0002t0003g0279 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.263+2860C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166163126 | ||||||
| chr1:166163131
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.263+2855A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166163131 | ||||||
| chr1:166163170
|
C | T | 1 | a0001c0001t0001g0049 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.263+2816G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166163170 | ||||||
| chr1:166163289
|
G | A | 1 | a0001c0001t0006g0180 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.263+2697C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166163289 | ||||||
| chr1:166163340
|
T | C | 1 | a0001c0001t0001g0280 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.263+2646A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166163340 | ||||||
| chr1:166163397
|
A | G | 3 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006 | 3 | HG03579.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.263+2589T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166163397 | ||||||
| chr1:166163583
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.263+2403G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166163583 | ||||||
| chr1:166163591
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.263+2395A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166163591 | ||||||
| chr1:166163617
|
A | T | 3 | a0001c0002t0001g0046a0001c0002t0001g0047a0001c0002t0001g0048 | 3 | HG02970.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.263+2369T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166163617 | ||||||
| chr1:166163805
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.263+2181C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166163805 | ||||||
| chr1:166163869
|
A | T | 17 | a0001c0001t0023g0298a0001c0002t0005g0299a0001c0002t0005g0300others(14): Show | 17 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+2117T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166163869 | ||||||
| chr1:166164107
|
T | C | 5 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0186others(2): Show | 5 | HG00544.hp2 HG00621.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.263+1879A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166164107 | ||||||
| chr1:166164247
|
C | T | 36 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(33): Show | 36 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(33): Show |
intron_variant | MODIFIER | c.263+1739G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166164247 | ||||||
| chr1:166164573
|
A | T | 36 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(33): Show | 36 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(33): Show |
intron_variant | MODIFIER | c.263+1413T>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166164573 | ||||||
| chr1:166164576
|
G | C | 36 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(33): Show | 36 | HG00544.hp1 HG01192.hp1 HG01261.hp1 others(33): Show |
intron_variant | MODIFIER | c.263+1410C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166164576 | ||||||
| chr1:166164613
|
C | T | 110 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0039others(107): Show | 110 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.263+1373G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166164613 | ||||||
| chr1:166164737
|
G | C | 1 | a0001c0001t0002g0281 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.263+1249C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166164737 | ||||||
| chr1:166164792
|
T | C | 10 | a0001c0001t0001g0282a0001c0001t0001g0286a0001c0001t0001g0287others(7): Show | 10 | HG00438.hp2 HG00673.hp1 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.263+1194A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166164792 | ||||||
| chr1:166164917
|
G | A | 2 | a0001c0001t0009g0296a0001c0001t0009g0297 | 2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.263+1069C>T | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166164917 | ||||||
| chr1:166164941
|
T | C | 19 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(16): Show | 19 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.263+1045A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166164941 | ||||||
| chr1:166165156
|
T | C | 100 | a0001c0001t0001g0035a0001c0001t0001g0194a0001c0001t0001g0203others(97): Show | 100 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.263+830A>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166165156 | ||||||
| chr1:166165220
|
G | C | 4 | a0001c0001t0002g0292a0001c0001t0002g0293a0001c0001t0002g0295others(1): Show | 4 | HG01358.hp1 HG01515.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.263+766C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166165220 | ||||||
| chr1:166165327
|
C | T | 1 | a0001c0001t0001g0035 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.263+659G>A | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166165327 | ||||||
| chr1:166165405
|
G | C | 5 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0006others(2): Show | 5 | HG02922.hp1 HG03130.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.263+581C>G | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166165405 | ||||||
| chr1:166165855
|
A | G | 1 | a0001c0002t0003g0034 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.263+131T>C | FAM78B | ENSG00000188859.7 | transcript | ENST00000354422.4 | protein_coding | 1/1 | chr1 | 166165855 |